Biosynthesis of brazzein using the bacterial cell-free protein synthesis system

I. Kazlouski, I. Belskaya, А. Zinchenko
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Abstract

Feasibility of producing brazzein plant sweetener by the cell-free biosynthesis procedure as an alternative to the classical submerged fermentation method was assessed in the present investigation. Chimeric RNA polymerase of T7 bacteriophage, S30-cell extract of Escherichia coli and multicopy plasmid vector pET42mut with the inserted brazzein gene were included into the protein synthesis. The completed research resulted in the first successful demonstration of the sweet protein biosynthesis in the cell-free system. The volumetric brazzein yield under optimized process conditions was 2 mg/ml of the reaction mixture, exceeding 57 times the maximum values that had been achieved in the previous studies applying whole-cell expression systems.
利用细菌无细胞蛋白合成系统合成铜黄蛋白
本研究评估了无细胞生物合成工艺替代传统的深层发酵法生产brazinin植物甜味剂的可行性。利用T7噬菌体的嵌合RNA聚合酶、大肠杆菌s30细胞提取物和插入brazzein基因的多拷贝质粒载体pET42mut进行蛋白合成。该研究首次成功地证明了甜蛋白在无细胞系统中的生物合成。在优化的工艺条件下,反应混合物的体积产率为2 mg/ml,超过了先前应用全细胞表达系统所取得的最大值的57倍。
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