Tantong Supaluk, Incharoensakdi Aran, Sirikantaramas Supaart, Lindblad Peter
Program in Biotechnology, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand; Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.
Department of Biochemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.
Protein Expr Purif. 2016 May;121:163-8. doi: 10.1016/j.pep.2016.01.020. Epub 2016 Feb 1.
Selected model strains of phototrophic cyanobacteria have been genetically engineered for heterologous expression of numerous enzymes. In the present study, we initially explored the heterologous expression of enzymes involved in trans-resveratrol production, namely, the production of tyrosine ammonia-lyase, coumaroyl CoA-ligase, and stilbene synthase, in the unicellular cyanobacterium Synechocystis PCC 6803. Under the promoters Ptrc1Ocore and Ptrc1O, the respective genes were transcribed and translated into the corresponding soluble proteins at concentrations of 16-34 μg L(-1). The expression levels of these enzymes did not affect the growth rate of the cyanobacterial cells. Interestingly, coumaroyl CoA-ligase expression slightly increased the chlorophyll a content of the cells. Overall, our results suggest that the complete pathway of trans-resveratrol production can be engineered in Synechocystis PCC 6803.
已对选定的光合蓝细菌模型菌株进行基因工程改造,以实现多种酶的异源表达。在本研究中,我们首先探索了参与反式白藜芦醇生产的酶,即酪氨酸解氨酶、香豆酰辅酶A连接酶和芪合酶在单细胞蓝细菌聚球藻PCC 6803中的异源表达。在启动子Ptrc1Ocore和Ptrc1O的控制下,相应的基因被转录并翻译成浓度为16 - 34 μg L(-1)的相应可溶性蛋白质。这些酶的表达水平并未影响蓝细菌细胞的生长速率。有趣的是,香豆酰辅酶A连接酶的表达略微增加了细胞的叶绿素a含量。总体而言,我们的结果表明,反式白藜芦醇生产的完整途径可以在聚球藻PCC 6803中构建。