Morris J G
Institute of Biological Sciences, University of Wales, Penglais, Aberystwyth, UK.
Appl Biochem Biotechnol. 1994 Aug;48(2):75-106. doi: 10.1007/BF02796164.
New obligately anaerobic bacteria are being discovered at an accelerating rate and it is becoming very evident that the diversity of anoxic biotransformations has been greatly underestimated. Furthermore, among contemporary anaerobes there are many that thrive in extreme environments including, for example, an impressive array of both archaebacterial and eubacterial hyperthermophiles. Free energy for growth and reproduction may be conserved not only via fermentations but also by anoxygenic photophosphorylation and other modes of creating transmembrane proton potential. Thus forms of anaerobic respiration in which various inorganic oxidants (or indeed carbon dioxide) serve as terminal electron acceptors have greatly extended the natural habitats in which such organisms may predominate. Anaerobic bacteria are, however, often found in nature as members of close microbial communities (consortia) that, although sustained by syntrophic and other relations between component species, are liable to alter their composition and character in response to environmental changes, e.g., availability of terminal oxidants. It follows that the biotechnological exploitation of obligately anaerobic bacteria must be informed by knowledge both of their biochemical capacities and of their normal environmental roles. It is against this background that illustrative examples of the activities of anaerobic bacteria are considered under three heads: 1. Biodegradation/Bioremediation, with special reference to the anaerobic breakdown of aromatic and/or halogenated organic substances; 2. Biosynthesis/Bioproduction, encompassing normal and modified fermentations; and 3. Biotransformations, accomplished by whole or semipermeabilized organisms or by enzymes derived therefrom, with particular interest attaching to the production of chiral compounds by a number of procedures, including electromicrobial reduction.
新的专性厌氧菌正以越来越快的速度被发现,而且越来越明显的是,缺氧生物转化的多样性被大大低估了。此外,在当代厌氧菌中,有许多在极端环境中茁壮成长,例如,包括一系列令人印象深刻的古细菌和真细菌嗜热菌。生长和繁殖所需的自由能不仅可以通过发酵来保存,还可以通过无氧光合磷酸化和其他产生跨膜质子电位的方式来保存。因此,以各种无机氧化剂(或实际上是二氧化碳)作为末端电子受体的厌氧呼吸形式极大地扩展了这类生物可能占主导地位的自然栖息地。然而,厌氧菌在自然界中通常作为紧密微生物群落(共生体)的成员被发现,这些群落虽然由组成物种之间的互营和其他关系维持,但容易因环境变化(例如末端氧化剂的可用性)而改变其组成和特性。因此,对专性厌氧菌的生物技术开发必须基于对其生化能力及其正常环境作用的了解。正是在这种背景下,厌氧菌活动的示例在以下三个方面进行了考虑:1. 生物降解/生物修复,特别提及芳香族和/或卤代有机物质的厌氧分解;2. 生物合成/生物生产,包括正常发酵和改良发酵;3. 生物转化,由完整或半透性生物体或从中衍生的酶完成,特别关注通过多种程序(包括电微生物还原)生产手性化合物。