Artilysation' of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci
| dc.contributor.author | Rodríguez-Rubio, Lorena | |
| dc.contributor.author | Chang, Wai-Ling | |
| dc.contributor.author | Gutiérrez, Diana | |
| dc.contributor.author | Lavigne, Rob | |
| dc.contributor.author | Martínez, Beatriz | |
| dc.contributor.author | Rodríguez, Ana | |
| dc.contributor.author | Govers, Sander K. | |
| dc.contributor.author | Aertsen, Abram | |
| dc.contributor.author | Hirl, Christine | |
| dc.contributor.author | Biebl, Manfred | |
| dc.contributor.author | Briers, Yves | |
| dc.contributor.author | García, Pilar | |
| dc.date.accessioned | 2018-11-09T16:15:56Z | |
| dc.date.available | 2018-11-09T16:15:56Z | |
| dc.date.issued | 2016-10-24 | |
| dc.date.updated | 2018-11-09T16:15:56Z | |
| dc.description.abstract | Endolysins constitute a promising class of antibacterials against Gram-positive bacteria. Recently, endolysins have been engineered with selected peptides to obtain a new generation of lytic proteins, Artilysins, with specific activity against Gram-negative bacteria. Here, we demonstrate that artilysation can also be used to enhance the antibacterial activity of endolysins against Gram-positive bacteria and to reduce the dependence on external conditions. Art-240, a chimeric protein of the anti-streptococcal endolysin λSa2lys and the polycationic peptide PCNP, shows a similar species specificity as the parental endolysin, but the bactericidal activity against streptococci increases and is less affected by elevated NaCl concentrations and pH variations. Time-kill experiments and time-lapse microscopy demonstrate that the killing rate of Art-240 is approximately two-fold higher compared to wildtype endolysin λSa2lys, with a reduction in viable bacteria of 3 log units after 10min. In addition, lower doses of Art240 are required to achieve the same bactericidal effect. | |
| dc.format.extent | 11 p. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.idgrec | 680685 | |
| dc.identifier.issn | 2045-2322 | |
| dc.identifier.pmid | 27775093 | |
| dc.identifier.uri | https://hdl.handle.net/2445/125974 | |
| dc.language.iso | eng | |
| dc.publisher | Nature Publishing Group | |
| dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.1038/srep35382 | |
| dc.relation.ispartof | Scientific Reports, 2016, vol. 6, num. 35382 | |
| dc.relation.uri | https://doi.org/10.1038/srep35382 | |
| dc.rights | cc-by (c) Rodriguez Rubio, Lorena et al., 2016 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es | |
| dc.source | Articles publicats en revistes (Genètica, Microbiologia i Estadística) | |
| dc.subject.classification | Estreptococs | |
| dc.subject.classification | Enzims microbians | |
| dc.subject.classification | Bacteriòfags | |
| dc.subject.other | Streptococcus | |
| dc.subject.other | Microbial enzymes | |
| dc.subject.other | Bacteriophages | |
| dc.title | Artilysation' of endolysin λSa2lys strongly improves its enzymatic and antibacterial activity against streptococci | |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion |
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