MICROORGANISM CAPABLE OF PRODUCING IMPROVED POLYHYDROXYALKANOATE AND METHOD OF PRODUCING POLYHYDROXYALKANOATE BY USING THE SAME
The present invention relates to a microorganism which is capable of producing a polyhydroxyalkanoate (PHA) and satisfies the requirements: (1) expression of a phbA gene is repressed or a catalytic activity of an enzyme encoded by the gene is repressed; (2) expression of a bktB gene is enhanced or a catalytic activity of an enzyme encoded by the gene is increased; and (3) a polyhydroxyalkanoate synthase gene and a crotonyl-CoA reductase gene are introduced thereinto. Culture of this microorganism enables efficient production of P(3HB-co-3HH), which is a PHA having excellent flexibility and being applied to a variety of applications, with an inexpensive carbon source.
1 . A microorganism, satisfying the following requirements (1) to (3):
(1) expression of a phbA gene is repressed or a catalytic activity of an enzyme encoded by the gene is repressed;
(2) expression of a bktB gene is enhanced or a catalytic activity of an enzyme encoded by the gene is increased; and
(3) a polyhydroxyalkanoate synthase gene and/or a crotonyl-CoA reductase gene are introduced thereinto.
2 . The microorganism according to claim 1 ,
wherein the expression of the phbA gene is repressed or the catalytic activity of the enzyme encoded by the gene is repressed, by at least one of the following manipulations (1) to (6):
(1) introduction of an additional termination codon between the initiation codon and the termination codon of the phbA gene;
(2) introduction of a mutation that causes reduction in a ribosome-binding activity into a ribosomal binding site of the phbA gene;
(3) introduction of a mutation that causes reduction in the catalytic activity of the enzyme encoded by the phbA gene into the inside of the phbA gene;
(4) utilization of RNA interference;
(5) insertion of a transposon into the inside of the phbA gene; and
(6) deletion of part or all of the phbA gene.
3 . The microorganism according to claim 1 ,
wherein the expression of the bktB gene is enhanced by additional insertion of a promoter having an activity of inducing transcription of the bktB gene into upstream of the bktB gene.
4 . The microorganism according to claim 3 ,
wherein the additionally inserted promoter is the following DNA (1) or (2):
(1) a DNA that, upstream of the bktB gene, has a sequence identity of 70% or higher with a DNA of the base sequence under SEQ ID No. 1 or 2, and has an activity of inducing transcription of the bktB gene; and
(2) a DNA that, upstream of the bktB gene, hybridizes with a DNA complementary with the DNA of the base sequence under SEQ ID No. 1 or 2 under a stringent condition, and has an activity of inducing transcription of the bktB gene.
5 . The microorganism according to claim 1 ,
wherein at least one of the following polyhydroxyalkanoate synthase genes and/or crotonyl-CoA reductase genes (1) to (4) is introduced:
(1) a gene that has a sequence identity of 70% or higher with a DNA of the base sequence under SEQ ID No. 3, and codes for an enzyme having an activity of reducing crotonyl-CoA to produce butyryl-CoA;
(2) a gene that hybridizes with a DNA complementary with the DNA of the base sequence under SEQ ID No. 3 under a stringent condition, and codes for an enzyme having an activity of reducing crotonyl-CoA to produce butyryl-CoA;
(3) a gene that has a sequence identity of 70% or higher with a DNA of the base sequence under SEQ ID No. 4, and codes for an enzyme having an activity of synthesizing a polyhydroxyalkanoate; and
(4) a gene that hybridizes with a DNA complementary with the DNA of the base sequence under SEQ ID No. 4 under a stringent condition, and codes for an enzyme having an activity of synthesizing a polyhydroxyalkanoate.
6 . A microorganism, which is capable of producing a polyhydroxyalkanoate by use of a vegetable oil or fat as a carbon source with achieving a dry cell amount of 150 g/L or more, a polymer content of 70% or higher, and a 3-hydroxyhexanoate content of 12 mol % or higher.
7 . The microorganism according to claim 5 , which is produced by gene recombination.
8 . The microorganism according to claim 1 , which is capable of producing a polyhydroxyalkanoate by use of a vegetable oil or fat as a carbon source with achieving a dry cell amount of 150 g/L or more, a polymer content of 70% or higher, and a 3-hydroxyhexanoate content of 12 mol % or higher.
9 . The microorganism according to claim 1 ,
wherein the polyhydroxyalkanoate is a polyester having 3-hydroxybutyrate and 3-hydroxyhexanoate as structural units.
10 . (canceled)
11 . (canceled)
12 . A method for producing a polyhydroxyalkanoate having a 3-hydroxyhexanoate unit, the method comprising:
cultivating the microorganism according to claim 1 with a vegetable oil or fat as a carbon source.
13 . The microorganism according to claim 1 , which is derived from Cupriavidus necator.
14 . The microorganism according to claim 10 , which is derived from Cupriavidus necator H16.
15 . The microorganism according to claim 2 , which is capable of producing a polyhydroxyalkanoate by use of a vegetable oil or fat as a carbon source with achieving a dry cell amount of 150 g/L or more, a polymer content of 70% or higher, and a 3-hydroxyhexanoate content of 12 mol % or higher.
16 . The microorganism according to claim 3 , which is capable of producing a polyhydroxyalkanoate by use of a vegetable oil or fat as a carbon source with achieving a dry cell amount of 150 g/L or more, a polymer content of 70% or higher, and a 3-hydroxyhexanoate content of 12 mol % or higher.
17 . The microorganism according to claim 4 , which is capable of producing a polyhydroxyalkanoate by use of a vegetable oil or fat as a carbon source with achieving a dry cell amount of 150 g/L or more, a polymer content of 70% or higher, and a 3-hydroxyhexanoate content of 12 mol % or higher.
18 . The microorganism according to claim 5 , which is capable of producing a polyhydroxyalkanoate by use of a vegetable oil or fat as a carbon source with achieving a dry cell amount of 150 g/L or more, a polymer content of 70% or higher, and a 3-hydroxyhexanoate content of 12 mol % or higher.
19 . The microorganism according to claim 2 , wherein the polyhydroxyalkanoate is a polyester having 3-hydroxybutyrate and 3-hydroxyhexanoate as structural units.
20 . The microorganism according to claim 3 , wherein the polyhydroxyalkanoate is a polyester having 3-hydroxybutyrate and 3-hydroxyhexanoate as structural units.
21 . The microorganism according to claim 4 , wherein the polyhydroxyalkanoate is a polyester having 3-hydroxybutyrate and 3-hydroxyhexanoate as structural units.
22 . The microorganism according to claim 5 , wherein the polyhydroxyalkanoate is a polyester having 3-hydroxybutyrate and 3-hydroxyhexanoate as structural units.