Ontology highlight
ABSTRACT:
SUBMITTER: McBrayer DN
PROVIDER: S-EPMC5551036 | biostudies-literature | 2017 Jun
REPOSITORIES: biostudies-literature
McBrayer Dominic N DN Gantman Brooke K BK Cameron Crissey D CD Tal-Gan Yftah Y
Organic letters 20170607 12
The development of an entirely solid-phase peptide synthesis (SPPS)-based synthesis of the quorum sensing signal gelatinase biosynthesis-activating pheromone (GBAP) from Enterococcus faecalis is reported. The method was used to prepare three libraries of analogues to investigate the structure-activity relationships (SARs) of the GBAP signal. The SAR studies revealed new characteristics of the GBAP signal and uncovered the most potent quorum sensing activator in E. faecalis known to date. ...[more]