Literature DB >> 1694554

Metabolic growth rate control in Escherichia coli may be a consequence of subsaturation of the macromolecular biosynthetic apparatus with substrates and catalytic components.

K F Jensen1, S Pedersen.   

Abstract

In this paper, the Escherichia coli cell is considered as a system designed for rapid growth, but limited by the medium. We propose that this very design causes the cell to become subsaturated with precursors and catalytic components at all levels of macromolecular biosynthesis and leads to a molecular sharing economy at a high level of competition inside the cell. Thus, the promoters compete with each other in the binding of a limited amount of free RNA polymerase and the ribosome binding sites on the mRNA chains compete with each other for the free ribosomes. The macromolecular chain elongation reactions sequester a considerable proportion of the total amount of RNA polymerase and ribosomes in the cells. We propose that the degree of subsaturation of the macromolecular biosynthetic apparatus renders a variable fraction of RNA polymerase and ribosomes unavailable for the initiation of new chain synthesis and that this, at least in part, determines the composition of the cell as a function of the growth rate. Thus, at rapid growth, the high speed of the elongation reactions enables the cell to increase the concentrations of free RNA polymerase and ribosomes for initiation purposes. Furthermore, it is proposed that the speed of RNA polymerase movement is adjusted to the performance speed of the ribosomes. Mechanistically, this adjustment of the coupling between transcription and translation involves transcriptional pause sites along the RNA chains, the adjustment of the saturation level of RNA polymerase with the nucleoside triphosphate substrates, and the concentration of ppGpp, which is known to inhibit RNA chain elongation. This model is able to explain the stringent response and the control of stable RNA and of ribosome synthesis in steady states and in shifts, as well as the rate of overall protein synthesis as a function of the growth rate.

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Year:  1990        PMID: 1694554      PMCID: PMC372765          DOI: 10.1128/mr.54.2.89-100.1990

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  84 in total

1.  DNA determinants of rRNA synthesis in E. coli: growth rate dependent regulation, feedback inhibition, upstream activation, antitermination.

Authors:  R L Gourse; H A de Boer; M Nomura
Journal:  Cell       Date:  1986-01-17       Impact factor: 41.582

2.  Genetic dissection of stringent control and nutritional shift-up response of the Escherichia coli S10 ribosomal protein operon.

Authors:  L P Freedman; J M Zengel; L Lindahl
Journal:  J Mol Biol       Date:  1985-10-20       Impact factor: 5.469

Review 3.  Ribosomal genes in Escherichia coli.

Authors:  L Lindahl; J M Zengel
Journal:  Annu Rev Genet       Date:  1986       Impact factor: 16.830

4.  Changes in the half-life of ribosomal protein messenger RNA caused by translational repression.

Authors:  J R Cole; M Nomura
Journal:  J Mol Biol       Date:  1986-04-05       Impact factor: 5.469

5.  Feedback regulation of rRNA synthesis in Escherichia coli. Requirement for initiation factor IF2.

Authors:  J R Cole; C L Olsson; J W Hershey; M Grunberg-Manago; M Nomura
Journal:  J Mol Biol       Date:  1987-12-05       Impact factor: 5.469

6.  Stringent and growth control of rRNA synthesis in Escherichia coli are both mediated by ppGpp.

Authors:  E Baracchini; H Bremer
Journal:  J Biol Chem       Date:  1988-02-25       Impact factor: 5.157

7.  Basal ppGpp level adjustment shown by new spoT mutants affect steady state growth rates and rrnA ribosomal promoter regulation in Escherichia coli.

Authors:  E Sarubbi; K E Rudd; M Cashel
Journal:  Mol Gen Genet       Date:  1988-08

8.  Feedback regulation of rRNA synthesis. A mutational alteration in the anti-Shine-Dalgarno region of the 16 S rRNA gene abolishes regulation.

Authors:  M Yamagishi; H A de Boer; M Nomura
Journal:  J Mol Biol       Date:  1987-12-05       Impact factor: 5.469

9.  Translation rate modification by preferential codon usage: intragenic position effects.

Authors:  H Liljenström; G von Heijne
Journal:  J Theor Biol       Date:  1987-01-07       Impact factor: 2.691

10.  Saturation mutagenesis of an Escherichia coli rRNA promoter and initial characterization of promoter variants.

Authors:  T Gaal; J Barkei; R R Dickson; H A deBoer; P L deHaseth; H Alavi; R L Gourse
Journal:  J Bacteriol       Date:  1989-09       Impact factor: 3.490

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  55 in total

Review 1.  The origin of eukaryotes: the difference between prokaryotic and eukaryotic cells.

Authors:  T Vellai; G Vida
Journal:  Proc Biol Sci       Date:  1999-08-07       Impact factor: 5.349

2.  Compartmentalization of transcription and translation in Bacillus subtilis.

Authors:  P J Lewis; S D Thaker; J Errington
Journal:  EMBO J       Date:  2000-02-15       Impact factor: 11.598

3.  Positive growth rate-dependent regulation of the pdxA, ksgA, and pdxB genes of Escherichia coli K-12.

Authors:  Andrew J Pease; Benjamin R Roa; Wen Luo; Malcolm E Winkler
Journal:  J Bacteriol       Date:  2002-03       Impact factor: 3.490

Review 4.  Regulation of ribosome biosynthesis in Escherichia coli and Saccharomyces cerevisiae: diversity and common principles.

Authors:  M Nomura
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

5.  Role of SeqA and Dam in Escherichia coli gene expression: a global/microarray analysis.

Authors:  Anders Løbner-Olesen; Martin G Marinus; Flemming G Hansen
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-07       Impact factor: 11.205

6.  Depletion of pre-16S rRNA in starved Escherichia coli cells.

Authors:  G A Cangelosi; W H Brabant
Journal:  J Bacteriol       Date:  1997-07       Impact factor: 3.490

7.  Coupling the cell cycle to cell growth.

Authors:  Erik Boye; Kurt Nordström
Journal:  EMBO Rep       Date:  2003-08       Impact factor: 8.807

Review 8.  Control of rRNA synthesis in Escherichia coli: a systems biology approach.

Authors:  Patrick P Dennis; Mans Ehrenberg; Hans Bremer
Journal:  Microbiol Mol Biol Rev       Date:  2004-12       Impact factor: 11.056

9.  Estimating the growth rate of slowly growing marine bacteria from RNA content.

Authors:  P F Kemp; S Lee; J Laroche
Journal:  Appl Environ Microbiol       Date:  1993-08       Impact factor: 4.792

10.  Growth-rate-dependent partitioning of RNA polymerases in bacteria.

Authors:  Stefan Klumpp; Terence Hwa
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-10       Impact factor: 11.205

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