Pesticidal proteine and nucleotide sequence encoding the same

The present invention relates to a pesticide protein and nucleotide sequence that encodes it, used to control pests, insects or plants.

Harmful insects are a major factor that causes the loss of significant quantities of agricultural crops worldwide. Broad-spectrum chemical pesticides have been used extensively to combat or eradicate agricultural pests. There is, however, a substantial interest in developing new, effective alternative pesticides.

Microbial pesticides have played an important role as an alternative to chemical pest control. The most commonly used microbial product is based on Bacillus thuringiensis bacteria. Bacillus thuringiensis is a gram-positive spore that produces a crystalline insecticidal protein (known as ICP)

Numerous types of Bacillus thuringiensis are known to produce more than 25 related but different types of crystalline insecticidal protein. The crystalline insecticidal proteins formed by Bacillus thuringiensis are toxic to the larvae of certain insects of the Lepidoptera, Diptera and Coleoptera classes. In general, when the crystalline insecticidal protein is ingested by an insect, the crystal is dissolved and transformed into a toxic substance by 50% in the digestive system of the insect. However, none of the crystalline insecticidal proteins known to be active against beetle larvae have shown significant effects on the Diabrotica species, in particular, Diabrotica virgifera virgifer, western corn rootworm (WCRW) or Diabrotica longicornus barberi, vier of the root of corn.

Bacillus thuringiensis is a close relative of Bacillus cereus (Bc). A major feature that differentiates them is the lack of a parasporic crystal in Bacillus cereus.

Bacillus cereus is a widespread bacterium that is commonly found in soil and has been isolated from a variety of foods and medicines. The body has been involved in food degradation.

Although Bacillus thuringiensis has been very useful in combating harmful insects, there is a need to expand the number of potential biological agents for pest control in agriculture.

Because it has been recognized that proteins with pesticide effects can be isolated from the vegetative growth phase of Bacillus, other strains can be isolated by standardized techniques and their action tested against certain plants and harmful insects. In general, Bacillus strains can be isolated from any sample of the environment, including soil, plants, insects, silo dust and others, by methods known in the art. See, for example, Travers et al. (1987) Appl. Environ. Microbiol. 53: 1263-1266; Saleh et al. (1969) Can J. Microbiol. 15: 1101-1104; DeLucca et al. (1981) Can J. Microbiol. 27: 865-870; and Norris et al. (1981) "The geera Bacillus and Sporolactobacillus, in Starr et al. (eds.), The Prokariotes: A Handbook on Habitats, Isolation, and Identification of Bacteria, Vol. II, Springer-Verlag Berlin Heidelberg. After isolation, the strains can be tested for pesticide action during their vegetative growth. In this way, new Bacillus proteins and strains with pesticide effects can be identified.

Processes for isolating proteins are known in the art. In general, proteins can be purified by conventional chromatography, which includes gel filtration, ion exchange, and immuno-affinity chromatography, by phase chromatography.

RO 117111 High performance liquid bl, such as high performance liquid phase chromatography with inverted phase, high performance liquid chromatography with ion exchange, high performance chromatographic filtration through stationary phase of known size, chromatography focusing by hydrophobic interaction, etc., separation by electrophoresis, such as, one-dimensional gel electrophoresis, two-dimensional gel electrophoresis, etc. Such separation processes are known in the art. See for example Current Protocols in Molecular Biology, vol. 1 and 2, Ausbel et al. (eds), John Wiley & Sons, NY (1988). In addition, antibodies against proteins can be obtained on highly pure preparations thereof. See, for example, Radka et al. (1983) J. Immunol. 128: 2804; and Radka et al. (1984) Immunogenetics 19:63.

Any combination of processes can be used to purify proteins with pesticide properties. As indicated in the process, the pesticide action is determined after each purification step. 60

Such purification steps will result in a highly purified amount of protein. "Highly purified" or "substantially pure" means a protein that does not contain absolutely any compound normally associated with that protein in its natural state. The quality of the "substantially pure protein preparations" can be appreciated by the absence of other spots of the detectable protein sequences 65 following SDS-PAGE, determined visually or by densimetric scanning. On the other hand, the lack of other amino-terminal sequences or N-terminal residues in a purified preparation may indicate the degree of purity . The purity can be verified by chromatography of the "pure" preparations showing the absence of other peaks through ion exchange, inverted phase or capillary electrophoresis. The terms "substantially pure or" highly purified 70 do not exclude artificial or synthetic mixtures of proteins with other compounds. Also, the terms do not exclude the presence of minor impurities that do not interfere with the biological action of the protein and which may be present, for example, due to incomplete purification.

Some proteins are single-polypeptide sequences, while many proteins 75 contain more than one polypeptide sequence. Once the purified protein is isolated, the protein or polypeptides it is made of can be characterized and ordered by standard methods known in the art. For example, the purified protein, or the polypeptides it is made of, can be fragmented with cyanogen bromide or proteases, such as , papain, chymotrypsin, trypsin, C-lysyl endopeptidase, etc. 80 (Oike et al. (1982) J. Biol. Chem. 257: 9751-9758; Liu et al. (1983) Int. J. Pept. Protein Res. 21: 209-215). The resulting peptides are separated, preferably by HPLC, or by gel dissolution and electroabsorption on PVDF membranes, and subjected to sequential ordering of amino acids. To fulfill this task, the peptides are preferably analyzed by automatic sequence sorters. It is known that N-terminal, C-terminal or internal amino acid sequences can be determined.

It is known that proteins can vary in molecular weight, vary in the number of component peptides, in their action against pests and in other characteristics. However, by the procedures that will be shown below, active proteins 90 against a variety of pests can be isolated and characterized.

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Once the purified protein has been isolated and characterized, it is known that it can be modified in various ways, including substitutions, deletions and amino acid insertions. The processes for such manipulations are known in the art. For example, variants of pesticide protein amino acid sequences can be prepared by DNA mutations. Such variants obtained will have the desired pesticide effect. Obviously, the mutations that will be made in the DNA, encoding the variant, do not have to place the sequence outside the reading frame and, preferably, will not create complementary regions that could produce secondary mRNA structures (EP Patent Application Publication no. 75444). .

It is known that polypeptide components or protein fragments that stop the pesticide effect can be produced. These fragments include shortened sequences as well as N-terminal, C-terminal sequences, internal amino acid sequences of proteins and amino acids or deleted amino acid sequences within the proteins.

Most deleted sequences, insertions, and substitutions in protein sequences do not usually produce radical changes in pesticide protein characteristics. However, when it is difficult to predict the exact effect of substitution, deletion or insertion, before performing the operation, a person skilled in the art will appreciate that the effect is evaluated by routine sorting tests.

Good alternative methods are known for obtaining nucleotide and amino acid sequences of the present proteins. For example, to obtain the nucleotide sequence that encodes the pesticide protein, clones of the cosmid, which express an active pesticide protein, can be isolated from the genetic information of the genome. From large clones of active cosmids, smaller subclones can be created and tested for effect. In this way, clones expressing an active pesticide protein can be arranged so as to determine the nucleotide sequence of the gene. Then, an amino acid sequence can be deduced to form the protein. For general molecular donation procedures, see, for example, Molecular Cloning, A Laboratory Manual, Second Edition, vol. 1-3, Sambrook et al. (eds) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY (1989), and references cited here.

Pesticide genes can be optimized to have a greater effect on plants. See, for example, US Application Serial no. 07/951715; EPA 0359472; EPA 0385962; WO 91/16432; Perlak et al (1991) Proc. Natl. Acad. Sci. USA 88: 3324-3328; and Murray et al (1989) Nucleic Acids Research 17: 477-498. In this way, genes can be synthesized using plant-approved codons.

Thus the preferred codon for a particular host is the only codon most often encoding the amino acid in that host. The preferred corn codon, for example, for a particular amino acid may be derived from a known gene sequence of corn. The use of maize codon for 28 maize genes is found in the work of Murray et al. (1989), Nucleic Acids Research 17: 477-498. Synthetic genes can also be created based on the distribution of codons that a particular host uses for a particular amino acid.

In this way, nucleotide sequences can be optimized, in effect, in any plant. It is known that any part or the entire sequence of a gene can be optimized or synthesized. This means that synthetic or partially optimized sequences can also be used.

Similarly, nucleotide sequences can be optimized in any microorganism. For the use of the preferred codon of Bacillus, see for example,

US Patent no. 5024837 and Johansen et al (1988) Gene 65: 293-304.

Methodologies for constructing expression plants in plants as well as introducing foreign DNA into plants are described in the prior art. Such expression cassettes may include promoters, terminators, enhancers, driving sequences and other regulatory sequences that operate in connection with the pesticide protein coding sequence.

In general, for the introduction of foreign DNA into plants, 145 Ti plasmid vectors have been used, as well as the direct use of DNA, liposomes, electroporation, micro-injection and the use of microprojects. Such methods have been published in the specialized journals. See, for example, Guerche et al (1987) Plant Science 52: 111-116; Neuhause et al (1987) Theor. Appl. Genet. 75: 30-36; Klein et al (1987) Nature 327: 70-73; Howell et al (1980) Science 208: 1265; Horsch et al 150 (1985) Science 227: 1229-1231; DeBlock et al (1989) Plant physiology 91: 694-701; Methods for Plant Molecular Biology (Weissbach and Weissbach, eds.) Academic Press, Inc. (1988); and Methods in Plant Molecular Biology (Schuler and Zielinsky, eds) Academic Press, Inc. (1989). See also US Patent Application Serial no. 08/008374. See also EPA 0193259 and EPA 0451878A1. 155

It is understood that the method of transformation will depend on the cell of the plant to be transformed.

It is known that the components of the expression box can be modified to increase the effect of the expression. For example, shortened sequences, nucleotide substitutions or other modifications may be used. See, for example, Perlak et al (1991) 160

Proc. Natl. Acad. Sci. USA 88: 3324-3328; Murray et al (1989) Nucleic Acids Research 17: 477-498; and WO 91/16432.

The assembly may also comprise any other required regulators such as, terminators, (Guerineau etal (1991), Mol. Gen. Genet., 226: 141-144; Proudfoot, (1991), Ce //, 64: 671-674; Sanfacon etal (1991), GenesDev5: 141 -149; Mogen et 165 al (1990), PlantCell, 2: 1261-1272; Munroe etal (1990) Gene, 91: 151-158; Ballas et al (1989), Nucleic Acids Res., 17: 7891-7903; Joshi et al (1987) Nucleic Acid Res., 15: 9627-9639; translational plant sequences (Joshi, CP, (1987), Nucleic Acids Research, 15: 6643-6653), introns (Luehrsen ad Walbot, (1991), Mol.

Gender. Genet., 225: 81-93) and the like, which operate in connection with the 170 nucleotide sequence. It may be advantageous to include 12.5 cm conducting sequences (primer sequences) in the expression box assembly. Such conductive sequences may act to increase translation.

Translational leaders are known in the art and include:

- Picornavirus conductors, for example, EMCV [Encephalomyocarditis 175 5-inch non-coding region) conductor (Elroy-Stein, 0., Fuerst, TR, and Moss, B. (1989) PNAS USA 86: 6126-6130);

- Potyvirus conductors, for example, VTE [Tobacco Etch Virus - recorded tobacco virus) (Alliso et al (1986); MDMV (dwarf tobacco mosaic virus); Virology, 154: 9-20, and 180

- human immunoglobulin heavy chain (BiP) binding protein, (Macejak, DG, and Sarnow.P., (1991), Nature, 353: 90-94;

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- the untranslated conductor of the mRNA protein of the alpha-alpha mosaic virus (AMV RNA 4), (Jobling, SA., and Gehrke, L., (1987), Nature, 325: 622-625;

- conducting tobacco mosaic virus (TMV), (Gallie, DR, et al (1989), Molecular Biology of RNA, pages 237-256; and

- conducting chlorinated corn virus virus (MCMV) (Lommel, SA, et al, (1991), Virology, 81: 382-385. See also Della-Ciopa et al (1987), Plant Physiology, 84 : 965-968.

A plant terminator can be used in the expression box. See Rosenberg et al (1987), Gene 56: 125; Guerineau et al (1991) Mol. Gender. Genet. 226: 141-144; Proudfoot, (1991), Cell 64: 671-674; Sanfacon et al (1991), Genes Oev5: 141-149; Mogen etal (1990), PlantCell, 2: 1261-1272; Munroe etal (1990), Gene 91: 151-158; Ballas et al (1989), Nucleic Acids Res., 17: 7891-7903; Joshi et al (1987), Nucleic Acid Rea., 15: 9627-9639.

For tissue-specific expression, nucleotide sequences can be linked to specific tissue promoters. See, for example, US Application Serial no. 07/951715.

It is known that genes encoding pesticide proteins can be used to transform insect-sensitive organisms. Such organisms include Baculoviruses, fungi, protozoa, bacteria and nematodes.

Several ways of introducing the pesticide-expressing gene into the host microorganism are possible, under conditions that allow stable gene expression and maintenance. For example, expression cassettes including DNA assemblies of interest, operatively linked to transcriptional and translational regulatory signals for expressing DNA configurations and a homologous DNA chain with a chain of the host organism, through which integration will take place, can be constructed, and / or an identical system that is functional in the host, through which stable integration or maintenance will take place.

Transcriptional and translational regulatory signals include, but are not limited to promoters, transcriptional initiation starting positions, operators, activators, amplifiers, other regulatory elements, ribosomal binding positions, initiation codons, termination signals, and the like. See, for example, US Patent 5039523; US Patent 4853331; EPO 0480762 A2; Sambrook et al. over; Molecular Cloning, The Laboratory Manual, Maniatis et al (eds) Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1982); Advanced Bacterial Genetica, Davis et al (eds) Cold Spring Harbor, NY (198O); and the references cited in this paper.

Suitable host cells, cells containing pesticides treated to prolong the action of the toxin in the cell, when the treated cell is applied in the target pest environment, may include either prokaryotes or eukaryotes, normally being limited to those cells that do not produce toxic substances for higher organisms, such as mammals. However, organisms that produce toxic substances for higher organisms could be used where the toxin is unstable or the level of application low enough so as to avoid any possibility of intoxication of a mammal. As hosts, of particular interest will be prokaryotes and lower eukaryotes, such as fungi.

Examples of both gram-negative and gram-positive prokaryotes include Enterobacteriaceae, such as, Escherichia, Erwinia, Shigella, Salmonella, and Proteus: Bacillaceae: Rhizobiceae, such as, Rhizobium: Spirillaceae, such as, photobacterium, Zymomonas, Serratia, Aeromonas, Vibrio, Desulfovibrio, Spirillum;

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Lactobacillaceae; Pseudomonadaceae, such as, Pseudomonas and Acetobacter; Azotobacteraceae and Nitrobacteraceae. Among eukaryotes are fungi such as Phycomycetes and Ascomycetes, which include yeasts such as Saccharomyces and Schizosaccharomyces; and yeast Basidiomycetes, such as, Rhodotorula, Aureobasidium, Sporobolomyces and the like.

Features of particular interest in the selection of the host cell for production purposes include: ease of insertion of the protein gene into the host, availability of expression systems, efficiency of expression, stability of the protein in the host, and presence of auxiliary genetic capabilities. Features of interest for use as a pesticide capsule include: the protective qualities of the pesticide cell, such as, the thick walls of the cell, pigmentation and the formation or packaging of inclusion bodies; affinity to leaves; lack of toxicity to mammals; specific attractiveness to be ingested by pests; ease of destruction and fixation without damaging the toxin. Other features include the ease of obtaining preparations containing the pesticide and their handling, the economics and stability of the storage of the preparations, etc.

Host organisms of particular interest include yeast, such as, Rhodotorula sp., Aureobasidium sp., Saccharomyces sp. and Sporobolomyces sp .; filoplane organisms such as, Pseudomonas sp., Erwinia sp. and Flavobacterium sp .; or other organisms such as Escherichia, Lactobacillus sp., Bacillus sp. and the like. Specific organisms include Pseudomonas aeurginosa, Pseudomonas fluorescens, Saccharomyces cerevisiae, Bacillus thuringiensis, Escherichia coli, Bacillus subtilis and others.

General methods for using microorganisms in the control of pesticide substances or in designing other organisms as pesticides are known in the art. See, for example, US Patent 5039523 and EP 0480762 A2.

Alternatively, pesticides are produced by introducing a heterologous gene into a host cell. Expression of the heterologous gene results, directly or indirectly, in the production and maintenance of intracellular pesticide. These cells are then treated under conditions that prolong the action of the toxin produced in the cell when the cell is applied to the target pest environment. The resulting product retains the toxin's toxicity (it naturally encapsulates it).

These naturally encapsulated pesticides can then be conditioned in the form of compositions in different preparations, in accordance with conventional techniques for application in a host-target environment, for example soil, water and plant foliage. See, for example, EPA 0192319.

The present invention relates to a pesticide protein isolated during the vegetative growth phase of a strain of Bacillus spp. or analogous and active fragments thereof and which is capable of destroying selected pests among insects, fungi, bacteria, nematodes, pathogenic protozoa, animal parasites and the like, in particular, insects of the classes Coleoptera, Diptera, Hymenoptera, Lepidoptere, Homoptera , Hemiptera, Orthoptera, Thysanoptera, Dermaptera, Isoptera, Mallophaga, Anoplura, Siphonaptera, or Trichoptera, this protein according to the invention has the amino acid sequence reproduced in SEQ.ID.N0: 7, with a molecular weight of 60-100 kDa, substantially purified and isolated during the period prior to the onset of sporulation in Bacillus cereus, namely the strain Bacillus cereus AB78 deposited under accession number NRRL B-21058 at the Agricultural Research Service, Patent Culture Collection (NRRL) , Northern

230

235

240

245

250

255

260

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Regional Research Center, 1815 North University Street, Peoria, IL 61604, USA or is isolated prior to the production of crystalline insecticidal protein from the strains of Bacillus thuringiensis AB6 having accession number NRRL B-21060, Bacillus thuringiensis AB88 AB289, AB294 and AB359 having accession numbers , NRRL B-21225, NRRL B-21227, NRRL B-21229, NRRL B-21226, as well as Bacillus thuringiensis strains AB59 and AB256 with accession numbers NRRL B-21228 and B-2123O, respectively All strains were submitted to the Agricultural Research Service, Patent Culture Collection (NRRL), Northern Regional Research Center, 1815 North University Street, Peoria, Illinois 61604, USA.

According to the invention, the DNA sequence encoding the substantially pure pesticide protein contained in the strain of Bacillus cereus AB78 and in the strains of Bacillus thuringiensis AB6, AB88, AB289, AB294, AB359, AB59 and AB256, is mainly the sequence of clone P5-4 of E. coli with accession number NRRL B-21O59 or the sequence of clone P3-12 of E. sheets with accession number NRRL B-21061, both of which are filed with the Agricultural Research Service Patent Culture Collection (NRRL) The nucleotide sequence is contained in clone pCIB6O22 of E schools with the accession number NRRL B-21222 filed with the Agricultural Research Service, Patent Culture Collection, (NRRL), Northern Regional Research Center, 1815 North University Street, Peoria, Illinois 61604, USA. The nucleotide sequence is presented as VIP-1 in SEQ ID N0: 4.

