The cloning and sequencing of the UDP-galactose 4-epimerase gene (galE) from Avibacterium paragallinarum.

Yolande Roodt, Robert Bragg, Jacobus Albertyn
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引用次数: 4

Abstract

The putative uridine diphosphate (UDP)-galactose 4-epimerase encoding gene, galE, was isolated from Avibacterium paragallinarum with the use of degenerate primers, colony hybridization and inverse PCR. The data revealed an open reading frame of 1017 bp encoding a protein of 338 amino acids with a molecular weight of 37 kDa and an isoelectric point of 5.5. High sequence homology was obtained with an 87, 91 and 89% sequence identity on protein level towards the galE genes from Actinobacillus pleuropneumoniae, Haemophilus influenza and Pasteurella multocida, respectively. To verify that the cloned galE gene encodes for a UDP-galactose 4-epimeras, this gene was cloned into the pYES-2 expression vector, followed by transformation in a Saccharomyces cerevisiae gal10 deletion strain. Complementation of the gal10 deletion mutant with the galE gene confirmed that this gene encodes a UDP-galactose 4-epimerase.

副翼鸟芽胞杆菌(Avibacterium paragallinarum) udp -半乳糖4- epimase基因(galE)的克隆与测序。
采用简并引物、集落杂交和反相PCR技术,从副伞鸟芽胞杆菌中分离得到了推测为UDP -半乳糖4- epimase编码基因galE。数据显示,一个1017 bp的开放阅读框编码一个338个氨基酸的蛋白,分子量为37 kDa,等电点为5.5。与胸膜肺炎放线杆菌、流感嗜血杆菌和多杀性巴氏杆菌的galE基因在蛋白水平上同源性较高,分别为87%、91%和89%。为了验证克隆的galE基因是否编码一段udp -半乳糖4-表肽,我们将该基因克隆到pies -2表达载体中,然后在酿酒酵母gal10缺失菌株中进行转化。gal10缺失突变体与galE基因的互补证实了该基因编码一种udp -半乳糖4- epimase。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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