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  • 09월 03일 23시 이후 : 초록수정 불가능, 일정확인 및 검색만 가능

제122회 대한화학회 학술발표회, 총회 및 기기전시회 안내 Photosynthesis and Photoprotection in Plant and Artificial Cells

등록일
2018년 10월 1일 12시 35분 18초
접수번호
2708
발표코드
PHYS1-1 이곳을 클릭하시면 발표코드에 대한 설명을 보실 수 있습니다.
발표시간
목 15시 : 40분
발표형식
분과기념
발표분야
Physical Chemistry - Recent Trends in Energy Harvesting/Storage Systems
저자 및
공동저자
Tae Kyu Ahn
Department of Energy Science, Sungkyunkwan University, Korea

Complex metabolic reactions in cells are distributed in organelle modular compartments. Reactions in organelles have been reproduced in vitro by reconstituting functional protein machinery into membrane systems. We tested harvest organelle design, if switchable, to provide both a sustainable energy source and means to induce bladder response.[1] ATP (ATP) sinter agent and two light converters (plant-derived photochemical system II and proteorhodopsin derived from bacteria) enable ATP synthesis. It depends on two optical conversion devices, and it enables optical control to dynamically control ATP synthesis. Red light and green light interfere with ATP synthesis. We encapsulated giant vesicle light synthesizing organelle to form one cell line and showed two ATP dependent responses, optical control of carbon fixation and actin polymerization, changing the morphology of the vesicle. We hope to develop a full biomimetic vesicular system with a regulatory network showing switchable photosynthetic organelle homeostasis.
We applied fluorescence spectromicroscopy to Arabidopsis mesophyll protoplasts in order to observe in vivo changes in fluorescence spectra of granal and stromal thylakoid regions during the state transition, a photoprotection method. [2] State transition in chloroplasts of plants, is an important regulatory mechanism to maintain the excitation balance between PSI and PSII in the thylakoid membrane. Light-harvesting complex II (LHCII) plays a key role as the regulated energy distributor between PSI and PSII. The microscopic fluorescence spectra obtained from a few sections with different depths were decomposed into PSI and PSII spectra and self-absorption effects were removed. We determined amplitude changes of PSI and PSII in fluorescence spectra solely due to state transition. Subdomain analysis of granal and stromal thylakoid regions clarified variant behaviors in the different regions.
[1] Lee et al. Nature Biotechnology 2018, 36, 530–535.
[2] Kim et al. Plant Cell & Physiology 2015, 56, 759-768


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