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dc.contributor.authorEsteban, Pedro Felipe-
dc.contributor.authorGarcía, Raúl-
dc.contributor.authorDueñas, Encarnación-
dc.contributor.authorSánchez-Pérez, Miguel-
dc.contributor.authorVázquez de Aldana, Carlos R.-
dc.contributor.authorRey Iglesias, Francisco del-
dc.date.accessioned2009-02-06T11:00:14Z-
dc.date.available2009-02-06T11:00:14Z-
dc.date.issued2005-11-16-
dc.identifier.citationCurrent Microbiology 51(6): 385-392 (2005)en_US
dc.identifier.issn0343-8651-
dc.identifier.urihttp://hdl.handle.net/10261/10383-
dc.description8 pages, 5 figures.-- et al.en_US
dc.description.abstractThe Candida albicans CaENG1 gene encoding an endo-1,3-β-glucanase was cloned by screening a genomic library with a DNA probe obtained by polymerase chain reaction using synthetic oligonucleotides designed according to conserved regions found between two Saccharomyces cerevisiae endo-1,3-β-glucanases (Eng1p and Eng2p). The gene contains a 3435-bp open reading frame (ORF), capable of encoding a protein of 1145 amino acids (124,157 Da), that contains no introns. Comparison of the ScEng1p sequence with partial C. albicans genomic sequences revealed the presence of a second protein with sequence similarity (the product of the Ca20C1.22c ORF, which was named CaENG2). Disruption of the CaENG1 gene in C. albicans had no dramatic effects on the growth rate of the strains, but it resulted in the formation of chains of cells, suggesting that the protein is involved in cell separation. Expression of CaENG1 in S. cerevisiae cells afforded a 12-fold increase in the 1,3-β-glucanase activity detected in culture supernatants, showing that the protein has similar enzymatic activity to that of the S. cerevisiae Eng1p. In addition, when the C. albicans protein was expressed under its native promoter in S. cerevisiae eng1 mutant cells, it was able to complement the separation defect of this mutant, indicating that these two proteins are true functional homologues.en_US
dc.description.sponsorshipThis research was supported by grants from the Comisión Interministerial de Ciencia y Tecnología (Grant Nos. 1FD97-1897-C02-02 and BIO2000-1573) and from the European Community (Grant No. QKL3-2000-01537). P. F. E., I. R., and R. G. were recipients of a fellowship from Ministerio de Educación y Ciencia (Spain).en_US
dc.format.extent376553 bytes-
dc.format.mimetypeapplication/pdf-
dc.language.isoengen_US
dc.publisherSpringer Natureen_US
dc.rightsclosedAccessen_US
dc.titleCharacterization of the CaENG1 gene encoding an endo-1,3-β-glucanase involved in cell separation in Candida albicansen_US
dc.typeartículoen_US
dc.identifier.doi10.1007/s00284-005-0066-2-
dc.description.peerreviewedPeer revieweden_US
dc.relation.publisherversionhttp://dx.doi.org/10.1007/s00284-005-0066-2en_US
dc.identifier.e-issn1432-0991-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeartículo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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