Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Polypeptide compositions toxic to anthonomus insects, and methods of use

a technology of polypeptide compositions and anthonomus insects, applied in the field of molecular biology, to achieve the effect of increasing or enhancing the resistance of such a plant to attack

Inactive Publication Date: 2003-12-11
MONSANTO TECH LLC
View PDF4 Cites 23 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Cry3 proteins generally display coleopteran activity, however, these generally have limited host range specificity and are not significantly toxic to target pests unless ingested in very high doses.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Polypeptide compositions toxic to anthonomus insects, and methods of use
  • Polypeptide compositions toxic to anthonomus insects, and methods of use
  • Polypeptide compositions toxic to anthonomus insects, and methods of use

Examples

Experimental program
Comparison scheme
Effect test

example 1

5.1 Example 1

[0196] Bacillus thuringiensis Stains with Sequences Related to CryET70

[0197] We previously identified a B. thuringiensis strain expressing a protein which we designated CryET70. The CryET70 protein had effective coleopteran specific bioactivity when provided in bioassay feeding studies to western corn rootworm larvae, but not against southern corn rootworm larvae. We were interested in identifying additional B. thuringiensis strains which contained DNA encoding CryET70 and closely related genes. Colony blot hybridization experiments were completed as indicated below, using a probe prepared from cryET70 DNA. Wild-type B. thuringiensis strains were patched onto LB plates and incubated at 30.degree. C. for four hours. A Nytran.RTM. Maximum-Strength Plus (Schleicher and Schuell, Keene, N.H.) circular (82 mm) membrane filter was then placed on the plates and the plates and filters were incubated at 25.degree. C. overnight. The filters, which contained an exact replica of the...

example 2

5.2 Example 2

[0199] Production of Antibody to CryET70

[0200] CryET70 specific polyclonal antibody was prepared so that proteins containing CryET70-related epitopes could be identified using immunological methods. Recombinant B. thuringiensis strain EG11839 containing plasmid pEG1648 expressing CryET70 was grown in C2 medium for four days at 25.degree. C. The resulting spores and crystals were washed in 2.5.times. volume H.sub.2O and resuspended at 1 / 20 the original volume in 0.005% Triton X-100.RTM.. The spore-crystal suspension was then loaded on a sucrose step gradient consisting of 79%, 72% and 55% sucrose. The gradient was spun overnight in a Beckman SW28 at 18,000 RPM. CryET70 crystals banded between the 79% and the 72% sucrose layers. CryET70 crystals were washed several times in H.sub.2O and resuspended in 0.005% Triton X-100.RTM.. The purified crystals were then solubilized in 50 mM sodium carbonate (pH 10), 5 mM DTT, and any contaminating vegetative cells or spores were remo...

example 3

5.3 Example 3

[0201] Southern and Western Blot Analyses

[0202] Strains identified in Example 1 as containing sequences related to cryET70 were examined further by Southern and Western blot analyses.

[0203] Total DNA was prepared from the strains by the following procedure. Vegetative cells were resuspended in a lysis buffer containing 50 mM glucose, 25 mM Tris-HCl (pH8.0), 10 mM EDTA, and 4 mg / ml lysozyme. The suspension was incubated at 37.degree. C. for one hr. Following incubation, SDS was added to 1%. The suspension was then extracted with an equal volume of phenol:chloroform:isoamyl alcohol (50:48:2). DNA was precipitated from the aqueous phase by the addition of one-tenth volume 3 M sodium acetate, and two volumes of 100% ethanol. The precipitated DNA was collected with a glass rod, washed with 70% ethanol, and resuspended in dH.sub.2O.

[0204] Total DNA was digested with EcoRI and separated on a 0.8% agarose gel in TAE buffer (40 mM Tris-acetate, 2 mM Na.sub.2EDTA, pH 8). The DNA ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

A novel gene encoding a Coleopteran inhibitory Bacillus thuringiensis insecticidal crystal protein is disclosed. The protein, tIC851, is insecticidally active and provides plant protection from at least cotton boll weevil, Anthomomus grandis, when applied to plants in an insecticidally effective composition.

Description

1.0 BACKGROUND OF THE INVENTION[0001] 1.1 Field of the Invention[0002] The present invention relates generally to the fields of molecular biology. Methods and compositions comprising DNA sequences, and polypeptides derived from Bacillus thuringiensis for use in insecticidal formulations and the development of transgenic insect-resistant plants are provided. Novel nucleic acids obtained from Bacillus thuringiensis that encode coleopteran-toxic polypeptides are disclosed. Various methods for making and using these nucleic acids, synthetically modified DNA sequences encoding tIC851 polypeptides, and native and synthetic polypeptide compositions are also disclosed. The use of DNA sequences as diagnostic probes and templates for protein synthesis, and the use of polypeptides, fusion proteins, antibodies, and peptide fragments in various insecticidal, immunological, and diagnostic applications are also disclosed, as are methods of making and using nucleic acid sequences in the development...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): A01N63/50C07K14/325C12N15/32C12N15/82
CPCA01N63/00C12N15/8286C07K14/325A01N63/02Y02A40/146A01N63/50A01N63/23
Inventor ISAAC, BARBARAELYSIA K.METTUS, ANNE-MARIE LIGHTMOSHIRI, FARHADSIVASUPRAMANIAN, SAKUNTALA
Owner MONSANTO TECH LLC
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com