Phenomenon of Transient Repression in Escherichia coli

Journal of Bacteriology
1966.0

Abstract

<jats:p> <jats:sc>Paigen, Kenneth</jats:sc> (Roswell Park Memorial Institute, Buffalo, N.Y.). Phenomenon of transient repression in <jats:italic>Escherichia coli</jats:italic> . J. Bacteriol. <jats:bold>91:</jats:bold> 1201–1209. 1966.—A family of mutants has been obtained in <jats:italic>Escherichia coli</jats:italic> K-12 in which β-galactosidase is not inducible for approximately one cell generation after the cells are transferred to glucose from other carbon sources. After that period; the enzyme can be induced at the level appropriate to glucose-grown cultures of the parent cells. Among a wide variety of carbon sources, the only one capable of eliciting a state of transient repression is glucose. Conversely, transient repression occurs when cells are transferred to glucose from any of a variety of other carbon sources. The only exceptions to this so far discovered are lactose, gluconate, and xylose. Susceptibility to transient repression in mutants can also be induced in glucose-grown cells by a period of starvation. Mutant cells which have become susceptible to transient repression lose susceptibility in the presence of glucose only when they are under conditions which permit active protein synthesis. The presence of an inducer of β-galactosidase is not required during this time, nor does pre-induction for β-galactosidase diminish the susceptibility of mutants. At least two other catabolite repression-sensitive enzymes (galactokinase and tryptophanase) are also sensitive to transient repression, and the two phenomena are probably related. The absolute specificity of glucose and the pattern of response seen after growth in different carbon sources suggest that the endogenous metabolite which produces these repressions is far more readily derived from glucose in metabolism than it is from any other exogenous carbon source.

Knowledge Graph

Similar Paper

Phenomenon of Transient Repression in <i>Escherichia coli</i>
Journal of Bacteriology 1966.0
Cyclic 3′,5′-Adenosine Monophosphate and <i>N</i> -Acetyl-glucosamine-6-Phosphate as Regulatory Signals in Catabolite Repression of the <i>lac</i> Operon in <i>Escherichia coli</i>
Journal of Bacteriology 1970.0
Catabolite repression in <i>Streptomyces venezuelae</i>. Induction of β-galactosidase, chloramphenicol production, and intracellular cyclic adenosine 3′,5′-monophosphate concentrations
Canadian Journal of Microbiology 1982.0
Multivalent Repression of Aspartic Semialdehyde Dehydrogenase in <i>Escherichia coli</i> K-12
Journal of Bacteriology 1972.0
Control of Uridine Diphosphate-Glucose Dehydrogenase Synthesis and Uridine Diphosphate-Glucuronic Acid Accumulation by a Regulator Gene Mutation in <i>Escherichia coli</i> K-12
Journal of Bacteriology 1970.0
A bactericidal product obtained from a mutant of escherichia coli
Biochemical and Biophysical Research Communications 1970.0
A new carbon catabolite repression mutation of Escherichia coli, mlc∗, and its use for producing isobutanol
Journal of Bioscience and Bioengineering 2012.0
ISOLATION AND PROPERTIES OF A PUTRESCINE-DEGRADING MUTANT OF <i>ESCHERICHIA COLI</i>
Journal of Bacteriology 1963.0
Control of differentiation in streptomycetes: involvement of extrachromosomal deoxyribonucleic acid and glucose repression in aerial mycelia development
Journal of Bacteriology 1976.0
Transcriptional Organization and Regulation of the <scp>l</scp> -Idonic Acid Pathway (GntII System) in <i>Escherichia coli</i>
Journal of Bacteriology 2004.0