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Authordc.contributor.authorAllende, Jorge E. 
Authordc.contributor.authorAllende, Catherine C. 
Authordc.contributor.authorGatica, Marta 
Authordc.contributor.authorMatamala, María 
Admission datedc.date.accessioned2019-01-29T14:14:04Z
Available datedc.date.available2019-01-29T14:14:04Z
Publication datedc.date.issued1964
Cita de ítemdc.identifier.citationBiochemical and Biophysical Research Communications, Volumen 16, Issue 4, 2018, Pages 342-346
Identifierdc.identifier.issn10902104
Identifierdc.identifier.issn0006291X
Identifierdc.identifier.other10.1016/0006-291X(64)90037-3
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/160319
Abstractdc.description.abstractThe aminoacyl-RNA synthetases have been shown to carry out the following two-step reaction: 1. 1) amino acid + ATP + enzyme ⇌ aminoacyl-AMP-enzyme + PPi 2. 2) aminoacyl-AMP-enzyme + sRNA ⇌ aminoacyl-sRNA + AMP + enzyme. Evidence for the formation of the intermediate aminoacyl-AMP-enzyme complex has been reported by several investigators (Hoagland, 1955, De Moss and Novelli, 1955, Berg, 1956). Tryptophanyl adenylate (Karasek, et, al., 1958) and seryl adenylate (Webster and Davie, 1961) were isolated in trichloroacetic acid supernatant fractions after incubation of amino acid and ATP with substrate amounts of the respective enzymes. The present communication describes the isolation of enzyme-bound threonyl adenylate and the capacity of this complex to transfer the threonine directly to sRNA. © 1964.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceBiochemical and Biophysical Research Communications
Keywordsdc.subjectBiophysics
Keywordsdc.subjectBiochemistry
Keywordsdc.subjectMolecular Biology
Keywordsdc.subjectCell Biology
Títulodc.titleIsolation of threonyl adenylate-enzyme complex
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile