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PMID: 6252191 Published · ppublish English Journal Article

Suppression of defects in cyclic adenosine 3',5'-monophosphate metabolism in Escherichia coli.

Journal of bacteriology ·Vol. 144 ·No. 1 ·1980-10-00 ·Pages 205-9

Alexander JK

Abstract

Strain MM6-13 (ptsI suc lacI sup) of Escherichia coli contains a suppressor of the succinate-negative phenotype. In MM6-13, sup caused enhanced growth in glycerol, maltose, melibiose, and succinate media and increased activity of beta-galactosidase and tryptophanase relative to an isogenic strain without sup. In strain A61 (cya sup), sup partially suppressed cya. Cyclic guanosine monophosphate increased beta-galactosidase activity sevenfold in A61 and enabled this strain to grow on maltose, galactose, succinate, and arabinose. Strain A61 responded to much lower concentrations of cyclic adenosine monophosphate than cyclic guanosine monophosphate. It appears that sup is located in the crp locus. These results suggest that sup mutants have an altered cyclic adenosine monophosphate receptor protein which is activated by cyclic guanosine monophosphate and has an increased affinity for cyclic adenosine monophosphate.

MeSH Terms
Carbohydrate Metabolism Cyclic AMP/metabolism,pharmacology Cyclic GMP/pharmacology Escherichia coli/genetics,metabolism Mutation Succinates/metabolism Suppression, Genetic beta-Galactosidase/metabolism
Chemicals
Succinates Cyclic AMP beta-Galactosidase Cyclic GMP
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Alexander J K
References (12)
12 references, click to expand
  1. Repression of beta-galactosidase synthesis by glucose in phosphotransferase mutants of Escherichia coli. Repression in the absence of glucose phosphorylation.
    J Biol Chem. 1969 Nov 10;244(21):5836-42 PMID: 4310826
  2. Suppression of a pleiotropic mutant affecting glycerol dissimilation.
    Biochem Biophys Res Commun. 1970 Jan 23;38(2):272-8 PMID: 4313930
  3. Transport of succinate in Escherichia coli. I. Biochemical and genetic studies of transport in whole cells.
    J Biol Chem. 1972 Oct 10;247(19):6323-31 PMID: 4346810
  4. A mutant transcription factor that is activated by 3':5'-cyclic guanosine monophosphate.
    Proc Natl Acad Sci U S A. 1973 Apr;70(4):1017-21 PMID: 4352217
  5. Abnormally high rate of cyclic AMP excretion from an Escherichia coli mutant deficient in cyclic AMP receptor protein.
    Biochem Biophys Res Commun. 1974 Mar 25;57(2):379-85 PMID: 4364238
  6. Genetic analysis of succinate utilization in enzyme I mutants of the phosphoenolpyruvate: sugar phosphotransferase system in Escherichia coli.
    J Bacteriol. 1975 Oct;124(1):252-61 PMID: 170246
  7. Cyclic adenosine 5'-monophosphate in Escherichia coli.
    Bacteriol Rev. 1976 Sep;40(3):527-51 PMID: 186018
  8. The Escherichia coli adenylate cyclase complex. Regulation by enzyme I of the phosphoenolpyruvate:sugar phosphotransferase system.
    Arch Biochem Biophys. 1978 May;188(1):47-55 PMID: 354532
  9. The cyclic 3',5'-adenosine monophosphate receptor protein and regulation of cyclic 3',5'-adenosine monophosphate synthesis in Escherichia coli.
    Mol Gen Genet. 1978 Sep 20;165(1):47-56 PMID: 213702
  10. The Escherichia coli adenylate cyclase complex: activation by phosphoenolpyruvate.
    J Supramol Struct. 1978;9(2):219-30 PMID: 219294
  11. Lysis of Escherichia coli mutants by lactose.
    J Bacteriol. 1979 Nov;140(2):643-8 PMID: 40961
  12. Protein measurement with the Folin phenol reagent.
    J Biol Chem. 1951 Nov;193(1):265-75 PMID: 14907713
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1980-10-00
Pages
205-9
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC294622
Subset
IM
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