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首页> 外文期刊>BMC Plant Biology >Cell-specific expression of tryptophan decarboxylase and 10-hydroxygeraniol oxidoreductase, key genes involved in camptothecin biosynthesis in Camptotheca acuminata Decne (Nyssaceae)
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Cell-specific expression of tryptophan decarboxylase and 10-hydroxygeraniol oxidoreductase, key genes involved in camptothecin biosynthesis in Camptotheca acuminata Decne (Nyssaceae)

机译:喜树生物中喜树碱生物合成关键基因色氨酸脱羧酶和10-羟基香叶醇氧化还原酶的细胞特异性表达

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Background Camptotheca acuminata is a major natural source of the terpenoid indole alkaloid camptothecin (CPT). At present, little is known about the cellular distribution of the biosynthesis of CPT, which would be useful knowledge for developing new strategies and technologies for improving alkaloid production. Results The pattern of CPT accumulation was compared with the expression pattern of some genes involved in CPT biosynthesis in C. acuminata [i.e., Ca-TDC1 and Ca-TDC2 (encoding for tryptophan decarboxylase) and Ca-HGO (encoding for 10-hydroxygeraniol oxidoreductase)]. Both CPT accumulation and gene expression were investigated in plants at different degrees of development and in plantlets subjected to drought-stress. In all organs, CPT accumulation was detected in epidermal idioblasts, in some glandular trichomes, and in groups of idioblast cells localized in parenchyma tissues. Drought-stress caused an increase in CPT accumulation and in the number of glandular trichomes containing CPT, whereas no increase in epidermal or parenchymatous idioblasts was observed. In the leaf, Ca-TDC1 expression was detected in some epidermal cells and in groups of mesophyll cells but not in glandular trichomes; in the stem, it was observed in parenchyma cells of the vascular tissue; in the root, no expression was detected. Ca-TDC2 expression was observed exclusively in leaves of plantlets subjected to drought-stress, in the same sites described for Ca-TDC1 . In the leaf, Ca-HGO was detected in all chlorenchyma cells; in the stem, it was observed in the same sites described for Ca-TDC1 ; in the root, no expression was detected. Conclusions The finding that the sites of CPT accumulation are not consistently the same as those in which the studied genes are expressed demonstrates an organ-to-organ and cell-to-cell translocation of CPT or its precursors.
机译:背景喜树喜树碱是萜类吲哚生物碱喜树碱(CPT)的主要天然来源。目前,关于CPT的生物合成的细胞分布知之甚少,这对于开发改进生物碱生产的新策略和技术将是有用的知识。结果比较了CPT积累的模式和一些参与CPT生物合成的基因在C. acuminata中的表达模式(即Ca-TDC1和Ca-TDC2(编码色氨酸脱羧酶)和Ca-HGO(编码10-羟基香叶醇氧化还原酶) )]。在不同发育程度的植物和遭受干旱胁迫的幼苗中都研究了CPT的积累和基因表达。在所有器官中,在表皮成纤维细胞,某些腺毛状体以及位于薄壁组织中的成纤维细胞组中都检测到了CPT的积累。干旱胁迫导致CPT积累和含有CPT的腺毛的数量增加,而未观察到表皮或实质性成纤维细胞的增加。在叶片中,在一些表皮细胞和叶肉细胞组中检测到Ca-TDC1表达,但在腺毛状体中未检测到。在茎中,在血管组织的薄壁细胞中观察到。在根中,未检测到表达。 Ca-TDC2的表达仅在遭受干旱胁迫的小植株的叶子中,在与Ca-TDC1相同的位置观察到。在叶片中,在所有绿藻细胞中都检测到了Ca-HGO。在茎中,在与Ca-TDC1所述的相同位置观察到了该酶;在根中,未检测到表达。结论CPT积累的位点与所研究基因表达的位点不一致,这一发现表明CPT或其前体在器官之间和细胞之间转移。

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