利用乳酸菌表達大腸桿菌之酸性磷酸

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Title:	利用乳酸菌表達大腸桿菌之酸性磷酸
Authors:	曾季清;Chih-Ching Tseng
Contributors:	生命科學研究所
Keywords:	大腸桿菌;酸性磷酸;電穿孔;植酸酵素;乳酸菌;Escherichia coli;acid phosphatase;electroporation;phytase;Lactobacillus
Date:	2000-07-18
Issue Date:	2009-09-22 10:15:54 (UTC+8)
Publisher:	國立中央大學圖書館
Abstract:	本研究藉由基因重組技術，將植酸?與乳酸菌二者相結合，欲促使乳酸菌群在動物體內多了一項代謝植酸的功能，希望藉此能幫助加強宿主動物營養份吸收，並間接達到減少以植酸的形式隨動物體的排遺排出體外之無機磷所造成的環境污染問題。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。 In this study, an acid phosphatase gene coding for phytase activity was obtained from Escherichia coli B strain and transferred to several species of Lactobacillus using recombinant technology. This process was expected to provide the increase of nutrient absorption and decrease of phytates excretion for the animals that harbor these genetically engineered bacteria carrying extra phytase activity. The 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.
Appears in Collections:	[Graduate Institute of Life Science] Electronic Thesis & Dissertation

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