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Improvement of sucrose tolerance of bakers yeast, Saccharomyces cerevisiae by mating : 미생물 교배를 이용한 제빵용 효모 Saccharomyces cerevisiae의 당 내성 형질 개량

DC Field Value Language
dc.contributor.advisor서진호-
dc.contributor.author오혜원-
dc.date.accessioned2018-05-29T03:54:35Z-
dc.date.available2021-04-13T02:35:54Z-
dc.date.issued2018-02-
dc.identifier.other000000149334-
dc.identifier.urihttps://hdl.handle.net/10371/141772-
dc.description학위논문 (석사)-- 서울대학교 대학원 : 농업생명과학대학 농생명공학부, 2018. 2. 서진호.-
dc.description.abstractABSTRACT

Bakers yeast, Saccharomyces cerevisiae, used as a starter in fermentation during a baking process is the main determinant of bread quality. S. cerevisiae SPC-SNU 70-1, isolated from Nuruk has excellent fermentation characteristics such as good leavening ability, generating volatile organic acids which affect a mild flavor and delaying the aging of bread. S. cerevisiae SPC-SNU 70-1 was able to show a good fermentability in lean (0% sucrose) and regular dough (8% sucrose), though, CO2 production decreased significantly in sweet dough containing 20 % sucrose. It is necessary to improve traits of the SPC-SNU 70-1 strain in high sucrose concentrations for various applications, while maintaining the inherent fermentation characteristics.
Eight novel strains to be mated with SPC-SNU 70-1 were isolated from Nuruk and grape. Those strains have high sucrose tolerance but poor fermentation activity in lean dough. Among 8 strains isolated, N1, N2, N5 and N6 strains with excellent leavening ability in sweet dough were selected for mating, but the N1 strain was excluded because it was impossible to form spores which is the first step of mating. The selected strains underwent sporulation, tetrad dissection and analysis. The isolated spores maintained haploids, thus the genetic sequences of the HO gene (HOmothallic switching endonuclease gene, encoding HO endonuclease that changes the mating type) were analyzed. All selected strains were found to be heterothallism. The haploid strains for mating were selected by the MAT locus PCR, barcode PCR and leavening ability. After mating, the same selection process was repeated to select mated strains.
Total 17 strains were selected and checked for the amount of CO2 production in lean, regular and sweet doughs. The strains with high industrial capability are designated as S-HW2, S-HW8, S-HW9, S-HW11 and S-HW16, S-HW17. Among them, the S-HW16 was selected based the fermentation ability in three different doughs. The amount of CO2 production of the S-HW16 strain increases 1.1-folds in lean dough, 1.3-folds in regular dough and 1.8-folds in sweet dough compared with that of SPC-SNU 70-1. The amount of fragrance components also increases. In sweet dough, the amount of esters which give a sweet flavor increases 10.6-folds and the amount of acetoin which give a buttery flavor increases 2.1-folds. This study demonstrated that mating was successfully used to develop new yeast strains with desired characteristics for baking.
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dc.description.tableofcontentsI. INTRODUCTION 1
1. Bakers yeast isolated from Nuruk 2
2. Mating 5
2.1. Saccharomyces cerevisiae life cycle 5
2.2. Different strain improvement techniques using hybridization 6
2.3. Direct mating 7
3. Research Objectives 11
II. MATERIALS AND METHODS 12
1. Strains 13
2. Isolation of Saccharomyces cerevisiae 15
2.1. Isolation by maltose subculture 15
2.2. Genomic DNA extraction 15
2.3. Strain-specific Polymerase Chain Reaction (PCR) 16
2.4. Random amplified polymorphism DNA (RAPD) PCR 18
2.5. Ploidy determination by PCR 19
2.6. SPC-SNU 70-1 strain-specific barcode PCR 19
3. Tetrad dissection and mating 22
3.1. Sporulation 22
3.2. Micromanipulator 22
3.3. Sequencing HO gene 24
4. Analysis of baking ability of S. cerevisiae 25
4.1. Preparation of yeast cell for dough fermentation 25
4.2. Liquid dough (LD) medium 26
4.3. Flour-based dough 27
4.4. Determination of leavening ability 27
4.5. Volatile fragrance assay 28
III. RESULTS AND DISCUSSIONS 29
1.Isolation of S. cerevisiae 30
1.1. Identification of new strains 30
1.2. Strains analysis by PCR 33
1.3. Determination of homo or heterothallism 35
1.4. Selection by leavening ability 37
2. Tetrad dissection 40
2.1. Sporulation 40
2.2. Determination of ploidy 40
2.3. Selection by barcode PCR 41
2.4. Selection by leavening ability 43
3. Mating 46
3.1. Determination of ploidy 46
3.2. Selection by barcode PCR 51
3.3. Selection by leavening ability 53
4. Application to baking 59
4.1. Analysis of dough fermentation characteristics 59
4.2. Analysis of fragrance components in dough fermentation 67
IV. CONCLUSIONS 72
V. REFERENCES 73
국 문 초 록 77
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dc.formatapplication/pdf-
dc.format.extent2083061 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectBaker’s yeast-
dc.subjectSaccharomyces cerevisiae-
dc.subjectindustrial strain-
dc.subjectnovel isolated strain-
dc.subjecthigh sucrose tolerance-
dc.subjectleavening ability-
dc.subjectsporulation-
dc.subjecttetrad analysis-
dc.subjectmating-
dc.subjectindustry applicability-
dc.subject.ddc630-
dc.titleImprovement of sucrose tolerance of bakers yeast, Saccharomyces cerevisiae by mating-
dc.title.alternative미생물 교배를 이용한 제빵용 효모 Saccharomyces cerevisiae의 당 내성 형질 개량-
dc.typeThesis-
dc.contributor.AlternativeAuthorHyewon Oh-
dc.description.degreeMaster-
dc.contributor.affiliation농업생명과학대학 농생명공학부-
dc.date.awarded2018-02-
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