Lynd L H, Zeikus J G
J Bacteriol. 1983 Mar;153(3):1415-23. doi: 10.1128/jb.153.3.1415-1423.1983.
The fermentative metabolism of Butyribacterium methylotrophicum grown on either H2-CO2, methanol, glucose, or CO is described. The following reaction stoichiometries were obtained: 1.00 H2 + 0.52 CO2 leads to 0.22 acetate + 0.06 cell C; 1 methanol + 0.18 CO2 + 0.01 acetate leads to 0.24 butyrate + 0.29 cell C; and 1.00 glucose leads to 0.31 CO2 + 1.59 acetate + 0.21 butyrate + 0.13 H2 + 1.58 cell C. Cell yields of 1.7 g (dry weight) per mol of H2, 8.2 g (dry weight) per mol of methanol, 42.7 g (dry weight) per mol of glucose, and 3.0 g (dry weight) per mol of CO were obtained from linear plots of cell synthesis and substrate consumption. Doubling times of 9.0, 9.0, and 3 to 4 h were observed during batch growth on H2-CO2, methanol, and glucose, respectively. Indicative of a growth factor limitation, glucose fermentation in defined medium displayed a lower cell synthesis efficiency than when yeast extract (0.05%) was present. B. methylotrophicum fermentation displayed atypically high substrate/cell carbon synthesis conversion ratios for an anaerobe, as greater than 24% of the carbon was assimilated into cells during growth on methanol or glucose. The data indicate that B. methylotrophicum conserves carbon-bound electrons during growth on single-carbon or multicarbon substrates.
描述了嗜甲基丁酸杆菌在H₂-CO₂、甲醇、葡萄糖或CO上生长时的发酵代谢。获得了以下反应化学计量关系:1.00 H₂ + 0.52 CO₂生成0.22乙酸盐 + 0.06细胞碳;1甲醇 + 0.18 CO₂ + 0.01乙酸盐生成0.24丁酸盐 + 0.29细胞碳;以及1.00葡萄糖生成0.31 CO₂ + 1.59乙酸盐 + 0.21丁酸盐 + 0.13 H₂ + 1.58细胞碳。通过细胞合成和底物消耗的线性图,得到每摩尔H₂的细胞产量为1.7 g(干重)、每摩尔甲醇为8.2 g(干重)、每摩尔葡萄糖为42.7 g(干重)、每摩尔CO为3.0 g(干重)。在H₂-CO₂、甲醇和葡萄糖分批培养过程中,观察到的倍增时间分别为9.0、9.0和3至4小时。在限定培养基中葡萄糖发酵显示出比存在酵母提取物(0.05%)时更低的细胞合成效率,这表明存在生长因子限制。嗜甲基丁酸杆菌发酵对于厌氧菌而言表现出异常高的底物/细胞碳合成转化率,因为在甲醇或葡萄糖上生长期间超过24%的碳被同化为细胞。数据表明嗜甲基丁酸杆菌在单碳或多碳底物上生长时保留碳结合电子。