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首页> 外文期刊>World Journal of Microbiology and Biotechnology >Specific dechlorinase activity in lindane degradation by Streptomyces sp. M7
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Specific dechlorinase activity in lindane degradation by Streptomyces sp. M7

机译:链霉菌属林丹降解中的特定脱氯酶活性。 M7

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摘要

Synthesis of dechlorinase in Streptomyces sp. M7 was induced when the microorganism was grown in the presence of lindane (γ-hexachlorocyclohexane) as the only carbon source. Activity of cells grown with lindane was about four and half times higher compared to cells grown with glucose. Maximum dechlorinase activity was observed at 30°C in alkaline conditions pH (7.9) and the enzyme did not show cation dependency. Sodium dodecyl sulfate polyacrylamide gel electrophoresis revealed one differential band with a molecular weight similar to serum albumin (M r 66,200), which corresponded to polynucleotide phosphorylase, an enzyme that plays an important role in the regulation system and could be involved in the regulation of the dechlorinase gene. Detected in cell-free extracts were γ-pentachlorocyclohexene and 1,3,4,6-tetrachloro-1,4-cyclohexadiene, both being products of the dechlorinase activity. This is the first time that the presence of an enzyme with dechlorinase activity has been demonstrated in an actinomycete strain isolated in Tucumán, Argentina. Characteristics of this enzyme revealed that Streptomyces sp. M7 could be useful in the future in bioremediation of soil or as a biosensor.
机译:链霉菌中脱氯酶的合成当微生物在林丹(γ-六氯环己烷)作为唯一碳源存在下生长时,会诱导M7。与用葡萄糖生长的细胞相比,用林丹生长的细胞的活性高约四倍半。在碱性条件下(pH值为7.9)在30°C时观察到最大的脱氯酶活性,该酶没有阳离子依赖性。十二烷基硫酸钠聚丙烯酰胺凝胶电泳显示一条分子量与血清白蛋白相似的差异带(M rsub 66200),与多核苷酸磷酸化酶相对应,多核苷酸磷酸化酶在调节系统中起重要作用,可能参与其中。脱氯酶基因的调控。在无细胞提取物中检测到的都是脱氯酶活性的产物γ-五氯环己烯和1,3,4,6-四氯-1,4-环己二烯。这是首次在阿根廷Tucumán分离的放线菌菌株中证实具有脱氯酶活性的酶的存在。该酶的特征显示链霉菌sp。 M7可能会在将来对土壤进行生物修复或作为生物传感器使用。

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