Prolonged stationary-phase incubation selects for lrp mutations in Escherichia coli K-12

被引:89
作者
Zinser, ER [1 ]
Kolter, R [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Microbiol & Mol Genet, Boston, MA 02115 USA
关键词
D O I
10.1128/JB.182.15.4361-4365.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Evolution by natural selection occurs in cultures of Escherichia coli maintained under carbon starvation stress. Mutants of increased fitness express a growth advantage in stationary phase (GASP) phenotype, enabling them to grow and displace the parent as the majority population. The first GASP mutation was identified as a loss-of-function allele of rpoS, encoding the stationary-phase global regulator, sigma(S) (M. M. Zambrano, D. A. Siegele, M. A. Almiron, A. Tormo, and R. Kelter, Science 259:1757-1760, 1993). We now report that a second global regulator, Lrp, can also play a role in stationary-phase competition. We found that a mutant that took over an aged culture of an rpoS strain had acquired a GASP mutation in lrp. This GASP allele, lrp-1141, encodes a mutant protein lacking the critical glycine in the turn of the helix-turn-helix DNA-binding domain. The lrp-1141 allele behaves as a null mutation when in single copy and is dominant negative when overexpressed. Hence, the mutant protein appears to retain stability and the ability to dimerize but lacks DNA-binding activity. We also demonstrated that a Ipp null allele generated by a transposon insertion has a fitness gain identical to that of the lrp-1141 allele, verifying that cells lacking Lrp activity have a competitive advantage during prolonged starvation. Finally, we tested by genetic analysis the hypothesis that the lrp-1141 GASP mutation confers a fitness gain by enhancing amino acid catabolism during carbon starvation. We found that while amino acid catabolism may play a role, it is not necessary for the lrp GASP phenotype, and hence the lrp GASP phenotype is due to more global physiological changes.
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页码:4361 / 4365
页数:5
相关论文
共 44 条
[1]   ANALYSIS OF CELL-SIZE AND DNA CONTENT IN EXPONENTIALLY GROWING AND STATIONARY-PHASE BATCH CULTURES OF ESCHERICHIA-COLI [J].
AKERLUND, T ;
NORDSTROM, K ;
BERNANDER, R .
JOURNAL OF BACTERIOLOGY, 1995, 177 (23) :6791-6797
[2]   ALTERED AMINO-ACID-METABOLISM IN LRP MUTANTS OF ESCHERICHIA-COLI K12 AND THEIR DERIVATIVES [J].
AMBARTSOUMIAN, G ;
DARI, R ;
LIN, RT ;
NEWMAN, EB .
MICROBIOLOGY-UK, 1994, 140 :1737-1744
[3]   Characterization of an lrp-like (lrpC) gene from Bacillus subtilis [J].
Beloin, C ;
Ayora, S ;
Exley, R ;
Hirschbein, L ;
Ogasawara, N ;
Kasahara, Y ;
Alonso, JC ;
LeHegarat, F .
MOLECULAR & GENERAL GENETICS, 1997, 256 (01) :63-71
[4]  
BRENNAN RG, 1989, J BIOL CHEM, V264, P1903
[5]  
CAETANOANOLLES G, 1993, PCR METH APPL, V3, P85
[6]   THE LEUCINE-RESPONSIVE REGULATORY PROTEIN, A GLOBAL REGULATOR OF METABOLISM IN ESCHERICHIA-COLI [J].
CALVO, JM ;
MATTHEWS, RG .
MICROBIOLOGICAL REVIEWS, 1994, 58 (03) :466-490
[7]   Cloning and identification of the Sulfolobus solfataricus lrp gene encoding an archaeal homologue of the eubacterial leucine-responsive global transcriptional regulator Lrp [J].
Charlier, D ;
Roovers, M ;
Thia-Toong, TL ;
Durbecq, V ;
Glansdorff, N .
GENE, 1997, 201 (1-2) :63-68
[8]   AN ESCHERICHIA-COLI PROMOTER INDUCED BY THE CESSATION OF GROWTH [J].
CONNELL, N ;
HAN, Z ;
MORENO, F ;
KOLTER, R .
MOLECULAR MICROBIOLOGY, 1987, 1 (02) :195-201
[9]   The leucine-responsive regulatory protein (Lrp) from Escherichia coli - Stoichiometry and minimal requirements for binding to DNA [J].
Cui, YH ;
Midkiff, MA ;
Wang, Q ;
Calvo, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (12) :6611-6617
[10]   REGULATION OF THE GLTBDF OPERON OF ESCHERICHIA-COLI - HOW IS A LEUCINE-INSENSITIVE OPERON REGULATED BY THE LEUCINE-RESPONSIVE REGULATORY PROTEIN [J].
ERNSTING, BR ;
DENNINGER, JW ;
BLUMENTHAL, RM ;
MATTHEWS, RG .
JOURNAL OF BACTERIOLOGY, 1993, 175 (22) :7160-7169