首页> 外文期刊>Journal of bacteriology >Dichloromethane dehalogenase with improved catalytic activity isolated from a fast-growing dichloromethane-utilizing bacterium.
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Dichloromethane dehalogenase with improved catalytic activity isolated from a fast-growing dichloromethane-utilizing bacterium.

机译:从快速生长的利用二氯甲烷的细菌中分离出具有改善的催化活性的二氯甲烷脱卤酶。

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A methylotrophic bacterium, denoted strain DM11, was isolated from groundwater and shown to utilize dichloromethane or dibromomethane as the sole carbon and energy source. The new isolate grew at the high rate of 0.22 h-1 compared with 11 previously characterized dichloromethane-utilizing bacteria (micromax, 0.08 h-1). The dichloromethane dehalogenase from strain DM11 (group B enzyme) was purified by anion-exchange chromatography. It was shown to be substantially different from the set of dichloromethane dehalogenases from the 11 slow-growing strains (group A enzymes) that had previously been demonstrated to be identical. The Vmax for the group B enzyme was 97 mkat/kg of protein, some 5.6-fold higher than that of the group A enzymes. The group A dehalogenases showed hyperbolic saturation with the cosubstrate glutathione, whereas the group B enzyme showed positive cooperativity in glutathione binding. Only 1 of 15 amino acids occupied common positions at the N termini, and amino acid contents were substantially different in group A and group B dehalogenases. Immunological assays demonstrated weak cross-reactivity between the two enzymes. Despite the observed structural and kinetic differences, there is potentially evolutionary relatedness between group A and group B enzymes, as indicated by (i) hybridization of DM11 DNA with a gene probe of the group A enzyme, (ii) a common requirement for glutathione in catalysis, and (iii) similar subunit molecular weights of about 34,000.
机译:从地下水中分离出一种甲基营养细菌,命名为DM11菌株,并证明其利用二氯甲烷或二溴甲烷作为唯一的碳和能源。与11种先前表征的利用二氯甲烷的细菌(micromax,0.08 h-1)相比,新分离株以0.22 h-1的高速率生长。通过阴离子交换色谱法纯化来自菌株DM11的二氯甲烷脱卤酶(B组酶)。结果表明,它与11种缓慢生长的菌株(A组酶)中的二氯甲烷脱卤化酶组完全不同,先前已证明它们是相同的。 B组酶的Vmax为97 mkat / kg蛋白质,比A组酶的Vmax高5.6倍。 A组脱卤素酶与共底物谷胱甘肽呈双曲线饱和,而B组酶与谷胱甘肽结合呈正协同作用。 15个氨基酸中只有1个在N末端占据共同位置,并且A组和B组脱卤素酶的氨基酸含量基本不同。免疫学分析表明两种酶之间的交叉反应性较弱。尽管观察到了结构和动力学上的差异,但A组和B组酶之间可能存在进化相关性,如(i)DM11 DNA与A组酶基因探针的杂交;(ii)谷胱甘肽在(iii)约34,000的相似亚基分子量。

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