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兼性厌氧菌腐败希瓦氏菌通过元素硫还原进行生长。

Growth of the facultative anaerobe Shewanella putrefaciens by elemental sulfur reduction.

作者信息

Moser D P, Nealson K H

机构信息

Center for Great Lakes Studies, University of Wisconsin-Milwaukee 53204, USA.

出版信息

Appl Environ Microbiol. 1996 Jun;62(6):2100-5. doi: 10.1128/aem.62.6.2100-2105.1996.

Abstract

The growth of bacteria by dissimilatory elemental sulfur reduction is generally associated with obligate anaerobes and thermophiles in particular. Here we describe the sulfur-dependent growth of the facultatively anaerobic mesophile Shewanella putrefaciens. Six of nine representative S. putrefaciens isolates from a variety of environments proved able to grow by sulfur reduction, and strain MR-1 was chosen for further study. Growth was monitored in a minimal medium (usually with 0.05% Casamino Acids added as a growth stimulant) containing 30 mM lactate and limiting concentrations of elemental sulfur. When mechanisms were provided for the removal of the metabolic end product, H2S, measurable growth was obtained at sulfur concentrations of from 2 to 30 mM. Initial doubling times were ca. 1.5 h and substrate independent over the range of sulfur concentrations tested. In the cultures with the highest sulfur concentrations, cell numbers increased by greater than 400-fold after 48 h, reaching a maximum density of 6.8 x 10(8) cells ml-1. Yields were determined as total cell carbon and ranged from 1.7 to 5.9 g of C mol of S(0) consumed-1 in the presence of the amino acid supplement and from 0.9 to 3.4 g of C mol of S(0-1) in its absence. Several lines of evidence indicate that cell-to-sulfur contact is not required for growth. Approaches for the culture of sulfur-metabolizing bacteria and potential ecological implications of sulfur reduction in Shewanella-like heterotrophs are discussed.

摘要

通过异化性元素硫还原进行细菌生长通常与专性厌氧菌尤其是嗜热菌有关。在此,我们描述了兼性厌氧嗜温菌腐败希瓦氏菌依赖硫的生长情况。从各种环境中分离出的9株具有代表性的腐败希瓦氏菌菌株中,有6株被证明能够通过硫还原进行生长,我们选择了MR-1菌株作进一步研究。在含有30 mM乳酸盐和限量元素硫的基本培养基(通常添加0.05%的酪蛋白氨基酸作为生长刺激剂)中监测生长情况。当提供去除代谢终产物硫化氢的机制时,在硫浓度为2至30 mM的条件下可获得可测量的生长。初始倍增时间约为1.5小时,在所测试的硫浓度范围内与底物无关。在硫浓度最高的培养物中,48小时后细胞数量增加了400多倍,达到最大密度6.8×10⁸个细胞/毫升。产量以总细胞碳来确定,在添加氨基酸的情况下,每消耗1摩尔零价硫产生的细胞碳量为1.7至5.9克,不添加氨基酸时为0.9至3.4克。几条证据表明生长不需要细胞与硫接触。文中讨论了硫代谢细菌的培养方法以及类似希瓦氏菌的异养菌中硫还原的潜在生态意义。

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