English  |  正體中文  |  简体中文  |  Items with full text/Total items : 76531/76531 (100%)
Visitors : 29684198      Online Users : 215
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version

    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/6300

    Title: Actinomycetes H12所產轉麩胺酸醯胺基?之生產、特性及加工製程之探討;Production, characterization and procession of transglutaminase produced by Actinomycetes H12
    Authors: 許寶月;Pao-Yueh Hsu
    Contributors: 生命科學研究所
    Keywords: Actinomycetes H12;轉麩胺酸醯胺基酶;鈷六十;Actinomycetes H12;transglutaminase;Co 60
    Date: 2004-01-06
    Issue Date: 2009-09-22 10:17:12 (UTC+8)
    Publisher: 國立中央大學圖書館
    Abstract: 摘要 本研究由50多個土壤樣品中分離出15,000株放線菌,其中以Actinomycetes H12有最高之轉麩胺酸醯胺基酶酵素活性。Actinomycetes H12於最適化液態培養條件下,培養可得轉麩胺酸醯胺基酶產量2.7 U/ml,較原始培養(TSB)條件下之轉麩胺酸醯胺基酶產量提高1.4倍,較S. ladakanum CCRC 12422之轉麩胺酸醯胺基酶高1.8倍,而與日本生產轉麩胺酸醯胺基酶之菌株Streptoverticillium sp. S-8112 產量2.5 U/ml相似。 Actinomycetes H12 之轉麩胺酸醯胺基酶蛋白質特性分析:其最適作用溫度40℃,熱穩定性在50℃下加熱30分鐘仍保有50%活性,最適作用pH 6-8。此轉麩胺酸醯胺基酶活性會受到Cu2+、 Zn2+明顯之抑制,但一價離子、Fe3+與Ca2+則不影響其活性。 Actinomycetes H12發酵槽液態培養至40-48小時,此時其酵素分泌至胞外比率仍低,利用此特性將發酵液高速離心後,可直接回收帶有酵素之菌泥,不經純化下其收率為85%,經冷凍乾燥後其活性不變,但發現有Escherichia coli,因之再輔以Co 60-10kGy照射殺死病原菌及生產菌,然其活性下降至65%,即使照射時加入抗氧化劑(β-carotene, ascorbic acid)亦不能改善提高其殘留活性。 We isolated 15,000 Actinomycetes strains from over 50 soil samples, one isolated strain H12 have the highest TGase activity. The TGase activity (2.7U/ml) under the optimal conditions was about 1.4-fold than the TSB medium condition and 1.8-fold than the TGase from S. ladakanum CCRC 12422, but it is similar to the enzyme from Streptovertecillium sp. S-8112 (2.5 U/ml). The crude TGase from Actinomycetes H12 had the optimum pH and temperature being pH 6-8 and 40℃, respectively. The stable pH range was 5-9 and thermal stability of the crude TGase remained 50% activity after treatment at 50℃ for 30 min. The metal ions, Cu2+ and Zn2+, inhibited the activity of TGase. The addition of monovalence, Fe3+ and Ca2+ did not affect the activity of TGase. When Actinomycetes H12 was cultured on fermentor after 40-48 hr, the extracellular TGase still low. So we centrifuged the culture fluid in a single step and with high yields (85%), then the TGase activity didn’t decrease after freeze-dry. There were contaminants in products, therefore we treatment with Co 60-10 kGy killing germs and Actinomycetes H12, but the enzyme activity is decreased (65%). It didn’t improve to raise the activity, even thought added β-carotene and ascorbic acid.
    Appears in Collections:[生命科學研究所 ] 博碩士論文

    Files in This Item:

    File SizeFormat

    All items in NCUIR are protected by copyright, with all rights reserved.

    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