Biokinetics of cadmium and zinc in a marine bacterium: Influences of metal interaction and pre-exposure

被引:21
作者
Chen, Dongshi [1 ]
Qian, Pei-Yuan [1 ]
Wang, Wen-Xiong [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Dept Biol, Kowloon, Hong Kong, Peoples R China
关键词
marine bacteria; cadmium; zinc; interaction; biokinetics;
D O I
10.1897/07-565.1
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The uptake kinetics of Cd and Zn, as influenced by metal interaction and metal pre-exposure, was examined in the ram-positive marine bacterium Bacillus firmus over a wide range of ambient free-Cd and -Zn concentrations. Bacteria were exposed to experimental media with different concentrations of Cd and Zn over a short, 15-min period. Zinc was found to be an effective competitive inhibitor of Cd uptake when the Zn(2+) concentration ([Zn(2+)]) was increased to 10(-8) M, whereas the Cd concentration (ranging from 10(-9) to 10(-6) M) did not affect Zn uptake. Inhibition of Cd uptake was dependent on [Zn(2+)] instead of the [Zn2+] to Cd(2+). concentration ratio. Cadmium uptake at different [Zn(2+)] was significantly inhibited by a sulfur ligand (SH) blocker (N-ethylmaleimide) and a Ca-channel blocker (lanthanum), suggesting that competition between Cd and Zn most likely occurred via binding to the same transport sites. Cadmium efflux also was determined in the presence of different [Zn(2+)]. A biphasic depuration of Cd was found when [Zn(2+)] was greater than 10-8 M, whereas the calculated Cd efflux rate was independent of [Zn(2+)]. We further exposed B. firmus at different Cd or Zn concentrations for 24 h, then determined the metal uptake and efflux kinetics as well as the metallothionein (MT) induction. Both the Cd and Zn cellular concentrations increased with greater exposed metal concentration, but the MT levels and efflux were little affected by the elevated metal concentration. To some extent, however, the Cd uptake was reduced with an elevated intracellular Zn concentration, suggesting that at high Cd concentrations, intracellular Zn can suppress the Cd uptake in B. firmus. These results help to understand the interactions of metals in the marine environments.
引用
收藏
页码:1794 / 1801
页数:8
相关论文
共 35 条
[1]   Different transport mechanisms for cadmium and mercury in Caco-2 cells: inhibition of Cd uptake by Hg without evidence for reciprocal effects [J].
Aduayom, I ;
Campbell, PGC ;
Denizeau, F ;
Jumaire, C .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 189 (01) :56-67
[2]   Characteristics of zinc transport by two bacterial cation diffusion facilitators from Ralstonia metallidurans CH34 and Escherichia coli [J].
Anton, A ;
Weltrowski, A ;
Haney, CJ ;
Franke, S ;
Grass, G ;
Rensing, C ;
Nies, DH .
JOURNAL OF BACTERIOLOGY, 2004, 186 (22) :7499-7507
[3]   Acute study of interaction among cadmium, calcium, and zinc transport along the rat nephron in vivo [J].
Barbier, O ;
Jacquillet, G ;
Tauc, M ;
Poujeol, P ;
Cougnon, M .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 287 (05) :F1067-F1075
[4]   Uptake and efflux of Cd and Zn by the green mussel Perna viridis after metal preexposure [J].
Blackmore, G ;
Wang, WX .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2002, 36 (05) :989-995
[5]   Fermentation product butane 2,3-diol induces Ca2+ transients in E. coli through activation of lanthanum-sensitive Ca2+ channels [J].
Campbell, Anthony K. ;
Naseem, Riffat ;
Wann, Kenneth ;
Holland, I. Barry ;
Matthews, Stephanie B. .
CELL CALCIUM, 2007, 41 (02) :97-106
[6]   Metal bioavailability to phytoplankton -: applicability of the biotic ligand model [J].
Campbell, PGC ;
Errécalde, O ;
Fortin, C ;
Hiriart-Baer, WR ;
Vigneault, B .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2002, 133 (1-2) :189-206
[7]   Kinetic study of the antiport mechanism of an Escherichia coli zinc transporter, ZitB [J].
Chao, Y ;
Fu, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (13) :12043-12050
[8]   PLASMIDS FOR HEAVY-METAL RESISTANCE IN ALCALIGENES-EUTROPHUS CH34 - MECHANISMS AND APPLICATIONS [J].
COLLARD, JM ;
CORBISIER, P ;
DIELS, L ;
DONG, Q ;
JEANTHON, C ;
MERGEAY, M ;
TAGHAVI, S ;
VANDERLELIE, D ;
WILMOTTE, A ;
WUERTZ, S .
FEMS MICROBIOLOGY REVIEWS, 1994, 14 (04) :405-414
[9]  
Endo T, 1996, BIOL PHARM BULL, V19, P944
[10]  
FAGAN MJ, 1994, J MOL EVOL, V38, P57