Herein we report the development of a direct and continuous spectrophotometric method for determining transglutaminase (TGase) activity by using N,Ndimethyl-1,4-phenylenediamine (DMPDA) as a ␥-glutamyl acceptor substrate and carbobenzyloxy-Lglutamylglycine (Z-Gln-Gly) as a typical peptide ␥-glutamyl
Continuous spectrophotometric assay of pantetheinase activity
✍ Scribed by Silvestro Duprè; Roberta Chiaraluce; Mirella Nardini; Carlo Cannella; Giorgio Ricci; Doriano Cavallini
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 539 KB
- Volume
- 142
- Category
- Article
- ISSN
- 0003-2697
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✦ Synopsis
A continuous spectrophotometric assay for pantetheinase determination using S-pantetheine-3-pyruvate as substrate is described. The enzymatic hydrolysis of this new substrate leads to the formation of S-cysteamine-3-pyruvate, which cyclizes in a non-rate-limiting step to give 2H-1 +thiazin-5,6dihydro-3-carboxylic acid (aminoethylcysteine ketimine), a compound exhibiting a strong absorption at 296 nm. The assay is optimized with respect to pH, buffer, and substrate concentration. Prereduction of the enzyme and some properties of the reaction are also studied. The assay is simple, rapid, very sensitive, and specific. Q 1984 Academic mess, IX
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