Use of Fluorescein Diacetate (FDA) as a Single-Cell Probe of Metabolic Activity in Dinoflagellate Cultures

R. Selvin, B. Reguera, I. Bravo, C. M. Yentsch
{"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}
引用次数: 10

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 ...
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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
目的是确定在环境相关的培养条件下细胞保持代谢活性的百分比。该方法结合了荧光显微镜和/或标准台式荧光仪,加上探针荧光素二乙酸酯(FDA)。当最终浓度为10 μM时,该染色剂在溶液中无色。它很容易穿透细胞膜,一旦进入细胞,酯酶就会裂解乙酸酯形成荧光素。在10分钟内,代谢活跃的细胞变成明亮的黄绿色(荧光测量在515-530 nm),而不活跃的细胞不发出荧光或只有弱荧光。FDA检测不会降解叶绿素a荧光信号(>675 nm),也不会在大多数情况下干扰正常运动或碳吸收。本研究对30个鞭毛藻无性系进行了检测。我们发现该试验有助于(1)优化培养条件和转移时间表;(2)评估转移到新媒体的创伤;测试……
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
A Note on the Feeding, Growth, and Reproduction of the Epipelagic Scyphomedusa Pelagia noctiluca (Forskål) The Control of Marine Phytoplankton. Use of Quine's View of “Object” in Assessing Productivity and Control Biology of Myctophid Fishes (Family Myctophidae) in the Rockall Trough, Northeastern Atlantic Ocean The Availability of Iron in Seawater: A Perspective Toward a Cladistic View of Phytoplankton Physiological Ecology
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1