Abstract
Katalaz, kısmi indirgenmiş oksijen türleri ve H2O2 nin yükseltgen etkisinden dokuların korunmasında önemli rol oynar. Tavuk karaciğer katalazı, (NH4)2SO4 çöktürmesi, etonol-kloroform muamelesi, CM-Selükoz ve Sephadeks G-200 kromotografisi kullanılarak saflaştırıldı. Jel filitrasyon kromotografisi ile tavuk karaciğer katalazının molekül ağırlığı yaklaşık olarak 235000 Da bulundu. SDS-jel elektroforezi sonucu tavuk karaciğer katalazının molekül ağırlığı 57500 Da olarak bulundu ve 4 alt birimden oluştuğu tespit edildi. Spesifik aktivite 55765.5 U/mg olarak saptandı. Hem içeriğinin kabaca ölçülmesini sağlayan A407/A270 oranı 0.52 olarak bulundu. Enzim için Km değeri 100 mM olarak belirlendi. Enzimin 7.0-10.0 aralığında geniş bir pH optimumuna sahip olduğu görüldü. Tavuk karaciğer katalaz enziminin optimum sıcaklığı 25 °C olarak tespit edildi. Saflaştırılmış enzim aktivitesi KCN, NaN3, β-merkaptoetanol, DTT, iyodoasetamit tarafından inhibe edildi, fakat sodyum dietilditiyokarbamatın enzimi inhibe etmediği görüldü.
Keywords
Purification and Partial Characterisation of Catalase from Chicken Liver and the Inhibition Effects of Some Chemicals on the Enzyme Activity
Abstract
Catalase plays a major role in the protection of tissues from oxydizing effects of H2O2 and partially reduced oxygen species. It was purified chicken liver by (NH4)2SO4 precipitation, ethanolchloroform treatment, CM-cellulose and Sephadex G-200 chromatography. The molecular weight of the native chicken liver catalase was estimated by gel filtration to be approximately 235000 Da. SDSgel electrophoresis results indicated that chicken liver catalase consists of four apparently identical sub-units, with a molecular weight of about 57500 Da. The specific activity was found to be 55765,3 U/mg. The optical spectrum of the purified enzyme shows a Soret band at 407 nm which is the characteristic for heme and there was apparent reduction by dithionite. The Km was found to be 100 mM. The maximal activity of the enzyme was observed between pH 7.0 and 10.0. The enzyme has a optimum reaction temperature at 25 °C. The activity of purified catalase was inhibited by azide, cyanide, β-mercaptoethanol, DTT, GSH and iodoacetamide.
Details
| Other ID | JA58SD59HP |
|---|---|
| Journal Section | Research Articles |
| Authors | |
| Publication Date | December 1, 2003 |
| Submission Date | December 1, 2003 |
| Published in Issue | Year 2003 Volume: 1 Issue: 21 |
Cite
Journal Owner: On behalf of Selçuk University Faculty of Science, Rector Prof. Dr. Metin AKSOY
Selcuk University Journal of Science Faculty accepts articles in Turkish and English with original results in basic sciences and other applied sciences. The journal may also include compilations containing current innovations.
It was first published in 1981 as "S.Ü. Fen-Edebiyat Fakültesi Dergisi" and was published under this name until 1984 (Number 1-4).
In 1984, its name was changed to "S.Ü. Fen-Edeb. Fak. Fen Dergisi" and it was published under this name as of the 5th issue.
When the Faculty of Letters and Sciences was separated into the Faculty of Science and the Faculty of Letters with the decision of the Council of Ministers numbered 2008/4344 published in the Official Gazette dated 3 December 2008 and numbered 27073, it has been published as "Selcuk University Journal of Science Faculty" since 2009.
It has been scanned in DergiPark since 2016.
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