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氰化物水合酶和氰化物二水合酶:氰化物生物降解和生物检测中的新兴工具。

Cyanide hydratases and cyanide dihydratases: emerging tools in the biodegradation and biodetection of cyanide.

作者信息

Martínková Ludmila, Veselá Alicja Barbara, Rinágelová Anna, Chmátal Martin

机构信息

Laboratory of Biotransformation, Institute of Microbiology, Academy of Sciences of the Czech Republic, Vídeňská 1083, CZ-142 20, Prague, Czech Republic.

Department of Biochemistry, Charles University in Prague, Hlavova 8, CZ-128 40, Prague, Czech Republic.

出版信息

Appl Microbiol Biotechnol. 2015 Nov;99(21):8875-82. doi: 10.1007/s00253-015-6899-0. Epub 2015 Sep 2.

Abstract

The purpose of this study is to summarize the current knowledge of the enzymes which are involved in the hydrolysis of cyanide, i.e., cyanide hydratases (CHTs; EC 4.2.1.66) and cyanide dihydratases (CynD; EC 3.5.5.1). CHTs are probably exclusively produced by filamentous fungi and widely occur in these organisms; in contrast, CynDs were only found in a few bacterial genera. CHTs differ from CynDs in their reaction products (formamide vs. formic acid and ammonia, respectively). Several CHTs were also found to transform nitriles but with lower relative activities compared to HCN. Mutants of CynDs and CHTs were constructed to study the structure-activity relationships in these enzymes or to improve their catalytic properties. The effect of the C-terminal part of the protein on the enzyme activity was determined by constructing the corresponding deletion mutants. CynDs are less active at alkaline pH than CHTs. To improve its bioremediation potential, CynD from Bacillus pumilus was engineered by directed evolution combined with site-directed mutagenesis, and its operation at pH 10 was thus enabled. Some of the enzymes have been tested for their potential to eliminate cyanide from cyanide-containing wastewaters. CynDs were also used to construct cyanide biosensors.

摘要

本研究的目的是总结目前关于参与氰化物水解的酶的知识,即氰化物水合酶(CHTs;EC 4.2.1.66)和氰化物二水合酶(CynD;EC 3.5.5.1)。CHTs可能仅由丝状真菌产生,并广泛存在于这些生物体中;相比之下,CynDs仅在少数细菌属中发现。CHTs与CynDs的反应产物不同(分别为甲酰胺与甲酸和氨)。还发现几种CHTs能转化腈类,但与HCN相比,其相对活性较低。构建了CynDs和CHTs的突变体,以研究这些酶的结构-活性关系或改善其催化特性。通过构建相应的缺失突变体,确定了蛋白质C末端部分对酶活性的影响。CynDs在碱性pH下的活性低于CHTs。为了提高其生物修复潜力,通过定向进化结合定点诱变对短小芽孢杆菌的CynD进行了改造,从而使其能够在pH 10下运行。已经对其中一些酶从含氰废水中去除氰化物的潜力进行了测试。CynDs还被用于构建氰化物生物传感器。

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