首页> 外文期刊>Journal of bacteriology >Purification and sequence analysis of a novel NADP(H)-dependent type III alcohol dehydrogenase from Thermococcus strain AN1.
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Purification and sequence analysis of a novel NADP(H)-dependent type III alcohol dehydrogenase from Thermococcus strain AN1.

机译:嗜热球菌菌株AN1的新型NADP(H)依赖型III型醇脱氢酶的纯化和序列分析。

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An NADP(H)-dependent alcohol dehydrogenase was isolated from the hyperthermophilic archaeon Thermococcus strain AN1. This enzyme is a homotetramer with a subunit molecular weight of 46,700. The enzyme oxidizes a series of primary linear alcohols but not methanol. The pH and temperature optima with ethanol as the substrate are 6.8 to 7.0 and 85 degrees C, respectively. The enzyme readily reduced acetaldehyde with NADPH as the cofactor. The gene encoding this enzyme has been cloned and sequenced. An open reading frame of 1,218 bp, starting with ATG and ending with TGA, was identified and corresponded to 406 amino acids. Sequence comparisons show that this Thermococcus strain AN1 enzyme has significant homologies with enzymes from the newly defined type III alcohol dehydrogenase family. Thermococcus strain AN1 alcohol dehydrogenase is the first archaeal enzyme belonging to this family.
机译:从超嗜热古细菌Thermococcus菌株AN1中分离出NADP(H)依赖的醇脱氢酶。该酶是亚基分子量为46,700的高四聚体。该酶氧化一系列伯直链醇,但不氧化甲醇。以乙醇为底物的最适pH和温度分别为6.8至7.0和85℃。该酶容易以NADPH作为辅因子还原乙醛。编码该酶的基因已被克隆并测序。鉴定了从ATG开始到TGA结束的1,218bp的开放阅读框,其对应于406个氨基酸。序列比较显示,该嗜热球菌菌株AN1酶与新定义的III型醇脱氢酶家族的酶具有显着的同源性。嗜热球菌菌株AN1醇脱氢酶是该家族的第一个古细菌。

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