Literature DB >> 27504

Use of fluorescamine-labeled casein as a substrate for assay of proteinases.

K Sogawa, K Takahashi.   

Abstract

Conditions have been investigated for the use of fluorescamine-labeled casein as a substrate for fluorometric assay of proteinases. Fluorescamine-labeled casein can be prepared simply by mixing solutions of casein and fluorescamine at pH 8.0 and used without removal of the excess reagent or its hydrolysis product. The fluorescence of the labeled casein and its enzymatic digest is moderately stable in the range of pH 7.0 to 10.0. Activities can be determined by measuring the fluorescence of the hydrolysis products soluble in 0.1 M trichloro acetic acid solution at pH 4.0 after adjusting the pH of the acid-soluble fraction to 7.7. This method is suited for assay of proteinases active at neutral to slightly alkaline pH values, and is capable of quantitating about 0.05 microgram of trypsin or 0.5 microgram of alpha-chymotrypsin or papain. The assay can be done in the presence of large amounts of contaminating amino acid, protein and/or exopeptidases which may interfere with the ordinary assay of proteinases.

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Year:  1978        PMID: 27504     DOI: 10.1093/oxfordjournals.jbchem.a132094

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  7 in total

1.  Monoclonal Antibodies to the Cell-Wall-Associated Proteinase of Lactococcus lactis subsp. cremoris Wg2.

Authors:  H Laan; E J Smid; L de Leij; E Schwander; W N Konings
Journal:  Appl Environ Microbiol       Date:  1988-09       Impact factor: 4.792

2.  Autoproteolysis of the Extracellular Serine Proteinase of Lactococcus lactis subsp. cremoris Wg2.

Authors:  H Laan; W N Konings
Journal:  Appl Environ Microbiol       Date:  1991-09       Impact factor: 4.792

3.  Cell Wall-Associated Proteases of Streptococcus cremoris Wg2.

Authors:  J Hugenholtz; D van Sinderen; J Kok; W N Konings
Journal:  Appl Environ Microbiol       Date:  1987-04       Impact factor: 4.792

4.  Detection of Specific Strains and Variants of Streptococcus cremoris in Mixed Cultures by Immunofluorescence.

Authors:  J Hugenholtz; H Veldkamp; W N Konings
Journal:  Appl Environ Microbiol       Date:  1987-01       Impact factor: 4.792

5.  The Proteolytic Systems of Streptococcus cremoris: an Immunological Analysis.

Authors:  J Hugenholtz; F Exterkate; W N Konings
Journal:  Appl Environ Microbiol       Date:  1984-12       Impact factor: 4.792

6.  Mechanism of Proteinase Release from Lactococcus lactis subsp. cremoris Wg2.

Authors:  H Laan; W N Konings
Journal:  Appl Environ Microbiol       Date:  1989-12       Impact factor: 4.792

7.  Binding of human plasminogen to Borrelia burgdorferi.

Authors:  L T Hu; G Perides; R Noring; M S Klempner
Journal:  Infect Immun       Date:  1995-09       Impact factor: 3.441

  7 in total

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