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在野生型酿酒酵母中,葡萄糖浓度在0至500毫克/升之间时对葡萄糖转运蛋白基因的体内调控。

In vivo regulation of glucose transporter genes at glucose concentrations between 0 and 500 mg/L in a wild type of Saccharomyces cerevisiae.

作者信息

Klockow Christine, Stahl Frank, Scheper Thomas, Hitzmann Bernd

机构信息

Institute of Technical Chemistry, Leibniz University of Hannover, 30167 Hannover, Germany.

出版信息

J Biotechnol. 2008 Jun 1;135(2):161-7. doi: 10.1016/j.jbiotec.2008.03.009. Epub 2008 Mar 29.

Abstract

When the yeast Saccharomyces cerevisiae consumes glucose, the expression of the genes for the glucose transport is controlled via signal transduction pathways and sensor molecules. Most publications describe the behavior of deletion strains while little is published about the in vivo regulation of glucose transporters in a wild type of S. cerevisiae. Here a global gene expression analysis via microarray experiments from cultivations with glucose concentrations of 50, 70, 100 and 500 mg/L is presented. This permits the observation of the fine-tuning of gene expression in dependency on the glucose concentration. We detected indications that the transport system for high glucose concentrations is activated at glucose concentrations between 50 and 100 mg/L. The regulation of genes coding enzymes for the signal pathways and of those encoding the transporters themselves supports this assumption. The expression of sensor-, signal- and transporter genes will be discussed in detail. In addition, new information about the behavior of the so far little described carriers HXT8, HXT12, HXT13, HXT17 and GAL2 will be given. According to our findings, HXT13 is active during starvation. HXT12, HXT17 and GAL2 are used at low glucose concentrations. The carrier HXT8 supports the glucose transport both during starvation and at low glucose concentrations.

摘要

当酿酒酵母消耗葡萄糖时,葡萄糖转运基因的表达通过信号转导途径和传感分子进行调控。大多数出版物描述的是缺失菌株的行为,而关于野生型酿酒酵母中葡萄糖转运蛋白的体内调控的报道很少。本文通过微阵列实验对葡萄糖浓度分别为50、70、100和500 mg/L的培养物进行了全局基因表达分析。这使得我们能够观察到基因表达如何根据葡萄糖浓度进行微调。我们检测到有迹象表明,高葡萄糖浓度的转运系统在葡萄糖浓度介于50至100 mg/L之间时被激活。对信号途径中编码酶的基因以及转运蛋白本身编码基因的调控支持了这一假设。将详细讨论传感、信号和转运蛋白基因的表达。此外,还将给出关于目前描述较少的载体HXT8、HXT12、HXT13、HXT17和GAL2行为的新信息。根据我们的研究结果,HXT13在饥饿期间具有活性。HXT12、HXT17和GAL2在低葡萄糖浓度时发挥作用。载体HXT8在饥饿期间和低葡萄糖浓度时均有助于葡萄糖转运。

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