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本文引用的文献

1
Novel twin-arginine translocation pathway-dependent phenotypes of Bacillus subtilis unveiled by quantitative proteomics.定量蛋白质组学揭示枯草芽孢杆菌新型双精氨酸转运途径相关表型。
J Proteome Res. 2013 Feb 1;12(2):796-807. doi: 10.1021/pr300866f. Epub 2013 Jan 11.
2
Transmembrane insertion of twin-arginine signal peptides is driven by TatC and regulated by TatB.双精氨酸信号肽的跨膜插入由 TatC 驱动,并受 TatB 调节。
Nat Commun. 2012;3:1311. doi: 10.1038/ncomms2308.
3
Structure of the TatC core of the twin-arginine protein transport system.双精氨酸蛋白转运系统 TatC 核心结构。
Nature. 2012 Dec 13;492(7428):210-4. doi: 10.1038/nature11683. Epub 2012 Dec 2.
4
Mapping the twin-arginine protein translocation network of Bacillus subtilis.绘制枯草芽孢杆菌双精氨酸蛋白易位网络。
Proteomics. 2013 Mar;13(5):800-11. doi: 10.1002/pmic.201200416. Epub 2013 Jan 21.
5
The LIKE system, a novel protein expression toolbox for Bacillus subtilis based on the liaI promoter.基于 liaI 启动子的枯草芽孢杆菌新型蛋白表达工具盒 LIKE 系统。
Microb Cell Fact. 2012 Oct 30;11:143. doi: 10.1186/1475-2859-11-143.
6
Building the repertoire of dispensable chromosome regions in Bacillus subtilis entails major refinement of cognate large-scale metabolic model.构建枯草芽孢杆菌非必需染色体区域的文库需要对同源的大规模代谢模型进行重大改进。
Nucleic Acids Res. 2013 Jan 7;41(1):687-99. doi: 10.1093/nar/gks963. Epub 2012 Oct 29.
7
High-salinity growth conditions promote Tat-independent secretion of Tat substrates in Bacillus subtilis.高盐生长条件促进枯草芽孢杆菌中 Tat 非依赖性 Tat 底物的分泌。
Appl Environ Microbiol. 2012 Nov;78(21):7733-44. doi: 10.1128/AEM.02093-12. Epub 2012 Aug 24.
8
Degradation of the twin-arginine translocation substrate YwbN by extracytoplasmic proteases of Bacillus subtilis.枯草芽孢杆菌胞外蛋白酶对双精氨酸转运蛋白 YwbN 的降解作用。
Appl Environ Microbiol. 2012 Nov;78(21):7801-4. doi: 10.1128/AEM.02023-12. Epub 2012 Aug 24.
9
Rational improvement of the engineered isobutanol-producing Bacillus subtilis by elementary mode analysis.通过基本模式分析对工程化的丁醇生产枯草芽孢杆菌进行合理改进。
Microb Cell Fact. 2012 Aug 3;11:101. doi: 10.1186/1475-2859-11-101.
10
Characterization and optimization of Bacillus subtilis ATCC 6051 as an expression host.枯草芽孢杆菌 ATCC 6051 的特性分析及其作为表达宿主的优化。
J Biotechnol. 2013 Jan 20;163(2):97-104. doi: 10.1016/j.jbiotec.2012.06.034. Epub 2012 Jul 10.

枯草芽孢杆菌:从土壤细菌到超级分泌细胞工厂。

Bacillus subtilis: from soil bacterium to super-secreting cell factory.

机构信息

Department of Medical Microbiology, University of Groningen, University Medical Center Groningen, Hanzeplein 1, P,O, box 30001, Groningen, 9700 RB, the Netherlands.

出版信息

Microb Cell Fact. 2013 Jan 14;12:3. doi: 10.1186/1475-2859-12-3.

DOI:10.1186/1475-2859-12-3
PMID:23311580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3564730/
Abstract

The biotechnology industry has become a key element in modern societies. Within this industry, the production of recombinant enzymes and biopharmaceutical proteins is of major importance. The global markets for such recombinant proteins are growing rapidly and, accordingly, there is a continuous need for new production platforms that can deliver protein products in greater yields, with higher quality and at lower costs. This calls for the development of next-generation super-secreting cell factories. One of the microbial cell factories that can meet these challenges is the Gram-positive bacterium Bacillus subtilis, an inhabitant of the upper layers of the soil that has the capacity to secrete proteins in the gram per litre range. The engineering of B. subtilis into a next-generation super-secreting cell factory requires combined Systems and Synthetic Biology approaches. In this way, the bacterial protein secretion machinery can be optimized from the single molecule to the network level while, at the same time, taking into account the balanced use of cellular resources. Although highly ambitious, this is an achievable objective due to recent advances in functional genomics and Systems- and Synthetic Biological analyses of B. subtilis cells.

摘要

生物技术产业已成为现代社会的重要组成部分。在这个行业中,重组酶和生物制药蛋白的生产具有重要意义。此类重组蛋白的全球市场正在迅速增长,因此,不断需要新的生产平台,以更高的产量、更高的质量和更低的成本提供蛋白产品。这就需要开发下一代超分泌细胞工厂。能够应对这些挑战的微生物细胞工厂之一是革兰氏阳性细菌枯草芽孢杆菌,它是土壤上层的一种栖息者,能够在每升范围内分泌蛋白。将枯草芽孢杆菌工程化为下一代超分泌细胞工厂需要结合系统和合成生物学方法。通过这种方式,可以从单个分子到网络水平优化细菌蛋白分泌机制,同时考虑到细胞资源的平衡利用。尽管这一目标极具挑战性,但由于近年来在枯草芽孢杆菌细胞的功能基因组学和系统及合成生物学分析方面取得了进展,这一目标是可以实现的。