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Cloning and sequence analysis of a partial L-lactate dehydrogenase gene of Bacillus coagulans Tl-4v

机译:凝结芽孢杆菌Tl-4v的部分L-乳酸脱氢酶基因的克隆和序列分析

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Bacillus coagulans TL-4 strain is a thermophilic bacterium for high L-lactate production. We reported here that its 779-bp partial NAD+-dependent L-lactate dehydrogenase (LDH) gene sequence (GenBank accession no. GU354320) encoding a deduced 259 amino acid peptide was cloned by using one pair of designed degenerate primers. The amino acid sequence alignment and the built phylogenetic tree revealed that this partial LDH of B. coagulans TL-4 shared high homology with the conserved LDH stretches from 59.17% to 74.70% among other 10 Bacillus species and 48.81% to that of Lactobacillus sp. MD-1. Furthermore, three highly conservative LDH regions, one (Val1∼Asp34) for NADH binding site and two (Asp59∼Ile86 and Asn107∼Arg139) for the distinct active sites, were also found in this NAD+-dependent LDH stretch.
机译:凝结芽孢杆菌TL-4菌株是用于高产L-乳酸的嗜热细菌。我们在这里报告说,通过使用一对cDNA克隆了其779-bp的部分NAD + -依赖性L-乳酸脱氢酶(LDH)基因序列(GenBank登录号GU354320),其编码推导的259个氨基酸肽被克隆。设计的简并引物。氨基酸序列比对和构建的系统进化树显示,凝结芽孢杆菌TL-4的该部分LDH与保守的LDH延伸率高,在其他10种芽孢杆菌中从59.17%至74.70%,与乳酸杆菌属的48.81%。 MD-1。此外,还有三个高度保守的LDH区,其中一个(Val1〜Asp 34 )用于NADH结合位点,两个(Asp 59 〜Ile 86 和Asn在依赖NAD + 的LDH片段中也发现了不同活性位点的 107 〜Arg 139 )。

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