Your browser doesn't support javascript.
loading
C-5(6) sterol desaturase from tetrahymena thermophila: Gene identification and knockout, sequence analysis, and comparison to other C-5(6) sterol desaturases.
Nusblat, Alejandro D; Najle, Sebastián R; Tomazic, Mariela L; Uttaro, Antonio D; Nudel, Clara B.
Afiliação
  • Nusblat AD; Cátedra de Biotecnología y Microbiología Industrial, Universidad de Buenos Aires, Junin, Argentina. anusblat@ffyb.uba.ar
Eukaryot Cell ; 8(8): 1287-97, 2009 Aug.
Article em En | MEDLINE | ID: mdl-19525418
ABSTRACT
The gene coding for a C-5(6) sterol desaturase in Tetrahymena thermophila, DES5A, has been identified by the knockout of the TTHERM_01194720 sequence. Macronucleus transformation was achieved by biolistic bombardment and gene replacement through phenotypic assortment, using paromomycin as the selective agent. A knockout cell line (KO270) showed a phenotype consistent with that of the DES5A deletion mutant. KO270 converted only 6% of the added sterol into the C-5 unsaturated derivative, while the wild type accumulated 10-fold larger amounts under similar conditions. The decreased desaturation activity is specific for the C-5(6) position of lathosterol and cholestanol; other desaturations, namely C-7(8) and C-22(23), were not affected. Analysis by reverse transcription-PCR reveals that DES5A is transcribed both in the presence and absence of cholestanol in wild-type cells, whereas the transcribed gene was not detected in KO270. The growth of KO270 was undistinguishable from that of the wild-type strain. Des5Ap resembles known C-5(6) sterol desaturases, displaying the three typical histidine motifs, four hydrophobic transmembrane regions, and two other highly conserved domains of unknown function. A phylogenetic analysis placed T. thermophila's enzyme and Paramecium orthologues in a cluster together with functionally characterized C-5 sterol desaturases from vertebrates, fungi, and plants, although in a different branch.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxirredutases / Proteínas de Protozoários / Tetrahymena thermophila Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Oxirredutases / Proteínas de Protozoários / Tetrahymena thermophila Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Ano de publicação: 2009 Tipo de documento: Article