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I 型 II 基于限制的组合调制技术用于代谢途径优化。

Type IIs restriction based combinatory modulation technique for metabolic pathway optimization.

机构信息

Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, People's Republic of China.

Key Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin, 300308, People's Republic of China.

出版信息

Microb Cell Fact. 2017 Mar 16;16(1):47. doi: 10.1186/s12934-017-0659-z.

Abstract

BACKGROUND

One of the most important research subjects of metabolic engineering is pursuing a balanced metabolic pathway, which is the basis of an efficient cell factory. In this work, we dedicated to develop a simple and efficient technique to modulate expression of multiple genes simultaneously, and select for the optimal regulation pattern.

RESULTS

A Type IIs restriction based combinatory modulation (TRCM) technique was designed and established in the research. With this technique, a plasmid library containing variably regulated mvaE, mvaS, mvaK , mvaD and mvaK of the mevalonate (MVA) pathway were obtained and transformed into E. coli DXS37-IDI46 to obtain a β-carotene producer library. The ratio of successfully assembled plasmids was determined to be 35%, which was increased to 100% when color based pre-screening was applied. Representative strains were sequenced to contain diverse RBSs as designed to regulate expression of MVA pathway genes. A relatively balanced MVA pathway was achieved in E. coli cell factory to increase the β-carotene yield by two fold. Furthermore, the approximate regulation pattern of this optimal MVA pathway was illustrated.

CONCLUSIONS

A TRCM technique for metabolic pathway optimization was designed and established in this research, which can be applied to various applications in terms of metabolic pathway regulation and optimization.

摘要

背景

代谢工程的重要研究课题之一是追求平衡的代谢途径,这是高效细胞工厂的基础。在这项工作中,我们致力于开发一种简单有效的同时调节多个基因表达的技术,并选择最佳的调节模式。

结果

设计并建立了一种基于 I 型限制性内切酶的组合调节(TRCM)技术。利用该技术,构建了一个包含可变调节 mvaE、mvaS、mvaK、mvaD 和 mvaK 的丙二酰辅酶 A(MVA)途径的质粒文库,并将其转化到 E. coli DXS37-IDl46 中,获得了β-胡萝卜素生产库。成功组装质粒的比例确定为 35%,当应用颜色初筛时,该比例增加到 100%。对代表性菌株进行测序,发现它们含有多种设计用于调节 MVA 途径基因表达的 RBS。在大肠杆菌细胞工厂中实现了相对平衡的 MVA 途径,使 β-胡萝卜素的产量增加了两倍。此外,还说明了这种最佳 MVA 途径的近似调节模式。

结论

本研究设计并建立了一种用于代谢途径优化的 TRCM 技术,可应用于代谢途径调节和优化的各种应用。

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