請用此 Handle URI 來引用此文件:
http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/43545完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 許輔(Fu Sheu) | |
| dc.contributor.author | Zih-Shiou Lin | en |
| dc.contributor.author | 林姿秀 | zh_TW |
| dc.date.accessioned | 2021-06-15T02:23:10Z | - |
| dc.date.available | 2009-08-20 | |
| dc.date.copyright | 2009-08-20 | |
| dc.date.issued | 2009 | |
| dc.date.submitted | 2009-08-18 | |
| dc.identifier.citation | 王宜慧,1998。幾丁質酶基因導入枯草桿菌及其表現分析。國立台灣大學植物病蟲害學研究所碩士論文。
王堂凱,2000。幾丁分解性桿菌屬細菌拮抗灰黴病菌活性之分析及幾丁質酶基因之選殖。國立台灣大學植物病理研究所碩士論文。 李豐在,2001。芽孢桿菌屬細菌幾丁質酶基因表現於螢光單胞細菌及其抗菌活性。國立台灣大學植物病理研究所碩士論文。 洪啓章,1994。Bacillus cereus NTU-FC-4菌株之幾丁質酶及幾丁聚醣酶之研究。台灣大學農業化學研究所碩士論文。 陳俊任,1993。Aeromonas sp. No. 16 所生產幾丁質酶之研究。台灣大學農業化學研究所碩士論文。 陳美菁,1995。Bacillus cereus NTU-FC-4幾丁聚醣酶之研究。台灣大學農業化學研究所碩士論文。 鄭茜茹,2000。由Aspergillus flavus NTU-FC-8生產幾丁聚醣酶之研究。台灣大學農業化學研究所碩士論文。 蘇甯茱,2001。枯草桿菌幾丁聚醣酶之純化與生化性質之研究。國立台灣大學農業化學研究所碩士論文。 蘇南維,1995。Listonella damsela NTU-FC-6幾丁質酶之研究。國立台灣大學農業化學研究所碩士論文。 Atkins E. D. T. 1985. Conformation in polysaccharides and complex carbohydrates. J Biosci. 8: 375-87. Atkins E. D. T, Dlugosz J., and Foord S. 1979. Electron diffraction and electron microscopy of crystalline a-chitin from the grasping spines of the marine worm Sagitta. Int J Biol Macromol 1: 29-32. Baek, J. M., Howell, C. B., and Kenerley, C. M. 1999. The role of an extracellular chitinase from Trichoderma virens Gv29-8 in the biocontrol of Rhizoctonia solani. Curr Genet. 35: 41-50. Blaak, H., Schnellmann, J., Walter, S., Henrissa, B., and Schrempf, H. 1993. Characteristics of an exochitinase from Streptomyces olivaceoviridis, its corresponding gene, putative protein domains and relationship to other chitinases. Eur. J. Biochem. 214: 659-669. Boller T., Gehri A., Mauch F. and Vogeli U. 1983. Chitinase in bean leaves: induction by ethylene, purification, properties, and possible function. Planta 157: 22-31. Blackwell J. 1973. Chitin. In: Walton AG, Blackwell J, editors. Biopolymers. New York: Academic Press. 474-489. Chanzy H. 1998. Chitin crystals. In: Domard A, Roberts GAF, Va˚rum KM, editors. Advances in chitin science. Lyon, France: Jacques Andre´. 11-21. Chre´tiennot-Dinet M-J, Giraud-Guille M-M, Vaulot D, Putaux J-L, Chanzy H. 1997. The chitinous nature of filament ejected by Phaeocystis (Prymnesiophycae). J Phycol. 33:666-672. Chen, J. P., Nagayama, F., and Chang, M. C. 1991. Cloning and expression of a chitinase gene from Aeromonas hydropila in Escherichia coli. Appl. Environ. Microbiol. 57: 2428-2436. Chernin, L. S., Fuente, L. D. L., Sobolev, V. Haran S., Vorgias, C. E., Oppenhein, A. B., and Chet, I. 1997. Molecular cloning, structural analysis, and expression in Escherichia coli of a Chitinase genr from Enterobacter agglomerans. Appl. Environ. Microbiol. 63: 834-839. Chernin, L., Ismailov, Z., Haran, S. and Chet, I. 1995. Chitinolytic Enterobacter agglomerans antagonistic to fungal plant pathogens. Appl. Environ. Microbiol. 61: 1720-1726. Fuchs, R. L., Mcpherson, S. A., and Drahos, D. J. 1985. Cloning of a Serratia marcescens gene encoding chitinase. Appl. Environ. Microbiol. 