Microorganism having regulated expression of (R)-specific enoyl-coa hydratase gene and method for producing polyhydroxyalkanoate copolymer using same
This invention relates to a microorganism that produces a polyhydroxyalkanoate (PHA) copolymer with a regulated monomer composition ratio and comprises a (R)-specific enoyl-CoA hydratase gene in the genome DNA, wherein a nucleotide sequence upstream of the (R)-specific enoyl-CoA hydratase gene comprises a modification consisting of a substitution(s), a deletion(s), an insertion(s), and/or an addition(s) of one or a plurality of nucleotides so that the expression of the (R)-specific enoyl-CoA hydratase gene is regulated, and to a method for producing a PHA copolymer using the microorganism.
1. A method for producing a polyhydroxyalkanoate (PHA) copolymer having at least 5 mol % of 3-hydroxyhexanoate (3HH) monomer, the method comprising:
culturing a microorganism comprising a (R)-specific enoyl-CoA hydratase gene in the genome DNA, wherein a nucleotide sequence upstream of the (R)-specific enoyl-CoA hydratase gene in the genome DNA of the microorganism comprises a modification that comprises a substitution, a deletion, an insertion, and/or an addition of at least one nucleotide so that expression of the (R)-specific enoyl-CoA hydratase gene is regulated, and further comprising a polyhydroxyalkanoate synthase gene, wherein the modification comprises a modification of at least one nucleotide in a promoter sequence and/or a Shine-Dalgarno (SD) sequence originally existing upstream of the (R)-specific enoyl-CoA hydratase gene in the genome DNA; or an insertion or substitution of an expression regulatory DNA comprising a promoter sequence and/or SD sequence, at a site upstream of the (R)-specific enoyl-CoA hydratase gene in the genome DNA, so that the mol % of the 3HH monomer is higher than a control without the modification;
wherein the modification comprises an insertion or substitution of an E. coli -derived promoter sequence selected from the group consisting of a trc promoter sequence, a lacUV5 promoter sequence, and a trp promoter sequence; and
recovering a polyhydroxyalkanoate copolymer from the microorganism.
2. The method of claim 1 , wherein the polyhydroxyalkanoate copolymer comprises, as a constitutive unit, from 8 to 13 mol % of 3-hydroxyhexanoic acid (3HH) monomer.
3. The method of claim 2 , wherein the polyhydroxyalkanoate copolymer is a poly(3-hydroxybutyrate-co-3-hydroxyhexanoate.
4. The method of claim 1 , wherein the insertion or substitution is at a position within 10,000 nucleotides upstream of the (R)-specific enoyl-CoA hydratase gene.
5. The method of claim 1 , wherein the polyhydroxyalkanoate synthase gene is from Aeromonas caviae.
6. The method of claim 1 , wherein the microorganism belongs to the genus Cupriavidus.
7. The method of claim 6 , wherein the microorganism is Cupriavidus necator.
8. The method of claim 1 , wherein the microorganism belongs to the genus Aeromonas.
9. The method of claim 8 , wherein the microorganism is Aeromonas hydrophila.
10. The method of claim 1 , wherein the (R)-specific enoyl-CoA hydratase gene forms an operon with another gene.
11. The method of claim 1 , wherein the expression regulatory DNA further comprises a Shine-Dalgarno (SD) sequence of the phaC1 gene or a modified SD sequence thereof, wherein the SD sequence or modified SD sequence comprises a nucleotide sequence selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 51, 52, and 60 to 66.
12. The method of claim 1 , wherein the microorganism comprises an expression regulatory DNA, which comprises a promoter comprising a nucleotide sequence selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 47, 48, and 50 and an SD sequence comprising a nucleotide sequence selected from the group consisting of the nucleotide sequences of SEQ ID NOs: 51, 52, and 60 to 66.
13. The method of claim 1 , wherein the microorganism comprises an expression regulatory DNA comprising a nucleotide sequence selected from the group consisting nucleotide sequences of SEQ ID NOs: 38-40 and 43-45.
14. The method of claim 1 , wherein the trc promoter sequence comprises the nucleotide sequence of SEQ ID NO: 47.
15. The method of claim 1 , wherein the trp promoter sequence comprises the nucleotide sequence of SEQ ID NO: 48.
16. The method of claim 1 , wherein the lacUV5 promoter sequence comprises the nucleotide sequence of SEQ ID NO: 50.