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首页> 外文期刊>Journal of proteomics >Comparative proteome analysis of A- and B-type starch granule-associated proteins in bread wheat (Triticum aestivum L.) and Aegilops crassa
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Comparative proteome analysis of A- and B-type starch granule-associated proteins in bread wheat (Triticum aestivum L.) and Aegilops crassa

机译:面包小麦(Aticiloes aestivum L.)和埃及山羊草(Aegilops crassa)A型和B型淀粉颗粒相关蛋白的蛋白质组比较分析

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摘要

Starch is the main component in the wheat endosperm and exists in two forms including A- and B-type granules. A bread wheat line CB037A and an Aegilops line Aegilops crassa were studied for the underlying starch biosynthesis mechanism in relation to granule types. The wheat line contains both types of starch granules while the Aegilops line only has the A-type. Differential starch granule development patterns of these two species were observed at the morphological level. A total of 190 differentially expressed proteins (DEPs) were detected between the two lines based on 2-D electrophoresis, among which 119 DEPs were identified, representing 13 unique proteins. Gene ontology annotation analysis indicated that both molecular functions and biological processes of the identified proteins are highly conserved. Different phosphorylation modification levels between the A- and B-type starch granules were found. Real-time quantitative reverse transcription PCR analysis revealed that a number of key genes including starch synthase I-1, pullulanase, isoamylase and starch branching enzyme Ha were differentially expressed between the two species. Our results demonstrated that the large granule size is associated with higher activities of multiple starch biosynthesis enzymes. The phosphorylation of starch biosynthesis enzymes is related with the formation of B-type starch granules.
机译:淀粉是小麦胚乳的主要成分,以两种形式存在,包括A型和B型颗粒。研究了面包小麦品系CB037A和Aegilops品系Aegilops crassa与颗粒类型相关的潜在淀粉生物合成机理。小麦品系包含两种类型的淀粉颗粒,而Aegilops品系仅具有A型。在形态学水平上观察到这两种物种的差异淀粉颗粒发育模式。基于2-D电泳,在两条细胞系之间共检测到190种差异表达蛋白(DEP),其中鉴定出119种DEP,代表13种独特蛋白。基因本体注释分析表明,所鉴定蛋白质的分子功能和生物学过程均高度保守。发现A型和B型淀粉颗粒之间的磷酸化修饰水平不同。实时定量逆转录PCR分析表明,两个关键基因包括淀粉合酶I-1,支链淀粉酶,异淀粉酶和淀粉分支酶Ha均差异表达。我们的结果表明,大颗粒与多种淀粉生物合成酶的较高活性有关。淀粉生物合成酶的磷酸化与B型淀粉颗粒的形成有关。

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