Home LiteratureArticle Details
PMID: 6359164 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Kinetic characterization and regulation of phosphoenolpyruvate-dependent methyl alpha-D-glucopyranoside transport by Salmonella typhimurium membrane vesicles.

Liu KD, Roseman S

Abstract

Membrane vesicles from Salmonella typhimurium SB3507 were used to study the kinetics of methyl alpha-D-glucopyranoside (MeGlc) transport by the phosphoenolpyruvate: glycose phosphotransferase system (PTS). During the first minute of phosphoenolpyruvate-dependent MeGlc transport, two distinct rates were observed; an initial rapid rate, V1 (Vmax, 7.4-8.4 nmol X mg-1 X min-1; Km, 8.2-11.2 X 10(-6)M), followed by a second slower rate, V2 (Vmax, 4-4.6 nmol X mg-1 X min-1; Km, 3.4-6.4 X 10(-6) M). The change in rate occurred when the intravesicular MeGlc phosphate concentration was 0.2 mM or less, depending on the external MeGlc concentration. The rate-limiting component in MeGlc transport was found to be enzyme II-BGlc, not phosphoenolpyruvate uptake or the PTS proteins enzyme I, HPr, and IIIGlc. The change from V1 to V2 thus suggests that the PTS is regulated in intact vesicles. However, this regulation was completely relieved by permeabilizing the vesicles with toluene. That is, the toluene-treated vesicles showed only V1 for MeGlc phosphorylation. Evidence was obtained to show that pyruvate and its metabolic products generated by the vesicles exerted no effect on the rate of MeGlc transport. Furthermore, the result from a dual-label experiment excluded exchange transphosphorylation as the mechanism for regulating MeGlc transport by the vesicles. Possible mechanisms for regulation of the PTS are discussed.

MeSH Terms
Biological Transport Cell Membrane/metabolism Kinetics Methylglucosides/metabolism Methylglycosides/metabolism Phosphoenolpyruvate/pharmacology Phosphorylation Salmonella typhimurium/metabolism
Chemicals
Methylglucosides Methylglycosides methylglucoside Phosphoenolpyruvate
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Liu K D
Roseman S
References (17)
17 references, click to expand
  1. Sugar transport. VII. Lactose transport in Staphylococcus aureus.
    J Biol Chem. 1973 Feb 10;248(3):966-74 PMID: 4684717
  2. Fine control of sugar uptake by Escherichia coli.
    Symp Soc Exp Biol. 1973;27:175-93 PMID: 4588142
  3. Utilization of gluconate by Escherichia coli. Uptake of D-gluconate by a mutant impaired in gluconate kinase activity and by membrane vesicles derived therefrom.
    Biochem J. 1974 May;140(2):193-203 PMID: 4375960
  4. Phosphorylation of D-glucose in Escherichia coli mutants defective in glucosephosphotransferase, mannosephosphotransferase, and glucokinase.
    J Bacteriol. 1975 Jun;122(3):1189-99 PMID: 1097393
  5. A transport system for phosphoenolpyruvate, 2-phosphoglycerate, and 3-phosphoglycerate in Salmonella typhimurium.
    J Biol Chem. 1975 Jul 10;250(13):5089-96 PMID: 238977
  6. The nature and control of carbohydrate uptake by Escherichia coli.
    FEBS Lett. 1976 Mar 15;63(1):3-9 PMID: 770191
  7. Sugar transport. Properties of mutant bacteria defective in proteins of the phosphoenolpyruvate: sugar phosphotransferase system.
    J Biol Chem. 1976 Nov 10;251(21):6584-97 PMID: 789368
  8. The bacterial phosphoenolpyruvate: sugar phosphotransferase system.
    Biochim Biophys Acta. 1976 Dec 14;457(3-4):213-57 PMID: 187249
  9. Kinetic analyses of the sugar phosphate:sugar transphosphorylation reaction catalyzed by the glucose enzyme II complex of the bacterial phosphotransferase system.
    J Biol Chem. 1978 Nov 10;253(21):7595-7 PMID: 359550
  10. Modified assay procedures for the phosphotransferase system in enteric bacteria.
    Anal Biochem. 1979 May;95(1):293-304 PMID: 386829
  11. Sugar transport by the bacterial phosphotransferase system. Phosphoryl transfer reactions catalyzed by enzyme I of Salmonella typhimurium.
    J Biol Chem. 1982 Dec 10;257(23):14477-91 PMID: 6754730
  12. Sugar transport by the bacterial phosphotransferase system. Isolation and characterization of a glucose-specific phosphocarrier protein (IIIGlc) from Salmonella typhimurium.
    J Biol Chem. 1982 Dec 10;257(23):14526-37 PMID: 6754734
  13. Sugar transport by the bacterial phosphotransferase system. The glucose receptors of the Salmonella typhimurium phosphotransferase system.
    J Biol Chem. 1982 Dec 10;257(23):14543-52 PMID: 6292227
  14. Sugar transport by the bacterial phosphotransferase system. Preparation and characterization of membrane vesicles from mutant and wild type Salmonella typhimurium.
    J Biol Chem. 1982 Dec 10;257(23):14565-75 PMID: 6754736
  15. [Galactoside-permease of Escherichia coli].
    Ann Inst Pasteur (Paris). 1956 Dec;91(6):829-57 PMID: 13395026
  16. PHOSPHATE BOUND TO HISTIDINE IN A PROTEIN AS AN INTERMEDIATE IN A NOVEL PHOSPHO-TRANSFERASE SYSTEM.
    Proc Natl Acad Sci U S A. 1964 Oct;52:1067-74 PMID: 14224387
  17. Galactose transport in Escherichia coli. I. General properties as studied in a galactokinaseless mutant.
    J Biol Chem. 1960 Jun;235:1580-5 PMID: 14403098
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1983-12-00
Pages
7142-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC390009
Subset
IM
Grants
NCI NIH HHS · CA 21901 · United States
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