首页> 外文期刊>Applied and Environmental Microbiology >Benzoate Fermentation by the Anaerobic BacteriumSyntrophus aciditrophicus in the Absence of Hydrogen-Using Microorganisms
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Benzoate Fermentation by the Anaerobic BacteriumSyntrophus aciditrophicus in the Absence of Hydrogen-Using Microorganisms

机译:缺氢微生物在无氢细菌的作用下发酵厌氧细菌苯甲酸

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The anaerobic bacterium Syntrophus aciditrophicusmetabolized benzoate in pure culture in the absence of hydrogen-utilizing partners or terminal electron acceptors. The pure culture of S. aciditrophicus produced approximately 0.5 mol of cyclohexane carboxylate and 1.5 mol of acetate per mol of benzoate, while a coculture of S.aciditrophicus with the hydrogen-using methanogenMethanospirillum hungatei produced 3 mol of acetate and 0.75 mol of methane per mol of benzoate. The growth yield of theS. aciditrophicus pure culture was 6.9 g (dry weight) per mol of benzoate metabolized, whereas the growth yield of the S. aciditrophicus-M. hungatei coculture was 11.8 g (dry weight) per mol of benzoate. Cyclohexane carboxylate was metabolized by S. aciditrophicus only in a coculture with a hydrogen user and was not metabolized by S. aciditrophicus pure cultures. Cyclohex-1-ene carboxylate was incompletely degraded by S. aciditrophicus pure cultures until a free energy change (ΔG′) of ?9.2 kJ/mol was reached (?4.7 kJ/mol for the hydrogen-producing reaction). Cyclohex-1-ene carboxylate, pimelate, and glutarate transiently accumulated at micromolar levels during growth of an S. aciditrophicus pure culture with benzoate. High hydrogen (10.1 kPa) and acetate (60 mM) levels inhibited benzoate metabolism byS. aciditrophicus pure cultures. These results suggest that benzoate fermentation by S. aciditrophicus in the absence of hydrogen users proceeds via a dismutation reaction in which the reducing equivalents produced during oxidation of one benzoate molecule to acetate and carbon dioxide are used to reduce another benzoate molecule to cyclohexane carboxylate, which is not metabolized further. Benzoate fermentation to acetate, CO2, and cyclohexane carboxylate is thermodynamically favorable and can proceed at free energy values more positive than ?20 kJ/mol, the postulated minimum free energy value for substrate metabolism.
机译:在没有使用氢的伙伴或末端电子受体的情况下,纯培养中的厌氧细菌嗜酸腐殖质代谢苯甲酸酯。嗜酸链霉菌的纯培养物每摩尔苯甲酸酯产生大约0.5摩尔环己烷羧酸盐和1.5摩尔乙酸盐,而嗜酸链霉菌与使用氢的产甲烷菌共培养产生的嗜酸甲烷单螺旋菌产生3摩尔乙酸盐和0.75摩尔甲烷每摩尔苯甲酸酯。 S的生长产量。嗜酸胃单胞菌纯培养物为每摩尔代谢的苯甲酸酯6.9 g(干重),而嗜酸链球菌M的生长产量。 Hangatei共培养物为每摩尔苯甲酸酯11.8 g(干重)。环己烷羧酸盐仅在与氢气使用者共培养的情况下才被嗜酸链球菌代谢,而不会被嗜酸链球菌纯培养物代谢。嗜酸链霉菌纯培养物不完全降解环己-1-烯羧酸盐,直到达到约9.2 kJ / mol的自由能变化(ΔG')(制氢反应的约4.7 kJ / mol)。在带有苯甲酸根的嗜酸链霉菌纯培养物生长过程中,环己烯-1-烯的羧酸根,庚二酸和戊二酸以微摩尔水平瞬时积累。高氢(10.1 kPa)和乙酸盐(60 mM)水平抑制了苯甲酸酯的新陈代谢。嗜酸营养菌纯培养物。这些结果表明,在没有氢使用者的情况下,嗜酸链球菌发酵苯甲酸酯的过程是通过歧化反应进行的,在该歧化反应中,一个苯甲酸酯分子氧化成乙酸盐和二氧化碳的过程中产生的还原当量用于将另一个苯甲酸酯分子还原成环己烷羧酸酯。不被进一步代谢。苯甲酸发酵成乙酸盐,CO2和环己烷羧酸盐在热力学上是有利的,并且可以在大于约20 kJ / mol的正能量(假定为底物代谢的最小自由能值)上进行。

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