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Cloning and characterisation of a novel 2,4-dichlorophenol hydroxylase from a metagenomic library derived from polychlorinated biphenyl-contaminated soil

机译:从多氯联苯污染土壤衍生的宏基因组文库中克隆和表征新型2,4-二氯苯酚羟化酶

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摘要

A novel 2,4-dichlorophenol hydroxylase (TfdB, EC 1.14.13.20) gene, designated as tfdB-JLU, was identified from a metagenome constructed from polychlorinated biphenyl-contaminated soil by functional screening and heterologously expressed in Escherichia coli. The deduced amino acid sequence of tfdB-JLU exhibited less than 48% homology with other known TfdBs. The enzyme exhibited a wider substrate spectrum than the previously reported TfdBs and higher relative activity towards ortho-substituted dichlorophenols, 2-chlorophenol, and 3-chlorophenol than towards 2,4-dichlorophenol, the preferred substrate of other known TfdBs. The enzyme had a K m of 5 μM for 2,4-dichlorophenol and 6 μM for NADPH. The optimal temperature and pH of the enzyme were 25°C and 7.5, respectively. Activity of the purified TfdB-JLU was slightly enhanced by Ca2+, Mn2+, Co2+, and Fe2+, and completely inhibited by Cu2+, Hg2+, and Zn2+. This study is the first report to identify a novel TfdB from a metagenome.
机译:一个新的2,4-二氯苯酚羟化酶(TfdB,EC 1.14.13.20)基因,被命名为tfdB-JLU,是通过功能筛选从多氯联苯污染土壤构建的一个基因组中鉴定出来的,并在大肠杆菌中异源表达。推定的tfdB-JLU氨基酸序列与其他已知的TfdBs的同源性低于48%。该酶显示出比以前报道的TfdBs更宽的底物谱,并且对邻位取代的二氯苯酚,2-氯苯酚和3-氯苯酚的相对活性比对2,4-二氯苯酚(其他已知TfdBs的优选底物)更高。该酶对2,4-二氯苯酚的K m 为5μM,对NADPH为6μM。该酶的最佳温度和pH分别为25°C和7.5。 Ca 2 + ,Mn 2 + ,Co 2 + 和Fe 2略微提高了纯化的TfdB-JLU的活性+ ,并被Cu 2 + ,Hg 2 + 和Zn 2 + 完全抑制。这项研究是从元基因组中鉴定新型TfdB的第一份报告。

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