51: 504-509. Genta F. A., Lucas B., Plínio T. C., Claudimir L. D. L., Walter R. T., Clélia F. 2006. Purification, characterization and molecular cloning of the major chitinase from Tenebrio molitor larval midgut. Insect Biochemistry and Molecular Biology. 36: 789-800. Gardner K.H., Blackwell J. 1975. Refinement of the structure of β-chitin. Biopolymers. 14: 1581-1595. Gao X. A., Ju W. T., Jung W. J, Park R. D. 2008. Purification and characterization of chitosanase from Bacillus cereus D-11. Carbohydrate Polymers. 72: 513-520 Hirano S., Midorikawa T. 1998. Novel method for the preparation of N-acylchitosan fiber and N-acylchitosan–cellulose fiber. Biomaterials. 19: 293-297. Haran, S., Schickler, H., and Chet, I. 1996a. Molecular mecganisms of lytic enzymes involved in the biocontrol activity of Trichoderma harzianum. Microbiol. 142: 2321-2331. Hirano S., Nakahira T., Nakagawa M., Kim S. K. 1999. The preparation and applications of functional fibres from crab shell chitin. J Biotechnol. 70: 373-377. Hudson S. M. 1998. Applications of chitin and chitosan as fiber and textile chemicals. In: Domard A, Roberts GAF, Va˚rum KM, editors. Advances in chitin science, vol. 2. Lyon (France): Jacques Andre´ Publ. 590-599. Hudson S. M. 1999. The applications of chitin and chitosan to fiber and textile products. In: Chen RH, Chen HC, editors. Advances in chitin science, vol. 3. Taiwan: National Taiwan Ocean University. 80-87. Hudson S. M., Jenkins D. W. 2003. Chitin and chitosan. In:Mark HF, editor. EPST. vol. 1. 3rd ed. New York: Wiley; 569-580. Inbar, J. and Chet, I. 1991. Evidence that chitinase produced by Aeromonas caviae is involved in the biological control of soil-borne plant pathogens by this bacterium. Soil. Biol. Biochem. 23: 973-978. Ito M., Matahira Y., Sakai K. 1998. The application of chitinchitosan to bone filling materials, vol. 4. Kichin, Kitosan Kenkyu: Publ. Nippon Kichin, Kitosan Gakkai. 142-143. Jeuniaux C. 1964. Free chitin and masked chitin in invertebrate skeletal structures. Arch.Int. Physiol. Biochem. 72(2): 329-330. Jones, J. D. G., Grady, K. L., Suslow, T. V., and Bedbrook, J. R. 1986. Isolation and characterization of gene s encoding two chitinase enzymes from Serratia marcescens. EMBO J. 5: 467-473. Joshi, S. Kozlowski, M., Selvaraj, G., Iyer, V. N., and Davies, R. W. 1988. Cloning of the genes of the chitin utilization regulon of Serratia liquefaciens. J. Bacteriol. 170: 2984-2988. Kobayashi, D. Y., Guglielmoni, M., and Clarke, B. B. 1995. Isolation of the chitinolytic bacteria Xanthomonas maltophilia and Serratia marcescens as biological control agents for summer patch disease of turfgrass. Soil. Biol. Biochem. 27: 1479-1487. Kuranda, M. J. and Robbins, P. W. 1991. Chitianse is required for cell separation during growth of Saccharomyces cerevisiae. J. Biol. Chem. 266: 19758-19767. Krajewska B. 2004. Application of chitin- and chitosan-based materials for enzyme immobilizations: a review. Enzyme Microbiol Technol. 