The advantages of the present invention are the following:

- the crystalline insecticidal protein active against the beetle larvae, obtained according to the invention, has shown significant effects on the species Diabrotîca, in particular, Diabrotîca virgifera virgifer. western corn rootworm (WCRW) or Diabrotîca longicornus barberi, northern corn rootworm;

- The protein or other polypeptide components described in the present invention can be used singly or in combination, and certain proteins of the present invention enhance the effect of pesticide proteins;

- a nucleotide sequence, isolated according to the invention, can be synthesized and used as a sample for the purpose of isolating the gene encoding the pesticide protein;

- The new strain, according to the invention, Bacillus cereus AB78, showed a significantly different spectrum of insecticidal action compared to the delta-endotoxins active on coleopters known based on Bacillus thuringiensis:

- The protein, according to the invention, has a much more selective action against beetles than the known strains of Bacillus thuringiensis active on beetles, in particular against Diabrotîca spp;

- a mixture of cells containing pCIB6203 (VIP-1 shifted and VIP-2) and cells containing pCIB6O23 (VIP-1 only) exhibit appreciable increased action against western corn rootworm.

The present invention comprises the pesticide protein, as well as its components and fragments for combating harmful plants and insects.

In particular, new pesticide proteins produced during the vegetative growth of Bacillus strains are revealed and which can be isolated in this state prior to the onset of sporulation. In the present invention, Bacillus strains, proteins and genes encoding proteins are presented. Genes encoding such proteins can be isolated, cloned and transformed into different supply vehicles for use in pest control programs.

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Although, it is known that pesticide proteins are produced during the vegetative growth of Bacillus strains, in this invention by vegetative growth is defined only that period of time before the beginning of sporulation. In the case of Bacillus thuringiensis, this vegetative growth is defined as that before the production of crystalline insecticidal protein.

In this invention, pests can be insects, fungi, bacteria, nematodes, pathogenic protozoa, parasitic liverworms and the like, but are not limited to them. Harmful insects include insects selected from the classes Coleoptera, Diptera, Hymenoptera, Lepidoptera, Mallophaga, Homoptera, Thysanoptera, Dermaptera, Isoptera, Anoplura, Siphonaptera, Trichoptera, Hemiptera, Orthoptera, etc.

Tables 1-10 provide the list of pests, associated with the crops of major importance; the list also contains pests of human and veterinary importance. Such pests are included in the scope of the present invention.

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Table 1 Lepidoptera (butterflies and moths)

Corn

Ostrinia nubilalis, (European corn drill)

Agrotis ipsilon, (black-cut worm) Helicoverpa zea, (maize spike worm) Sodoptera frugiperda, (autumn larvae of moths in stock) Diatraea grandiosella, (south-western broom of maize) Elasmopalpus of tealuselus corn ) Diatraea saccharalis, (the cane of sugar cane)

sorghum

Chilo partellus, (sorghum drill)

Spodoptera frugiperda, (autumn larvae of moths in the flock)

Helicoverpa zea, (the corn worm)

Elasmopalpus lignosellus, (dwarf drill of corn stalk)

Feltia subterranea, (the cutting worm that shatters)

Wheat

Pseudaletia unipunctata, (moth larvae in stol)

Spodoptera frugiperda, (autumn larvae of moths in the flock)

Elasmopalpus lignosellus, (dwarf drill of corn stalk)

Agrotis orthogonia, (western yellow-cut worm)

Sunflower

Suleima helianthana, (moth of the sunflower cup)

Homoeosoma electellum, (sunflower moth)

Cotton

Heliothis virescens, (cotton seed worm) Helicoverpa zea, (cotton seed worm) Spodoptera exigua, (root worm) Pectinophora gossypiella, (pink worm)

340

345

350

355

360

365

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Rice

Diatraea saccharais, (the reed of sugar cane)

Spodoptera frugiperda, (autumn worm)

Helicoverpa zea, (corn worm's worm)

Soy beans

Pseudoplusia includens, (soft worm for soy beans)

Anticarsia gemmatalis, (omida bean fodder)

Plathypena scabra, (green clover worm)

Ostrinia nubilalis, (European corn drill)

Agrotis ipsilon, (black cut off)

Spodoptera exigua, (root larvae of stol moths)

Heliothis virescens, (larva of the cotton seed moth making coconut)

Helicoverpa zea, (larva of cotton seed moth making coconut)

Barley

Ostrinia nubilalis, (European corn drill)

Agrotis ipsilon, (black cut off)

Table 2

Beetles (cockroaches)

Corn

Diabrotica virgifera virgifera, (western corn rootworm)

Diabrotica longicoris barberi, (southern corn rootworm)

Howardi undecimpuncta diabrotica, (southern corn rootworm) Melanotus spp., (Thin worm with hard body)

Cyclocephala borealis, (northern non-apparent cockroach - white larva)

Cyclocephala immacuata, (southern non-apparent beetle - white larva)

Popilia japonica, (Japanese beetle)

Chaetocnema pulicaria, (corn flea beetle)

Sphenophorus maidis, (corn beetle)

sorghum

Phyllophaga crinita, (white beetle larva)

Eleodes, Conoderus, and Aeous spp, (thin worm)

Oulema melanopus, (cereal leaf beetle)

Chaetocema pulicaria, (corn fleas)

Sphenophorus maidis, (corn beetle)

Wheat

Oulema melanopus, (cereal leaf beetle)

Hypera punctata, (clover leaf beetle)

Diabrotica udecimpunctata howardi, (Southern corn rootworm) Sunflower

Zygograma exclamationis, (sunflower beetle)

Bothyrus gibbosus, (carrot beetle)

Cotton

Anthonomus grandis (the gray cockroach that destroys the immature cotton seed shell)

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415

Rice

Colaspis brunnea (the grape beetle)

Lissorhoptrus oryzophilus (rice cockroach)

Sitophilus oryzae (rice beetle)

Soy bean

Epilachna varivestis (Mexican bean beetle)

Table 3

Homoptera (Muscles, Tiny Insects)

Corn

Rhopalosiphum maidis (the tiny insect of the corn leaf that sucks the juice of the plant) Anuraphis maidiradicis (the tiny insect of the root of corn)

sorghum

Rhopalosiphum maidis (the tiny insect of the corn leaf)

Sipha flava (the tiny yellow insect of the sugar cane)

Wheat

The tiny Russian wheat insect

Schizaphis graminum (green beetle)

Macrosiphum avenae (the tiny English wheat insect)

Cotton

Aphis gossypii (the tiny insect of cotton)

Pseudatomoscelis seriatus (fleas of cotton leaf)

Trialeurodes abutilonea (winged muscularis)

Rice

Nephotettix nigropictus (rice leaf fleas)

Soy bean

Myzus persicae (the tiny green peach insect)

Empoasca fabae (potato leaf fleas)

Barley

Schizaphis graminum (green beetle)

Rape

Brevicoryne brassicae (tiny cabbage-headed insect)

420

425

430

435

440

Table 4

445

Hemiptera (cockroaches)

Corn

Blissus leucopterus leucopterus (black cockroach sucking its juice)

sorghum

Blissus leucopterus leucopterus (black cockroach sucking its juice]

Cotton

Lyngus lineolaris (the beetle that stains plants) Rice

Blissus leucopterus leucopterus (black cockroach sucking its juice) with wings with wings white white wings which attacking attacks attacking plants planting plants

450

455

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Acrosternum hilare (the nasty green cockroach with the body of a shield)

Soy bean

Acrosternum hilare (the nasty green cockroach with the body of a shield)

Barley

Blissus leucopterus leucopterus (black cockroach with white wings attacking the plant sucking its juice)

Acrosternum hilare (the nasty green beetle with the body of a shield) Euschistus servus (the nasty brown beetle)

Table 5

Orthoptera (locusts, crickets and cockroaches)

Corn

Melanoplus femurrubrum (red-footed locust)

Melanoplus sanguinipes (migratory locust)

Wheat

Melanoplus femurrubrum (red-footed locust)

Melanoplus differentialis (locust)

Melanoplus sanguinipes (migratory locust)

Cotton

Melanoplus femurrubrum (red-footed locust)

Melanoplus differentialis (locust)

Soy bean

Melanoplus femurrubrum (red-footed locust)

Melanoplus differentialis (locust) in the household

American Periplaneta (American beetle)

Blattella germanica (German beetle)

Blatta orientalis (oriental beetle)

Table 6

Diptera (Muscles and Mosquitoes)

Corn

Hylemya platura (worms without legs - like larvae - attacking the corn seed)

Agromyza parvicornis (spotted corn leaf worm)

sorghum

Contarinia sorghicola (sorghum muscle)

Wheat

Mayetiola destructor (Hessian muscle)

Sitodiplosis mosellana (wheat moss)

American Meromyza (Wheat Stem Worm)

Hylemya coarctata (wheat root moss)

Sunflower

Neolasioptera murtfeldtiana (sunflower seed muscle)

Soy bean

Hylemya platura (corn seed worm)

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Barley

Hylemya platura (worm of corn seed) 505

Mayetiola destructor (Hessian muscle)

Insects that attack humans and animals and carry microbes Aedes aegypti (yellow fever mosquito)

Aedes albopictus (the daytime mosquito of the forest)

Phlebotomus papatasii (sand muscle)

Domestic fly (housefly)

Tabanus atratus (the black muscle of the horses)

Cochliomyia hominivorax (Muscle that enters the skin)

Thysanoptera (insect)

Corn

Anaphothrips obscurus (grass insect)

Wheat

Frankliniella fusca (tobacco insect)

Cotton

Thrips tabaci (onion insect)

Frankliniella fusca (tobacco insect)

Soy bean

Sericothrips variabilis (soy and bean insects)

Thrips tabaci (onion insect)

510

515

Table 7

520

525

Table 8

Hymenoptera (cuticles, ants, wasps, etc.) 530

Corn

Solenopsis milesta (thistle ant) ​​Wheat

Cephus cinctus (wheat stalk cutter)

535

Table 9

Other representative species and species

Dermaptera (ears)

Auricularia (European ear)

Isoptera (termites) 540

Reticulitermes flavipes (underground eastern termite)

Mallophaga (biting lice)

Cuclotogaster heterographa (head lice)

Bovicola bovis (lice of cattle)

Anoplura (suckling lice) 545

Pediculus humanus (head and body lice)

Siphonaptera (fleas)

Ctenocephalides felis (cat fleas)

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Table 10

Mites (tiny spiders and ticks)

Corn

Tetranychus urticae (the tiny double-spotted spider) Sorg

Tetranychus cinnabarinus (the tiny red-crimson spider)

Tetranychus urticae (the tiny double-spotted spider) Wheat

Aceria tulipae (the spiral worm of wheat)

Cotton

Tetranychus cinnabarius (the tiny red-crimson spider)

Tetranychus urticae (tiny spotted double spider) Soya beans

Tetranychus turkestani (tiny spider of strawberries) Tetraychus urticae (double-spotted tiny spider) Barley

Petrobia latens (brown wheat mite)

Important mites of animals and humans

Demacentor variabilis (American dog tick) Argas persicus (poultry tick) Dermatophagoides farinae (American dust mite) Dermatophagoides pteronyssimus (European dust mite)

None of the crystalline insecticidal proteins active against known coleopteran larvae have shown significant effects on the species Diabrotica, in particular, Diabrotica virgifera virgifer, western corn rootworm (WCRW) or Diabrotica longicornus barberi, northern worm. herein refers to such pesticide proteins.

In this invention, vegetative growth is defined as that period of time before sporulation begins. In the case of Bacilius thuringiensis, this vegetative growth occurs before the production of crystalline insecticidal protein.

The present invention also comprises nucleotide sequences from microorganisms, other than Bacilius, where the denucleotide sequences are isolated by hybridization with nucleotide sequences of the Bacilius strains according to the invention. Such nucleotide sequences can be tested in pesticide action.

The invention also comprises nucleotide sequences encoding pesticide proteins.

Moreover, the invention comprises proteins obtained from organisms other than Bacilius where the protein interacts with antibodies that fight against the proteins of the invention. Also, such isolated proteins can be tested for pesticide effect by the processes disclosed in the present invention.

given the nucleotide sequences encoding the pesticide proteins of the invention, they can be manipulated and used to enhance the protein in a variety of hosts including other organisms, microorganisms and plants.

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From the amino acid sequence of the purified protein, a nucleotide sequence can be synthesized and used as a sample to help isolate the gene encoding the 595 pesticide protein.

The pesticide genes of the invention can be optimized by known methods to have an increased effect in plants.

The genes that encode such proteins can be isolated, cloned and transformed into different supply vehicles for use in 600 pest control programs.

Thus, the Bacillus microorganisms that find their use, according to the present invention, include Bacillus cereus and Bacillus Thuringiensis, as well as the other Bacillus species, listed in Table 11:

605 Table 11

List of Bacillus species

<td>Morphological group 1</td><td colspan="2">Unassigned stems</td>

<td>B. megaterium</td><td>Subgroup A</td><td></td>

<td>B. cereus *</td><td>B. apiarus *</td><td> 610</td>

<td>B. cereus var. mycoides</td><td>B. filicolonicus</td><td></td>

<td>B. thuringiensis *</td><td>B. thiaminolyticus</td><td></td>

<td>B. licheniformis</td><td>B. alkalophilus</td><td></td>

<td>B. subtilis *</td><td>Subgroup B</td><td></td>

<td>B. pumnilus</td><td>B. cirroflagellosus</td><td> 615</td>

<td>B. firmus *</td><td>B. chitinosporus</td><td></td>

<td>B. coagulans Morphological group 2</td><td>B. lentus</td><td></td>

<td>B. polymyxa</td><td>Subgroup C</td><td></td>

<td>B. macerans</td><td>B. badius</td><td> 620</td>

<td>B. circulans</td><td>B. aneurinolyticus</td><td></td>

<td>B. stearothermophilus</td><td>B. macroides</td><td></td>

<td>B. alvei *</td><td>B. freundenreichii</td><td></td>

<td>B. laterosporus *</td><td>Subgroup D</td><td></td>

<td>B. brevis</td><td>B. pantothenticus</td><td> 625</td>

<td>B. pulvifaciens</td><td>B. epiphytus</td><td></td>

<td>B. popilliae *</td><td>Subgroup E1</td><td></td>

<td>B. lentimorbus *</td><td>B. aminovorans</td><td></td>

<td>B. larvae *</td><td>B. globisporus</td><td></td>

<td>Morphological group 3</td><td>B. insolitus</td><td> 630</td>

<td>B. sphaericus *</td><td>B. psychrophilus</td><td></td>

<td>B. pastry</td><td>Subgroup E2 B. psychrosaccharolyticus</td><td></td>

<td colspan="2">* Those Bacillus strains that were previously discovered in insects.</td><td></td>

The group was formed according to Parry, JM et al. (1983) Color Atlas of 635 Bacillus species, Wolfe Medical Publications, London.

The pesticide protein, according to the invention, produced during vegetative growth, can be isolated from Bacillus strains at the times indicated by this invention. In one case, insecticidal proteins produced during vegetative growth, called VIP (insecticidal vegetative proteins) can be isolated. 640

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The proteins or other polypeptide components described in the present invention can be used singly or in combination. That is, more proteins can be used to combat various harmful insects. In addition, certain proteins of the present invention enhance the effect of pesticide proteins. These proteins are called “auxiliary proteins. While the mechanism of action is not absolutely certain, when the auxiliary proteins and pesticide proteins we are interested in are together, the insecticidal properties of the pesticide proteins are increased several times.

The pesticide proteins of the present invention may vary in molecular weight, having polypeptide components with a molecular weight of at least 30 kDa or greater, preferably about 50 kDa or greater.

Bacillus strains, according to the invention, can be used to protect pests from agricultural crops and their products. Alternatively, a gene encoding the pesticide may be introduced by a suitable vector into a microbial host, and this host may be applied to the environment or to plants or animals. Hosts of microorganisms can be selected from those that occupy the "phytosphere (phylloplane, phillosphere, rhizosphere, and / or rhizoplana) of one or more crops of interest. These microorganisms are selected so as to be able to successfully compete in a particular environment, with wild type microorganisms, to maintain and maintain stable expression of the gene expressing the polypeptide pesticide and, desirable, to provide enhanced protection. of the pesticide against its degradation and inactivation due to the environment.

Such microorganisms include bacteria, algae, fungi. Of particular interest are microorganisms such as, Pseudomonas, Erwinia, Serratia, Klebsiella, Xanthomonas, Streptomyces, Rhizobium, Rhodopseudomonas, Methylius, Agrobacterium, Acetobacter, Lactobacillus, Arthrobacter, Azotobacter, Leuconostoj fungi, and in particular alkaligen, for example, Saccharomyces, Cryptococcus, Kluyveromyces, Sporobolomyces, Rhodotoruia and Aureobasidium. Of particular interest are species of bacteria in the phytosphere, such as, Pseudomonas syringae, Pseudomonas fluorescens, Serratia marcesces, Acetobacter xilinum, Agrobacteria, Rhodopseudomonas spheroides, Xanthomonas campestris, Rhizobium melioti, Alcaligenes entrophus, Clavibacter; and yeast species from the phytosphere, such as, Rhodotoruia rubra, R. glutinis, R. marina, R. aurantiaca, Cryptococcus albidus, C. diffluens, C. laurentii, Saccharomyces rosei, S. pretoriensis,

S. cerevisiae, Sporobolomyces rosues, S. odorus, Kluyveromyces veronae and Aureobasidium polluans. Of particular interest are pigmented microorganisms.

Bacillus strains, according to the invention, or microorganisms that have been genetically modified to contain the pesticide gene and protein, can be used to protect crops and agricultural products from pests. In one aspect of the invention, the entire cell of a pesticide toxin-producing organism is treated with reagents that prolong the action of the toxin produced in the cell, when the cell is applied in the target pest environment.

The active ingredients of the present invention are normally applied in the form of compositions and can be applied on the crop surface or on the plant to be treated, simultaneously or successively with other compounds. These compounds can be either fertilizers or micronutrient donors, as well as other compositions that influence the growth of the plant. They can also be selective herbicides, insecticides, fungicides, bactericides, nematocides,

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690 molluscocides or mixtures of several such compositions, if desired, together with other acceptable carriers for agriculture, surfactants or accelerating aids commonly used in the compositions technique. Suitable carriers and adjuvants may be solid or liquid and correspond to substances commonly used in compositions technology, for example, natural or regenerated mineral substances, solvents, dispersants, wetting agents, binders or fertilizers.

