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Aquaporins and hexose transporters in a wine strain of Saccharomyces cerevisiae.

机译:酿酒酵母(Saccharomyces cerevisiae)酒菌株中的水通道蛋白和己糖转运蛋白。

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摘要

Proteins are important components of the plasma membrane in the yeast Saccharomyces cerevisiae. In this research two classes of membrane proteins were studied in a wine yeast strain: Aquaporins (AQY1 and AQY2) and the Hexose Transporters (HXTI-HXT17 ). These proteins play different roles in the membrane of this organism. Although several functions have been attributed to Aqy1p in laboratory yeast strains, no clear role for Aqy1p in the wine yeast UCD 932 could be defined. The AQY1 gene form UCD 932 was found to be functional in a heterologous expression system but deletion of this gene showed no effect on the ability of the strain to ferment synthetic grape juice media, to resist ethanol challenges, or on the formation/germination of spores. AQY 2 was found to be nonfunctional in UCD 932, as expected.; The hexose transporters play very important roles in the utilization of sugars over a wide concentration range. The first seven hexose transporter genes have been described as the major sugar transporters during fermentation. Of these major hexose transporters during fermentation, HXT1, HXT3 , and HXTS were found to be the most abundant hexose transporters in UCD 932 using Green Fluorescent Protein tagging. Deletion of HXT1, HXT3, or HXT5 in UCD 932 did not affect the ability of the strain to ferment synthetic media. When these deletion strains were grown in media containing ethanol, the strain lacking HXT3 was not able to complete the fermentation to the same extent as the other deletion strains. The role of HXT3 in this ethanol sensitivity was not clearly defined, but the insertion of a functional HXT3 into the HXT5 locus was not able to overcome this defect and restore wild-type growth.
机译:蛋白质是酿酒酵母中质膜的重要组成部分。在这项研究中,在葡萄酒酵母菌株中研究了两类膜蛋白:水通道蛋白(AQY1和AQY2)和己糖转运蛋白(HXTI-HXT17)。这些蛋白质在该生物体的膜中扮演不同的角色。尽管实验室酵母菌株中的Aqy1p具有多种功能,但尚不能确定Aqy1p在葡萄酒酵母UCD 932中的明确作用。发现来自UCD 932的AQY1基因在异源表达系统中起作用,但是该基因的缺失对菌株发酵合成葡萄汁培养基的能力,抗乙醇挑战或孢子形成/发芽的能力没有影响。 。如预期的那样,在UCD 932中发现AQY 2无法正常工作。己糖转运蛋白在宽浓度范围内的糖利用中起着非常重要的作用。前七个己糖转运蛋白基因已被描述为发酵过程中的主要糖转运蛋白。在发酵过程中这些主要的己糖转运蛋白中,使用绿色荧光蛋白标记法发现HXT1,HXT3和HXTS是UCD 932中最丰富的己糖转运蛋白。在UCD 932中删除HXT1,HXT3或HXT5不会影响菌株发酵合成培养基的能力。当这些缺失菌株在含有乙醇的培养基中生长时,缺乏HXT3的菌株无法以与其他缺失菌株相同的程度完成发酵。 HXT3在这种乙醇敏感性中的作用尚未明确定义,但是将功能性HXT3插入HXT5基因座无法克服该缺陷并恢复野生型生长。

著录项

  • 作者

    Karpel, Jonathan Earl.;

  • 作者单位

    University of California, Davis.;

  • 授予单位 University of California, Davis.;
  • 学科 Biology Molecular.
  • 学位 Ph.D.
  • 年度 2006
  • 页码 150 p.
  • 总页数 150
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;
  • 关键词

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