{"title":"双醋酸荧光素(FDA)作为鞭毛藻培养物代谢活性单细胞探针的应用","authors":"R. Selvin, B. Reguera, I. Bravo, C. M. Yentsch","doi":"10.1080/01965581.1988.10749548","DOIUrl":null,"url":null,"abstract":"AbstractOur goal was to determine what percentage of cells remain metabolically active under environmentally relevant culture conditions. The approach combines epifluorescence microscopy and/or a standard bench-top fluorometer, plus the probe fluorescein diacetate (FDA). This stain is colorless in solution when added at a final concentration of 10 μM. It readily penetrates the cell membrane, and once inside the cell esterases cleave acetates to form fluorescein. Within 10 minutes, metabolically active cells become brilliantly yellow-green (fluorescence measured at 515–530 nm) while inactive cells do not fluoresce or are only weakly fluorescent. The FDA assay does not degrade the chlorophyll a fluorescence signal (>675 nm) nor does it interfere with normal motility or carbon uptake in most instances. Thirty clones of dinoflagellates were examined in this study. We found this assay useful to (1) optimize culture conditions and transfer schedules; (2) evaluate trauma of transfer into new media; (3) test for ...","PeriodicalId":262997,"journal":{"name":"Biological oceanography","volume":"28 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2013-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"10","resultStr":"{\"title\":\"Use of Fluorescein Diacetate (FDA) as a Single-Cell Probe of Metabolic Activity in Dinoflagellate Cultures\",\"authors\":\"R. Selvin, B. Reguera, I. Bravo, C. M. Yentsch\",\"doi\":\"10.1080/01965581.1988.10749548\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"AbstractOur goal was to determine what percentage of cells remain metabolically active under environmentally relevant culture conditions. The approach combines epifluorescence microscopy and/or a standard bench-top fluorometer, plus the probe fluorescein diacetate (FDA). This stain is colorless in solution when added at a final concentration of 10 μM. It readily penetrates the cell membrane, and once inside the cell esterases cleave acetates to form fluorescein. Within 10 minutes, metabolically active cells become brilliantly yellow-green (fluorescence measured at 515–530 nm) while inactive cells do not fluoresce or are only weakly fluorescent. The FDA assay does not degrade the chlorophyll a fluorescence signal (>675 nm) nor does it interfere with normal motility or carbon uptake in most instances. Thirty clones of dinoflagellates were examined in this study. We found this assay useful to (1) optimize culture conditions and transfer schedules; (2) evaluate trauma of transfer into new media; (3) test for ...\",\"PeriodicalId\":262997,\"journal\":{\"name\":\"Biological oceanography\",\"volume\":\"28 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"10\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biological oceanography\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/01965581.1988.10749548\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biological oceanography","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/01965581.1988.10749548","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Use of Fluorescein Diacetate (FDA) as a Single-Cell Probe of Metabolic Activity in Dinoflagellate Cultures
AbstractOur goal was to determine what percentage of cells remain metabolically active under environmentally relevant culture conditions. The approach combines epifluorescence microscopy and/or a standard bench-top fluorometer, plus the probe fluorescein diacetate (FDA). This stain is colorless in solution when added at a final concentration of 10 μM. It readily penetrates the cell membrane, and once inside the cell esterases cleave acetates to form fluorescein. Within 10 minutes, metabolically active cells become brilliantly yellow-green (fluorescence measured at 515–530 nm) while inactive cells do not fluoresce or are only weakly fluorescent. The FDA assay does not degrade the chlorophyll a fluorescence signal (>675 nm) nor does it interfere with normal motility or carbon uptake in most instances. Thirty clones of dinoflagellates were examined in this study. We found this assay useful to (1) optimize culture conditions and transfer schedules; (2) evaluate trauma of transfer into new media; (3) test for ...