National Changhua University of Education Institutional Repository : Item 987654321/16772
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 6507/11669
造访人次 : 29999918      在线人数 : 390
RC Version 3.2 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 进阶搜寻

jsp.display-item.identifier=請使用永久網址來引用或連結此文件: http://ir.ncue.edu.tw/ir/handle/987654321/16772

题名: Characterization of Fe/Mn-Superoxide Dismutase from Diatom Thallassiosira weissflogii: Cloning, Expression, and Property
作者: Ken, Chuian-Fu;Hsiung, Tung-Ming;Huang, Zong-Xian;Juang, Rong-Huay;Lin, Chi-Tsai
贡献者: 生物學系
关键词: Diatom;Thallassiosira weissflogii;Expression;Cambialistic-superoxide dismutase (Fe/Mn−SOD)
日期: 2005
上传时间: 2013-06-05T08:48:13Z
出版者: American Chemical Society
摘要: A cDNA clone of 1114 bp encoding a putative Mn−superoxide dismutase (Mn−SOD) from diatom Thallassiosira weissflogii was cloned by the PCR technique. Nucleotide sequence analysis of this cDNA clone revealed that it was translated into 201 amino acid residues. When the sequence was compared with Mn−SODs from Vibrio mimicus and Escherichia coli, as well as two Fe−SODs from E. coli and Photobacterium leiognathi, this SOD showed higher homology to Mn−SOD. The amino acid residues required to coordinate the single manganese ion were conserved in all reported Mn−SOD sequences. This cDNA was introduced in an expression vector, pET-20b(+), and transformed into E. coli BL21(DE3)pLysS. The expressed SOD protein was then purified by a His-tag column. The recombinant enzyme was heated at 55 °C with a time-dependent assay; the time interval for 50% inactivation was 23 min, and its thermal inactivation rate constant Kd was 3.03 × 10-2 min-1. The enzyme was inactivated either in acidic pH (below 4.0) or in the presence of imidazole (above 1.6 M) and had only a moderate effect under SDS (above 4%), whereas it was not affected under an alkaline pH (above 9.0). The atomic absorption spectrometric assay showed that 0.6 atom of iron/manganese (3:1) was present in each subunit of SOD. Reconstitution study was suggested that diatom SOD was cambialistic (Fe/Mn)−SOD. The finding of this SOD cDNA could be used for a reference in comparing the differences among marine phytoplankton species and as a probe to detect the transcription level of this enzyme, which can be applied in cosmetics for skin protection or defending unesthetic effects caused by oxygen-containing free radicals.
關聯: J. Agric. Food chem., 53(5): 1470-1474
显示于类别:[生物學系] 期刊論文

文件中的档案:

档案 大小格式浏览次数
index.html0KbHTML625检视/开启


在NCUEIR中所有的数据项都受到原著作权保护.

 


DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