Literature DB >> 9534243

Stationary phase, amino acid limitation and recovery from stationary phase modulate the stability and translation of chloramphenicol acetyltransferase mRNA and total mRNA in Escherichia coli.

Ann E S Kuzj, Poonam S Medberry, Janet L Schottel.   

Abstract

The functional stability of the chloramphenicol acetyltransferase (cat) mRNA, as well as the functional stability of the total mRNA pool, change during the course of Escherichia coli culture growth. mRNA half-lives are long during lag phase, decrease during the exponential phase and increase again during the stationary phase of the bacterial growth cycle. The half-lives of cat mRNA and total mRNA also increase three- to fourfold during amino acid starvation when compared to exponential culture growth. Even though the stability of the cat message changes about fourfold during culture growth, the amount of cat mRNA per cell mass does not vary significantly between the culture growth phases, indicating that there are compensating changes in cat gene transcription. Translation of cat mRNA also changes during culture growth. In exponential phase, the rate of cat translation is about 14-fold higher than when the culture is in stationary phase. This is in contrast to the fourfold increase in stability of cat mRNA in the stationary-phase culture compared to the exponentially growing culture and indicates that active translation is not correlated with increased mRNA stability. When a stationary-phase culture was diluted into fresh medium, there was a five- to sevenfold increase in CAT synthesis and a threefold increase in total protein synthesis in the presence or absence of rifampicin. These results suggest that while mRNA becomes generally more stable and less translated in the stationary-phase culture, the mRNA is available for immediate translation when nutrients are provided to the culture even when transcription is inhibited.

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Year:  1998        PMID: 9534243     DOI: 10.1099/00221287-144-3-739

Source DB:  PubMed          Journal:  Microbiology (Reading)        ISSN: 1350-0872            Impact factor:   2.777


  7 in total

1.  Massive presence of the Escherichia coli 'major cold-shock protein' CspA under non-stress conditions.

Authors:  A Brandi; R Spurio; C O Gualerzi; C L Pon
Journal:  EMBO J       Date:  1999-03-15       Impact factor: 11.598

2.  The anatomy of microbial cell state transitions in response to oxygen.

Authors:  Amy K Schmid; David J Reiss; Amardeep Kaur; Min Pan; Nichole King; Phu T Van; Laura Hohmann; Daniel B Martin; Nitin S Baliga
Journal:  Genome Res       Date:  2007-09-04       Impact factor: 9.043

3.  Transcription of all amoC copies is associated with recovery of Nitrosomonas europaea from ammonia starvation.

Authors:  Paul M Berube; Ram Samudrala; David A Stahl
Journal:  J Bacteriol       Date:  2007-03-23       Impact factor: 3.490

4.  Complementary roles of initiation factor 1 and ribosome recycling factor in 70S ribosome splitting.

Authors:  Michael Y Pavlov; Ayman Antoun; Martin Lovmar; Måns Ehrenberg
Journal:  EMBO J       Date:  2008-05-22       Impact factor: 11.598

5.  Toxic introns and parasitic intein in Coxiella burnetii: legacies of a promiscuous past.

Authors:  Rahul Raghavan; Linda D Hicks; Michael F Minnick
Journal:  J Bacteriol       Date:  2008-07-07       Impact factor: 3.490

6.  An RpoS-dependent sRNA regulates the expression of a chaperone involved in protein folding.

Authors:  Inês Jesus Silva; Alvaro Darío Ortega; Sandra Cristina Viegas; Francisco García-Del Portillo; Cecília Maria Arraiano
Journal:  RNA       Date:  2013-07-26       Impact factor: 4.942

7.  The stability of an mRNA is influenced by its concentration: a potential physical mechanism to regulate gene expression.

Authors:  Sébastien Nouaille; Sophie Mondeil; Anne-Laure Finoux; Claire Moulis; Laurence Girbal; Muriel Cocaign-Bousquet
Journal:  Nucleic Acids Res       Date:  2017-11-16       Impact factor: 16.971

  7 in total

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