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PMID: 15215149 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

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

Antimicrobial agents and chemotherapy ·Vol. 48 ·No. 7 ·2004-07-00 ·Pages 2778-81

Saavedra L, Minahk C, de Ruiz Holgado AP, Sesma F

Abstract

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.

MeSH Terms
Amino Acid Sequence Bacteriocins/chemistry,genetics,pharmacology DNA Primers Drug Synergism Enterococcus/genetics Listeria/drug effects Membrane Potentials/drug effects Microbial Sensitivity Tests Molecular Sequence Data Peptides/chemical synthesis,pharmacology Reverse Transcriptase Polymerase Chain Reaction
Chemicals
Bacteriocins DNA Primers Peptides enterocin CRL35
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Saavedra Lucila
Centro de Referencia para Lactobacilos (CERELA-CONICET), S.M. de Tucumán (4000), Chacabuco 145, Tucumán, Argentina.
Minahk Carlos
de Ruiz Holgado Aída P
Sesma Fernando
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19 references, click to expand
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Article Info
Journal
Antimicrobial agents and chemotherapy
Abbr.
Antimicrob Agents Chemother
ISSN
0066-4804
Published
2004-07-00
Pages
2778-81
Language
English
Region
United States
NLM ID
0315061
PMCID
PMC434193
Subset
IM
Grants
PHS HHS · AY 398693 · United States
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