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电子传递至琥珀酸沃林氏菌的周质硝酸还原酶(NapA)与NapC蛋白无关。

Electron transport to periplasmic nitrate reductase (NapA) of Wolinella succinogenes is independent of a NapC protein.

作者信息

Simon Jörg, Sänger Monica, Schuster Stephan C, Gross Roland

机构信息

Institut für Mikrobiologie, Johann Wolfgang Goethe-Universität, Marie-Curie-Str. 9, D-60439 Frankfurt am Main, Germany.

出版信息

Mol Microbiol. 2003 Jul;49(1):69-79. doi: 10.1046/j.1365-2958.2003.03544.x.

Abstract

The rumen bacterium Wolinella succinogenes grows by respiratory nitrate ammonification with formate as electron donor. Whereas the enzymology and coupling mechanism of nitrite respiration is well known, nitrate reduction to nitrite has not yet been examined. We report here that intact cells and cell fractions catalyse nitrate and chlorate reduction by reduced viologen dyes with high specific activities. A gene cluster encoding components of a putative periplasmic nitrate reductase system (napA, G, H, B, F, L, D) was sequenced. The napA gene was inactivated by inserting a kanamycin resistance gene cassette. The resulting mutant did not grow by nitrate respiration and did not reduce nitrate during growth by fumarate respiration, in contrast to the wild type. An antigen was detected in wild-type cells using an antiserum raised against the periplasmic nitrate reductase (NapA) from Paracoccus pantotrophus. This antigen was absent in the W. succinogenes napA mutant. It is concluded that the periplasmic nitrate reductase NapA is the only respiratory nitrate reductase in W. succinogenes, although a second nitrate-reducing enzyme is apparently induced in the napA mutant. The nap cluster of W. succinogenes lacks a napC gene whose product is thought to function in quinol oxidation and electron transfer to NapA in other bacteria. The W. succinogenes genome encodes two members of the NapC/NirT family, NrfH and FccC. Characterization of corresponding deletion mutants indicates that neither of these two proteins is required for nitrate respiration. A mutant lacking the genes encoding respiratory nitrite reductase (nrfHA) had wild-type properties with respect to nitrate respiration. A model of the electron transport chain of nitrate respiration is proposed in which one or more of the napF, G, H and L gene products mediate electron transport from menaquinol to the periplasmic NapAB complex. Inspection of the W. succinogenes genome sequence suggests that ammonia formation from nitrate is catalysed exclusively by periplasmic respiratory enzymes.

摘要

瘤胃细菌琥珀酸沃氏菌以甲酸作为电子供体,通过呼吸性硝酸盐氨化作用进行生长。虽然亚硝酸盐呼吸的酶学和偶联机制已为人熟知,但硝酸盐还原为亚硝酸盐的过程尚未得到研究。我们在此报告,完整细胞和细胞组分能以高比活性催化还原紫精染料介导的硝酸盐和氯酸盐还原反应。对一个推定的周质硝酸盐还原酶系统(napA、G、H、B、F、L、D)的编码组件的基因簇进行了测序。通过插入卡那霉素抗性基因盒使napA基因失活。与野生型相比,所得突变体不能通过硝酸盐呼吸生长,在延胡索酸呼吸生长过程中也不能还原硝酸盐。使用针对泛养副球菌周质硝酸盐还原酶(NapA)产生的抗血清,在野生型细胞中检测到了一种抗原。在琥珀酸沃氏菌napA突变体中不存在这种抗原。结论是,周质硝酸盐还原酶NapA是琥珀酸沃氏菌中唯一的呼吸性硝酸盐还原酶,尽管在napA突变体中显然诱导产生了第二种硝酸盐还原酶。琥珀酸沃氏菌的nap基因簇缺少napC基因,其产物被认为在其他细菌中参与醌的氧化以及向NapA的电子传递。琥珀酸沃氏菌基因组编码NapC/NirT家族的两个成员,即NrfH和FccC。对相应缺失突变体的表征表明,这两种蛋白质对于硝酸盐呼吸都不是必需的。一个缺乏编码呼吸性亚硝酸盐还原酶基因(nrfHA)的突变体在硝酸盐呼吸方面具有野生型特性。提出了一个硝酸盐呼吸电子传递链模型,其中napF、G、H和L基因产物中的一个或多个介导从甲基萘醌到周质NapAB复合物的电子传递。对琥珀酸沃氏菌基因组序列的检查表明,硝酸盐形成氨的过程仅由周质呼吸酶催化。

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