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Extracellular Reduction of Hexavalent Chromium by Cytochromes MtrC and OmcA of Shewanella oneidensis MR-1

机译:拟南芥希瓦氏菌MR-1的细胞色素MtrC和OmcA对六价铬的胞外还原作用

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To characterize the roles of cytochromes MtrC and OmcA of Shewanella oneidensis MR-1 in Cr(VI) reduction, the effects of deleting the mtrC and/or omcA gene on Cr(VI) reduction and the cellular locations of reduced Cr(III) precipitates were investigated. Compared to the rate of reduction of Cr(VI) by the wild type (wt), the deletion of mtrC decreased the initial rate of Cr(VI) reduction by 43.5%, while the deletion of omcA or both mtrC and omcA lowered the rate by 53.4% and 68.9%, respectively. In wt cells, Cr(III) precipitates were detected by transmission electron microscopy in the extracellular matrix between the cells, in association with the outer membrane, and inside the cytoplasm. No extracellular matrix-associated Cr(III) precipitates, however, were found in the cytochrome mutant cell suspension. In mutant cells without either MtrC or OmcA, most Cr(III) precipitates were found in association with the outer membrane, while in mutant cells lacking both MtrC and OmcA, most Cr(III) precipitates were found inside the cytoplasm. Cr(III) precipitates were also detected by scanning election microscopy on the surfaces of the wt and mutants without MtrC or OmcA but not on the mutant cells lacking both MtrC and OmcA, demonstrating that the deletion of mtrC and omcA diminishes the extracellular formation of Cr(III) precipitates. Furthermore, purified MtrC and OmcA reduced Cr(VI) with apparent k_(cat) values of 1.2 ± 0.2 (mean ± standard deviation) and 10.2 ± 1 s~(?1) and K_(m) values of 34.1 ± 4.5 and 41.3 ± 7.9 μM, respectively. Together, these results consistently demonstrate that MtrC and OmcA are the terminal reductases used by S. oneidensis MR-1 for extracellular Cr(VI) reduction where OmcA is a predominant Cr(VI) reductase.
机译:为了表征Shewanella oneidensis MR-1的细胞色素MtrC和OmcA在Cr(VI)还原中的作用,删除mtrC和/或omcA基因对Cr(VI)还原的作用以及还原的Cr(III)沉淀的细胞位置被调查了。与野生型(wt)降低Cr(VI)的速率相比,删除mtrC可以使Cr(VI)的初始还原速率降低43.5%,而删除omcA或删除mtrC和omcA都可以降低速率分别增长53.4%和68.9%。在wt细胞​​中,通过透射电子显微镜在细胞之间,与外膜相关以及在细胞质内部的细胞外基质中检测到了Cr(III)沉淀。但是,在细胞色素突变细胞悬浮液中未发现细胞外基质相关的Cr(III)沉淀。在没有MtrC或OmcA的突变细胞中,发现大多数Cr(III)沉淀物与外膜结合,而在既没有MtrC也没有OmcA的突变细胞中,大多数Cr(III)沉淀物发现于细胞质内。 Cr(III)沉淀物也可以通过扫描电子显微镜在wt和没有MtrC或OmcA的突变体的表面上检测到,但在缺乏MtrC和OmcA的突变体细胞上都没有,这表明mtrC和omcA的缺失减少了Cr的细胞外形成(III)沉淀。此外,纯化的MtrC和OmcA还原了Cr(VI),表观k_(cat)值为1.2±0.2(均值±标准偏差)和10.2±1 s〜(?1),K_(m)值为34.1±4.5和41.3分别为±7.9μM。在一起,这些结果一致证明,MtrC和OmcA是S.oneidensis MR-1用于胞外Cr(VI)还原的末端还原酶,其中OmcA是主要的Cr(VI)还原酶。

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