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Thermostable glycerol kinase from Thermus flavus: cloning, sequencing, and expression of the enzyme gene

机译:来自黄热栖热菌的热稳定甘油激酶:该酶基因的克隆,测序和表达

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摘要

The thermostable glycerol kinase (EC 2.7.1.30) gene from Thermus flavus was cloned and expressed in Escherichia coli DH5α. An open reading frame of 1488 bp for the glycerol kinase gene (glpK) starting with an ATG methionine codon was found, which encodes a protein of 496 amino acid residues whose calculated molecular weight is 54,835. The amino acid sequence of T. flavus glycerol kinase is 80.6% and 64.1% identical with those of Bacillus subtilis and E. coli. Transformants of E. coli DH5α harboring plasmid pGYK12 with a 1505 bp chromosomal DNA fragment containing the T. flavus glycerol kinase gene showed about 23.87-fold higher glycerol kinase activity than T. flavus.
机译:克隆了黄热栖热菌的热稳定甘油激酶(EC 2.7.1.30)基因,并在大肠杆菌DH5α中表达。发现了一个以ATG甲硫氨酸密码子为起始的甘油激酶基因(glpK)的1488 bp开放阅读框,该编码框编码一个496个氨基酸残基的蛋白质,其计算分子量为54,835。黄曲霉甘油激酶的氨基酸序列与枯草芽孢杆菌和大肠杆菌的氨基酸序列相同,分别为80.6%和64.1%。带有质粒pGYK12的大肠杆菌DH5α转化子含有一个含有黄曲霉甘油激酶基因的1505 bp染色体DNA片段,其转化率比黄曲霉高约23.87倍。

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