博碩士論文 87622003 完整後設資料紀錄

DC 欄位 語言
DC.contributor生命科學系zh_TW
DC.creator曾季清zh_TW
DC.creatorChih-Ching Tsengen_US
dc.date.accessioned2000-7-18T07:39:07Z
dc.date.available2000-7-18T07:39:07Z
dc.date.issued2000
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=87622003
dc.contributor.department生命科學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract本研究首先利用聚合?鏈鎖反應(PCR)的方式成功的篩選出大腸桿菌(Escherichia coli B strain CCRC 12567)之酸性磷酸?基因,其長度為1237 bp;接著將該基因送入大腸桿菌之蛋白質表現系統(pET system),並證明所篩選出之基因的確能轉譯成具有能夠分解抗營養因子植酸之酵素。 然後將酸性磷酸?基因與穿梭載體pGIT032重新構築後,以電穿孔(electroporation)將此重組載體送入Lactobacillus plantarum CCRC 10069、Lactobacillus casei subsp. rhamnosus GG、Lactobacillus casei Shirota等三種不同乳酸菌。結果顯示轉殖後之菌種胞內酵素活性表現以Lactobacillus casei subsp. rhamnosus GG轉殖株之植酸?表現最高,達未轉殖單一宿主菌株之62.4倍,而Lactobacillus casei Shirota之轉殖株之植酸?表現亦分別為2倍,但Lactobacillus plantarum的活性幾乎與對照菌株相同。 最後將此三種轉殖菌株進行模擬體內消化道環境酸度、膽鹽耐受性試驗。在酸度耐受性試驗方面,三種轉殖株經pH 2.0之Rogosa and Sharpe(MRS)處理、培養後均不生長;但經pH 3.0處理後,任一轉殖菌均發現當酸度處理時間愈長,其菌液於培養皿內培養後之生成菌落數愈少。此外,三種菌轉殖株均不具0.3和0.5%Oxygall膽鹽之耐受性。zh_TW
dc.description.abstractThe acid phosphatase gene of Escherichia coli B strain was cloned using polymerase chain reaction (PCR) technique. Subsequently, the gene was transferred into pET expression system using BL21 cells as host. The recombinant Escherichia coli successfully expressed fused protein affirmatively carrying phytase activity. The same gene was set to transform the Lactobacillus using shuttle vector pGIT032. After the recombinant vector was constructed, it was transferred to Lactobacillus plantarum, Lactobacillus casei subsp. rhamnosus GG and Lactobacillus casei Shirita using electroporation technique. The results showed the intracellular phytase activity of the transformants of Lactobacillus casei subsp. rhamnosus GG increased 62.4 times and Lactobacillus casei Shirita increased 2 times while Lactobacillus plantarum remained unchanged. All three different transformed Lactobacillus were subjected to simulation tests for gastrointestinal tract in animals including acid tolerance and bile-salt tolerance. In pH 2.0, all three showed no tolerance. In pH 3.0, the tolerance decreased as the incubation time increased. Furthermore, no tolerance was observed in the treatments by bile salt of 0.3 and 0.5% of Oxygall.en_US
DC.subject大腸桿菌zh_TW
DC.subject酸性磷酸zh_TW
DC.subject電穿孔zh_TW
DC.subject植酸酵素zh_TW
DC.subject乳酸菌zh_TW
DC.subjectEscherichia colien_US
DC.subjectacid phosphataseen_US
DC.subjectelectroporationen_US
DC.subjectphytaseen_US
DC.subjectLactobacillusen_US
DC.title利用乳酸菌表達大腸桿菌之酸性磷酸zh_TW
dc.language.isozh-TWzh-TW
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

若有論文相關問題,請聯絡國立中央大學圖書館推廣服務組 TEL:(03)422-7151轉57407,或E-mail聯絡  - 隱私權政策聲明