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Pure-Culture Growth of Fermentative Bacteria Facilitated by H2 Removal: Bioenergetics and H2 Production

机译:去除H2促进发酵细菌的纯培养生长:生物能和H2的产生

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摘要

We used an H2-purging culture vessel to replace an H2-consuming syntrophic partner, allowing the growth of pure cultures of Syntrophothermus lipocalidus on butyrate and Aminobacterium colombiense on alanine. By decoupling the syntrophic association, it was possible to manipulate and monitor the single organism's growth environment and determine the change in Gibbs free energy yield (ΔG) in response to changes in the concentrations of reactants and products, the purging rate, and the temperature. In each of these situations, H2 production changed such that ΔG remained nearly constant for each organism (−11.1 ± 1.4 kJ mol butyrate−1 for S. lipocalidus and −58.2 ± 1.0 kJ mol alanine−1 for A. colombiense). The cellular maintenance energy, determined from the ΔG value and the hydrogen production rate at the point where the cell number was constant, was 4.6 × 10−13 kJ cell−1 day−1 for S. lipocalidus at 55°C and 6.2 × 10−13 kJ cell−1 day−1 for A. colombiense at 37°C. S. lipocalidus, in particular, seems adapted to thrive under conditions of low energy availability.
机译:我们使用净化H2的培养容器代替消耗H2的同养伴侣,从而使丁酸乳突肌纯培养物在丁酸和丙氨酸氨基杆菌上生长。通过解除同养关系的耦合,可以操纵和监视单一生物的生长环境,并根据反应物和产物的浓度,净化速率和温度的变化确定吉布斯自由能产率(ΔG)的变化。在上述每种情况下,H2的产生都发生了变化,使得每种生物的ΔG几乎保持不变(脂毛链霉菌的-11.1±1.4 kJ mol丁酸盐 -1 和丙氨酸<-58.2±1.0 kJ mol丙氨酸 -1 表示A. colombiense)。由ΔG值和恒定的氢生成速率确定的细胞维持能量为4.6×10 −13 kJ cell -1 −1 在55°C和6.2×10 −13 kJ细胞 −1 day −1 对于37°C时的哥伦比亚杆菌。 lipocalidus似乎特别适合在能量利用率低的条件下壮成长。

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