Claims
- 1. A plant, the genome of which comprises introduced DNAs encoding the following enzymes:
- a .beta.-ketothiolase that condenses acetyl-CoA and propionyl-CoA to produce .beta.-ketovaleryl-CoA;
- a .beta.-ketothiolase that condenses two molecules of acetyl-CoA to produce acetoacetyl-CoA;
- a .beta.-ketoacyl-CoA reductase that reduces acetoacetyl-CoA and a .beta.-ketovaleryl-CoA to produce .beta.-hydroxybutyryl-CoA and .beta.-hydroxyvaleryl-CoA, respectively;
- a polyhydroxyalkanoate synthase that incorporates .beta.-hydroxybutyryl-CoA and .beta.-hydroxyvaleryl-CoA into P(3HB-co-3HV) copolymer; and
- a wild type or deregulated threonine deaminase enzyme,
- wherein each of said introduced DNAs is operatively linked to regulatory signals that cause expression of said introduced DNAs and
- wherein said plant produces P(3HB-co-3HV) copolymer.
- 2. A plant, the genome of which comprises introduced DNAs encoding the following enzymes:
- a .beta.-ketothiolase that condenses acetyl-CoA and propionyl-CoA to produce .beta.-ketovaleryl-CoA and that condenses two molecules of acetyl-CoA to produce acetoacetyl-CoA;
- a .beta.-ketoacyl-CoA reductase that reduces acetoacetyl-CoA and .beta.-ketovaleryl-CoA to produce .beta.-hydroxybutyryl-CoA and .beta.-hydroxyvaleryl-CoA, respectively;
- a polyhydroxyalkanoate synthase that incorporates .beta.-hydroxybutyryl-CoA and .beta.-hydroxyvaleryl-CoA into P(3HB-co-3HV) copolymer; and
- a wild type or deregulated threonine deaminase enzyme,
- wherein each of said introduced DNAs is operatively linked to regulatory signals that cause expression of said introduced DNAs and
- wherein said plant produces P(3HB-co-3HV) copolymer.
- 3. The plant of claim 1 or 2, wherein said deregulated threonine deaminase is E. coli threonine deaminase wherein leucine at amino acid position 447 is replaced with an amino acid selected from the group consisting of alanine, isoleucine, valine, proline, phenylalanine, tryptophan, and methionine.
- 4. The plant of claim 1 or 2, wherein said deregulated threonine deaminase is E. coli threonine deaminase wherein leucine at amino acid position 447 is replaced with phenylalanine.
- 5. The plant of claim 1 or 2, wherein said deregulated threonine deaminase is E. coli threonine deaminase wherein leucine at amino acid position 481 is replaced with an amino acid selected from the group consisting of alanine, isoleucine, valine, proline, phenylalanine, tryptophan, and methionine.
- 6. The plant of claim 1 or 2, wherein said deregulated threonine deaminase is E. coli threonine deaminase wherein leucine at amino acid position 481 is replaced with phenylalanine.
- 7. The plant of claim 1 or 2, wherein said deregulated threonine deaminase is E. coli threonine deaminase wherein leucine at amino acid position 447 is replaced with an amino acid selected from the group consisting of alanine, isoleucine, valine, proline, phenylalanine, tryptophan, and methionine, and wherein leucine at amino acid position 481 is replaced with an amino acid selected from the group consisting of alanine, isoleucine, valine, proline, phenylalanine, tryptophan, and methionine.
- 8. The plant of claim 1 or 2, wherein said deregulated threonine deaminase is E. coli threonine deaminase wherein leucine at amino acid position 447 is replaced with phenylalanine and wherein leucine at amino acid position 481 is replaced with phenylalanine.
- 9. The plant of claim 1, wherein said .beta.-ketothiolase that condenses acetyl-CoA and propionyl-CoA to produce .beta.-ketovaleryl-CoA is Alcaligenes eutrophus BktB .beta.-ketothiolase.
- 10. The plant of claim 2, wherein said .beta.-ketothiolase is Alcaligenes eutrophus BktB .beta.-ketothiolase.