Preferred methods of applying an active ingredient or agrochemical composition according to the invention, which contains at least one of the pesticide proteins produced by the bacterial strains according to the invention, are: leaf application, seed coating and soil application. The number of applications and their frequency depend on the intensity of the infestation with the corresponding pest.

In one embodiment of the invention, a Bacillus cereus microorganism has been isolated capable of destroying Diabrotica virgifera virgifera and Diabrotica longicornis barberi.

The new strain is the Bacillus cereus strain AB78 and was submitted to the Agricultural Research Service, Patent Culture Collection (NRRL), Northern Regional Research Center, 1815 North University Street, Peoria, IL 61604, USA and has accession number RRL B-21058.

A protein was substantially purified from a Bacillus cereus strain. The purification of the protein was verified by SDS-PAGE and biological action. The protein has a molecular weight of about 60 ... 100 kDa, in particular 70 ... 90 kDa, and more particularly about 80 kDa.

The amino-terminal sequence reveals the following amino acid chain: NH2-Lys-Arg-GluIle-Asp-Glu-Asp-Thr-Asp-Thr-Asx-Gly-Asp-Ser-lle-Pro- (SEQ ID N0: 8), where Asx represents either Asp or Asn. The entire amino acid chain is given in SEQ ID NO: 7.

An oligonucleotide sample was generated for the portion of the gene encoding amino acids 3-9 of the NH2- terminus. The sample was synthesized based on the delta-endotoxin gene codon from Bacillus thuringiensis (Bt). The nucleotide sequence of the oligonucleotide sample used for southern hybridization was as follows:

5'ΌΑΑ AK GAT CAA GAT ACN GAT-3 '(SEQ ID NO: 9) where N represents any base.

In addition, the DNA sample for the Bacillus cereus AB78 VIP-1 gene described in the present invention allows the sorting of any Bacillus strain or other organisms for the purpose of determining whether the VIP-1 gene (or a related gene) is naturally present or whether a particular transformed organism includes the VIP-I gene.

Examples of embodiments of the invention are given below, without limiting the invention, as are also the construction of amino acid sequences in connection with the invention, sequences which all form an integral part of the present invention and depict parts of the invention. pesticide proteins or nucleotide sequences that encode these proteins.

Example 1. Isolation and characterization of Bacillus cereus strain AB78

Bacillus cereus strain AB78 was isolated from a contaminated laboratory plate, in T3 medium (per liter: 3 g tripton, 2 g tryptose, 1.5 g yeast extract, 0.05 M sodium phosphate (pH = 6, 8], 0.005 g MnCl₂; middle Travers, RS 1983). AB78 presented a significant action against the western corn rootworm. Antibiotic action against gram-positive Bacillus spp. (Table 12) was also demonstrated.

695

700

705

710

715

720

725

730

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Table 12

Antibiotic action of the culture supernatant of strain AB78

<td rowspan="2">Bacteria tested</td><td colspan="2">Inhibition zone (cm)</td>

<td>AB78</td><td>Streptomycin</td>

<td>E.coli</td><td> 0,0</td><td> 3,0</td>

<td>B.megaterium</td><td> 1,1</td><td> 2,2</td>

<td>B.mycoides</td><td> 1,3</td><td> 2,1</td>

<td>B. cereus CB</td><td> 1,0</td><td> 2,0</td>

<td>B. cereus 11950</td><td> 1,3</td><td> 2,1</td>

<td>B. cereus 14579</td><td> 1,0</td><td> 2,4</td>

<td>B. cereus AB78</td><td> 0,0</td><td> 2,2</td>

<td>Bt var. isrealensis</td><td> 1.1</td><td> 2,2</td>

<td>Bt. var tenebrionis</td><td> 0.9</td><td> 2,3</td>

The morphological characteristics of the Bacillus cereus strain AB78 are as follows: Vegetable sticks with a length of 3.1 - 5.0 mm and a width of 0.2 - 2.0 mm. Cells with round heads, single in short chains. A single subterminal, cylindrical-oval endospore formed in each cell. No parasporal crystal formation. Colonies opaque, eroded, lobed and flat. No pigment production. Motile cells. Flagella present.

The growth characteristics are as follows:

Optionally aerobic, with optimum growth temperature, 21 - 3 ° C. It grows to 15, 20, 25, 30 and 37 ° C. It does not increase at temperatures above 4 ° C. Increases in NaCl 5-7%.

Table 13 shows the biochemical profile of Bacillus cereus strain AB78.

Table 13

Biochemical characteristics of B. cereus strain AB78

<td>L-arabinose acid</td><td> -</td><td>Methylene blue reoxidized</td><td> +</td>

<td>L-arabinose gas</td><td> -</td><td>Low nitrogen</td><td> +</td>

<td>D-xylose acid</td><td> -</td><td>Nitrogen reduced to N0₂</td><td> +</td>

<td>D-xylose gas</td><td> -</td><td>VP</td><td> +</td>

<td>D-glucose acid</td><td> +</td><td>H₂0₂ decomposed</td><td> +</td>

<td>D-glucose gas</td><td> -</td><td>indole</td><td> -</td>

<td>Lactose acid</td><td> -</td><td>Decomposed tyrosine</td><td> +</td>

<td>Lactose gas</td><td> -</td><td>Oihidroxiacetoa</td><td> -</td>

<td>Sucrose acid</td><td> -</td><td>Sunflower lactic acid</td><td> -</td>

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Table 13 (continued)

<td>Sucrose gas</td><td> -</td><td>Sunflower coagulated milk</td><td> -</td>

<td>D-mannitol acid</td><td> -</td><td>Sunflower Alkaline Milk</td><td> -</td>

<td>D-mannitol gas</td><td> -</td><td>Sunflower peptonised milk</td><td> -</td>

<td>Use of propionate</td><td> +</td><td>Reduced sunflower milk</td><td> -</td>

<td>Using encryption</td><td> +</td><td>Casein hydrolyzate</td><td> +</td>

<td>Hydrolyzed hyphae</td><td>W</td><td>Hydrolyzed from starch</td><td> +</td>

<td>Low methylene blue</td><td> +</td><td>Liquefied gelatin with lecithinase production</td><td>W</td>

\ N - weak reaction 780

Example 2. Bacterial cultures Subculture of Bacillus cereus strain AB78 was used to inoculate the following medium, known as "TB soup:

Tryptone ......

Yeast Glycerol Extract ......

KH2P04 .....

K2HP04 .....

pH = 7.4 g / l 785 g / l ml / l

2.1 g / l

14.7 g / l

790

After cooling, potassium phosphate was added "autoclaved soup. The containers were kept in the incubator, at 3 ° C, on a rotating vibrator, at 250 rpm, for 24 to 36 h.

The above procedure can be adapted for large users, through procedures well known in the art. 795 during vegetative growth, usually 24 ... 36 h after culture start, AB78 bacteria were centrifuged from the culture supernatant. The culture supernatant, which contains the active protein, was used in biological samples.

Example 3. Biological samples with insects

The strain of Bacillus cereus AB78 has been tested against numerous insects 800 described below.

Northern, western and southern roots of maize, Diabrotica virgifera virgifera, D. longicornis barberi and D. undecempunctata howardi: Dilutions were made from culture supernatant of strain AB78, grown 24 ... 36 h, by mixing with the liquid artificial culture medium (Marrone et al (1985) J. of Economic 805 Entomology 78: 290-293] and letting it solidify The solidified culture medium was cut and placed in the plates. Newborn larvae were placed on composition and kept at 3 ° C. After 6 ... 8 days the death of the larvae was recorded.

E. coli donated biological sample: E. coli was grown overnight in L-Amp 100, at 37 ° C. Ten ml of culture were subjected to ultrasound 3 times, 20 s, 810 each time. 500 ml of gently treated culture were added to the liquid culture medium for western rootworm of maize.

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Colorado potato beetle, Leptinotarsa ​​decemlineata: dilutions in Triton X-1OO (to give a final concentration of 0.1% TX-1OO) were made from the culture supernatant of strain AB78, raised 24 ... 36 h 5 cm² portions of potato leaf were soaked in these dilutions, dried in air and placed on filter paper soaked in plastic plates. Newborn larvae were placed on the leaf portions and kept at 3 ° C. The death of the larvae was recorded after 3 to 5 days.

Yellow table worm, Tenebrio molitor. dilutions were made from AB78 strain culture supernatant increased 24 ... 36 h, by mixing with liquid culture medium (Bioserv # F924O) and resting for solidification. The solidified culture medium was cut and placed in plastic plates. Newborn larvae were placed on the culture medium and kept at 3 ° C. Larval mortality was recorded after 6 ... 8 days.

European corn drill, black-cut worm, tobacco bud worm, tobacco horn worm and beet worm; Ostrinia nubilalis, Agrotis ipsilon, Heliothis virescens, Manduca sexta and Spodoptera exigua respectively: dilutions, in TX-1OO (to give a final concentration of 0.1% TX-1OO), made from cultured supernatant of strain AB78 grown 24. ..36 h. 100 ml supernatant was pipetted on a surface of 18 cm² solidified culture medium (Bioserv # F924O] and allowed to air dry. The larvae in the early stages of development were then placed on the surface of the culture medium and kept at 30 ° C. Larval mortality was recorded after 3. ..6 days.

Northern houseplant, Culex pipiens: dilutions were made from culture supernatant of strain B78 grown 24 ... 36 h. 100 ml was pipetted in 10 ml water, in a 30 ml plastic cup. Three larvae were added to the water and kept at room temperature. Larval mortality was recorded after 24 ... 48 h. The spectrum of AB78 strain activity is given in table 14.

Table 14

AB78 strain culture supernatant action against different insect species

<td>Insect species</td><td>The order</td><td>The action</td>

<td>Western worm root of corn (Diabrotica virgifera virgifera)</td><td>Col</td><td> +++</td>

<td>Northern root worm of corn (Diabrotica longicornis barberi)</td><td>Col</td><td> +++</td>

<td>Southern root root of corn (Diabrotica undecimpunctata howardi)</td><td>Col</td><td> -</td>

<td>Potato beetle [Leptinotarsa ​​decemlineata)</td><td>Col</td><td> -</td>

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Table 14 (continued)

860

<td>Insect species</td><td>The order</td><td>The action</td>

<td>Yellow table worm [Tenebrio molitor)</td><td>Col</td><td></td>

<td>European corn drill (Ostrinia nubilalis]</td><td>Lep</td><td> -</td>

<td>Tobacco worms (Heliothis virescens)</td><td>Lep</td><td></td>

<td>Worms with tobacco horns (Manduca sexta)</td><td>Lep</td><td></td>

<td>Beetle worms [Spodoptera exigua]</td><td>Lep</td><td> -</td>

<td>Black cutter worm (Agrotis ipsilon)</td><td>Lep</td><td> -</td>

<td>Northern house mosquito (Culex pipiens)</td><td> -</td><td> -</td>

865

870

The novel isolated strain, according to the invention, Bacillus cereusAB78, showed a significantly different spectrum of insecticidal action compared to delta-endotoxins active on coleopters known from Bacillus thuringiensis.

In particular, the AB7B strain, according to the invention, showed a more selective action against cockroaches, than the known strains of Bacillus thuringiensis active on beetles, in that it was more active against Diabrotica spp. The most active was against D. virgifera virgifera and D. longicornis barberi, but not against D. undecimpunctata howardi.

A number of Bacillus strains have been biologically tested for their action during vegetative growth (Table 15) against western corn root worm. The results show that the AB78 strain, according to the invention, is unique in terms of action against western rootworm of maize, which is not a general phenomenon.

Table 15

875

880

885

890

The action of culture supernatants from different strains of Bacillus spp against the western root worm

<td>Bacillus strain</td><td>Mortality percentage</td>

<td>B.cereus Ab 78 (Bat. 1)</td><td>1CO</td>

<td>B.cererus AB 78 (Bat. 2)</td><td>1OO</td>

<td>B.cererus (Carolina Bio.)</td><td> 12</td>

<td>B.cereus ATCC 11950</td><td> 12</td>

<td>B.cereus ATCC 14579</td><td> 8</td>

895

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Table 15 (continued)

<td>B. mycoides [Carolina Bio.)</td><td> 30</td>

<td>B.popillia</td><td> 28</td>

<td>B. thuringiensis HD 135</td><td> 41</td>

<td>B. thuringiensis HD 191</td><td> 9</td>

<td>B. thuringiensis GC 91</td><td> 4</td>

<td>B. thuringiensis isrealensis</td><td> 24</td>

<td>Water control</td><td> 4</td>

The specific action of strain AB78, according to the invention, against the western rootworm is shown in table 16.

Table 16

AB78 strain culture supernatant action against western rootworm of corn

<td>Culture supernatant concentration (pl / ml)</td><td>Mortality percentage</td>

<td> 100</td><td> 100</td>

<td> 25</td><td> 87</td>

<td> 10</td><td> 80</td>

<td> 5</td><td> 40</td>

<td> 2,5</td><td> 20</td>

<td> 1</td><td> 6</td>

<td> 0</td><td> 0</td>

For western root worms of maize, LC 50 was calculated to be 6.2 µl of culture supernatant per milliliter of composition.

Example 4. Isolation and purification of the active protein for maize root worm from strain AB78

The culture medium without cells and cell debris was treated at 70% saturation by adding 472 g / l of solid ammonium sulfate. The dissolution was done, at room temperature, followed by cooling in an ice bath and centrifugation, at 1OOOO xg, for 30 minutes for the precipitated proteins to appear in agglomerated form.

The supernatant was removed and the precipitate was dissolved in 1/10 of the initial volume with 20 mM TRIS-HCl buffer solution, at pH = 7.5.

The salts embedded in the precipitate were removed from the solution, either by dialysis in 20 mM TRIS-HCl solution, pH = 7.5, or by passing through a purification column.

The protein solution thus obtained was titrated, at pH = 3.5, with 20 mM sodium citrate pH = 2.5. After an incubation, for 30 minutes, at room temperature, the solution was centrifuged at 3000 xg, for 10 minutes. At this stage, the supernatant contained the highest amount of active protein.

Following the neutralization of the solution at pH = 7, O, the supernatant was passed over an anionic Mono-Q exchanger, column equilibrated with 20 mM TRIS, pH = 7.5, at a flow rate of 940, 300 ml / min. . The column was eluted with a linear and stepwise gradient, using

400 mM NaCl, in 20 mM TRIS, pH = 7.5.

The biological samples of the portions of the eluate and the SDS-PAGE analysis were used to confirm the active portions. SDS-PAGE analysis identified the biologically active protein as having a molecular weight of 80 kDa. 945

Example 5. Sequence analysis of the maize root worm active protein

The 80 kDa protein isolated by SDS-PAGE was transferred to the PVDF electrophoresis membrane and subjected to amino-terminal sequencing, performed by repeated Edman cycles on the ABI 470 liquid-pulsing computer. The transfer was performed 950 in 10 mM CAPS buffer. , with 10% methanol, pH = 11.0 as follows:

Incubation of the gel following electrophoresis was done in the transfer buffer for 5 min.

The ProBlott PVDF membrane was briefly moistened with 100% MeOH, then equilibrated in the transfer buffer. 955

The multilayer was arranged between foamy sponges and filter paper squares with the configuration of a Cathode-Gel-Membrane-Anode.

The transfer was carried out at a constant voltage of 70 V, for one hour.

After transfer, the membrane was rinsed with water and stained for 2 min with 0.25% Coomassie Blue R-250 in 50% MeOH. Dye removal was performed by 960 successive rinses with 50% MeOH, 40% water, 10% acetic acid.

After cleaning, the membrane was dried in air before extracting the strips for sequence analysis. Blott Cartridge and appropriate cycles have been used to achieve maximum efficiency and productivity. Data analysis was performed using 610 Sequence Analysis software to identify and quantify 965 PTH amino acid derivatives for each sequential cycle.

The N-terminal sequence was determined to be: NH2-Lys-Arg-Glu-lle-Asp-Glu-Asp-ThrAsp-Thr-Asx-Gly-Asp-Ser-lle-Pro- (SEQ ID NO: 8], where Asx represents Asp or Asn.

Example 6. Construction of the 970 DNA sample

An oligonucleotide sample was generated for the region of the gene encoding amino acids 3-9 of the N-terminal sequence (example 5). The sample was synthesized based on the codon role of the delta-endotoxin gene of Bacillus thuringiensis (Bt). The 5'-GAA nucleotide sequence ATT GAT CAA GAT ACN GAT-3 '(SEQ ID NO: 9) was used as a sample in southern hybridizations. The oligonucleotide was synthesized using 975 standard equipment and procedures.

Example 7. Determination of the isoelectric point of the corn rootworm active protein

The purified protein from Example 5 of the purification process was analyzed on an isoelectric focused gel 3-9 µl, using the Phastgel 980 electrophoresis system (Pharmacia). The standard operating procedures were followed by separation and staining with silver, the pl approximated to 4.9.

Example 8. PCR data on strain AB78

PCR analysis (See, for example, US Patent Application Serial No. 08/008006; Carozzi et al (1991) Appl. Environ. Microbio 1. 57 (11): 3057-3061, 985

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AB78 did not contain any genes for the insecticidal crystalline protein of the strain

Bacillus thuringiensis or Bacillus. sphaericus (Table 17).

Table 17

Bacillus insecticidal crystalline protein gene primers tested by PCR against AB78 DNA

<td>First tested</td><td>Result product</td>

<td>2 sets specific to CrylllA</td><td>Negative</td>

<td>CrylllB</td><td>Negative</td>

<td>2 specific sets for CrylA</td><td>Negative</td>

<td>CryIA (a)</td><td>Negative</td>

<td>CrylA (b) specific</td><td>Negative</td>

<td>cryIB</td><td>Negative</td>

<td>CrylC specific</td><td>Negative</td>

<td>CrylE specific</td><td>Negative</td>

<td>2 specific sets for B.sphaericus</td><td>Negative</td>

<td>2 sets for CrylV</td><td>Negative</td>

<td>Control with Bacillus (PI-PLC)</td><td>Positive</td>

Example 9. Cloning of the entire DNA cosmid from the B. cereus strain AB78

The VIP-1 gene was cloned from all DNA prepared from strain AB78, as follows:

Isolation of DNA from strain AB78 was performed as follows:

1. Cultivation of bacteria overnight, in 10 ml solution L (Sterile centrifugal tube, 50 ml).

2. Add 25 ml of fresh L-solution and ampicillin (30 mg / ml).

3. The growth of the cells, with agitation, 2 ... 6 h, at a temperature of 3 ° C.

4. Rotate the cells in a 50 ml polypropylene tube in a clinical centrifuge IEC, at 3/4 of the speed.

5. Resuspended cell agglomeration, in 10 ml TES

6. Add 30 mg lyzozym and incubate for 2 h at 37 ° C.

7. 200 ml 20% SDS and 400 ml Proteinase K (20 mg / ml) are added. Incubate at 37 ° C.

8. Add 200 ml of fresh Proteinase K. Incubate for one hour at 55 ° C. Add 5 ml of TES (TES = 50mM, pH = 8, O, 100 mM EDTA, 15 mM NaCl) so that finally it is a volume of 15 ml.

