한국해양대학교

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Myxococcus sp.YH667이 생산하는 항균물질의 분리 및 구조 동정

DC Field Value Language
dc.contributor.author 정해슬 -
dc.date.accessioned 2017-02-22T02:24:39Z -
dc.date.available 2017-02-22T02:24:39Z -
dc.date.issued 2009 -
dc.date.submitted 2009-01-15 -
dc.identifier.uri http://kmou.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000002174351 ko_KR
dc.identifier.uri http://repository.kmou.ac.kr/handle/2014.oak/8357 -
dc.description.abstract Myxobacteria are unique gram-negative bacteria characterized by the gliding and fruiting body forming nature. Myxobacteria especially attract many researchers, since they have many possibilities of producing undiscovered bioactive substances. Recently new antobiotics such as myxin, inhibitoty lipid-factors, anbruticin, G1499-2, myxocidins, myxothiazol, pyrrolntrin, antibiotic TA, myxovirescins, myxovalargins, corallopyronins were reported to be produced by these organisms. Isolation and purification of myxobacteria from nature, however, are very difficult due to their complicated life cycle. In our search for the bioactive metabolites from myxobacteria, strain YH667, belonging to the genus Myxococcus, was found to produce antimicrobial compound. The producing strain, Myxococcus sp. YH667, was isolated from a soil sample collected at Je-ju island in Korea. The organic extracts from the culture broth and cell mass were prepared by solvent partitioning. Guided by the results of antimicrobial test and ¹H-NMR analysis, the moderately polar fractions were separated by silica, ODS, and sephadex LH-20 column chromatography followed by ODS HPLC to yield compound 1 as a colorless oil. The structure of compound 1 was determined as myxovirescin C₁ using combined spectroscopic methods and by comparison with reference data. Compound 1(Myxovirescin C₁) possessed high activity against Escherichia coli, and weak activity against Staphylococcus aureus. -
dc.description.tableofcontents Ⅰ. 서론 = 3 Ⅱ. 실험재료 및 방법 = 6 1. 시약 및 기기 = 6 1.1 시약 및 충진제 = 6 1.2 기기 = 6 2. 용매 = 7 3. 점액세균의 분리 = 7 3.1 공시토양 = 7 3.2 점액세균의 분리법 = 8 3.3 먹이균의 종류 = 9 3.4 선정된 먹이균의 배양 = 11 3.5 점액세균 배지 = 12 3.6 균주분리 = 14 4. 항생물질 생산균주의 스크리닝 = 16 4.1 점액세균의 스크리닝 배양 = 16 4.2 배지 = 16 4.3 생장억제활성의 측정 = 16 5. 균주 YH667이 생산하는 항생물질의 정제 = 18 5.1 배양 = 18 5.2 대사산물의 추출 및 분리 정제 = 20 6. 활성물질의 구조결정 = 24 6.1 TLC 등색시약 = 24 6.2 분광학 기기 = 26 7. 활성물질의 생물학적 활성 = 26 Ⅲ. 결과 및 고찰 = 27 1. 용균성 점액세균의 분리 = 27 1.1 공시토양 = 27 1.2 먹이균 선정 = 27 1.3 점액세균의 분리 = 28 2. 대사산물의 스크리닝 = 33 3. 균주 YH667의 동정 = 38 4. 균주 YH667의 대량 배양 = 41 5. 균주 YH667이 생산하는 항생물질의 분리 정제 = 41 5.1 추출 및 분획 = 41 5.2 분리 정제 = 42 6. 균주 YH667이 생산하는 항생물질의 구조 결정 = 46 7. 균주 YH667이 생산하는 항생물질의 항균활성 = 57 Ⅳ. 결론 = 58 Ⅴ. 참고문헌 = 60 -
dc.language kor -
dc.publisher 한국해양대학교 대학원 -
dc.title Myxococcus sp.YH667이 생산하는 항균물질의 분리 및 구조 동정 -
dc.title.alternative Isolation and Identification of Antimicrobial Compound from, Myxococcus sp. YH667 -
dc.type Thesis -
dc.date.awarded 2009-02 -
dc.contributor.alternativeName Jeong -
dc.contributor.alternativeName Hae-Seul -
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해양생명환경학과 > Thesis
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