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Molecular cloning and functional characterisation of a glucose transporter, CaHGT1, of Candida albicans.
Varma, A; Singh, B B; Karnani, N; Lichtenberg-Fraté, H; Höfer, M; Magee, B B; Prasad, R.
Afiliação
  • Varma A; School of Life Sciences, Jawaharlal Nehru University, New Delhi, India.
FEMS Microbiol Lett ; 182(1): 15-21, 2000 Jan 01.
Article em En | MEDLINE | ID: mdl-10612724
We have cloned the first glucose transporter CaHGT1 (Candida albicans high-affinity glucose transporter) of a pathogenic yeast, Candida albicans. The DNA sequence (GenBank accession number Y16834) analysis revealed an ORF encoding a novel protein of 545 amino acids with a predicted molecular mass of 60.67 kDa. The putative protein with 12 transmembrane domains has 51% identity with Kluyveromyces lactis high-affinity glucose transporter, HGT1. The protein signatures which are conserved and distinctive of the sugar transporters belonging to the major facilitator superfamily (MFS) were also found in CaHgt1p. When heterologously expressed, the ORF functionally complemented a mutant strain of Saccharomyces cerevisiae RE700A which was deleted in seven hexose transporter genes and thus was unable to grow or transport glucose. The expression of CaHGT1 in C. albicans showed a transcript of 1.6 kb which was enhanced in response to the human steroid hormone progesterone. Interestingly, the transcript levels were also enhanced in the presence of drugs, e.g. cycloheximide, chloramphenicol and benomyl. The results suggest that CaHGT1, which encodes a MFS protein, could be linked to the drug resistance phenomenon in C. albicans.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte de Monossacarídeos / Candida albicans / Clonagem Molecular Idioma: En Revista: FEMS Microbiol Lett Ano de publicação: 2000 Tipo de documento: Article País de afiliação: Índia
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Transporte de Monossacarídeos / Candida albicans / Clonagem Molecular Idioma: En Revista: FEMS Microbiol Lett Ano de publicação: 2000 Tipo de documento: Article País de afiliação: Índia