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首页> 外文期刊>Applied and Environmental Microbiology >Application of the Synechococcus nirA Promoter To Establish an Inducible Expression System for Engineering the Synechocystis Tocopherol Pathway
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Application of the Synechococcus nirA Promoter To Establish an Inducible Expression System for Engineering the Synechocystis Tocopherol Pathway

机译:应用synechococcus nirA启动子建立可诱导表达系统以工程化拟蓝藻生育酚途径

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摘要

Tocopherols are important antioxidants in lipophilic environments. They are synthesized by plants and some photosynthetic bacteria. Recent efforts to analyze and engineer tocopherol biosynthesis led to the identification of Synechocystis sp. strain PCC 6803 as a well-characterized model system. To facilitate the identification of the rate-limiting step(s) in the tocopherol biosynthetic pathway through the modulation of transgene expression, we established an inducible expression system in Synechocystis sp. strain PCC 6803. The nirA promoter from Synechococcus sp. strain PCC 7942, which is repressed by ammonium and induced by nitrite (S.-I. Maeda et al., J. Bacteriol. 180:4080-4088, 1998), was chosen to drive the expression of Arabidopsis thaliana p-hydroxyphenylpyruvate dioxygenase. The enzyme catalyzes the formation of homogentisic acid from p-hydroxyphenylpyruvate. Expression of this gene under inducing conditions resulted in up to a fivefold increase in total tocopherol levels with up to 20% of tocopherols being accumulated as tocotrienols. The culture supernatant of these cultures exhibited a brown coloration, a finding indicative of homogentisic acid excretion. Enzyme assays, functional complementation, reverse transcription-PCR, and Western blot analysis confirmed transgene expression under inducing conditions only. These data demonstrate that the nirA promoter can be used to control transgene expression in Synechocystis and that homogentisic acid is a limiting factor for tocopherol synthesis in Synechocystis sp. strain PCC 6803.
机译:生育酚是亲脂环境中的重要抗氧化剂。它们是由植物和一些光合细菌合成的。分析和工程设计生育酚生物合成的最新努力导致鉴定了集胞藻。 PCC 6803应变作为一个很好表征的模型系统。为了促进通过调节转基因表达来确定生育酚生物合成途径中的限速步骤,我们在Synechocystis sp。中建立了可诱导的表达系统。菌株Synechococcus sp。的nirA启动子。选择菌株PCC 7942,其被铵抑制并被亚硝酸盐诱导(S.I. Maeda等人,J。Bacteriol。180:4080-4088,1998),以驱动拟南芥对羟基苯丙酮酸双加氧酶的表达。 。该酶催化由对羟基苯丙酮酸形成高纯酸。该基因在诱导条件下的表达导致总生育酚水平增加多达五倍,其中最多20%的生育酚以生育三烯酚的形式积累。这些培养物的培养物上清液显示出褐色,这表明尿黑酸排泄。酶测定,功能互补,逆转录PCR和蛋白质印迹分析仅在诱导条件下证实了转基因表达。这些数据表明,nirA启动子可用于控制集胞藻中转基因的表达,而高纯酸是集胞藻sp中生育酚合成的限制因素。株PCC 6803。

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