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作 者:窦维泽 姜雯 冯艺川 金卓 全雪丽[2] 吴松权[1,2] Dou Weize;Jiang Wen;Feng Yichuan;Jin Zhuo;Quan Xueli;Wu Songquan(College of Integration Science,Yanbian University,Yanji 133000,Jilin,China;Agricultural College,Yanbian University,Yanji 133000,Jilin,China)
机构地区:[1]延边大学融合学院,吉林延吉133000 [2]延边大学农学院,吉林延吉133000
出 处:《作物杂志》2024年第1期48-56,共9页Crops
基 金:吉林省自然科学基金(YDZJ202101ZYTS197);国家自然科学基金(21462044)。
摘 要:H2O2处理能显著增加膜荚黄芪不定根中毛蕊异黄酮葡萄糖苷(CG)的含量。为探究其生物合成机制,以膜荚黄芪不定根为试验材料,经H_(2)O_(2)处理后进行转录组测序筛选差异表达基因。选取上调基因进行功能和代谢通路分析,用qRT-PCR验证,并对相关生理生化指标进行测定。结果表明,差异表达基因的筛选和基因功能注释表明,H_(2)O_(2)处理引起了氧化胁迫,为抵消氧化胁迫,膜荚黄芪不定根通过激活乙烯信号通路,诱导苯丙烷异黄酮生物合成途径中的全部结构基因,从而显著增加CG的含量。此外,为了增加CG,H_(2)O_(2)处理也会诱导苯丙氨酸的生物合成。试验结果进一步揭示了膜荚黄芪不定根中CG的积累机制,为今后规模化生产黄芪CG奠定理论依据。Hydrogen peroxide(H 2 O 2)significantly enhanced the content of calycosin-7-O-β-D-glucoside(CG)in Astragalus membranaceus adventitious roots(AMARs).To discover its biosynthetic mechanism of CG,AMARs were used to screen the differentially expressed genes(DEGs)through transcriptome sequencing after H_(2)O_(2) treatment.The function and metabolic pathways were analyzed by using up-regulated genes,verified them by qRT-PCR method,and measured the relevant physiological and biochemical parameters.The results showed that AMARs activated ethylene signaling,induced all structural genes in the phenylpropane-isoflavone biosynthesis pathway,significantly increased the content of CG to counteract the oxidative stress caused by H_(2)O_(2 )treatment.Furthermore,H_(2)O_(2) treatment also induced phenylalanine biosynthesis in order to increase the content of CG.These results revealed the accumulation mechanism of CG in AMARs which laid a theoretical basis for large-scale production of CG in the future.
关 键 词:H_(2)O_(2) 氧化胁迫 膜荚黄芪 转录组测序 毛蕊异黄酮葡萄糖苷
分 类 号:S567.239[农业科学—中草药栽培]
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