35:126-139. Kobayashi Y., Nishiyama M., Matsuo R., Tokura S., Nishi N. 1982. Application of chitin and its derivatives to paper industry. In: Hirano S, Tokura S, editors. Chitin chitosan. In: Proceeding of the International Conference, 2d. Jpn Soc Chitin Chitosan, Tattori, Japan. 244-247. Kosyakov V. N., Yakovlev N. G., Veleshko I. E. 2002. Application of chitin-containing fiber material ‘‘mycoton’’ for actinide adsorption. J Nucl Sci Technol (suppl. 3). 508-511. Kanke M., Katayama H., Tsuzuki S., Kuramoto H. 1989. Application of chitin and chitosan to pharmaceutical preparations. Chem Pharm Bull. 37:523-528. Kato Y., Onishi H., Machida Y. 2003. Application of chitin and chitosan derivatives in the pharmaceutical field. Curr Pharm Biotechnol. 4: 303-309. Kurakake M., Shou Yo-u, Kiyomi N., Minako S., Toshiaki K. 2000. Properties of chitosanase from Bacillus cereus S1. Current microbiology. 40: 6-9. Koga D., Tsukamoto T., Sueshige N., Usumi T. and Ide A. 1989. Kinetics of chitinase form yam, Dioscorea oppsita thunb. Agric. Biol. Chem. 54(1): 2505-2512. LaVallie, E.R., DiBlasio, E.A., Kovacic, S., Grant, K.L., Schendel, P.F. and McCoy, J.M. 1993. Bio/Technology. 11: 187–193. Lim, H. S., Kim, Y. S., and Kim, S. D. 1991. Pseudomonas stutzeri YPL-1 genetic transformation and antifungal mechanism against Fusarium soani, an agent of plant rot. Appl. Environ. Microbiol. 57: 510-516. Limon, M. C., Pintor-Toro, J. A., and Benitez, T. 1999. Increased antifungal activity of Trichoderma hrazianum transformants that overexpress a 33-kDa chitinase. Phytopathology. 89: 254-261. Lorito, M., Di Pietro, A., Hayes, C. K., Woo, S. L., and Harman, G. E. 1993a. Antifungal, synergistic interaction between chitinolytic enzymes from Trichoderma harzianum and Enterobacter cloacae. Phytopathology. 83: 721-728. Lorito, M., Haeman, G. E., Hayes, C. K., Broadway, R. M., Tronsmo, A., Woo, S. L., and Di Pietro, A. 1993b. Chitinnolytic Enzymes Produced by Trichiderma harzianum:Amtifungal Activity of Purified Endochitinase and Chitobiosidase. Phytopathology. 83: 302-307. Lorito, M., Hayes, C. K., Di Pietro, A., Woo, S. L. and Harman, G. E. 1994a. Purification, characterization , and synergistic activity of a glucan 1,3-p-glucoisdase and an N-acetyl-p-glucosaminidase from Trichoderma harzianum. Phytopathology. 84: 398-405. Lorito, M., Peterbauer, C., Hayes, C. K., and Harman, G. E. 1994. Synergistic interaction between fungal cell wall degrading enzymes and different antifungal compounds enhances inhibition of spore germination. Microbiology. 140: 623-629. Lorito, M., Woo, S. L., D’Ambrosio, M., Harman, G. E. Hayes, C. K., Kubicek, C.P., and Scala, F. 1996. Synergistic interaction between cell wall degrading enzymes and membrane affecting compounds. Mol. Plant-Microbe Interact. 9: 206-213. Monaghan, R. L., D. E. Eveleigh, R. P. Tewari, and E. T. Reese. 1973. Chitosanase, a novel enzyme. Nature New Biology. 245: 78-80. Minke R., Blackwell J. 1978. The structure of α-chitin. J Mol Biol. 120: 167-181. Mavingui, P. and Heulin, T. 1994. In vitro chitinase and antifungal activity of a soil, rhizosphere and rhizoplane population of Bacillus polymyxa. Soil/ Biol . Biochem. 