Glutathione transferase isoenzymes from Bufo bufo embryos at an early developmental stage

Author:

Di Ilio C1,Aceto A1,Bucciarelli T1,Dragani B1,Angelucci S1,Miranda M2,Poma A2,Amicarelli F2,Barra D3,Federici G4

Affiliation:

1. Istituto di Scienze Biochimiche Facolta' di Medicina, Università ‘G. D'Annunzio’, Chieti, Italy

2. Dipartimento di Biologia e Fisiologia Cellulare Università dell'Aquila, L'Aquila, Italy

3. Dipartimento di Scienze Biochimiche e Centro di Biologia Molecolare del Consiglio Nazionale delle Ricerche, Università di Roma ‘La Sapienza’, Roma, Italy

4. Dipartimento di Biologia, Università di Roma ‘Tor Vergata’, Roma, Italy

Abstract

Six forms of glutathione transferase (GST) were resolved from the cytosolic fraction of Bufo bufo embryos at developmental stage 4 by GSH-Sepharose affinity chromatography followed by f.p.l.c. chromatofocusing in the 9-6 pH range. They have apparent isoelectric points at pH 8.37 (GST I), 8.22 (GST II), 8.10 (GST III), 7.84 (GST IV), 7.37 (GST V) and 7.12 (GST VI), and each displayed an apparent subunit molecular mass of 23 kDa by SDS/PAGE. The Bufo bufo embryo enzymes showed very similar structural, catalytic and immunological properties, as indicated by their substrate-specificities, inhibition characteristics, c.d. spectra, h.p.l.c. elution profiles and immunological reactivities, as well as by their N-terminal amino acid sequences. Although Bufo bufo embryo GSTs do not correspond to any other known GSTs, the results of our experiments indicate that amphibian GSTs could be included in the Pi family of GSTs. This conclusion is supported by the analysis of c.d. spectra, and by the fact that mammalian Pi class GSTs and amphibian GSTs showed about 80% identity in their N-terminal amino acid sequences. Furthermore, antisera prepared against Bufo bufo GST III cross-reacted in immunoblotting analysis with Pi class GSTs, and vice versa.

Publisher

Portland Press Ltd.

Subject

Cell Biology,Molecular Biology,Biochemistry

Cited by 30 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Bioconcentration and metabolism of pesticides and industrial chemicals in the frog;Journal of Pesticide Science;2014

2. Marine Glutathione S-Transferases;Marine Biotechnology;2007-08-09

3. Uptake and Effects on Detoxication Enzymes of Cypermethrin in Embryos and Tadpoles of Amphibians;Archives of Environmental Contamination and Toxicology;2004-10

4. Molecular cloning, expression and characterization of glutathione S-transferase from Mytilus edulis;Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology;2004-10

5. Amphibian transition to the oxidant terrestrial environment affects the expression of glutathione S-transferases isoenzymatic pattern;Biochimica et Biophysica Acta (BBA) - Molecular Cell Research;2004-05

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3