Easy and Rapid Purification of Highly Active Nisin

Author:

Abts André1,Mavaro Antonino1,Stindt Jan1,Bakkes Patrick J.1,Metzger Sabine2,Driessen Arnold J. M.3,Smits Sander H. J.1,Schmitt Lutz1

Affiliation:

1. Institute of Biochemistry, Heinrich Heine University Düsseldorf, Universitätsstrabe 1, 40225 Düsseldorf, Germany

2. Biological and Medical Research Center, Heinrich Heine University Düsseldorf, Universitätsstrabe 1, 40225 Düsseldorf, Germany

3. Department of Molecular Microbiology, Groningen Biomolecular Sciences and Biotechnology Institute, Zernike Institute for Advanced Materials and the Kluyver Centre for the Genomics of Industrial Microorganisms, University of Groningen, Nijenborgh 7, 9747 AG Groningen, The Netherlands

Abstract

Nisin is an antimicrobial peptide produced and secreted by several L. lactis strains and is specifically active against Gram-positive bacteria. In previous studies, nisin was purified via cation exchange chromatography at low pH employing a single-step elution using 1 M NaCl. Here, we describe an optimized purification protocol using a five-step NaCl elution to remove contaminants. The obtained nisin is devoid of impurities and shows high bactericidal activity against the nisin-sensitive L. lactis strain NZ9000. Purified nisin exhibits an IC50 of ~3 nM, which is a tenfold improvement as compared to nisin obtained via the one-step elution procedure.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Hindawi Limited

Subject

Biochemistry

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