Methods of sustaining culture viability
View Patent ↗The present invention relates to methods for sustaining a microbial culture during periods of limited substrate supply. In accordance with the methods of the invention, a microbial culture comprising carboxydotrophic bacteria can be sustained during periods of limited substrate supply by maintaining the temperature of the microbial culture at a temperature below an optimum operating temperature. Examples of periods of limited substrate supply include when the microbial culture is transported to a remote location or during time when it is stored.
1. A method of sustaining viability of a microbial culture of a carboxydotrophic bacterium in a continuous fermentation process, the method comprising: providing a gaseous substrate comprising CO as the sole carbon source to a bioreactor comprising a fermentation broth comprising a culture of said bacterium suspended in a liquid nutrient medium; fermenting the gaseous substrate to alcohols and acids at an optimum operating temperature; monitoring the CO concentration in the fermentation broth; and when the CO concentration is determined to be limiting lowering the temperature of the fermentation broth below the optimum operating temperature such that viability of the bacterium is maintained, where the CO is determined to be limited when the rate of transfer of CO into the fermentation broth is less than the uptake of CO by the culture of the bacterium.
2. The method of claim 1 where the culture is maintained at a temperature of at least 5° C. below the optimum operating temperature.
3. The method of claim 1 where the culture is maintained at a temperature of at least 10° C. below the optimum operating temperature.
4. The method of claim 1 further comprising increasing the temperature of the fermentation broth to its optimum operating temperature in response to the CO concentration no longer being limiting.
5. The method of claim 1 where the culture is maintained at a temperature below the optimum operating temperature for a time of at least 3 hours.
6. The method of claim 1 where the carboxydotrophic bacterium is selected from the group consisting of Clostridium, Moorella, Pyrococcus, Eubacterium, Desulfobacterium, Carboxydothermus, Acetogenium, Acetobacterium, Acetoanaerobium, Butyribaceterium and Peptostreptococcus.
7. The method of claim 6 , wherein the carboxydotrophic bacterium is Clostridium autoethanogenum.
8. A method of transporting a viable microbial culture of a carboxydotrophic bacterium comprising: transferring a fermentation broth comprising said bacterium, suspended in a liquid nutrient medium and at the bacterium's optimum operating temperature, from a bioreactor to a transportation vessel; pressurizing the transportation vessel with a gaseous substrate comprising CO; lowering the temperature of the vessel below the bacterium's optimum operating temperature; transporting the vessel to a remote location; the bacterium characterized in that it is capable of fermenting a gaseous substrate comprising CO as the sole carbon source to alcohols and acids.
9. The method of claim 8 where the temperature is lowered to at least 5° C. below the optimum operating temperature.
10. The method of claim 8 where the microbial culture is stirred during transport.
11. The method of claim 8 further comprising increasing the temperature of the transportation vessel at the remote location to the optimum operating temperature of the bacterium and inoculating a bioreactor with the microbial culture.
12. The method of claim 8 further comprising inoculating a bioreactor with the microbial culture at the remote location and increasing the temperature of the bioreactor to the optimum operating temperature of the bacterium.
13. The method of claim 8 where the carboxydotrophic bacterium is selected from the group consisting of Clostridium, Moorella, Pyrococcus, Eubacterium, Desulfobacterium, Carboxydothermus, Acetogenium, Acetobacterium, Acetoanaerobium, Butyribaceterium and Peptostreptococcus.
14. The method of claim 13 where the carboxydotrophic bacterium is Clostridium autoethanogenum.
15. A method of storing a viable microbial culture of a carboxydotrophic bacterium comprising: transferring a microbial culture comprising said bacterium, suspended in a liquid nutrient medium and at the bacterium's optimum operating temperature, to a storage vessel; pressurizing the storage vessel with a gaseous substrate comprising CO; lowering the temperature of the storage vessel below the optimum operating temperature of the bacterium; storing the microbial culture for a selected period of time; the bacterium characterized in that it is capable of fermenting the gaseous substrate comprising CO as the sole carbon source to alcohols and acids.
16. The method of claim 15 where the culture is stored at a temperature at least 5° C. below the optimum operating temperature.
17. The method of claim 15 where the culture is stored at a temperature of at least 10° C. below the optimum operating temperature.
18. The method of claim 15 where the culture is stored at a temperature below the optimum operating temperature for a time of at least 3 hours.
19. The method of claim 15 where the carboxydotrophic bacterium is selected from the group consisting of Clostridium, Moorella, Pyrococcus, Eubacterium, Desulfobacterium, Carboxydothermus, Acetogenium, Acetobacterium, Acetoanaerobium, Butyribaceterium and Peptostreptococcus.
20. The method of claim 19 , wherein the carboxydotrophic bacterium is Clostridium autoethanogenum.