9. It is extracted in two rows with phenol (10 ml phenol, rotated at room temperature, at 3/4 of the speed, in a clinical centrifuge type IEC). Transfer the supernatant to a clean tube fitted with a large diameter pipette.

10. It extracts 1: 1 at once. phenol: chloroform / isoamyl alcohol (ratio 24: 1).

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1030

11. The DNA is precipitated with an equal volume of cold isopropanol; is centrifuged for plaque agglomeration of DNA.

12. The agglomerate was resuspended in 5 ml TE.

13. The DNA was precipitated with 0.5 ml 3M NaOAc, pH = 5.2 and 11 ml 95% ethanol. Store at -20 ° C for 2 hours.

14. Hook the DNA from the tube with a plastic frame, transfer it to a microfuge tube, centrifuge, pipette excess ethanol, dry in vacuo.

15. Resuspended in 0.5 ml TE. Incubate at 90 ° C for 90 minutes to help the DNA pass through the solution.

16. The concentration is determined using standard procedures.

Cloning of the AB78 stem cosmid

All procedures (unless otherwise indicated) were performed in accordance with Stratagene Protocol, Supercos 1 Instruction Manual, Cat. no. 251 301.

In general, the stages were as follows:

A. Partial restriction digestion Or 3A of the DNA of strain AB78.

B. Preparation of the DNA vector

C. DNA binding and wrapping

D. Titration of the genetic information of the cosmid

1. Prepare a culture of HB cells by placing a culture grown overnight in 5 ml of TB with 0.2% maltose. Incubate for 3.5 h at 37 ° C.

2. Centrifuge the cells and resuspend, in 0.5 ml 10 mM MgSO₄.

3. Interfere:

100 ml cells

100 ml diluted coating mixture

100 10 mM MgSO₄ ml TB

4. It is absorbed at room temperature for 30 minutes without stirring.

5. Add 1 ml TB and mix gently. Incubate for 30 minutes at 37 ° C.

6. Spread 200 ml on the L-amp plates. Incubate overnight at 37 ° C.

At least 400 clones of the cosmid were selected for action against the western corn root worm described in Example 3. DNA from 5 active clones and 5 inactive clones was used in southern hybridization. The results demonstrated that the hybridization using the oligonucleotide sample described above is correlated with the action of the western root root of the corn (Table 18).

Clones of cosmid P3-12 and P5-4 were submitted to the Agricultural Research Service Patent Culture Collection (NRRL) and were given access numbers B-21061 and B-21059, respectively.

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1040

1045

1050

1055

1060

1065

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Table 18

Action of clones of the AB78 stem cosmid against the western corn root worm

<td>clone</td><td>Average percentage of mortality (N = 4)</td>

<td>Clones that hybridize with the sample</td><td></td>

<td>P1-73</td><td> 47</td>

<td>P1-83</td><td> 64</td>

<td>P2-2</td><td> 69</td>

<td>P3-12</td><td> 85</td>

<td>P5-4</td><td> 97</td>

<td>Clones that do not hybridize with the sample</td><td></td>

<td>P1-2</td><td> 5</td>

<td>P3-8</td><td> 4</td>

<td>P3-9</td><td> 12</td>

<td>P3-18</td><td> 0</td>

<td>P4-6</td><td> 9</td>

Example 10. Identifying a 6 kb Active Region Against Western Root Corn Worm

DNA from P3-12 was partially digested with the restriction enzyme or 3A, and bound in the pUCI9 vector of E. coli and transformed into lysates. An 80 kDa protein-specific DNA sample was synthesized by PCR amplification of a portion of P3-12 DNA. The oligonucleotides MK113 and MK117, which hybridize to VIP-1 portions, were synthesized by using the partial amino acid sequence of the 80 kDa protein. Plasmid subclones were identified by colony hybridization of the PCR sample and tested for their action against western rootworm. One of these clones, PL2, hybridizes to the PCR fragment and is active against the western root corn worm, according to the biological sample described above.

A 6kb Cla I restriction fragment from PL2 was cloned into Sma I of the pHT31O1 oscillatory vector of E. coli-Bacillus (Lereclus, D. et al, 1989, FEMS Microbiology Letters 60: 211-218) to obtain pCIB6201. This configuration confers western root root worm anti-worm action on both Bacillus and coli strains, in any orientation.

pCIB6O22 contains the same 6 kb Cla I fragment in pBluescript SK (+) (Stratagene), produces the equivalent VIP-1 protein, and is also active against western corn rootworm.

The nucleotide sequence of pCIP6O22 was determined by Stanger's dideoxy termination method, Proc. Natl. Acad. Sci. USA, 74: 5463-5467 (1977), using PRISM Ready Reaction Dye Deoxy Terminator Cycle Sequencing Kits and PRISM Sequenase Terminator Double-StrandedADN Sequencing Kit and analyzed on the ABI 373 automatic computer. The sequence is given in SEQ ID NO: I comprising SEQ ID NO: 4 encoding VIP-1 protein, of 1OOkDa defined in the sequence SEQ ID N0: 5.

RO 117111 Bl pCIB6O22 was filed with the Agricultural Research Service, Patent Culture

Collection, (NRRL), Northern Regional Research Center, 1815 North University 1110

Street, Peoria, Illinois 61604, USA, and was given access number NRRL B-21222.

Example 11. Functional dissection of the VIP-1 region of DNA

To confirm the need for the VIP-1 open reading frame (ORF) for insecticidal action, a mutation was created in the gene. Bgl II restriction enzyme recognizes a single locus located 1758 bp in the coding region of VIP-1. pCIB6201 1115 was digested with Bgl II and single-stranded ends filled with DNA polymerase (Klenow fragment) and dNTPS.PIasmida was relegated and transformed into E. coli. The resulting plasmid, pCIB6203, contains a 4-nucleotide insert in the coding region of VIP-1.

pCIB6203 does not confer insecticidal action, confirming that VIP-1 is an 1120 essential component of the action of the western corn rootworm.

To further define the region required for VIP-1 coding, subclones of VIP-1 and VIP-2 (auxiliary protein) regions were constructed and tested for their ability to complete the mutation in pCIB6203.

pCIB6023 contains the 3.7 kb Xba I-EcoRV fragment in pBluescript SK (+) 1125 (Stratagene). Western blot analysis indicates that pCIB6023 produces VIP-1 protein in the same amount and size as clones PL2 and pCIB6022.

pCIB6023 contains the entire 80 kd protein gene.

pCIB6023 was submitted to the Agricultural Research Service, Patent Culture Collection, (NRRL), Northern Regional Research Center, 1815 North University 1130 Street, Peoria, Illinois 61604, USA, and was given accession number NRRL B-21223.

pCIB6O23 presents some action. However, the level of action is lower than that of pCIB6022. A mixture of cells containing pCIB6203 (VIP-1 shifted and VIP-2) and cells containing pCIB6023 (VIP-1 only) exhibit increased action against western corn rootworm. Thus, pCIB6023 must produce 1135 VIP-1 functional genetic product and pCIB6203 must produce VIP-2 functional genetic product. These results suggest an additional demand for a genetic product from the VIP-2 region, in combination with VIP-1, to confer maximum action against western corn rootworm. (See Table 19).

Table 191140

Characterization of pCIB 6022 cxsmb vn »irv c

1

JOOlp

1-----------------------------------------------------------------------------1

IT

<img file="RO117111B1_D0001.tif" />

J

<td>Test configurations</td><td colspan="2">Action against WCRW</td>

<td>pCIB6022</td><td> +++</td><td> 1145</td>

<td>pCIB6023</td><td colspan="2"> +</td>

<td>PCIB6203</td><td></td><td> 1150</td>

pCIB6203 pCIB6023 +++

RO 117111 Bl

The framed regions represent the amount of VIP-1. Light colored portions indicate the regions encoding the 80 kDa peptide observed in Bacillus. The dark-colored portions represent the N-terminal amino acids established in the DNA sequence of VIP-1.

Arrows represent configurations transcribed by the beta-galactosidase promoter.

Restriction places: C-Cla; X-Xba I; S-Sca I; Rl-Eco Rl; B-Bgl II; RV Eco RV.

Example 12. Antibody production of strain AB78

Antibody production was initiated in two Lewis strain rats to allow both of them to produce hybridoma cell lines and also to produce sufficient serum for limited selection of cDNA information. Another factor was the very limited amount of antigen available and the fact that it could be purified only by PAGE and then by electrotransfer on nitrocellulose.

Due to the limited availability of the antigen on nitrocellulose, the latter was emulsified in DMSO and injected into the hind paws of the animals to promote B-cell production in the popliteal lymph nodes just above. A serum with strong reaction was produced by western analysis in the first production obtained by bleeding. Several consecutive injections and bleeding produced enough serum to make the necessary selection.

Then, hybridoma production was initiated with one of the rats. The popliteal lymph nodes were extracted, macerated and the resulting cells were mixed with myeloma mouis P3x63Ag8,653. Further cell selection was performed as described below. Four initial sources were selected to be agitated giving the strongest emulsified antigen reaction at limited dilution donation. Ten additional sources were chosen for expression and cold storage.

Procedure for emulsifying the AB78 strain on nitrocellulose in DMSO for ELISA type selection:

After electrotransferring the samples of the AB78 strains and transferring them by PAGE into nitrocellulose, the reversible strain Ponceanus is used to visualize all the transferred proteins.

The toxin band corresponding to strain AB78, previously identified and ordered Nterminal, is identified and extracted from nitrocellulose. Each strip has a size of 1 mm x 5 mm in order to minimize the amount of emulsified nitrocellulose. A single tape is placed in a centrifugal tube with 250 µl of DMSO and macerated with a plastic gun (Kontes, Vineland, NJ). To help emulsify, the DMSO mixture is heated for 2 to 3 minutes. , the temperature of 37 ... 45 ° C. 0 further maceration may be required after heating; however, all nitrocellulose should be emulsified. Once emulsified, sample AB78 is placed on ice. In microtiter preparation, the plate is coated with emulsified antigen and the sample should be diluted in borate saline buffer solution as follows: 1: 5, 1:10, 1:15, 1:20, 1:30, 1: 5O, 1: 100 and O. The coating antigen should be prepared immediately before use.

ELISA Protocol;

1. Coating with AB78 / DMS0 in BBS. Incubation overnight, at a temperature of 4 ° C.

2. Wash the 3X plate with 1X ELISA wash buffer.

3. Hold for 30 minutes at room temperature (1% BSA &amp; 0.05% Tween 20 in BPS).

4. Wash the 3X plate with 1X ELISA wash buffer.

RO 117111 Bl

1205

5. Add rat serum. Incubate at 37 ° C.

6. Wash the 3X plate with 1X ELISA wash buffer.

7. An anti-rat rat prepared with a concentration of 2 pg / ml in diluent ELISA is added. Incubate for one hour at 37 ° C.

8. Wash the 3X plate with 1X ELISA wash buffer.

9. Add anti-goat alkaline phosphatase prepared in rabbit with concentration 2 pg / ml in ELISA diluent.

10. 3X wash with 1X ELISA wash buffer.

11. Substrate is added. Incubate for 30 minutes at room temperature.

12. After 30 minutes the incubation with NaOH 3N solution is stopped.

Example 13. Activation of insecticidal action of inactive Bacillus thuringiensis strains using AB78 VIP clones

By adding pCIB6203 to the culture supernatant of a Bacillus thuringiensis GC91 strain, 100% mortality of Diabrotica virgifera virgifera occurs. Taken separately, neither pCIB6203 nor GC91 are active against Diabrotica virgifera virgifera. The data are presented below:

1210

1215

<td>The material tested</td><td>Mortality in percentage of Diabrotica</td>

<td>PCIB62O3</td><td> 0</td>

<td>GC91</td><td> 16</td>

<td>+ GC91 PCIB62O3</td><td> 100</td>

<td>Control</td><td> 0</td>

1220

Example 14. Isolation and biological action of B. cereus strain AB81

A second Bacillus cereus strain, called ΑΒΘ1, was isolated from silo dust samples using standard methodologies. A subculture of strain AB81 was grown and prepared to be the biological sample, as described in example 2. The biological action was evaluated, as described in example 3. The results are as follows:

1225

1230

<td>Insect species tested</td><td>Mortality percentage</td>

<td>Ostrinia nubilalis</td><td> 0</td>

<td>Aggrieved YES</td><td> 0</td>

<td>Diabrotica virgifera virgifera</td><td> 55</td>

1235

Example 15. Isolation and biological action of B. thuringiensis strain AB6

A Bacillus thuringiensis strain, named AB6, was isolated from silo dust samples by standard methods known in the art. A subculture of strain AB6 was grown and prepared for biological testing as described in Example 2. Half of the sample was autoclaved for 15 min to test for beta-exotoxin.

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RO 117111 Bl

The biological action was evaluated as described in Example 3.

The results are as follows:

<td>Insect species tested</td><td>Mortality percentage</td>

<td>Ostrinia nubilalis</td><td>A</td>

<td>Aggrieved YES</td><td>1OO</td>

<td>Agrotis ipsilon [autoclaved sample]</td><td> 0</td>

<td>Diabrotica virgifera virgifera</td><td> 0</td>

The AB6 strain was submitted to the Agricultural Research Service, Patent Culture Collection (NRRL), Northern Regional Research Center, 1815 North University Street, Peoria, Illinois 61604, USA, and has accession number NRRL B-21O6O.

Example 16. Isolation and biological action of B. thurigiensis strain AB88 The strain Bacillus thuringiensis, termed AB88, was isolated from silage dust samples by standard methods. A strain strain AB88 was grown and prepared for biological testing, as described in Example 2. Half of the sample was autoclaved for 15 min to test for beta-toxin. The biological action was evaluated against a number of insect species described in Example 3. The results are as follows:

<td rowspan="2">Insect species tested</td><td rowspan="2">Class</td><td colspan="2">Percentage mortality of the culture supernatant</td>

<td>Neautoclavat</td><td>autoclave</td>

<td>Aggrieved YES</td><td>Lepidoptera</td><td> 100</td><td> 5</td>

<td>Ostrinia nubilalis</td><td>Lepidoptera</td><td> 100</td><td> 0</td>

<td>Spodoptera frugiperda</td><td>Lepidoptera</td><td> 100</td><td> 4</td>

<td>Helicoverpa zea</td><td>Lepidoptera</td><td> 100</td><td> 12</td>

<td>Heliothis virescens</td><td>Lepidoptera</td><td> 100</td><td> 12</td>

<td>Leptinotarsa ​​decemlineata</td><td>beetles</td><td> 0</td><td> 0</td>

<td>Diabrotica virgifera virgifera</td><td>Coleoptera</td><td> 0</td><td> 5</td>

The delta-endotoxin crystals were purified from strain AB88 by standard methods. No action on the part of the pure crystals was observed against

Agrotis ipsilon, when tested biologically.

RO 117111 Bl

1285

Example 17. VIP purification from strain AB88

Bacterial fluid culture was increased overnight at 3 ° C in TB medium. The cells were removed and the supernatant was kept. The proteins were precipitated with ammonium sulphate (70% saturation), centrifuged and the sediment thus obtained was preserved. The sediment was resuspended in the initial volume of 20 mM Tris, pH = 7.5 and dialyzed on the same buffer. The dialysate of strain AB88 is more turbid than other comparable material obtained from strain AB78. AB88 strain proteins were separated after clarification by several different methods, including isoelectric focusing (Rotofor, BioRad, Hercules, CA), precipitation at pH = 4.5, ion exchange chromatography, stationary phase chromatography and ultrafiltration .

The active protein against the European corn borer remained in the sediment obtained by precipitating the dialysate, at pH = 4.5. When the preparative IEF was made on dialysis, using ampholytes pH = 3 ... 1O, the insecticidal action of ECB was found in all fractions with pH value 7 or higher.

SDS-PAGE of these fractions showed approximately equal molecular weight protein bands, with 60 kDa and about 80 kDa. The 60 kDa and 80 kDa bands were separated by HPLC ion exchange on a Poros-Q column (PerSeptive Biosystems, Cambridge, MA). The N-terminal sequence was obtained from two fractions containing slightly different molecular mass proteins, but both having a size of about 60 kDa. The sequences obtained are similar, both with each other and with some delta-endotoxins.

Anion exchange fraction 23 (lower): xEPFVSAxxxQxxx (SEQ ID NO: 10)

Anion exchange fraction 28 (higher): xEYENVEPFVSAx (SEQ ID NO: 11) When the (active) sediment with pH = 4.5 was further separated by anion exchange on a Poros-Q column, the action was found only in fractions with a major band, about 60 kDa.

The active protein against the black cutter worm also remained. in the sediment, when the dialysate of strain AB88 was lowered, to pH = 4.5.

Using ampholite pH = 3 ... 10 in the preparative IEF, the action was not detected in the ECB-active IEF fractions; instead, it had a larger fraction, pH = 4.5 ... 5.0.

Its major compounds have molecular weights of approximately 35 and 80 kDa.

The sediment, with pH = 4.5 was separated by exchange of HPLC anions in fractions containing only the material, of 35 kDa and fractions containing, both bands, of 35 kDa and 80 kDa.

Example 18. VIP characterization of strain AB88

Fractions containing the various plant proteins active against Lepidopterans were generated as described in Example 17. Analysis of the active fractions showed that different VIPs are responsible for the action against different species, by Lepidopterans.

The action of Agrotis ipsilon is due to a protein, 80 kDa or 35 kDa, which is single or in combination. These proteins are not related to any of the delta-endotoxins Bacillus thuringiensis, as evidenced by the lack of sequence homology to the known delta-endotoxin sequences. Also, these proteins are not found in the delta-endotoxin crystal AB88. The N-terminal sequences of major delta-endotoxins were compared with the N-terminal sequences of VIPs, 80 kDa and 35 kDa, and no sequence homology was found. The summary of results is as follows:

1290

1295

1300

1305

1310

1315

1320

1325

RO 117111 Bl

<td>Agrotis VIP N-terminal sequences</td><td>N-terminal sequence of major proteins endotoxins</td>

<td>80 kDa</td><td>130 kDa MDNNPNINE (SEQ ID NO: 14) 80 kDa</td>

<td>MNKNNTKLPTRALP (SEQ ID NO: 12]</td><td>MDNNPNINE (SEQ ID NO: 15) 60 kDa</td>

<td>35 kDa ALSENTGKDGGYIVP [SEQ ID NO: 13)</td><td></td>

The action of Ostriniei nubilalis is due to a VIP of 60 kDa and the action of the Spodoptera frugiperda is due to a VIP of unknown size.

Bacillus thuringiensis strain AB88 was submitted to the Agricultural Research Service, Patent Culture Collection (NRRL), Northern Regional Research Center, 1815 North University Street, Peoria, Illinois 61604, USA and has accession number NRRL B-21225.

