An enzymatic lysine electrode is developed for the potentiometric analysis of lysine (Lys). This lysine biosensor consists of a chemically immobilized lysine oxidase membrane attached to an all-solid-state ammonium electrode. In this system, the enzymatic degradation of lysine produces ammonia, which is then detected with the ammonium electrode. The influence of immobilization conditions on the potentiometric response and the lifetime of the electrode was studied. Under optimal conditions, the relationship between the potentiometric response and the log [Lys] was linear between 3x10(-5) and 10(-3) M, the sensitivity was 50 mV/decade, the repeatability 1.4%, and the response time t(95%) was 15 s. (C) 1998 Elsevier Science B.V, All rights reserved.
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King Mongkuts Univ Technol North Bangkok, Fac Sci Appl, Dept Ind Chem, Bangkok 10800, Thailand
Chulalongkorn Univ, Petr & Petrochem Coll, Conduct & Electroact Polymers Res Unit, Bangkok 10330, ThailandKing Mongkuts Univ Technol North Bangkok, Fac Sci Appl, Dept Ind Chem, Bangkok 10800, Thailand
Prissanaroon-Ouajai, Walaiporn
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Sirivat, Anuvat
Pigram, Paul J.
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La Trobe Univ, Ctr Mat & Surface Sci, Dept Phys, Bundoora, Vic 3086, AustraliaKing Mongkuts Univ Technol North Bangkok, Fac Sci Appl, Dept Ind Chem, Bangkok 10800, Thailand
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School of Agriculture and Wine Science, Charles Sturt University, Wagga, Wagga NSW 2678, AustraliaSchool of Agriculture and Wine Science, Charles Sturt University, Wagga, Wagga NSW 2678, Australia
Lawal, A.T.
Adeloju, S.B.
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Water and Sensor Research Group, School of Applied Science and Engineering, Monash University, Gippsland Campus, Churchill Vic 3842, AustraliaSchool of Agriculture and Wine Science, Charles Sturt University, Wagga, Wagga NSW 2678, Australia