Peroxidase from Catharanthus roseus (L.) G. Don and the biosynthesis of alpha-3 ',4 '-anhydrovinblastine: a specific role for a multifunctional enzyme

• Type: Article in International Scientific Journal
• Date: 2003

Authors

Sottomayor, M (Author) FCUP; Barcelo, AR (Author) Other

Journal

Title: Protoplasma

Vol. 222

Pages: 97-105

ISSN: 0033-183X

Publisher: Springer Nature

Indexing

ISI Web of Knowledge - 38 Citations

Scopus - 49 Citations

Scientific classification

FOS: Natural sciences > Biological sciences

Other information

Authenticus ID: P-000-KJ8

DOI: 10.1007/s00709-003-0003-9

Abstract (EN): We have characterized a basic peroxidase with alpha-3',4'-anhydrovinblastine (AVLB) synthase activity, which was purified from Catharanthus roseus leaves. This enzyme was the single peroxidase isoenzyme detected in C. roseus leaves, and the single AVLB synthase activity detected in C roseus extracts. It was observed that the monomeric substrates of AVLB, vindoline and catharanthine, are both suitable electron donors for the oxidizing intermediates of the basic peroxidase compounds I and II. Results also showed that the reaction proceeds by a radical-propagated mechanism. Substrate specificity studies of the enzyme revealed that it was also able to oxidize several common peroxidase substrates, indicating a broad range of substrate specificity that is characteristic of class III plant peroxidases. Cytochemical studies showed that the enzyme is localized in C. roseus mesophyll vacuoles, in individual spots at the inner surface of the tonoplast. This particular location suggests a meaningful spatial organization that led to the proposal of a metabolic channeling model for the peroxidase-mediated synthesis of AVLB. The importance of this type of mechanism in the regulation of peroxidase isoenzyme functions in vivo is discussed. In view of the results obtained it is concluded that the basic peroxidase present in C. roseus leaves fulfills all the requirements to be considered as an AVLB synthase, and it is proposed that this specific function of this multifunctional enzyme is determined by metabolic channeling resulting from specific protein-protein interactions.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 9