dc.creatorSegato, Fernando
dc.creatorBerto, Gabriela L.
dc.creatorAraújo, Evandro Ares de
dc.creatorMuniz, João Renato Carvalho
dc.creatorPolikarpov, Igor
dc.date.accessioned2016-09-21T13:32:22Z
dc.date.accessioned2018-07-04T17:09:23Z
dc.date.available2016-09-21T13:32:22Z
dc.date.available2018-07-04T17:09:23Z
dc.date.created2016-09-21T13:32:22Z
dc.date.issued2014-02
dc.identifierActa Crystallographica F, Chester : International Union of Crystallography - IUCr, v. 70, part. 2, p. 267-270, Feb. 2014
dc.identifier2053-230X
dc.identifierhttp://www.producao.usp.br/handle/BDPI/50831
dc.identifier10.1107/S2053230X13034936
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1645413
dc.description.abstractEndoglucanases are important enzymes that are involved in the modification and degradation of cellulose. Filamentous fungi such as Aspergillus terreus are effective biomass degraders in nature owing to their capacity to produce an enzymatic arsenal of glycoside hydrolases, including endoglucanase from glycoside hydrolase family 12 (GH12). The A. terreus GH12 endoglucanase was cloned and overexpressed in A. nidulans, purified and crystallized. A single crystal was obtained from a solution consisting of 2 M ammonium sulfate, 5%(v/v) 2-propanol. X-ray diffraction data were collected to a resolution of 1.85 Å using synchrotron radiation and a preliminary molecular-replacement solution was obtained in the trigonal space group P3221. The unit-cell parameters were a=b= 103.24, c=48.96 Å.
dc.languageeng
dc.publisherInternational Union of Crystallography - IUCr
dc.publisherChester
dc.relationActa Crystallographica F
dc.rightsCopyright International Union of Crystallography
dc.rightsopenAccess
dc.titleExpression, purification, crystallization and preliminary X-ray diffraction analysis of Aspergillus terreus endo-β-1,4-glucanase from glycoside hydrolase family 12
dc.typeArtículos de revistas


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