Literature DB >> 877580

Phenylketonuria: a new method for the simultaneous determination of plasma phenylalanine and tyrosine.

R S Shen, C W Abell.   

Abstract

This quantitative spectrophotometric method is based on the conversion of phenylalanine and tyrosine by phenylalanine ammonia-lyase to trans-cinnamic acid and trans-coumaric acid, respectively. Neither deproteinization nor prior incubation of the sample is required, and the entire procedure can be performed in 20 minutes. The method is sensitive to 1-micromolar concentrations of the two compounds, and only 20 microliters of plasma or serum is required to determine both phenylalanine and tyrosine simultaneously. These amino acids were determined between molar ratios (phenylalanine to tyrosine) of 0.1 to 40 in the serum or plasma of healthy individuals and plasma of phenylketonuric patients.

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Year:  1977        PMID: 877580     DOI: 10.1126/science.877580

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  3 in total

1.  hph-1: a mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.

Authors:  V C Bode; J D McDonald; J L Guenet; D Simon
Journal:  Genetics       Date:  1988-02       Impact factor: 4.562

2.  Predicting the phenylalanine blood concentration from urine analyses. An approach to noninvasive monitoring of patients with phenylketonuria.

Authors:  U Langenbeck; F Baum; A Mench-Hoinowski; H Luthe; A W Behbehani
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

3.  Artificial cell-microencapsulated phenylalanine ammonia-lyase.

Authors:  L Bourget; T M Chang
Journal:  Appl Biochem Biotechnol       Date:  1984       Impact factor: 2.926

  3 in total

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