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  1. NTU Theses and Dissertations Repository
  2. 醫學院
  3. 微生物學科所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/9833
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dc.contributor.advisor李昆達
dc.contributor.authorPei-Chun Luen
dc.contributor.author盧佩君zh_TW
dc.date.accessioned2021-05-20T20:44:07Z-
dc.date.available2011-07-23
dc.date.available2021-05-20T20:44:07Z-
dc.date.copyright2008-07-23
dc.date.issued2008
dc.date.submitted2008-07-16
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Hammonds, T.R., Denyer, S.P., Jackson, D.E., and Irving, W.L. (1996). Studies to show that with podophyllotoxin the early replicative stages of herpes simplex virus type 1 depend upon functional cytoplasmic microtubules. J Med Microbiol 45, 167-172.
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Lim, Y.H., Leem, M.J., Shin, D.H., Chang, H.B., Hong, S.W., Moon, E.Y., Lee, D.K., Yoon, S.J., and Woo, W.S. (1999). Cytotoxic constituents from the roots of Anthriscus sylvestris. Archives of pharmacal research 22, 208-212.
MacRae, W.D., Hudson, J.B., and Towers, G.H. (1989). The antiviral action of lignans. Planta Med 55, 531-535.
Markos, A.R. (2001). The successful treatment of molluscum contagiosum with podophyllotoxin (0.5%) self-application. Int J STD AIDS 12, 833.
Miyata, M., Itoh, K., and Tachibana, S. (1998). Extractives of Juniperus chinensis L. I: Isolation of podophyllotoxin and yatein from the leaves of J. chinensis. Journal of Wood Science 44, 397-400.
Moraes-Cerdeira, R.M., Burandt, C.L., Jr., Bastos, J.K., Nanayakkara, N.P., and McChesney, J.D. (1998). In vitro propagation of Podophyllum peltatum. Planta Med 64, 42-45.
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Nakatsubo, T., Mizutani, M., Suzuki, S., Hattori, T., and Umezawa, T. (2008). Characterization of Arabidopsis thaliana Pinoresinol Reductase, a New Type of Enzyme Involved in Lignan Biosynthesis. J Biol Chem 283, 15550-15557.
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Schwartz, J., and Norton, S.A. (2002). Useful plants of dermatology. VI. The mayapple (Podophyllum). J Am Acad Dermatol 47, 774-775.
Sicilia, T., Niemeyer, H.B., Honig, D.M., and Metzler, M. (2003). Identification and stereochemical characterization of lignans in flaxseed and pumpkin seeds. J Agric Food Chem 51, 1181-1188.
Sudo, K., Konno, K., Shigeta, S., and Yokota, T. (1998). Inhibitory effects of podophyllotoxin derivatives on herpes simplex virus replication. Antivir Chem Chemother 9, 263-267.
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Syed, T.A., Lundin, S., and Ahmad, M. (1994). Topical 0.3% and 0.5% podophyllotoxin cream for self-treatment of molluscum contagiosum in males. A placebo-controlled, double-blind study. Dermatology 189, 65-68.
Syed, T.A., Cheema, K.M., Khayyami, M., Ahmad, S.A., Ahmad, S.H., and Ahmad, S. (1995). Human leukocyte interferon-alpha versus podophyllotoxin in cream for the treatment of genital warts in males. A placebo-controlled, double-blind, comparative study. Dermatology 191, 129-132.
Truedsson, L., Sjoholm, A.G., and Sturfelt, G. (1985). Complement activating rheumatoid factors in rheumatoid arthritis studied by haemolysis in gel: relation to antibody class and response to treatment with podophyllotoxin derivatives. Clin Exp Rheumatol 3, 29-37.
Udino, L., Abaul, J., Bourgeois, P., Gorrichon, L., Duran, H., and Zedde, C. (1999). Lignans from the Seeds of Hernandia sonora. Planta Med 65, 279-281.
Umezawa, T. (2003). Diversity in lignan biosynthesis. Phytochemistry Reviews 2, 371-390.
Van Uden, W., Bos, J.A., Boeke, G.M., Woerdenbag, H.J., and Pras, N. (1997). The Large-Scale Isolation of Deoxypodophyllotoxin from Rhizomes of Anthriscus sylvestris Followed by Its Bioconversion into 5-Methoxypodophyllotoxin b-D-Glucoside by Cell Cultures of Linum flavum. J. Nat. Prod. 60, 401-403.
