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Outer Membrane c-Type Cytochromes Required for Fe(III) and Mn(IV) Oxide Reduction in Geobacter sulfurreducens

机译:减少土壤细菌硫还原剂中的Fe(III)和Mn(IV)氧化物还原所需的外膜c型细胞色素

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The potential role of outer membrane proteins in electron transfer to insoluble Fe(III) oxides by Geobacter sulfurreducens was investigated because this organism is closely related to the Fe(III) oxide-reducing organisms that are predominant in many Fe(III)-reducing environments. Two of the most abundant proteins that were easily sheared from the outer surfaces of intact cells were c-type cytochromes. One, designated OmcS, has a molecular mass of ca. 50 kDa and is predicted to be an outer membrane hexaheme c-type cytochrome. Transcripts for omcS could be detected during growth on Fe(III) oxide, but not on soluble Fe(III) citrate. The omcS mRNA consisted primarily of a monocistronic transcript, and to a lesser extent, a longer transcript that also contained the downstream gene omcT, which is predicted to encode a second hexaheme outer membrane cytochrome with 62.6% amino acid sequence identity to OmcS. The other abundant c-type cytochrome sheared from the outer surface of G. sulfurreducens, designated OmcE, has a molecular mass of ca. 30 kDa and is predicted to be an outer membrane tetraheme c-type cytochrome. When either omcS or omcE was deleted, G. sulfurreducens could no longer reduce Fe(III) oxide but could still reduce soluble electron acceptors, including Fe(III) citrate. The mutants could reduce Fe(III) in Fe(III) oxide medium only if the Fe(III) chelator, nitrilotriacetic acid, or the electron shuttle, anthraquinone 2,6-disulfonate, was added. Expressing omcS or omcE in trans restored the capacity for Fe(III) oxide reduction. OmcT was not detected among the sheared proteins, and genetic studies indicated that G. sulfurreducens could not reduce Fe(III) oxide when omcT was expressed but OmcS was absent. In contrast, Fe(III) oxide was reduced when omcS was expressed in the absence of OmcT. These results suggest that OmcS and OmcE are involved in electron transfer to Fe(III) oxides in G. sulfurreducens. They also emphasize the importance of evaluating mechanisms for Fe(III) reduction with environmentally relevant Fe(III) oxide, rather than the more commonly utilized Fe(III) citrate, because additional electron transfer components are required for Fe(III) oxide reduction that are not required for Fe(III) citrate reduction.
机译:研究了外膜蛋白在土壤还原性硫还原剂将电子转移至不溶性Fe(III)氧化物中的潜在作用,因为该生物与在许多Fe(III)还原环境中占主导地位的Fe(III)氧化物还原生物密切相关。 。从完整细胞的外表面容易剪切出的两种最丰富的蛋白质是c型细胞色素。一种称为OmcS,分子量约为。 50 kDa,预计是外膜六血红素c型细胞色素。 omcS的转录本可以在Fe(III)氧化物上生长期间检测到,但在可溶性柠檬酸Fe(III)上则不能检测到。 omcS mRNA主要由单顺反子转录本组成,在较小程度上由较长的转录本组成,该转录本还包含下游基因omcT,该基因预计编码具有与OmcS相同的62.6%氨基酸序列同一性的第二个六血红素外膜细胞色素。从G.sulfreducens外表面剪下的另一种丰富的c型细胞色素,称为OmcE,分子量约为1。 30 kDa,预计是外膜四血红素c型细胞色素。当删除omcS或omcE时,G.sulfreducens不再能够还原Fe(III)氧化物,但仍可以还原可溶性电子受体,包括柠檬酸Fe(III)。仅当添加Fe(III)螯合剂次氮基三乙酸或电子穿梭蒽醌2,6-二磺酸盐时,突变体才能还原Fe(III)氧化物介质中的Fe(III)。反式表达omcS或omcE可以恢复还原Fe(III)的能力。在剪切的蛋白中未检测到OmcT,遗传研究表明,表达omcT但不存在OmcS时,硫还原菌不能还原Fe(III)氧化物。相反,当在没有OmcT的情况下表达omcS时,Fe(III)氧化物被还原。这些结果表明OmcS和OmcE参与电子转移到G.sulfreducens中的Fe(III)氧化物。他们还强调了评估与环境相关的Fe(III)氧化物而不是更常用的柠檬酸Fe(III)还原Fe(III)的机制的重要性,因为氧化Fe(III)还原需要额外的电子转移成分柠檬酸铁(III)还原不需要。

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