首页 | 本学科首页   官方微博 | 高级检索  
     


Performances of three bacterial assays in toxicity assessment
Authors:Reteuna  C.  Vasseur  P.  Cabridenc  R.
Affiliation:(1) Centre des Sciences de l'Environnement, 1, rue des Récollets, 57000 Metz, France;(2) I.R.CH.A., Rue Lavoisier, 91710 Vert-Le-Petit, France
Abstract:Three differing bacterial toxicity assays were compared: the lsquoMicrotoxrsquo test, (Photobacterium phosphoreum luminescence inhibition assay), the lsquooxygen consumption of activated sludgersquo assay (ISO 8192), and the lsquoGlucose U-14C mineralizationrsquo assay (the rate of release of 14CO2 by lsquoEscherichia colirsquo ). Metals, amines, halogenated alcans, chlorophenols, aromatic hydrocarbons, surfactants, and pesticides were screened for their toxic activity.Results showed satisfactory repeatability of the three bacterial assays with variation coefficients between 5 and 32%. The lsquoMicrotoxrsquo assay was the most sensitive test evaluated under our conditions. The lower sensitivity of the lsquooxygen consumptionrsquo assay may have been due to high concentrations of substrates which modify toxicant bioavailability, and also to a high biomass/toxic substances ratio. The lsquoGlucose U-14C mineralizationrsquo assay was selective, and low in sensitivity; but the specific species used in this test — Escherichia coli — may have been responsible for this selectivity.The lsquoMicrotoxrsquo test appears to be well adapted to the detection of aquatic environmental pollution, and to the toxicity screening of complex solid waste effluents and/or leachates. The lsquooxygen consumptionrsquo assay can be advantageously used to measure the impact of sewage on activated sludge in biological treatment plants. The lsquoGlucose U-14C mineralizationrsquo assay, which does not require high biomass, can be useful for in situ studies using field microorganisms.
Keywords:bacterial assays  toxicity assessment  microtox test  oxygen consumption assay  glucose mineralization assay  bioavailability
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号