Early changes in membrane potential of Saccharomyces cerevisiae induced by varying extracellular K(+), Na (+) or H (+) concentrations
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- buněčná membrána metabolismus MeSH
- draslík metabolismus MeSH
- fluorescenční barviva chemie MeSH
- fluorometrie MeSH
- kationty jednomocné metabolismus MeSH
- koncentrace vodíkových iontů MeSH
- membránové potenciály účinky léků MeSH
- Saccharomyces cerevisiae účinky léků metabolismus MeSH
- sodík metabolismus MeSH
- vodík metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- draslík MeSH
- fluorescenční barviva MeSH
- kationty jednomocné MeSH
- sodík MeSH
- vodík MeSH
Recently we introduced a fluorescent probe technique that makes possible to convert changes of equilibrium fluorescence spectra of 3,3'-dipropylthiadicarbocyanine, diS-C3(3), measured in yeast cell suspensions under defined conditions into underlying membrane potential differences, scaled in millivolts (Plasek et al. in J Bioenerg Biomembr 44: 559-569, 2012). The results presented in this paper disclose measurements of real early changes of plasma membrane potential induced by the increase of extracellular K(+), Na(+) and H(+) concentration in S. cerevisiae with and without added glucose as energy source. Whereas the wild type and the ∆tok1 mutant cells exhibited similar depolarization curves, mutant cells lacking the two Trk1,2 potassium transporters revealed a significantly decreased membrane depolarization by K(+), particularly at lower extracellular potassium concentration [K(+)]out. In the absence of external energy source plasma membrane depolarization by K(+) was almost linear. In the presence of glucose the depolarization curves exhibited an exponential character with increasing [K(+)]out. The plasma membrane depolarization by Na(+) was independent from the presence of Trk1,2 transporters. Contrary to K(+), Na(+) depolarized the plasma membrane stronger in the presence of glucose than in its absence. The pH induced depolarization exhibited a fairly linear relationship between the membrane potential and the pHo of cell suspensions, both in the wild type and the Δtrk1,2 mutant strains, when cells were energized by glucose. In the absence of glucose the depolarization curves showed a biphasic character with enhanced depolarization at lower pHo values.
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Biochim Biophys Acta. 2000 Mar 10;1469(1):1-30 PubMed
J Membr Biol. 1991 Aug;123(2):171-82 PubMed
Mol Cell Biol. 1999 May;19(5):3328-37 PubMed
Microbiology (Reading). 1998 Oct;144 ( Pt 10):2749-2758 PubMed
Biotechnol Bioeng. 2004 Mar 30;85(7):776-89 PubMed
FEMS Yeast Res. 2010 Aug 1;10(5):508-17 PubMed
Mol Cell Biochem. 1996 May 24;158(2):121-4 PubMed
Nature. 1998 Jul 9;394(6689):192-5 PubMed
Mol Biol Cell. 2005 Mar;16(3):1396-405 PubMed
Arch Biochem Biophys. 1984 May 15;231(1):217-25 PubMed
J Membr Biol. 1998 Mar 1;162(1):67-80 PubMed
Folia Microbiol (Praha). 2011 Jan;56(1):23-8 PubMed
FEMS Yeast Res. 2012 Jun;12(4):439-46 PubMed
Microbiol Mol Biol Rev. 2010 Mar;74(1):95-120 PubMed
J Bioenerg Biomembr. 2010 Oct;42(5):419-32 PubMed
J Biol Chem. 1998 Jun 12;273(24):14838-44 PubMed
FEMS Yeast Res. 2006 Nov;6(7):1039-46 PubMed
PLoS Comput Biol. 2013;9(1):e1002879 PubMed
Yeast. 1998 Sep 30;14(13):1189-97 PubMed
Fungal Biol. 2010 Feb-Mar;114(2-3):144-50 PubMed
J Theor Biol. 1974 Nov;48(1):11-18 PubMed
J Biol Chem. 2009 Jan 30;284(5):2795-2802 PubMed
Yeast. 1998 Jan 30;14(2):115-32 PubMed
J Bioenerg Biomembr. 2012 Oct;44(5):559-69 PubMed
Cell Mol Life Sci. 2010 Aug;67(15):2511-32 PubMed