Example 19. Isolation and biological action of other Bacillus species

Other Bacillus species have been isolated that produce insecticidal proteins during vegetative growth. These strains were isolated from environmental samples by standard methods. The isolated strains were prepared for biological study and then tested as described in Examples 2 and 3 respectively. Isolated strains that produced insecticidal proteins during vegetative growth, with action against Agrotis ipsilon, are given in the table below:

<td>Bacillus isolated</td><td>Presence of deltaendotoxin crystal</td><td>Mortality percentage</td>

<td>AB6</td><td> +</td><td> 100</td>

<td>AB53</td><td> -</td><td> 80</td>

<td>AB88</td><td> +</td><td> 100</td>

<td>AB195</td><td> -</td><td> 60</td>

<td>AB211</td><td> -</td><td> 70</td>

<td>AB217</td><td> -</td><td> 83</td>

<td>AB272</td><td> -</td><td> 80</td>

<td>AB279</td><td> -</td><td> 70</td>

<td>AB289</td><td> +</td><td> 100</td>

<td>AB292</td><td> +</td><td> 80</td>

<td>AB294</td><td> -</td><td> 100</td>

<td>AB300</td><td> -</td><td> 80</td>

<td>AB359</td><td> -</td><td> 100</td>

RO 117111 Bl

Isolated strains AB289, AB294 and AB359 were submitted to Agricultural

Research Service, Patent Culture Collection (NRRL), Northern Regional Research 1370

Center, 1815 North University Street, Peoria, Illinois 61604, USA, and have access numbers NRRL B-21227, NRRL B-21229 and NRRL B-21226, respectively.

Bacillus strains that produce insecticidal proteins during vegetative growth, with action against Diabrotica virgifera virgifera are given in the table below. 1375

<td>Bacillus isolated</td><td>Presence of deltaendotoxin crystal</td><td>Mortality percentage</td>

<td>AB52</td><td> -</td><td> 50</td>

<td>AB59</td><td> -</td><td> 71</td>

<td>AB68</td><td> +</td><td> 60</td>

<td>AB78</td><td> -</td><td> 100</td>

<td>AB122</td><td> -</td><td> 57</td>

<td>AB218</td><td> -</td><td> 64</td>

<td>AB256</td><td> -</td><td> 64</td>

1380

1385

Isolated strains AB59 and AB256 were submitted to the Agricultural Research Service, Patent Culture Collrctio (NRRL), Northern Regional Research Center, 1815 North University Street, Peoria, Illinois 61604, USA, and have accession numbers NRRL B-21228 and B- respectively. 21230.

The following warehouses were established at the Agricultural Research Service, Patent Culture Collection (NRRL), Northern Regional Research Center, 1815 North University Street, Peoria, Illinois 61604, USA:

1390

<td>1. E. coli PL 2</td><td colspan="2">no. access NRRL B-21221</td>

<td>2. E. coli pCIB 6022</td><td>no. access NRRL B-21222</td><td> 1395</td>

<td>3. E. coli pCIB 6023</td><td>no. access NRRL B-21223</td><td></td>

<td>4. Bacillus thuringiensis HD73-78 VIP</td><td>no. access NRRL B-21224</td><td></td>

<td>5. Bacillus thuringiensis AB88</td><td>no. access NRRL B-21225</td><td></td>

<td>6. Bacillus thuringiensis AB359</td><td>no. access NRRL B-21226</td><td></td>

<td>7. Bacillus thuringiensis AB289</td><td>no. access NRRL B-21227</td><td> 1400</td>

<td>8. Bacillus sp. AB59</td><td>no. access NRRL B-21228</td><td></td>

<td>9. Bacillus sp. AB294</td><td>no. access NRRL B-21229</td><td></td>

<td>10. Bacillus sp. AB256</td><td>no. access NRRL B-21230</td><td></td>

<td>11. E. coli P 5-4</td><td>no. access NRRL B-21059</td><td></td>

<td>12. E. coli P 3-12</td><td>no. access NRRL B-21061</td><td> 1405</td>

<td>13. Bacillus cereus AB78</td><td>no. access NRRL B-21058</td><td></td>

<td>14. Bacillus thuringiensis AB6</td><td>no. access NRRL B-21060</td><td></td>

RO 117111 Bl

List of pesticide protein sequences (1) General information:

(1) Owner: CIBA-GEIGY AG, CH-4OO2 Klybeckstrasse 191, Basel, Switzerland (A) Inventors: Gregory W. Warren, USA; Michael G. Koziel, USA; Martha A. Mullins, USA; Gordon J. Nye, USA; Brian Carr, USA; Nalini Manaj Desai, USA and N. Kristy Kostichka, USA.

(ii) Title of the invention: New pesticide proteins and varieties (iii) Number of sequences: 18 (vi) Date of priority of the application:

(A) No. Application: US O8 / O37O57; (B) Date of filing: March 25, 1993 (2) Information for SEQ ID NO: 1:

(i) sequence characteristics:

(a) length: 6106 base pairs (b) type: nucleic acid (c) winding: simple (d) topology: linear (ii) molecule type: DNA (genomic) (vi) original source:

(a) organism: Bacillus cereus (b) variety: AB78 (c) individual isolate: NRRL B-21058 (ix) characteristics:

(a) name / key: CDS (b) location: 1082 ... 1810 (d) other information: / product = "VIP-2" / label = orf-1 (ix) characteristics:

(a) name / key: CDS (b) location: 1925 ... 2470 (d) other information: / product = 'vip-2 / label = orf-2 (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 1:

ATCGATACAA TGIIGI11 IA CTTAGACCGG TAGTCTCTGT AATTTGTTTA ATGCTATATT 60

CTTTACTTTG ATACATTTTA ATAGCCATTT CAACCTTATC AGTATGTTTT

TGTGGTCTTC120

CTCCTTT111 TCCACGAGCT CTAGCTGCGT TTAATCCTGT TTTGGTACGT

TCGCTAATAA180

TATCTCTTTC TAATTCTGGA ATACTTGCCA TCATTCGAAA GAAGAATTTC CCCATAGCAT 240

TAGAGGTATC AATGTTGTCA TGAATAGAAA TAAAATCTAC ACCTAGCTCT TTGAATTITT 300

CACTTAACTC AATTAGGTGT TTTGTAGAGC GAGAAATTCG ATCAAGTTTG TAAACAACTA

360

RO 117111 Bl

TCTTATCGCCTTTACGTAAT ACTTTTAGCA ACTCTTCGAG TTGAGGGCGC TCTTI A IA 420

TTCCTGTTAT TTTCTCCTGA TATAGCCTTT CTACACCATA TTGTTGCAAA GCATCTATT480 GCATATCGAG ΑΓΙ ΙIGTICTTCTGTGCTGA CACGAGCATA ACCAAAAATC AAAKGGTTT 540

CACTTCCTAT CTAAATATAT CTATTAAAAT AGCACCAAAA ACCTTATTAA ATTAAAATAA

600

GGAACTTTGT TTTTGGATAT GGATTKGGT ACTCAATATG GATGAGTTTT TAACGCTTTT

660

GTTAAAAAAC AAACAAGTGC CATAAACGGT CGI Π II GGG ATGACATAAT AAATAATCTG 720

TTTGATTAAC CTAACCTTGT ATCCTTACAG CCCAGTTTTA TTTGTACTTC AACTGACTGA

780

ATATGAAAAC AACATGAAGG TTTCATAAAA ΠΤΑΤΑΤΑΚ KCCATAACG GATGCTCTAT 840

CTTTAGGTTA TAGTTAAATT ATAAGAAAAA AACAAACGGA GGGAGTGAAA

AAAAGCATCT 900

TCTCTATAAT TTTACAGGCT CTTTAATAAG AAGGGGGGAG ATTAGATAAT AAATATGAAT 960

ATCTATCTAT AATTGTTTGC KCTACAATA ACTTATCTAA CTTTCATATA CAACAACAAA 1020

ACAGACTAAA TCCAGAKGT ATAKCAKT TCAGKGKC CKTATAAAA TAATTTCATA 1080

ATG AAA AGA ATG GAG GGA AAG KG KT ATG GTG TCA AAA AAA TTA1126

Met Lys Arg Met Glu Gly Lys Leu Phe Met Val Ser Lys Lys Leu 15 1015

CAA GTA GTT ACT AAA ACT GTA TTG CTT AGT ACA GTT TTC TCT ATA TCT 1174

Gin Val Val Thr Lys Thr Val Leu Leu Ser Thr Val Phe Ser lle Ser

2530

TTA TTA AAT AAT GAA GTG ATA AAA GCT GAA CAA TTA AAT ΑΤΑ AAT TCT 1222

Leu Leu Asn Asn Glu Val lle Lys Ala Glu Gin Leu Asn lle Asn Ser

4045

CAA AGT AAA TAT ACT AAC KG CAA AAT CTA AAA ATC ACT GAC AAG GTA 1270

Gin Ser Lys Tyr Thr Asn Leu Gin Asn Leu Lys lle Thr Asp Lys Val

5560

GAG GAT TTT AAA GAA GAT AAG GAA AAA GCG AAA GAA TGG GGG AAA GAA 1318

Glu Asp Phe Lys Glu Asp Lys Glu Lys Ala Lys Glu Trp Gly Lys Glu

70 75

AAA GAA AAA GAG TGG AAA CTA ACT GCT ACT GAA AAA GGA AAA ATG AAT 1366

Lys Glu Lys Glu Trp Lys Leu Thr Ala Thr Glu Lys Gly Lys Met Asn

85 90 95

AAT KT KA GAT AAT AAA AAT GAT ATA NAG ACA AAT TAT AAA GAA AK 1414

Asn Phe Leu Asp Asn Lys Asn Asp lle Xaa Thr Asn Tyr Lys Glu lle

100 105 110

1455

1460

1465

1470

1475

1480

1485

1490

1495

RO 117111 Bl

1462

1510

1558

1606

1654

1702

1750

1798

ACT TTT TCT ATG GCA GGC TCA TTT GAA GAT GAA ATA AAA GAT TTA AAA

Thr Phe Ser Met Ala Gly Ser Phe Glu Asp Glu Ile Lys Asp Leu Lys

115 120125

GAA ATT GAT AAG ATG TTT GAT AAA ACC AAT CTA TCA AAT TCT ATT ATC

Glu Hair Asp Lys Met Phe Asp Lys Thr Asn Leu Ser Asn Ser Hair Hair

130 135140

ACC TAT AAA AAT GTG GAA CCG ACA ACA ATT GGA TTT AAT AAA TCT TTA

Thr Tyr Lys Asn Val Glu Pro Thr Thr Ile Gly Phe Asn Lys Ser Leu

145 150155

ACA GAA GGT AAT ACG ATT AAT TCT GAT GCA ATG GCA CAG TTT AAA GAA

Thr Glu Gly Asn Thr Ile Asn Ser Asp Ala Met Ala Gin Phe Lys Glu

160 165 170175

CAA TTT TTA GAT AGG GAT ATT AAG TTT GAT AGT TAT CTA GAT ACG CAT

Gin Phe Leu Asp Arg Asp Ile Lys Phe Asp Ser Tyr Leu Asp Thr His

180 185190

TTA ACT GCT CAA CAA GTT TCC AGT AAA GAA AGA GTT ATT TTG AAG GTT

Leu Thr Ala Gin Gin Val Ser Ser Lys Glu Arg Val Ile Leu Lys Val

195 200205

ACG GTT CCG AGT GGG AAA GGT TCT ACT ACT CCA ACA AAA GCA GGT GTC

Thr Val Pro Ser Gly Lys Gly Ser Thr Thr Pro Thr Lys Ala Gly Val

210 215220

ATT TTA AAT AAT AGT GAA TAC AAA ATG CTC ATT GAT AAT GGG TAT ATG

Hair Leu Asn Asn Ser Glu Tyr Lys Met Leu Hair Asp Asn Gly Tyr Met

225 230235

GTC CAT GTA GAT TAAGGTATCA AAAGTGGTGA AAAAAGGGGG TGGAGTGCCT

Val His Val Asp

240

TACAAATTGA AGGGACTTTA AAAAAGAGTC TTGACTTTAA AAATGATATA AATGCTGAAG 1910

CGCATAGCTG GGGT ATG AAG AAT TAT GAA GAG TGG GCT AAA GAT TTA ACC 1960

Met Lys Asn Tyr Glu Glu Trp Ala Lys Asp Leu Thr

510

GAT TCG CAA AGG GAA GCT TTA GAT GGG TAT GCT AGG CAA GAT TAT AAA

Asp Ser Gin Arg Glu Ala Leu Asp Gly Tyr Ala Arg Gin Asp Tyr Lys

2025

GAA ATC AAT AAT TAT TTA AGA AAT CAA GGC GGA AGT GGA AAT GAA AAA

Glu Hair Asn Asn Tyr Leu Arg Asn Gin Gly Gly Ser Gly Asn Glu Lys

3540

CTA GAT GCT CAA ATA AAA AAT ATT TCT GAT GCT TTA GGG AAG AAA CCA

Leu Asp Ala Gin Hair Lys Asn Ile Ser Asp Ala Leu Gly Lys Lys Pro

50 5560

ATA CCG GAA AAT ACT ACT GTG TAT AGA TGG TGT GGC ATG CCG GAA TTT

Hair Pro Glu Asn Hair Thr Val Tyr Arg Trp Cys Gly Met Pro Glu Phe

7075

1850

2008

2056

2104

2152

RO 117111 Bl

GGT TAT CAA ATT AGT GAT CCG TTA CCT TCT TTA AAA GAT TTT GAA GAA

Gly Tyr Gin Ile Ser Asp Pro Leu Pro Ser Leu Lys Asp Phe Glu Glu

85 90

CAA TTT TTA AAT ACA ATC AAA GAA GAC AAA GGA TAT ATG AGT ACA AGC

Gin Phe Leu Asn Thr Ile Lys Glu Asp Lys Gly Tyr Met Ser Thr Ser

100 105

TTA TCG AGT GAA CGT CTT GCA GCT TTT GGA TCT AGA AAA ATT ATA TTA

2200

2248

2296

1545

1550

Leu Ser Ser Glu Arg Leu Ala Ala Phe Gly Ser Arg Lys Ile Ile Leu

110 115120

CGA TTA CAA GTT CCG AAA GGA AGT ACG GGT GCG TAT TTA AGT GCC ATT 2344

Arg Leu Gin Val Pro Lys Gly Ser Thr Gly Ala Tyr Leu Ser Ala Hair

125 130 135140

GGT GGA TTT GCA AGT GAA AAA GAG ATC CTACTT GAT AAA GAT AGT AAA 2392

Gly Gly Phe Ala Ser Glu Lys Glu Ile Leu Leu Asp Lys Asp Ser Lys

145 150155

1555

TAT CAT ACT GAT AAA GTA ACA GAG GTA ACT ATT AAA GGT GTT AAG CGA 2440

1560

Tyr His Hair Asp Lys Val Thr Glu Val Ile Hair Lys Gly Val Lys Arg

160 165 170

TAT GTA GTG GAT GCA ACA TTA TTA ACA AAT TAAGGAGATG AAAAATATGA 2490

Tyr Val Val Asp Ala Thr Leu Leu Thr Asn

175 180

AGAAAAAGTT AGCAAGTGTT GTAACGTGTA CGTTATTAGC TCCTATGTTT TTGAATGGAA

1565

2550

ATGTGAATGC TGTTTACGCA GACAGCAAAA CAAATCAAAT TTCTACAACA

CAGAAAAATC 2610

AACAGAAAGA GATGGACCGA AAAGGATTAC TTGGGTATTA TTTCAAAGGA

AAAGATTTTA 2670

GTAATCTTAC TATGTTTGCA CCGACACGTG ATAGTACTCT TATTTATGAT CAACAAACAG

1570

2730

CAAATAAACT ATTAGATAAA AAACAACAAG AATATCAGTC TATTCGTTGG ATTGGTTTGA

2790

TTCAGAGTAA AGAAACGGGA GATTTCACAT TTAACTTATC TGAGGATGAA CAGGCAATTA 2850

TAGAAATCAA TGGGAAAATT ATTTCTAATA AAGGGAAAGA AAAGCAAGTT GTCCATTTAG

2910

AAAAAGGAAA ATTAGTTCCA ATCAAAATAG AGTATCAATC AGATACAAAA TTTAATATTG

1575

1580

2970

ACAGTAAAAC ATTTAAAGAA CTTAAATTAT TTAAAATAGA TAGTCAAAAC CAACCCCAGC

3030

AAGTCCAGCA AGATGAACTG AGAAATCCTG AATTTAACAA GAAAGAATCA

CAGGAATTCT 3090

TAGCGAAACC ATCGAAAATA AATCTTTTCA CTCAAMAAAT GAAAAGGGAA

ATTGATGAAG 3150

ACACGGATAC GGATGGGGAC TCTATTCCTG ACCTTTGGGA AGAAAATGGG TATACGATTC 3210

AMAATAGAAT CGCTGTAAAG TGGGACGATT CTCTAGCAAG TAAAGGGTAT

1585

1590

ACGAAATTTG 3270

RO 117111 Bl

TTTCAAATCC ACTAGAAAGT CACACAGTTG GTGATCCTTA TACAGATTAT GAAAAGGCAG

3330

CAAGAGATCT AGATTTGTCA AATGCAAAGG AAACGTTTAA CCCATTGGTA GCTGCTTTTC 3390

CAAGTGTGAA TGTTAGTATG GAAAAGGTGA TATTATCACC AAATGAAAAT TTATCCAATA 3450

GTGTAGAGTC TCATTCATCC ACGAATTGGT CTTATACAAA TACAGAAGGT GCTTCTGTTG 3510

AAGCGGGGAT TGGACCAAAA GGTATTTCGT TCGGAGTTAG CGTAAACTAT CAACACTCTG 3570

AAACAGTTGC ACAAGAATGG GGAACATCTA CAGGAAATAC TTCGCAATTC

AATACGGCTT 3630

CAGCGGGATA TTTAAATGCA AATGTTCGAT ATAACAATGT AGGAACTGGT GCCATCTACG 3690

ATGTAAAACC TACAACAAGT TTTGTATTAA ATAACGATAC TATCGCAACT ATTACGGCGA 3750

AATCTAATTC TACAGCCTTA AATATATCTC CTGGAGAAAG TTACCCGAAA AAAGGACAAA 3810

ATGGAATCGC AATAACATCA ATGGATGATT TTAATTCCCA TCCGATTACA TTAAATAAAA 3870

AACAAGTAGA TAATCTGCTA AATAATAAAC CTATGATGTT GGAAACAAAC CAAACAGATG 3930

GTGTTTATAA GATAAAAGAT ACACATGGAA ATATAGTAAC TGGCGGAGAA

TGGAATGGTG 3990

TCATACAACA AATCAAGGCT AAAACAGCGT CTATTATTGT GGATGATGGG GAACGTGTAG 4050

CAGAAAAACG TGTAGCGGCA AAAGATTATG AAAATCCAGA AGATAAAACA

CCGTCTTTAA 4110

CTTTAAAAGA TGCCCTGAAG CTTTCATATC CAGATGAAAT AAAAGAAATA GAGGGATTAT 4170

TATATTATAA AAACAAACCG ATATACGAAT CGAGCGTTAT GACTTACTTA GATGAAAATA 4230

CAGCAAAAGA AGTGACCAAA CAATTAAATG ATACCACTGG GAAATTTAAA

GATGTAAGTC 4290

ATTTATATGA TGTAAAACTG ACTCCAAAAA TGAATGTTAC AATCAAATTG TCTATACTTT 4350

ATGATAATGC TGAGTCTAAT GATAACTCAA TTGGTAAATG GACAAACACA AATATTGTTT 4410

CAGGTGGAAA TAACGGAAAA AAACAATATT CTTCTAATAA TCCGGATGCT AATTTGACAT 4470

TAAATACAGA TGCTCAAGAA AAATTAAATA AAAATCGTGA CTATTATATA ACTTTATATA 9530

TGAAGTCAGA AAAAAACACA CAATGTGAGA TTACTATAGA TGGGGAGATT

TATCCGATCA 4590

CTACAAAAAC AGTGAATGTG AATAAAGACA ATTACAAAAG ATTAGATATT ATAGCTCATA

4650

1640

RO 117111 Bl

ATATAAAAAG TAATCCAATT TCTTCACTTC ATATTAAAAC GAATGATGAA ATTAACTTTAT

4710

TTTGGGATGA TATTTCTATA ACAGATGTAG CATCAATAAA ACCGGAAAAT TTAACAGATT 4770

CAGAAATTAA ACAGATTTAT AGTAGGTATG GTATTAAGTT AGAAGATGGA ATCCTTATTG 4830 ataaaaaagg tgggattcat tatggtgaat ttattaatga agctagtttt aatattgaac

