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集胞藻PCC 6803中脂肪酸激活酶Slr1609互作蛋白的鉴定
引用本文:徐乐,巫琴,晋虎,陈磊,张卫文. 集胞藻PCC 6803中脂肪酸激活酶Slr1609互作蛋白的鉴定[J]. 生物工程学报, 2015, 31(8): 1194-1202
作者姓名:徐乐  巫琴  晋虎  陈磊  张卫文
作者单位:天津大学化工学院 合成微生物学实验室,天津 300072,天津大学化工学院 合成微生物学实验室,天津 300072,天津大学化工学院 合成微生物学实验室,天津 300072,天津大学化工学院 合成微生物学实验室,天津 300072,天津大学化工学院 合成微生物学实验室,天津 300072
基金项目:国家重点基础研究发展计划 (973计划) (Nos. 2012CB721101, 2011CBA00803) 资助。
摘    要:集胞藻中slr1609是编码脂肪酸激活酶的基因,对与其相关的重要功能伴侣蛋白进行研究,可以完善对脂肪酸合成模块的认识,为进一步通过合成生物学技术改造蓝细菌提供理论支持。本研究在集胞藻PCC 6803中建立了蛋白质复合体分析及鉴定技术:利用氯霉素抗性基因筛选,构建带有3×FLAG标签的Slr1609突变株,通过RT-PCR优化重组蛋白表达条件;同时对突变株进行了Western blotting鉴定,以及利用Native-PAGE验证了蛋白质复合体的存在。最后,LC-MS/MS质谱鉴定获得了Slr1609蛋白复合体中的可能伴侣蛋白。

关 键 词:slr1609,脂肪酸,蛋白质复合体,蓝细菌
收稿时间:2014-10-20

Identification and characterization of partner proteins interacting with fatty acid activation enzyme Slr1609 in Synechocystis sp. PCC 6803
Le Xu,Qin Wu,Hu Jin,Lei Chen and Weiwen Zhang. Identification and characterization of partner proteins interacting with fatty acid activation enzyme Slr1609 in Synechocystis sp. PCC 6803[J]. Chinese journal of biotechnology, 2015, 31(8): 1194-1202
Authors:Le Xu  Qin Wu  Hu Jin  Lei Chen  Weiwen Zhang
Affiliation:Laboratory of Synthetic Microbiology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China,Laboratory of Synthetic Microbiology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China,Laboratory of Synthetic Microbiology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China,Laboratory of Synthetic Microbiology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China and Laboratory of Synthetic Microbiology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, China
Abstract:To understand molecular modules related to polyunsaturated fatty acids (PUFA) synthesis and eventually produce PUFA at high efficiency, we developed a protein complex analysis technology in Synechocystis sp. PCC 6803, and applied it to identify possible partner proteins interacting with the key enzymes that catalyze PUFA biosynthesis. We first constructed a recombinant expression of protein of slr1609 encoding the fatty acid activation enzyme, by fusing 3×FLAG tag with the target protein. Then we verified its expression by Western blotting targeting 3×FLAG tag. To maximize purification of Slr1609 protein complex, we optimized the protein expression conditions of Slr1609 in Synechocystis in a 5 L fermenter by monitoring its gene expression using RT-qPCR. The purification of the Slr1609 protein complexes was demonstrated by a Native-PAGE analysis. Finally, LC-MS/MS proteomic analysis allowed identification of the possible partner proteins interacting with Slr1609.
Keywords:slr1609   fatty acid   protein complex   cyanobacterium
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