Martínez-Martínez Irene, Montoro-García Silvia, Lozada-Ramírez José Daniel, Sánchez-Ferrer Alvaro, García-Carmona Francisco
Department of Biochemistry and Molecular Biology, Faculty of Biology, University of Murcia, E-30071 Murcia, Spain.
Anal Biochem. 2007 Oct 15;369(2):210-7. doi: 10.1016/j.ab.2007.06.030. Epub 2007 Jun 22.
A bromothymol blue-based colorimetric assay has been devised to screen for acetyl xylan esterase or cephalosporin C (CPC) deacetylase activities using 7-amino cephalosporanic acid (7-ACA), CPC, or acetylated xylan as substrate. These enzymes are not screened with their natural substrates because of the tedious procedures available previously. Acetyl xylan esterase from Bacillus pumilus CECT 5072 was cloned, expressed in Escherichia coli Rosetta (DE3), and characterized using this assay. Similar K(M) values for 7-ACA and CPC were obtained when compared with those described using HPLC methods. The assay is easy to perform and can be carried out in robotic high-throughput colorimetric devices normally used in directed evolution experiments. The assay allowed us to detect improvements in activity at a minimum of twofold with a very low coefficient of variance in 96-well plates. This method is significantly faster and more convenient to use than are known HPLC and pH-stat procedures.
已设计出一种基于溴百里酚蓝的比色测定法,以7-氨基头孢烷酸(7-ACA)、头孢菌素C(CPC)或乙酰化木聚糖为底物,筛选乙酰木聚糖酯酶或头孢菌素C(CPC)脱乙酰酶活性。由于先前可用的程序繁琐,这些酶未用其天然底物进行筛选。克隆了短小芽孢杆菌CECT 5072的乙酰木聚糖酯酶,在大肠杆菌Rosetta (DE3) 中表达,并使用该测定法进行表征。与使用HPLC方法描述的K(M)值相比,7-ACA和CPC的K(M)值相似。该测定法易于操作,可在定向进化实验中常用的机器人高通量比色设备中进行。该测定法使我们能够在96孔板中以非常低的变异系数检测到至少两倍的活性提高。该方法比已知的HPLC和pH计程序显著更快且更易于使用。