4.7 Article

Construction and development of an auto-regulatory gene expression system in Bacillus subtilis

期刊

MICROBIAL CELL FACTORIES
卷 14, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s12934-015-0341-2

关键词

Bacillus subtilis; Protein expression system; Promoter; Quorum sensing; Auto-inducible; Auto-regulatory; Over-production; srf operon

资金

  1. Priority Academic Program Development of Jiangsu Higher Education Institutions
  2. 111 Project [111-2-06]
  3. Jiangsu province Collaborative Innovation Center for Advanced Industrial Fermentation industry development program
  4. National High Technology Research and Development Program of China (863 Program) [2014AA021304]
  5. Fundamental Research Funds for the Central Universities [JUSRP51411B]
  6. National Natural Science Foundation of China [31400058]
  7. Natural Science Foundation of Jiangsu Province [BK20130139]
  8. Public Project for Key Laboratory of Industrial Biotechnology, Ministry of Education [KLIB-KF201306]

向作者/读者索取更多资源

Background: Bacillus subtilis is an all-important Gram-positive bacterium of valuable biotechnological utility that has been widely used to over-produce industrially and pharmaceutically relevant proteins. There are a variety of expression systems in terms of types of transcriptional patterns, among which the auto-inducible and growth-phase-dependent promoters are gaining increasing favor due to their inducer-independent feature, allowing for the potential to industrially scale-up. To expand the applicability of the auto-inducible expression system, a novel auto-regulatory expression system coupled with cell density was constructed and developed in B. subtilis using the quorum-sensing related promoter srfA (P-srfA). Results: The promoter of the srf operon was used to construct an expression plasmid with the green fluorescent protein (GFP) downstream of PsrfA. The expression displayed a cell-density-dependent pattern in that GFP had a fairly low expression level at the early exponential stage and was highly expressed at the late exponential as well as the stationary stages. Moreover, the recombinant system had a similar expression pattern in wild-type B. subtilis 168, WB600, and WB800, as well as in B. subtilis 168 derivative strain 1681, with the complete deletion of PsrfA, indicating the excellent compatibility of this system. Noticeably, the expression strength of PsrfA was enhanced by optimizing the -10 and -35 core sequence by substituting both sequences with consensus sequences. Importantly, the expression pattern was successfully developed in an auto-regulatory cell-density coupling system by the simple addition of glucose in which GFP could not be strongly expressed until glucose was depleted, resulting in a greater amount of the GFP product and increased cell density. The expression system was eventually tested by the successful over-production of aminopeptidase to a desired level. Conclusion: The auto-regulatory cell density coupling system that is mediated by PsrfA is a novel expression system that has an expression pattern that is split between cell-growth and over-expression, leading to an increase in cell density and elevating the overall expression levels of heterologously expressed proteins. The broad applicability of this system and inducer-free expression property in B. subtilis facilitate the industrial scale-up and medical applications for the over-production of a variety of desired proteins.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据