Literature DB >> 6508735

Kinetic analysis of chemical reactions coupled to an enzymic step. Application to acid phosphatase assay with Fast Red.

J Escribano, F García-Carmona, F García-Cánovas, J L Iborra, J A Lozano.   

Abstract

Acid phosphatase assay with alpha-naphthyl phosphate as substrate and the use of diazonium salt (Fast Red TR) for chromophore formation was kinetically analysed as a system of two chemical reactions coupled to an enzymic reaction. This system follows a mechanism defined as enzymic-chemical-chemical (EzCC). The accumulation of chromophore with reaction time presented a marked lag period, which was only dependent on the rate constants of the chemical reactions and was independent of the enzymic step. The specific rate constants of each chemical step were determined in 3.8-5.0 pH and 10-35 degrees C temperature ranges. Thermodynamic parameters of the chemical steps were also obtained. Measurement of acid phosphatase activity can be carried out in the pH range 3.8-5.0 (4.8 was optimal pH) without the need to eliminate the lag period.

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Year:  1984        PMID: 6508735      PMCID: PMC1144346          DOI: 10.1042/bj2230633

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  13 in total

1.  An automated continuous-monitoring procedure for the determination of acid phosphatase activity in serum.

Authors:  R J Warren; D W Moss
Journal:  Clin Chim Acta       Date:  1977-06-01       Impact factor: 3.786

2.  A rapid assay for catechol oxidase and lactase using 2-nitro-5-thiobenzoic acid.

Authors:  H Esterbauer; E Schwarzl; M Hayn
Journal:  Anal Biochem       Date:  1977-02       Impact factor: 3.365

3.  An optimized continuous-monitoring procedure for semiautomated determination of serum acid phosphatase activity.

Authors:  R Bais; J B Edwards
Journal:  Clin Chem       Date:  1976-12       Impact factor: 8.327

4.  A new and rapid colorimetric determination of acetylcholinesterase activity.

Authors:  G L ELLMAN; K D COURTNEY; V ANDRES; R M FEATHER-STONE
Journal:  Biochem Pharmacol       Date:  1961-07       Impact factor: 5.858

5.  [Continuous photometric measurement of prostate acid phosphatase activity].

Authors:  G Hillmann
Journal:  Z Klin Chem Klin Biochem       Date:  1971-05

6.  A generalized theory of the transition time for sequential enzyme reactions.

Authors:  J S Easterby
Journal:  Biochem J       Date:  1981-10-01       Impact factor: 3.857

7.  [Coupling of 1-naphthol with fast-red-TR. Studies on the optimization of a continuous determination of acid phosphatase, I. (author's transl)].

Authors:  G Gundlach; B Mühlhausen
Journal:  J Clin Chem Clin Biochem       Date:  1980-10

8.  The steady-state kinetics of peroxidase with 2,2'-azino-di-(3-ethyl-benzthiazoline-6-sulphonic acid) as chromogen.

Authors:  R E Childs; W G Bardsley
Journal:  Biochem J       Date:  1975-01       Impact factor: 3.857

9.  Interference with the kinetic determination of acid phosphatase.

Authors:  G T Sanders; P Serné; F J Hoek
Journal:  Clin Chim Acta       Date:  1978-11-01       Impact factor: 3.786

10.  The metabolic pathway catalyzed by the tyrosinase of Agaricus bisporus.

Authors:  K Boekelheide; D G Graham; P D Mize; P W Jeffs
Journal:  J Biol Chem       Date:  1980-05-25       Impact factor: 5.157

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  2 in total

1.  A kinetic study of the suicide inactivation of an enzyme measured through coupling reactions. Application to the suicide inactivation of tyrosinase.

Authors:  J Escribano; J Tudela; F Garcia-Carmona; F Garcia-Canovas
Journal:  Biochem J       Date:  1989-09-01       Impact factor: 3.857

2.  A kinetic study of hypoxanthine oxidation by milk xanthine oxidase.

Authors:  J Escribano; F Garcia-Canovas; F Garcia-Carmona
Journal:  Biochem J       Date:  1988-09-15       Impact factor: 3.857

  2 in total

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