Choma C T, Yamazaki H
Can J Microbiol. 1981 May;27(5):547-50. doi: 10.1139/m81-081.
Benzylpenicillin was clearly separated from benzylpenicilloic acid by ascending chromatography on a diethylaminoethyl cellulose paper using 0.1 M ammonium acetate as a solvent. Using this chromatographic system, penicillinase was assayed by measuring the formation of [14C]benzylpenicilloic acid from [14C]benzylpenicillin. This assay remedies the lack of specificity of the commonly used iodometric assays. Periplasmic penicillinase was released from Escherichia coli by suspension in a mixture of 1% phenethyl alcohol and 5 mM ethylenediaminetetraacetate (pH 7.0). This simple extraction method not only facilitates the assay of penicillinase in an E. coli culture, but will also be useful for large-scale purification of periplasmic penicillinase.
使用0.1M醋酸铵作为溶剂,在二乙氨基乙基纤维素纸上进行上行色谱法,可将苄青霉素与苄青霉素酸清晰分离。利用该色谱系统,通过测量[¹⁴C]苄青霉素生成[¹⁴C]苄青霉素酸的量来测定青霉素酶。该测定方法弥补了常用碘量法缺乏特异性的不足。通过将大肠杆菌悬浮于1%苯乙醇和5mM乙二胺四乙酸(pH 7.0)的混合物中,可释放出周质青霉素酶。这种简单的提取方法不仅便于测定大肠杆菌培养物中的青霉素酶,还将有助于大规模纯化周质青霉素酶。