Insecticidal proteins from
View Patent ↗The invention pertains to novel insecticidal compounds derived from Bacillus thuringiensis strains. New proteins designated Cry1Jd, Cry9Fa, and Cry1Bf, and insecticidal fragments thereof are provided, as well as DNA sequences encoding these proteins or their insecticidal fragments. Further provided are recombinant hosts expressing such proteins, particularly plant cells and plants.
1. An recombinant DNA encoding an insecticidal protein, comprising an amino acid sequence with at least 95% sequence identity to the amino acid sequence of SEQ ID No. 4 from amino acid position 1 to amino acid position 596.
2. The DNA of claim 1 , encoding a protein comprising the amino acid sequence of SEQ ID No. 4 from amino acid position 1 to amino acid position 596.
3. The DNA of claim 2 , encoding a protein comprising the amino acid sequence of SEQ ID No. 4.
4. The DNA of claim 1 , wherein said DNA hybridizes under stringent hybridization conditions to the DNA of SEQ ID No. 3, wherein said stringent hybridization is by:
a) immobilizing DNA on a filter, and prehybridizing said filter for 1 to 2 hours in prehybridization fluid comprised of either 50% formamide, 5% SSPE, 2×Denhardt's reagent and 0.1% SDS at 42 ° C., or 6×SSC, 2×Denhardt′s reagent and 0.1% SDS at 68 ° C.;
b) adding a denatured labeled probe comprising DNA of SEQ ID No. 3 directly to the prehybridization fluid and incubating for 16 to 24 hours at 42 ° C. if that was the temperature used in step a), or at 68 ° C. if that was the temperatuve used in step a);
c) after incubation, washing the filters for 20 minutes at room temperature in 1×SSC, 0.1% SDS, followed by three washes of 20 minutes each at 68 ° C. in 0.2 ×SSC and 0.1% SDS;
d) establishing an autoradiograph by exposing the filters for 24 to 48 hours to X-ray film at −70 ° C. with an intensifying screen.
5. The DNA of claim 1 , comprising an artificial DNA sequence having a different codon usage compared to the DNA sequence of SEQ ID NO: 3.
6. A chimeric gene comprising the DNA of claim 1 , operably-linked to a plant-expressible promoter.
7. A plant cell, plant or seed transformed to contain the chimeric gene of claim 6 .
8. The plant cell, plant or seed of claim 7 , comprising said chimeric gene integrated in the nuclear or chloroplast DNA of their cells.
9. The plant cell, plant or seed of claim 8 , which is selected from the group consisting of: corn, cotton, rice, oilseed rape, Brassica species, eggplant, soybean, potato, sunflower, tomato, sugarcane, tea, beans, tobacco, strawberry, clover, cucumber, watermelon, pepper, oat, barley, wheat, dahlia, gladiolus, chrysanthemum, sugarbeet, sorghum, alfalfa, and peanut cells, plants or seeds.
10. A micro-organism, transformed to contain the DNA of claim 1 .
11. The micro-organism of claim 10 , which is selected from the genus Agrobacterium, Escherichia , or Bacillus.
12. A process for controlling insects, said process comprising expressing the DNA of claim 1 , or a chimeric gene comprising said DNA operably-linked to a plant-expressible promoter, in host cells, and contacting insects with said host cells.
13. A process for obtaining a plant with resistance to insects, said process comprising transforming plant cells with the DNA of claim 1 , or with a chimeric gene comprising said DNA operably-linked to a plant-expressible promoter, and regenerating transformed plants and progeny thereof which are resistant to insects.
14. The process of claim 12 , wherein said insects are larvae of Heliothis virescens.
15. The process of claim 13 , wherein said insects are larvae of Heliothis virescens.
16. The process of claim 13 , further comprising obtaining seed from said plants comprising said DNA.