Determination of Some Flavonoid Derivatives Inhibitory Effect on Bovine Milk Lactoperoxidase Enzyme
Öz
Peroxidases (PODs) are a group of enzymes that are commonly found in bacteria, fungi, plants and animals and have important uses in the food, pharmaceutical industry and clinical diagnostics. Lactoperoxidase (LPO) enzyme, which is included in peroxidase enzyme class, is found milk, saliva and tears in mammals. With thiocyanate and hydrogen peroxide, it forms one of the body's defense systems against infections. Flavonoid derivatives are abundant in plants and constitute an important part of the diet. These derivatives, which are produced synthetically or naturally, have many pharmacological activities. In this study, the effect of some flavonoid derivatives (5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4H-chromen-4-one (a), 3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one (b), 7-Hydroxy-4'-nitroisoflavone (c), 6-Fluoroflavone (d), 7-Hydroxy-3-(4-methoxyphenyl)-4H-chromen-4-one (e), 7-Methoxy-2-phenyl-4H-chromen-4-one (f)) on the lactoperoxidase enzyme was investigated. Firstly, by using Sepharose-4B-L-tyrosine-sulfanilamide affinity chromatography, the LPO enzyme was purified 65 fold (with a yield of 23%) from bovine milk and kinetic studies were carried out with flavonoid derivatives using this enzyme. The Ki values of six molecules were found in ranging from 7.85 µM to 0.023 μM. 6-Fluoroflavone was the most effective inhibitor with Ki value of 0.023 μM.
Anahtar Kelimeler
Kaynakça
- Galende, P.P., et al., Purification and structural stability of white Spanish broom (Cytisus multiflorus) peroxidase. 2015. 72: p. 718-723.
- Thomas, E.J.P.i.c. and biology, Lactoperoxidase: structure and catalytic properties. 1991. 1: p. 123-142.
- Naidu, A., Lactoperoxidase, in Natural food antimicrobial systems. 2000, CRC Press. p. 116-145.
- Koes, R., W. Verweij, and F.J.T.i.p.s. Quattrocchio, Flavonoids: a colorful model for the regulation and evolution of biochemical pathways. 2005. 10(5): p. 236-242.
- Li, R.-S., et al., Design, synthesis and evaluation of flavonoid derivatives as potential multifunctional acetylcholinesterase inhibitors against Alzheimer’s disease. 2013. 23(9): p. 2636-2641.
- Birt, D.F. and E. Jeffery, Flavonoids. Advances in Nutrition, 2013. 4(5): p. 576-577.
- Hoensch, H.P. and R.J.W.j.o.g.o. Oertel, Emerging role of bioflavonoids in gastroenterology: Especially their effects on intestinal neoplasia. 2011. 3(5): p. 71.
- Haenen, G.R. and A. Bast, [50] Nitric oxide radical scavenging of flavonoids, in Methods in enzymology. 1999, Elsevier. p. 490-503.
Ayrıntılar
Birincil Dil
İngilizce
Konular
-
Bölüm
Araştırma Makalesi
Yazarlar
Aykut Öztekin
*
0000-0003-1418-179X
Türkiye
Yayımlanma Tarihi
16 Mayıs 2019
Gönderilme Tarihi
13 Şubat 2019
Kabul Tarihi
30 Mart 2019
Yayımlandığı Sayı
Yıl 2019 Cilt: 4 Sayı: 1