Literature DB >> 9449773

Three fluorescent probes for the flow-cytometric assessment of membrane potential in Saccharomyces cerevisiae.

B Denksteinová1, K Sigler, J Plaásek.   

Abstract

Three fluorescent probes, tetramethyl rhodamine ethyl ester (TMRE), 3,3'-dipropylthiacarbocyanine iodide (diS-C3(3)) and 3,3'-dipropyloxacarbocyanine iodide (diO-C3(3)), were tested for their suitability as fluorescent indicators of membrane potential in Saccharomyces cerevisiae in studies performed by flow cytometry. For all these dyes the intensity of fluorescence of stained cells increased with probe concentration in the range of 60-3000 nmol/L. The optimum staining period was 15-20 min for diS-C3(3). Depolarization of cells by increased extracellular potassium level and by valinomycin elicited with all probes a drop in fluorescence intensity. In some yeast batches this depolarization was accompanied by a separation of subpopulations with different fluorescence properties.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 9449773     DOI: 10.1007/bf02814623

Source DB:  PubMed          Journal:  Folia Microbiol (Praha)        ISSN: 0015-5632            Impact factor:   2.099


  7 in total

1.  Assessment of membrane potential using confocal microspectrofluorimetry.

Authors:  J Plasek; B Denksteinova; F Sureau
Journal:  J Fluoresc       Date:  1993-09       Impact factor: 2.217

Review 2.  Potential-sensitive molecular probes in membranes of bioenergetic relevance.

Authors:  J C Smith
Journal:  Biochim Biophys Acta       Date:  1990-03-15

Review 3.  Slow fluorescent indicators of membrane potential: a survey of different approaches to probe response analysis.

Authors:  J Plásek; K Sigler
Journal:  J Photochem Photobiol B       Date:  1996-04       Impact factor: 6.252

4.  Transmembrane potentials in cells: a diS-C3(3) assay for relative potentials as an indicator of real changes.

Authors:  J Plásek; R E Dale; K Sigler; G Laskay
Journal:  Biochim Biophys Acta       Date:  1994-12-30

5.  Transient hyperpolarization of yeast by glucose and ethanol.

Authors:  J B van de Mortel; D Mulders; H Korthout; A P Theuvenet; G W Borst-Pauwels
Journal:  Biochim Biophys Acta       Date:  1988-12-07

6.  Fluorescent staining with bromocresol purple: a rapid method for determining yeast cell dead count developed as an assay of killer toxin activity.

Authors:  H Kurzweilová; K Sigler
Journal:  Yeast       Date:  1993-11       Impact factor: 3.239

7.  Comparison of three different methods for determining yeast killer toxin K1 activity and standardisation of units.

Authors:  H Kurzweilová; K Sigler
Journal:  Experientia       Date:  1995-01-15
  7 in total
  1 in total

1.  Coding and non-coding roles of MOCCI (C15ORF48) coordinate to regulate host inflammation and immunity.

Authors:  Cheryl Q E Lee; Baptiste Kerouanton; Sonia Chothani; Shan Zhang; Ying Chen; Chinmay Kumar Mantri; Daniella Helena Hock; Radiance Lim; Rhea Nadkarni; Vinh Thang Huynh; Daryl Lim; Wei Leong Chew; Franklin L Zhong; David Arthur Stroud; Sebastian Schafer; Vinay Tergaonkar; Ashley L St John; Owen J L Rackham; Lena Ho
Journal:  Nat Commun       Date:  2021-04-09       Impact factor: 14.919

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.