Method for enhancing production of isoprenoid compounds
View Patent ↗The present invention provides methods of producing an isoprenoid or an isoprenoid precursor in a genetically modified host cell. The methods generally involve modulating the level of hydroxymethylglutaryl-CoA (HMG-CoA) in the cell, such that the level of HMG-CoA is not toxic to the cell and/or does not substantially inhibit cell growth, but is maintained at a level that provides for high-level production of mevalonate, IPP, and other downstream products of an isoprenoid or isoprenoid pathway, e.g., polyprenyl diphosphates and isoprenoid compounds. The present invention further provides genetically modified host cells that are suitable for use in a subject method. The present invention further provides recombinant nucleic acid constructs for use in generating a subject genetically modified host cell, including recombinant nucleic acid constructs comprising nucleotide sequences encoding one or more mevalonate pathway enzymes, and recombinant vectors (e.g., recombinant expression vectors) comprising same. The present invention further provides methods for identifying nucleic acids that encode HMG-CoA reductase (HMGR) variants that provide for relief of HMG-CoA accumulation-induced toxicity. The present invention further provides methods for identifying agents that reduce intracellular accumulation of HMG-CoA.
1. A method for producing an isoprenoid or isoprenoid precursor via a mevalonate pathway in Escherichia coli , the method comprising:
(i) culturing in a suitable medium an E. coli cell genetically modified to produce heterologous hydroxymethylglutaryl-CoA (HMG-CoA) synthase (HMGS) and heterologous HMG-CoA reductase (HMGR), wherein the relative activity level of the HMGR produced in the genetically modified E. coli cell is higher than the relative activity level of the HMGS produced in the genetically modified E. coli cell, and wherein the genetically modified E. coli cell is further genetically modified to produce one or more additional heterologous mevalonate pathway enzymes selected from:
(a) an acetoacetyl-CoA thiolase;
(b) a mevalonate kinase;
(c) a phosphomevalonate kinase; and
(d) a mevalonate pyrophosphate decarboxylase;
wherein the genetically modified E. coli cell produces the isoprenoid or isoprenoid precursor at a level at least as high as the level produced in a control E. coli strain expressing pBAD33MevT sequence shown in SEQ ID NO:2, and wherein the genetically modified E. coli cell exhibits less HMG-CoA induced growth inhibition compared to the control E. coli strain; and
(ii) recovering the produced isoprenoid or isoprenoid precursor.
2. The method of claim 1 , wherein the acetoacetyl-CoA thiolase is heterologous to the genetically modified E. coli cell.
3. The method of claim 1 , wherein the genetically modified E. coli cell comprises two or more copies of a heterologous nucleic acid comprising a nucleotide sequence encoding the HMGR.
4. The method of claim 1 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 50% higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
5. The method of claim 1 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 2-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
6. The method of claim 1 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 5-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
7. The method of claim 1 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 10-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
8. The method of claim 1 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 50-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
9. A method for producing an isoprenoid or isoprenoid precursor via a mevalonate pathway in Escherichia coli , the method comprising: (i) culturing in a suitable medium an E. coli cell genetically modified to produce heterologous hydroxymethylglutaryl-CoA (HMG-CoA) synthase (HMGS) and heterologous HMG-CoA reductase (HMGR), wherein the relative activity level of the HMGR produced in the genetically modified E. coli cell is higher than the relative activity level of the HMGS produced in the genetically modified E. coli cell, and wherein the genetically modified E. coli cell is further genetically modified to produce one or more additional heterologous mevalonate pathway enzymes selected from:
(a) an acetoacetyl-CoA thiolase;
(b) a mevalonate kinase;
(c) a phosphomevalonate kinase; and
(d) a mevalonate pyrophosphate decarboxylase;
wherein the genetically modified E. coli cell produces the isoprenoid or isoprenoid precursor at a level at least as high as the level produced in a control E. coli strain expressing pBAD24MevT sequence shown in SEQ ID NO:1, and wherein the genetically modified E. coli cell exhibits less HMG-CoA induced growth inhibition compared to the control E. coli strain; and
(ii) recovering the produced isoprenoid or isoprenoid precursor.
10. The method of claim 9 , wherein the acetoacetyl-CoA thiolase is heterologous to the genetically modified E. coli cell.
11. The method of claim 9 , wherein the genetically modified E. coli cell comprises two or more copies of a heterologous nucleic acid comprising a nucleotide sequence encoding the HMGR.
12. The method of claim 9 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 50% higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
13. The method of claim 9 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 2-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
14. The method of claim 9 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 5-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
15. The method of claim 9 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 10-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.
16. The method of claim 9 , wherein the level of isoprenoid or isoprenoid precursor produced in the genetically modified E. coli cell is at least about 50-fold higher than the level of isoprenoid or isoprenoid precursor produced in the control E. coli strain.