Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
, 321 ( Pt 2) (Pt 2), 487-95

Mechanism of Glucose and Maltose Transport in Plasma-Membrane Vesicles From the Yeast Candida Utilis


Mechanism of Glucose and Maltose Transport in Plasma-Membrane Vesicles From the Yeast Candida Utilis

P J van den Broek et al. Biochem J.


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.

Similar articles

See all similar articles


    1. Biochim Biophys Acta. 1983 Oct 4;760(1):143-8 - PubMed
    1. J Biol Chem. 1983 Mar 25;258(6):3608-14 - PubMed
    1. Biochemistry. 1984 Nov 20;23(24):5675-81 - PubMed
    1. Proc Natl Acad Sci U S A. 1985 Nov;82(22):7555-9 - PubMed
    1. Eur J Biochem. 1986 Jan 15;154(2):375-81 - PubMed

Publication types