4890

CATTGCCAAA TTATGTGACC AAATATGAAG TTACTTATAG TAGTGAGTTA GGACCAAACG 9950

TGAGTGACAC ACTTGAAAGT GATAAAATTT ACAAGGATGG GACAATTAAA TTTGATTTTA 5010

CCAAATATAG TAAAAATGAA CAAGGATTAT TTTATGACAG TGGATTAAAT TGGGACTTTA 5070

AAATTAATGC TATTACTTAT GATGGTAAAG AGATGAATGT TTTTCATAGA TATAATAAAT 5130

TGGTGCTAAA GATAGTGTAA AAGTTAATAT ACTGTAGGAT 5190 TCTATGAAGC

TGTAATAAAA GTAATGG AAT TGATATCGTA CTTTGGAGTG GGGGATACTT TGTAAATAGT 5250

TCTATCAGAA ACATTAGACT AAGAAAAGTT ACTACCCCCA CTTGAAAATG AAGATTCAAC 5310

TGATTACAAA CAACCTGTTA AATATTATAA GGTTTTAACA AAATATTAAA CTCTTTATGT 5370

TAATACTGTA ATATAAAGAG TTTAATTGTA TTCAAATGAA GCTTTCCCAC AAAATTAGAC 5430

TGATTATCTA ATGAAATAAT CAGTCTAATT TTGTAGAACA GGTCTGGTAT TATTGTACGT 5490

GGTCACTAAA AGATATCTAA TATTATTGGG CAAGGCGTTC CATGATTGAA TCCTCGAATG 5550

TCTTGCCCTT TTCATTTATT TAAGAAGGAT TGTGGAGAAA nATGGTTTA GATAATGAAG 5610

AAAGACTTCA CTTCTAATH TTGATGTTAA ATAAATCAAA ATTTGGCGAT TCACATTGTT

5670

TAATCCACTG ATAAAACATA CTGGAGTGTT CTTAAAAAAT CAGUI11111 CTTTATAAAA 5730

TTTTGCTTAG CGTACGAAAT TCGTGTTTTG TTGGTGGGAC CCCATGCCCA TCAACTTAAG 5790

AGTAAATTAG TAATGAACTT TCGTTCATCT GGATTAAAAT AACCTCAAAT TAGGACATGT 5850

TTTTAAAAAT AAGCAGACCA AATAAGCCTA GAATAGGTAT CATTTTTAAA AATTATGCTG 5910

Five 11IG TTTTCCAAAT CCATTATACT CATAAGCAAC ACCCATAATG TCAAAGACTG 5970

TTTTTGTCTC ATATCGATAA GCTTGATATC GAATTCCTGC AGCCCGGGGG ATCCACTAGT

6030

1645

1650

1655

1660

1665

1670

1675

1680

RO 117111 Bl

TCTAGAGCGG CCGCCACCGC GGTGGAGCTC CAGCTTTTGT TCCCTTTAGT GAGGGTTAAG

6090

TTCGAGCTTG TCGTGG

6106 (2) Information for SEQ ID NO: 2:

(i) sequence characteristics:

(a) length: 243 amino acids (b) type: amino acid (d) topology: linear (ii) molecule type: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 2:

Met Lys Arg Met Glu Gly Lys Leu Phe Met Val Ser Lys Lys Leu Gin

1015

Val Val Thr Lys Thr Val Leu Leu Ser Thr Val Phe Ser lle Ser Leu

2530

Leu Asn Asn Glu Val lle Lys Ala Glu Gin Leu Asn lle Asn Ser Gin

4045

Ser Lys Tyr Thr Asn Leu Gin Asn Leu Lys lle Thr Asp Lys Val Glu

5560

Asp Phe Lys Glu Asp Lys Glu Lys Ala Lys Glu Trp Gly Lys Glu Lys

70 7580

Glu Lys Glu Trp Lys Leu Thr Ala Thr Glu Lys Gly Lys Met Asn Asn

9095

Phe Leu Asp Asn Lys Asn Asp lle Xaa Thr Asn Tyr Lys Glu lle Thr

100 105110

Phe Ser Met Ala Gly Ser Phe Glu Asp Glu lle Lys Asp Leu Lys Glu

115 120125 le Asp Lys Met Phe Asp Lys Thr Asn Leu Ser Asn Ser le Le Thr

130 135140

Tyr Lys Asn Val Glu Pro Thr Thr lle Gly Phe Asn Lys Ser Leu Thr

145 150 155160

Glu Gly Asn Thr lle Asn Ser Asp Ala Met Ala Gin Phe Lys Glu Gin

165 170175

Phe Leu Asp Arg Asp lle Lys Phe Asp Ser Tyr Leu Asp Thr His Leu

180 185190

Thr Ala Gin Gin Val Ser Ser Lys Glu Arg Val lle Leu Lys Val Thr

195 200205

Val Pro Ser Gly Lys Gly Ser Thr Thr Pro Thr Lys Ala G1y Va1 lle

210 215220

Leu Asn Asn Ser Glu Tyr Lys Met Leu lle Asp Asn Gly Tyr Met Val

225 230 235240

His Val

RO 117111 Bl (2) Information for SEQ ID NO: 3:

(i) sequence characteristics:

(a) length: 182 amino acids (b) type: amino acid (D) topology: linear (ii) molecule type: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO; 3:

Met Lys Asn Tyr Glu Glu Trp Ala Lys Asp Leu Thr Asp Ser Gin Arg

5 1015

Glu Ala Leu Asp Gly Tyr Ala Arg Gin Asp Tyr Lys Glu lle Asn Asn

2530

Tyr Leu Arg Asn Gin Gly Gly Ser Gly Asn Glu Lys Leu Asp Ala Gin

4045 le Lys Asn lle Ser Asp Ala Leu Gly Lys Lys Pro le Pro Glu Asn

5560 lle Thr Val Tyr Arg Trp Cys Gly Met Pro Glu Phe Gly Tyr Gin lle

70 7580

Ser Asp Pro Leu Pro Ser Leu Lys Asp Phe Glu Glu Gin Phe Leu Asn

9095

Thr lle Lys Glu Asp Lys Gly Tyr Met Ser Thr Ser Leu Ser Ser Glu 100 105110

Arg Leu Ala Ala Phe Gly Ser Arg Lys leu Arg Leu Gin Val

115 120125

Pro Lys Gly Ser Thr Gly Ala Tyr Leu Ser Ala lle Gly Gly Phe Ala

130 135140

Ser Gys Lys Glu Leu Leu Leu Asp Lys Asp Ser Lys Tyr His lle Asp 145 150 155160

Lys Val Thr Glu Val lle lle Lys Gly Val Lys Arg Tyr Val Val Asp

165 170175

Ala Thr Leu Leu Thr Asn

180 (2) Information for SEQ ID NO: 4:

(i) sequence characteristics:

(a) length: 2655 base pairs (b) type: nucleic acid (c) winding: simple (d) topology: linear (ii) molecule type: DNA (genomic) (iii) hypothetical: no

1730

1735

1740

1745

1750

1755

1760

1765 (iii) anti-sense: no

1770

RO 117111 Bl (vi) original source:

(a) organism: Bacillus cereus (b) variety: AB78 (c) isolated individually: NRRL B-21O58 (ix) characteristics:

(a) name / key: CDS (b) location: 1 ... 2652 (c) identification method: experimental (d) other information / product: = "VIP-1 protein, 10O kDa" / evidence = experimental ( xi) DESCRIPTION OF THE SEQUENCE: SEQ ID NO: 4:

ATG AAA AAT ATG AAG AAA AAG TTA GCA AGT GTT GTA ACG TGT ACG TTA 48

Met Lys Asn Met Lys Lys Lys Leu Ala Ser Val Val Thr Cys Thr Leu

5 1015

TTA GCT CCT ATG TTT TTG AAT GGA AAT GTG AAT GCT GTT TAC GCA GAC 96

Leu Ala Pro Met Phe Leu Asn Gly Asn Val Asn Ala Val Tyr Ala Asp

2530

AGC AAA ACA AAT CAA ATT TCT ACA ACA CAG AAA AAT CAA CAG AAA GAG 144

Ser Lys Thr Asn Gin lle Ser Thr Thr Gin Lys Asn Gin Gin Lys Glu

4045

ATG GAC CGA AAA GGA TTA CTT GGG TAT TAT TTC AAA GGA AAA GAT TTT 192

Met Asp Arg Lys Gly Leu Leu Gly Tyr Tyr Phe Lys Gly Lys Asp Phe

5560

AGT AAT CTT ACT ATG TTT GCA CCG ACA CGT GAT AGT ACT CH ATT TAT 240

Ser Asn Leu Thr Met Phe Ala Pro Thr Arg Asp Ser Thr Leu lle Tyr

70 7580

GAT CAA CAA ACA GCA AAT AAA CTA TTA GAT AAA AAA CAA CAA GAA TAT 288

Asp Gin Gin Thr Ala Asn Lys Leu Leu Asp Lys Lys Gin Gin Glu Tyr

9095

CAG TCT ATT CGT TGG ATT GGT TTG ATT CAG AGT AAA GAA ACG GGA GAT 336

Gin Ser lle Arg Trp lle Gly Leu lle Gin Ser Lys Glu Thr Gly Asp

100 105110

TTC ACA TTT AAC TTA TCT GAG GAT GAA CAG GCA ATT ATA GAA ATC AAT 384

Phe Thr Phe Asn Leu Ser Glu Asp Glu Gin Allah li Glu li Asn

115 120125

GGG AAA ATT ATT TCT AAT AAA GGG AAA GAA AAG CAA GTT GTC CAT TTA 432

Gly Lys Him Ser Asn Lys Gly Lys Glu Lys Gin Val Val His Leu

130 135140

GAA AAA GGA AAA TTA GTT CCA ATC AAA ATA GAG TAT CAA TCA GAT ACA 480

Glu Lys Gly Lys Leu Val Pro lle Lys lle Glu Tyr Gin Ser Asp Thr

145 150 155160

AAA TTT AAT ATT GAC AGT AAA ACA TTT AAA GAA CTT AAA TTA TTT AAA 528

Lys Phe Asn lle Asp Ser Lys Thr Phe Lys Glu Leu Lys Leu Phe Lys

165 170175

RO 117111 Bl

ΑΤΑ GAT AGT CAA AAC CAA CCC CAG CAA GTC CAG CAA GAT GAA CTG AGA 576 lle Asp Ser Gin Asn Gin Pro Gin Gin Val Gin Gin Asp Glu Leu Arg 180 185190

AAT CCT GAA TTT AAC AAG AAA GAA TCA CAG GAA TTC TTA GCG AAA CCA

Asn Pro Glu Phe Asn Lys Lys Glu Ser Gin Glu Phe Leu Ala Lys Pro

195 200205

TCG AAA ATA AAT CTT TTC ACT CAA MAA ATG AAA AGG GAA ATT GAT GAA

Ser Lys lle Asn Leu Phe Thr Gin Xaa Met Lys Arg Glu lle Asp Glu

210 215220

GAC ACG GAT ACG GAT GGG GAC TCT ATT CCT GAC CTT TGG GAA GAA AAT

Asp Thr Asp Thr Asp Gly Asp Ser lle Pro Asp Leu Trp Glu Glu Asn

225 230 235240

GGG TAT ACG ATT CAM AAT AGA ATC GCT GTA AAG TGG GAC GAT TCT CTA Gly Tyr Thr lle Xaa Asn Arg lle Ala Val Lys Trp Asp Asp Ser Leu

245 250255

GCA AGT AAA GGG TAT ACG AAA TTT GTT TCA AAT CCA CTA GAA AGT CAC

Ala Ser Lys Gly Tyr Thr Lys Phe Val Ser Asn Pro Leu Glu Ser His

260 265270

ACA GTT GGT GAT CCT TAT ACA GAT TAT GAA AAG GCA GCA AGA GAT CTA

Thr Val Gly Asp Pro Tyr Thr Asp Tyr Glu Lys Ala Ala Arg Asp Leu

275 280285

GAT TTG TCA AAT GCA AAG GAA ACG TTT AAC CCA TTG GTA GCT GCT TTT

Asp Leu Ser Asn Ala Lys Glu Thr Phe Asn Pro Leu Val Ala Ala Phe

290 295300

CCA AGT GTG AAT GTT AGT ATG GAA AAG GTG ATA TTA TCA CCA AAT GAA

Pro Ser Val Asn Val Ser Met Glu Lys Val lle Leu Ser Pro Asn Glu

305 310 315320

AAT TTA TCC AAT AGT GTA GAG TCT CAT TCA TCC ACG AAT TGG TCT TAT Asn Leu Ser Asn Ser Val Glu Ser His Ser Ser Thr Asn Trp Ser Tyr 325 330335

ACA AAT ACA GAA GGT GCT TCT GTT GAA GCG GGG ATT GGA CCA AAA GGT

Thr Asn Thr Glu Gly Ala Ser Val Glu Ala Gly lle Gly Pro Lys Gly

340 345350

ATT TCG TTC GGA GTT AGC GTA AAC TAT CAA CAC TCT GAA ACA GTT GCA lle Ser Phe Gly Val Ser Val Asn Tyr Gin His Ser Glu Thr Val Ala

355 360365

CAA GAA TGG GGA ACA TCT ACA GGA AAT ACT TCG CAA TTC AAT ACG GCT

Gin Glu Trp Gly Thr Ser Thr Gly Asn Thr Ser Gin Phe Asn Thr Ala

370 375 380

TCA GCG GGA TAT TTA AAT GCA AAT GTT CGA TAT AAC AAT GTA GGA ACT

Ser Ala Gly Tyr Leu Asn Ala Asn Val Arg Tyr Asn Asn Val Gly Thr

385 390 395 400

GGT GCC ATC TAC GAT GTA AAA CCT ACA ACA AGT TTT GTA TTA AAT AAC

Gly Ala lle Tyr Asp Val Lys Pro Thr Thr Ser Phe Val Leu Asn Asn

405 410 415

1820

624

672

720

768

816

864

912

960

1008

1056

1104

1152

1200

1825

1830

1835

1840

1845

1850

1855

1860

1248

RO 117111 Bl

GAT ACT ATC GCA ACT ATT ACG GCG AAA TCT AAT TCT ACA GCC TTA AAT Asp Thr Ile Ala Thr Ile Thr Ala Lys Ser Asn Ser Thr Ala Leu Asn

420 425430

ATA TCT CCT GGA GAA AGT TAC CCG AAA AAA GGA CAA AAT GGA ATC GCA Ile Ser Pro Gly Glu Ser Tyr Pro Lys Lys Gly Gin Asn Gly Ile Ala

435 440445

ATA ACA TCA ATG GAT GAT TTT AAT TCC CAT CCG ATT ACA TTA AAT AAA Ile Thr Ser Met Asp Asp Phe Asn Ser His Pro Ile Thr Leu Asn Lys

450 455460

AAA CAA GTA GAT AAT CTG CTA AAT AAT AAA CCT ATG ATG TTG GAA ACA Lys Gin Val Asp Asn Leu Leu Asn Asn Lys Pro Met Met Leu Glu Thr 465 470 475480

AAC CAA ACA GAT GGT GTT TAT AAG ATA AAA GAT ACA CAT GGA AAT ATA Asn Gin Thr Asp Gly Val Tyr Lys Ile Lys Asp Thr His Gly Asn Ile

485 430495

GTA ACT GGC GGA GAA TGG AAT GGT GTC ATA CAA CAA ATC AAG GCT AAA Val Thr Gly Gly Glu Trp Asn Gly Val ile Gin Gin Ile Lys Ala Lys

500 505510

ACA GCG TCT ATT ATT GTG GAT GAT GGG GAA CGT GTA GCA GAA AAA CGT Thr Ala Ser Ile Ile Val Asp Asp Gly Glu Arg Val Ala Glu Lys Arg

515 520525

GTA GCG GCA AAA GAT TAT GAA AAT CCA GAA GAT AAA ACA CCG TCT TTA Val Ala Ala Lys Asp Tyr Glu Asn Pro Glu Asp Lys Thr Pro Ser Leu

530 535540

ACT TTA AAA GAT GCC CTG AAG CTT TCA TAT CCA GAT GAA ATA AAA GAA Thr Leu Lys Asp Ala Leu Lys Leu Ser Tyr Pro Asp Glu Ile Lys Glu 545 550 555560

ATA GAG GGA TTA TTA TAT TAT AAA AAC ZXAA CCG ATA TAC GAA TCG AGC Ile Glu Gly Leu Leu Tyr Tyr Lys Asn Lys Pro Ile Tyr Glu Ser Ser

565 570575

GTT ATG ACT TAC TTA GAT GAA AAT ACA GCA AAA GAA GTG ACC AAA CAA

Val Met Thr Tyr Leu Asp Glu Asn Thr Ala Lys Glu Val Thr Lys Gin

580 585590

TTA AAT GAT ACC ACT GGG AAA TTT AAA GAT GTA AGT CAT TTA TAT GAT Leu Asn Asp Thr Thr Gly Lys Phe Lys Asp Val Ser His Leu Tyr Asp

