Suppr超能文献

一种具有超过10000倍动态范围的工程诱导型启动子系统。

An Engineered Inducible Promoter System with over 10 000-Fold Dynamic Range.

作者信息

Castillo-Hair Sebastian M, Fujita Masaya, Igoshin Oleg A, Tabor Jeffrey J

机构信息

Department of Bioengineering , Rice University , 6100 Main Street , Houston , Texas 77005 , United States.

Department of Biology and Biochemistry , University of Houston , 4800 Calhoun Road , Houston , Texas 77004 , United States.

出版信息

ACS Synth Biol. 2019 Jul 19;8(7):1673-1678. doi: 10.1021/acssynbio.8b00469. Epub 2019 Jun 28.

Abstract

is the leading model Gram-positive bacterium, and a widely used chassis for industrial protein production. However, research is limited by a lack of inducible promoter systems with low leakiness and high dynamic range. Here, we engineer an inducible promoter system based on the T7 RNA Polymerase (T7 RNAP), the lactose repressor LacI, and the chimeric promoter P, integrated as a single copy in the genome. In the absence of IPTG, LacI strongly represses T7 RNAP and P and minimizes leakiness. Addition of IPTG derepresses P and simultaneously induces expression of T7RNAP, which results in very high output expression. Using green fluorescent and β-galactosidase reporter proteins, we estimate that this LacI-T7 system can regulate expression with a dynamic range of over 10 000, by far the largest reported for an inducible promoter system. Furthermore, LacI-T7 responds to similar IPTG concentrations and with similar kinetics as the widely used P IPTG-inducible system, which we show has a dynamic range of at most 300 in a similar genetic context. Due to its superior performance, our LacI-T7 system should have broad applications in fundamental biology studies and biotechnology.

摘要

是革兰氏阳性菌的主要模型,也是工业蛋白质生产中广泛使用的底盘。然而,研究受到缺乏低渗漏率和高动态范围的诱导型启动子系统的限制。在这里,我们构建了一种基于T7 RNA聚合酶(T7 RNAP)、乳糖阻遏物LacI和嵌合启动子P的诱导型启动子系统,该系统作为单拷贝整合到基因组中。在没有异丙基-β-D-硫代半乳糖苷(IPTG)的情况下,LacI强烈抑制T7 RNAP和P,并将渗漏率降至最低。添加IPTG可解除对P的抑制,并同时诱导T7RNAP的表达,从而导致非常高的输出表达。使用绿色荧光蛋白和β-半乳糖苷酶报告蛋白,我们估计这个LacI-T7系统可以在超过10000的动态范围内调节表达,这是迄今为止报道的诱导型启动子系统中最大的动态范围。此外,LacI-T7对IPTG浓度的响应和动力学与广泛使用的P IPTG诱导系统相似,我们发现在相似的遗传背景下,该系统的动态范围最多为300。由于其卓越的性能,我们的LacI-T7系统应该在基础生物学研究和生物技术中有广泛的应用。

相似文献

1
An Engineered Inducible Promoter System with over 10 000-Fold Dynamic Range.
ACS Synth Biol. 2019 Jul 19;8(7):1673-1678. doi: 10.1021/acssynbio.8b00469. Epub 2019 Jun 28.
2
Development of inducer-free expression plasmids based on IPTG-inducible promoters for Bacillus subtilis.
Microb Cell Fact. 2017 Jul 25;16(1):130. doi: 10.1186/s12934-017-0747-0.
3
A T7 promoter-specific, inducible protein expression system for Bacillus subtilis.
Mol Gen Genet. 1996 Feb 5;250(2):230-6. doi: 10.1007/BF02174183.
4
Efficient Protein Expression and Biosynthetic Gene Cluster Regulation in Driven by a T7-BOOST System.
ACS Synth Biol. 2023 Nov 17;12(11):3328-3339. doi: 10.1021/acssynbio.3c00331. Epub 2023 Oct 26.
5
Protein expression systems combining a flavonoid-inducible promoter and T7 RNA polymerase in Bacillus subtilis.
Biosci Biotechnol Biochem. 2023 Aug 23;87(9):1017-1028. doi: 10.1093/bbb/zbad072.
8
T7 RNA polymerase-driven inducible cell lysis for DNA transfer from Escherichia coli to Bacillus subtilis.
Microb Biotechnol. 2017 Nov;10(6):1797-1808. doi: 10.1111/1751-7915.12843. Epub 2017 Aug 16.
10
Building an Inducible T7 RNA Polymerase/T7 Promoter Circuit in Synechocystis sp. PCC6803.
ACS Synth Biol. 2019 Apr 19;8(4):655-660. doi: 10.1021/acssynbio.8b00515. Epub 2019 Apr 3.

