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Cloning of d-lactate dehydrogenase genes of Lactobacillus delbrueckii subsp. bulgaricus and their roles in d-lactic acid production

机译:德氏乳杆菌亚种的d-乳酸脱氢酶基因的克隆。保加利亚及其在d-乳酸生产中的作用

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摘要

Lactobacillus delbrueckii subsp. bulgaricus is a heterogenous lactic acid bacterium that converts pyruvate mainly to d-lactic acid using d-lactate dehydrogenases (d-LDHs), whose functional properties remain poorly characterized. Here, the d-LDHs genes (ldb0101, ldb0813, ldb1010, ldb1147 and ldb2021) were cloned and overexpressed in Escherichia coli JM109 from an inducible pUC18 vector, respectively, and the resulting strains were compared in terms of d-lactic acid production. The strain expressing ldb0101 and ldb1010 gene individually produced more d-lactate than other three strains. Further study revealed that Ldb0101 activity was down-regulated by the oxygen and, therefore, achieved a highest titer of d-lactate (1.94 g/L) under anaerobic condition, and introduction of ldb1010 gene enhanced d-lactate formation (0.94 and 0.85 g/L, respectively) both in aerobic and anaerobic conditions due to a relatively stable q d-lactate. Our results suggested that the enzyme Ldb0101 and Ldb1010 played a role of more importance in d-lactate formation. To the best of our knowledge, we demonstrate for the first time the roles of different d-LDH homologs from L. bulgaricus in d-lactic acid production.
机译:德氏乳杆菌亚种。保加利亚是一种异质乳酸细菌,它使用d-乳酸脱氢酶(d-LDHs)主要将丙酮酸转化为d-乳酸,其功能特性仍然很差。在此,分别从可诱导的pUC18载体在大肠杆菌JM109中克隆和过表达d-LDHs基因(ldb0101,ldb0813,ldb1010,ldb1147和ldb2021),并比较了产生的菌株的乳酸产量。表达ldb0101和ldb1010基因的菌株比其他三个菌株分别产生更多的d-乳酸。进一步的研究表明Ldb0101的活性受到氧气的下调,因此在厌氧条件下达到了最高的d-乳酸(1.94 g / L)滴度,而导入ldb1010基因增强了d-乳酸的形成(0.94和0.85 g / d)由于相对稳定的q d-乳酸,因此在有氧和厌氧条件下均可使用。我们的结果表明,酶Ldb0101和Ldb1010在d-乳酸的形成中起着更重要的作用。据我们所知,我们首次证明了来自保加利亚乳杆菌的不同d-LDH同源物在d-乳酸生产中的作用。

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