Physiological Studies of <i>Escherichia coli</i> Strain MG1655: Growth Defects and Apparent Cross-Regulation of Gene Expression

Eric Soupène(University of California, Berkeley), Wally C. van Heeswijk(University of California, Berkeley), Jacqueline Plumbridge(Centre National de la Recherche Scientifique), Valley Stewart(University of California, Davis), Daniel Bertenthal(University of California, Berkeley), Haidy Lee(University of California, Berkeley), Prasad Gyaneshwar(University of California, Berkeley), Oleg Paliy(University of California, Berkeley), Parinya Charernnoppakul(University of California, Berkeley), Sydney Kustu(University of California, Berkeley)
Journal of Bacteriology
August 29, 2003
Cited by 224Open Access
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Abstract

Escherichia coli strain MG1655 was chosen for sequencing because the few mutations it carries (ilvG rfb-50 rph-1) were considered innocuous. However, it has a number of growth defects. Internal pyrimidine starvation due to polarity of the rph-1 allele on pyrE was problematic in continuous culture. Moreover, the isolate of MG1655 obtained from the E. coli Genetic Stock Center also carries a large deletion around the fnr (fumarate-nitrate respiration) regulatory gene. Although studies on DNA microarrays revealed apparent cross-regulation of gene expression between galactose and lactose metabolism in the Stock Center isolate of MG1655, this was due to the occurrence of mutations that increased lacY expression and suppressed slow growth on galactose. The explanation for apparent cross-regulation between galactose and N-acetylglucosamine metabolism was similar. By contrast, cross-regulation between lactose and maltose metabolism appeared to be due to generation of internal maltosaccharides in lactose-grown cells and may be physiologically significant. Lactose is of restricted distribution: it is normally found together with maltosaccharides, which are starch degradation products, in the mammalian intestine. Strains designated MG1655 and obtained from other sources differed from the Stock Center isolate and each other in several respects. We confirmed that use of other E. coli strains with MG1655-based DNA microarrays works well, and hence these arrays can be used to study any strain of interest. The responses to nitrogen limitation of two urinary tract isolates and an intestinal commensal strain isolated recently from humans were remarkably similar to those of MG1655.


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