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首页> 外文期刊>International Journal of Molecular Sciences >Genome-Wide Identification, 3D Modeling, Expression and Enzymatic Activity Analysis of Cell Wall Invertase Gene Family from Cassava (Manihot esculenta Crantz)
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Genome-Wide Identification, 3D Modeling, Expression and Enzymatic Activity Analysis of Cell Wall Invertase Gene Family from Cassava (Manihot esculenta Crantz)

机译:木薯(Manihot esculenta Crantz)细胞壁转化酶基因家族的全基因组鉴定,3D建模,表达和酶活性分析

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The cell wall invertases play a crucial role on the sucrose metabolism in plant source and sink organs. In this research, six cell wall invertase genes (MeCWINV1-6) were cloned from cassava. All the MeCWINVs contain a putative signal peptide with a predicted extracellular location. The overall predicted structures of the MeCWINV1-6 are similar to AtcwINV1. Their N-terminus domain forms a β-propeller module and three conserved sequence domains (NDPNG, RDP and WECP(V)D), in which the catalytic residues are situated in these domains; while the C-terminus domain consists of a β-sandwich module. The predicted structure of Pro residue from the WECPD (MeCWINV1, 2, 5, and 6), and Val residue from the WECVD (MeCWINV3 and 4) are different. The activity of MeCWINV1 and 3 were higher than other MeCWINVs in leaves and tubers, which suggested that sucrose was mainly catalyzed by the MeCWINV1 and 3 in the apoplastic space of cassava source and sink organs. The transcriptional levels of all the MeCWINVs and their enzymatic activity were lower in tubers than in leaves at all the stages during the cassava tuber development. It suggested that the major role of the MeCWINVs was on the regulation of carbon exportation from source leaves, and the ratio of sucrose to hexose in the apoplasts; the role of these enzymes on the sucrose unloading to tuber was weaker.
机译:细胞壁转化酶在植物源和汇器官中的蔗糖代谢中起关键作用。在这项研究中,从木薯中克隆了六个细胞壁转化酶基因(MeCWINV1-6)。所有的MeCWINV都包含具有预测的细胞外位置的推定信号肽。 MeCWINV1-6的总体预测结构与AtcwINV1相似。它们的N末端结构域形成一个β-螺旋桨模块和三个保守的序列结构域(NDPNG,RDP和WECP(V)D),其中催化残基位于这些结构域中;而C末端域由β三明治模块组成。来自WECPD的Pro残基(MeCWINV1、2、5和6)和来自WECVD的Val残基(MeCWINV3和4)的预测结构不同。 MeCWINV1和3在叶片和块茎中的活性高于其他MeCWINV,这表明蔗糖主要由木薯源和汇器官的质外性空间中的MeCWINV1和3催化。在木薯块茎发育的所有阶段,块茎中所有MeCWINVs的转录水平及其酶活性均低于叶片。这表明MeCWINVs的主要作用是调控源叶碳的出口,以及质外体中蔗糖与己糖的比例。这些酶对蔗糖向块茎卸载的作用较弱。

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