von Heimendahl, C.B., Schafer, K.M., Eklund, P., Sjoholm, R., Schmidt, T.J., and Fuss, E. (2005). Pinoresinol-lariciresinol reductases with different stereospecificity from Linum album and Linum usitatissimum. Phytochemistry 66, 1254-1263.
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Xia, Z.Q., Costa, M.A., Pelissier, H.C., Davin, L.B., and Lewis, N.G. (2001). Secoisolariciresinol dehydrogenase purification, cloning, and functional expression. Implications for human health protection. J Biol Chem 276, 12614-12623.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/9833-
dc.description.abstract鬼臼素 (Podophyllotoxin) 對癌細胞具強效毒殺作用,其化學衍生物已應用於臨床抗癌藥物之使用。本研究從台灣八角蓮 (Podophyllum pleianthum Hance)中選殖出鬼臼素生合成路徑中之pinoresinol lariciresinol reductase 基因 PLR (將 pinoresinol 先轉化為 lariciresinol,再轉化為 secoisolariciresinol) 以及 secoisolariciresinol dehydrogenase 基因 SDH (可將 secoisolariciresinol 轉化為 matairesinol)。選殖 sdh 是以台灣八角蓮 RNA為材料,經反轉錄-聚合酶連鎖反應 (RT-PCR) 得到 cDNA 序列,此序列與美洲八角蓮Podophyllum peltatum 之 sdh cDNA 序列進行比對後,達到 98.1% 的一致性,其胺基酸序列的一致性亦達 98.2%。選定在25 oC、0.01 mM isopropyl--D-1-thiogalactopyranoside (IPTG) 誘導 9 小時為重組蛋白 SDH 於大腸桿菌表現之最適條件。變性膠體電泳 (Sodium dodecyl sulfate polyacrylamide gel electrophoresis, SDS-PAGE) 分析可以清楚看到與 SDH-His tag 蛋白質 (34 kDa) 分子量大小相同之重組蛋白之生成。重組蛋白轉化的結果以高效能液相層析 (High performance liquid chromatography, HPLC) 系統進行分析,比較其反應產物 matairesinol 之滯留時間 (23.97分鐘) 及其UV全波長吸收光譜,皆和標準品相吻合。故可確認台灣八角蓮 sdh 之cDNA序列已成功選殖,並可在大腸桿菌內進行具有酵素活性之表現。此外,由台灣八角蓮經由cDNA末端快速擴增技術(Rapid amplification of cDNA ends, RACE)PCR 與 RT-PCR得到之 plr 序列,與美國金鐘連翹 (Forsythia intermedia) 之 plr cDNA 序列比對後,達到 68.9% 的一致性,其胺基酸序列的一致性亦達 75.2% 一致性與 85% 的相似度。西方墨點結果顯示目標蛋白質已表現於大腸桿菌,可以清楚看到與 PLR-His tag 蛋白質 (39 kDa) 分子量大小相同之重組蛋白之生成。zh_TW
dc.description.abstractPodophyllotoxin possesses strong tumor-specific cytotoxicity, and its chemical derivatives have been employed in clinical cancer treatment. From Podophyllum pleianthum Hance, pinoresinol lariciresinol reductase (PLR) gene was cloned, which can convert pinoresinol to lariciresinol and consequently to secoisolariciresinol, and secoisolariciresinol dehydrogenase (SDH) gene, which can convert secoisolariciresinol to matairesinol. The total RNA of Podophyllum pleianthum Hance was used as the material for sdh cloning by using reverse transcriptase PCR (RT-PCR). The cDNA sequence of sdh which got from Podophyllum pleianthum Hance aligned with sdh cDNA sequence from Podophyllum peltatum. It reached to 98.1% identity. The alignment of amino acid sequence reached to 98.2%. The optimum conditions was used 0.01 mM IPTG inducting 9 hours at 25oC for expression of SDH in E. coli. The result showed a 34 kDa of protein in SDS-PAGE, the same size for sdh with a SDH-Histag design. The conversion of recombinant enzyme reaction was further analyzed by HPLC, the retention time (23.97 min) and the UV absorption spectrum matched with the characters of authentic matairesinol. It indicated that the cDNA sequence of sdh was cloned from Podophyllum pleianthum Hance and expressed in E.coli functionally. Meanwhile, cDNA of plr got from Podophyllum pleianthum Hance by using rapid amplification of cDNA ends PCR (RACE PCR) and RT-PCR, was aligned with plr cDNA sequence from Forsythia intermedia, and it reached to 68.9% identity. Alignment of amino acid sequence also reached to 75.2% identity and 85% similarity. Western blotting proved the expression of target protein PLR in E. coli. The results showed a 39 kDa of recombinant protein expressed in SDS-PAGE, the same size for sdh with a PLR-His tag design.en
dc.description.provenanceMade available in DSpace on 2021-05-20T20:44:07Z (GMT). No. of bitstreams: 1
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Previous issue date: 2008
en
dc.description.tableofcontents口試委員申請書………………………………………………………………………II
中文摘要…………………………………………………………………………III
Abstract…………………………………………………………………………IV
Abbreviation…………………………………………………………………VI
中英文專有名詞對照表………………………………………………VII
Contents…………………………………………………………………………VIII
Contents of figures………………………………………………X

