SYSTEM AND METHOD FOR CONTROLLING METABOLITE PRODUCTION IN A MICROBIAL FERMENTATION
A method is provided for controlling a metabolic profile of an anaerobic microbial fermentation culture. In particular, a metabolic profile of a fermentation process is controlled by controlling the amount of dissolved CO2 provided to a culture. Further provided is a method of producing one or more products by microbial fermentation of a gaseous substrate through feeding tail gas CO2 from a reactor to a second reactor, or by recycling tail gas CO2 to the same reactor.
1 . A method for controlling the metabolic profile of a fermentation culture comprising at least one carboxydotrophic acetogenic microorganism, the method comprising:
a. flowing a gaseous substrate comprising CO and CO 2 to a bioreactor comprising a culture of the microorganism in a liquid nutrient medium to produce at least one product derived from acetyl CoA and at least one product derived from pyruvate; and
b. adjusting the amount of CO 2 dissolved in the liquid nutrient medium such that the production of at least one product derived from pyruvate is controlled.
2 . The method of claim 1 , wherein the amount of CO 2 dissolved in the medium is increased such that the production of at least one product derived from pyruvate is increased.
3 . The method of claim 1 , wherein the amount of CO 2 dissolved in the medium is decreased such that the production of at least on product derived from pyruvate is decreased.
4 . The method of claim 1 , wherein the amount of CO 2 dissolved in the medium is adjusted by controlling the flow of CO 2 to the bioreactor.
5 . The method of claim 1 , wherein the CO 2 partial pressure is adjusted in order to adjust the amount of CO 2 dissolved in the liquid nutrient medium.
6 . The method of claim 1 , wherein the fermentation is carried out at a pressure of greater than 250 kPag such that the concentration of CO 2 dissolved in the liquid nutrient medium is increased.
7 . The method of claim 1 , wherein the fermentation is carried out at a pressure of less than 200 kPag such that the concentration of CO 2 dissolved in the liquid nutrient medium is reduced.
8 . The method of claim 1 , wherein the concentration of CO 2 in the gaseous substrate provided to the bioreactor is from about 15% to about 65%.
9 . The method of claim 1 wherein the concentration of CO 2 in the gaseous substrate provided to the bioreactor is gradually increased over time.
10 . The method of claim 1 , wherein the at least one product derived from pyruvate is selected from the group consisting of 2,3-butanediol, lactate, succinate, methyl ethyl ketone (MEK), 2-butanol, propanediol, 2-propanol, isopropanol, acetoin, isobutanol, citramalate, butadiene and poly lactic acid (PLA).
11 . The method of claim 1 , further comprising monitoring the CO 2 concentration in an exit stream exiting the bioreactor in order to monitor the amount of CO 2 utilised by the culture within the bioreactor.
12 . The method of claim 1 , wherein adjusting the amount of CO 2 dissolved in the liquid nutrient medium controls the ratio of pyruvate derived products to acetyl CoA derived products.
13 . A method for producing one or more products by microbial fermentation of a gaseous substrate, the method comprising:
a. receiving a gaseous substrate comprising CO in a first bioreactor comprising a culture of at least one carboxydotrophic acetogenic microorganism in a liquid nutrient medium;
b. fermenting the gaseous substrate comprising CO to produce one or more liquid products and an exit gas comprising CO 2 ;
c. passing the exit gas comprising CO 2 either back to the first bioreactor or to a second bioreactor, wherein said second bioreactor comprises a culture of at least one carboxydotrophic acetogenic microorganism in a liquid nutrient medium; and
d. fermenting the exit gas comprising CO 2 in the first or second bioreactor to produce at least one product.
14 . The method of claim 13 , wherein the exit gas comprising CO 2 is blended with at least one gaseous substrate prior to being fed to the second bioreactor.
15 . The method of claim 14 , wherein at least one additional gaseous substrate is fed to the second bioreactor for use as a substrate in the fermentation.
16 . The method of claim 13 , wherein the first bioreactor produces acetyl CoA derived products and pyruvate derived products and the ratio of acetyl CoA derived products to pyruvate derived products is from about 30:1 to about 20:1.
17 . The method of claim 13 , wherein the second bioreactor produces a lower ratio of acetyl CoA derived products to pyruvate derived products than the first bioreactor.
18 . The method of claim 13 , wherein the at least one product derived from pyruvate is selected from the group comprising 2,3-butanediol, lactate, succinate, methyl ethyl ketone (MEK), 2-butanol, propanediol, 2-propanol, isopropanol, acetoin, isobutanol, citramalate, butadiene and poly lactic acid (PLA).
19 . The method of claim 13 , further comprising taking a tail gas stream produced from the second bioreactor and passing it to the first bioreactor for use as a substrate.
20 . A method for controlling the metabolic profile of a fermentation culture comprising at least one carboxydotrophic acetogenic microorganism, the method comprising;
a. flowing a gaseous substrate comprising CO to a bioreactor comprising a culture of the microorganism in a liquid nutrient medium to provide a fermentation broth; and
b. increasing a rate of CO oxidation via a ferredoxin dependent carbon monoxide dehydrogenase to increase a level of reduced ferredoxin in the fermentation broth;
wherein the increased level of reduced ferredoxin increases a rate of pyruvate fermentation from acetyl CoA.
21 . The method of claim 1 , wherein the at least one carboxydotrophic acetogenic microorganism is selected from the group consisting of Moorella, Clostridium, Ruminococcus, Acetobacterium, Eubacterium, Butyribacterium, Oxobacter, Methanosarcina , and Desulfotomaculum.
22 . The method of claim 1 , wherein the at least one microorganism is selected from the group consisting of Clostridium autoethanogenum, Clostridium ljundgahlii, Clostridium ragsdalei, Clostridium carboxydivorans and Clostridium coskatii.