In recent years it has become clear that the production of N-acyl homo
serine lactones (N-AHLs) is widespread in Gram-negative bacteria. Thes
e molecules act as diffusible chemical communication signals (bacteria
l pheromones) which regulate diverse physiological processes including
bioluminescence, antibiotic production, plasmid conjugal transfer and
synthesis of exoenzyme virulence factors in plant and animal pathogen
s. The paradigm for N-AHL production is in the bioluminescence (lux) p
henotype of Photobacterium fischeri (formerly classified as Vibrio fis
cheri) where the signalling molecule N-(3-oxohexanoyl)-L-homoserine la
ctone (OHHL) is synthesized by the action of the Luxl protein. OHHL is
thought to bind to the LuxR protein, allowing it to act as a positive
transcriptional activator in an autoinduction process that physiologi
cally couples cell density (and growth phase) to the expression of the
bioluminescence genes. Based on the growing information on Luxl and L
uxR homologues in other N-AHL-producing bacterial species such as Erwi
nia carotovora, Pseudomonas aeruginosa, Yersinia enterocolitica, Agrob
acterium tumefaciens and Rhizobium leguminoserum, it seems that analog
ues of the P. fischeri lux autoinducer sensing system are widely distr
ibuted in bacteria. The general physiological function of these simple
chemical signalling systems appears to be the modulation of discrete
and diverse metabolic processes in concert with cell density. In an ev
olutionary sense, the elaboration and action of these bacterial pherom
ones can be viewed as an example of multicellularity in prokaryotic po
pulations.