Literature DB >> 2776579

Rapid analytical technique for the assessment of cell metabolic activity in marine microalgae.

J Dorsey1, C M Yentsch, S Mayo, C McKenna.   

Abstract

A standard method for the assessment of cell viability has been developed for marine phytoplankton using an inexpensive stain, fluorescein diacetate (FDA), at .75 microM for 10 min. A flow cytometer was used as the fluorescence detector, providing an assessment of viability for each individual particle. Cell size and chlorophyll fluorescence per cell were assessed simultaneously, permitting an assignment of viability to specific subpopulations, thus increasing the power of the technique. A reasonable correspondence between FDA mean fluorescence intensity per cell and an independent metabolic indicator, photosynthetic capacity measured by 14C, was found. Both FDA mean fluorescence intensity and photosynthetic capacity vary as a function of cell volume. Recovery after extended periods of darkness indicate that cells that are FDA negative may not be dead, but merely quiescent or inactive.

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Year:  1989        PMID: 2776579     DOI: 10.1002/cyto.990100518

Source DB:  PubMed          Journal:  Cytometry        ISSN: 0196-4763


  11 in total

1.  Quantitative assessment of marine sponge cells in vitro: development of improved growth medium.

Authors:  R Willoughby; S A Pomponi
Journal:  In Vitro Cell Dev Biol Anim       Date:  2000-03       Impact factor: 2.416

2.  Green autofluorescence in dinoflagellates, diatoms, and other microalgae and its implications for vital staining and morphological studies.

Authors:  Ying Zhong Tang; Fred C Dobbs
Journal:  Appl Environ Microbiol       Date:  2007-02-02       Impact factor: 4.792

3.  Direct measurements of natural planktonic bacterial community viability by flow cytometry.

Authors:  J Porter; J Diaper; C Edwards; R Pickup
Journal:  Appl Environ Microbiol       Date:  1995-07       Impact factor: 4.792

4.  A new insight into allelopathic effects of Alexandrium minutum on photosynthesis and respiration of the diatom Chaetoceros neogracile revealed by photosynthetic-performance analysis and flow cytometry.

Authors:  Aurélie Lelong; Hansy Haberkorn; Nelly Le Goïc; Hélène Hégaret; Philippe Soudant
Journal:  Microb Ecol       Date:  2011-07-05       Impact factor: 4.552

5.  Flow cytometric analysis to evaluate physiological alterations in herbicide-exposed Chlamydomonas moewusii cells.

Authors:  Raquel Prado; Carmen Rioboo; Concepción Herrero; Paula Suárez-Bregua; Angeles Cid
Journal:  Ecotoxicology       Date:  2011-10-05       Impact factor: 2.823

6.  Diatom-associated bacteria are required for aggregation of Thalassiosira weissflogii.

Authors:  Astrid Gärdes; Morten H Iversen; Hans-Peter Grossart; Uta Passow; Matthias S Ullrich
Journal:  ISME J       Date:  2010-09-09       Impact factor: 10.302

7.  Use of a microscope photometer to analyze in vivo fluorescence intensity of epilithic microalgae grown on artificial substrata.

Authors:  G Becker; H Holfeld; A T Hasselrot; D M Fiebig; D A Menzler
Journal:  Appl Environ Microbiol       Date:  1997-04       Impact factor: 4.792

8.  Sorting inhibitors (Sortins): Chemical compounds to study vacuolar sorting in Arabidopsis.

Authors:  Jan Zouhar; Glenn R Hicks; Natasha V Raikhel
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-09       Impact factor: 11.205

9.  Comparing Acute Effects of a Nano-TiO2 Pigment on Cosmopolitan Freshwater Phototrophic Microbes Using High-Throughput Screening.

Authors:  Chu Thi Thanh Binh; Christopher G Peterson; Tiezheng Tong; Kimberly A Gray; Jean-François Gaillard; John J Kelly
Journal:  PLoS One       Date:  2015-04-29       Impact factor: 3.240

10.  Classification of phytoplankton cells as live or dead using the vital stains fluorescein diacetate and 5-chloromethylfluorescein diacetate.

Authors:  Hugh L MacIntyre; John J Cullen
Journal:  J Phycol       Date:  2016-04-28       Impact factor: 2.923

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