Compositions and methods for the biosynthesis of 1,4-butanediol and its precursors
The invention provides a non-naturally occurring microbial biocatalyst including a microbial organism having a 4-hydroxybutanoic acid (4-HB) biosynthetic pathway having at least one exogenous nucleic acid encoding 4-hydroxybutanoate dehydrogenase, succinyl-CoA synthetase, CoA-dependent succinic semialdehyde dehydrogenase, or α-ketoglutarate decarboxylase, wherein the exogenous nucleic acid is expressed in sufficient amounts to produce monomeric 4-hydroxybutanoic acid (4-HB). Also provided is a non-naturally occurring microbial biocatalyst including a microbial organism having 4-hydroxybutanoic acid (4-HB) and 1,4-butanediol (BDO) biosynthetic pathways, the pathways include at least one exogenous nucleic acid encoding 4-hydroxybutanoate dehydrogenase, succinyl-CoA synthetase, CoA-dependent succinic semialdehyde dehydrogenase, 4-hydroxybutyrate:CoA transferase, 4-butyrate kinase, phosphotransbutyrylase, α-ketoglutarate decarboxylase, aldehyde dehydrogenase, alcohol dehydrogenase or an aldehyde/alcohol dehydrogenase, wherein the exogenous nucleic acid is expressed in sufficient amounts to produce 1,4-butanediol (BDO). Additionally provided are methods for the production of 4-HB and BDO.
1. A non-naturally occurring microbial organism having a 4-hydroxybutanoic acid (4-HB) biosynthetic pathway, said pathway comprising exogenous nucleic acids encoding a) an α-ketoglutarate decarboxylase, or an α-ketoglutarate dehydrogenase and a CoA-dependent succinic semialdehyde dehydrogenase, or a glutamate:succinate semialdehyde transaminase and a glutamate decarboxylase; and b) a 4-hydroxybutanoate dehydrogenase, wherein said exogenous nucleic acids are expressed and the microbial organism secretes monomeric 4-HB.
2. The non-naturally occurring microbial organism of claim 1 , wherein the exogenous nucleic acids encode a) an α-ketoglutarate decarboxylase, and b) a 4-hydroxybutanoate dehydrogenase.
3. The non-naturally occurring microbial organism of claim 1 , wherein the exogenous nucleic acids encode a) an α-ketoglutarate dehydrogenase and a CoA-dependent succinic semialdehyde dehydrogenase, and b) a 4-hydroxybutanoate dehydrogenase.
4. The non-naturally occurring microbial organism of claim 1 , wherein the exogenous nucleic acids encode a) a glutamate:succinate semialdehyde transaminase and a glutamate decarboxylase, and b) a 4-hydroxybutanoate dehydrogenase.
5. The non-naturally occurring microbial organism of claim 1 , wherein said monomeric 4-HB is expressed at an intracellular concentration of about 5 mM or more.
6. The non-naturally occurring microbial organism of claim 1 , wherein said monomeric 4-HB is expressed at an intracellular concentration of about 10 mM or more.
7. The non-naturally occurring microbial organism of claim 1 , wherein said microbial organism is a bacterium.
8. The non-naturally occurring microbial organism of claim 1 , wherein the bacterium is Escherichia coli.
9. A method for the production of 4-hydroxybutanoic acid (4-HB) comprising culturing the non-naturally occurring microbial organism of claim 1 under conditions and for a sufficient period of time to produce monomeric 4-HB.
10. The method of claim 9 , wherein the exogenous nucleic acids encode a) an α-ketoglutarate decarboxylase, and b) a 4-hydroxybutanoate dehydrogenase.
11. The method of claim 9 , wherein the exogenous nucleic acids encode a) an α-ketoglutarate dehydrogenase and a CoA-dependent succinic semialdehyde dehydrogenase, and b) a 4-hydroxybutanoate dehydrogenase.
12. The method of claim 9 , wherein the exogenous nucleic acids encode a) a glutamate:succinate semialdehyde transaminase and a glutamate decarboxylase, and b) a 4-hydroxybutanoate dehydrogenase.
13. The method of claim 9 , wherein said monomeric 4-HB is expressed at an intracellular concentration of about 5 mM or more.
14. The method of claim 9 , wherein said monomeric 4-HB is expressed at an intracellular concentration of about 10 mM or more.
15. The method of claim 9 , wherein said microbial organism is a bacterium.
16. The method of claim 9 , wherein the bacterium is Escherichia coli.
17. The method of claim 9 , further comprising the step of isolating the 4-HB.
18. The method of claim 17 , wherein the isolated 4-HB is a salt form.
19. The method of claim 18 , wherein the salt form is a sodium salt.
20. The method of claim 18 , wherein the salt form is a potassium salt.
21. The method of claim 17 , wherein the isolated 4-HB is an acid.
22. The method of claim 17 , wherein the 4-HB is isolated by solvent extraction.
23. A method for producing γ-butyrolactone (GBL), comprising chemically converting 4-HB to GBL, wherein the 4-HB is produced by the method of claim 9 and wherein the GBL is produced by fermentation.
24. A method for producing tetrahydrofuran (THF), comprising chemically converting 4-HB to THF, wherein the 4-HB is produced by the method of claim 9 , and wherein the THF is produced by fermentation and the chemical reduction of 4-HB and/or GBL.
25. A method for producing 1,4-butanediol (BDO), comprising chemically converting 4-HB to BDO, wherein the 4-HB is produced by the method of claim 9 and wherein the BDO is produced by fermentation.
26. A method for producing pyrrolidone, comprising chemically converting 4-HB to pyrrolidone, wherein the 4-HB is produced by the method of claim 9 , and wherein the pyrrolidone is produced by amination of GBL.
27. A method for producing N-methyl-pyrrolidone, comprising chemically converting 4-HB to N-methyl-pyrrolidone, wherein the 4-HB is produced by the method of claim 9 , and wherein the N-methyl-pyrrolidone is produced by amination of GBL.