Department of Microbiology, Wageningen Agricultural University, Hesselink van Suchtelenweg 4, 6703 CT Wageningen, and Department of Environmental Technology, Wageningen Agricultural University, Wageningen, The Netherlands.
Appl Environ Microbiol. 1992 Jan;58(1):346-52. doi: 10.1128/aem.58.1.346-352.1992.
Thermophilic propionate-oxidizing, proton-reducing bacteria were enriched from the granular methanogenic sludge of a bench-scale upflow anaerobic sludge bed reactor operated at 55 degrees C with a mixture of volatile fatty acids as feed. Thermophilic hydrogenotrophic methanogens had a high decay rate. Therefore, stable, thermophilic propionate-oxidizing cultures could not be obtained by using the usual enrichment procedures. Stable and reproducible cultivation was possible by enrichment in hydrogen-pregrown cultures of Methanobacterium thermoautotrophicum DeltaH which were embedded in precipitates of FeS, achieved by addition of FeCl(2) to the media. The propionate-oxidizing bacteria formed spores which resisted pasteurization for 30 min at 90 degrees C or 10 min at 100 degrees C. Highly purified cultures were obtained with either M. thermoautotrophicum DeltaH or Methanobacterium thermoformicicum Z245 as the syntrophic partner organism. The optimum temperature for the two cultures was 55 degrees C. Maximum specific growth rates of cultures with M. thermoautotrophicum DeltaH were somewhat lower than those of cultures with M. thermoformicicum Z245 (0.15 and 0.19 day, respectively). Growth rates were even higher (0.32 day) when aceticlastic methanogens were present as well. M. thermoautotrophicum DeltaH is an obligately hydrogen-utilizing methanogen, showing that interspecies hydrogen transfer is the mechanism by which reducing equivalents are channelled from the acetogens to this methanogen. Boundaries of hydrogen partial pressures at which propionate oxidation occurred were between 6 and 34 Pa. Formate had a strong inhibitory effect on propionate oxidation in cultures with M. thermoautotrophicum. Inhibition by formate was neutralized by addition of the formate-utilizing methanogen or by addition of fumarate. Results indicate that formate inhibited succinate oxidation to fumarate, an intermediate step in the biochemical pathway of propionate oxidation.
从 55°C 的上流式厌氧污泥床反应器的颗粒状产甲烷污泥中富集了嗜热丙酸氧化、质子还原细菌,该反应器以挥发性脂肪酸混合物为进料。嗜热氢营养型产甲烷菌的衰减速率很高。因此,通过通常的富集程序无法获得稳定的嗜热丙酸氧化培养物。通过在嵌入 FeS 沉淀物中的 Methanobacterium thermoautotrophicum DeltaH 预生长培养物中富集,并且通过向培养基中添加 FeCl(2)来实现稳定和可重复的培养,这是可能的。丙酸氧化细菌形成孢子,能够抵抗 90°C 下 30 分钟或 100°C 下 10 分钟的巴氏消毒。使用 Methanobacterium thermoautotrophicum DeltaH 或 Methanobacterium thermoformicicum Z245 作为共培养物,可以获得高度纯化的培养物。两种培养物的最佳温度均为 55°C。与 Methanobacterium thermoformicicum Z245 相比,与 Methanobacterium thermoautotrophicum DeltaH 共培养的最大比生长速率略低(分别为 0.15 和 0.19 天)。当存在乙酸营养型产甲烷菌时,生长速率甚至更高(0.32 天)。Methanobacterium thermoautotrophicum DeltaH 是一种专性利用氢气的产甲烷菌,表明种间氢气转移是将还原当量从产乙酸菌传递到这种产甲烷菌的机制。丙酸氧化发生的氢气分压边界在 6 到 34 Pa 之间。在与 Methanobacterium thermoautotrophicum 共培养的体系中,甲酸盐对丙酸氧化具有强烈的抑制作用。通过添加利用甲酸盐的产甲烷菌或添加延胡索酸盐,可以中和甲酸盐对丙酸氧化的抑制作用。结果表明,甲酸盐抑制了琥珀酸盐氧化为延胡索酸盐,这是丙酸氧化生物化学途径中的中间步骤。