通过mtrC基因克隆和硝酸盐还原途径破坏优化重组阿塞拜疆谢瓦内拉细菌的金属生物还原过程。

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Molecular Biotechnology Pub Date : 2024-11-01 Epub Date: 2023-11-02 DOI:10.1007/s12033-023-00920-x
Elham Rastkhah, Faezeh Fatemi, Parvaneh Maghami
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引用次数: 0

摘要

随着人口的增长、工业化和城市化,环境污染日益严重。阿塞拜疆谢瓦内拉菌是一种高效的金属生物修复细菌。选择mtrC基因作为克隆靶点,以改善EET(细胞外电子转移)途径中的电子通量链。使用SDM(定点突变)技术,这种独特的基因组装的特点是mtrC基因夹在两个napD/B基因之间,以破坏硝酸盐还原途径,而硝酸盐还原是主要的金属还原竞争对手。将Shew-mtrC基因构建转移到表达宿主菌(E.coli BL21和S.azerbaijanica)中的表达质粒pET28a(+)中,在pUC57中,将克隆质粒转移到克隆宿主菌E.coli Top10和S.azerbaijanica中。所有克隆程序(即合成、插入、转化、克隆和蛋白质表达)都通过精确的测试进行了验证和确认。使用ATR-FTIR分析、CD、蛋白质印迹、亲和层析、SDS-PAGE和其他技术来确认MtrC蛋白的表达和结构。基因组序列和引物是根据提交的谢瓦内拉oneidensis MR-1基因组设计的,该基因组是与该本土物种最相似的细菌。作为一种可持续的策略,重组阿塞拜疆S.azerbaijanica细菌在金属生物修复中的性能需要更多的研究来验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Optimizing the Metal Bioreduction Process in Recombinant Shewanella azerbaijanica Bacteria: A Novel Approach via mtrC Gene Cloning and Nitrate-Reducing Pathway Destruction.

Optimizing the Metal Bioreduction Process in Recombinant Shewanella azerbaijanica Bacteria: A Novel Approach via mtrC Gene Cloning and Nitrate-Reducing Pathway Destruction.

Environmental pollution is growing every day in terms of the increase in population, industrialization, and urbanization. Shewanella azerbaijanica is introduced as a highly potent bacterium in metal bioremediation. The mtrC gene was selected as a cloning target to improve electron flux chains in the EET (extracellular electron transfer) pathway. Using the SDM (site-directed mutagenesis) technique, the unique gene assembly featured the mtrC gene sandwiched between two napD/B genes to disrupt the nitrate reduction pathway, which serves as the primary metal reduction competitor. Shew-mtrC gene construction was transferred to expression plasmid pET28a (+) in the expression host bacteria (E. coli BL21 and S. azerbaijanica), in pUC57, cloning plasmid, which was transferred to the cloning host bacteria E. coli Top10 and S. azerbaijanica. All cloning procedures (i.e., synthesis, insertion, transformation, cloning, and protein expression) were verified and confirmed by precise tests. ATR-FTIR analysis, CD, western blotting, affinity chromatography, SDS-PAGE, and other techniques were used to confirm the expression and structure of the MtrC protein. The genome sequence and primers were designed according to the submitted Shewanella oneidensis MR-1 genome, the most similar bacteria to this native species. The performance of recombinant S. azerbaijanica bacterium in metal bioremediation, as sustainable strategy, has to be verified by more research.

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来源期刊
Molecular Biotechnology
Molecular Biotechnology 医学-生化与分子生物学
CiteScore
4.10
自引率
3.80%
发文量
165
审稿时长
6 months
期刊介绍: Molecular Biotechnology publishes original research papers on the application of molecular biology to both basic and applied research in the field of biotechnology. Particular areas of interest include the following: stability and expression of cloned gene products, cell transformation, gene cloning systems and the production of recombinant proteins, protein purification and analysis, transgenic species, developmental biology, mutation analysis, the applications of DNA fingerprinting, RNA interference, and PCR technology, microarray technology, proteomics, mass spectrometry, bioinformatics, plant molecular biology, microbial genetics, gene probes and the diagnosis of disease, pharmaceutical and health care products, therapeutic agents, vaccines, gene targeting, gene therapy, stem cell technology and tissue engineering, antisense technology, protein engineering and enzyme technology, monoclonal antibodies, glycobiology and glycomics, and agricultural biotechnology.
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