Kaya E.D.Söyüt H.Beydemir T.20.04.20192019-04-2020.04.20192019-04-2020131382-6689https://dx.doi.org/10.1016/j.etap.2013.05.019https://hdl.handle.net/20.500.12403/849Many studies have shown that metal ions may lead to oxidative stress in biological systems. Accordingly, DNA damage, protein modification, enzyme inhibition and activation, lipid peroxidation and many other effects may occur in living organisms. Many different formations of metal ions may enter human cells along with water, air, and various foods, and humans are negatively affected by these conditions, either directly or indirectly. These effects may cause irreversible damage to human metabolism. In this study, the toxicological effects of heavy metals on carbonic anhydrase enzyme activity from the gilthead sea bream liver were investigated. The carbonic anhydrase enzyme was purified via affinity chromatography and had a specific activity of 6775.5EUmg-1. The kinetics and characteristic properties, such as optimum pH, stable pH, optimum temperature, activation energy (Ea), activation enthalpy (?H), Q10, Km, and Vmax, were determined for the purified enzyme SDS-polyacrylamide gel electrophoresis showed a single band and molecular weight of the subunit was approximately 25kDa. Cd(II), Cu(II), Ni(II) and Ag(I) inhibited the enzyme activity in vitro. The type of inhibition and Ki values for these metals were calculated from Lineweaver-Burk plots as 17.74mM, 36.20mM, 12.85mM and 0.025mM for Cd(II), Cu(II), Ni(II) and Ag(I), respectively. All the metals were noncompetitive inhibitors. © 2013 The Authors.eninfo:eu-repo/semantics/openAccessCarbonic anhydraseFishHeavy metalsInhibitionLivercadmiumcarbonate dehydratasecopperheavy metalnickelsilveraffinity chromatographyanimal tissuearticlecontrolled studyenergyenthalpyenzyme activityenzyme analysisenzyme kineticsenzyme purificationenzyme stabilityheavy metal poisoningin vitro studylivermolecular weightnonhumanoxidative stresspH measurementpollutionpolyacrylamide gel electrophoresispriority journalSparus auratatemperature measurementCAcarbonic anhydraseCarbonic anhydraseFishHeavy metalsInhibitionLivermolecular weightMWrainbow troutRTSDS-PAGEsodium dodecyl sulfate polyacrylamide gel electrophoresisAnimalsCarbonic Anhydrase InhibitorsCarbonic AnhydrasesChromatography, AffinityDose-Response Relationship, DrugFish ProteinsKineticsLiverMetals, HeavyModels, BiologicalSea BreamWater Pollutants, ChemicalArchosargus rhomboidalisSparus aurataCarbonic anhydraseFishHeavy metalsInhibitionLivercadmiumcarbonate dehydratasecopperheavy metalnickelsilveraffinity chromatographyanimal tissuearticlecontrolled studyenergyenthalpyenzyme activityenzyme analysisenzyme kineticsenzyme purificationenzyme stabilityheavy metal poisoningin vitro studylivermolecular weightnonhumanoxidative stresspH measurementpollutionpolyacrylamide gel electrophoresispriority journalSparus auratatemperature measurementCAcarbonic anhydraseCarbonic anhydraseFishHeavy metalsInhibitionLivermolecular weightMWrainbow troutRTSDS-PAGEsodium dodecyl sulfate polyacrylamide gel electrophoresisAnimalsCarbonic Anhydrase InhibitorsCarbonic AnhydrasesChromatography, AffinityDose-Response Relationship, DrugFish ProteinsKineticsLiverMetals, HeavyModels, BiologicalSea BreamWater Pollutants, ChemicalArchosargus rhomboidalisSparus aurataArticle36251452110.1016/j.etap.2013.05.019238111082-s2.0-84879768228N/AWOS:000324082900031Q2