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dc.contributor.authorHuang, CYen_US
dc.contributor.authorYang, YSen_US
dc.date.accessioned2014-12-08T15:41:51Z-
dc.date.available2014-12-08T15:41:51Z-
dc.date.issued2002-10-04en_US
dc.identifier.issn0006-291Xen_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0006-291X(02)02330-6en_US
dc.identifier.urihttp://hdl.handle.net/11536/28461-
dc.description.abstractImidase catalyzes the hydrolysis of a variety of imides. The removal of metal from imidase eliminates its activity but does not affect its tetrameric and secondary structure. The reactivation of the apoenzyme with transition metal ions Co2+, Zn2+, Mn2+, and Cd2+ shows that imidase activity is linearly dependent on the amount of metal ions added. Ni2+ and Cu2+ are also inserted, one per enzyme subunit, into the apoimidase, but do not restore imidase activity. Enzyme activity with different metal replaced imidase varies significantly. However, the changes of the metal contents do not appear to affect the pK(a)s obtained from the bell-shaped pH profiles of metal reconstituted imidase. The metal-hydroxide mechanism for imidase action is not supported based on the novel findings from this study. It is proposed that metal ion in mammalian imidase functions as a Lewis acid, which stabilizes the developing negative charge of imide substrate in transition state.en_US
dc.language.isoen_USen_US
dc.subjectimidaseen_US
dc.subjectpH profileen_US
dc.subjectmetal replacementen_US
dc.subjecttransition metalen_US
dc.titleThe role of metal on imide hydrolysis: metal content and pH profiles of metal ion-replaced mammalian imidaseen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0006-291X(02)02330-6en_US
dc.identifier.journalBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONSen_US
dc.citation.volume297en_US
dc.citation.issue4en_US
dc.citation.spage1027en_US
dc.citation.epage1032en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000178569700051-
dc.citation.woscount17-
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