dc.creatorBORGES, Keyller Bastos
dc.creatorBONATO, Pierina Sueli
dc.creatorPUPO, Mônica Tallarico
dc.date.accessioned2012-03-26T14:02:24Z
dc.date.accessioned2018-07-04T13:59:32Z
dc.date.available2012-03-26T14:02:24Z
dc.date.available2018-07-04T13:59:32Z
dc.date.created2012-03-26T14:02:24Z
dc.date.issued2011
dc.identifierQuímica Nova, v.34, n.8, p.1354-1357, 2011
dc.identifier0100-4042
dc.identifierhttp://producao.usp.br/handle/BDPI/5856
dc.identifier10.1590/S0100-40422011000800011
dc.identifierhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422011000800011
dc.identifierhttp://www.scielo.br/pdf/qn/v34n8/11.pdf
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1604430
dc.description.abstractThe enantioselective biotransformation of propranolol (Prop) by the endophytic fungi Phomopsis sp., Glomerella cingulata, Penicillium crustosum, Chaetomium globosum and Aspergillus fumigatus was investigated by studying the kinetics of the aromatic hydroxylation reaction with the formation of 4-hydroxypropranolol (4-OH-Prop). Both Prop enantiomers were consumed by the fungi in the biotransformation process, but the 4-hydroxylation reaction yielded preferentially (-)-(S)-4-OH-Prop. The quantity of metabolites biosynthesized varied slightly among the evaluated endophytic fungi. These results show that all investigated endophytic fungi could be used as biosynthetic tools in biotransformation processes to obtain the enantiomers of 4-OH-Prop.
dc.languageeng
dc.publisherSociedade Brasileira de Química
dc.relationQuímica Nova
dc.rightsCopyright Sociedade Brasileira de Química
dc.rightsopenAccess
dc.subjectEnantioselective biotransformation
dc.subjectPropranolol
dc.subjectEndophytic fungi
dc.titleEnantioselective biotransformation of propranolol to the active metabolite 4-hydroxypropranolol by endophytic fungi
dc.typeArtículos de revistas


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