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酿酒酵母戊糖磷酸途径非氧化部分前两个基因的克隆与特性分析。

Cloning and characterization of the first two genes of the non-oxidative part of the Saccharomyces cerevisiae pentose-phosphate pathway.

作者信息

Miosga T, Zimmermann F K

机构信息

Institut für Mikrobiologie und Genetik, Technische Hochschule Darmstadt, Schnittspahnstrasse 10, D-64287 Darmstadt, Germany.

出版信息

Curr Genet. 1996 Nov;30(5):404-9. doi: 10.1007/s002940050149.

Abstract

We have cloned and characterized the two remaining unknown genes of the non-oxidative part of the pentose-phosphate pathway of Saccharomyces cerevisiae encoding the enzymes D-ribulose-5-phosphate 3-epimerase (Rpe1p) and D-ribose-5-phosphate ketol-isomerase (Rki1p). Rpe1p has an unexpected high specific activity of 2148 mU x (mg protein)-1 in crude extracts. Deletion mutants of RPE1 show no enzyme activity and are unable to grow on D-xylulose. Unexpectedly, haploid rki1 deletion mutants are not viable. Functional expression of RKI1 was demonstrated following an increase of gene dosage in the haploid rki1 deletion mutant, which restored viability and specific D-ribose-5-phosphate ketol-isomerase activity. Both enzymes show high similarity to the deduced protein sequences of various open reading frames, expressed sequence tags or cDNAs from different organisms.

摘要

我们已经克隆并鉴定了酿酒酵母戊糖磷酸途径非氧化部分中剩余的两个未知基因,它们分别编码D-核糖-5-磷酸3-差向异构酶(Rpe1p)和D-核糖-5-磷酸酮醇异构酶(Rki1p)。在粗提物中,Rpe1p具有2148 mU x (mg蛋白)-1 这一意外的高比活性。RPE1的缺失突变体没有酶活性,并且无法在D-木酮糖上生长。出乎意料的是,单倍体rki1缺失突变体无法存活。在单倍体rki1缺失突变体中增加基因剂量后,证明了RKI1的功能表达,这恢复了其活力和特定的D-核糖-5-磷酸酮醇异构酶活性。这两种酶与来自不同生物体的各种开放阅读框、表达序列标签或cDNA的推导蛋白质序列具有高度相似性。

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