Please use this identifier to cite or link to this item: http://repositorio.ufc.br/handle/riufc/63380
Type: Artigo de Periódico
Title: Screening of Bothrops snake venoms for L-Amino acid oxidase activity
Authors: Pessatti, Marcos L.
Fontana, José D.
Furtado, Maria F. D.
Guimarães, Manuel F.
Zanette, Lorenzo Roberto Sgobaro
Costa, Walliana
Baron, Madalena
Issue Date: 1995
Publisher: Applied Biochemistry and Biotechnology
Citation: PESSATTI, Marcos L. et al. Screening of Bothrops snake venoms for L-Amino acid oxidase activity. Applied Biochemistry and Biotechnology, [s. l.], v. 51-52, p. 197-210, 1995.
Abstract: Toxins, enzymes, and biologically active peptides are the main components of snake venoms from the genus Bothrops. Following the venom inoculation, the local effects are hemorrhage, edema, and myonecrosis. Nineteen different species of Brazilian Bothrops were screened for protein content and L-amino acid oxidase activity. B. cotiara, formerly found in the South of Brazil, is now threatened with extinction. Its venom contains a highly hemorrhagic fraction and, as expected from the deep yellow color of the corresponding lyophilized powder, a high L-amino acid oxidase CLAO) activity was also characterized. Flavin adenine dinucleotide (FAD) is its associate coenzyme. B. cotiara venom LAO catalyzed the oxidative deamination of several L-amino acids, and the best substrates were methionine, leucine, tryptophan, and phenylalanine, hence, its potential application for the use in biosensors for aspartame .determination and for the removal of amino acids from plasma. High levels for LAO were also found in other species than B. cotiara. In addition, the technique of isoelectric focusing (IEF) was employed as a powerful tool to study the iso- or multienzyme distribution for LAO activity in the B. cotiara snake venom.
URI: http://www.repositorio.ufc.br/handle/riufc/63380
Access Rights: Acesso Aberto
Appears in Collections:DBIO - Artigos publicados em revista científica

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