Fluorescein Derivatives as Antibacterial Agents Acting via Membrane Depolarization
Pavel A. Nazarov,
Roman S. Kirsanov,
Stepan S. Denisov,
Ljudmila S. Khailova,
Marina V. Karakozova,
Konstantin G. Lyamzaev,
Galina A. Korshunova,
Konstantin A. Lukyanov,
Elena A. Kotova,
Yuri N. Antonenko
Affiliations
Pavel A. Nazarov
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia
Roman S. Kirsanov
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia
Stepan S. Denisov
Department of Biochemistry, University of Maastricht, Cardiovascular Research Institute Maastricht, Universiteitssingel 50, 6229 ER Maastricht, The Netherlands
Ljudmila S. Khailova
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia
Marina V. Karakozova
Center of Life Sciences, Skolkovo Institute of Science and Technology, 121205 Moscow, Russia
Konstantin G. Lyamzaev
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia
Galina A. Korshunova
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia
Konstantin A. Lukyanov
Center of Life Sciences, Skolkovo Institute of Science and Technology, 121205 Moscow, Russia
Elena A. Kotova
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia
Yuri N. Antonenko
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119991 Moscow, Russia
Appending a lipophylic alkyl chain by ester bond to fluorescein has been previously shown to convert this popular dye into an effective protonophoric uncoupler of oxidative phosphorylation in mitochondria, exhibiting neuro- and nephroprotective effects in murine models. In line with this finding, we here report data on the pronounced depolarizing effect of a series of fluorescein decyl esters on bacterial cells. The binding of the fluorescein derivatives to Bacillus subtilis cells was monitored by fluorescence microscopy and fluorescence correlation spectroscopy (FCS). FCS revealed the energy-dependent accumulation of the fluorescein esters with decyl(triphenyl)- and decyl(tri-p-tolyl)phosphonium cations in the bacterial cells. The latter compound proved to be the most potent in suppressing B. subtilis growth.