| Literature DB >> 30340682 |
Chieh Lin1, Yung-Cheng Jair2, Yi-Chieh Chou1, Pai-Shan Chen3, Yi-Chun Yeh4.
Abstract
Clinicians require a simple quantitative method for the detection of both phenylalanine and tyrosine to facilitate the diagnosis of phenylketonuria, a common inherited disorder of amino acid metabolism. In this study, we developed a novel whole-cell biosensor for the quantification of phenylalanine and tyrosine through the expression of red and green fluorescent proteins. The proposed system responds specifically and sensitively to phenylalanine/tyrosine without interferences from other amino acids. Furthermore, the precision of the biosensor was evaluated using specimens of normal human urine by LC-MS.Entities:
Keywords: E; Phenylalanine; Phenylketonuria; Tyrosine; coli; tyrR
Mesh:
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Year: 2018 PMID: 30340682 DOI: 10.1016/j.aca.2018.08.053
Source DB: PubMed Journal: Anal Chim Acta ISSN: 0003-2670 Impact factor: 6.558