26: 801-803. Miyashita, K., Fuji, T., and Sawada, Y. 1991. Molceular cloning and characterization of chitinase genes from Streptomyces lividans 66. J. Gen. Microbiol. 137: 2065-2072. Morimoto, K., Karita, S., Kimura, T., Sakka, K., and Ohmiya, K. 1997. Cloning , sequence, and expression of the gene encoding Clostridium paraputrificum chitinase ChiB and analysis of the functions of novel cadherin-like domains and a chitin-binding domain. J. Bacteriol. 179: 7306-7314. Olivera B. M., Hillyard D. R., Marsh M., Yoshikami D. 1995. Combinatorial peptide libraries in drug design: lesson from venomous cone snails. Tibtech. 13: 422-426. Pleban, S., Chernin, l., and Chet, I. 1997. Chitinolytic activity of an endophytic strain of Bacillus cereus. Lett. In Appl. Microbiol. 25:284-288. Rinaudo M. 2006. Chitin and chitosan: Properties and applications. Prog. Polym. Sci. 31: 603-632. Robbins P. W., Alberight C. And Benfield B. 1988. Cloning and expression of a Streptomyces plicatus chitinase (chitinase-63) in Escherichia coli. J.Biol. chem.. 263(1): 443-447. Rudall K. M., Kenchington W. 1973.The chitin system. Biol Rev. 40: 597-636. Rudall K. M. 1969. Chitin and its association with other molecules. J Polym Sci Part C. 28: 83-102. Rathke T. D., Hudson S. M. 1994. Review of chitin and chitosan as fiber and film formers. Rev Macromol Chem Phys. 34: 375-437. Sahai A. S. 1993. Chitinase of fungi and plants:their involvement in morphogenesis ans host-parasite interaction. FEMS Microbiol. Rev. 11: 317-338. Saito Y., Okano T., Chanzy H., Sugiyama J. 1995. Structural study of a-chitin from the grasping spine of the arrow worm (Sagitta spp.). J Struct Biol. 114: 218-228. Shapira, R., Ordentlich, A., Chet, I., and Oppenheim, A. B. 1989. Control of plant diseases by chitinase expressed from cloned DNA in Escherichia coli. Phytopathology. 79: 1246-1249. Songkroah C., Nakbanpote W., Thiravetyan P. 2004. Recovery of silver–thiosulfate complexes with chitin. Process Biochem. 39: 1553-1559. Shiro, M., Ueda, M., Kawaguchi, T., and Arai, M. 1996. Cloning of a cluster of chitinase genes from Aeromonas sp. No. 10S-24 Biochim. Biophy. Acta. 1305: 44-48. Sundheim, L., Poplawsky, A. R., and Ellingboe, A. H. 1988. Molecular control of two chitinase genes from Serratia marcescens and their expression in Pseudomonas species. Physiol. Mol. Plant Pathol. 33: 483-491. Tokura S., Nishi N. 1982. Preparation and properties of alkylchitin fibers. In: Hirano S, Tokura S, editors. Chitin chitosan. In: Proceeding of the international conference, 2d. Jpn. Soc. Chitin Chitosan, Tattori, Japan. 244-247. Ueda, M., Kawaguchi, T., and Arai, M. 1994. Molecular cloning and nucleotide sequence of the gene encoding chitinase II from Aeromonas sp. NO. 10S-24. J. Ferment. Bioeng. 78: 205-211. van Aalten D. M. F., D. Komander, B. Synstad, S. Gåseidnes, M. G. Peter, and V. G. H. Eijsink. 2001. Structural insights into the catalytic mechanism of a family 18 exo-chitinase. PNAS. 98(16): 8979-8984. Wu G. J., Guo J. T. 2007. Chitooligosaccharides in combination with interferon-γ increase nitric oxide production via nuclear factor-κB activation in murine RAW264.7 macrophages. Food and Chemical Toxicology. 