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Potential of Synechocystis PCC 6803 as a novel cyanobacterial chassis for heterologous expression of enzymes in the trans-resveratrol biosynthetic pathway

机译:蓝藻PCC 6803作为新型蓝藻底盘在反白藜芦醇生物合成途径中异源表达酶的潜力

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摘要

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 mu g 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. (C) 2016 Elsevier Inc. All rights reserved.
机译:已经对光养性蓝细菌的选定模型菌株进行了基因工程改造,以用于多种酶的异源表达。在本研究中,我们最初探讨了单细胞蓝藻Synechocystis PCC 6803中反式白藜芦醇生产中涉及的酶的异源表达,即酪氨酸氨解酶,香豆酰CoA连接酶和二苯乙烯合酶的生产。 Ptrc1Ocore和Ptrc10分别被转录并以16-34μgL-1的浓度翻译成相应的可溶性蛋白。这些酶的表达水平不影响蓝细菌细胞的生长速率。有趣的是,香豆酰基辅酶A连接酶的表达略微增加了细胞中叶绿素a的含量。总体而言,我们的结果表明,可以在Synechocystis PCC 6803中设计反式白藜芦醇生产的完整途径。(C)2016 Elsevier Inc.保留所有权利。

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