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Development of a Novel Biosensor-Driven Mutation and Selection System via in situ Growth of Corynebacterium crenatum for the Production of L-Arginine

机译:通过原位生长的新型生物传感器驱动突变和选择系统的开发,用于生产L-精氨酸的床杆菌

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The high yield mutants require a high-throughput screening method to obtain them quickly. Here, we developed an L-arginine biosensor (ARG-Select) to obtain increased L-arginine producers among a large number of mutant strains. This biosensor was constructed by ArgR protein and argC promoter, and could provide the strain with the output of bacterial growth via the reporter gene sacB; strains with high L-arginine production could survive in 10 % sucrose screening. To extend the screening limitation of 10 % sucrose, the sensitivity of ArgR protein to L-arginine was decreased. Corynebacterium crenatum SYPA5-5 and its systems pathway engineered strain Cc6 were chosen as the original strains. This biosensor was employed, and L-arginine hyperproducing mutants were screened. Finally, the HArg1 and DArg36 mutants of C. crenatum SYPA5-5 and Cc6 could produce 56.7 g L-1 and 95.5 g L-1 of L-arginine, respectively, which represent increases of 35.0 % and 13.5 %. These results demonstrate that the transcription factor (TF)-based biosensor could be applied in high yield strains selection as an effective high-throughput screening method.
机译:高产量突变体需要高通量的筛选方法以快速获得它们。在这里,我们开发了L-精氨酸生物传感器(Arg-SELECT),以获得大量突变菌株中的增加的L-精氨酸生产商。该生物传感器由ARGR蛋白和ARGC启动子构建,并且可以通过报告基因Sacb提供细菌生长的产量的菌株;具有高L-精氨酸产量的菌株可以在10%蔗糖筛查中存活。为了延长10%蔗糖的筛选限制,降低了ARGR蛋白对L-精氨酸的敏感性。选择CoryneBacterium Crenatum Sypa5-5及其系统途径工程菌株CC6作为原始菌株。使用这种生物传感器,筛选L-精氨酸超级突变体。最后,C. crenatum Sypa5-5和CC6的Harg1和Darg36突变体分别可以分别产生56.7g L-1和95.5g L-1的L-精氨酸,其增加的增加35.0%和13.5%。这些结果表明,基于转录因子(TF)的生物传感器可以在高产菌株选择中应用作为一种有效的高通量筛选方法。

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