The dynamic microbe: green fluorescent protein brings bacteria to light
- PMID: 12207688
- DOI: 10.1046/j.1365-2958.2002.03089.x
The dynamic microbe: green fluorescent protein brings bacteria to light
Abstract
The demonstration that the green fluorescent protein (GFP) from the jellyfish Aequorea victoria required no jellyfish-specific cofactors and could be expressed as a fluorescent protein in heterologous hosts including both prokaryotes and eukaryotes sparked the development of GFP as one of the most common reporters in use today. Over the past several years, the utility of GFP as a reporter has been optimized through the isolation and engineering of variants with increased folding rates, different in vivo stabilities and colour variants with altered excitation and emission spectral properties. One of the great utilities of GFP is as a probe for characterizing spatial and temporal dynamics of gene expression, protein localization and protein-protein interactions in living cells. The innovative application of GFP as a reporter in bacteria has made a significant contribution to microbial cell biology. This review will highlight recent studies that demonstrate the potential of GFP for real-time analysis of gene expression, protein localization and the dynamics of signalling transduction pathways through protein-protein interactions.
Similar articles
-
The molecular determinants of the efficiency of green fluorescent protein mutants.Histol Histopathol. 2000 Jan;15(1):101-7. doi: 10.14670/HH-15.101. Histol Histopathol. 2000. PMID: 10668201 Review.
-
New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria.Appl Environ Microbiol. 1998 Jun;64(6):2240-6. doi: 10.1128/AEM.64.6.2240-2246.1998. Appl Environ Microbiol. 1998. PMID: 9603842 Free PMC article.
-
Mutations that suppress the thermosensitivity of green fluorescent protein.Curr Biol. 1996 Dec 1;6(12):1653-63. doi: 10.1016/s0960-9822(02)70789-6. Curr Biol. 1996. PMID: 8994830
-
Green fluorescent protein--a bright idea for the study of bacterial protein localization.FEMS Microbiol Lett. 2001 Oct 16;204(1):9-18. doi: 10.1111/j.1574-6968.2001.tb10854.x. FEMS Microbiol Lett. 2001. PMID: 11682170 Review.
-
Green fluorescent protein.Photochem Photobiol. 1995 Oct;62(4):651-6. doi: 10.1111/j.1751-1097.1995.tb08712.x. Photochem Photobiol. 1995. PMID: 7480149 Review.
Cited by
-
Vectors for ligation-independent construction of lacZ gene fusions and cloning of PCR products using a nicking endonuclease.Plasmid. 2011 Sep;66(3):180-5. doi: 10.1016/j.plasmid.2011.07.007. Epub 2011 Aug 10. Plasmid. 2011. PMID: 21854804 Free PMC article.
-
Characterization of Bacillus subtilis Colony Biofilms via Mass Spectrometry and Fluorescence Imaging.J Proteome Res. 2016 Jun 3;15(6):1955-62. doi: 10.1021/acs.jproteome.6b00127. Epub 2016 May 11. J Proteome Res. 2016. PMID: 27136705 Free PMC article.
-
Development and optimization of an EGFP-based reporter for measuring the general stress response in Listeria monocytogenes.Bioeng Bugs. 2012 Mar-Apr;3(2):93-103. doi: 10.4161/bbug.19476. Epub 2012 Mar 1. Bioeng Bugs. 2012. PMID: 22539028 Free PMC article.
-
Use of fluorescent-protein tagging to determine the subcellular localization of mycoplasma pneumoniae proteins encoded by the cytadherence regulatory locus.J Bacteriol. 2004 Oct;186(20):6944-55. doi: 10.1128/JB.186.20.6944-6955.2004. J Bacteriol. 2004. PMID: 15466048 Free PMC article.
-
Stable Expression of Modified Green Fluorescent Protein in Group B Streptococci To Enable Visualization in Experimental Systems.Appl Environ Microbiol. 2018 Aug 31;84(18):e01262-18. doi: 10.1128/AEM.01262-18. Print 2018 Sep 15. Appl Environ Microbiol. 2018. PMID: 30006391 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous