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  1. NTU Theses and Dissertations Repository
  2. 生物資源暨農學院
  3. 園藝暨景觀學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/41338
完整後設資料紀錄
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dc.contributor.advisor許明仁
dc.contributor.authorWei-Zhu Shien
dc.contributor.author施瑋筑zh_TW
dc.date.accessioned2021-06-15T00:16:08Z-
dc.date.available2011-06-23
dc.date.copyright2009-06-23
dc.date.issued2009
dc.date.submitted2009-06-08
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/41338-
dc.description.abstract檄樹 (Morinda citrifolia L.) 又名諾麗 (noni),其果實之發酵屬於自然發酵,過程中並未額外添加菌酛。然而,對於諾麗果於發酵過程中的菌相變化至今尚未有文獻報告。因此,本篇研究擬同時應用目前可探知最完整菌群結構之方法— PCR-DGGE 分子生物技術及傳統培養技術進行鑑定,以了解諾麗果實於發酵過程中菌群之結構及其變化情況,並比較兩種鑑定方法之間的差異性。此外,亦同時進行一般成分的分析,以期能夠了解菌相和成分變化之間的關聯性。
由結果發現,諾麗果於未發酵時之 pH 值、可溶性固形物含量、可滴定酸含量,分別於 4.67、5.9 °Brix、0.3% 左右;經發酵八週後則分別維持在 3.6-4.0、4.8-5.2 °Brix、1.0-1.3%之間。諾麗果中乳酸、醋酸、酒精皆於發酵第三天時開始產生,分別於第 14、24、21 天時達到最高峰:0.215、1.767、6.290 g/L。發酵八週後則分別維持在:0.1-0.2、1.6、5.0-5.5 g/L 之間。此外,諾麗果於發酵過程中總生菌數、乳酸菌數、總真菌數皆於發酵第一週時達到最高峰,菌數維持在106 CFU/mL 左右。第 2 至 7 週處於恆定期,菌數維持在 105 CFU/mL 左右。在進入第 8 週後,菌數則開始大幅下降至 103 CFU/mL 左右,之後則維持恆定。
由鑑定結果發現,諾麗果發酵期間細菌部份是以醋酸菌為主,可能的菌屬有:Swaminathamia、Acetobacter、Acidomonas、Gluconobacter、Gluconacetobacter、Asaia、Kozakia 共七種,其中又以 Acetobacter 為主導發酵的菌屬。且並不是由單幾株菌主導發酵,而是由許多不同種的 Acetobacter 一起共同進行發酵作用。
關鍵字:諾麗果、菌相、PCR-DGGE、醋酸菌Acetobacter
zh_TW
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Previous issue date: 2009
en
dc.description.tableofcontents誌謝………………………………………………………………………I
中文摘要…………………………………………………………………II
英文摘要………………………………………………………………III
目錄……………………………………………………………………IV
圖次……………………………………………………………………VII
表次……………………………………………………………………IX
壹、前言…………………………………………………………………1
貳、文獻回顧……………………………………………………………3
一、諾麗果……………………………………………………………3
(一) 諾麗果簡介……………………………………………………3
(二) 諾麗果加工製品………………………………………………3
(三) 諾麗果汁之營養成分…………………………………………4
(四) 諾麗果汁之發酵………………………………………………9
二、傳統微生物分類與鑑定…………………………………………13
(一) 發展背景………………………………………………………13
(二) 傳統細菌分類與鑑定系統……………………………………13
(三) 限制與瓶頸……………………………………………………15
三、分子生物技術於微生物分類與鑑定之發展……………………16
(一) 發展背景………………………………………………………16
(二) 發展現況簡介…………………………………………………16
四、利用 PCR-DGGE 技術應用於食品微生物菌群結構的探討……17
(一) 16S rDNA 在細菌分類與鑑定上的獨特性及應用……………17
(二) 聚合酶連鎖反應………………………………………………19
(三) 變性梯度膠體電泳……………………………………………22
參、材料與方法………………………………………………………29
一、實驗架構…………………………………………………………29
二、實驗材料…………………………………………………………30
(一) 諾麗果原料……………………………………………………30
(二) 藥品……………………………………………………………30
(三) 儀器設備………………………………………………………32
三、實驗方法…………………………………………………………33
(一) 原料前處理……………………………………………………33
(二) 八週發酵………………………………………………………33
(三) 分析樣品製備…………………………………………………34
(四) 傳統培養菌相分析……………………………………………34
(五) PCR-DGGE菌相分析……………………………………………35
(六) 一般成分分析…………………………………………………47
肆、結果與討論………………………………………………………54
一、傳統培養菌相分析………………………………………………54
二、一般成分分析……………………………………………………57
(一) pH 值之變化…………………………………………………57
(二) 可溶性固形物之變化…………………………………………60
(三) 可滴定酸之變化………………………………………………63
(四) 乳酸含量之變化………………………………………………67
(五) 醋酸含量之變化………………………………………………69
(六) 酒精含量之變化………………………………………………72
三、PCR-DGGE菌相分析………………………………………………75
(一) 微生物 genomic DNA 萃取結果……………………………75
(二) 16S rDNA 之 PCR 條件確立及反應結果……………………78
(三) 垂直 DGGE 電泳圖譜結果……………………………………85
(四) 水平 DGGE 電泳圖譜結果……………………………………88
(五) 16S rDNA V3 region 序列比對與分析結果………………96
(六) 綜合討論……………………………………………………110
伍、結論………………………………………………………………115
陸、參考文獻…………………………………………………………116
柒、附錄………………………………………………………………124
dc.language.isozh-TW
dc.subject醋酸菌Acetobacterzh_TW
dc.subject諾麗果zh_TW
dc.subject菌相zh_TW
dc.subjectPCR-DGGEzh_TW
dc.subjectMicrofloraen
dc.subjectMorinda citrifoliaen
dc.subjectAcetobacteren
dc.subjectPCR-DGGEen
dc.title檄樹果實自然發酵過程中菌相與果汁成分變化之研究zh_TW
dc.titleStudies on the Changes of Microflora and Chemical Constituents in the Noni (Morinda citrifolia L.) Fruit Juices during Natural Fruit Fermentation.en
dc.typeThesis
dc.date.schoolyear97-2
dc.description.degree碩士
dc.contributor.coadvisor曾文聖
dc.contributor.oralexamcommittee徐源泰
dc.subject.keyword諾麗果,菌相,PCR-DGGE,醋酸菌Acetobacter,zh_TW
dc.subject.keywordMorinda citrifolia,Microflora,PCR-DGGE,Acetobacter,en
dc.relation.page129
dc.rights.note有償授權
dc.date.accepted2009-06-10
dc.contributor.author-college生物資源暨農學院zh_TW
dc.contributor.author-dept園藝學研究所zh_TW
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