Microbial fermentation for the production of terpenes
The invention provides a method for producing a terpene or a precursor thereof by microbial fermentation. Typically, the method involves culturing a recombinant bacterium in the presence of a gaseous substrate whereby the bacterium produces a terpene or a precursor thereof, such as mevalonic acid, isopentenyl pyrophosphate, dimethylallyl pyrophosphate, isoprene, geranyl pyrophosphate, farnesyl pyrophosphate, and/or farnesene. The bacterium may comprise one or more exogenous enzymes, such as enzymes in mevalonate, DXS, or terpene biosynthesis pathways.
1. A recombinant C1-fixing microorganism capable of producing mevalonic acid, or a terpene precursor, from a carbon source comprising a nucleic acid encoding a group of exogenous enzymes comprising thiolase, 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) synthase, and HMG-CoA reductase, wherein the microorganism is from Clostridium or Moorella.
2. The microorganism according to claim 1 , further comprising a nucleic acid encoding a group of enzymes comprising mevalonate kinase, phosphomevalonate kinase, and mevalonate diphosphate decarboxylase.
3. The microorganism according to claim 2 , wherein the terpene precursor is isopentenyl diphosphate.
4. The microorganism according to claim 2 , further comprising a nucleic acid encoding an exogenous enzyme selected from the group consisting of isopentenyl diphosphate isomerase and geranyltranstransferase.
5. The microorganism according to claim 4 , wherein the terpene precursor is dimethylallyl pyrophosphate or geranyl pyrophosphate.
6. The microorganism according to claim 4 , further comprising a nucleic acid encoding an exogenous enzyme comprising isoprene synthase.
7. The microorganism according to claim 6 , wherein the nucleic acid encoding isoprene synthase comprises SEQ ID NO: 21.
8. The microorganism according to claim 4 , wherein the terpene precursor is farnesyl pyrophosphate.
9. The microorganism according to claim 4 , further comprising a nucleic acid encoding an exogenous enzyme comprising farnesene synthase.
10. The microorganism according to claim 9 , wherein the nucleic acid encoding farnesene synthase comprises SEQ ID NO: 57.
11. The microorganism according to claim 2 , further comprising a nucleic acid encoding both an exogenous enzyme isopentenyl diphosphate isomerase and an exogenous enzyme geranyltranstransferase.
12. The microorganism according to claim 1 , wherein the microorganism is selected from the group consisting of Clostridium autoethanogenum, Clostridium ljungdahlii, Clostridium ragsdalei, Clostridium carboxidivorans, Clostridium drakei, Clostridium scatologenes, Clostridium aceticum, Clostridium formicoaceticum, Clostridium magnum, Moorella thermoacetica , and Moorella thermautotrophica.
13. The microorganism according to claim 1 , wherein the carbon source is at least one C1 compound selected from the group consisting of carbon monoxide and carbon dioxide as the carbon source.
14. The microorganism according to claim 1 , wherein the mevalonic acid, or the terpene precursor, is converted to a terpene selected from the group consisting of terpenoids, isoprene, pinene, limonene, farnesene, and any combination thereof.
15. The microorganism according to claim 1 , having carbon monoxide dehydrogenase.
16. The microorganism according to claim 1 , further comprising a nucleic acid encoding at least one enzyme acting in a 1-deoxy-D-xylulose-5-phosphate synthase (DXS) pathway.
17. The microorganism according to claim 16 , wherein the DXS pathway is that of a different organism than the microorganism.
18. The microorganism according to claim 1 , wherein the exogenous enzymes are derived from a plant.
19. The microorganism according to claim 1 , wherein the nucleic acid encoding the exogenous enzymes is codon optimized.
20. The microorganism according to claim 1 , wherein the nucleic acid encoding the exogenous enzymes is integrated into the genome of the microorganism.
21. The microorganism according to claim 1 , wherein the nucleic acid encoding the exogenous enzymes is incorporated in a plasmid.
22. The microorganism according to claim 1 , wherein the nucleic acid encoding the exogenous enzymes is regulated by one or more constitutive promoters.
23. A method for producing mevalonic acid, or a terpene precursor, by culturing the recombinant C1-fixing microorganism according to claim 1 using at least one C1 compound selected from the group consisting of carbon monoxide and carbon dioxide as a carbon source, to allow the recombinant C1-fixing microorganism to produce mevalonic acid, or a terpene precursor.
24. The method according to claim 23 , wherein the microorganism is provided with a gas comprising hydrogen.
25. The method according to claim 23 , wherein the mevalonic acid, or terpene precursor, is recovered.
26. The method of claim 23 , wherein the C1 compound is derived from an industrial process selected from the group consisting of ferrous metal products manufacturing, non-ferrous products manufacturing, petroleum refining, coal gasification, electric power production, carbon black production, ammonia production, methanol production, and coke manufacturing.
27. The method of claim 23 , wherein the C1 compound is syngas. 26 . The bacteria according to claim 7 , wherein the nucleic acid encoding isoprene synthase comprises SEQ ID NO: 21 .
28. A method for producing a terpene precursor by providing at least one C1 compound selected from the group consisting of carbon monoxide and carbon dioxide into contact with the recombinant C1-fixing microorganism according to claim 1 , to allow the microorganism to produce a terpene precursor from the C1 compound.
29. The method according to claim 28 , wherein the microorganism is provided with a gas comprising hydrogen.
30. The method according to claim 28 , wherein the terpene precursor is recovered.