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Acidithiobacillus ferrooxidans is one of the main acidophilic chemolithotrophic bacteria involved in the bioleaching of metal sulfide ores. The bacterium-mineral interaction requires the development of biofilms, whose formation is regulated in many microorganisms by type AI-1 quorum sensing. Here, we report the existence and characterization of a functional type AI-1 quorum-sensing system in A. ferrooxidans. This microorganism produced mainly acyl-homoserine lactones (AHL) with medium and large acyl chains and different C-3 substitutions, including 3-hydroxy-C 8 -AHL, 3-hydroxy-C 10 -AHL, C 12 -AHL, 3-oxo-C 12 -AHL, 3-hydroxy-C 12 -AHL, C 14 -AHL, 3-oxo-C 14 -AHL, 3-hydroxy-C 14 -AHL, and 3-hydroxy-C 16 -AHL. A quorum-sensing genetic locus that includes two open reading frames, afeI and afeR, which have opposite orientations and code for proteins with high levels of similarity to members of the acyl synthase (I) and transcriptional regulator (R) protein families, respectively, was identified. Overexpression of AfeI in Escherichia coli and the associated synthesis of AHLs confirmed that AfeI is an AHL synthase. As determined by reverse transcription-PCR, the afeI and afeR genes were transcribed in A. ferrooxidans. The transcription levels of the afeI gene were higher in cells grown in sulfur and thiosulfate media than in iron-grown cells. Phosphate starvation induced an increase in the transcription levels of afeI which correlated with an increase in AHL levels. Two afe boxes which could correspond to the AfeR binding sites were identified upstream of the afeI gene. This is the first report of a functional type AI-1 quorum-sensing system in an acidophilic chemolithotrophic microorganism, and our results provide a very interesting opportunity to explore the control and regulation of biofilm formation during the bioleaching process.Quorum sensing (QS) is a widespread phenomenon that enables bacterial cells to establish cell-cell communication and to regulate the expression of specific genes in response to local changes in cell density (6,48,49). QS provides the means to coordinate the activities of cells so that they function as a multicellular unit and communicate with eukaryotic hosts (6,20,48,49). In gram-negative bacteria, depending on the autoinductor (AI) molecule, two QS processes have been described: type AI-1, which is involved mainly in intraspecies communication, and type AI-2, which is related to interspecies communication (20,49).The type AI-1 QS regulatory system is composed of four elements: (i) a transcriptional regulator (protein family R); (ii) a cis-acting DNA palindromic sequence; (iii) an acyl-homoserine lactone (AHL), which is the signaling molecule or autoinducer (AI-1); and (iv) the AHL synthase protein (protein family I), which synthesizes the AI (6,20,48,49). It is currently accepted that AI-1 diffuses freely between the cellular and external environments and complexes with the R protein only at a high cell density. The AHL-R complex binds through the R carboxyl domain to the specific site...

Lantibiotics are antimicrobial peptides from the bacteriocin family, secreted by Gram-positive bacteria. These peptides differ from other bacteriocins by the presence of (methyl)lanthionine residues, which result from enzymatic modification of precursor peptides encoded by structural genes. Several groups of lantibiotics have been distinguished, the largest of which is the lacticin 481 group. This group consists of at least 16 members, including lacticin 481, streptococcin A-FF22, mutacin II, nukacin ISK-1, and salivaricins. We present the first review devoted to this lantibiotic group, knowledge of which has increased significantly within the last few years. After updating the group composition and defining the common properties of these lantibiotics, we highlight the most recent developments. The latter concern: transcriptional regulation of the lantibiotic genes; understanding the biosynthetic machinery, in particular the ability to perform in vitro prepeptide maturation; characterization of a novel type of immunity protein; and broad application possibilities. This group differs in many aspects from the best known lantibiotic group (nisin group), but shares properties with less-studied groups such as the mersacidin, cytolysin and lactocin S groups.