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  1. NTU Theses and Dissertations Repository
  2. 生命科學院
  3. 生化科學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/60243
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor吳世雄
dc.contributor.authorChih-Hsien Suen
dc.contributor.author蘇誌賢zh_TW
dc.date.accessioned2021-06-16T10:14:08Z-
dc.date.available2013-08-25
dc.date.copyright2013-08-25
dc.date.issued2013
dc.date.submitted2013-08-19
dc.identifier.citationReference
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16. Gao, X.L., M. Nakadai, and B.B. Snider, Synthesis of (-)-TAN-2483A. Revision of the structures and syntheses of (+/-)-FD-211 (Waol A) and (+/-)-FD-212 (Waol B). Organic Letters, 2003. 5(4): p. 451-454.
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34. Kiyotaka Koyama, S.N., further characterizationof seven Bis(naphtho-gama-pyrone) congners of Ustilaginoidins, coloring matters of Claviceps virens(Ustilaginoidea virens). Chem. Pharm. Bull, 1988. 36(1): p. 146-152.
35. Ugaki, N., et al., New isochaetochromin, an inhibitor of triacylglycerol synthesis in mammalian cells, produced by Penicillium sp FKI-4942: I. Taxonomy, fermentation, isolation and biological properties. Journal of Antibiotics, 2012. 65(1): p. 15-19.
36. Agatsuma, T., et al., UCS1025A and B, new antitumor antibiotics from the fungus Acremonium species. Organic Letters, 2002. 4(25): p. 4387-4390.
37. Nakai, R., et al., UCS1025A, a novel antibiotic produced by Acremonium sp. Journal of Antibiotics, 2000. 53(3): p. 294-296.
38. Du, L.C. and L.L. Lou, PKS and NRPS release mechanisms. Natural Product Reports, 2010. 27(2): p. 255-278.
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40. He, H.Y., et al., Pyrrocidines A and B, new antibiotics produced by a filamentous fungus. Tetrahedron Letters, 2002. 43(9): p. 1633-1636.
41. Marfori, E.C., et al., Trichosetin, a novel tetramic acid antibiotic produced in dual culture of Trichoderma harzianum and Catharanthus roseus Callus. Zeitschrift Fur Naturforschung C-a Journal of Biosciences, 2002. 57(5-6): p. 465-470.
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/60243-
dc.description.abstract本研究的目的在於尋找真菌Myceliophthora heterothallica中具有生物活性
的天然物,並且期望可以得到過去文獻未發現的新化合物,Myceliophthora
heterothallica 的培養溫度為45℃,初步的活性測試顯示此真菌的乙酸乙酯萃取物有良好的抗癌和抗菌活性,為了瞭解Myceliophthora heterothallica 具有生物活性的化合物為何,在研究中以大量培養的方式以取得較為大量的萃取物,之後再以不同的純化方式進行純化,並以質譜和核磁共振的方式解出化合物的結構。

研究中得到了十二個化合物,其中包含了十一個已知化合物及一個先前未被發表的化合物。而除了分離和純化之外,這些純化後的化合物進行了包括了抗癌活性和抗菌活性生物活性的測試, 實驗結果發現其中有一個化合物具有抗菌的活性是先前未被報導過的,之後這些化合物的其他生物活性或是作用機制或許可以在之後的研究中繼續探討。
zh_TW
dc.description.abstractThe aim of this research is to search for bioactive secondary metabolites from the fungus Myceliophthora heterothallica in order to obtain compounds not previously reported in the literature. Myceliophthora heterothallica was cultured at 45 ℃. Preliminary bioactivity tests showed that the EtOAc crude extract showed good bioactivity on anti-cancer and anti-bacteria bioassays. In order to identify the bioactive compounds of Myceliophthora heterothallica, the fungi was large-scale cultured to obtain large amounts of fungi extract. After extraction, various purification methods (gel filtration, SiO2 open column, HPLC) were applied to purify the bioactive compounds and the purified compounds were identified by NMR and mass spectroscopy.
