Microbial engineering for the production of chemical and pharmaceutical products from the isoprenoid pathway
The invention relates to the production of one or more terpenoids through microbial engineering, and relates to the manufacture of products comprising terpenoids.
1. A method for making a pharmaceutical product, the method comprising:
providing an Escherichia coli ( E. coli ) that produces isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) through an upstream methylerythritol pathway (MEP) and converts the IPP and DMAPP to squalene or derivative thereof through a recombinantly expressed downstream synthesis pathway comprising farnesyl diphosphate synthase and squalene synthase;
culturing the E. coli to produce the squalene or derivative thereof, wherein the accumulation of indole in the culture is controlled to below 100 mg/L to thereby increase production of squalene or derivative thereof; and
incorporating the squalene or derivative thereof, into a pharmaceutical product.
2. The method of claim 1 , wherein accumulation of indole in the culture is controlled by balancing the upstream MEP pathway with the downstream terpenoid synthesis pathway.
3. The method of claim 1 , further comprising measuring the amount or concentration of indole continuously or intermittently.
4. The method of claim 1 , wherein accumulation of indole in the culture is maintained to below 50 mg/L.
5. The method of claim 1 , wherein accumulation of indole in the culture is maintained to below 10 mg/L.
6. The method of claim 1 , wherein the squalene or derivative thereof is produced at 10 mg/L or more.
7. The method of claim 1 , wherein the squalene or derivative thereof is produced at 100 mg/L or more.
8. The method of claim 1 , wherein the E. coli has additional copies of one or more of the dxs, idi, ispD, and ispF genes of the MEP pathway.
9. The method of claim 8 , wherein the E. coli has a heterologous dxs-idi-ispDF operon.
10. A method for making a terpenoid, the method comprising:
providing an Escherichia coli ( E. coli ) that produces isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) through an upstream methylerythritol pathway (MEP) and converts the IPP and DMAPP to squalene or derivative thereof through a recombinantly expressed downstream synthesis pathway comprising farnesyl diphosphate synthase and squalene synthase; and
culturing the E. coli to produce the squalene or derivative thereof, wherein the accumulation of indole in the culture is controlled to below 100 mg/L to thereby increase terpenoid production; and recovering the squalene or derivative thereof.
11. The method of claim 10 , wherein accumulation of indole in the culture is controlled by balancing the upstream MEP pathway with the downstream terpenoid synthesis pathway.
12. The method of claim 10 , further comprising, measuring the amount or concentration of indole continuously or intermittently.
13. The method of claim 10 , wherein accumulation of indole in the culture is maintained to below 50 mg/L.
14. The method of claim 10 , wherein accumulation of indole in the culture is maintained to below 10 mg/L.
15. The method of claim 10 , wherein the squalene or derivative thereof is produced at 10 mg/L or more.
16. The method of claim 10 , wherein the squalene or derivative thereof is produced at 100 mg/L or more.
17. The method of claim 10 , wherein the E. coli has additional copies of one or more of the dxs, idi, ispD and ispF genes of the MEP pathway.
18. The method of claim 10 , wherein the E. coli has a heterologous dxs-idi-ispDF operon.