4.7 Article

Enhancement of the enterocin CRL35 activity by a synthetic peptide derived from the NH2-terminal sequence

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ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
卷 48, 期 7, 页码 2778-2781

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AMER SOC MICROBIOLOGY
DOI: 10.1128/AAC.48.7.2778-2781.2004

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  1. PHS HHS [AY 398693] Funding Source: Medline

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The enterocin CRL35 biosynthetic gene cluster was cloned and sequenced. The sequence was revealed to be highly identical to that of the mundticin KS gene cluster (S. Kawamoto, J. Shima, R. Sato, T. Eguchi, S. Ohmomo, J. Shibato, N. Horikoshi, K. Takeshita, and T. Sameshima, Appl. Environ. Microbiol. 68:3830-3840, 2002). Short synthetic peptides were designed based on the bacteriocin sequence and were evaluated in antimicrobial competitive assays. The peptide KYYGNGVSCNKKGCS produced an enhancement of enterocin CRL35 antimicrobial activity in a buffer system.

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