Artigo Revisado por pares

Optimisation of a coupled enzymatic assay of glutathione peroxidase activity in bovine milk and whey

2000; Elsevier BV; Volume: 10; Issue: 5-6 Linguagem: Inglês

10.1016/s0958-6946(00)00057-1

ISSN

1879-0143

Autores

J Chen, Helena Lindmark‐Månsson, B. Åkesson,

Tópico(s)

Garlic and Onion Studies

Resumo

Glutathione peroxidase (GSHPx) may have important functions in milk but studies of its activity during dairy processing are hampered by the lack of suitable assays. Thus, a coupled enzymatic assay of GSHPx activity was developed for bovine milk and whey. The reaction mixture contained reduced glutathione, tert-butylhydroperoxide, glutathione reductase and NADPH in phosphate buffer. The effect of reaction conditions on enzymatic and non-enzymatic NADPH consumption was studied, and blanks without added GSHPx sample or complete incubations containing 4 mmol L−1 mercaptosuccinate as an inhibitor of GSHPx were used. With increasing pH and glutathione concentration the reaction rates increased both in the complete incubation and the blank but optimal GSHPx activity was attained at a glutathione concentration of 0.63 mmol L−1. A pH of 7.6 was chosen to attain near-optimal activity without reaching high blanks. Application of the new procedure showed that bulk whey samples had rather constant GSHPx activity with an average (SD) of 36.1 (2.9) U mL−1, but whey samples prepared from individual cows showed a two-fold variation (range 24.5–50.6 U mL−1). The procedure described was more reproducible and precise than previous methods and will be employed in further studies of dairy products.

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