中大機構典藏-NCU Institutional Repository-提供博碩士論文、考古題、期刊論文、研究計畫等下載:Item 987654321/68197
English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 80990/80990 (100%)
造訪人次 : 41665174      線上人數 : 1530
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧:
  • 您可在西文檢索詞彙前後加上"雙引號",以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋,建議至進階搜尋限定作者欄位,可獲得較完整資料
  • 進階搜尋


    請使用永久網址來引用或連結此文件: http://ir.lib.ncu.edu.tw/handle/987654321/68197


    題名: 硫化屬古生菌中的酮醇酸還原異構酶結構分析;Structural analysis of ketol-acid reductoisomerase from Sulfolobus solfataricus
    作者: 汪致霖;Wang,Chih-lin
    貢獻者: 生命科學系
    關鍵詞: 酮醇酸還原異構酶;硫化屬古生菌;蛋白質結構;Sulfolobus solfataricus;ketol-acid reductoisomerase;Structural analysis
    日期: 2015-08-25
    上傳時間: 2015-09-23 10:53:02 (UTC+8)
    出版者: 國立中央大學
    摘要: 酮醇酸還原異構酶可以在植物、真菌和細菌體內找到,而動物體內則沒有此酵素存在。酮醇酸還原異構酶可以應用在產生支鏈形胺基酸、生質能源以及除草劑。酮醇酸還原異構酶是支鏈形胺基酸生合成反應第二個反應的酵素,可以將乙酰乳酸轉變成2,3-二羥基異戊酸。此轉變過程包含了兩個反應,先依靠鎂離子將烷基轉移,之後在消耗菸鹼醯胺腺嘌呤二核苷酸磷酸(NADPH)還原兩個酮基。我們發現硫化屬古生菌(Sulfolobus solfataricus)中具有三個酮醇酸還原異構酶,分別是酮醇酸還原異構酶-1、酮醇酸還原異構酶-2和酮醇酸還原異構酶-3。這三個酮醇酸還原異構酶的基因序列之間並不完全相同,但是具有相同屬於酮醇酸還原異構酶的保守基因,且尚未了解其在生物體內分別的作用。在我的研究中,以大腸桿菌BL21(DE3)來大量表現酮醇酸還原異構酶-3,並利用快速蛋白質液相層析系統純化此蛋白質,我們發現酮醇酸還原異構酶-3在溶液中是以十二聚體的形式存在,並成功得到此十二聚體蛋白質的晶體,但晶體繞射訊號不佳。因此我們從電顯影像中,利用單分子重建法得到此十二聚體的三維平均結構,並用模擬的原子結構模型代入三維平均結構,嘗試以此方法來預測其四級結構組成,我們發現以單分子三維重構法重建出的酮醇酸還原異構酶-3結構與同一類的酮醇酸還原異構酶非常相似,在未來我們希望利用這個模擬的原子結構來探究其功能。;Ketol-acid reductoisomerase (KARI) enzyme which is found in plants, fungi and bacteria but not in animals has attracted much interest for production of amino acids, biofuels and development of antimicrobial agents. The KARI is the second enzyme in the branched-chain amino acid biosynthesis pathway, which conversion of 2-acetolactate into 2,3-dihydroxyisovalerate. The conversion involves an Mg2+-dependent alkyl migration followed by a Nicotinamide adenine dinucleotide phosphate (NADPH)-dependent reduction of the 2-keto group. We have found that there are three homologs, IlvC1, IlvC2 and IlvC3 from sulfolobus solfataricus. The amino acid sequences of these three KARIs possess conserved regions despite they are not highly similar to one another and their function in vivo is not clear. In my study, ilvc3 were overexpressed in E. coli BL21 (DE3) and purified by FPLC. The ilvc3 was a dodecamer in solution with molecular weight ~450 kDa. We successfully found the condition of crystallize, however the diffraction of ilvc3 crystal was poor. Therefore, we built a 3D map of Ilvc3 by single particle 3D reconstruction atomic model, which could help us to determine the quaternary structure. It was discovered that the modeling structure of ilvc3 was similar to the other KARI in different species. In future, we attempt to study the function by the modeling atomic structure.
    顯示於類別:[生命科學研究所 ] 博碩士論文

    文件中的檔案:

    檔案 描述 大小格式瀏覽次數
    index.html0KbHTML470檢視/開啟


    在NCUIR中所有的資料項目都受到原著作權保護.

    社群 sharing

    ::: Copyright National Central University. | 國立中央大學圖書館版權所有 | 收藏本站 | 設為首頁 | 最佳瀏覽畫面: 1024*768 | 建站日期:8-24-2009 :::
    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 隱私權政策聲明