This study is aimed at identifying the proteins that are up-regulated during astaxanthin accumulation in Haematococcus lacustris. For this H. lacustris cells were cultivated in photobioreactors under normal light irradiance of 40μEm<SUP>-2<...
http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
https://www.riss.kr/link?id=A107600900
2009
-
SCOPUS,SCIE
학술저널
241-246(6쪽)
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
This study is aimed at identifying the proteins that are up-regulated during astaxanthin accumulation in Haematococcus lacustris. For this H. lacustris cells were cultivated in photobioreactors under normal light irradiance of 40μEm<SUP>-2<...
This study is aimed at identifying the proteins that are up-regulated during astaxanthin accumulation in Haematococcus lacustris. For this H. lacustris cells were cultivated in photobioreactors under normal light irradiance of 40μEm<SUP>-2</SUP>s<SUP>-1</SUP> for 6 days and then induced to accumulate astaxanthin for 3 days further by exposure to continuous high irradiance of 200μEm<SUP>-2</SUP>s<SUP>-1</SUP> with fluorescent lamps as light source after the cells reached the stationary phase in a nitrogen-depleted condition. Under this condition, the average astaxanthin content per cell increased from 91mg/l up to 406mg/l after 3 days of induction. The proteomics data from a two-dimensional electrophoretic comparison demonstrated that a combination of nitrogen source depletion and 1h high light have significantly changed the pattern of protein expression in H. lacustris. A total of 49 protein spots were picked after 1h of stress induction. They consisted of 13 down-regulated proteins and 36 up-regulated proteins. Fifteen proteins which had highly up-regulated expression were further analyzed by matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). The results will point toward interesting proteins that can be pursued for further analysis of astaxanthin biosynthesis pathway.
Synthesis, structural analysis and application of novel acarbose-fructoside using levansucrase