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通过结合转录调控和密码子使用算法提高大肠杆菌中外源膜蛋白的产量。

Improving heterologous membrane protein production in Escherichia coli by combining transcriptional tuning and codon usage algorithms.

作者信息

Claassens Nico J, Siliakus Melvin F, Spaans Sebastiaan K, Creutzburg Sjoerd C A, Nijsse Bart, Schaap Peter J, Quax Tessa E F, van der Oost John

机构信息

Laboratory of Microbiology, Wageningen University and Research, Wageningen, The Netherlands.

Laboratory of Systems and Synthetic Biology, Wageningen University and Research, Wageningen, The Netherlands.

出版信息

PLoS One. 2017 Sep 13;12(9):e0184355. doi: 10.1371/journal.pone.0184355. eCollection 2017.

Abstract

High-level, recombinant production of membrane-integrated proteins in Escherichia coli is extremely relevant for many purposes, but has also been proven challenging. Here we study a combination of transcriptional fine-tuning in E. coli LEMO21(DE3) with different codon usage algorithms for heterologous production of membrane proteins. The overexpression of 6 different membrane proteins is compared for the wild-type gene codon usage variant, a commercially codon-optimized variant, and a codon-harmonized variant. We show that transcriptional fine-tuning plays a major role in improving the production of all tested proteins. Moreover, different codon usage variants significantly improved production of some of the tested proteins. However, not a single algorithm performed consistently best for the membrane-integrated production of the 6 tested proteins. In conclusion, for improving heterologous membrane protein production in E. coli, the major effect is accomplished by transcriptional tuning. In addition, further improvements may be realized by attempting different codon usage variants, such as codon harmonized variants, which can now be easily generated through our online Codon Harmonizer tool.

摘要

在大肠杆菌中高水平重组生产膜整合蛋白对许多目的而言都极为重要,但也已被证明具有挑战性。在此,我们研究了在大肠杆菌LEMO21(DE3)中进行转录微调与使用不同密码子使用算法相结合,用于异源生产膜蛋白。比较了野生型基因密码子使用变体、商业密码子优化变体和密码子协调变体对6种不同膜蛋白的过表达情况。我们表明,转录微调在提高所有测试蛋白的产量中起主要作用。此外,不同的密码子使用变体显著提高了一些测试蛋白的产量。然而,没有一种算法在6种测试蛋白的膜整合生产中始终表现最佳。总之,为提高大肠杆菌中异源膜蛋白的产量,主要作用是通过转录调控实现的。此外,通过尝试不同的密码子使用变体,如密码子协调变体,可能会实现进一步的改进,现在可以通过我们的在线密码子协调工具轻松生成这些变体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/460a/5597330/b9b49d780800/pone.0184355.g001.jpg

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