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首页> 外文期刊>Indian Journal of Biochemistry & Biophysics >Pichia pastoris INO1 gene expression affects intracellular maltase activity and MAL1(+) gene expression in Schizosaccharomyces pombe
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Pichia pastoris INO1 gene expression affects intracellular maltase activity and MAL1(+) gene expression in Schizosaccharomyces pombe

机译:毕赤酵母的INO1基因表达影响粟酒裂殖酵母的细胞内麦芽糖酶活性和MAL1(+)基因表达

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摘要

In our previous study, we found that the transfonnant Sch.p944 which contains the plasmid pADH-INO synthesized higher inositol than the transfonnant Sch.p1025 which contains the plasmid pSPIN-22. In this study, we examined the influence of 1N01 gene expression on intracellular maltase activity and MAL1(+) gene expression in these two transfonnants. The highest specific maltase activity was observed when Sch.p944 was grown in the synthetic medium containing initial 2.0% (w/v) glucose, whereas glucose repression of maltase activity occurred when Sch.p1025 was cultivated in the same medium containing glucose more than initial 0.5% (w/v), suggesting that synthesis of the maltase was derepressed in Sch.p944. Also, higher mRNA encoding intracellular maltase activity was found in Sch.p944 than that in Sch.p 1025 after 32 h of cell growth in the media containing initial 2.0% glucose, indicating that the derepression occurred at the transcriptional level. Furthermore, higher phosphatidylinositol (PI) content was detected in Sch.p944 cells grown in the medium containing initial 2.0% (w/v) glucose for 32 h than in Sch.p1025 cells grown under the sane conditions, inclicating that PI might be involved in derepression of MAL1(+) gene expression and intracellular maltase activity.
机译:在我们先前的研究中,我们发现包含质粒pADH-INO的透明糖蛋白Sch.p944的合成比包含质粒pSPIN-22的透明糖蛋白Sch.p1025合成的肌醇更高。在这项研究中,我们检查了这两个透明糖中1N01基因表达对细胞内麦芽糖酶活性和MAL1(+)基因表达的影响。当Sch.p944在含有初始2.0%(w / v)葡萄糖的合成培养基中生长时,观察到最高的比麦芽糖酶活性,而当Sch.p1025在含有比初始葡萄糖多的葡萄糖的相同培养基中培养时,则发生了麦芽糖酶活性的葡萄糖抑制。 0.5%(w / v),表明麦芽糖酶的合成在Sch.p944中被抑制。同样,在含有初始2.0%葡萄糖的培养基中,细胞生长32小时后,在Sch.p944中发现的编码细胞内麦芽糖酶活性的mRNA高于Sch.p 1025,这表明去抑制发生在转录水平。此外,与在正常条件下生长的Sch.p1025细胞相比,在含有初始2.0%(w / v)葡萄糖的培养基中培养32 h的Sch.p944细胞中检测到的磷脂酰肌醇(PI)含量更高。抑制MAL1(+)基因表达和细胞内麦芽糖酶活性。

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