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1 ide and possibly the secretion of the mature autoinducing peptide.
2 and AgrB and AgrD are required to produce an autoinducing peptide.
3 ay whose activating ligand is an agr-encoded autoinducing peptide.
5 st agr were noncompetitive inhibitors of the autoinducing peptide (AIP) activated AgrC receptor, by a
6 via agr-dependent quorum sensing in which an autoinducing peptide (AIP) activates AgrC, a histidine p
8 transduction module that is activated by an autoinducing peptide (AIP) encoded within the agr locus
9 e AgrC receptor histidine kinase detects its autoinducing peptide (AIP) ligand and generates an intra
11 coccus aureus, AgrD is the propeptide for an autoinducing peptide (AIP) pheromone that triggers the A
12 ce factors via the production and sensing of autoinducing peptide (AIP) signal molecules by the agr l
14 pportunistic pathogen, and the binding of an autoinducing peptide (AIP) signal to its cognate transme
15 S. epidermidis strains, but only one of the autoinducing peptide (AIP) signals has been identified (
16 reus is a major human pathogen that utilizes autoinducing peptide (AIP) signals to mediate QS and the
17 due thiolactone-containing peptide called an autoinducing peptide (AIP) that is biosynthesized from t
18 e, is initiated by the binding of a specific autoinducing peptide (AIP) to the extracellular domain o
19 agr, activated upon binding of a self-coded autoinducing peptide (AIP) to the receptor-histidine kin
20 bitory activity suggested that the S. caprae autoinducing peptide (AIP) was responsible, and mass spe
21 rference: each agr type synthesizes a cyclic autoinducing peptide (AIP) with a distinct sequence that
22 n RNAIII-activating protein (RAP) and by the autoinducing peptide (AIP), and is inhibited by RNAIII-i
23 naling activity of a secreted pheromone, the autoinducing peptide (AIP), generated following the ribo
24 a polytopic receptor, AgrC, activated by an autoinducing peptide (AIP), to coordinate quorum sensing
27 we recently developed analogues of a native autoinducing peptide (AIP-III) signal that can inhibit A
28 sensing system, staphylococci secrete unique autoinducing peptides (AIPs) and detect their concentrat
30 aureus virulence is regulated when secreted autoinducing peptides (AIPs) are recognized by a membran
32 ococci, for example, most of these so-called autoinducing peptides (AIPs) contain a conserved thiolac
33 charomyces cerevisiae and the elucidation of autoinducing peptides (AIPs) from supernatants of pathog
34 " which involves generation and secretion of autoinducing peptides (AIPs) into the surrounding enviro
35 f 10 truncated analogues based on the parent autoinducing peptides (AIPs) of Staphylococcus lugdunens
36 regulated by macrocyclic peptide signals (or autoinducing peptides (AIPs)) and their cognate transmem
37 of small signaling pheromones is the cyclic autoinducing peptides (AIPs), which regulate expression
39 Thus, oxidant-mediated inactivation of an autoinducing peptide from S. aureus is a critical innate
40 d the regulation of a virulence factor by an autoinducing peptide in pneumococci has been demonstrate
41 addition to the quorum sensing effect of the autoinducing peptide of agr, the sarT-sarU pathway may r
42 s to detect delta-hemolysin activity and agr autoinducing peptide production indicated that 15 ( appr
43 ntation of the culture medium with synthetic autoinducing peptide (sAIP) significantly increased Agr
44 N-terminal region, is the propeptide for an autoinducing peptide that is the ligand for AgrC; and Ag
45 us comprises the secretion and sensing of an autoinducing peptide to activate its own expression via
46 enes are essential for the production of the autoinducing peptide, which functions as a signal for th