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Saccharomyces cerevisiae has a single glutamate synthase gene coding for a plant-like high-molecular-weight polypeptide.
Cogoni, C; Valenzuela, L; González-Halphen, D; Olivera, H; Macino, G; Ballario, P; González, A.
Afiliación
  • Cogoni C; Dipartimento di Biopatologia Umana Policlinico Umberto I. Universitá di Roma La Sapienza, Italy.
J Bacteriol ; 177(3): 792-8, 1995 Feb.
Article en En | MEDLINE | ID: mdl-7836314
ABSTRACT
Purification of the glutamate synthase (GOGAT) enzyme from Saccharomyces cerevisiae showed that it is an oligomeric enzyme composed of three identical 199-kDa subunits. The GOGAT structural gene was isolated by screening a yeast genomic library with a yeast PCR probe. This probe was obtained by amplification with degenerate oligonucleotides designed from conserved regions of known GOGAT genes. The derived amino-terminal sequence of the GOGAT gene was confirmed by direct amino-terminal sequence analysis of the purified protein of 199 kDa. Northern (RNA) analysis allowed the identification of an mRNA of about 7 or 8 kb. An internal fragment of the GOGAT gene was used to obtain null GOGAT mutants completely devoid of GOGAT activity. The results show that S. cerevisiae has a single NADH-GOGAT enzyme, consisting of three 199-kDa monomers, that differs from the one found in prokaryotic microorganisms but is similar to those found in other eukaryotic organisms such as alfalfa.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Genes Fúngicos / Glutamato Sintasa Idioma: En Revista: J Bacteriol Año: 1995 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Saccharomyces cerevisiae / Genes Fúngicos / Glutamato Sintasa Idioma: En Revista: J Bacteriol Año: 1995 Tipo del documento: Article País de afiliación: Italia