There were twelve compounds obtained in this study, including eleven known and one compound never reported previously. In addition to purification of compounds, anti-bacteria and anti-cancer bioactivity was tested. A known compound was shown to exhibit previously unreported anti-bacterial activity which warrants further research into its mechanism and biochemistry.
en
dc.description.provenanceMade available in DSpace on 2021-06-16T10:14:08Z (GMT). No. of bitstreams: 1
ntu-102-R00b46016-1.pdf: 3580453 bytes, checksum: 51723b58713e7da1edcf9c2a4ffa1cee (MD5)
Previous issue date: 2013
en
dc.description.tableofcontents摘要 II
Abstract III
致謝 V
Contents VI
Content of Figures IX
Content of Tables XIV
Chapter 1 1
INTRODUCTION 1
1.1 Thermophilic Fungi 1
1.2 Myceliophthora heterothallica 2
1.3 Literature Review of Myceliophthora 4
Waol A and B: 4
Estatin A and B: 5
Myceliothermophins A–E: 5
1.4 Objective 7
Chapter 2 9
MATERIALS AND METHODS 9
2.1 Materials 9
2.1.1 Fungi Strains 9
2.1.2 Medium for Myceliophthora heterothallica 9
2.1.3 Instruments 10
2.2 Methods 11
2.2.1 Flow Chart 11
2.2.2 Bioactivity Screening 11
2.2.3 Extraction, Isolation and Purification 12
2.2.4 Bacteria Culture 14
2.2.5 ITS region sequence identification for fungi 14
Chapter 3 16
RESULTS 16
Bioactivity-guided Compound Purification 16
Chapter 4 20
Structure Elucidation and Their Bioactivities 20
4.1 Cyclo(Ile-Pro) (1) 20
4.2 Cyclo(Val-Pro) (2) 24
4.3 Cyclo(Tyr-Pro) (3) 28
4.4 Cyclo(Phe-Pro) (4) 32
4.5 Cyclo(Phe-Leu) (5) 36
4.6 Bisdethiobis(methylthio)gliotoxin (6) 40
4.7 Phenylacetic acid (7) 44
4.8 4-Hydroxy-benzaldehyde (8) 47
4.9 Demethylmacrosporine (9) 49
4.10 Chaetochromin (10) 52
4.11 UCS1025B (11) 56
4.12 Compound 12 (12) 63
4.13 Pure compound Biological Activities 68
4.13.1 Anti-bacteria activity 68
4.13.2 Anti-cancer activity 69
Chapter 5 71
Discussion 71
Reference 75
dc.language.isoen
dc.subject嗜熱性真菌zh_TW
dc.subjectMyceliophthora heterothallicazh_TW
dc.subject抗癌活性zh_TW
dc.subject抗菌活性zh_TW
dc.subject天然物純化zh_TW
dc.subjectMyceliophthora heterothallicaen
dc.subjectthermophilic fungusen
dc.subjectnatural product purificationen
dc.subjectanti-bacteria activityen
dc.subjectanti-cancer activityen
dc.title嗜熱性真菌 Myceliophthora heterothallica 之化學成分及其生物活性研究zh_TW
dc.titleStudies on the Chemical Constituents and Their Biological Activities of the Thermophilic Fungus, Myceliophthora heterothallicaen
dc.typeThesis
dc.date.schoolyear101-2
dc.description.degree碩士
dc.contributor.oralexamcommittee楊玉良,鄭偉杰
dc.subject.keyword嗜熱性真菌,Myceliophthora heterothallica,抗癌活性,抗菌活性,天然物純化,zh_TW
dc.subject.keywordMyceliophthora heterothallica,thermophilic fungus,natural product purification,anti-bacteria activity,anti-cancer activity,en
dc.relation.page78
dc.rights.note有償授權
dc.date.accepted2013-08-19
dc.contributor.author-college生命科學院zh_TW
dc.contributor.author-dept生化科學研究所zh_TW
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