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dc.contributor.authorOliveira, Camila M.-
dc.contributor.authorSilva, Geraldo H.-
dc.contributor.authorRegasini, Luis O.-
dc.contributor.authorZanardi, Lisineia M.-
dc.contributor.authorEvangelista, Alana H.-
dc.contributor.authorYoung, Maria C. M.-
dc.contributor.authorBolzani, Vanderlan da Silva-
dc.contributor.authorAraújo, Angela Regina-
dc.date.accessioned2014-05-20T14:20:11Z-
dc.date.accessioned2016-10-25T17:41:28Z-
dc.date.available2014-05-20T14:20:11Z-
dc.date.available2016-10-25T17:41:28Z-
dc.date.issued2009-11-01-
dc.identifierhttp://www.znaturforsch.com/ac/v64c/c64c.htm-
dc.identifier.citationZeitschrift Fur Naturforschung Section C-a Journal of Biosciences. Tubingen: Verlag Z Naturforsch, v. 64, n. 11-12, p. 824-830, 2009.-
dc.identifier.issn0939-5075-
dc.identifier.urihttp://hdl.handle.net/11449/26059-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/26059-
dc.description.abstractIn the course of our continuous search for bioactive metabolites from endophytic fungi living in plants from the Brazilian flora, leaves of Alibertia macrophylla (Rubiaceae) were submitted to isolation of endophytes, and two species of Penicillium were isolated. The acetonitrile fraction obtained in corn from a culture of Penicillium sp.1 afforded orcinol (1). on the other hand, Penicillium sp.1 cultivated in potato-dextrose-broth furnished two different compounds, cyclo-(L-Pro-L-Val) (2) and uracil (3). The chromatographic fractionation of the acetonitrile fraction obtained from Penicillium sp.2 led to three dihydroisocoumarins, 4-hydroxymellein (4), 8-methoxymellein (5) and 5-hydroxymellein (6). Compounds 5 and 6 were obtained from the Penicillium genus for the first time. Additionally, metabolites 1-6 were evaluated for their antifungal and acetylcholinesterase (AChE) inhibitory activities. The most active compounds 1. and 4 exhibited detection limits of 5.00 and 10.0 mu g against Cladosporium. cladosporioides and C. sphaerospermum, respectively. Compound 2 showed a detection limit of 10.0 mu g, displaying potent AChE inhibitory activity.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.format.extent824-830-
dc.language.isoeng-
dc.publisherVerlag Z Naturforsch-
dc.sourceWeb of Science-
dc.subjectPenicilliumen
dc.subjectAlibertia macrophyllaen
dc.subjectEndophytic Fungien
dc.subjectAcetylcholinesteraseen
dc.titleBioactive Metabolites Produced by Penicillium sp.1 and sp.2, Two Endophytes Associated with Alibertia macrophylla (Rubiaceae)en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de Sergipe (UFS)-
dc.contributor.institutionInstituto de Botânica-
dc.description.affiliationUniv Estadual Paulista, Nucleo Bioensaios Biossintese & Ecofisiol Prod Na, Dept Quim Organ, Inst Quim, BR-14800900 São Paulo, Brazil-
dc.description.affiliationUniv Fed Sergipe, BR-49500000 Itabaiana, Sergipe, Brazil-
dc.description.affiliationInst Bot, Secao Fisiol & Bioquim Plantas, BR-04301902 São Paulo, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Nucleo Bioensaios Biossintese & Ecofisiol Prod Na, Dept Quim Organ, Inst Quim, BR-14800900 São Paulo, Brazil-
dc.description.sponsorshipIdFAPESP: 03/02176-7-
dc.identifier.wosWOS:000274113500012-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-74049141976.pdf-
dc.relation.ispartofZeitschrift fur Naturforschung - Section C Journal of Biosciences-
dc.identifier.scopus2-s2.0-74049141976-
dc.identifier.orcid0000-0001-7616-9652pt
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