Literature DB >> 9020885

Mechanism of glucose and maltose transport in plasma-membrane vesicles from the yeast Candida utilis.

P J van den Broek1, A E van Gompel, M A Luttik, J T Pronk, C C van Leeuwen.   

Abstract

Transport of glucose and maltose was studied in plasma-membrane vesicles from Candida utilis. The yeast was grown on a mixture of glucose and maltose in aerobic carbon-limited continuous cultures which enabled transport to be studied for both sugars with the same vesicles. Vesicles were prepared by fusion of isolated plasma membranes with proteoliposomes containing bovine heart cytochrome c oxidase as a proton-motive-force-generating system. Addition of reduced cytochrome c generated a proton-motive force, consisting of a membrane potential, negative inside, and a pH gradient, alkaline inside. Energization led to accumulation of glucose and maltose in these vesicles, reaching accumulation ratios of about 40-50. Accumulation also occurred in the presence of valinomycin or nigericin, but was prevented by a combination of the two ionophores or by uncoupler, showing that glucose and maltose transport are dependent on the proton-motive force. Comparison of sugar accumulation with quantitative data on the proton-motive force indicated a 1:1 H+/sugar stoichiometry for both transport systems. Efflux of accumulated glucose was observed on dissipation of the proton-motive force. Exchange and counterflow experiments confirmed the reversible character of the H+-glucose symporter. In contrast, uncoupler or a mixture of valinomycin plus nigericin induced only a slow efflux of accumulated maltose. Moreover under counterflow conditions, the expected transient accumulation was small. Thus the H+-maltose symporter has some characteristics of a carrier that is not readily reversible. It is concluded that in C. utilis the transport systems for glucose and maltose are both driven by the proton-motive force, but the mechanisms are different.

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Year:  1997        PMID: 9020885      PMCID: PMC1218095          DOI: 10.1042/bj3210487

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  44 in total

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Authors:  P Viitanen; M J Newman; D L Foster; T H Wilson; H R Kaback
Journal:  Methods Enzymol       Date:  1986       Impact factor: 1.600

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Authors:  W de Vrij; A J Driessen; K J Hellingwerf; W N Konings
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Authors:  A J Driessen; J Kodde; S de Jong; W N Konings
Journal:  J Bacteriol       Date:  1987-06       Impact factor: 3.490

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Authors:  J P Tijssen; T M Dubbelman; J Van Steveninck
Journal:  Biochim Biophys Acta       Date:  1983-10-04

5.  Electrochemical potential and ion transport in vesicles of yeast plasma membrane.

Authors:  M Calahorra; J Ramírez; S M Clemente; A Peña
Journal:  Biochim Biophys Acta       Date:  1987-05-29

6.  Fluorescence method for measuring the kinetics of fusion between biological membranes.

Authors:  D Hoekstra; T de Boer; K Klappe; J Wilschut
Journal:  Biochemistry       Date:  1984-11-20       Impact factor: 3.162

7.  The isolation of plasma membrane and characterisation of the plasma membrane ATPase from the yeast Candida albicans.

Authors:  M J Hubbard; R Surarit; P A Sullivan; M G Shepherd
Journal:  Eur J Biochem       Date:  1986-01-15

8.  Glucose transport in vesicles reconstituted from Saccharomyces cerevisiae membranes and liposomes.

Authors:  R Ongjoco; K Szkutnicka; V P Cirillo
Journal:  J Bacteriol       Date:  1987-07       Impact factor: 3.490

9.  Glucose transport activity in isolated plasma membrane vesicles from Saccharomyces cerevisiae.

Authors:  A J Franzusoff; V P Cirillo
Journal:  J Biol Chem       Date:  1983-03-25       Impact factor: 5.157

10.  Incorporation of beef heart cytochrome c oxidase as a proton-motive force-generating mechanism in bacterial membrane vesicles.

Authors:  A J Driessen; W de Vrij; W N Konings
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

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  1 in total

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