The Debaryomyces hansenii NHA1 gene encodes a plasma membrane alkali-metal-cation antiporter with broad substrate specificity
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
16303259
DOI
10.1016/j.gene.2005.10.007
PII: S0378-1119(05)00608-6
Knihovny.cz E-zdroje
- MeSH
- Ascomycota genetika fyziologie MeSH
- chlorid sodný MeSH
- DNA fungální MeSH
- fyziologická adaptace MeSH
- geny hub * MeSH
- kationty metabolismus MeSH
- koncentrace vodíkových iontů MeSH
- kovy metabolismus MeSH
- membránové proteiny genetika MeSH
- molekulární sekvence - údaje MeSH
- Na(+)-H(+) antiport genetika MeSH
- plazmidy MeSH
- proteiny přenášející kationty genetika MeSH
- Saccharomyces cerevisiae - proteiny genetika MeSH
- sekvence aminokyselin MeSH
- sekvence nukleotidů MeSH
- substrátová specifita MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- chlorid sodný MeSH
- DNA fungální MeSH
- kationty MeSH
- kovy MeSH
- membránové proteiny MeSH
- Na(+)-H(+) antiport MeSH
- NHA1 protein, S cerevisiae MeSH Prohlížeč
- proteiny přenášející kationty MeSH
- Saccharomyces cerevisiae - proteiny MeSH
Debaryomyces hansenii is a yeast species often found in salty environments. Its genome sequence is known completely, but the mechanisms behind its halotolerance are poorly understood. In the D. hansenii genome, there is a gene strongly homologous to the Saccharomyces cerevisiae NHA1 gene (encoding a plasma membrane Na+/H+ antiporter). We isolated this DhNHA1 gene from two D. hansenii strains (CBS 767 and CBS 1793) differing in their osmotolerance. Both DhNHA1 alleles were heterologously expressed in a S. cerevisiae strain lacking its own systems for the efflux of alkali metal cations (BW31a, ena1-4delta nha1delta). D. hansenii Na+/H+ antiporters were localized in the plasma membrane of BW31a cells, their presence increased BW31a tolerance to sodium, potassium, lithium and also rubidium. Measurements of Na+ and K+ efflux from S. cerevisiae cells expressing DhNHA1 alleles show that the D. hansenii antiporters efficiently transported both cations out of cells. The sodium and potassium transport activity of Nha1 antiporters from both D. hansenii strains was almost identical, indicating that plasma membrane antiporter activity is not one of the factors determining the different levels of halotolerance in the two strains.
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