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The Pichia pastoris transmembrane protein GT1 is a glycerol transporter and relieves the repression of glycerol on AOX1 expression

机译:巴斯德毕赤酵母跨膜蛋白GT1是甘油转运蛋白,可减轻甘油对AOX1表达的抑制作用

摘要

Promoter of alcohol oxidase I (PAOX1) is the most efficient promoter involved in the regulation of recombinant protein expression in Pichia pastoris (P. pastoris). PAOX1 is tightly repressed by the presence of glycerol in the culture medium; thus, glycerol must be exhausted before methanol can be taken up by P. pastoris and the expression of the heterologous protein can be induced. In this study, a candidate glycerol transporter (GT1, GeneID: 8197545) was identified, and its role was confirmed by further studies (e.g. bioinformatics analysis, heterologous complementation in Schizosaccharomyces pombe (S. pombe)). When GT1 is co-expressed with enhanced green fluorescent protein (EGFP), it localizes to the membrane and S. pombe carrying gt1 but not the wild-type strain can grow on medium containing glycerol as the sole carbon source. The present study is the first to report that AOX1 in the X-33gt1 mutant can achieve constitutive expression in medium containing glycerol; thus, knocking down gt1 can eliminate the glycerol repression of PAOX1 in P. pastoris. These results suggest that the glycerol transporter may participate in the process of PAOX1 inhibition in glycerol medium.
机译:醇氧化酶I(PAOX1)的启动子是参与巴斯德毕赤酵母(P. pastoris)重组蛋白表达调控的最有效启动子。培养基中甘油的存在会严格抑制PAOX1;因此,必须先用尽甘油,然后甲醇才能被巴斯德毕赤酵母吸收,并诱导异源蛋白的表达。在这项研究中,确定了候选的甘油转运蛋白(GT1,GeneID:8197545),并通过进一步的研究(例如生物信息学分析,粟酒裂殖酵母(S. pombe)中的异源互补)确认了其作用。当GT1与增强型绿色荧光蛋白(EGFP)共表达时,它定位于膜和带有gt1的粟酒裂殖酵母,但野生型菌株不能在含有甘油作为唯一碳源的培养基上生长。本研究首次报道X-33gt1突变体中的AOX1可以在含甘油的培养基中实现组成型表达。因此,敲低gt1可以消除巴斯德毕赤酵母中PAOX1的甘油抑制。这些结果表明,甘油转运蛋白可能参与了PAOX1在甘油培养基中的抑制作用。

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