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粟酒裂殖酵母中编码γ-谷氨酰转肽酶I的基因受不可发酵碳源和氮饥饿的调控。

The Schizosaccharomyces pombe gene encoding gamma-glutamyl transpeptidase I is regulated by non-fermentable carbon sources and nitrogen starvation.

作者信息

Kim Hong-Gyum, Park Hey-Jung, Kang Hyun-Jung, Lim Hye-Won, Kim Kyunghoon, Park Eun-Hee, Ahn Kisup, Lim Chang-Jin

机构信息

Division of Life Sciences, Kangwon National University, Chuncheon 200-701, Republic of Korea.

出版信息

J Microbiol. 2005 Feb;43(1):44-8.

Abstract

In our previous study, the first structural gene (GGTI) encoding g-glutamyl transpeptidase was cloned and characterized from the fission yeast Schizosaccharomyces pombe, and its transcription, using the GGTI-lacZ fusion gene, containing the 1,085 bp upstream region from the translational initiation point, was found to be enhanced by sodium nitroprusside and L-buthionine-(S,R)-sulfoximine (BSO). In the present work, regulation of the GGTI gene was further elucidated. Non-fermentable carbon sources, such as acetate and ethanol, markedly enhanced the synthesis of beta-galactosidase from the GGTI-lacZ fusion gene. However, its induction by non-fermentable carbon sources appeared to be independent of the presence of the Pap1 protein. Nitrogen starvation also gave rise to induction of GGTI gene expression in a Pap1-independent manner. The three additional fusion plasmids, carrying 754, 421 and 156 bp regions, were constructed. The sequence responsible for the induction by non-fermentable carbon sources and nitrogen starvation was identified to exist within a -421 bp region of the GGTI gene. Taken together, the S. pombe GGTI gene is regulated by non-fermentable carbon sources and nitrogen starvation.

摘要

在我们之前的研究中,从裂殖酵母粟酒裂殖酵母中克隆并鉴定了编码γ-谷氨酰转肽酶的第一个结构基因(GGTI),并且使用包含翻译起始点上游1085 bp区域的GGTI-lacZ融合基因发现其转录受到硝普钠和L-丁硫氨酸-(S,R)-亚砜亚胺(BSO)的增强。在本研究中,对GGTI基因的调控进行了进一步阐明。不可发酵的碳源,如乙酸盐和乙醇,显著增强了GGTI-lacZ融合基因中β-半乳糖苷酶的合成。然而,其由不可发酵碳源诱导的过程似乎与Pap1蛋白的存在无关。氮饥饿也以不依赖Pap1的方式诱导GGTI基因表达。构建了另外三个携带754、421和156 bp区域的融合质粒。确定负责由不可发酵碳源和氮饥饿诱导的序列存在于GGTI基因的-421 bp区域内。综上所述,粟酒裂殖酵母GGTI基因受不可发酵碳源和氮饥饿的调控。

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