The ability of Shewanella decolorationis S12 to obtain energy for growth by coupling the oxidation of various electron donors to dissimilatory azoreduction was investigated. This microorganism can reduce a variety of azo dyes by use of formate, lactate, pyruvate, or H2 as the electron donor. Furthermore, strain S12 grew to a maximal density of 3.0 × 107 cells per ml after compete reduction of 2.0 mM amaranth in a defined medium. This was accompanied by a stoichiometric consumption of 4.0 mM formate over time when amaranth and formate were supplied as the sole electron acceptor and donor, respectively, suggesting that microbial azoreduction is an electron transport process and that this electron transport can yield energy to support growth. Purified membranous, periplasmic, and cytoplasmic fractions from S12 were analyzed, but only the membranous fraction was capable of reducing azo dyes with formate, lactate, pyruvate, or H2 as the electron donor. The presence of 5 μM Cu2+ ions, 200 μM dicumarol, 100 μM stigmatellin, and 100 μM metyrapone inhibited anaerobic azoreduction activity by both whole cells and the purified membrane fraction, showing that dehydrogenases, cytochromes, and menaquinone are essential electron transfer components for azoreduction. These results provide evidence that the microbial anaerobic azoreduction is linked to the electron transport chain and suggest that the dissimilatory azoreduction is a form of microbial anaerobic respiration. These findings not only expand the number of potential electron acceptors known for microbial energy conservation but also elucidate the mechanisms of microbial anaerobic azoreduction.
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机译:研究了希瓦氏菌S12脱色通过将各种电子供体的氧化与异化偶氮还原偶联而获得生长所需能量的能力。通过使用甲酸盐,乳酸盐,丙酮酸盐或H2作为电子供体,该微生物可以还原多种偶氮染料。此外,在限定的培养基中竞争减少2.0 mM mar菜后,菌株S12生长到最大密度为每毫升3.0×107个细胞。当a菜和甲酸分别作为唯一的电子受体和供体供应时,随着时间的推移,化学计量消耗4.0 mM的甲酸,这表明微生物的偶氮还原是一个电子传输过程,并且这种电子传输可以产生能量来支持生长。分析了来自S12的纯化的膜,周质和细胞质级分,但只有膜级分能够还原甲酸酯,乳酸,丙酮酸或H2作为电子供体的偶氮染料。 5μM的Cu2 +离子,200μM的杜马洛尔,100μM的柱菌素和100μM的甲吡酮的存在抑制了整个细胞和纯化膜部分的厌氧偶氮还原活性,表明脱氢酶,细胞色素和甲萘醌是偶氮还原的重要电子转移成分。这些结果提供了微生物厌氧还原作用与电子传输链相关的证据,并表明异化氮还原作用是微生物厌氧呼吸的一种形式。这些发现不仅扩大了已知用于微生物节能的潜在电子受体的数量,而且阐明了微生物厌氧偶氮还原的机理。
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