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首页> 外文期刊>Tropical Agriculture and Development >Characterization and Expression Analysis of a Putative a-L-Arabinofuranosidase/p-D-xylosidase Gene Derived from Avocado
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Characterization and Expression Analysis of a Putative a-L-Arabinofuranosidase/p-D-xylosidase Gene Derived from Avocado

机译:鳄梨衍生的α-L-阿拉伯呋喃糖苷酶/ p-D-木糖苷酶基因的表征和表达分析

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Cell wall is an important component which decides growth, volume, shape of plant cells. Alternation of its structure also affects various aspects of plant development. In this study, we obtained a cDNA clone encoding an a-L-arabinofuranosidase/ (3-D-xylosidase from avocado fruit. The clone, designated as PaArf/Xyl3A, contained 3,002 nucleotides which encoded 777 amino acid residues with a calculated molecular mass of 83.4 kDa. The deduced amino acid sequence contained a putative signal peptide. Calculated molecular mass of the truncated protein was 80 kDa consisting of 745 amino acid residues. In addition, there were two potential N-linked glycosylation sites, suggesting that PaArf/Xyl3A would be exported to the apoplast where the enzyme could hydrolyze on cell wall polysaccharides. Phylogenetic analysis showed that PaArf/Xyl3A clustered near other plant a-L-arabinofuranosidases/p-D-xylosidases exhibiting a preferential arabinosyl hydrolyzing activity against natural polysaccharides. These resultsindicated that the protein would be secreted from cytosol to cell wall (apoplast) and might act as an a-L-arabinofuranosidase against natural polysaccharides. Accumulation of the mRNA was detected in the fruit right after harvest and other active growingorgans such as immature leaves, expanded young leaves, germinating seedling and roots. According to the expression pattern and the phylogenetic relationship, PaArf/Xyl3A might be involved in arabinose metabolism and change to cell-to-cell contact of avocado during cell division/proliferation stage.
机译:细胞壁是决定植物细胞生长,体积,形状的重要组成部分。其结构的变化也影响植物发育的各个方面。在这项研究中,我们从鳄梨果实中获得了编码aL-阿拉伯呋喃糖苷酶/(3-D-木糖苷酶)的cDNA克隆。命名为PaArf / Xyl3A的克隆包含3,002个核苷酸,编码777个氨基酸残基,计算分子量为83.4。 kDa。推导的氨基酸序列包含一个推定的信号肽,截短蛋白的计算分子量为80 kDa,由745个氨基酸残基组成,此外,还有两个潜在的N-联糖基化位点,表明PaArf / Xyl3A可能是系统发育分析表明,PaArf / Xyl3A聚簇在其他植物aL-阿拉伯呋喃糖苷酶/ pD-木糖苷酶附近,对天然多糖具有优先的阿拉伯糖基水解活性,这些结果表明该蛋白将被分泌。从细胞质到细胞壁(质外体),并可能作为天然多糖的aL-阿拉伯呋喃糖苷酶s。收获后立即在水果和其他活跃的生长器官如未成熟的叶子,膨胀的幼叶,发芽的幼苗和根中检测到mRNA的积累。根据表达模式和系统发育关系,PaArf / Xyl3A可能参与了阿拉伯糖的代谢,并在细胞分裂/增殖阶段改变了鳄梨的细胞间接触。

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