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Biosynthetic relationship between C-28-brassinosteroids and C-29-brassinosteroids in rice (Oryza sativa) seedlings

机译:水稻幼苗中C-28-油菜素类固醇与C-29-油菜素类固醇之间的生物合成关系

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A crude enzyme solution was prepared from young rice seedlings, and the metabolism of C-29-brassinosteroids identified from the seedlings was examined. When 28-homoteasterone was added as a substrate, 28-homotyphasterol, teasterone, and 26-nor-28-homoteasterone were characterized as enzyme products by GC-MS/SIM analysis. With 28-homotyphasterol, 28-homoteasterone, typhasterol, 28-homocastasterone, and 26-nor-28-homotyphasterol were formed and identified as products. When 28-homocastasterone was used, castasterone and 26-nor-28-homocastasterone were identified as products. Together with the reduced biological activity of C-29-brassinosteroids and their metabolites in the rice lamina inclination assay, these metabolic studies suggest a biosynthetic sequence, 28-homoteasterone <-> 28-homotyphasterol -> 28-homocastasterone for C-29-brassinosteroid biosynthesis is connected to the biosynthetic sequence teasterone <-> typhasterol -> castasterone for C-28-brassinosteroids by C-28 demethylation, i.e., in order to increase biological activity in the rice plant. Additionally, the C-29-brassinosteroids seem to bio-degrade their C-26 demethylated C-28-brassinosteroid analogs to reduce brassinosteroid activity in planta. In conclusion, the biosynthesis of C-29-brassinosteroids is a likely alternative route to the biologically-active brassinosteroid, castasterone, in rice. (C) 2014 Elsevier Ltd. All rights reserved.
机译:从年轻的水稻幼苗中制备粗酶溶液,并检查从幼苗中鉴定出的C-29-油菜素类固醇的代谢。当添加28-高纯甾酮作为底物时,通过GC-MS / SIM分析将28-高同甾醇,茶甾酮和26-去-28-高纯甾酮表征为酶产物。与28-同型甾醇,28-同型甾酮,邻苯二酚,28-同型异体甾酮和26-去-28-同型甾醇形成并鉴定为产物。当使用28-高雌甾酮时,鉴定出了雌甾烷酮和26-去-28-高雌甾酮。这些代谢研究表明,C-29-油菜甾醇及其代谢产物的生物活性降低,在水稻薄层倾斜试验中,这些生物合成序列表明,C-29-油菜甾醇的生物合成序列为28-高纯甾烯酮<-> 28-同型胆固醇-> 28-高古甾酮。生物合成通过C-28脱甲基作用连接到C-28-油菜甾醇的生物合成序列茶甾酮-香豆酚->甾酮,即为了增加水稻植株的生物活性。此外,C-29-油菜素类固醇似乎可以生物降解其C-26脱甲基的C-28-油菜素类固醇类似物,从而降低植物中油菜素类固醇的活性。总之,在水稻中,C-29-油菜甾醇的生物合成可能是具有生物活性的油菜素甾体,雌甾酮的替代途径。 (C)2014 Elsevier Ltd.保留所有权利。

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