Determination of L-Amino Acids and L-Amino Acid Oxidase Activity Using Luminol Chemiluminescence
- 1 January 1977
- journal article
- research article
- Published by Taylor & Francis in Analytical Letters
- Vol. 10 (12) , 931-943
- https://doi.org/10.1080/00032717708059249
Abstract
A quantitative enzymatic method has been developed for analysis of most of the naturally occurring L-amino acids as well as the enzyme L-amino acid oxidase. The method is based on the reaction of L-amino acid oxidase with L-amino acids to generate hydrogen peroxide. The peroxide is then determined by reacting it with excess luminol and ferricyanide and measuring the resulting chemiluminescence. The lower limit of detection for any particular amino acid is related to the specific activity of the enzyme for that substrate. Concentrations as low as 5.0 × 10−8 M are measurable for some amino acids. Using L-phenylalanine as a substrate, enzyme activity can be measured in the range of 0.012 to 0.21 U. of enzyme.Keywords
This publication has 10 references indexed in Scilit:
- Glucose oxidase chemiluminescence measurement of glucose in urine compared with the hexokinase method.Clinical Chemistry, 1976
- Quantitative determination of blood glucose using enzyme induced chemiluminescence of luminolAnalytical Chemistry, 1975
- Chemiluminescent enzyme method for glucoseAnalytical Chemistry, 1975
- Enzyme-Induced Chemiluminescence-Determination of Blood Glucose Using LuminolAnalytical Letters, 1974
- Chemiluminescence and bioluminescence in chemical analysisAnalytical Chemistry, 1974
- Chemiluminescence in analytical chemistryAnalytica Chimica Acta, 1974
- An Automated Procedure for the Sensitive and Specific Determination of ATPClinical Chemistry, 1969
- Crystalline l-Amino Acid Oxidase of Crotalus adamanteusJournal of Biological Chemistry, 1960