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

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

摘要

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。
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 ...
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