45: 250-258. Wang Z., Lanhong Z., Shaoli Y., Rongli N., Edward C., Xiukun L. 2007. N-Acetylchitooligosaccharide is a potent angiogenic inhibitor both in vivo and in vitro. Biochemical and Biophysical Research Communications. 357: 26-31. Wang S. Yi, Moyne A. L., George T., Wu S. J., Robert D. L., Narendra K. S. 2001. Purification and characterization of a Bacillus cereus exochitinase. Enzyme and Microbial Technology. 28: 492-498 Wang S.Y., Wu S. J., George T., Robert D. L., AND Narendra K. S. 2001. Molecular cloning and structural analysis of the gene encoding Bacillus cereus exochitinase Chi36 Journal of bioscience and bioengineering. 92(1): 59-66. Watanabe, T., Oyanagi, W., Suzuki, K., and Tanaka, H. 1990a. Chitinase system of Bacillus circulans WL-12 and importance of chitinase A1 in chitin degradation. J. Bacteriol. 172: 4017-4022. Watanabe, T., Suzuki., Oyanagi, W. Ohnishi, K., and Tanaka, H. 1990b. Gene cloning of chitinase A1 from Bacillus circulans Wl-12 revealed its evolutionary relationship to Serratia chitinase and to the type III homology units of fibronectin. J. Biol. Chem. 265: 15659-15665. Wilhelm, E., Arthofer, W., Schafleitner, R., and Kerbs, B. 1998. Bacillus subtilis an endophyte of chestnut (Castanea sativa) as antagonist against chestnut blight (Cryphonectria parasitica). Plant Cell Tissue Organ Cult. 52: 105-108. Wortman, A. T., Somerville, C. C., and Colwell, R. R. 1986. Chitinase determinants of Vibrio vulnificus : gene cloning and application of a chitinase probe. Appl. Environ. Microbiol. 52: 142-145. Yoshino H., Ishii S., Nishimura S., Kurita K. 1992. Preparation and characterization of mercapto-chitin derivatives. In: Brine CJ, Sandford PA, Zikakis JP, editors. Advances in chitin and chitosan. London and New York: Elsevier. 565-570. Yusof N. L., Wee A., Lim L. Y., Khor E. 2003. Flexible chitin films as potential wound-dressing materials: wound model studies. J Biomed Mater Res A. 66: 224-232. | |
| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/43545 | - |
| dc.description.abstract | 葡萄糖胺與幾丁寡糖為幾丁質 (chitin) 之水解產物,在許多工業及生物技術方面佔有重要角色。葡萄糖胺與幾丁寡糖可由幾丁質酶分解幾丁質而獲得,因而本研究主要之目的為純化、轉殖並於大腸桿菌系統表現仙人掌桿菌屬 Bacillus cereus BCRC 11026 中之幾丁質酶。實驗上自仙人掌桿菌屬之 B. cereus BCRC 11026 萃取粗蛋白,經硫酸銨沉澱、快速蛋白質液相層析及活性測試等步驟,分離出具有幾丁質分解能力之幾丁質水解酶,經由 SDS-PAGE 分析結果顯示蛋白質分子量約為 61 kDa,後續進行 N 端胺基酸序列分析,發現其 N 端胺基酸序列為 SDIKY。之後以 B. cereus BCRC 11026 之全 DNA 為模板,以N 端胺基酸序列搜尋基因庫所得之同源基因序列為引子進行聚合酶連鎖反應,獲得 B. cereus BCRC 11026 之幾丁質酶基因 GD1A4,並構築成含有幾丁質酶基因的質體 pET32a-GD1A。將 pET32a-GD1A 轉殖入 Escherichia coli BL-21 表現後,進行 SDS-PAGE 與 western blotting 分析,顯示此重組蛋白分子量約為 38.5 kDa。分析發現此重組幾丁質水解酶之純化倍率為 48.78,回收率為 1.67 %,比活性為 12.536 U/mg,其最適反應溫度約為 60℃,最適反應 pH 值為 6.0,在 60 ℃以下熱安定。此幾丁質水解酶可利用於葡萄糖胺與幾丁寡糖之生產。 | zh_TW |
