Instability of the acetamide-inducible expression vector pJAM2 in Mycobacterium tuberculosis
- PMID: 16125237
- DOI: 10.1016/j.plasmid.2005.06.005
Instability of the acetamide-inducible expression vector pJAM2 in Mycobacterium tuberculosis
Abstract
The Escherichia coli-mycobacterium shuttle vector pJAM2 has been used to inducibly express genes in mycobacteria. The vector carries the promoter region from the highly inducible acetamidase gene of Mycobacterium smegmatis which is used to drive expression of heterologous genes. We used pJAM2 to over-express the Mycobacterium tuberculosis gene Rv2868c, a homologue of gcpE. In M. smegmatis the plasmid was stable, but the promoter region was readily deleted when the parental vector or recombinant plasmids were transformed into M. tuberculosis. We mapped the deletion by sequencing and found that it encompassed the entire acetamidase promoter and adjacent sequence totalling approximately 7.3 kb and occurred very soon after introduction into M. tuberculosis. This is the first report of instability of a vector carrying the acetamidase promoter in M. tuberculosis.
Similar articles
-
A versatile vector for mycobacterial protein production with a functional minimized acetamidase regulon.Protein Sci. 2017 Nov;26(11):2302-2311. doi: 10.1002/pro.3288. Epub 2017 Sep 25. Protein Sci. 2017. PMID: 28857325 Free PMC article.
-
Expression systems for study of mycobacterial gene regulation and development of recombinant BCG vaccines.Biochem Biophys Res Commun. 1998 May 29;246(3):797-804. doi: 10.1006/bbrc.1998.8724. Biochem Biophys Res Commun. 1998. PMID: 9618292
-
A new Gateway vector and expression protocol for fast and efficient recombinant protein expression in Mycobacterium smegmatis.Protein Expr Purif. 2008 Jan;57(1):81-7. doi: 10.1016/j.pep.2007.08.015. Epub 2007 Sep 14. Protein Expr Purif. 2008. PMID: 17949993
-
Gene Transfer in Mycobacterium tuberculosis: Shuttle Phasmids to Enlightenment.Microbiol Spectr. 2014 Apr;2(2):10.1128/microbiolspec.MGM2-0037-2013. doi: 10.1128/microbiolspec.MGM2-0037-2013. Microbiol Spectr. 2014. PMID: 26105819 Free PMC article. Review.
-
[Advances in Mycobacterium tuberculosis proteomics].Zhonghua Jie He He Hu Xi Za Zhi. 2009 Jul;32(7):527-9. Zhonghua Jie He He Hu Xi Za Zhi. 2009. PMID: 19954008 Review. Chinese. No abstract available.
Cited by
-
Sensitive detection of gene expression in mycobacteria under replicating and non-replicating conditions using optimized far-red reporters.PLoS One. 2010 Mar 23;5(3):e9823. doi: 10.1371/journal.pone.0009823. PLoS One. 2010. PMID: 20352111 Free PMC article.
-
Construction of an overexpression library for Mycobacterium tuberculosis.Biol Methods Protoc. 2018;3(1):bpy009. doi: 10.1093/biomethods/bpy009. Epub 2018 Aug 20. Biol Methods Protoc. 2018. PMID: 30197930 Free PMC article.
-
The application of tetracyclineregulated gene expression systems in the validation of novel drug targets in Mycobacterium tuberculosis.Front Microbiol. 2015 Aug 4;6:812. doi: 10.3389/fmicb.2015.00812. eCollection 2015. Front Microbiol. 2015. PMID: 26300875 Free PMC article. Review.
-
Molecular characterization of AmiC, a positive regulator in acetamidase operon of Mycobacterium smegmatis.Cell Stress Chaperones. 2018 Jul;23(4):539-550. doi: 10.1007/s12192-017-0861-2. Epub 2017 Dec 22. Cell Stress Chaperones. 2018. PMID: 29273966 Free PMC article.
-
Emerging applications of riboswitches - from antibacterial targets to molecular tools.J Appl Genet. 2016 Nov;57(4):531-541. doi: 10.1007/s13353-016-0341-x. Epub 2016 Mar 28. J Appl Genet. 2016. PMID: 27020791 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources