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论文题目: Design of an ectoine-responsive AraC mutant and its application in metabolic engineering of ectoine biosynthesis
作者: Chen Wei#, Zhang Shan#, Jiang Peixia#, Yao Jun, He Yongzhi, Chen Lincai, Gui Xiwu, Dong Zhiyang*, and Tang Shuang-Yan*.
联系作者:
刊物名称: Metab Eng
期: 30
卷:
页: 149-155
年份: 2015
影响因子: 6.714
论文下载: http://www.sciencedirect.com/science/article/pii/S109671761500066X
摘要: Advanced high-throughput screening methods for small molecules may have important applications in the metabolic engineering of the biosynthetic pathways of these molecules. Ectoine is an excellent osmoprotectant that has been widely used in cosmetics. In this study, the Escherichia coli regulatory protein AraC was engineered to recognize ectoine as its non-natural effector and to activate transcription upon ectoine binding. As an endogenous reporter of ectoine, the mutated AraC protein was successfully incorporated into high-throughput screening of ectoine hyper-producing strains. The ectoine biosynthetic cluster from Halomonas elongata was cloned into E. coli. By engineering the rate-limiting enzyme l-2,4-diaminobutyric acid (DABA) aminotransferase (EctB), ectoine production and the specific activity of the EctB mutant were increased. Thus, these results demonstrated the effectiveness of engineering regulatory proteins into sensitive and rapid screening tools for small molecules and highlighted the importance and efficacy of directed evolution strategies applied to the engineering of genetic components for yield improvement in the biosynthesis of small molecules.