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微生物降解六氯环己烷的生物化学及生物修复展望。

Biochemistry of microbial degradation of hexachlorocyclohexane and prospects for bioremediation.

机构信息

Department of Zoology, University of Delhi, Delhi 110007, India.

出版信息

Microbiol Mol Biol Rev. 2010 Mar;74(1):58-80. doi: 10.1128/MMBR.00029-09.

Abstract

Lindane, the gamma-isomer of hexachlorocyclohexane (HCH), is a potent insecticide. Purified lindane or unpurified mixtures of this and alpha-, beta-, and delta-isomers of HCH were widely used as commercial insecticides in the last half of the 20th century. Large dumps of unused HCH isomers now constitute a major hazard because of their long residence times in soil and high nontarget toxicities. The major pathway for the aerobic degradation of HCH isomers in soil is the Lin pathway, and variants of this pathway will degrade all four of the HCH isomers although only slowly. Sequence differences in the primary LinA and LinB enzymes in the pathway play a key role in determining their ability to degrade the different isomers. LinA is a dehydrochlorinase, but little is known of its biochemistry. LinB is a hydrolytic dechlorinase that has been heterologously expressed and crystallized, and there is some understanding of the sequence-structure-function relationships underlying its substrate specificity and kinetics, although there are also some significant anomalies. The kinetics of some LinB variants are reported to be slow even for their preferred isomers. It is important to develop a better understanding of the biochemistries of the LinA and LinB variants and to use that knowledge to build better variants, because field trials of some bioremediation strategies based on the Lin pathway have yielded promising results but would not yet achieve economic levels of remediation.

摘要

林丹,六氯环己烷(HCH)的γ-异构体,是一种有效的杀虫剂。在 20 世纪后半叶,提纯的林丹或未提纯的林丹和 HCH 的α-、β-和δ-异构体的混合物被广泛用作商业杀虫剂。由于其在土壤中的停留时间长和高非靶毒性,大量未使用的 HCH 异构体现在构成了一个主要的危险。HCH 异构体在土壤中的好氧降解的主要途径是林途径,尽管速度较慢,但该途径的变体可以降解所有四种 HCH 异构体。途径中林 A 和林 B 酶的一级结构差异在决定它们降解不同异构体的能力方面起着关键作用。林 A 是脱氯化氢酶,但对其生物化学知之甚少。林 B 是一种水解脱氯酶,已被异源表达和结晶,并对其底物特异性和动力学的序列-结构-功能关系有了一定的了解,尽管也存在一些显著的异常。一些林 B 变体的动力学报告称,即使对其首选异构体,其动力学也很慢。重要的是要更好地了解林 A 和林 B 变体的生物化学,并利用这些知识来构建更好的变体,因为基于林途径的一些生物修复策略的现场试验已经取得了有希望的结果,但还没有达到经济修复水平。

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