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Novel Biochemical Properties and Physiological Role of the Flavin Mononucleotide Oxidoreductase YhdA from Bacillus subtilis

机译:来自芽孢杆菌枯草芽孢杆菌的黄素单核苷酸氧化还原酶YHDA的新生物化学特性和生理作用

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Cr(VI) is mutagenic and teratogenic and considered an environmental pollutant of increasing concern. The use of microbial enzymes that convert this ion into its less toxic reduced insoluble form, Cr(III), represents a valuable bioremediation strategy. In this study, we examined the Bacillus subtilis YhdA enzyme, which belongs to the family of NADPH-dependent flavin mononucleotide oxide reductases and possesses azo-reductase activity as a factor that upon overexpression confers protection on B. subtilis from the cytotoxic effects promoted by Cr(VI) and counteracts the mutagenic effects of the reactive oxygen species (ROS)-promoted lesion 8-OxoG. Further, our in vitro assays unveiled catalytic and biochemical properties of biotechnological relevance in YhdA; a pure recombinant His_(10)-YhdA protein efficiently catalyzed the reduction of Cr(VI) employing NADPH as a cofactor. The activity of the pure oxidoreductase YhdA was optimal at 30°C and at pH 7.5 and displayed K_(m) and V _(max) values of 7.26?mM and 26.8?μmol·min~(?1)·mg~(?1) for Cr(VI), respectively. Therefore, YhdA can be used for efficient bioremediation of Cr(VI) and counteracts the cytotoxic and genotoxic effects of oxygen radicals induced by intracellular factors and those generated during reduction of hexavalent chromium.IMPORTANCE Here, we report that the bacterial flavin mononucleotide/NADPH-dependent oxidoreductase YhdA, widely distributed among Gram-positive bacilli, conferred protection to cells from the cytotoxic effects of Cr(VI) and prevented the hypermutagenesis exhibited by a MutT/MutM/MutY-deficient strain. Additionally, a purified recombinant His_(10)-YhdA protein displayed a strong NADPH-dependent chromate reductase activity. Therefore, we postulate that in bacterial cells, YhdA counteracts the cytotoxic and genotoxic effects of intracellular and extracellular inducers of oxygen radicals, including those caused by hexavalent chromium.
机译:Cr(vi)是致突变性和致畸性的,并且被认为是越来越多的环境污染物。使用微生物酶将该离子转化为其较小的毒性减少的不溶性形式Cr(III)表示有价值的生物化反应策略。在这项研究中,我们研究了枯草芽孢杆菌YhDA酶,其属于NADPH依赖性黄蛋白单核苷酸还原酶的家族,并具有偶氮还原酶活性,作为在过度表达赋予B.枯草芽孢杆菌免受CR促进的细胞毒性作用的因素的因素。来自CR促进的细胞毒性效应(vi)并抵消反应性氧物种(ROS)的致致抗体效果 - α-α-氧化症8-氧气。此外,我们的体外测定揭开了Yhda的生物技术相关性的催化和生化特性;纯重组His_(10)-yHDA蛋白有效地催化了使用NADPH作为辅因子的Cr(VI)的还原。纯氧化还原酶YHDA的活性在30℃和pH7.5时最佳,显示K_(m)和v _(max)值为7.26Ωmm和26.8Ω·mm〜(?1)·mg〜(? 1)分别为Cr(vi)。因此,YHDA可用于Cr(VI)的有效生物修复,并抵消细胞内因子诱导的氧自由基的细胞毒性和遗传毒性效应,并且在减少六价铬期间产生的那些。在此报告细菌黄蛋白单核苷酸/ NADP-依赖于氧化还原酶YHDA,广泛分布在革兰氏阳性杆菌中,从Cr(vi)的细胞毒性作用赋予细胞的保护,并防止了由mut / mutm / uty缺陷的菌株表现出的高培训。另外,纯化的重组His_(10)-yHDA蛋白显示出强烈的NADPH依赖性铬酸盐还原酶活性。因此,我们假设在细菌细胞中,Yhda抵消了氧自由基细胞内和细胞外诱导剂的细胞毒性和遗传毒性作用,包括由六价铬引起的那些。

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