595 600605

GTA AAA CTG ACT CCA AAA ATG AAT GTT ACA ATC AAA TTG TCT ATA CTT Val Lys Leu Thr Pro Lys Met Asn Val Thr Ile Lys Leu Ser Ile Leu

610 615620

TAT GAT AAT GCT GAG TCT AAT GAT AAC TCA ATT GGT AAA TGG ACA AAC Tyr Asp Asn Ala Glu Ser Asn Asp Asn Ser Ile Gly Lys Trp Thr Asn 625 630 635640

ACA AAT ATT GTT TCA GGT GGA AAT AAC GGA AAA AAA CAA TAT TCT TCT Thr Asn Ile Val Ser Gly Gly Asn Asn Gly Lys Lys Gys Tyr Ser Ser

645 650655

1296

1344

1392

1440

1488

1536

1584

1632

1680

1728

1776

1824

1-872

1920

1968

RO 117111 Bl

2016

1910

2064

AAT AAT CCG GAT GCT AAT TTG ACA TTA AAT ACA GAT GCT CAA GAA AAA

Asn Asn Pro Asp Ala Asn Leu Thr Leu Asn Thr Asp Ala Gin Glu Lys

660 665 670

TTA AAT AAA AAT CGT GAC TAT TAT ATA AGT TTA TAT ATG AAG TCA GAA

Leu Asn Lys Asn Arg Asp Tyr Tyr Ile Ser Leu Tyr Met Lys Ser Glu

675 680685

AAA AAC ACA CAA TGT GAG ATT ACT ATA GAT GGG GAG ATT TAT CCG ATC Lys Asn Thr Gin Cys Glu Ile Thr Ile Asp Gly Glu Ile Tyr Pro Ile

690 695700

ACT ACA AAA ACA GTG AAT GTG AAT AAA GAC AAT TAC AAA AGA TTA GAT Thr Thr Lys Thr Val Asn Val Asn Lys Asp Asn Tyr Lys Arg Leu Asp

705 710 715720

ACT ATA GCT CAT AAT ATA AAA AGT AAT CCA ATT TCT TCA CTT CAT ATT Ile Ile Ala His Asn Ile Lys Ser Asn Pro Ile Ser Ser Leu His Ile

725 730735

AAA ACG AAT GAT GAA ATA ACT TTA ΤΓΤ TGG GAT GAT ATT TCT ATA ACA Lys Thr Asn Asp Glu Ile Thr Leu Phe Trp Asp Asp Ile Ser Ile Thr

740 745750

GAT GTA GCA TCA ATA AAA CCG GAA AAT TTA ACA GAT TCA GAA ATT AAA Asp Val Ala Ser Ile Lys Pro Glu Asn Leu Thr Asp Ser Glu Ile Lys

755 760765

CAG ATT TAT AGT AGG TAT GGT ATT AAG TTA GAA GAT GGA ATC CTT ATT Gin Ile Tyr Ser Arg Tyr Gly Ile Lys Leu Glu Asp Gly Ile Leu Ile

770 775780

GAT AAA AAA GGT GGG ATT CAT TAT GGT GAA TTT ATT AAT GAA GCT AGT Asp Lys Lys Gly Gly Ile His Tyr Gly Glu Phe Ile Asn Glu Ala Ser

785 790 795800

TTT AAT ATT GAA CCA TTG CCA AAT TAT GTG ACC AAA TAT GAA GTT ACT Phe Asn Ile Glu Pro Leu Pro Asn Tyr Val Thr Lys Tyr Glu Val Thr

805 810815

TAT AGT AGT GAG TTA GGA CCA AAC GTG AGT GAC ACA CTT GAA AGT GAT Tyr Ser Ser Glu Leu Gly Pro Asn Val Ser Asp Thr Leu Glu Ser Asp

820 825830

AAA ATT TAC AAG GAT GGG ACA ATT AAA TTT GAT TTT ACC AAA TAT AGT Lys Ile Tyr Lys Asp Gly Thr Ile Lys Phe Asp Phe Thr Lys Tyr Ser

835 840845

AAA AAT GAA CAA GGA TTA TTT TAT GAC AGT GGA TTA AAT TGG GAC TTT Lys Asn Glu Gin Gly Leu Phe Tyr Asp Ser Gly Leu Asn Trp Asp Phe

850 855 860

AAA ATT AAT GCT ATT ACT TAT GAT GGT AAA GAG ATG AAT GTT TTT CAT

Lys Hair Asn Ala Hair Thr Tyr Asp Gly Lys Glu Met Asn Val Phe His

865 870 875 880

AGA TAT AAT AAA TAG

Arg Tyr Asn Lys

2112

2160

2208

2256

2304

2352

2400

2448

2496

2544

2592

2640

1915

1920

1925

1930

1935

1940

1945

1950

2655

RO 117111 Bl (2) Information for SEQ ID NO: 5:

(i) sequence characteristics:

(a) length: 884 amino acids (b) type: amino acid (d) topology: linear (ii) molecule type: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 5:

Met Lys Asn Met Lys Lys Lys Leu Ala Ser Val Val Thr Cys Thr Leu 15 1015

Leu Ala Pro Met Phe Leu Asn Gly Asn Val Asn Ala Val Tyr Ala Asp 20 2530

Ser Lys Thr Asn Gin lle Ser Thr Thr Gin Lys Asn Gin Gin Lys Glu

4045

Met Asp Arg Lys Gly Leu Leu Gly Tyr Tyr Phe Lys Gly Lys Asp Phe 50 5560

Ser Asn Leu Thr Met Phe Ala Pro Thr Arg Asp Ser Thr Leu lle Tyr 65 70 7580

Asp Gin Gin Thr Ala Asn Lys Leu Leu Asp Lys Lys Gin Gin Glu Tyr 85 9095

Gin Ser lle Arg Trp lle Gly Leu lle Gin Ser Lys Glu Thr Gly Asp 100 105110

Phe Thr Phe Asn Leu Ser Glu Asp Glu Gin Ala li Glu lle Asn 115 120125

Gly Lys lle lle Ser Asn Lys Gly Lys Glu Lys Gin Val Val His Leu 130 135140

Glu Lys Gly Lys Leu Val Pro lle Lys lle Glu Tyr Gin Ser Asp Thr 145 150 155160

Lys Phe Asn lle Asp Ser Lys Thr Phe Lys Glu Leu Lys Leu Phe Lys 165 170175 lle Asp Ser Gin Asn Gin Pro Gin Gin Val Gin Gin Asp Glu Leu Arg 180 185190

Asn Pro Glu Phe Asn Lys Lys Glu Ser Gin Glu Phe Leu Ala Lys Pro 195 200205

Ser Lys lle Asn Leu Phe Thr Gin Xaa Met Lys Arg Glu lle Asp Glu 210 215220

Asp Thr Asp Thr Asp Gly Asp Ser lle Pro Asp Leu Trp Glu Glu Asn 225 230 235240

Gly Tyr Thr lle Xaa Asn Argle Ala Val Lys Trp Asp Asp Ser Leu 245 250255

A1 a Ser Lys Gly Tyr Thr Lys Phe Val Ser Asn Pro Leu Glu Ser His 260 265270

Thr Val Gly Asp Pro Tyr Thr Asp Tyr Glu Lys Ala Ala Arg Asp Leu

275 280285

RO 117111 Bl

Asp Leu Ser Asn Ala Lys Glu Thr Phe Asn Pro Leu Val Ala Ala Phe 290 295300

Pro Ser Val Asn Val SerMet Glu Lys Val Ile Leu Ser Pro Asn Glu 305 310 315320

Asn Leu Ser Asn Ser Val Glu Ser His Ser Ser Thr Asn Trp Ser Tyr 325 330335

Thr Asn Thr Glu Gly Ala Ser Val Glu Ala Gly Hair Gly Pro Lys Gly

340 345350

Ile Ser Phe Gly Val Ser Val Asn Tyr Gin His Ser Glu Thr Val Ala 355 360365

Gin Glu Trp Gly Thr Ser Thr Gly Asn Thr Ser Gin Phe Asn Thr Ala 370 375380

Ser Ala Gly Tyr Leu Asn Ala Asn Val Arg Tyr Asn Asn Val Gly Thr 385 390 395400

Gly Ala Ile Tyr Asp Val Lys Pro Thr Thr Ser Phe Val Leu Asn Asn

405 410415

Asp Thr Ile Ala Thr Ile Thr Ala Lys Ser Asn Ser Thr Ala Leu Asn 420 425430

Hair Ser Pro Gly Glu Ser Tyr Pro Lys Lys Gly Gin Asn Gly Ile Ala 435 440445

Hair Thr Ser Met Asp Asp Phe Asn Ser His Pro Hair Thr Leu Asn Lys 450 455460

Lys Gin Val Asp Asn Leu Leu Asn Asn Lys Pro Met Met Leu Glu Thr 465 970 975480

Asn Gin Thr Asp Gly Val Tyr Lys Hair Lys Asp Thr His Gly Asn Hair

485 490495

Val Thr Gly Gly Glu Trp Asn Gly Val Hair Gin Gin Hair Lys Ala Lys

500 505510

Thr Ala Ser Ile Ile Val Asp Asp Gly Glu Arg Val Ala Glu Lys Arg 515 520525

Val Ala Ala Lys Asp Tyr Glu Asn Pro Glu Asp Lys Thr Pro Ser Leu 530 535540

Thr Leu Lys Asp Ala Leu Lys Leu Ser Tyr Pro Asp Glu Ile Lys Glu 545 550 555560

Hair Glu Gly Leu Leu Tyr Tyr Lys Asn Lys Pro Hair Tyr Glu Ser Ser

565 570575

Val Met Thr Tyr Leu Asp Glu Asn Thr Ala Lys Glu Val Thr Lys Gin 580 585590

Leu Asn Asp Thr Thr Gly Lys Phe Lys Asp Val Ser His Leu Tyr Asp 595 600605

Val Lys Leu Thr Pro Lys Met Asn Val Thr Ile Lys Leu Ser Ile Leu 610 615620

Tyr Asp Asn Ala Glu Ser Asn Asp Asn Ser Ile Gly Lys Trp Thr Asn 625 630 635640

Thr Asn Ile Val Ser Gly Gly Asn Asn Gly Lys Lys Gin Tyr Ser Ser

645 650655

2000

2005

2010

2015

2020

2025

2030

2035

2040

RO 117111 Bl

Asn Asn Pro Asp Ala Asn Leu Thr Leu Asn Thr Asp Ala Gin Glu Lys

660 665 670

Leu Asn Lys Asn Arg Asp Tyr Tyr Ile Ser Leu Tyr Met Lys Ser Glu

675 680 685

Lys Asn Thr Gin Cys Glu Hair Thr Hair Asp Gly Glu Hair Tyr Pro Hair

690 695700

Thr Thr Lys Thr Val Asn Val Asn Lys Asp Asn Tyr Lys Arg Leu Asp 705 710 715720

Hair Hair Ala His Asn Hair Lys Ser Asn Pro Hair Ser Ser Leu His Hair

725 730735

Lys Thr Asn Asp Glu Ile Thr Leu Phe Trp Asp Asp Ile Ser Ile Thr 740 745750

Asp Val Ala Ser Ile Lys Pro Glu Asn Leu Thr Asp Ser Glu Ile Lys

755 760765

Gin Hair Tyr Ser Arg Tyr Gly Hair Lys Leu Glu Asp Gly Hair Leu Hair

770 775780

Asp Lys Lys Gly Gly Ile His Tyr Gly Glu Phe Ile Asn Glu Ala Ser

785 790 795800

Phe Asn Ile Glu Pro Leu Pro Asn Tyr Val Thr Lys Tyr Glu Val Thr

805 810815

Tyr Ser Ser Glu Leu Gly Pro Asn Val Ser Asp Thr Leu Glu Ser Asp 820 825830

Lys Ile Tyr Lys Asp Gly Thr Ile Lys Phe Asp Phe Thr Lys Tyr Ser 835 840845

Lys Asn Glu Gin Gly Leu Phe Tyr Asp Ser Gly Leu Asn Trp Asp Phe 850 855860

Lys Ile Asn Ala Ile Thr Tyr Asp Gly Lys Glu Met Asn Val Phe His 865 870 875880

ArgTyrAsn Lys (2) Information for SEQ ID NO: 6:

(i) sequence characteristics:

(a) length: 2004 base pairs (b) type: nucleic acid (c) winding: simple (d) topology: linear (ii) molecule type: DNA (genomic) (iii) hypothetical: not (iii) anti-sense : not (vi) original source:

(a) organism: Bacillus cereus (b) variety: AB78 (c) individual isolate: NRRL B-21058

RO 117111 Bl

2090 (ix) characteristics:

(a) name / key: CDS (b) location: 1 ... 2001 (c) identification method: experimental (d) other information: / product = .80 kda VIP-1 protein / / evidence = experimental

2095 (xi) DESCRIPTION OF THE SEQUENCE: SEQ ID NO: 6:

ATG AAA AGG GAA ATT GAT GAA GAC ACG GAT ACG GAT GGG GAC TCT ATT Met Lys Arg Glu lle Asp Glu Asp Thr Asp Thr Asp Gly Asp Ser lle

5 1015

CCT GAC CTT TGG GAA GAA AAT GGG TAT ACG ATT CAM AAT AGA ATC GCT

Pro Asp Leu Trp Glu Glu Asn Gly Tyr Thr lle Xaa Asn Arg lle Ala

2530

GTA AAG TGG GAC GAT TCT CTA GCA AGT AAA GGG TAT ACG AAA TTT GTT

Val Lys Trp Asp Asp Ser Leu Ala Ser Lys Gly Tyr Thr Lys Phe Val

4045

TCA AAT CCA CTA GAA AGT CAC ACA GTT GGT GAT CCT TAT ACA GAT TAT

Ser Asn Pro Leu Glu Ser His Thr Val Gly Asp Pro Tyr Thr Asp Tyr

5560

GAA AAG GCA GCA AGA GAT CTA GAT TTG TCA AAT GCA AAG GAA ACG TTT

Glu Lys Ala Ala Arg Asp Leu Asp Leu Ser Asn Ala Lys Glu Thr Phe

70 7580

AAC CCA TTG GTA GCT GCT TTT CCA AGT GTG AAT GTT AGT ATG GAA AAG Asn Pro Leu Val Ala Ala Phe Pro Ser Val Asn Val Ser Met Glu Lys

9095

GTG ΑΤΑ TTA TCA CCA AAT GAA AAT TTA TCC AAT AGT GTA GAG TCT CAT Val leu Le Pro Ser Asn Glu Asn Leu Ser Asn Ser Val Glu Ser His

100 105110

TCA TCC ACG AAT TGG TCT TAT ACA AAT ACA GAA GGT GCT TCT GTT GAA

Ser Ser Thr Asn Trp Ser Tyr Thr Asn Thr Glu Gly Ala Ser Val Glu

115 120125

GCG GGG ACT GGA CCA AAA GGT ATT TCG TTC GGA GTT AGC GTA AAC TAT

Ala Gly le Gly Pro Lys Gly le Ser Phe Gly Val Ser Val Asn Tyr

130 135140

CAA GAC TCT GAA ACA GTT GCA CAA GAA TGG GGA ACA TCT ACA GGA AAT

Gin His Ser Glu Thr Val Ala Gin Glu Trp Gly Thr Ser Thr Gly Asn

145 150 155160

ACT TCG CAA TTC AAT ACG GCT TCA GCG GGA TAT TTA AAT GCA AAT GTT Thr Ser Gin Phe Asn Thr Ala Ser Ala Gly Tyr Leu Asn Ala Asn Val

165 170 175

CGA TAT AAC AAT GTA GGA ACT GGT GCC ATC TAC GAT GTA AAA CCT ACA

Arg Tyr Asn Asn Val Gly Thr Gly Ala lle Tyr Asp Val Lys Pro Thr

180 185 190

ACA AGT TTT GTA TTA AAT AAC GAT ACT ATC GCA ACT ATT ACG GCG AAA

Thr Ser Phe Val Leu Asn Asn Asp Thr lle Ala Thr lle Thr Ala Lys

195 200 205

144

192

240

288

336

384

432

480

528

576

2100

2105

2110

2115

2120

2125

2130

624

2135

RO 117111 Bl

TCT AAT TCT ACA GCC TTA AAT ATA TCT CCT GGA GAA AGT TAC CCG AAA

Ser Asn Ser Thr A1 a Leu Asn lle Ser Pro Gly Glu Ser Tyr Pro Lys

210 215220

AAA GGA CAA AAT GGA ATC GCA ATA ACA TCA ATG GAT GAT TTT AAT TCC

Lys Gly Gin Asn Gly li Ala lle Thr Ser Met Asp Asp Phe Asn Ser

225 230 235240

CAT CCG ATT ACA TTA AAT AAA AAA CAA GTA GAT AAT CTG CTA AAT AAT His Pro lle Thr Leu Asn Lys Lys Gin Val Asp Asn Leu Leu Asn Asn

245 250255

AAA CCT ATG ATG TTG GAA ACA AAC CAA ACA GAT GGT GTT TAT AAG ATA Lys Pro Met Met Leu Glu Thr Asn Gin Thr Asp Gly Val Tyr Lys lle

260 265270

AAA GAT ACA CAT GGA AAT ATA GTA ACT GGC GGA GAA TGG AAT GGT GTC Lys Asp Thr His Gly Asn lle Val Thr Gly Gly Glu Trp Asn Gly Val

275 280285

ATA CAA CAA ATC AAG GCT AAA ACA GCG TCT ATT ATT GTG GAT GAT GGG le Gin Gin le Lys A1a Lys Thr Ala Serile le Val Asp Asp Gly

290 295300

GAA CGT GTA GCA GAA AAA CGT GTA GCG GCA AAA GATTAT GAA AAT CCA Glu Arg Val Ala Glu Lys Arg Val Ala Ala Lys Asp Tyr Glu Asn Pro

305 310 315320

GAA GAT AAA ACA CCG TCT TTA ACT TTA AAA GAT G ~ C CTG AAG CTT TCA

Glu Asp Lys Thr Pro Ser Leu Thr Leu Lys Asp Ala Leu Lys Leu Ser

325 330335

TAC CCA GAT GAA ATA AAA GAA ATA GAG GGA TTA TTA TAT TAT AAA AAC

Tyr Pro Asp Glu le Lys Glu lle Glu Gly Leu Leu Tyr Tyr Lys Asn

340 345350

AAA CCG ATA TAC GAA TCG AGC GTT ATG ACT TAC TTA GAT GAA AAT ACA

Lys Pro lle Tyr Glu Ser Ser Val Met Thr Tyr Leu Asp Glu Asn Thr

355 360365

GCA AAA GAA GTG ACC AAA CAA TTA AAT GAT ACC ACT GGG AAA TTT AAA

Ala Lys Glu Val Thr Lys Gin Leu Asn Asp Thr Thr Gly Lys Phe Lys

370 375380

GAT GTA AGT CAT TTA TAT GAT GTA AAA CTG ACT CCA AAA ATG AAT GTT

Asp Val Ser His Leu Tyr Asp Val Lys Leu Thr Pro Lys Met Asn Val

385 390 395400

ACA ATC AAA TTG TCT ATA CTT TAT GAT AAT GCT GAG TCT AAT GAT AAC Thr lle Lys Leu Ser lle Leu Tyr Asp Asn Ala Glu Ser Asn Asp Asn

