Cypionka H
Institut für Chemie und Biologie des Meeres, Universität Oldenburg, D-26111 Oldenburg, Germany.
Annu Rev Microbiol. 2000;54:827-48. doi: 10.1146/annurev.micro.54.1.827.
Throughout the first 90 years after their discovery, sulfate-reducing bacteria were thought to be strict anaerobes. During the last 15 years, however, it has turned out that they have manifold properties that enable them to cope with oxygen. Sulfate-reducing bacteria not only survive oxygen exposure for at least days, but many of them even reduce oxygen to water. This process can be a true respiration process when it is coupled to energy conservation. Various oxygen-reducing systems are present in Desulfovibrio species. In Desulfovibrio vulgaris and Desulfovibrio desulfuricans, oxygen reduction was coupled to proton translocation and ATP conservation. In these species, the periplasmic fraction, which contains hydrogenase and cytochrome c3, was found to catalyze oxygen reduction with high rates. In Desulfovibrio gigas, a cytoplasmic rubredoxin oxidase was identified as an oxygen-reducing terminal oxidase. Generally, the same substrates as with sulfate are oxidized with oxygen. As additional electron donors, reduced sulfur compounds can be oxidized to sulfate. Sulfate-reducing bacteria are thus able to catalyze all reactions of a complete sulfur cycle. Despite a high respiration rate and energy coupling, aerobic growth of pure cultures is poor or absent. Instead, the respiration capacity appears to have a protective function. High numbers of sulfate-reducing bacteria are present in the oxic zones and near the oxic-anoxic boundaries of sediments and in stratified water bodies, microbial mats and termite guts. Community structure analyses and microbiological studies have shown that the populations in those zones are especially adapted to oxygen. How dissimilatory sulfate reduction can occur in the presence of oxygen is still enigmatic, because in pure culture oxygen blocks sulfate reduction. Behavioral responses to oxygen include aggregation, migration to anoxic zones, and aerotaxis. The latter leads to band formation in oxygen-containing zones at concentrations of </=20% air saturation.
在被发现后的最初90年里,硫酸盐还原菌被认为是严格厌氧菌。然而,在过去15年中,事实证明它们具有多种特性,使其能够应对氧气。硫酸盐还原菌不仅能在氧气环境中存活至少数天,而且其中许多甚至能将氧气还原为水。当该过程与能量守恒耦合时,它可以是一个真正的呼吸过程。脱硫弧菌属物种中存在各种氧还原系统。在普通脱硫弧菌和脱硫脱硫弧菌中,氧还原与质子转运和ATP守恒耦合。在这些物种中,发现含有氢化酶和细胞色素c3的周质部分能高效催化氧还原。在巨大脱硫弧菌中,一种细胞质红素氧化酶被鉴定为氧还原末端氧化酶。一般来说,与硫酸盐反应时相同的底物会被氧气氧化。作为额外的电子供体,还原态硫化合物可被氧化为硫酸盐。因此,硫酸盐还原菌能够催化完整硫循环的所有反应。尽管呼吸速率和能量耦合较高,但纯培养物的有氧生长较差或不存在。相反,呼吸能力似乎具有保护功能。在沉积物的有氧区域、有氧-缺氧边界附近以及分层水体、微生物垫和白蚁肠道中存在大量的硫酸盐还原菌。群落结构分析和微生物学研究表明,这些区域的种群特别适应氧气。在有氧气存在的情况下异化硫酸盐还原如何发生仍然是个谜,因为在纯培养中氧气会阻止硫酸盐还原。对氧气的行为反应包括聚集、迁移到缺氧区域和趋氧性。后者导致在空气饱和度≤20%的含氧区域形成条带。