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研究生: 劉慧屏
Hui Ping Liu
論文名稱: 建構乳酸菌載體及探討基因轉移的方法
Construct lactic acid bacterial vectors and study methods for gene transfer
指導教授: 林志侯
Thy-Hou Lin
口試委員:
學位類別: 碩士
Master
系所名稱: 生命科學暨醫學院 - 分子醫學研究所
Institute of Molecular Medicine
論文出版年: 2008
畢業學年度: 96
語文別: 中文
論文頁數: 86
中文關鍵詞: 乳酸菌電穿孔接合基因槍穿梭載體
外文關鍵詞: Lactobacillus rhamnosus TCELL-1, electroporation, conjugation, gene gun, shuttle vector
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  • 乳酸菌為一種益生菌,在自然界中廣泛地存在。本實驗利用廣域宿主複製源 pAMβ1 和 pUC origin 建構一個可在乳酸菌及大腸桿菌內複製的穿梭載體,並選用兩無帶質體的乳酸菌希望能做為此穿梭載體的宿主,測試結果可在乳酸球菌(Lactococcus lactis MG1363)複製。此外,亦利用此載體探討不同基因轉移方法如 electroporation、conjugation 和 gene gun 對乳酸菌的應用性。結果發現對 MG1363而言,使用 electroporation 或 conjugation 是可以成功的,但在基因槍法上可能受限於粒子大小而不適合太小的菌種。而在所選的乳酸桿菌(Lactobacillus rhamnosus TCELL-1)利用各種方法都沒有很好的結果,此種桿菌難以轉殖成功的原因不明仍有待後續之研究。


    Lactic acid bacterial is a kind of probiotic bacteria and wide exists in nature. In this research, we constructed a vector, pAC, which can exist between Lactic acid bacterial and E.coli. The pAC vector was constructed by using the pAMβ1 replicon and the pUC origin. In my result, pAC can exist in Lactococcus lactis MG1363 but not in Lactobacillus rhamnosus TCELL-1. In addition, we also use the pAC vector to study methods for gene transfer such as electroporation、conjugation and gene gun on the application of lactic acid bacteria. The result shows that electroporation and conjugation methods were successive in MG1363 but not in TCELL-1. And with gene gun method, it may be restricted by the Au or W particle size and not suitable for the species. The reason that TCELL-1 is difficult to be transformed is not known. It will require further study.

    目錄 1 中文摘要 5 Abstract 6 研究動機 7 序論 8 材料方法 17 一、材料 17 1. 本實驗所用到的菌株 17 2. 本實驗所用到的質體 17 3. 本實驗所用到的試劑、培養基 17 二、培養條件 17 三、方法 18 1.質體 DNA抽取 18 2.瓊脂膠電泳分析 20 3.DNA片段回收 21 4.DNA 純度鑑定及定量分析 22 5.聚合□連鎖反應 22 6.DNA 連接反應 23 7.質體的轉形作用 24 8.Conjugation 29 9.Lactic acid bacterial 全 DNA 的抽取 30 10.乳糖代謝測試 32 11.菌種鑑別 32 12.生長曲線測定 33 結果 34 一、乳酸去氫□基因的選殖 34 二、乳酸菌複製源的尋找 34 三、穿梭載體的構築 35 四、重組載體的構築 36 五、不同基因轉移方法在乳酸菌上的應用 36 六、乳糖代謝測試 39 七、菌種鑑別 39 討論 41 表一、本實驗所使用的菌株、培養基及來源 45 表二、本實驗所用到的質體及其來源 46 表三、實驗所使用的菌種和轉殖菌種、特徵、質體大小、由來 47 表四、菌種篩選標記 48 表五、TCELL-1測試過的緩衝液 49 表六、Electroporation 條件 50 表七、Gene gun測試條件 51 圖一:實驗流程圖 52 圖二:Electroporation 示意圖 53 圖三:革蘭氏陰性菌 conjugation示意圖 54 圖四:Gene gun儀器簡略圖及操作示意圖 55 圖五:已構築之 pSA 及pAC map 56 圖六:已構築之 pSA 及 pAC 限制酵素分析 57 圖七:已構築之 pGEL1 及 pGEL2 map 58 圖八:已構築之 pGEL1 及 pGEL2 限制酵素分析 59 圖九:Electroporation 轉型菌株抗性基因確認 60 圖十:Conjugation 轉殖菌株抗性基因確認 61 圖十一:乳糖代謝測試圖 62 圖十二:菌種鑑別 63 圖十三:SEM下Lactobacillus rhamnosus TCELL-1形態 64 圖十四:SEM下Lactococcus lactis MG1363形態 65 圖十五: SEM下0.6 μm 金粒子 66 圖十六: SEM下0.6 μm 金粒子與 DNA 混合後的圖 67 圖十七: SEM下0.6 μm 金粒子與 DNA 混合後的圖 68 圖十八、生長曲線 69 參考文獻 70 附錄 76

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