Chapter I. Introduction……………………………………………………1
1.1 Lignan………………………………………………………………………2
1.2 Podophyllotoxin……………………………………………………………2
1.3 Etoposide, Teniposide, Etopophos and new cytotoxin derivatives……………5
1.4 Biosynthesis of podophyllotoxin………………………………………………6
1.5 Secoisolariciresinol and matairesinol………………………………………9
1.6 Reasearch background……………………………………………………………10

Chapter II. Materials and Methods……………………………………13
2.1 Plants and microorganisms and vectors………………………………………14
2.2 Construction of plasmids…………………………… ………………………14
2.3 Construction of E. coli expression hosts……………………………………20
2.4 Expression of sdh and plr in E. coli…………………………………………21
2.5 Purificattion of recombinant protein…………………………………………21
2.6 Protein expression analysis…………………………………………………22

Chapter III. Results…………………………………………………………27
3.1 Gene cloning of sdh……………………………………………………………28
3.2 Expression of sdh in M15……………………………………………………28
3.3 Purification of recombinant SDH……………………………………………29
3.4 Biotransformation of rSDH in vitro…………………………………………30
3.5 Kinetic parameters of recombinant SDH………………………………………31
3.6 Gene cloning of plr……………………………………………………………31
3.7 Expression of plr in M15……………………………………………………32

Chapter IV. Discussion……………………………………………………35

Chapter V. Conclusion and Perspective…………………………………39
Figures……………………………………………………………………………42
References…………………………………………………………………………68
Appendices………………………………………………………………………74
dc.language.isoen
dc.title台灣八角蓮 Pinoresinol lariciresinol reductase 與 Secoisolariciresinol dehydrogenase 之基因選殖與表現zh_TW
dc.titleGene Cloning and Heterologous Expression of Pinoresinol Lariciresinol Reductase and Secoisolariciresinol Dehydrogenase Gene from Podophyllum pleianthum Hanceen
dc.typeThesis
dc.date.schoolyear96-2
dc.description.degree碩士
dc.contributor.oralexamcommittee蘇遠志,黃鵬林,劉祖惠,杜宜殷
dc.subject.keyword鬼臼素,台灣八角蓮,美洲八角蓮,大腸桿菌,美國金鐘連翹,zh_TW
dc.subject.keywordPodophyllotoxin,Podophyllum pleianthum Hance,Podophyllum peltatum,Escherichis coli,Forsythia intermedia,en
dc.relation.page73
dc.rights.note同意授權(全球公開)
dc.date.accepted2008-07-17
dc.contributor.author-college生命科學院zh_TW
dc.contributor.author-dept微生物與生化學研究所zh_TW
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