한국해양대학교

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키틴분해 박테리아 Bacillus idriensis (CGH18)의 항산화 활성

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dc.contributor.author 정명은 -
dc.date.accessioned 2017-02-22T02:14:25Z -
dc.date.available 2017-02-22T02:14:25Z -
dc.date.issued 2012 -
dc.date.submitted 2012-04-25 -
dc.identifier.uri http://kmou.dcollection.net/jsp/common/DcLoOrgPer.jsp?sItemId=000002174143 ko_KR
dc.identifier.uri http://repository.kmou.ac.kr/handle/2014.oak/8094 -
dc.description.abstract Salt-fermented seafood sauce, called jeot-gal is one of the popular Korean traditional sauses and has been used to season other Korean food. It is made with various seafoods, such as shrimp, oyster, shellfish, fish, fish eggs, crab, and fish intestine. The seafood is salted and fermented for 2-3 months; then spices are added later to give its distinctive flavor. We considered that salt-fermented seafood' s high storability would be greatly contributed by antioxidizing capacity of microorganism that inhabits oxidation in salt fermented-seafood. This capacity to avert spoilage would also be due to the antioxidant produced by the microorganism. Crab, one of people' s favorite types of seafood, is one ingredient founf in salt-fermented seafood sauces. Its shell contains a polysaccharide called as chitin which is slow to decompose. Therefore, the problem is that consumption of crab generates crab shell as a waste, and this waste pollutes the environment. Therefore, salt-fermented food sauce made with crab will be a good source of a microorganism that may decompose chitin and prevent oxidation of seafood. The research team tried to isolate microorganisms to show antioxidizing and chitin-decomposing activities in colloidal chitin culture medium. As a result, a bacterium CGH18 was isolated from crab marinated in Soy Sauce and identified as Bacillus idriensis by 16S rDNA sequence homology search. B. idriensis exhibited optimal growth condition of pH, temperature, and culture time at 7.0, 25℃ and 48 h, respectively. The culture broth was extracted repeatedly with EtOAc for 1 hour using sonication. Its crude extracts were partitioned between n-BuOH and H2O. The organic layer was further partitioned between CH2Cl2 and H2O. Antioxidant activities of crude extract and its solvent fractions were evaluated using five different activity tests, including the degree of occurrence of intracellular reactive oxygen species (ROS), peroxynitrite (ONOO−), and lipid peroxidation, as well as the extent of GSH level, and oxidative damage of genomic DNA. All fractions exhibited significant antioxidant activity in bioassay systems used. In particular, the CH2Cl2 fraction showed the strongest antioxidant activity among the solvent fractions. Further purification of the CH2Cl2 fraction by various chromatographic methods resulted in the isolation of two diketopiperazine (compounds 1-2). Their chemical structures were determined by extensive 2D NMR experiments such as 1H gDQCOSY, TOCSY, NOESY, gHMQC, and gHMBC, and by comparison with published spectral data. -
dc.description.tableofcontents List of schemes ------------------------------------------------------- ⅰ List of tables ----------------------------------------------------------- ⅱ List of figures ---------------------------------------------------------- ⅲ List of abbreviations ------------------------------------------------- ⅴ List of symbols -------------------------------------------------------- ⅵ Abstract ----------------------------------------------------------------- 1 1 서론 -------------------------------------------------------------------- 3 2 재료 및 방법 --------------------------------------------------------- 6 2-1. 재료 ----------------------------------------------------------- 6 (1) 시료 ---------------------------------------------------------- 6 2-2. 시약 ----------------------------------------------------------- 6 (1) 배양 및 선발을 위한 배지 -------------------------------------- 6 (2) 추출, 분획 및 분리 ----------------------------------------------- 6 (3) 활성 ----------------------------------------------------------------- 7 2-3. 기기 ----------------------------------------------------------------- 8 2-4. 배지 ----------------------------------------------------------------- 9 (1) 균주의 분리 및 동정을 위한 고체 배지 --------------------- 9 (2) 균주의 액체 배양 및 보관을 위한 배지 --------------------- 9 (3) 선발을 위한 Colloidal chitin 배지 ---------------------------- 9 (3-1) 수산가공부산물인 홍게 껍질을 사용한 Chitin 제조 -- 9 (3-2) Colloidal chitin의 제조 ------------------------------------- 10 (3-2) Colloidal chitin의 배지 제조 ------------------------------ 10 2-5. 균주의 선발 ------------------------------------------------------ 12 (1) 젓갈 미생물 1차 선발 ------------------------------------------ 12 (2) 2차 선발 ---------------------------------------------------------- 12 (3) 3차 선발 ---------------------------------------------------------- 12 2-6. 선정 균주의 균학적 특성 ------------------------------------- 13 (1) 형태 및 생화학적 특성 ---------------------------------------- 13 (2) 분리균의 동정 및 분류 ---------------------------------------- 13 (3) 선정 균주의 최적 배양 조건 --------------------------------- 14 2-7. 추출, 분획 및 분리 --------------------------------------------- 15 (1) 추출 및 분획 ----------------------------------------------------- 15 (2) 화학물의 분리 --------------------------------------------------- 17 2-8. 항산화 활성 실험 ------------------------------------------------ 19 (1) Peroxynitrite 소거 활성----------------------------------------- 19 2-9. 세포수준에서의 활성 실험 ------------------------------------ 22 (1) 세포배양 ----------------------------------------------------------- 22 (2) Cell vuability의 측정 -------------------------------------------- 22 (3) ROS (total free radical 측정) --------------------------------- 25 (4) TBARS법을 이용한 lipid peroxidation 측정 --------------- 27 (5) Genomic DNA 추출 및 Genomic DNA의 산화 생성물 측정 - 27 (6) GSH(Glutathione) 함량 측정 --------------------------------- 28 3 결과 및 고찰 -------------------------------------------------------- 29 3-1. 최종 선발 균주의 형태 및 생화학적 특성규명 --------- 29 (1) 형태 및 생화학적 측성규명--------------------------------- 29 (2) 최적 배양 조건 ------------------------------------------------ 33 3-2. B. idriensis에서 분리한 화합물들의 구조 결정 -------- 37 3-3. 항산화 활성 실험 --------------------------------------------- 47 (1) Peroxynitrite 소거 활성 ------------------------------------- 47 3-4. 세포 수준에서의 활성 실험 -------------------------------- 50 (1) HT-1080 세포를 대한 MTT assay 효과 ----------------- 50 (2) ROS (total free radical 측정) ------------------------------ 52 (3) TBARS법을 이용한 lipid peroxidation 측정 ------------ 60 (4) Genomic DNA 추출 및 Genomic DNA의 산화 생성물 측정 - 62 (5) GSH(Glutathione) 함량 측정 ------------------------------- 64 (6) 인체 유래 암세포에 대한 세포 독성 효과 --------------- 66 (6-1) HT-1080 세포 독성 효과 -------------------------------- 66 (6-2) MCF-7 세포 독성 효과 ---------------------------------- 66 (6-3) HT-29 세포 독성 효과 ---------------------------------- 66 4 요약 및 결론 -------------------------------------------------------- 70 5 참고문헌 ------------------------------------------------------------ 72 6 부록 ---------------------------------------------------------------- 77 -
dc.language kor -
dc.publisher 한국해양대학교 대학원 -
dc.title 키틴분해 박테리아 Bacillus idriensis (CGH18)의 항산화 활성 -
dc.title.alternative Antioxidant Activity of a Chitin-degrading Bacterium Bacillus idriensis (CGH18) -
dc.type Thesis -
dc.date.awarded 2012-02 -
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해양생명환경학과 > Thesis
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