Determination of l-Phenylalanine Based on an NADH-Detecting Biosensor

• Published in: Analytical chemistry (Washington) 1998-03, Vol.70 (5), p.991-997
• Main Authors: Huang, Tina, Warsinke, Axel, Kuwana, Theodore, Scheller, Frieder W
• Format: Article
• Language: English
• Subjects: Amino Acid Oxidoreductases; Benzoquinones - chemistry; Biochemistry; Biological and medical sciences; Biosensing Techniques; Biosensors; Biotechnology; Carbon; Catechols - chemistry; Electrochemistry; Enzymes; Enzymes, Immobilized; Fundamental and applied biological sciences. Psychology; Humans; Hydrogen-Ion Concentration; Methods. Procedures. Technologies; Mixed Function Oxygenases; Monophenol Monooxygenase; NAD - analysis; Phenylalanine - analysis; Phenylalanine - blood; Tyrosine - chemistry; Various methods and equipments
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac971010u

An enzyme carbon paste electrode containing three different enzymes was developed for the determination of l-phenylalanine. This sensor is based on the enzymatic/electrochemical recycling of tyrosinase in combination with salicylate hydroxylase and l-phenylalanine dehydrogenase (PADH). The enzymes salicylate hydroxylase and tyrosinase were coimmobilized first in a carbon paste electrode for the sensitive detection of NADH. The principle of the bienzyme scheme is as follows:  the first enzyme, salicylate hydroxylase, converts salicylate to catechol in the presence of oxygen and NADH. The second enzyme, tyrosinase, then oxidizes the catechol to o-quinone, which is electrochemically detected and reduced back to catechol at the electrode at an E appl = −50 mV vs Ag/AgCl. This results in an amplified signal due to the recycling of the catechol and o-quinone between tyrosinase and the surface of the electrode. Prior to adding PADH, the salicylate hydroxylase−tyrosinase carbon paste electrode was characterized in terms of its sensitivity to NADH, pH dependence, buffer composition, interferences, and stability. Interference from ascorbic acid and uric acid was found to be minimal. Human serum was used to investigate whether this bienzyme system was suitable for the detection of NADH in serum and blood samples. The sensitivity for NADH was increased by a factor of 33 times using the bienzyme amplification scheme (electroreduction of o-quinone at E appl = −50 mV) as opposed to the salicylate hydroxylase single-enzyme system (at which catechol would have been oxidized at E appl = +150 mV vs Ag/AgCl). The detection limit for NADH achieved by the bienzyme carbon paste electrode was 1 vs 100 μM for the single-enzyme carbon paste electrode. The salicylate hydroxylase−tyrosinase system was then coupled with phenylalanine dehydrogenase for l-phenylalanine determination. This multienzyme sensor was able to achieve a linear range of 20−150 μM and a detection limit of 5 μM for l-phenylalanine. The sensitivity is sufficient since the reference clinical range for l-phenylalanine is 78−206 μM.