Le Guével R, Pakdel F
Université de Rennes, Rennes, France.
Biotechniques. 2001 May;30(5):1000-4. doi: 10.2144/01305st05.
Here, we describe a rapid, convenient, and quantitative beta-galactosidase assay in liquid culture of recombinant yeast that expresses the estrogen receptor. This assay allows large-scale screening of chemicals (more than 600 samples/day) for the evaluation of their direct estrogenic potency and accurate determination of their EC50 with minimal manipulations. The assay, which is based on digestion of the yeast cell wall by lyticase (zymolase), a beta-glucanase isolated from Arthrobacter luteus, followed by a hypoosmotic shock lysis, is performed completely in 96-well plates. This protocol for using recombinant yeast with the two-hybrid technology significantly advances recombinant yeast manipulation.
在此,我们描述了一种在表达雌激素受体的重组酵母液体培养物中进行快速、便捷且定量的β-半乳糖苷酶测定方法。该测定方法允许对化学物质进行大规模筛选(每天超过600个样本),以评估其直接雌激素活性,并通过最少的操作准确测定其半数有效浓度(EC50)。该测定方法基于从藤黄节杆菌分离出的β-葡聚糖酶溶菌酶(zymolase)消化酵母细胞壁,随后进行低渗休克裂解,整个过程在96孔板中完全完成。这种使用重组酵母和双杂交技术的方案显著推进了重组酵母操作。