Kinetoplastid glucose transporters

被引:73
作者
Tetaud, E [1 ]
Barrett, MP [1 ]
Bringaud, F [1 ]
Baltz, T [1 ]
机构
[1] UNIV BORDEAUX 2, MOL PARASITOL LAB, CNRS, UPRESA 5016, F-33076 BORDEAUX, FRANCE
关键词
D O I
10.1042/bj3250569
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Protozoa of the order kinetoplastida have colonized many habitats, and several species are important parasites of humans. Adaptation to different environments requires an associated adaptation at a cell's interface with its environment, i.e. the plasma membrane. Sugar transport by the kinetoplastida as a phylogenetically related group of organisms offers an exceptional model in which to study the ways by which the carrier proteins involved in this process may evolve to meet differing environmental challenges. Seven genes encoding proteins involved in glucose transport have been cloned from several kinetoplastid species, The transporters all belong to the glucose transporter superfamily exemplified by the mammalian erythrocyte transporter GLUT1. Some species, such as the African trypanosome Trypanosoma brucei, which undergo a life cycle where the parasites are exposed to very different glucose concentrations in the mammalian bloodstream and tsetse-fly midgut, have evolved two different transporters to deal with this fluctuation. Other species, such as the South American trypanosome Trypanosoma cruzi, multiply predominantly in conditions of relative glucose deprivation (intracellularly in the mammalian host, or within the reduviid bug midgut) and have a single, relatively high-affinity type, transporter. All of the kinetoplastid transporters can also transport D-fructose, and are relatively insensitive to the classical inhibitors of GLUT1 transport cytochalasin B and phloretin.
引用
收藏
页码:569 / 580
页数:12
相关论文
共 103 条
[91]   CHARACTERIZATION OF GLUCOSE-TRANSPORT AND CLONING OF A HEXOSE TRANSPORTER GENE IN TRYPANOSOMA-CRUZI [J].
TETAUD, E ;
BRINGAUD, F ;
CHABAS, S ;
BARRETT, MP ;
BALTZ, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) :8278-8282
[92]   CDNA SEQUENCE-ANALYSIS OF A 29-KDA CYSTEINE-RICH SURFACE-ANTIGEN OF PATHOGENIC ENTAMOEBA-HISTOLYTICA [J].
TORIAN, BE ;
FLORES, BM ;
STROEHER, VL ;
HAGEN, FS ;
STAMM, WE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (16) :6358-6362
[93]   MELIBIOSE-CATION COTRANSPORT SYSTEM OF ESCHERICHIA-COLI [J].
TSUCHIYA, T ;
WILSON, DM ;
WILSON, TH .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1985, 456 :342-349
[94]   ROLE OF DENOVO PROTEIN-SYNTHESIS IN THE INTERCONVERSION OF GLUCOSE-TRANSPORT SYSTEMS IN THE YEAST PICHIA-OHMERI [J].
VERMA, RS ;
SPENCERMARTINS, I ;
VANUDEN, N .
BIOCHIMICA ET BIOPHYSICA ACTA, 1987, 900 (01) :139-144
[95]   PHYSIOLOGICAL AND PATHOLOGICAL OBSERVATIONS ON 4 STRAINS OF TRYPANOSOMA-CRUZI [J].
VONBRAND, T ;
TOBIE, EJ ;
KISSLING, RE ;
ADAMS, G .
JOURNAL OF INFECTIOUS DISEASES, 1949, 85 (01) :5-16
[96]   Glucose uptake in Trypanosoma vivax and molecular characterization of its transporter gene [J].
Waitumbi, JN ;
Tetaud, E ;
Baltz, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 237 (01) :234-239
[97]  
Wandel S, 1995, N-S ARCH PHARMACOL, V353, P36
[98]   METABOLISM OF SCHIZOTRYPANUM CRUZI CHAGAS .2. GALACTOSE UTILIZATION [J].
WARREN, LG ;
KITZMAN, WB .
JOURNAL OF PARASITOLOGY, 1963, 49 (05) :808-&
[99]   Glucose uptake occurs by facilitated diffusion in procyclic forms of Trypanosoma brucei [J].
Wille, U ;
Seyfang, A ;
Duszenko, M .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1996, 236 (01) :228-233
[100]   IDENTIFICATION OF A SURFACE-MEMBRANE PROTON-TRANSLOCATING ATPASE IN PROMASTIGOTES OF THE PARASITIC PROTOZOAN LEISHMANIA-DONOVANI [J].
ZILBERSTEIN, D ;
DWYER, DM .
BIOCHEMICAL JOURNAL, 1988, 256 (01) :13-21