Organotin compounds and their interactions with microorganisms

被引:80
作者
White, JS
Tobin, JM [1 ]
Cooney, JJ
机构
[1] Dublin City Univ, Sch Biotechnol, Dublin 9, Ireland
[2] Univ Massachusetts, Environm Coastal & Ocean Sci Program, Boston, MA 02125 USA
关键词
inorganic tin; organotins; microorganisms; organotin resistance; biosorption; biotransformation;
D O I
10.1139/cjm-45-7-541
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
Organotin compounds are ubiquitous in the environment. The general order of toxicity to microorganisms increases with the number and chain length of organic groups bonded to the tin atom. Tetraorganotins and inorganic tin have little toxicity. Because of their lipophilicity, organotins are regarded as membrane active. There is evidence that the site of action of organotins may be both at the cytoplasmic membrane and intracellular level. Consequently, it is not known whether cell surface adsorption or accumulation within the cell, or both is a prerequisite for toxicity. Biosorption studies on a fungus, cyanobacteria, and microalgae indicates that cell surface binding alone occurred in these organisms, while studies on the effects of TBT (tributyltin) on certain microbial enzymes indicated that in some bacteria TBT can interact with cytosolic enzymes. Microorganism-organotin interactions are influenced by environmental conditions. In aquatic systems, both pH and salinity can determine organotin speciation and therefore reactivity. These environmental factors may also alter selectivity for resistant microorganisms in polluted systems. Tin-resistant microorganisms have been identified, and resistance can be either plasmid or chromosomally mediated. In one TBT-resistant organism, an Altermonas sp., an efflux system was suggested as the resistance mechanism. Biotransformation of organotin compounds by debutylation or methylation has been observed. These reactions may influence the toxicity, mobility, and environmental fate of organotin compounds.
引用
收藏
页码:541 / 554
页数:14
相关论文
共 89 条
[1]  
Ambrosini A, 1996, APPL ORGANOMET CHEM, V10, P53, DOI 10.1002/(SICI)1099-0739(199602)10:1<53::AID-AOC477>3.3.CO
[2]  
2-2
[3]   Cd2+-induced damage to yeast plasma membrane and its alleviation by Zn2+: Studies on Schizosaccharomyces pombe cells and reconstituted plasma membrane vesicles [J].
Assmann, S ;
Sigler, K ;
Hofer, M .
ARCHIVES OF MICROBIOLOGY, 1996, 165 (04) :279-284
[4]  
ASTRUC M, 1989, METAL SPECIATION SEP, V2, P263
[5]   BIOSORPTION OF TRIBUTYLTIN AND OTHER ORGANOTIN COMPOUNDS BY CYANOBACTERIA AND MICROALGAE [J].
AVERY, SV ;
CODD, GA ;
GADD, GM .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1993, 39 (06) :812-817
[6]  
AVERY SV, 1991, FEMS MICROBIOL LETT, V84, P205
[7]   MICROBIAL-DEGRADATION OF BIS(TRIBUTYLTIN) OXIDE [J].
BARUG, D .
CHEMOSPHERE, 1981, 10 (10) :1145-1154
[8]   ORGANOTINS IN SWISS LAKES AFTER THEIR BAN - ASSESSMENT OF WATER, SEDIMENT, AND DREISSENA-POLYMORPHA CONTAMINATION OVER A 4-YEAR PERIOD [J].
Becker-van Slooten, K ;
Tarradellas, J .
ARCHIVES OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1995, 29 (03) :384-392
[9]   ACCUMULATION AND FATE OF TRI-N-BUTYLTIN CATION IN ESTUARINE BACTERIA [J].
BLAIR, WR ;
OLSON, GJ ;
BRINCKMAN, FE ;
IVERSON, WP .
MICROBIAL ECOLOGY, 1982, 8 (03) :241-251
[10]  
BLUNDEN SJ, 1984, ENV CHEM, P46