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Amperometric bienzyme screen-printed biosensor for the determination of leucine.
Labroo, Pratima; Cui, Yue.
Afiliação
  • Labroo P; Department of Biological Engineering, Utah State University, Logan, UT, 84322, USA.
Anal Bioanal Chem ; 406(1): 367-72, 2014 Jan.
Article em En | MEDLINE | ID: mdl-24220759
ABSTRACT
Leucine plays an important role in protein synthesis, brain functions, building muscle mass, and helping the body when it undergoes stress. Here, we report a new amperometric bienzyme screen-printed biosensor for the determination of leucine, by coimmobilizing p-hydroxybenzoate hydroxylase (HBH) and leucine dehydrogenase (LDH) on a screen-printed electrode with NADP(+) and p-hydroxybenzoate as the cofactors. The detection principle of the sensor is that LDH catalyzes the specific dehydrogenation of leucine by using NADP(+) as a cofactor. The product, NADPH, triggers the hydroxylation of p-hydroxybenzoate by HBH in the presence of oxygen to produce 3,4-dihydroxybenzoate, which results in a change in electron concentration at the working carbon electrode, which is detected by the potentiostat. The sensor shows a linear detection range between 10 and 600 µM with a detection limit of 2 µM. The response is reproducible and has a fast measuring time of 5-10 s after the addition of a given concentration of leucine.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Leucina Desidrogenase / 4-Hidroxibenzoato-3-Mono-Oxigenase / Leucina Limite: Humans Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Técnicas Biossensoriais / Leucina Desidrogenase / 4-Hidroxibenzoato-3-Mono-Oxigenase / Leucina Limite: Humans Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos