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dc.contributor.advisor박진병-
dc.contributor.author서효실-
dc.creator서효실-
dc.date.accessioned2016-08-25T10:08:22Z-
dc.date.available2016-08-25T10:08:22Z-
dc.date.issued2010-
dc.identifier.otherOAK-000000057193-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/185508-
dc.identifier.urihttp://dcollection.ewha.ac.kr/jsp/common/DcLoOrgPer.jsp?sItemId=000000057193-
dc.description.abstractEnantioselective oxygenation of 2-(2’-acetoxyethyl)cyclohexanone into R-lipoic acid precursor, R-7-(2’-acetoxyethyl)-2-oxepanone has been investigated with recombinant Corynebacterium glutamicum expressing the chnB gene encoding cyclohexanone monooxygenase (CHMO) of Acinetobacter calcoaceticus NCIMB 9871. The recombinant biocatalyst produced R-7-(2’-acetoxyethyl)-2-oxepanone at a rate of over 60 U/g CDW (3.6 mmol/g CDW/h, 0.67 g/g CDW/h) in a whole-cell assay. The biocatalytic activity was maintained over 12 U/g CDW at a substrate concentration of over 25 g/L in the medium, pointing to high catalytic stability against substrate toxicity. Furthermore, biotransformation in a fed-batch culture mode allowed the biocatalyst to produce R-7-(2’-acetoxyethyl)-2-oxepanone at over 6.2 g/L in the medium. The specific and volumetric oxidation activity was 0.09 g/g CDW/h (8.14U/g CDW) and 277 U/L, respectively. These results indicate that the C. glutamicum-based biocatalyst is efficient for the selective oxygenation of 2-(2’-acetoxyethyl) cyclohexanone into R-7-(2’-acetoxyethyl)-2-oxepanone.;Acinetobacter calcoaceticus NCIMB 9871 유래의 cyclohexanone monooxygenase gene (chnB)이 발현된 재조합 Corynebacterium glutamicum의 생촉매 효율을 조사하였다. 유가식 배양에 기초한 생물전환에서 cyclohexanone으로부터 ε-caprolactone을 18.1 g/l로 생산할 수 있었다. Specific and volumetric productivities는 각각 0.13 g/g dry cells/h (19.3 U/g of dry cells) 와 1.34 g/L/h (196 U/L)이었다. 이는 유사한 반응 환경에서 A. calcoaceticus 유래의 chnB를 발현하는 재조합 Escherichia coli BL21 (DE3)의 결과와 비교하여 각각 6배와 1.6배 이상 높다. C. glutamicum 전세포 촉매의 Baeyer-Villiger oxidation 반응을 R-lipoic acid 전구체 생산에 응용하였을 때 유가식 배양에 기초한 생물전환에서 2-(2’-acetoxyethyl)cyclohexanone으로부터 R-7-(2’-acetoxyethyl)-2-oxepanone을 6.2 g/l로 생산할 수 있었다. 이 때 specific and volumetric productivities는 각각 0.09 g /g of dry cells/ h (8.14 U/g of dry cells) 와 3.1 g /L/h (277 U/L) 이었다. 종합적으로 재조합 C. glutamicum은 Baeyer-Villiger oxidation를 위한 뛰어난 차세대 생촉매라고 사료된다.-
dc.description.tableofcontents1. Introduction = 1 1.1 Oxidative biotransformation = 1 1.2 Recombinant biocatalyst = 1 1.3 C. glutamicum as a biocatalyst = 2 1.4 Biocatalytic Baeyer-Villiger oxidation = 7 1.5 Application of biocatalytic Baeyer-Villiger oxidations to synthesis of R-lipoic acid precursor = 11 2. Materials and Methods = 13 2.1 Construction of recombinant C. glutamicum-based biocatalyst = 13 2.2 Cultivation conditions of recombinant C. glutamicum = 14 2.3 Protein electrophoresis = 14 2.4 Whole cell CHMO activity assay = 15 2.5 Biotransformation = 15 2.6 Determination of glucose concentration = 16 2.7 Measurement of ketones and lactones concentration = 16 3. Results and Discussion = 17 3.1 Characterization of recombinant C. glutamicum-based biocatalyst = 17 3.1.1 Expression of chnB in C. glutamicum = 17 3.1.2 Whole cell CHMO activity = 23 3.2 Biotransformation of cyclic ketones into corresponding lactones = 27 3.2.1 Biotransformation of cyclohexanone into ε-caprolactone = 27 3.2.2 Biotransformation of 2-(2'acetoxyethyl)cyclohexanone into R-7-(2'-acetoxyethyl)-2-oxepanone = 33 4. Summary and Conclusions = 36 5. References = 37 Appendix : Isolation of a Fermenting Microorganism Involved in Formation of ortho -Dihydroxyisoflavones in Doenjang (Korean Fermented Soybean Paste) = 43 Abstract in Korean (국문초록) = 59-
dc.formatapplication/pdf-
dc.format.extent1323067 bytes-
dc.languageeng-
dc.publisher이화여자대학교 대학원-
dc.titleBiotransformation of 2-(2’acetoxyethyl)cyclohexanoneinto R-lipoic acid precursor, R-7-(2’-acetoxyethyl)-2-oxepanone with recombinant Corynebacterium glutamicum-
dc.typeMaster's Thesis-
dc.creator.othernameSeo, Hyo Seel-
dc.format.pageⅴ, 60 p.-
dc.identifier.thesisdegreeMaster-
dc.identifier.major대학원 식품공학과-
dc.date.awarded2010. 2-
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