Figure 1.

Three canonical quorum-sensing circuits in bacteria. (a) In Gram-negative bacteria, AHLs (red triangles) are produced by LuxI-like proteins and are detected by LuxR-type proteins. AHLs freely diffuse across the cell membrane and increase in concentration in the environment in proportion to cell growth. LuxR-type proteins, when bound to cognate autoinducers, bind specific promoter DNA elements and activate transcription of target genes (xyz). (b) Gram-positive bacteria synthesize oligopeptides (red wavy lines) that are typically modified at specific amino acids and are actively secreted. Detection occurs via a two-component signal transduction circuit, leading to the phosphorylation of a response regulator protein, which can bind promoter DNA and regulate transcription of target genes (xyz). (c) Quorum sensing in Vibrio harveyi. Two parallel two-component systems detect AI-1 (blue triangles), an AHL synthesized by LuxLM, and AI-2 (red circles), a furanosyl borate diester, which is synthesized by LuxS. In the absence of autoinducer, the sensors act as kinases and autophosphorylate at a conserved histidine residue, H1, and the phosphate is transferred to a conserved aspartate residue, D1, in the response regulator domain. Phosphate is sequentially transferred to the conserved histidine (H2) of the phosphotransferase LuxU and then to the conserved aspartate (D2) of the response regulator LuxO. Phospho-LuxO indirectly represses transcription of luxCDABE, the enzymes encoding luciferase. Binding of the autoinducers by LuxN and LuxPQ leads to the dephosphorylation of LuxU and LuxO. Dephosphorylation of LuxO relieves repression of luxCDABE. A transcriptional activator called LuxR (not similar to LuxR in a) is required for expression of luxCDABE.