首页> 外文期刊>Phytochemistry >Involvement of pectin methyl-esterase during the ripening of grapeberries: partial cDNA isolation, transcript expression and changes in thedegree of methyl-esterification of cell wall pectins
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Involvement of pectin methyl-esterase during the ripening of grapeberries: partial cDNA isolation, transcript expression and changes in thedegree of methyl-esterification of cell wall pectins

机译:果胶甲基酯酶在葡萄成熟过程中的作用:部分cDNA分离,转录本表达和细胞壁果胶甲基酯化程度的变化

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Grape berries (Vitis vinifera L., ev Ugni blanc) were harvested at 12 different weeks of development in 1996 and 1997. Ripening was induced at veraison, the crucial stage of berry softening, and was followed by a rapid accumulation of glucose and fructose and an increase of pH. Total RNAs, crude proteins and cell wall material were isolated from each developmental stage. A partial length cDNA (pme 1, accession number AF 159122, GenBank (TM)) encoding a pectin methyl-esterase (PME, EC 3. 1. 1.11) was cloned by RT-PCR with degenerate primers. Northern blots revealed that mRNAs coding for PME accumulate from one week before the onset of ripening until complete maturity, indicating that this transcript represents an early marker of veraison and could be involved in berry softening. However, PME activity was detected during all developmental stages. Total activity per berry increased, whereas "specific" activity, on a fresh weight basis, decreased during development. The amount of cell wall material (per berry and per g of berry) followed the same pattern as that of PME activity (total and "specific" respectively), indicating they were tightly correlated and that PME levels varied very little in the cell walls. Nevertheless, the degree of methyl-esterification of insoluble pectins decreased throughout the development from 68% in green stages to less than 20% for the ripe berries, and this observation is consistent with the induction of PME mRNAs during ripening. Relations between transcript expression, PME activity, the DE of insoluble pectic polysaccharides and their involvement in grape berry ripening are discussed.
机译:葡萄浆果(Vitis vinifera L.,ev Ugni blanc)分别在1996和1997年的12个不​​同发育周中收获。成熟期是在浆果软化的关键阶段-发芽期诱导的,随后迅速积累了葡萄糖和果糖, pH值升高。从每个发育阶段分离总RNA,粗蛋白和细胞壁材料。用简并引物通过RT-PCR克隆了编码果胶甲基酯酶(PME,EC 3.1.1.11)的部分长度cDNA(pme 1,登录号AF 159122,GenBank TM)。 Northern印迹显示,从成熟开始前的一个星期到完全成熟,编码PME的mRNA就会积累,这表明该转录物代表了早期的veraison标记,可能参与了浆果的软化。但是,在所有发育阶段均检测到PME活性。每个浆果的总活性增加,而以鲜重计的“特定”活性在发育过程中降低。细胞壁物质的数量(每浆果和每克浆果)遵循与PME活性相同的模式(分别为总和“特异”),表明它们紧密相关,并且细胞壁中PME的水平变化很小。然而,在整个发育过程中,不溶性果胶的甲基酯化程度从绿色阶段的68%下降到成熟浆果的20%以下,这一观察结果与成熟过程中对PME mRNA的诱导一致。讨论了转录表达,PME活性,不溶性果胶多糖的DE及其与葡萄浆果成熟之间的关系。

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