Construction of a modified penicillin-binding protein 2a from methicillin-resistant Staphylococcus aureus and purification by immobilized metal affinity chromatography.

Abstract:

:The mecA-27r gene, which encodes PBP2a-27r, was modified by site-specific mutagenesis, resulting in replacement of the N-terminal membrane anchor with a short chelating peptide (CP-PBP2a-27r). CP-PBP2a-27r retained the same binding affinity for beta-lactam antibiotics as the wild-type enzyme. Approximately 95% pure CP-PBP2a-27r was recovered in a single step by use of chelating-peptide-immobilized metal ion affinity chromatography.

journal_name

J Bacteriol

journal_title

Journal of bacteriology

authors

Wu CY,Blaszczak LC,Smith MC,Skatrud PL

doi

10.1128/jb.176.5.1539-1541.1994

subject

Has Abstract

pub_date

1994-03-01 00:00:00

pages

1539-41

issue

5

eissn

0021-9193

issn

1098-5530

journal_volume

176

pub_type

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