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dc.contributor.authorKırıcı, Mahinur
dc.contributor.authorAtamanalp, M.
dc.contributor.authorKırıcı, Mahinur
dc.contributor.authorBeydemir, Şükrü
dc.date.accessioned2019-10-18T18:43:18Z
dc.date.available2019-10-18T18:43:18Z
dc.date.issued2017
dc.identifier.issn2519-8521
dc.identifier.issn2520-2588
dc.identifier.urihttps://dx.doi.org/10.15421/021712
dc.identifier.urihttps://hdl.handle.net/11421/10183
dc.descriptionWOS: 000397159400012en_US
dc.description.abstractMany aquatic environmental problems have arisen in consequence of contamination of water by toxic metals and organic pollutants in the present age of technology. Metals play vital roles in enzyme activities and other metabolic events due to their bioaccumulative and nonbiodegradable properties among aquatic pollutants. The aim of this study was to evaluate the inhibitory effects of some metal ions (Ag+, Cu2+, Co2+, Ni2+, Pb2+ and Zn2+) on Capoeta trutta gill and liver glutathione reductase (EC: 1.8.1.7; GR). For this purpose, initially, GR was purified from C. trutta gill and liver. Purification procedure consisted of three steps; preparation of hemolysate, ammonium sulphate precipitation and 2', 5'-ADP Sepharose 4B affinity chromatography. Using this procedure, C. turtta gill GR, having the specific activity of 19.111 EU/mg proteins, was purified with a yield of 38.8% and 910.05-fold; C. trutta liver GR, having the specific activity of 16.167 EU/mg proteins, was purified with a yield of 21.1% and 734.86-fold. The purity of the enzymes was checked on sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) and each purified enzyme showed a single band on the gel. In addition, inhibitory effects of some metal ions (Ag+, Cu2+, Co2+, Ni2+, Pb2+ and Zn2+) on GR from gill and liver were investigated in vitro. Ki constants and IC50 values for metal ions which showed inhibition effects were determined by Lineweaver-Burk graps and plotting activity % vs. [I]. In conclusion, IC50 values for fish gill GR were 0.000625, 0.153, 0.220, 0.247 and 0.216 mM and Ki constants for fish gill GR were 0.00045 +/- 0.00008, 0.128 +/- 0.036, 0.182 +/- 0.138, 0.482 +/- 0.219 and 0.112 +/- 0.047 mM for Ag+, Cu2+, Co2+, Ni2+, Pb2+ and Zn2+, respectively. IC50 values for fish liver GR were 0.000437, 0.217, 0.185, 0.355 and 0.349 mM and Ki constants for fish liver GR were 0.00025 +/- 0.00013, 0.532 +/- 0.146, 0.123 +/- 0.066, 0.093 +/- 0.020 and 0.151 +/- 0.084 mM for Ag+, Cu2+, Co2+, Ni2+, Pb2+ and Zn2+, respectively. In vitro inhibition rank order was determined as Ag+ > Co2+ > Zn2+ > Ni2+ > Pb2+ for fish gill GR; Ag+ > Cu2+ > Co2+ > Pb2+ > Ni2+ for fish liver GR. From these results, we showed that Ag+ metal ion is the most potent inhibitor of GR enzyme on gill and liver tissues.en_US
dc.language.isoengen_US
dc.publisherOles Honchar Dnipropetrovsk Natl Universityen_US
dc.relation.isversionof10.15421/021712en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCapoeta Truttaen_US
dc.subjectGlutathione Reductaseen_US
dc.subjectLiveren_US
dc.subjectGillen_US
dc.subjectMetal Toxicityen_US
dc.titleIn vitro effects of some metal ions on glutathione reductase in the gills and liver of Capoeta truttaen_US
dc.typearticleen_US
dc.relation.journalRegulatory Mechanisms in Biosystemsen_US
dc.contributor.departmentAnadolu Üniversitesien_US
dc.contributor.authorIDKIRICI, Muammer/0000-0003-1888-4388en_US
dc.identifier.volume8en_US
dc.identifier.issue1en_US
dc.identifier.startpage66en_US
dc.identifier.endpage70en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorBeydemir, Şükrü


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