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RNA干扰对吗啡生物合成基因salAT的抑制作用及途径酶的关联证据。

RNAi suppression of the morphine biosynthetic gene salAT and evidence of association of pathway enzymes.

作者信息

Kempe Katja, Higashi Yasuhiro, Frick Susanne, Sabarna Khaled, Kutchan Toni M

机构信息

Donald Danforth Plant Science Center, 975 North Warson Road, St. Louis, MO 63132, USA.

出版信息

Phytochemistry. 2009 Mar;70(5):579-89. doi: 10.1016/j.phytochem.2009.03.002. Epub 2009 Apr 7.

Abstract

Papaver somniferum L. was transformed with an RNAi construct designed to reduce transcript levels of the gene encoding the morphine biosynthetic enzyme, salutaridinol 7-O-acetyltransferase (SalAT). RNA interference of salAT led to accumulation of the intermediate compounds, salutaridine and salutaridinol, in a ratio ranging from 2:1 to 56:1. Along the morphine biosynthetic pathway, salutaridine is stereospecifically reduced by salutaridine reductase (SalR) to salutaridinol, which is subsequently acetylated by SalAT. SalAT transcript was shown by quantitative PCR to be diminished, while salR transcript levels remained unaffected. Yeast two-hybrid and co-immunoprecipitation analyses indicated an interaction between SalR and SalAT, which suggested the occurrence of an enzyme complex and provided an explanation for the unexpected accumulation of salutaridine. Decreased concentrations of thebaine and codeine in latex were also observed, while the morphine levels remained constant compared to concentrations found in untransformed control plants.

摘要

用一种RNA干扰构建体转化罂粟(Papaver somniferum L.),该构建体旨在降低编码吗啡生物合成酶——羟基血根碱7 - O - 乙酰转移酶(SalAT)的基因的转录水平。SalAT的RNA干扰导致中间化合物羟基血根碱和羟基血根醇积累,其比例范围为2:1至56:1。在吗啡生物合成途径中,羟基血根碱被羟基血根碱还原酶(SalR)立体特异性地还原为羟基血根醇,随后羟基血根醇被SalAT乙酰化。定量PCR显示SalAT转录本减少,而SalR转录水平不受影响。酵母双杂交和免疫共沉淀分析表明SalR和SalAT之间存在相互作用,这表明存在一种酶复合物,并为羟基血根碱的意外积累提供了解释。同时观察到乳汁中蒂巴因和可待因的浓度降低,而与未转化对照植物中发现的浓度相比,吗啡水平保持不变。

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