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荚膜红假单胞菌暗发酵生长的生理学

Physiology of dark fermentative growth of Rhodopseudomonas capsulata.

作者信息

Madigan M T, Cox J C, Gest H

出版信息

J Bacteriol. 1980 Jun;142(3):908-15. doi: 10.1128/jb.142.3.908-915.1980.

Abstract

The photosynthetic bacterium Rhodopseudomonas capsulata can grow under anaerobic conditions with light as the energy source or, alternatively, in darkness with D-fructose or certain other sugars as the sole source of carbon and energy. Growth in the latter mode requires an "accessory oxidant" such as trimethylamine-N-oxide, and the resulting cells contain the photosynthetic pigments characteristic of R. capsulata (associated with intracytoplasmic membranes) and substantial deposits of poly-beta-hydroxybutyrate. In dark anaerobic batch cultures in fructose plus trimethylamine-N-oxide medium, trimethylamine formation parallels growth, and typical fermentation products accumulate, namely, CO2 and formic, acetic, and lactic acids. These products are also found in dark anaerobic continuous cultures of R. capsulata; acetic acid and CO2 predominate when fructose is limiting, whereas formic and lactic acids are observed at elevated concentrations when trimethylamine-N-oxide is the limiting nutrient. Evidence is presented to support the conclusions that ATP generation during anaerobic dark growth of R. capsulata on fructose plus trimethylamine-N-oxide occurs by substrate level phosphorylations associated with classical glycolysis and pyruvate dissimilation, and that the required accessory oxidant functions as an electron sink to permit the management of fermentative redox balance, rather than as a terminal electron acceptor necessary for electron transport-driven phosphorylation.

摘要

光合细菌荚膜红假单胞菌可以在厌氧条件下以光为能源进行生长,或者在黑暗中以D-果糖或某些其他糖类作为唯一的碳源和能源进行生长。后一种生长模式需要一种“辅助氧化剂”,如三甲胺-N-氧化物,由此产生的细胞含有荚膜红假单胞菌特有的光合色素(与胞内膜相关)以及大量的聚-β-羟基丁酸酯沉积物。在果糖加三甲胺-N-氧化物培养基中的黑暗厌氧分批培养中,三甲胺的形成与生长平行,并且典型的发酵产物会积累,即二氧化碳以及甲酸、乙酸和乳酸。这些产物在荚膜红假单胞菌的黑暗厌氧连续培养中也能找到;当果糖受到限制时,乙酸和二氧化碳占主导,而当三甲胺-N-氧化物是限制营养物时,甲酸和乳酸的浓度会升高。有证据支持以下结论:荚膜红假单胞菌在果糖加三甲胺-N-氧化物上进行厌氧黑暗生长期间,ATP的产生是通过与经典糖酵解和丙酮酸异化作用相关的底物水平磷酸化实现的,并且所需的辅助氧化剂起到电子阱的作用,以维持发酵性氧化还原平衡,而不是作为电子传递驱动的磷酸化所必需的末端电子受体。

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