Modified fluorimetric assay for estimating ampicilloate concentrations and its use for detecting beta-lactamase and penicillin acylase activity in bacteria

被引:9
作者
Baker, WL
机构
[1] School of Chemical Sciences, Swinburne University of Technology, Melbourne, Vic. 3122, John Street
关键词
beta-lactamase; penicillin acylase; ampicilloate; fluorescence assay; Lowry A reagent; ascorbate;
D O I
10.1039/a608053g
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Sodium ampicilloate concentrations were estimated fluorimetrically by heating solutions with ascorbic acid, EDTA and a modified Lowry A reagent which was prepared by including copper sulfate and potassium sodium tartrate in 0.5 mol dm(-3) acetate buffer at pH 4. A concentration range of 0.5-50 mu mol dm(-3) was used for the estimations, The reaction was used to estimate beta-lactamase activity on ampicillin but the substrate also showed some fluorescence and a calculation was required to determine the amount of ampicilloate formed when both substances were present in the one reaction mixture, The beta-lactamase was inhibited by treatment with trichloroacetic acid so the procedure could be used to assay the enzyme activity after a fixed time, 6-Aminopenicillanic acid did not fluoresce on treatment with the modified reagent and organisms which contained penicillin acylase lowered the amount of ampicillin which could be converted to ampicilloate. When penicillin acylase and beta-lactamase co-existed in the one organism, the respective activities were determined by use of the copper-ascorbate-EDTA fluorescence assay for ampicilloate coupled with a fluorescamine assay for 6-aminopenicillanic acid determinations, On prolonged incubation, some organisms containing penicillin acylases lowered the amount of ampicilloate which formed a fluorescent product, This effect was attributed to deacylation of ampicilloate by the penicillin acylases.
引用
收藏
页码:447 / 453
页数:7
相关论文
共 27 条
[2]   NOMOGRAPHS FOR FLUORIMETRIC ASSAY OF PENICILLIN ACYLASE ACTIVITY AGAINST ALPHA-AMINOBENZYLPENICILLIN DERIVATIVES [J].
BAKER, WL ;
HAVLICEK, PJ .
JOURNAL OF GENERAL AND APPLIED MICROBIOLOGY, 1985, 31 (01) :107-110
[4]   A NOTE ON THE DETECTION OF PENICILLIN ACYLASE ACTIVITY IN ESCHERICHIA-COLI BY THE REACTION OF AMPICILLIN WITH BIURET REAGENT [J].
BAKER, WL .
JOURNAL OF APPLIED BACTERIOLOGY, 1980, 49 (02) :225-229
[5]   ACTIVITY OF PENICILLIN ACYLASE PRODUCING BACTERIA AGAINST ALPHA-AMINOBENZYLPENICILLINS [J].
BAKER, WL .
ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY, 1983, 49 (06) :551-558
[6]   COEXISTENCE OF BETA-LACTAMASE AND PENICILLIN ACYLASE IN BACTERIA - DETECTION AND QUANTITATIVE-DETERMINATION OF ENZYME-ACTIVITIES [J].
BAKER, WL .
JOURNAL OF APPLIED BACTERIOLOGY, 1992, 73 (01) :14-22
[7]   ISOLATION AND IDENTIFICATION OF FLUORESCENT DEGRADATION PRODUCT OF SOME BETA-LACTAM ANTIBIOTICS [J].
BARBHAIYA, RH ;
BROWN, RC ;
PAYLING, DW ;
TURNER, P .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1978, 30 (04) :224-227
[8]   6-AMINOPENICILLANIC ACID .5. 6-AMINOPENICILLANIC ACID AS A SUBSTRATE FOR PENICILLINASE AND AN INDUCER OF PENICILLINASE FORMATION [J].
BATCHELOR, F ;
CAMERONWOOD, J ;
ROLINSON, GN ;
CHAIN, EB .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1961, 154 (957) :514-+
[9]   2 ANTIGENICALLY DIFFERENT STATES OF ACTIVE PENICILLINASE [J].
CITRI, N .
BIOCHIMICA ET BIOPHYSICA ACTA, 1958, 27 (02) :277-281
[10]   A COLORIMETRIC PROCEDURE FOR MEASURING BETA-LACTAMASE ACTIVITY [J].
COHENFORD, MA ;
ABRAHAM, J ;
MEDEIROS, AA .
ANALYTICAL BIOCHEMISTRY, 1988, 168 (02) :252-258