Peng T, Zhang Q, Guo L
Institute of Biophysics, Chinese Academy of Sciences, Beijing.
Yi Chuan Xue Bao. 1994;21(2):155-60.
Site-directed mutagenesis was performed at Ser177 of Penicillin G Acylase (PGA) gene of E. coli by gap duplex method. Screened by 2-nitro-5-phenylacetaminobenzoic acid (NIPAB) test paper assay and confirmed by DNA sequencing, the mutants Cys177, Gly177, Arg177 and Asn177 were obtained. They have no activity of PGA. The mutant enzyme was expressed and detected by PAGE. It is suggested that Ser177 is at the substrate binding center of PGA and can not be replaced.
采用缺口双链法对大肠杆菌青霉素G酰化酶(PGA)基因的Ser177位点进行定点诱变。通过2-硝基-5-苯乙酰氨基苯甲酸(NIPAB)试纸检测筛选,并经DNA测序确认,获得了突变体Cys177、Gly177、Arg177和Asn177。它们没有PGA活性。对突变酶进行表达并通过聚丙烯酰胺凝胶电泳(PAGE)检测。结果表明,Ser177位于PGA的底物结合中心,不能被取代。