A kinetic study into the hydrolysis of the ochratoxins and analogues by carboxypeptidase A

Autor: Maria A. Stander, van Der Westhuizen Fh, Steyn Ps, Payne Be
Rok vydání: 2001
Předmět:
Zdroj: Chemical research in toxicology. 14(3)
ISSN: 0893-228X
Popis: The hydrolyses of the ochratoxins and analogues by carboxypeptidase A were assessed. This was done by measuring the amount of phenylalanine formed with liquid chromatography coupled to tandem electrospray mass spectrometry. The kinetic data of ochratoxin A, ochratoxin B, and the synthetic bromo-ochratoxin B were compared to the values of a number of synthesized structure analogues, namely, ochratoxin A methyl ester, ochratoxin B methyl ester, N-(2-hydroxybenzoyl)phenylalanine, N-(5-chloro-2-hydroxybenzoyl)phenylalanine, N-(5-bromo-2-hydroxybenzoyl)phenylalanine, and N-(5-fluoro-2-hydroxybenzoyl)phenylalanine. The halogen-containing analogues had lower turnovers than their des-halo analogues. There are no substantial differences in the kinetic data between the different halogen-containing analogues.
Databáze: OpenAIRE