Syngas fermentation process and medium
View Patent ↗A process for fermenting syngas and a fermentation medium provides high ethanol productivity while removing medium components that were previously thought to be essential. The process is effective for providing a specific STY of at least about 1 g ethanol/(L·day·gram cells). In this aspect, the fermentation medium has less than about 1.04 ppm boron, less than about 0.16 ppm manganese, less than about 0.26 ppm molybdenum, or less than about 0.16 ppm copper.
1. A fermentation process comprising fermenting syngas in a fermentation medium with acetogenic bacteria, the process effective for providing a specific STY of at least about 1 gram of ethanol/(L·day·gram cells),
wherein the fermentation medium includes
at least 112 to 125 mg of nitrogen per gram of cells,
at least 10.5 to 15 mg of phosphorous per gram of cells, and
at least 26 to 36 mg of potassium per gram of cells,
wherein the fermentation medium has less than 0.025 ppm boron, less than 0.0025 ppm manganese, less than 0.001 ppm molybdenum, and less than 0.01 ppm copper and wherein the fermentation medium has less than 0.01 g/L carbohydrates and less than 0.01 g/L yeast extract.
2. The fermentation process of claim 1 wherein the nitrogen is provided from a nitrogen source selected from the group consisting of ammonium chloride, ammonium phosphate, ammonium sulfate, ammonium nitrate, and mixtures thereof, the phosphorous is provided from a phosphorous source selected from the group consisting of phosphoric acid, ammonium phosphate, potassium phosphate, and mixtures thereof, and the potassium is provided from a potassium source selected from the group consisting of potassium chloride, potassium phosphate, potassium nitrate, potassium sulfate, and mixtures thereof.
3. The fermentation process of claim 1 wherein the fermentation medium includes one or more of
at least about 2.7 mg of iron per gram of cells,
at least about 10 μg of tungsten per gram of cells,
at least about 34 μg of nickel per gram of cells,
at least about 9 μg of cobalt per gram of cells,
at least about 4.5 mg of magnesium per gram of cells,
at least about 11 mg of sulfur per gram of cells, and
at least about 6.5 μg of thiamine per gram of cells.
4. The fermentation process of claim 3 wherein the fermentation medium includes one or more of
about 2.7 to about 5 mg of iron per gram of cells,
about 10 to about 30 μg of tungsten per gram of cells,
about 34 to about 40 μg of nickel per gram of cells,
about 9 to about 30 μg of cobalt per gram of cells,
about 4.5 to about 10 mg of magnesium per gram of cells,
about 11 to about 20 mg of sulfur per gram of cells, and
about 6.5 to about 20 μg of thiamine per gram of cells.
5. The fermentation process of claim 4 wherein the iron is provided from an iron source selected from the group consisting of ferrous chloride, ferrous sulfate, and mixtures thereof, the tungsten is provided from a tungsten source selected from the group consisting of sodium tungstate, calcium tungstate, potassium tungstate, and mixtures thereof, the nickel is provided from a nickel source selected from the group consisting of nickel chloride, nickel sulfate, nickel nitrate, and mixtures thereof, the cobalt is provided from a cobalt source selected from the group consisting of cobalt chloride, cobalt fluoride, cobalt bromide, cobalt iodide, and mixtures thereof, the magnesium is provided from a magnesium source selected from the group consisting of magnesium chloride, magnesium sulfate, magnesium phosphate, and the sulfur is provided from a sulfur source selected from the group consisting of cysteine, sodium sulfide, and mixtures thereof.
6. The fermentation process of claim 1 wherein a pH of the fermentation medium is maintained in a range of about 4.2 to about 4.8.
7. The fermentation process of claim 1 wherein the syngas has a CO/CO 2 ratio of at least about 0.75.
8. The fermentation process of claim 1 wherein the acetogenic bacteria is selected from the group consisting of Acetogenium kivui, Acetoanaerobiun noterae, Acetobacterium woodii, Alkalibaculum bacchi CP11 ATCC BAA-1772, Blautia producta, Butyribacterium methylotrophicum, Caldanaerobacter subterraneous, Caldanaerobacter subterraneous pacificus, Carboxydothermus hydrogenoformans, Clostridium aceticum, Clostridium acetobutylicum, Clostridium autoethanogenum DSM 19630 of DSMZ Germany, Clostridium autoethanogenum DSM 10061 of DSMZ Germany, Clostridium autoethanogenum DSM 23693 of DSMZ Germany, Clostridium autoethanogenum DSM 24138 of DSMZ Germany, Clostridium carboxidivorans P7 ATCC PTA-7827 , Clostridium coskatii ATCC PTA-10522, Clostridium drakei, Clostridium ljungdahlii PETC ATCC 49587, Clostridium ljungdahlii ERI2 ATCC 55380, Clostridium ljungdahlii C-01 ATCC 55988 , Clostridium ljungdahlii O-52 ATCC 55889 , Clostridium magnum, Clostridium pasteurianum DSM 525 of DSMZ Germany, Clostridium ragsdali P11 ATCC BAA-622 , Clostridium scatologenes, Clostridium thermoaceticum, Clostridium ultunense, Desulfotomaculum kuznetsovii, Eubacterium limosum, Geobacter sulfurreducens, Methanosarcina acetivorans, Methanosarcina barkeri, Morrella thermoacetica, Morrella thermoautotrophica, Oxobacter pfennigii, Peptostreptococcus productus, Ruminococcus productus, Thermoanaerobacter kivui , and mixtures thereof.
9. The fermentation process of claim 1 wherein the process is effective for providing a cell density of at least about 1.0 g/L.
10. The fermentation process of claim 1 wherein the process is effective for providing a CO conversion of at least about 5 to about 99%.
11. The fermentation process of claim 1 wherein B, Mn, Mo or Cu sources are eliminated from medium preparations.