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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/39457
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dc.contributor.authorGiraldo, Marielle Aleixo-
dc.contributor.authorda Silva, Tony Marcio-
dc.contributor.authorSalvato, Fernanda-
dc.contributor.authorTerenzi, Hector Francisco-
dc.contributor.authorJorge, Joao Atilio-
dc.contributor.authorSouza Guimaraes, Luis Henrique-
dc.date.accessioned2014-05-20T15:30:00Z-
dc.date.accessioned2016-10-25T18:05:22Z-
dc.date.available2014-05-20T15:30:00Z-
dc.date.available2016-10-25T18:05:22Z-
dc.date.issued2012-02-01-
dc.identifierhttp://dx.doi.org/10.1007/s11274-011-0837-9-
dc.identifier.citationWorld Journal of Microbiology & Biotechnology. New York: Springer, v. 28, n. 2, p. 463-472, 2012.-
dc.identifier.issn0959-3993-
dc.identifier.urihttp://hdl.handle.net/11449/39457-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/39457-
dc.description.abstractThe filamentous fungus Paecylomices variotii was able to produce high levels of cell extract and extracellular invertases when grown under submerged fermentation (SbmF) and solid-state fermentation, using agroindustrial products or residues as substrates, mainly soy bran and wheat bran, at 40A degrees C for 72 h and 96 h, respectively. Addition of glucose or fructose (a parts per thousand yen1%; w/v) in SbmF inhibited enzyme production, while the addition of 1% (w/v) peptone as organic nitrogen source enhanced the production by 3.7-fold. However, 1% (w/v) (NH4)(2)HPO4 inhibited enzyme production around 80%. The extracellular form was purified until electrophoretic homogeneity (10.5-fold with 33% recovery) by DEAE-Fractogel and Sephacryl S-200 chromatography. The enzyme is a monomer with molecular mass of 102 kDa estimated by SDS-PAGE with carbohydrate content of 53.6%. Optima of temperature and pH for both, extracellular and cell extract invertases, were 60A degrees C and 4.0-4.5, respectively. Both invertases were stable for 1 h at 60A degrees C with half-lives of 10 min at 70A degrees C. Mg2+, Ba2+ and Mn2+ activated both extracellular and cell extract invertases from P. variotii. The kinetic parameters K-m and V-max for the purified extracellular enzyme corresponded to 2.5 mM and 481 U/mg prot(-1), respectively.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent463-472-
dc.language.isoeng-
dc.publisherSpringer-
dc.sourceWeb of Science-
dc.subjectInvertaseen
dc.subjectbeta-Fructofuranosidaseen
dc.subjectSucroseen
dc.subjectPaecylomycesen
dc.subjectFungien
dc.titleThermostable invertases from Paecylomyces variotii produced under submerged and solid-state fermentation using agroindustrial residuesen
dc.typeoutro-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUniv São Paulo, Dept Biol, Fac Filosofia Ciencias & Letras Ribeirao Preto, BR-14040901 São Paulo, Brazil-
dc.description.affiliationUniv Estadual Paulista, Inst Quim Araraquara, BR-14800900 São Paulo, Brazil-
dc.description.affiliationUniv São Paulo, Dept Genet, ESALQ, BR-13418900 São Paulo, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim Araraquara, BR-14800900 São Paulo, Brazil-
dc.identifier.doi10.1007/s11274-011-0837-9-
dc.identifier.wosWOS:000300014300007-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofWorld Journal of Microbiology & Biotechnology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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