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首页> 外文期刊>International Biodeterioration & Biodegradation >The function of an installed photosynthetic formaldehyde-assimilation pathway containing dihydroxyacetone synthase and dihydroxyacetone kinase enhanced formaldehyde removal from solution in transgenic geranium leaves
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The function of an installed photosynthetic formaldehyde-assimilation pathway containing dihydroxyacetone synthase and dihydroxyacetone kinase enhanced formaldehyde removal from solution in transgenic geranium leaves

机译:已安装的包含二羟基丙酮合酶和二羟基丙酮激酶的光合甲醛同化途径的功能增强了转基因天竺葵叶片中溶液中甲醛的去除

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摘要

In a previous study, we created transgenic geranium leaves installed with a photosynthetic formaldehyde (HCHO)-assimilation pathway containing dihydroxyacetone synthase (DAS) and dihydroxyacetone kinase (DAM). In the current study, DAS and DAM expression was confirmed in the leaves of three selected transgenic lines via RT-PCR analysis. C-13 NMR analysis showed that the actions of the DAS/DAK pathway completely inhibited the role of citrate-produced pathway during HCHO metabolism in transgenic geranium leaves treated with 2 mM (HCHO)-C-13 for 4 h. Further analysis indicated that HCHO uptake from this solution was always higher in the leaves of the three transgenic lines than in WT (untransformed) leaves during a 48-h treatment period. This result suggests that the role of the installed DAS/DAK pathway enhanced HCHO uptake from solution in transgenic geranium leaves. Moreover, the relationship between HCHO uptake and treatment time approached a linear function during the first 40-h treatment period due to the function of the installed pathway. Based on the (HCHO)-C-13 metabolic profile and the HCHO uptake curves, (HCHO)-C-13 metabolic pathways in transgenic leaves treated with 2 mM (HCHO)-C-13 were postulated and the contribution of the DAS/DAK pathway to HCHO uptake by transgenic leaves was quantitatively evaluated. (C) 2015 Elsevier Ltd. All rights reserved.
机译:在以前的研究中,我们创建了装有光合甲醛(HCHO)同化途径的转基因天竺葵叶,该途径包含二羟基丙酮合酶(DAS)和二羟基丙酮激酶(DAM)。在本研究中,通过RT-PCR分析证实了三种选择的转基因品系叶片中DAS和DAM的表达。 C-13 NMR分析表明,在2 mM(HCHO)-C-13处理4 h的转基因天竺葵叶片中,DAS / DAK途径的作用完全抑制了柠檬酸产生途径在HCHO代谢过程中的作用。进一步的分析表明,在48小时的处理过程中,三种转基因品系的叶子中该溶液对HCHO的吸收总是比WT(未转化)的叶子高。该结果表明,已安装的DAS / DAK途径的作用增强了转基因天竺葵叶片中HCHO从溶液中的吸收。此外,由于安装途径的功能,在最初的40小时治疗期间,HCHO摄取与治疗时间之间的关系接近线性函数。根据(HCHO)-C-13代谢曲线和HCHO吸收曲线,假设用2 mM(HCHO)-C-13处理的转基因叶片中的(HCHO)-C-13代谢途径以及DAS /定量评估了DAK途径对转基因叶片摄取HCHO的影响。 (C)2015 Elsevier Ltd.保留所有权利。

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