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首页> 外文期刊>Systematic and Applied Microbiology >Identification and cloning of a gene encoding tannase (tannin acylhydrolase) from Lactobacillus plantarum ATCC 14917 super(T)
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Identification and cloning of a gene encoding tannase (tannin acylhydrolase) from Lactobacillus plantarum ATCC 14917 super(T)

机译:植物乳杆菌ATCC 14917 super(T)编码鞣酸酶(单宁酸酰基水解酶)的基因的鉴定和克隆

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The gene tanLpl, encoding a novel tannase enzyme (TanLpl), has been cloned from Lactobacillus plantarum ATCC 14917 super(T). This is the first report of a tannase gene cloned from a bacterial source other than from Staphylococcus lugdunensis, which has been reported elsewhere. The open reading frame of tanLpl, spanning 1410bp, encoded a 469-amino-acid protein that showed 28.8% identity to the tannase of S. lugdunensis with several commonly conserved sequences. These sequences could not be found in putative tannases reported for other bacteria and fungi. TanLpl was expressed in Escherichia coli DH5 alpha from a pGEM-T expression system and purified. SDS-PAGE analysis indicated that purified TanLpl was a monomer polypeptide of approximately 50kDa in size. Subsequent enzymatic characterization revealed that TanLpl was most active in an alkaline pH range at 40 super(o)C, which was quite different from that observed for a fungal tannase of Aspergillus oryzae. In addition, the Michaelis-Menten constant of TanLpl was markedly lower than that of A. oryzae tannase. The evidence suggests that TanLpl should be classified into a novel family of tannases. electrophoresis
机译:从植物乳杆菌ATCC 14917 super(T)克隆了编码新型鞣酸酶(TanLpl)的基因tanLpl。这是第一个从细菌来源克隆的鞣酸酶基因的报道,而不是从其他葡萄球菌lugdunensis。 tanLpl的开放阅读框跨度为1410bp,编码一个469个氨基酸的蛋白质,该蛋白质与lugdunensis的鞣酸酶具有28.8%的同一性,并具有几个通常保守的序列。在其他细菌和真菌的推定鞣酸酶中找不到这些序列。从pGEM-T表达系统在大肠杆菌DH5α中表达TanLpl,并进行纯化。 SDS-PAGE分析表明纯化的TanLpl是大小约为50kDa的单体多肽。随后的酶学表征显示,TanLpl在40℃的碱性pH范围内活性最高,这与米曲霉的真菌鞣酸酶所观察到的完全不同。另外,TanLpl的Michaelis-Menten常数显着低于米曲霉丹参酶。有证据表明,TanLpl应该被归类为新的鞣酸酶家族。电泳

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