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Expression and subcellular localization of antiporter regulating protein OsARP in rice induced by submergence, salt and drought stresses

机译:淹水,干旱和盐胁迫诱导水稻反转运蛋白调控蛋白OsARP的表达和亚细胞定位

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We examined the expression and subcellular localization of antiporter regulating protein OsARPin a submergence tolerant rice (Oryza sativa?L.) cultivar FR13A. In the public databases, this protein was designated as putative Os02g0465900 protein. The cDNA containing the full-length sequence of?OsARP?gene was present in Gene Bank Accession no. AK071205 and this encoded 216 amino acids which had molecular mass of 25 kD. The?OsARP?gene was first expressed into?E. coli?and antibody was produced by using purified recombinant protein. The expression of OsARP protein was detected under submergence, salt and drought stresses. This protein was widely expressed in roots, shoots and leaves of rice under salt stress. To get an insight into the functional role of OsARP protein, subcellular localization was done using cell fractionation of rice leaves. Immuno-blotting of 3-day submergence rice leaves cell fractions detected the presence of OsARP protein in plasma-membrane fraction only. This indicates that OsARP is a membrane bound protein of rice which is expressed under submergence, salt and drought stresses.
机译:我们研究了抗转运蛋白OsARP在耐旱水稻品种FR13A中的表达和亚细胞定位。在公共数据库中,该蛋白被称为推定的Os02g0465900蛋白。含有“ OsARP”基因全长序列的cDNA存在于Gene Bank登录号No. AK071205和它编码了分子量为25 kD的216个氨基酸。 “ OsARP”基因首先被表达为“ E”。用纯化的重组蛋白生产大肠杆菌和抗体。在淹水,盐和干旱胁迫下检测到OsARP蛋白的表达。该蛋白在盐胁迫下在水稻的根,芽和叶中广泛表达。为了深入了解OsARP蛋白的功能作用,使用稻叶的细胞分离技术进行了亚细胞定位。 3天淹没水稻的免疫印迹分析显示,仅在血浆膜组分中检测到OsARP蛋白的存在。这表明OsARP是水稻的膜结合蛋白,在淹水,盐分和干旱胁迫下表达。

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