首页> 外文期刊>Mathematical research letters: MRL >Expression Profiles and Protein Complexes of Starch Biosynthetic Enzymes from White-Core and Waxy Mutants Induced from High Amylose Indica Rice
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Expression Profiles and Protein Complexes of Starch Biosynthetic Enzymes from White-Core and Waxy Mutants Induced from High Amylose Indica Rice

机译:淀粉生物合成酶的表达谱和蛋白质复合物来自高直链淀粉籼稻的白核和蜡质突变体

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Physicochemical properties of endosperm starches in milled rice determine its cooking and eating quality. Amylose is synthesized by granule-bound starch synthase I (GBSSI), whilst amylopectin is synthesized by the synergistic activities of starch synthases (SSs), branching enzymes (BEs) and debranching enzymes (DBEs). However, the complexes formed by starch biosynthetic enzymes are not well characterized. Gene expression profiles and protein complexes were determined in white-core (GM645) and waxy (GM077) mutants derived from a high amylose indica rice Guangluai 4 (GLA4). In GM645, genes including AGPS1, GBSSI, SSIIa, BEI, BEIIa, BEIIb, PUL, ISA1 and SP were significantly downregulated during seed development. In GM077, the expression levels of AGPL2, AGPS1, AGPS2b, SSIIIa, BEI, PUL and ISA1 were significantly upregulated. Co-immunoprecipitation assays revealed interactions of SSs-BEs, SSs-PUL and BEs-PUL in developing seeds. However, weak SSI-SSIIa interaction was detected in GM077, whilst SSI-PUL interaction was absent. Weak interaction signals for SSI-SSIIa, SSIIa-BEI, SSIIa-BEIIb, BEI-BEIIb and SSI-BEI were also observed in GM645. These results suggest that the protein-protein interactions for starch biosynthesis are modified in mutants, which provides insight into the mechanisms of starch biosynthesis, particularly in indica rice.
机译:碾磨稻米淀粉淀粉的物理化学性质确定其烹饪和饮食品质。通过颗粒结合的淀粉合酶I(GBSSI)合成直链淀粉,而通过淀粉合酶(SSS),支化酶(BES)和脱机酶(DBES)的协同活性合成淀粉蛋白。然而,淀粉生物合成酶形成的复合物具有很好的表征。基因表达谱和蛋白质复合物在白核(GM645)和衍生自高淀粉蛋白籼稻广油4(GLA4)的蜡质(GM077)突变体中测定。在GM645中,在种子发育期间,在种子发育期间显着下调包括AGPS1,GBSSI,SSIIA,Bei,Beiia,Beiib,Pul,Isa1和Sp的基因。在GM077中,显着上调了AGPL2,AGPS1,AGPS2B,SSIIIA,BEI,PUL和ISA1的表达水平。共免疫沉淀测定揭示了SSS-BES,SSS-培养物和BES-PUR的相互作用。然而,在GM077中检测到弱SSI-SSIIa相互作用,同时缺乏SSI-粉性互动。在GM645还观察到SSI-SSIIA,SSIIA-BEI,SSIIA-BEIIB,北贝和SSI-BEI的弱相互作用信号。这些结果表明,淀粉生物合成的蛋白质 - 蛋白质相互作用在突变体中改性,其洞察淀粉生物合成机制,特别是在籼稻中。

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