Suppr超能文献

一种用于革兰氏阳性菌中高表达基因变异体选择的合成生物学方法。

A synbio approach for selection of highly expressed gene variants in Gram-positive bacteria.

机构信息

Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800, Kgs. Lyngby, Denmark.

Department of Plant and Environmental Science, University of Copenhagen, 1871, Frederiksberg, Denmark.

出版信息

Microb Cell Fact. 2018 Mar 8;17(1):37. doi: 10.1186/s12934-018-0886-y.

Abstract

BACKGROUND

The market for recombinant proteins is on the rise, and Gram-positive strains are widely exploited for this purpose. Bacillus subtilis is a profitable host for protein production thanks to its ability to secrete large amounts of proteins, and Lactococcus lactis is an attractive production organism with a long history in food fermentation.

RESULTS

We have developed a synbio approach for increasing gene expression in two Gram-positive bacteria. First of all, the gene of interest was coupled to an antibiotic resistance gene to create a growth-based selection system. We then randomised the translation initiation region (TIR) preceding the gene of interest and selected clones that produced high protein titres, as judged by their ability to survive on high concentrations of antibiotic. Using this approach, we were able to significantly increase production of two industrially relevant proteins; sialidase in B. subtilis and tyrosine ammonia lyase in L. lactis.

CONCLUSION

Gram-positive bacteria are widely used to produce industrial enzymes. High titres are necessary to make the production economically feasible. The synbio approach presented here is a simple and inexpensive way to increase protein titres, which can be carried out in any laboratory within a few days. It could also be implemented as a tool for applications beyond TIR libraries, such as screening of synthetic, homologous or domain-shuffled genes.

摘要

背景

重组蛋白市场正在兴起,革兰氏阳性菌株被广泛用于此目的。枯草芽孢杆菌因其能够大量分泌蛋白质而成为一种有利的蛋白质生产宿主,而乳酸乳球菌则因其在食品发酵方面的悠久历史而成为一种有吸引力的生产生物。

结果

我们开发了一种合成生物学方法来提高两种革兰氏阳性细菌中的基因表达。首先,将目的基因与抗生素抗性基因连接,以创建基于生长的选择系统。然后,我们随机化了目的基因之前的翻译起始区(TIR),并选择了那些能够在高浓度抗生素下存活的克隆,这些克隆能够产生高蛋白滴度。使用这种方法,我们能够显著提高两种工业相关蛋白的产量;枯草芽孢杆菌中的唾液酸酶和乳酸乳球菌中的酪氨酸氨裂解酶。

结论

革兰氏阳性细菌被广泛用于生产工业酶。要使生产具有经济可行性,就需要高滴度。这里提出的合成生物学方法是一种简单且廉价的提高蛋白滴度的方法,可以在几天内完成。它也可以作为一种工具,用于 TIR 文库以外的应用,如合成、同源或结构域改组基因的筛选。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8dd6/5842541/0c6c73cdd6cc/12934_2018_886_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验