Fitness cost of the green fluorescent protein in gastrointestinal bacteria

被引:51
作者
Rang, C [1 ]
Galen, JE
Kaper, JB
Chao, L
机构
[1] Univ Calif San Diego, Div Biol, La Jolla, CA 92093 USA
[2] Univ Maryland, Ctr Vaccine Dev, Baltimore, MD 21201 USA
关键词
green fluorescent protein; protein cost; promoter activity;
D O I
10.1139/w03-072
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:531 / 537
页数:7
相关论文
共 45 条
[1]  
BENDER RA, 1996, CELLULAR MOL BIOL, V1, P4
[2]   Regulated antigen expression in live recombinant Salmonella enterica serovar typhimurium strongly affects colonization capabilities and specific CD4+-T-cell responses [J].
Bumann, D .
INFECTION AND IMMUNITY, 2001, 69 (12) :7493-7500
[3]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[4]   Bacterial plasmid conjugation on semi-solid surfaces monitored with green fluorescent protein (GFP) from Aequorea victoria as a marker [J].
Christensen, BB ;
Sternberg, C ;
Molin, S .
GENE, 1996, 173 (01) :59-65
[5]   FACS-optimized mutants of the green fluorescent protein (GFP) [J].
Cormack, BP ;
Valdivia, RH ;
Falkow, S .
GENE, 1996, 173 (01) :33-38
[6]   Gene transfer into stimulated and unstimulated T lymphocytes by HIV-1-derived lentiviral vectors [J].
Costello, E ;
Munoz, M ;
Buetti, E ;
Meylan, PRA ;
Diggelmann, H ;
Thali, M .
GENE THERAPY, 2000, 7 (07) :596-604
[7]  
Dahlberg C, 1998, APPL ENVIRON MICROB, V64, P2670
[8]   A vector for promoter trapping in Bacillus cereus [J].
Dunn, AK ;
Handelsman, J .
GENE, 1999, 226 (02) :297-305
[9]   Use of green fluorescent protein as a marker for ecological studies of activated sludge communities [J].
Eberl, L ;
Schulze, R ;
Ammendola, A ;
Geisenberger, O ;
Erhart, R ;
Sternberg, C ;
Molin, S ;
Amann, R .
FEMS MICROBIOLOGY LETTERS, 1997, 149 (01) :77-83
[10]   SecA membrane cycling at SecYEG is driven by distinct ATP binding and hydrolysis events and is regulated by SecD and SecF [J].
Economou, A ;
Pogliano, JA ;
Beckwith, J ;
Oliver, DB ;
Wickner, W .
CELL, 1995, 83 (07) :1171-1181