Academic Journal

Biochemical and Mutational Studies of the Bacillus cereus CECT 5050T Formamidase Support the Existence of a C-E-E-K Tetrad in Several Members of the Nitrilase Superfamily

التفاصيل البيبلوغرافية
العنوان: Biochemical and Mutational Studies of the Bacillus cereus CECT 5050T Formamidase Support the Existence of a C-E-E-K Tetrad in Several Members of the Nitrilase Superfamily
المؤلفون: Soriano-Maldonado, Pablo, Martínez-Gómez, Ana Isabel, Andújar-Sánchez, Montserrat, Neira, José L., Clemente-Jiménez, Josefa María, Las Heras-Vázquez, Francisco Javier, Rodríguez-Vico, Felipe, Martínez-Rodríguez, Sergio
المصدر: Applied and Environmental Microbiology ; volume 77, issue 16, page 5761-5769 ; ISSN 0099-2240 1098-5336
بيانات النشر: American Society for Microbiology
سنة النشر: 2011
الوصف: Formamidases (EC 3.5.1.49) are poorly characterized proteins. In spite of this scarce knowledge, ammonia has been described as playing a central role in the pathogenesis of human pathogens such as Helicobacter pylori , for which formamidase has been shown to participate in the nitrogen metabolic pathway. Sequence analysis has revealed that at least two different groups of formamidases are classified as EC 3.5.1.49: on the one hand, the derivatives of the FmdA-AmdA superfamily, which are the best studied to date, and on the other hand, the derivatives of Helicobacter pylori AmiF. Here we present the cloning, purification, and characterization of a recombinant formamidase from Bacillus cereus CECT 5050T (BceAmiF), the second member of the AmiF subfamily to be characterized, showing new features of the enzyme further supporting its relationship with aliphatic amidases. We also present homology modeling-based mutational studies confirming the importance of the Glu140 and Tyr191 residues in the enzymatic activities of the AmiF family. Moreover, we can conclude that a second glutamate residue is critical in several members of the nitrilase superfamily, meaning that what has consistently been identified as a C-E-K triad is in fact a C-E-E-K tetrad.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1128/aem.00312-11
DOI: 10.1128/AEM.00312-11
الاتاحة: http://dx.doi.org/10.1128/aem.00312-11
https://journals.asm.org/doi/pdf/10.1128/AEM.00312-11
Rights: https://journals.asm.org/non-commercial-tdm-license
رقم الانضمام: edsbas.1848F613
قاعدة البيانات: BASE