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首页> 外文期刊>Plant physiology >MOLECULAR CLONING, IMMUNOCHEMICAL LOCALIZATION TO THE VACUOLE, AND EXPRESSION IN TRANSGENIC YEAST AND TOBACCO OF A PUTATIVE SUGAR TRANSPORTER FROM SUGAR BEET
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MOLECULAR CLONING, IMMUNOCHEMICAL LOCALIZATION TO THE VACUOLE, AND EXPRESSION IN TRANSGENIC YEAST AND TOBACCO OF A PUTATIVE SUGAR TRANSPORTER FROM SUGAR BEET

机译:甜菜专用糖转运蛋白的分子克隆,免疫化学定位到液泡以及在转基因酵母和烟草中的表达

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摘要

Several plant genes have been cloned that encode members of the sugar transporter subgroup of the major facilitator superfamily of transporters. Here we report the cloning, expression, and membrane localization of one of these porters found in sugar beet (Beta vulgaris L.). This clone, cDNA-1, codes for a protein with 490 amino acids and an estimated molecular mass of 54 kD. The predicted membrane topology and sequence homology suggest that cDNA-1 is a member of the sugar transporter family. RNA gel blot analysis revealed that this putative sugar transporter is expressed in all vegetative tissues and expression increases with development in leaves. DNA gel blot analysis indicated that multiple gene copies exist for this putative sugar transporter in the sugar beet genome. Antibodies directed against small peptides representing the N- and C-terminal domains of the cDNA1 protein identified a 40-kD polypeptide in microsomes isolated from cDNA-1-transformed yeast (Saccharomyces cerevisiae). Moreover, the same protein was identified in sugar beet and transgenic tobacco (Nicotiana tobacum L.) membrane fractions. Detailed analysis of the transporter's distribution across linear sucrose gradients and flotation centrifugations showed that it co-migrates with tonoplast membrane markers. We conclude that this carrier is located on the tonoplast membrane and that it may mediate sugar partitioning between the vacuole and cytoplasmic compartments. [References: 58]
机译:已经克隆了几种植物基因,它们编码转运蛋白的主要促进子超家族的糖转运蛋白亚组的成员。在这里,我们报告在甜菜(Beta vulgaris L.)中发现的这些搬运工之一的克隆,表达和膜定位。该克隆cDNA-1编码具有490个氨基酸的蛋白质,估计分子量为54 kD。预测的膜拓扑和序列同源性表明cDNA-1是糖转运蛋白家族的成员。 RNA凝胶印迹分析表明,这种假定的糖转运蛋白在所有营养组织中均有表达,并且随着叶的发育而增加。 DNA凝胶印迹分析表明,甜菜基因组中该推定的糖转运蛋白存在多个基因拷贝。针对代表cDNA1蛋白N和C端结构域的小肽段的抗体,在从cDNA-1转化酵母(酿酒酵母)分离的微粒体中鉴定出40 kD多肽。此外,在甜菜和转基因烟草(Nicotiana tobacum L.)膜级分中鉴定出相同的蛋白质。对转运蛋白在线性蔗糖梯度和浮选离心中分布的详细分析表明,它与液泡膜标记一起迁移。我们得出的结论是,该载体位于液泡膜上,它可能介导液泡和细胞质区室之间的糖分配。 [参考:58]

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