Microbes and infection · 2002
Characterization of a gene which encodes a mannosyltransferase homolog of Paracoccidioides brasiliensis.
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Costa Alessandra A, Gómez Francisco J, Pereira Maristela, Felipe M Sueli S, Jesuino Rosália S A, Deepe George S, de Almeida Soares Célia M
Аннотация
We screened an expression library of the yeast form of Paracoccidioides brasiliensis with a pool of human sera that was pre-adsorbed with mycelium, from patients with paracoccidioidomycosis (PCM). A sequence (PbYmnt) was obtained and characterized. A genomic clone was obtained by PCR of P. brasiliensis total DNA. The sequence contained a single open reading frame (ORF) encoding a protein of 357 amino acid residues, with a molecular mass of 39.78 kDa. The deduced amino acid sequence exhibited identity to mannosyl- and glycosyltransferases from several sources. A DXD motif was present in the translated gene and this sequence is characteristic of the glycosyltransferases. Hydropathy analysis revealed a single transmembrane region near the amino terminus of the molecule that suggested a type II membrane protein. The PbYmnt was expressed preferentially in the yeast parasitic phase. The accession number of the nucleotide sequence of PbYmnt and its flanking regions is AF374353. A recombinant protein was generated in Escherichia coli. Our data suggest that PbYmnt encodes one member of a glycosyltransferase family of proteins and that our strategy was useful in the isolation of differentially expressed genes.
Предметные рубрики MeSH
Amino Acid MotifsAmino Acid SequenceBase SequenceCloning, MolecularFungal ProteinsHumansHydrophobic and Hydrophilic InteractionsMannosyltransferasesMolecular Sequence DataParacoccidioidesParacoccidioidomycosisPolymerase Chain ReactionRecombinant ProteinsSequence Analysis, DNASequence Homology, Amino Acid