| dc.description.abstract | N-acetyl-D-glucosamine (GlcNAc) and N-acetyl chitooligosaccharides, the products of chitin, are important to several industries and biotechnology sectors. They could be hydrolyzed from chitin by chitinase. The aim of this study was to purify and clone the gene encoding chitinase from Bacillus cereus BCRC 11026 and to perform recombinant expression in a prokaryotic E. coli system. Chitinase was purified from B. cereus BCRC 11026 through ammonium sulfate fractionation and Mono S ion-exchange chromatography. Its molecular mass was about 61 kDa, as determined by SDS-PAGE. The N-terminal amino acid sequence of the purified chitinase was further determined. Cloning was carried out using PCR technique, using the homogeneous gene sequences of the purified chitinase as the primers. The chitinase fragment (GD1A4) amplified from the genomic DNA of B. cereus BCRC 11026 was ligated with pET-32a (+) vector to generate an expression vector, pET32a-GD1A4. In order to achieve successful expression of the recombinant chitinase, the plasmid pET32a-GD1A4 was then transferred into E. coli BL-21 to produce the recombinant protein with a molecular weight of 38.5 kDa. Furthermore, the recombinant chitinase were purified and concentrated by 48.78 fold with a recovery of 1.67 % and a specific activity of 12.536 U/mg. The optimal pH and temperature for the recombinant chitinase wase 6.0 and 60 ℃, respectively, and the enzyme activity was relatively stable below 60 ℃. This chitinase could be utilized for the production of N-acetyl-D-glucosamine and N-acetyl chitooligosaccharides. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-15T02:23:10Z (GMT). No. of bitstreams: 1 ntu-98-R96628205-1.pdf: 2864710 bytes, checksum: 252fb11fd12deed6a4ce87f53bc6bdd4 (MD5) Previous issue date: 2009 | en |
| dc.description.tableofcontents | 目錄
壹、 中文摘要…………………………………………………………………… 1 貳、 英文摘要…………………………………………………………………… 2 參、 研究目的…………………………………………………………………… 3 肆、 研究背景…………………………………………………………………… 4 一、幾丁質與幾丁聚醣及其衍生物之介紹………………………………… 4 二、幾丁質酶與幾丁聚醣酶………………………………………………… 10 三、微生物幾丁質酶基因之選殖…………………………………………… 13 伍、材料與方法…………………………………………………………………… 15 一、Bacillus cereus BCRC 11026幾丁質酶之純化……………………… 15 二、Bacillus cereus BCRC 11026幾丁質酶基因之選殖………………… 22 三、重組蛋白質生化性質分析……………………………………………… 33 陸、實驗結果…………………………………………………………………… 35 一、Bacillus cereus BCRC 11026 幾丁質酶之純化、檢定 與胺基酸序列之分析…………………………………………………… 35 二、幾丁質基因之選殖……………………………………………………… 36 三、以 Escherichia coli表現幾丁質酶之生化性質…………………… 41 柒、討論…………………………………………………………………………… 43 捌、引用文獻…………………………………………………………………… 45 玖、圖表………………………………………………………………………… 56 | |
| dc.language.iso | zh-TW | |
| dc.subject | 幾丁質酶 | zh_TW |
| dc.subject | 幾丁質 | zh_TW |
| dc.subject | chitin | en |
| dc.subject | chititnase | en |
| dc.title | 仙人掌桿菌幾丁質酶基因選殖及表現之研究 | zh_TW |
| dc.title | Molecular Cloning and Gene Expression of the Chitinase from Bacillus cereus BCRC 11026 | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 97-2 | |
| dc.description.degree | 碩士 | |
| dc.contributor.oralexamcommittee | 周志輝(Chau Chi-Fai),劉?睿(Je-Ruei Liu),徐源泰(Yuan-Tay Shyu) | |
| dc.subject.keyword | 幾丁質,幾丁質酶, | zh_TW |
| dc.subject.keyword | chitin,chititnase, | en |
| dc.relation.page | 90 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2009-08-18 | |
| 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 |
| 顯示於系所單位: | 園藝暨景觀學系 | |
文件中的檔案:
| 檔案 | 大小 | 格式 | |
|---|---|---|---|
| ntu-98-1.pdf 未授權公開取用 | 2.8 MB | Adobe PDF |
系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。
