Enhanced xylitol production rate by engineering glycerol metabolic path-way and pentose phosphate pathway in Candida tropicalisGlycerol 대사 경로의 대사공학 기법을 이용한 Candida tropicalis에서 Xylitol 생산 증대

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dc.contributor.advisor김정회-
dc.contributor.advisorKim, Jung-Hoe-
dc.contributor.authorAhmad,Irshad-
dc.date.accessioned2013-09-11T01:06:04Z-
dc.date.available2013-09-11T01:06:04Z-
dc.date.issued2011-
dc.identifier.urihttp://library.kaist.ac.kr/search/detail/view.do?bibCtrlNo=482573&flag=dissertation-
dc.identifier.urihttp://hdl.handle.net/10203/179875-
dc.description학위논문(박사) - 한국과학기술원 : 생명과학과, 2011.8, [ viii, 88 p. ]-
dc.description.abstractThe yeast Candida tropicalis produces xylitol, a natural, low-calorie sweetener whose metabolism does not require insulin, by catalytic activity of NADPH-dependent xylose reductase. Extensive research has been carried out on the dietary and technological properties of xylitol because of its growing market and high added value. Glycerol can be used as a primary carbon source by yeasts, little is known regarding glycerol metabolism in C. tropicalis. In this study, gk gene which encodes glycerol kinase was disrupted from the genome of xylitol dehydrogenase gene (XYL2)-disrupted C. tropicalis strain BSXDH-3. The resulting gk knockout C. tropicalis strain, termed "IA", was incapable to grow on glycerol. The cells growth on glycerol was resumed by co-expressing Scheffersomyces stipitis gcy1, 2 and 3 genes, which respectively encode NADP+-dependent alcohol dehydrogenase 1, 2 and 3, under the control of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) promoter. NADPH-dependent xylitol production was higher in the engineered strain, termed "IA-3", than in BSXDH-3. Rates of xylitol production at 16 and 24 hr for IA-3 were 0.85 g l-1 h-1 and 1.28 g l-1 h-1 respectively; these values are 30% and 18% higher than corresponding rates for BSXDH-3. The oxidative pentose phosphate pathway (PPP) is a major basis of NADPH biosynthesis in C. tropicalis. In order to increase xylitol production rate, xylitol dehydrogenase gene (XYL2)-disrupted C. tropicalis strain BSXDH-3 was engineered to co-express zwf and gnd genes, which respectively encode glucose-6-phosphate dehydrogenase (G6PDH) and 6-phosphogluconate dehydrogenase (6-PGDH), under the control of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) promoter. NADPH-dependent xylitol production was higher in the engineered strain, termed "PP", than in BSXDH-3. In fermentation experiments using glycerol as a co-substrate with xylose, strain PP showed volumetric xylitol productivity of 1.25 g l-1 h-1...eng
dc.languageeng-
dc.publisher한국과학기술원-
dc.subject자일리톨-
dc.subject자일로오스-
dc.subject글리세롤 대사 경로-
dc.subject캔디다 트로피칼리스-
dc.subjectXylitol-
dc.subjectXylose-
dc.subjectGlycerol metabolic pathway-
dc.subjectCandida tropicalis-
dc.subjectScheffersomyces stipitis-
dc.subject캔디다 트로피칼리스-
dc.titleEnhanced xylitol production rate by engineering glycerol metabolic path-way and pentose phosphate pathway in Candida tropicalis-
dc.title.alternativeGlycerol 대사 경로의 대사공학 기법을 이용한 Candida tropicalis에서 Xylitol 생산 증대-
dc.typeThesis(Ph.D)-
dc.identifier.CNRN482573/325007 -
dc.description.department한국과학기술원 : 생명과학과, -
dc.identifier.uid020054524-
dc.contributor.localauthor김정회-
dc.contributor.localauthorKim, Jung-Hoe-
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