405 410415

TCA ATT GGT AAA TGG ACA AAC ACA AAT ATT GTT TCA GGT GGA AAT AAC

Ser le Gly Lys Trp Thr Asn Thr Asn le Val Ser Gly Gly Asn Asn

420 425430

GGA AAA AAA CAA TAT TCT TCT AAT AAT CCG GAT GCT AAT TTG ACA TTA

Gly Lys Lys Gin Tyr Ser Ser Asn Asn Pro Asp Ala Asn Leu Thr Leu

435 440445

672

720

768

816

864

912

960

1008

1056

1104

1152

1200

1248

1296

1344

RO 117111 Bl

1392

2185

1440

AAT ACA GAT GCT CAA GAA AAA TTA AAT AAA AAT CGT GAC TAT TAT ATA

Asn Thr Asp Ala Gin Glu Lys Leu Asn Lys Asn Arg Asp Tyr Tyr Ile

450 455 460

AGT TTA TAT ATG AAG TCA GAA AAA AAC ACA CAA TGT GAG ATT ACT ATA

Ser Leu Tyr Met Lys Ser Glu Lys Asn Thr Gin Cys Glu Ile Thr Ile

465 470 475480

GAT GGG GAG ATT TAT CCG ATC ACT ACA AAA ACA GTG AAT GTG AAT AAA

Asp Gly Glu Ile Tyr Pro Hair Thr Thr Lys Thr Val Asn Val Asn Lys

485 490495

GAC AAT TAC AAA AGA TTA GAT ATT ATA GCT CAT AAT ATA AAA AGT AAT

Asp Asn Tyr Lys Arg Leu Asp Hair Hair Ala His Asn Hair Lys Ser Asn

500 505510

CCA ATT TCT TCA CTT CAT ATT AAA ACG AAT GAT GAA ATA ACT TTA TTT

Pro Ile Ser Ser Leu His Ile Lys Thr Asn Asp Glu Ile Thr Leu Phe

515 520525

TGG GAT GAT ATT TCT ATA ACA GAT GTA GCA TCA ATA AAA CCG GAA AAT

Trp Asp Asp Ile Ser Ile Thr Asp Val Ala Ser Ile Lys Pro Glu Asn

530 535540

TTA ACA GAT TCA GAA ACT AAA GAG ATT TAT AGT AGG TAT GGT ATT AAG

Leu Thr Asp Ser Glu Ile Lys Gin Ile Tyr Ser Arg Tyr Gly Ile Lys

545 550 555560

TTA GAA GAT GGA ATC CTT ATT GAT AAA AAA GGT GGG ATT CAT TAT GGT

Leu Glu Asp Gly Hair Leu Hair Asp Lys Lys Gly Gly Ile His Tyr Gly

565 570575

GAA TTT ACT AAT GAA GCT AGT TTT AAT ACT GAA CCA KG CCA AAT TAT

Glu Phe Ile Asn Glu Ala Ser Phe Asn Ile Glu Pro Leu Pro Asn Tyr

580 585590

GTG ACC AAA TAT GAA GTT ACT TAT AGT AGT GAG TTA GGA CCA AAC GTG

Val Thr Lys Tyr Glu Val Thr Tyr Ser Ser Glu Leu Gly Pro Asn Val

595 600605

AGT GAC ACA CTT GAA AGT GAT AAA ATT TAC AAG GAT GGG ACA ATT AAA

Ser Asp Thr Leu Glu Ser Asp Lys Ile Tyr Lys Asp Gly Thr Ile Lys

610 615620

TTT GAT TTT ACC AAA TAT AGT AAA AAT GAA CAA GGA TTA TTT TAT GAC

Phe Asp Phe Thr Lys Tyr Ser Lys Asn Glu Gin Gly Leu Phe Tyr Asp

625 630 635640

AGT GGA TTA AAT TGG GAC TTT AAA ACT AAT GCT ACT ACT TAT GAT GGT

Ser Gly Leu Asn Trp Asp Phe Lys Ile Asn Ala Ile Thr Tyr Asp Gly

645 650655

AAA GAG ATG AAT GTT TTT CAT AGA TAT AAT AAA TAG

Lys Glu Met Asn Val Phe His Arg Tyr Asn Lys

660665

1488

1536

1584

1632

1680

1728

1776

1824

1872

1920

1968

2190

2195

2200

2205

2210

2215

2220 (2) Information for SEQ ID NO: 7:

(i) sequence characteristics:

(a) length: 667 amino acids

2004

2225

RO 117111 Bl (b) type: amino acid (d) topology: linear (ii) molecule type: protein (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 7:

Met Lys Arg Glu Ile Asp Glu Asp Thr Asp Thr Asp Gly Asp Ser Ile 15 1015

Pro Asp Leu Trp Glu Glu Asn Gly Tyr Thr Ile Xaa Asn Arg Hair Ala

2530

Val Lys Trp Asp Asp Ser Leu Ala Ser Lys Gly Tyr Thr Lys Phe Val 35 4045

Ser Asn Pro Leu Glu Ser His Thr Val Gly Asp Pro Tyr Thr Asp Tyr 50 5560

Glu Lys Ala Ala Arg Asp Leu Asp Leu Ser Asn Ala Lys Glu Thr Phe 65 70 7580

Asn Pro Leu Val Ala Ala Phe Pro Ser Val Asn Va1 Ser Met Glu Lys 85 9095

Val Ile Leu Ser Pro Asn Glu Asn Leu Ser Asn Ser Val Glu Ser His 100 105110

Ser Ser Thr Asn Trp Ser Tyr Thr Asn Thr Glu Gly Ala Ser Val Glu

115 120125

Ala Gly Ile Gly Pro Lys Gly Ile Ser Phe Gly Val Ser Val Asn Tyr

130 135140

Gin His Ser Glu Thr Val Ala Gin Glu Trp Gly Thr Ser Thr Gly Asn 145 150 155160

Thr Ser Gin Phe Asn Thr Ala Ser Ala Gly Tyr Leu Asn Ala Asn Val 165 170175

Arg Tyr Asn Asn Val Gly Thr Gly Ala Hair Tyr Asp Val Lys Pro Thr

180 185190

Thr Ser Phe Val Leu Asn Asn Asp Thr Ile Ala Thr Ile Thr Ala Lys 195 200205

Ser Asn Ser Thr Ala Leu Asn Ile Ser Pro Gly Glu Ser Tyr Pro Lys 210 215220

Lys Gly Gin Asn Gly Hair Ala Hair Thr Ser Met Asp Asp Phe Asn Ser 225 230 235240

His Pro Ile Thr Leu Asn Lys Lys Gin Val Asp Asn Leu Leu Asn Asn

245 250255

Lys Pro Met Met Leu Glu Thr Asn Gin Thr Asp Gly Val Tyr Lys Ile

260 265270

Lys Asp Thr His Gly Asn Ile Val Thr Gly Gly Glu Trp Asn Gly Val

275 280285

Hair Gin Gin Hair Lys Ala Lys Thr Ala Ser Hair Hair Val Asp Asp Gly

290 295300

Glu Arg Val Ala Glu Lys Arg Val Ala Ala Lys Asp Tyr Glu Asn Pro 305 310 315320

RO 117111 Bl

Glu Asp Lys Thr Pro Ser Leu Thr Leu Lys Asp Ala Leu Lys Leu Ser 325 330335

Tyr Pro Asp Glu le Lys Glu lle Glu Gly Leu Leu Tyr Tyr Lys Asn

340 345350

Lys Pro lle Tyr Glu Ser Ser Val Met Thr Tyr Leu Asp Glu Asn Thr 355 360365

Ala Lys Glu Val Thr Lys Gin Leu Asn Asp Thr Thr Gly Lys Phe Lys 370 375380

Asp Val Ser His Leu Tyr Asp Val Lys Leu Thr Pro Lys Met Asn Val 385 390 395400

Thr lle Lys Leu Ser lle Leu Tyr Asp Asn Ala Glu Ser Asn Asp Asn 405 410415

Ser Gly Lys Trp Thr Asn Thr Asn Ser Val Gly Gly Asn Asn 420 425430

Gly Lys Lys Gin Tyr Ser Ser Asn Asn Pro Asp Ala Asn Leu Thr Leu 435 440445

Asn Thr Asp Ala Gin Glu Lys Leu Asn Lys Asn Arg Asp Tyr Tyr lle 450 455460

Ser Leu Tyr Met Lys Ser Glu Lys Asn Thr Gin Cys Glu lle Thr lle 465 470 475480

Asp Gly Glu lle Tyr Pro lle Thr Thr Lys Thr Val Asn Val Asn Lys

485 490495

Asp Asn Tyr Lys Arg Leu Asp li Ala His Asn li Lys Ser Asn

500 505510

Pro le Ser Ser Leu His lle Lys Thr Asn Asp Glu lle Thr Leu Phe 515 520525

Trp Asp Asp Him Be Him Thr Asp Val Ala Be Him Lys Pro Glu Asn 530 535540

Leu Thr Asp Ser Glu lle Lys Gin lle Tyr Ser Arg Tyr Gly lle Lys 545 550 555560

Leu Glu Asp Gly le Leu le Asp Lys Lys Gly Gly le His Tyr Gly

565 570575

Glu Phe lle Asn Glu Ala Ser Phe Asn lle Glu Pro Leu Pro Asn Tyr 580 585590

Val Thr Lys Tyr Glu Val Thr Tyr Ser Ser Glu Leu Gly Pro Asn Val 595 600605

Ser Asp Thr Leu Glu Ser Asp Lys le Tyr Lys Asp Gly Thr le Lys 610 615620

Phe Asp Phe Thr Lys Tyr Ser Lys Asn Glu Gin Gly Leu Phe Tyr Asp 625 630 635640

Ser Gly Leu Asn Trp Asp Phe Lys lle Asn Ala lle Thr Tyr Asp Gly 645 650655

Lys Glu Met Asn Val Phe His Arg Tyr Asn Lys

660665

2275

2280

2285

2290

2295

2300

2305

2310

2315

RO 117111 Bl (2) Information for SEQ ID NO: 8:

(i) sequence characteristics:

(a) length: 16 amino acids (b) type: amino acid (c) winding: simple (d) topology: linear (ii) molecule type: peptide (iii) hypothetical: not (v) fragment type: N-terminal (vi) original source:

(a) organism: Bacillus cereus (b) variety: AB78 (c) individual isolate: NRRL B-21058 (ix) characteristics:

(a) name / key: peptides (b) localization: 1 ... 16 (d) other information: / notes = "N-terminal sequence of purified protein from strain AB78" (xi) DESCRIPTION OF SEQUENCE: SEQ ID NO: 8 :

Lys Arg Glu lle Asp Glu Asp Thr Asp Thr Asx Gly Asp Ser lle Pro 15 10 15 (2) Information for SEQ ID NO: 9:

(i) sequence characteristics:

(a) length: 21 base pairs (b) type: nucleic acid (c) winding: simple (d) topology: linear (ii) molecule type: DNA (genomic) (iii) hypothetical: not (iii) anti-sense : no (ix) characteristics:

(a) name / key: mise feature (b) location: 1 ... 21 (d) other information: / notes = 'sample of oligonucleotides based on amino acids 3 to 9 of SEQ ID NO: 8, using Bacillus strain codon thuringiensis (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 9:

GAAATTGATC AAGATACNGA T 21

RO 117111 Bl

2365 (2) Information for SEQ ID NO: 10:

(i) sequence characteristics:

(a) length: 14 amino acids (b) type: amino acid (c) winding: simple (d) topology: linear (ii) molecule type: peptide (iii) hypothetical: not (v) fragment type: N-terminal (vi) original source:

(a) organism: Bacillus thuringiensis (b) variety: AB88 (ix) characteristics:

(a) name / key: peptides (b) localization: 1 ... 14 (d) other information: / notes = "N-terminal amino acid sequence of protein known as anion exchanger of fraction 23 (smallest)" (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 10:

Xaa Glu Pro Phe Val Ser Ala Xaa Xaa Xaa Gin Xaa Xaa Xaa

5 10 (2) Information for SEQ ID NO: 11:

(i) sequence characteristics:

(a) length: 13 amino acids (b) type: amino acid (c) winding: simple (d) topology: linear (ii) molecule type: peptide (iii) hypothetical: no (v) fragment type: N-terminal (vi) original source:

(a) organism: Bacillus thuringiensis (b) variety: ΑΒ8Θ (ix) characteristics:

(a) name / key: peptides (b) localization: 1 ... 13 (d) other information: / notes = "N-terminal amino acid sequence of protein known as anion exchanger of fraction 23 (highest)" (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 11:

Xaa Glu Tyr Glu Asn Val Glu Pro Phe Val Ser Ala Xaa

5 10

2370

2375

2380

2385

2390

2395

2400

2405

RO 117111 Bl (2) Information for SEQ ID NO: 12:

(i) sequence characteristics:

(a) length: 14 amino acids (b) type: amino acid (c) winding: simple (d) topology: linear (ii) molecule type: peptide (iii) hypothetical: not (v) fragment type: N-terminal (vi) original source:

(a) organism: Bacillus thurigiensis (b) variety: AB88 (ix) characteristics:

(a) name / key: peptides (b) location: 1 ... 14 (d) other information: / notes = "N-terminal sequence of VIP 80 kDa active against Agrotis ipsilon (XI) DESCRIPTION OF SEQUENCE: SEQ ID NO: 12:

Met Asn Lys Asn Asn Thr Lys Leu Pro Thr Arg Ala Leu Pro

10 (2) Information for SEQ ID NO: 13:

(i) sequence characteristics:

(a) length: 15 amino acids (b) type: amino acid (c) winding: simple (d) topology: linear (ii) molecule type: peptide (iii) hypothetical: not (v) fragment type: N-terminal (vi ) original source:

(a) organism: Bacillus thuringiensis (b) variety: AB88 (ix) characteristics:

(a) name / key: peptides (b) localization: 1 ... 15 (d) other information: / notes = "N-terminal amino acid sequence of 35 kDa VIP active against Agrotis ipsilon (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 13:

Ala Leu Ser Glu Asn Thr Gly Lys Asp Gly Gly Tyr Ile Val Pro

10 15

RO 117111 Bl

2455 (2) Information for SEQ ID NO: 14:

(i) sequence characteristics:

(a) length: 9 amino acids (b) type: amino acid (c) winding: simple (d) topology: linear (ii) molecule type: peptide (iii) hypothetical: not (v) fragment type: N-terminal (vi) original source:

(A) organism: Bacillus thuringiensis (ix) characteristics:

(a) name / key: peptides (b) location: 1 ... 9 (d) other information: / notes = "N-terminal sequence of 130kda delta-endotoxins"

2460

2465 (xi) DESCRIPTION OF THE SEQUENCE: SEQ ID NO: 14: Met Asp Asn Asn Pro Asn lle Asn Glu

5

2470 (2) Information for SEQ ID NO: 15:

(i) sequence characteristics:

(a) length: 9 amino acids

2475 (b) type: amino acid (c) winding: simple (d) topology: linear (ii) molecule type: peptide (iii) hypothetical: not (v) fragment type: N-terminal (ix) characteristics:

2480 (a) name / key: peptides (b) location: 1 ... 9 (d) other information: / notes = 80 kDa endotoxin "" N-terminal sequence of delta2485 (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 15 : Met Asp Asn Asn Pro Asn lle Asn Glu

5 (2) Information for SEQ ID NO: 16:

(i) sequence characteristics:

(a) length: 11 amino acids (b) type: amino acid (c) winding: simple (d) topology: linear

2490

2495

RO 117111 Bl (ii) molecule type: peptide (iii) hypothetical: no (v) fragment type: N-terminal (vi) original source:

(A) organism: Bacillus thuringiensis (ix) characteristics:

(a) name / key: peptides (b) location: 1 ... 11 (d) other information: / notes = "N-terminal sequence of 60 kDa deltaendotoxin" (xi) DESCRIPTION OF SEQUENCE: SEQ ID NO: 16:

Met Asn Val Leu Asn Ser Gly Arg Thr Thr lle

5 10 (2) Information for SEQ ID NO: 17:

(i) sequence characteristics:

(a) length: 2655 base pairs (b) type: nucleic acid (c) winding: simple (d) topology: linear (ii) molecule type: DNA (genomic) (iii) hypothetical: not (iii) anti-sense : no (xi) SEQUENCE DESCRIPTION: SEQ ID NO: 17:

<td>ATGAAGAACA TGAAGAAGAA</td><td>GCTGGCCAGC</td><td>GTGGTGACCT</td><td>GCACCCTGCT</td>

<td>GGCCCCCATG 60 TTCCTGAACG GCAACGTGAA</td><td>CGCCGTGTAC</td><td>GCCGACAGCA</td><td>AGACCAACCA</td>

<td>GATCAGCACC 120 ACCCAGAAGA ACCAGCAGAA</td><td>GGAGATGGAC</td><td>CGCAAGGGCC</td><td>TGCTGGGCTA</td>

<td>CTACTTCAAG 180 GGCAAGGACT TCAGCAACCT</td><td>GACCATGTTC</td><td>GCCCCCACGC</td><td>GTGACAGCAC</td>

<td>CCTGATCTAC 240 GACCAGCAGA CCGCCAACAA</td><td>GCTGCTGGAC</td><td>AAGAAGCAGC</td><td>AGGAGTACCA</td>

<td>GAGCATCCGC 300 TGGATCGGCC TGATCCAGAG</td><td>CAAGGAGACC</td><td>GGCGACTTCA</td><td>CCTTCAACCT</td>

<td>GAGCGAGGAC 360 GAGCAGGCCA TCATCGAGAT</td><td>CAACGGCAAG</td><td>ATCATCAGCA</td><td>ACAAGGGCAA</td>

<td>GGAGAAGCAG 420 GTGGTGCACC TGGAGAAGGG</td><td>CAAGCTGGTG</td><td>CCCATCAAGA</td><td>TCGAGTACCA</td>

<td>GAGCGACACC 480 AAGTTCAACA TCGACAGCAA</td><td>GACCTTCAAG</td><td>GAGCTGAAGC</td><td>TTTTCAAGAT</td>

<td>CGACAGCCAG 540 AACCAGCCCC AGCAGGTGCA</td><td>GCAGGACGAG</td><td>CTGCGCAACC</td><td>CCGAGTTCAA</td>

<td>CAAGAAGGAG 600</td><td></td><td></td><td></td>