- 11. The plant of claim 1 or 2, wherein said .beta.-ketoacyl-CoA reductase is obtainable from a microorganism selected from the group consisting of Alcaligenes eutrophus, Alcaligenes faecalis, Aphanothece sp., Azotobacter vinelandii, Bacillus cereus, Bacillus megaterium, Beijerinkia indica, Derxia gummosa, Methylobacterium sp., Microcoleus sp., Nocardia corallina, Pseudomonas cepacia, Pseudomonas extorquens, Pseudomonas oleovorans, Rhodobacter sphaeroides, Rhodobacter capsulatus, Rhodospirillum rubrum, and Thiocapsa pfennigii.
- 12. The plant of claim 1 or 2, wherein said polyhydroxyalkanoate synthase is obtainable from a microorganism selected from the group consisting of Alcaligenes eutrophus, Alcaligenes faecalis, Aphanothece sp., Azotobacter vinelandii, Bacillus cereus, Bacillus megaterium, Beijerinkia indica, Derxia gummosa, Methylobacterium sp., Microcoleus sp., Nocardia corallina, Pseudomonas cepacia, Pseudomonas extorquens, Pseudomonas oleovorans, Rhodobacter sphaeroides, Rhodobacter capsulatus, Rhodospirillum rubrum, and Thiocapsa pfennigii.
- 13. The plant of claim 1 or 2, wherein each of said introduced DNAs is operatively linked to a transit peptide coding region that directs transport of the enzymes encoded by the introduced DNAs into a plastid.
- 14. The plant of claim 13, wherein said plastid is located in a seed of said plant.
- 15. A plant, the genome of which comprises introduced DNAs encoding the following enzymes:
- a wild-type or deregulated threonine deaminase;
- a .beta.-ketothiolase that condenses acetyl-CoA and propionyl-CoA to produce .beta.-ketovaleryl-CoA;
- an aceotacetyl-CoA reductase; and
- a polyhydroxyalkanoate synthase obtainable from a microorganism selected from the group consisting of Alcaligenes eutrophus, Alcaligenes faecalis, Aphanothece sp., Azotobacter vinelandii, Bacillus cereus, Bacillus megaterium, Beijerinkia indica, Derxia gummosa, Methylbacterium sp., Microcoleus sp., Nocardia corallina, Pseudomonas cepacia, Pseudomonas extorquens, Pseudomonas oleovorans, Rhodobacter sphaeroides, Rhodobacter capsulatus, Rhodospirillum rubrum, and Thiocapsa pfennigii,
- wherein each of said introduced DNAs is operatively linked to a transit peptide coding region that directs transport of the enzymes encoded by the introduced DNAs into a plastid, and regulatory signals that cause expression of said introduced DNAs in seeds of said plant; and
- wherein said plant produces P(3HB-co-3HV) copolymer in seeds thereof.
- 16. The plant of claim 15, wherein the .beta.-ketothiolase is the Alcaligenes eutrophus BktB .beta.-ketothiolase.
- 17. A method of producing P(3HB-co-3HV) copolymer, comprising growing said plant of claim 1 or 2 and recovering said P(3HB-co-3HV) copolymer produced thereby.
- 18. A method of producing P(3HB-co-3HV) copolymer, comprising growing said plant of claim 15 and recovering said P(3HB-co-3HV) copolymer produced thereby.
- 19. An isolated DNA molecule comprising a nucleotide sequence encoding a deregulated E. coli threonine deaminase wherein the leucine at amino acid position 447 is replaced with an amino acid selected from the group consisting of alanine, isoleucine, valine, proline, phenylalanine, tryptophan, and methionine.
- 20. The isolated DNA molecule of claim 19, comprising the nucleotide sequence shown in SEQ ID NO:5.
- 21. An isolated DNA molecule comprising a nucleotide sequence selected from the group consisting of:
- (a) the nucleotide sequence shown in SEQ ID NO:9 or the complement thereof; and
- (b) a nucleotide sequence encoding SEQ ID NO:11.
- 22. An isolated DNA molecule, comprising the nucleotide sequence shown in SEQ ID NO:9 or the complement thereof.
Parent Case Info
This application is a continuation of copending U.S. patent application Ser. No. 08/614,877 filed Mar. 13, 1996.
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Continuations (1)
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Number |
Date |
Country |
Parent |
614877 |
Mar 1996 |
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