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미세유체플랫폼 내 미세조류 배양 및 실시간 관찰 연구와 생체지질염색 방법 : Microfluidic Platform for Real-time Observation and Vital Lipid Staining of Microalgae

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dc.contributor.advisor전누리-
dc.contributor.author김민서-
dc.date.accessioned2017-07-14T03:46:09Z-
dc.date.available2017-07-14T03:46:09Z-
dc.date.issued2012-08-
dc.identifier.other000000002758-
dc.identifier.urihttps://hdl.handle.net/10371/123966-
dc.description학위논문 (석사)-- 서울대학교 대학원 : 기계항공공학부(멀티스케일 기계설계전공), 2012. 8. 전누리.-
dc.description.abstractIn recent years, one of the most promising alternative energy resources is biomass, which can be converted to biofuel, such as biodiesel and bioethanol. Microalgae are the next generation of green-fuel since they can produce neutral lipids and hydrocarbons in large quantities-
dc.description.abstractyet several challenges to the success of microalgal biofuel still exist-
dc.description.abstractthese include strain development, medium optimization, reactor design, metabolic engineering, and product purification.
The green microalgal capability of producing materials for biofuel is depending on many environmental factors of photosynthetic eukaryotes such as light exposure, CO2, nutrient concentration, temperature and pH. Microfluidic device can serve the precise spatial and temporal control by taking advantages of the basic characteristics of laminar flow and is easy to observe single cellular behaviors. Considering these facts, we have studied microalgae to newly focus on microfluidic platform. Among several meaningful microalgal species for biofuel, much of our current research is involved with Chlamydomonas reinhardtii, which is one of the model organisms.
In this paper, we introduce a microfluidic platform to cultivate and observe microalgae in real-time even after staining cells vitally. We have utilized microchannels of microfluidic platform to maintain location of cells and prevent cells from being lost. As a result of the process of photolithography, the height of the channel was 5 μm and it was reasonable to the average height of C. reinhardtii cells.
To estimate microalgal viability in a microfluidic platform, we observed cells after cell loading and imaging. On the conclusion, channels of microfluidic platform were effect to observe microalgal cell division or change in real-time even after vital lipid staining. We ultimately expect this microfluidic platform to bring out meaningful results from cells dedicating as microfluidic tool for the study of microalgae.
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dc.description.tableofcontents1. Introduction............................................................................1
2. Material and Methods....................................................................5
2.1 Algal Cultures................................................................5
2.1.1 Growth Conditions..................................................5
2.1.2 TAP medium.........................................................6
2.2 Microfluidic platform.........................................................6
2.2.1 Device design......................................................6
2.2.2 Photolithography...................................................8
2.2.3 Monolithic bonding.................................................8
2.3 Real-time observation.........................................................11
2.3.1 Morphological variation and reproduction...........................11
2.4 Vital lipid staining..........................................................11
2.4.1 BODIPY 505/515.....................................................12
2.4.2 BODIPY 500/510.....................................................13
3. Results and Discussion..................................................................14
3.1 Microfluidic platform.........................................................14
3.2 Real-time observation.........................................................14
3.2.1 Real-time observation of C. reinhardtii in microchannels...........14
3.3 Vital lipid staining..........................................................17
3.3.1 BODIPY 505/515.....................................................17
3.3.2 BODIPY 500/510.....................................................18
3.3.3 Real-time observation..............................................22
4. Conclusion..............................................................................24
5. References..............................................................................25
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dc.formatapplication/pdf-
dc.format.extent1325104 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectMicrofluidics-
dc.subjectMicroalgae-
dc.subjectBiodiesel-
dc.subjectVital lipid staining-
dc.subjectReal-time observation-
dc.subject.ddc621-
dc.title미세유체플랫폼 내 미세조류 배양 및 실시간 관찰 연구와 생체지질염색 방법-
dc.title.alternativeMicrofluidic Platform for Real-time Observation and Vital Lipid Staining of Microalgae-
dc.typeThesis-
dc.description.degreeMaster-
dc.citation.pagesvi, 26-
dc.contributor.affiliation공과대학 기계항공공학부(멀티스케일 기계설계전공)-
dc.date.awarded2012-08-
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