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首页> 外文期刊>Scientific reports. >Characterization and functional analysis of two novel 3-hydroxy-3-methylglutaryl-coenzyme A reductase genes (GbHMGR2 and GbHMGR3) from Ginkgo biloba
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Characterization and functional analysis of two novel 3-hydroxy-3-methylglutaryl-coenzyme A reductase genes (GbHMGR2 and GbHMGR3) from Ginkgo biloba

机译:两种新型3-羟基-3-甲基戊齐律 - 辅酶(GBHMGR2和GBHMGR3)的表征及功能分析来自银杏叶片的还原酶基因

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Terpene trilactones (TTLs) are the main secondary metabolites of Ginkgo biloba. As one of the rate-limiting enzymes in the mevalonic acid (MVA) pathway of TTL biosynthesis, 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGR) catalyzes the 3-hydroxy-3-methylglutaryl coenzyme A to form MVA. In this study, two cDNA sequences of HMGR genes, namely, GbHMGR2 and GbHMGR3, were cloned from G. biloba. The protein sequences of GbHMGR2 and GbHMGR3, which contain several functional domains, were analyzed. Regulatory elements related to light, hormone, and stress response were detected in the promoter regions of GbHMGR2 and GbHMGR3. The catalytic activity of these genes was verified by a functional complement experiment in yeast. Quantitative real-time PCR (qRT-PCR) showed the distinct expression patterns of the two genes in different organs. The TTL contents in the organs were detected by high-performance liquid chromatography- evaporative light scattering detector. GbHMGR2 and GbHMGR3 were responded to cold, dark, methyl jasmonate (MJ), abscisic acid (ABA), salicylic acid (SA), and ethephon (Eth) treatments. The TTL contents were also regulated by cold, dark, MJ, ABA, SA, and Eth treatment. In conclusion, GbHMGR2 and GbHMGR3 may participate in the MVA pathway of TTL biosynthesis.
机译:Terpene三碎石(TTL)是银杏叶的主要次级代谢物。作为TTL生物合成的甲醛酸(MVA)途径中的速率限制酶之一,3-羟基-3-甲基戊齐律 - 辅酶A还原酶(HMGR)催化3-羟基-3-甲基戊齐律辅酶A以形成MVA。在该研究中,从G.Biloba克隆了两个HMGR基因的CDNA序列,即GBHMGR2和GBHMGR3。分析了含有若干功能域的GBHMGR2和GBHMGR3的蛋白质序列。在GBHMGR2和GBHMGR3的启动子区域中检测到与光,激素和应力反应相关的调节元件。通过酵母中的功能补体实验验证了这些基因的催化活性。定量实时PCR(QRT-PCR)显示出不同器官中的两个基因的不同表达模式。通过高效液相色谱 - 蒸发光散射检测器检测器官中的TTL含量。 GBHMGR2和GBHMGR3响应冷,黑暗,茉莉酸酯(MJ),脱落酸(ABA),水杨酸(SA)和Ethephon(Eth)治疗。 TTL含量也受冷,暗,MJ,ABA,SA和Eth治疗调节。总之,GBHMGR2和GBHMGR3可以参与TTL生物合成的MVA途径。

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