Literature DB >> 14608419

Fitness cost of the green fluorescent protein in gastrointestinal bacteria.

Camilla Rang1, James E Galen, James B Kaper, Lin Chao.   

Abstract

There are surprisingly few studies that have successfully used the green fluorescent protein (GFP) as a quantitative reporter in selection experiments screening for inducible bacterial promoters. One explanation is that GFP expression may confer a fitness cost for bacteria. To test this possibility, we monitored the doubling time in enteric bacteria expressing GFP. Four bacterial species, Escherichia coli, enterohaemorrhagic E. coli, Shigella flexneri, Salmonella typhi, and Vibrio cholerae, were examined. The level of GFP expression was varied by using a salt-inducible promoter. After accounting for the increase in doubling time resulting from elevated osmolarity, the doubling time of all bacteria was found to increase proportionally with GFP expression, and some strains were more affected than others. Cultures of the bacteria most affected by GFP exhibited a proportion of elongated cells, which suggests that GFP production could interfere with cell division in these strains. The results in this study show that GFP is costly to bacteria and suggest that overly active promoters should be difficult to obtain from a genomic promoter library. They also suggest that the chances of succeeding in using GFP as a reporter in selection experiments are increased by growing the bacteria for the fewest number of generations and by subduing the expression of GFP whenever possible, such as by using a low copy vector to clone the library.

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Year:  2003        PMID: 14608419     DOI: 10.1139/w03-072

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  20 in total

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5.  Green fluorescent protein is superior to blue fluorescent protein as a quantitative reporter of promoter activity in E. coli.

Authors:  James L Lissemore; Joshua Bayes; Molly Calvey; Lucas Reineke; Anne Colagiavanni; Melissa Tscheiner; David P Mascotti
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6.  Gene Architectures that Minimize Cost of Gene Expression.

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7.  Reporter enzyme fluorescence (REF) imaging and quantification of tuberculosis in live animals.

Authors:  Ying Kong; Jeffrey D Cirillo
Journal:  Virulence       Date:  2010-11-01       Impact factor: 5.882

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Review 9.  Neurotransmitters: The Critical Modulators Regulating Gut-Brain Axis.

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Journal:  J Cell Physiol       Date:  2017-04-10       Impact factor: 6.384

10.  Allocation of gene products to daughter cells is determined by the age of the mother in single Escherichia coli cells.

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Journal:  Proc Biol Sci       Date:  2020-05-06       Impact factor: 5.349

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