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Metabolite profiling and molecular responses in a drought-tolerant savory Satureja rechingeri exposed to water deficit

机译:暴露于缺水的耐旱咸味香菜的代谢产物谱和分子响应

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摘要

This study aimed to determine the response of Satureja rechingeri to water deficit by quantifying the expression of three targeted genes and four traditional reference genes using quantitative real-time PCR analysis (RT-qPCR). Drought stress was imposed by withholding water 4 months after planting. Profiling of volatile and non-volatile compounds using gas chromatography/mass spectrometry (GC/MS) and high-performance thin layer chromatography (HPTLC) showed an increasing–decreasing trend of major phenolic and terpenoid compounds such as rosmarinic and caffeic acids, carvacrole, thymol and p-Cymene. Drought stress also lead to significant increases in oil yield, soluble sugars and proline as well as significant reductions in leaf water potential (LWP), relative water content (RWC), and pigments. Metabolite profiling revealed the strategies savory employed to generate different biochemical phenotypes. RT-qPCR analysis showed that up-regulation of the three genes [1-deoxy-d-xylulose 5-phosphate reductoisomerase (DXR), 3-hydroxy-3-methylglutaryl-coenzyme. A reductase (HMGR) and rosmarinic acid synthase: 4-coumaroyl-CoA (RAS)] selected from the phenylpropanoid and terpenoid biosynthesis pathways were markedly enhanced at the transcript levels of the regulatory steps and directly increased the production of secondary metabolites, including phenolic and terpenoid compounds. Actin protein (ACT), elongation factor 1-α (EF1α), glyceraldehyde-3-phosphate dehydrogenase cytosolic (GAPC) and ubiquitin-conjugating enzyme (UBC) were used as traditional reference genes. UBC’s suitability as the reference genes were verified in S. rechingeri. The study’s results provide the foundation for gene expression analysis of savory and other species of Lamiaceae. Thus, the effective application of drought stress before harvesting can increase the quantity and quality of raw material.Electronic supplementary materialThe online version of this article (10.1007/s13205-018-1491-9) contains supplementary material, which is available to authorized users.
机译:这项研究的目的是通过定量实时定量PCR分析(RT-qPCR)对三个靶向基因和四个传统参考基因的表达进行定量分析,从而确定Satureja rechingeri对缺水的反应。种植后4个月不浇水,造成干旱胁迫。使用气相色谱/质谱(GC / MS)和高性能薄层色谱(HPTLC)对挥发性和非挥发性化合物进行分析表明,主要的酚类和萜类化合物(如迷迭香和咖啡酸,木瓜酚,百里香酚和对伞花烃。干旱胁迫还导致油料产量,可溶性糖和脯氨酸的显着增加,以及叶水势(LWP),相对含水量(RWC)和色素的显着降低。代谢物谱分析揭示了可用于产生不同生化表型的策略。 RT-qPCR分析显示三个基因[1-脱氧-d-木酮糖5-磷酸还原异构酶(DXR),3-羟基-3-甲基戊二酰辅酶的上调。选自苯丙烷和萜类生物合成途径的还原酶(HMGR)和迷迭香酸合酶:4-香豆酰-CoA(RAS)]在调控步骤的转录水平上显着增强,并直接增加了次级代谢产物的生成,包括酚类和萜类化合物。肌动蛋白(ACT),延伸因子1-α(EF1α),甘油三磷酸脱氢酶胞质(GAPC)和泛素结合酶(UBC)被用作传统的参考基因。 UBC作为参考基因的适合性已在雷金氏酵母中得到验证。该研究结果为咸味科和其他唇形科的基因表达分析提供了基础。因此,在收获前有效地利用干旱胁迫可以增加原材料的数量和质量。电子补充材料本文的在线版本(10.1007 / s13205-018-1491-9)包含补充材料,授权用户可以使用。

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