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从耐盐酵母毕赤酵母中克隆和表征甘油-3-磷酸脱氢酶(NAD+)基因。

Cloning and characterization of a glycerol-3-phosphate dehydrogenase (NAD+) gene from the halotolerant yeast Pichia farinosa.

机构信息

Key Laboratory of Bio-Resources and Eco-Environment of Ministry of Education, College of Life Science, Sichuan University, Chengdu 610064, People's Republic of China.

出版信息

Yeast. 2010 Feb;27(2):115-21. doi: 10.1002/yea.1736.

Abstract

In this study, a novel glycerol-3-phosphate dehydrogenase (NAD(+)) (EC1.1.1.8) gene (PfGPD) was cloned from halotolerant yeast Pichia farinosa, using degenerate reverse transcription (RT)-PCR and rapid amplification of cDNA ends (RACE) methods. The full-length cDNA of the PfGPD gene is 1403 bp, which has an open reading frame (ORF) encoding 370 amino acids. PfGPD is conserved with other glycerol-3-phosphate dehydrogenase genes and presents a single copy in the P. farinosa genome. Transcriptional analysis revealed that PfGPD gene expression level was high after 2 h induction in a hyperosmotic environment containing 2 M NaCl and returned to normal within 6 h. These results suggest that the PfGPD gene is induced by salt stress. Yeast complementation experiment indicated that PfGPD complements gpd1 mutation in S. cerevisiae. The Accession No. for PfGPD in GenBank is EF601986.

摘要

在这项研究中,我们使用简并反转录(RT)-PCR 和快速扩增 cDNA 末端(RACE)方法,从耐盐酵母巴斯德毕赤酵母中克隆了一种新型甘油-3-磷酸脱氢酶(NAD(+))(EC1.1.1.8)基因(PfGPD)。PfGPD 全长 cDNA 为 1403bp,包含一个编码 370 个氨基酸的开放阅读框(ORF)。PfGPD 与其他甘油-3-磷酸脱氢酶基因保守,在毕赤酵母基因组中呈现单拷贝。转录分析表明,在含有 2 M NaCl 的高渗环境中诱导 2 小时后,PfGPD 基因表达水平较高,6 小时内恢复正常。这些结果表明 PfGPD 基因受到盐胁迫的诱导。酵母互补实验表明,PfGPD 可互补酿酒酵母 gpd1 突变。PfGPD 在 GenBank 中的登录号为 EF601986。

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