引用本文的文献

1
Engineering plant holobionts for climate-resilient agriculture.
ISME J. 2025 Jan 2;19(1). doi: 10.1093/ismejo/wraf158.
2
Innovations, Challenges and Future Directions of T7RNA Polymerase in Microbial Cell Factories.
ACS Synth Biol. 2025 May 16;14(5):1381-1396. doi: 10.1021/acssynbio.5c00139. Epub 2025 Apr 10.
3
A facile and robust T7-promoter-based high-expression of heterologous proteins in Bacillus subtilis.
Bioresour Bioprocess. 2022 May 18;9(1):56. doi: 10.1186/s40643-022-00540-4.
5
Synthetic Homoserine Lactone Sensors for Gram-Positive Using LuxR-Type Regulators.
ACS Synth Biol. 2024 Jan 19;13(1):282-299. doi: 10.1021/acssynbio.3c00504. Epub 2023 Dec 11.
6
Potent IPTG-inducible integrative expression vectors for production of recombinant proteins in Bacillus subtilis.
World J Microbiol Biotechnol. 2023 Apr 1;39(6):143. doi: 10.1007/s11274-023-03566-8.
8
Integrative expression vectors with P promoters for inducer-free overproduction of recombinant proteins in .
Biotechnol Rep (Amst). 2020 Oct 9;28:e00540. doi: 10.1016/j.btre.2020.e00540. eCollection 2020 Dec.
9
Positioning Bacillus subtilis as terpenoid cell factory.
J Appl Microbiol. 2021 Jun;130(6):1839-1856. doi: 10.1111/jam.14904. Epub 2020 Nov 20.
10
A regulated synthetic operon facilitates stable overexpression of multigene terpenoid pathway in Bacillus subtilis.
J Ind Microbiol Biotechnol. 2020 Feb;47(2):243-249. doi: 10.1007/s10295-019-02257-4. Epub 2020 Jan 1.

本文引用的文献

1
Phosphatase activity tunes two-component system sensor detection threshold.
Nat Commun. 2018 Apr 12;9(1):1433. doi: 10.1038/s41467-018-03929-y.
3
A part toolbox to tune genetic expression in Bacillus subtilis.
Nucleic Acids Res. 2016 Sep 6;44(15):7495-508. doi: 10.1093/nar/gkw624. Epub 2016 Jul 8.
4
An extraordinary stringent and sensitive light-switchable gene expression system for bacterial cells.
Cell Res. 2016 Jul;26(7):854-7. doi: 10.1038/cr.2016.74. Epub 2016 Jun 17.
5
6
Ion channels enable electrical communication in bacterial communities.
Nature. 2015 Nov 5;527(7576):59-63. doi: 10.1038/nature15709. Epub 2015 Oct 21.
7
Chromosomal Arrangement of Phosphorelay Genes Couples Sporulation and DNA Replication.
Cell. 2015 Jul 16;162(2):328-337. doi: 10.1016/j.cell.2015.06.012. Epub 2015 Jul 9.
8
Density of founder cells affects spatial pattern formation and cooperation in Bacillus subtilis biofilms.
ISME J. 2014 Oct;8(10):2069-79. doi: 10.1038/ismej.2014.52. Epub 2014 Apr 3.
10
Bacillus subtilis: from soil bacterium to super-secreting cell factory.
Microb Cell Fact. 2013 Jan 14;12:3. doi: 10.1186/1475-2859-12-3.

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