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萜类化合物合成相关的 1-脱氧-D-木酮糖-5-磷酸合酶(DXS)基因的特性与功能。

Characterization and Function of the 1-Deoxy-D-xylose-5-Phosphate Synthase (DXS) Gene Related to Terpenoid Synthesis in .

机构信息

Key Laboratory of Forest Genetics & Biotechnology of Ministry of Education, Nanjing Forestry University, Nanjing 210037, China.

出版信息

Int J Mol Sci. 2021 Jan 15;22(2):848. doi: 10.3390/ijms22020848.

Abstract

In the methyl-D-erythritol-4-phosphate (MEP) pathway, 1-deoxy-D-xylose-5-phosphate synthase (DXS) is considered the key enzyme for the biosynthesis of terpenoids. In this study, (MK970590) was isolated from . Bioinformatics analysis revealed homology of MK970590 with DXS proteins from other species. Relative expression analysis suggested that expression was higher in roots than in other plant parts, and the treatment of seedlings with mechanical injury via 15% polyethylene glycol 6000, 10 mM HO, 50 μM ethephon (ETH), 10 mM methyl jasmonate (MeJA), and 1 mM salicylic acid (SA) resulted in an increased expression of . pET28a- was expressed in TransB (DE3) cells, and stress analysis showed that the recombinant protein was involved in resistance to NaCl and drought stresses. The subcellular localization of was in the chloroplast. We also cloned a full-length 1024 bp promoter. expression was observed in roots, stems, and leaves. overexpression significantly increased carotenoid, chlorophyll a, and chlorophyll b contents and DXS enzyme activity, suggesting that is important in isoprenoid biosynthesis. This study provides a theoretical basis for molecular breeding for terpene synthesis regulation and resistance.

摘要

在甲基-D-赤藓醇-4-磷酸(MEP)途径中,1-脱氧-D-木酮糖-5-磷酸合酶(DXS)被认为是萜类化合物生物合成的关键酶。在这项研究中,从 中分离出 (MK970590)。生物信息学分析表明,MK970590 与来自其他物种的 DXS 蛋白具有同源性。相对表达分析表明, 在根中表达高于其他植物部位,并且通过 15%聚乙二醇 6000、10 mM HO、50 μM 乙烯利(ETH)、10 mM 茉莉酸甲酯(MeJA)和 1 mM 水杨酸(SA)处理 幼苗导致 的表达增加。pET28a-在 TransB(DE3)细胞中表达,应激分析表明重组蛋白参与耐 NaCl 和干旱应激。 的亚细胞定位在叶绿体中。我们还克隆了全长 1024 bp 的 启动子。 在 根、茎和叶中观察到 表达。过表达 显著增加类胡萝卜素、叶绿素 a 和叶绿素 b 的含量以及 DXS 酶活性,表明 在异戊二烯生物合成中很重要。这项研究为萜类化合物合成调控和抗性的分子育种提供了理论基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ff/7830437/cac34a135861/ijms-22-00848-g001.jpg

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