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Construction and Characterization of tetH Overexpression and Knockout Strains of Acidithiobacillus ferrooxidans

机译:铁氧化酸性硫杆菌的tetH过表达和敲除菌株的构建和鉴定

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摘要

Acidithiobacillus ferrooxidans is a major participant in consortia of microorganisms used for bioleaching. It can obtain energy from the oxidation of Fe2+, H2, S0, and various reduced inorganic sulfur compounds (RISCs). Tetrathionate is a key intermediate during RISC oxidation, hydrolyzed by tetrathionate hydrolase (TetH), and used as sole energy source. In this study, a tetH knockout (ΔtetH) mutant and a tetH overexpression strain were constructed and characterized. The tetH overexpression strain grew better on sulfur and tetrathionate and possessed a higher rate of tetrathionate utilization and TetH activity than the wild type. However, its cell yields on tetrathionate were much lower than those on sulfur. The ΔtetH mutant could not grow on tetrathionate but could proliferate on sulfur with a lower cell yield than the wild type's, which indicated that tetrathionate hydrolysis is mediated only by TetH, encoded by tetH. The ΔtetH mutant could survive in ferrous medium with an Fe2+ oxidation rate similar to that of the wild type. For the tetH overexpression strain, the rate was relatively higher than that of the wild type. The reverse transcription-quantitative PCR (qRT-PCR) results showed that tetH and doxD2 acted synergistically, and doxD2 was considered important in thiosulfate metabolism. Of the two sqr genes, AFE_0267 seemed to play as important a role in sulfide oxidation as AFE_1792. This study not only provides a substantial basis for studying the function of the tetH gene but also may serve as a model to clarify other candidate genes involved in sulfur oxidation in this organism.
机译:酸性氧化硫杆菌铁氧体是用于生物浸出的微生物联合体的主要参与者。它可以通过Fe 2 + ,H2,S 0 和各种还原的无机硫化合物(RISC)的氧化获得能量。四硫代酸盐是RISC氧化过程中的关键中间体,被四硫代酸盐水解酶(TetH)水解,并用作唯一的能源。在这项研究中,构建并鉴定了tetH基因敲除(ΔtetH)突变体和tetH过表达菌株。与野生型相比,tetH过表达菌株在硫和四硫代酸盐上生长更好,并具有更高的四硫代酸盐利用率和TetH活性。但是,其在四硫代酸盐上的细胞产率远低于在硫磺下的细胞产率。 ΔtetH突变体不能在四硫酸酯上生长,但可以在硫上增殖,其细胞产率低于野生型,这表明四硫酸酯水解仅由tetH编码,由tetH编码。 ΔtetH突变体可以在铁质培养基中生存,其Fe 2 + 的氧化速率与野生型相似。对于tetH过表达菌株,其发生率相对高于野生型。逆转录-定量PCR(qRT-PCR)结果表明,tetH和doxD2具有协同作用,并且doxD2被认为在硫代硫酸盐代谢中很重要。在两个sqr基因中,AFE_0267似乎在硫化物氧化中起着与AFE_1792同样重要的作用。该研究不仅为研究tetH基因的功能提供了坚实的基础,而且可以作为阐明该生物中涉及硫氧化的其他候选基因的模型。

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