Microbiologia

URI permanente desta comunidadehttps://locus.ufv.br/handle/123456789/11840

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Agora exibindo 1 - 2 de 2
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    Cloning and characterization of a gene encoding the endopolygalacturonase of Penicillium griseoroseum
    (Biotechnology Letters, 1999-05) Ribon, A. O. B.; Coelho, J. L. C.; Barros, E. G. de; Araújo, E. F.
    A conserved region of a polygalacturonase (PG) gene from Penicillium griseoroseum was PCR amplified and used to screen a genomic library from this fungus. The nucleotide sequence of the isolated clone (pggI) consisted of 1497 bp, including a coding region of 1251 bp. This region potentially encodes a protein of 376 amino acids, and is interrupted by two introns. Extensive homology was observed between this protein and several fungal endopolygalacturonases. DNA hybridization analyses revealed that there is a low copy number of pggI in the P. griseoroseum genome, probably one or two copies.
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    Production of pectin lyase by Penicillium griseoroseum as a function of the inoculum and culture conditions
    (World Journal of Microbiology and Biotechnology, 1992-10-09) Brumano, M. H. N.; Coelho, J. L. C.; Araújo, E. F.; Silva, D. O.
    Optimum activity of an extracellular pectin lyase produced by Penicillium griseoroseum in submerged culture was after 120 h using 0.1% (w/v) citrus pectin as substrate. Sucrose at 0.1% (w/v) stimulated enzyme production and citrus pectin gave the highest activity of enzyme per unit growth.