Home LiteratureArticle Details
PMID: 6155375 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Control of protein synthesis in Escherichia coli: strain differences in control of translational initiation after energy source shift-down.

Journal of bacteriology ·Vol. 142 ·No. 3 ·1980-06-00 ·Pages 888-98

Jacobson LA, Jen-Jacobson L

Abstract

We have studied the parameters of protein synthesis in a number of Escherichia coli strains after a shift-down from glucose-minimal to succinate-minimal medium. One group of strains, including K-12(lambda) (ATCC 10798) and NF162, showed a postshift translational yield of 50 to 65% and a 2- to 2.5-fold increase in the functional lifetime of general messenger ribonucleic acid. There was no change in the lag time for beta-galactosidase induction in these strains after the shift-down. A second group, including W1 and W2, showed no reduction in translational yield, no change in the functional lifetime of messenger ribonucleic acid, and a 50% increase in the lag time for beta-galactosidase induction. Evidence is presented which indicates that this increased lag time is not the result of a decreased rate of polypeptide chain propagation. A third group of strains, including NF161, CP78, and NF859, showed an intermediate pattern: translational yield was reduced to about 75% of normal, and the messenger ribonucleic acid functional lifetime was increased by about 50%. Calculation of the relative postshift rates of translational initiation gave about 0.2, 1.0, and 0.5, respectively, for the three groups. There was no apparent correlation between the ability to control translation and the genotypes of these strains at the relA, relX, or spoT loci. Measurements of the induction lag for beta-galactosidase during short-term glucose starvation or after a down-shift induced by alpha-methylglucoside indicated that these regimens elicit responses that are physiologically distinct from those elicited by a glucose-to-succinate shift-down.

MeSH Terms
Bacterial Proteins/biosynthesis Energy Metabolism Enzyme Induction Escherichia coli/metabolism Galactosidases/biosynthesis Glucose/metabolism Kinetics Peptide Chain Initiation, Translational RNA, Bacterial/metabolism RNA, Messenger/metabolism Species Specificity Succinates/metabolism Transcription, Genetic beta-Galactosidase/biosynthesis
Chemicals
Bacterial Proteins RNA, Bacterial RNA, Messenger Succinates Galactosidases beta-Galactosidase Glucose
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Jacobson L A
Jen-Jacobson L
References (17)
17 references, click to expand
  1. Control of messenger RNA synthesis and decay in Escherichia coli.
    J Mol Biol. 1966 Oct;20(3):559-73 PMID: 5338988
  2. Regulation of ribonucleic acid synthesis in Escherichia coli during diauxie lag: accumulation of heterogeneous ribonucleic acid.
    J Bacteriol. 1970 Jun;102(3):740-6 PMID: 4914078
  3. Initiation, elongation and inactivation of lac messenger RNA in Escherichia coli studied studied by measurement of its beta-galactosidase synthesizing capacity in vivo.
    J Mol Biol. 1971 Sep 28;60(3):453-72 PMID: 4938821
  4. Nucleotide changes and the regulation of ribonucleic acid accumulation during growth rate shifts in Escherichia coli.
    J Biol Chem. 1972 Feb 10;247(3):790-7 PMID: 4550760
  5. Induction kinetics of the L-arabinose operon of Escherichia coli.
    J Bacteriol. 1973 Jul;115(1):9-14 PMID: 4577756
  6. Intracistronic polarity during dissociation of translation from transcription in Escherichia coli.
    J Mol Biol. 1973 Jul 15;77(4):589-604 PMID: 4579450
  7. Accumulation of 70S monoribosomes in Escherichia coli after energy source shift-down.
    J Bacteriol. 1972 Jul;111(1):142-51 PMID: 4591472
  8. Control of protein synthesis of Escherichia coli. I. Translation and functional inactivation of messenger ribonucleic acid after energy source shift-down.
    J Biol Chem. 1974 Oct 10;249(19):6272-9 PMID: 4609047
  9. Simple downshift and resulting lack of correlation between ppGpp pool size and ribonucleic acid accumulation.
    J Bacteriol. 1975 May;122(2):585-91 PMID: 1092659
  10. Association of messenger ribonucleic acid with 70S monosomes from down-shifted Escherichia coli.
    J Bacteriol. 1976 Jul;127(1):637-43 PMID: 179981
  11. A novel nucleotide implicated in the response of E. coli to energy source downshift.
    Cell. 1976 Jan;7(1):75-84 PMID: 779954
  12. The amino acid sequence of beta-galactosidase of Escherichia coli.
    Proc Natl Acad Sci U S A. 1977 Apr;74(4):1507-10 PMID: 323855
  13. Control of protein synthesis in Escherichia coli: analysis of an energy source shift-down.
    J Bacteriol. 1977 Jul;131(1):18-29 PMID: 326760
  14. A gene involved in the metabolic control of ppGpp synthesis.
    Mol Gen Genet. 1978 Jan 17;158(3):271-7 PMID: 342913
  15. Control of protein synthesis in Escherichia coli: control of bacteriophage Q beta coat protein synthesis after energy source shift-down.
    J Virol. 1979 Apr;30(1):267-78 PMID: 384018
  16. A genetic locus for the regulation of ribonucleic acid synthesis.
    Proc Natl Acad Sci U S A. 1961 Dec 15;47:2005-14 PMID: 13916843
  17. FALSE FEEDBACK INHIBITION OF AROMATIC AMINO ACID BIOSYNTHESIS BY BETA-2-THIENYLALANINE.
    Biochim Biophys Acta. 1965 Jan 11;95:54-62 PMID: 14289034
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1980-06-00
Pages
888-98
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC294114
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com