| Literature DB >> 30793902 |
Noel M Lacerna1, Bailey W Miller2, Albebson L Lim1, Jortan O Tun1, Jose Miguel D Robes1, Mark Jeremiah B Cleofas1, Zhenjian Lin2, Lilibeth A Salvador-Reyes1, Margo G Haygood2, Eric W Schmidt2, Gisela P Concepcion1.
Abstract
Three new pyoluteorin analogues, mindapyrroles A-C (1-3), were purified from Pseudomonas aeruginosa strain 1682U.R.0a.27, a gill-associated bacterium isolated from the tissue homogenate of the giant shipworm Kuphus polythalamius. Mindapyrroles B and C inhibit the growth of multiple pathogenic bacteria, with mindapyrrole B (2) showing the most potent antimicrobial activity and widest selectivity index over mammalian cells. Preliminary structure-activity relationship analysis showed that dimerization of the pyoluteorin moiety through a C-C linkage is detrimental to the antimicrobial activity, but addition of an aerugine unit in the methylene bridge is favorable for both the antimicrobial activity and selectivity index.Entities:
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Year: 2019 PMID: 30793902 PMCID: PMC8188622 DOI: 10.1021/acs.jnatprod.8b00979
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050