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从耐渗透压酵母 Candida magnoliae 中克隆和鉴定乳清酸盐-5′-磷酸脱羧酶基因(URA3)。

Cloning and characterization of the orotidine-5'-phosphate decarboxylase gene (URA3) from the osmotolerant yeast Candida magnoliae.

机构信息

School of Biotechnology and Bioengineering, Kangwon National University, Chuncheon 200-701, Korea.

出版信息

J Microbiol Biotechnol. 2012 May;22(5):642-8. doi: 10.4014/jmb.1111.11071.

Abstract

We determined the nucleotide sequence of the URA3 gene encoding orotidine-5'-phosphate decarboxylase (OMPDCase) of the erythritol-producing osmotolerant yeast Candida magnoliae by degenerate polymerase chain reaction and genome walking. Sequence analysis revealed the presence of an uninterrupted open-reading frame of 795 bp, encoding a 264 amino acid residue protein with the highest identity to the OMPDCase of the yeast Kluyveromyces marxianus. Phylogenetic analysis of the deduced amino acid sequence revealed that it shared a high degree of identity with other yeast OMPDCase homologs. The cloned URA3 gene successfully complemented the ura3 null mutation in Saccharomyces cerevisiae, revealing that it encodes a functional OMPDCase in C. magnoliae. An enzyme activity assay and reverse transcription polymerase chain reaction indicated that the expression level of the C. magnoliae URA3 gene in S. cerevisiae was not as high as that of the S. cerevisiae URA3 gene. The GenBank accession number for C. magnoliae URA3 is JF521441.

摘要

我们通过简并聚合酶链反应和基因组步移法确定了产赤藓糖醇耐渗酵母 Candida magnoliae 的 URA3 基因,该基因编码乳清酸-5'-磷酸脱羧酶(OMPDCase)。序列分析表明,存在一个 795bp 的连续开放阅读框,编码一个 264 个氨基酸残基的蛋白质,与酵母 Kluyveromyces marxianus 的 OMPDCase 具有最高的同一性。推导的氨基酸序列的系统发育分析表明,它与其他酵母 OMPDCase 同源物具有高度的同一性。克隆的 URA3 基因成功地补充了酿酒酵母的 ura3 缺失突变,表明它在 C. magnoliae 中编码一种功能性的 OMPDCase。酶活性测定和反转录聚合酶链反应表明,C. magnoliae URA3 基因在酿酒酵母中的表达水平不如酿酒酵母 URA3 基因高。C. magnoliae URA3 的 GenBank 登录号为 JF521441。

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