Department of Biological Sciences, University of Texas at El Paso, El Paso, TX 79968, USA.
Sci Total Environ. 2010 Feb 15;408(6):1422-9. doi: 10.1016/j.scitotenv.2009.12.027. Epub 2010 Jan 13.
The assay described here represents an improved yeast bioassay that provides a rapid yet sensitive screening method for EDCs with very little hands-on time and without the need for sample preparation. Traditional receptor-mediated reporter assays in yeast were performed twelve to twenty four hours after ligand addition, used colorimetric substrates, and, in many cases, required high, non-physiological concentrations of ligand. With the advent of new chemiluminescent substrates a ligand-induced signal can be detected within thirty minutes using high picomolar to low nanomolar concentrations of estrogen. As a result of the sensitivity (EC(50) for estradiol is approximately 0.7nM) and the very short assay time (2-4h) environmental water samples can typically be assayed directly without sterilization, extraction, and concentration. Thus, these assays represent rapid and sensitive approaches for determining the presence of contaminants in environmental samples. As proof of principle, we directly assayed wastewater influent and effluent taken from a wastewater treatment plant in the El Paso, TX area for the presence of estrogenic activity. The data obtained in the four-hour yeast bioassay directly correlated with GC-mass spectrometry analysis of these same water samples.
这里描述的测定方法代表了一种改进的酵母生物测定法,它提供了一种快速而敏感的筛选 EDCs 的方法,所需的操作时间很少,而且不需要进行样品制备。传统的酵母中基于受体的报告基因测定法在配体添加后 12 至 24 小时进行,使用比色底物,并且在许多情况下,需要高生理非生理浓度的配体。随着新的化学发光底物的出现,可以在 30 分钟内使用高皮摩尔到低纳摩尔浓度的雌激素检测到配体诱导的信号。由于灵敏度高(雌二醇的 EC(50)约为 0.7nM),并且测定时间非常短(2-4 小时),因此通常可以直接对环境水样进行测定,而无需灭菌、提取和浓缩。因此,这些测定方法代表了快速灵敏的方法,可以确定环境样品中污染物的存在。作为原理验证,我们直接测定了来自德克萨斯州埃尔帕索地区的废水处理厂的废水进水和出水的雌激素活性。在四小时酵母生物测定中获得的数据与这些水样的 GC-质谱分析直接相关。