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首页> 外文期刊>Bioscience, Biotechnology, and Biochemistry >In Vitro Protein Import of a Putative Amino Acid Transporter from Arabidopsis thaliana into Chloroplasts and Its Suborganellar Localization
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In Vitro Protein Import of a Putative Amino Acid Transporter from Arabidopsis thaliana into Chloroplasts and Its Suborganellar Localization

机译:拟南芥中假定的氨基酸转运蛋白的体外蛋白导入叶绿体及其亚细胞定位

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摘要

We identified a gene product of At5g19500 (At5g19500p) from Arabidopsis thaliana that is homologous to EcTyrP, a tyrosine-specific transporter from Escherichia coli. Computational analyses of the amino acid sequence of At5g19500p predicted 11 transmembrane domains (TMDs) and a potential plastid targeting signal at its amino terminus. As a first step toward understanding the possible role of At5g19500p in plant cells, we attempted to determine the localization of At5g19500p by an in vitro chloroplastic import assay using At5g19500p translated in a cell-free wheat germ system (Madin et al., Proc. Natl. Acad. Sci. USA, 97,559-564 (2000)), followed by subfractionation of the chloroplasts. At5g19500p was successfully imported into chloroplasts, and the newly transported mature form of At5g19500p was recovered from the inner envelope membrane.
机译:我们从拟南芥中鉴定了At5g19500(At5g19500p)的基因产物,该产物与EcTyrP(大肠杆菌的酪氨酸特异性转运蛋白)同源。 At5g19500p氨基酸序列的计算分析预测了11个跨膜结构域(TMD)和在其氨基末端的潜在质体靶向信号。作为了解At5g19500p在植物细胞中可能作用的第一步,我们尝试通过在无细胞小麦胚芽系统中翻译的At5g19500p进行体外叶绿素导入测定,确定At5g19500p的定位(Madin等,Proc。Natl Acad。Sci。USA,97,559-564(2000)),然后将叶绿体细分。 At5g19500p已成功导入叶绿体中,并从内膜中回收了新运输的成熟形式的At5g19500p。

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