首页> 外文期刊>World Journal of Microbiology & Biotechnology >Enhancement of L-2-haloacid dehalogenase expression in Pseudomonas stutzeri DEH138 based on the different substrate specificity between dehalogenase-producing bacteria and their dehalogenases
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Enhancement of L-2-haloacid dehalogenase expression in Pseudomonas stutzeri DEH138 based on the different substrate specificity between dehalogenase-producing bacteria and their dehalogenases

机译:基于产生脱卤酶的细菌与其脱卤酶之间不同的底物特异性,增强斯图氏假单胞菌DEH138中L-2-卤酸脱卤酶的表达

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摘要

There was no direct correlation in substrate specificity between the metabolism of Pseudomonas stutzeri DEH138 and its corresponding dehalogenase. Dehalogenase substrates that could be dehalogenated might not be degraded by DEH138 or vice versa. Basing on this, different approaches to enhance L-2-haloacid dehalogenase (L-DEX) production in DEH138 via the combination of non-halogenated compounds with different inducers were applied. The optimum approach to obtain more L-DEX from DEH138 was the combination of DL-lactate and DL-2-chlorobutyrate, with 5.7-fold greater production and 11.7-fold greater productivity of the enzyme after optimization.
机译:Stutzeri假单胞菌DEH138的代谢与其相应的脱卤酶之间的底物特异性没有直接相关性。可能被脱卤的脱卤酶底物可能不会被DEH138降解,反之亦然。在此基础上,采用了不同的方法,通过非卤代化合物与不同诱导剂的结合来提高DEH138中L-2-卤代酸脱卤酶(L-DEX)的产量。从DEH138获得更多L-DEX的最佳方法是DL-乳酸和DL-2-氯丁酸酯的组合,优化后酶的产量增加5.7倍,生产率提高11.7倍。

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