Premium
Fiuorimetric assessment of Pseudomonas fluorescens viability after freeze‐thawing using ethidium bromide
Author(s) -
Puchkov E.O.,
Melkozernov A.N.
Publication year - 1995
Publication title -
letters in applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.698
H-Index - 110
eISSN - 1472-765X
pISSN - 0266-8254
DOI - 10.1111/j.1472-765x.1995.tb01083.x
Subject(s) - ethidium bromide , fluorescence , bacteria , viability assay , pseudomonas fluorescens , nucleic acid , permeability (electromagnetism) , biophysics , chemistry , chromatography , biology , biochemistry , cell , dna , genetics , physics , quantum mechanics , membrane
E.O. PUCHKOV AND A.N. MELKOZERNOV. 1995. The relationship between impairment of the Pseudomonas fluorescens cell envelope's permeability barrier for ethidium cation, the fluorescent moiety of ethidium bromide, and viability after freeze‐thawing was investigated. Ethidium fluorescence in the suspension of intact bacteria did not change. Disruption of the bacterial permeability barrier by cetyltrimethylammonium bromide (CTAB) led to ethidium fluorescence increase due to interaction of the fluorochrome with intracellular nucleic acids. In the suspension of freeze‐thawed cells, ethidium fluorescence increased and the subsequent treatment by CTAB resulted in further fluorescence increase up to the final level corresponding to that in CTAB‐treated intact bacteria. For bacteria exposed to different freeze‐thawing regimes, the relative ethidium fluorescence increase closely correlated with the relative number of fluorescing cells revealed microscopically. In the suspension of freeze‐thawed cells, the relative additional ethidium fluorescence increase after CTAB treatment closely correlated with viability evaluated by plate counts. It is concluded that the fluorimetric approach may be used as a means of rapidly evaluating bacterial viability after freeze‐thawing.