Purification of carbonic anhydrase from capoeta umbla (Heckel, 1843) gills and toxicological effects of some metals on enzyme activity [Capoeta umbla (Heckel, 1843) solungaç dokusundan karbonik anhidraz enziminin saflaştırılması ve bazı metallerin enzim aktivitesi üzerine toksikolojik etkilerinin İncelenmesi]
Date
2016Author
Kırıcı, M. and Kırıcı, M. and Beydemir, Ş. and Atamanalp, M.
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In this study, in vitroeffects of some metal ions(Fe3+, Cd2+, Pb2+ and Ni2+)on cytoplasmic carbonic anhydrase(CA, EC 4.2.1.1) from Capoeta umbla gill was investigated. CA was purified from the gills of C. umbla for the first time. It was purified with the Sepharose-4B-L-Tyrosine Sulphanilamide affinity chromatography method. The overall purification was approx. 31.69-fold with a yield of 53.33%, and a specific activity of 326.73 EU/mg proteins. Sodium dodecyl sulphate- polyacrylamide gel electrophoresis (SDS-PAGE) showed a single band corresponding to a molecular weight of approx. 29 kDa. The constants of the enzyme inhibitor complex (Ki) and 50% inhibitory values (IC50) for metal ions were determined by Lineweaver-Burk graphs and plotting activity % vs. [I], respectively. The Kiconstants and IC50 values were 0.012±0.0135 and 0.136 mM for Fe3+, 0.019±0.0113 and 0.191 mM for Cd2+, 0.041±0.0075 and 0.289 mM for Pb2+, and 0,120±0.034 and 0.924 mM for Ni2+. It was determined that Fe3+, Cd2+ and Pb2+ inhibited the enzyme competitively while Ni2+ inhibited the enzyme noncompetitively. The potential inhibitor for C. umbla gill CA was found as Fe3+ from these results. © Published by Central Fisheries Research Institute (CFRI) Trabzon, Turkey.
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https://www.scopus.com/inward/record.uri?eid=2-s2.0-84975809647&doi=10.4194%2f1303-2712-v16_1_17&partnerID=40&md5=5b8d711201373aacd7eac0e3ca741721http://acikerisim.bingol.edu.tr/handle/20.500.12898/4704
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