首页> 外文期刊>FEMS Microbiology Letters >Molecular cloning and characterization of two YGL039w genes encoding broad specificity NADPH-dependent aldehyde reductases from Kluyveromyces marxianus strain DMB1
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Molecular cloning and characterization of two YGL039w genes encoding broad specificity NADPH-dependent aldehyde reductases from Kluyveromyces marxianus strain DMB1

机译:两种YGL039W基因的分子克隆与表征编码宽特异性NADPH依赖性醛还原酶中的kluyveromyces marxianus菌株DMB1

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摘要

Two genes from Kluyveromyces marxianus strain DMB1, YGL039w1 and YGL039w2, encode putative uncharacterized oxidoreductases that respectively share 42 and 44% identity with the Saccharomyces cerevisiae S288c NADPH-dependent methylglyoxal reductase (EC 1.1.1.283). To determine the enzymatic characteristics of their products, the two genes were expressed in recombinant Escherichia coli cells, after which the YGL039w1 and YGL039w2 proteins were purified to homogeneity. In the presence of NADPH, both enzymes showed reductive activities toward at least nine aldehyde substrates, but no NADP(+)-dependent oxidative activities. These two YGL039w proteins thus appear to be aldehyde reductases. In addition, although both enzymes retained more than 70% of their activities after incubation for 30 min at temperatures below 40 degrees C or at pHs between 5.5 and 11.3, YGL039w2 was slightly more thermostable than YGL039w1.
机译:来自Kluyveromyces Marxianus菌株DMB1,YGL039W1和YGL039W2的两种基因,分别与酿酒酵母S288C NADPH依赖性甲基甘油还原酶(EC 1.1.1.283)分别分别分别分别占42和44%的同一性的诱导的无表氧化酶。 为了确定其产物的酶促特性,两种基因在重组大肠杆菌细胞中表达,之后将YgL039W1和YGL039W2蛋白质纯化为均匀性。 在NADPH的存在下,两种酶向至少九个醛底物显示还原活性,但没有NADP(+)依赖性氧化活性。 因此,这两个YG1039W蛋白似乎是醛还原酶。 此外,尽管在低于40℃或5.5和11.3的温度下孵育30分钟后,两种酶在温度下保留超过70%的活性,但在5.5和11.3之间,YGL039W2比YG1039W1略高。

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