» Articles » PMID: 26673679

Identification of a Highly Efficient Stationary Phase Promoter in Bacillus Subtilis

Overview
Journal Sci Rep
Specialty Science
Date 2015 Dec 18
PMID 26673679
Citations 25
Authors
Affiliations
Soon will be listed here.
Abstract

A promoter that enabled high-level expression of the target gene during the stationary phase in the absence of an inducer would facilitate the efficient production of heterogeneous proteins at a low cost. In this study, a genome-scale microarray-based approach was employed to identify promoters that induced high-level expression of the target genes in Bacillus subtilis from the late log phase to the stationary phase without an inducer. Eleven candidate promoters were selected based on B. subtilis microarray data and the quantitative PCR analysis. Among the selected promoters, Pylb exhibited the highest activity with the reporter bgaB during the stationary phase. Compared with P43 (a commonly used constitutive promoter), promoter Pylb could express two reporter genes (egfp and mApple), and the expression levels of EGFP and RFP were 7.8- and 11.3-fold higher than that of P43, respectively. This finding was verified by overexpression of the genes encoding pullulanase and organophosphorus hydrolase, the activities of which were 7.4- and 2.3-fold higher, respectively, when driven by Pylb compared with P43. Therefore, our results suggest that the Pylb promoter could be used to overexpress target genes without an inducer; this method could facilitate the identification and evaluation of attractive promoters in the genome.

Citing Articles

Enhancing High-Level Food-Grade Expression of Glutamate Decarboxylase and Its Application in the Production of γ-Aminobutyric Acid.

Zhang K, Lv H, Yu X, Zhu X, Chen S, Wu J J Microbiol Biotechnol. 2025; 35:e2410013.

PMID: 39849933 PMC: 11813360. DOI: 10.4014/jmb.2410.10013.


Delaying production with prokaryotic inducible expression systems.

De Baets J, De Paepe B, De Mey M Microb Cell Fact. 2024; 23(1):249.

PMID: 39272067 PMC: 11401332. DOI: 10.1186/s12934-024-02523-w.


The Construction of an Environmentally Friendly Super-Secreting Strain of through Systematic Modulation of Its Secretory Pathway Using the CRISPR-Cas9 System.

Ferrando J, Minana-Galbis D, Picart P Int J Mol Sci. 2024; 25(13).

PMID: 39000067 PMC: 11240994. DOI: 10.3390/ijms25136957.


Engineering a carbon source-responsive promoter for improved biosynthesis in the non-conventional yeast .

Bassett S, Da Silva N Metab Eng Commun. 2024; 18:e00238.

PMID: 38845682 PMC: 11153928. DOI: 10.1016/j.mec.2024.e00238.


Implementation of Fluorescent-Protein-Based Quantification Analysis in L-Form Bacteria.

Tian D, Liu Y, Zhang Y, Liu Y, Xia Y, Xu B Bioengineering (Basel). 2024; 11(1).

PMID: 38247958 PMC: 10813599. DOI: 10.3390/bioengineering11010081.


References
1.
Ming Y, Wei Z, Lin C, Sheng G . Development of a Bacillus subtilis expression system using the improved Pglv promoter. Microb Cell Fact. 2010; 9:55. PMC: 2908567. DOI: 10.1186/1475-2859-9-55. View

2.
Nicolas P, Mader U, Dervyn E, Rochat T, Leduc A, Pigeonneau N . Condition-dependent transcriptome reveals high-level regulatory architecture in Bacillus subtilis. Science. 2012; 335(6072):1103-6. DOI: 10.1126/science.1206848. View

3.
Nijland R, Lindner C, van Hartskamp M, Hamoen L, Kuipers O . Heterologous production and secretion of Clostridium perfringens beta-toxoid in closely related Gram-positive hosts. J Biotechnol. 2006; 127(3):361-72. DOI: 10.1016/j.jbiotec.2006.07.014. View

4.
Harwood C, Wipat A . Sequencing and functional analysis of the genome of Bacillus subtilis strain 168. FEBS Lett. 1996; 389(1):84-7. DOI: 10.1016/0014-5793(96)00524-8. View

5.
Lee S, Pan J, Park S, Choi S . Development of a stationary phase-specific autoinducible expression system in Bacillus subtilis. J Biotechnol. 2010; 149(1-2):16-20. DOI: 10.1016/j.jbiotec.2010.06.021. View