dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:17:29Z
dc.date.available2014-05-20T13:17:29Z
dc.date.created2014-05-20T13:17:29Z
dc.date.issued2004-01-01
dc.identifierBiochemistry and Molecular Biology Education. Bethesda: Amer Soc Biochemistry Molecular Biology Inc., v. 32, n. 1, p. 45-48, 2004.
dc.identifier1470-8175
dc.identifierhttp://hdl.handle.net/11449/3926
dc.identifier10.1002/bmb.2004.494032010311
dc.identifierWOS:000188380200011
dc.identifierWOS000188380200011.pdf
dc.identifier0147241723612464
dc.description.abstractThe present research describes an efficient procedure to obtain high levels of trypsinogen and chymotrypsinogen by using a simple, rapid, and easily reproducible method. The extraction process and the time-course of activation of zymogens can be carried out in a single laboratory period, without sophisticated equipment. The main objective was to prepare a laboratory class that would stimulate student interest in enzyme regulation, exploring the fact that the catalytic activity of some enzymes is regulated by different mechanisms. The regulation of proteolytic enzymes requires the synthesis of an inactive zymogen and its being irreversibly switched on by specific proteolytic cleavage.
dc.languageeng
dc.publisherAmer Soc Biochemistry Molecular Biology Inc
dc.relationBiochemistry and Molecular Biology Education
dc.relation1.036
dc.relation0,370
dc.rightsAcesso aberto
dc.sourceWeb of Science
dc.subjectzymogen
dc.subjecttrypsin
dc.subjectchymotrypsin
dc.subjectenteropeptidase
dc.subjectenzyme regulation
dc.subjectproteolytic cleavage
dc.titleThe zymogen-enteropeptidase system: A practical approach to study the regulation of enzyme activity by proteolytic cleavage
dc.typeArtículos de revistas


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