INVESTIGADORES
FISCHER sonia Elizabeth
congresos y reuniones científicas
Título:
Isolation and characterization of Pseudomonas sp. SF4c mutants impaired in bacteriocina production
Autor/es:
FISCHER, S; JOFRÉ, E; GODINO, A; MORI, G
Lugar:
Carloz Paz
Reunión:
Congreso; VI Congreso Argentino de Microbiologia General; 2009
Institución organizadora:
Samige
Resumen:
Bacteria living in a competitive environment are able to secrete proteinaceous toxins, known as bacteriocins, which can kill closely related bacterial competitors while causing little harm to the bacteriocinogenic cells. On the other hand, bacteriocins have potential as biological control agents that can be used against bacterial pathogens (Parret el at., 2005).Pseudomonas sp. SF4C (native strain isolated from wheat rhizosphere) produces a high-molecular-weight bacteriocin (resistant to proteinase K) that is active against Pseudomonas fluorescens CTR 212.To obtain mutants impaired in bacteriocin production, random transposon mutagenesis of Pseudomonas sp SF4c was carried out. Kanamycin-resistant Tn5-B20 mutants of strain SF4C that had lost the capacity to inhibit the growth of strain CTR 212 were isolated.The presence of a single Tn5-B20insertion in some mutants (496, 581, 634) was confirmed by Southern blot analysis. All the transconjugants analyzed showed hybridizing fragments of similar sizes. Therefore, it is possible that the transposon has been inserted at identical positions in the genomes of these mutants.An EcoRI fragment containing the Tn5-B20 insertion present in the mutant strain 634 was cloned into vector pBluescript to generate the plasmid pSF16. DNA sequence analysis of pSF16 revealed that the transposon was inserted into a gene encoding a putative phage tape-measure protein involved in the determination of tail length in phage. This gene belongs to Prophage 01 cluster from Pseudomonas fluorescens Pf0-1. Closely related prophages 01 exist in the genomes of P. fluorescens Pf-5, P. fluorescens Q8r1-96 and P. fluorescens SBW25. The homologous prophage elements from Pf-5 and Q8r1-96 are similar to F-type pyocins. These pyocins were first discovered in P. aeruginosa and represent a class of high-molecular weight protease- and nuclease-resistant bacteriocins that resemble flexible and non-contractile tails of bacteriophages. A prophage element found in the identical spot (between mutS and cinA) in the genome of P. fluorescens SBW25 has a similar overall organization but resembling another class of phage tail-like bacteriocins, the R-type pyocins of P. aeruginosa. Furthermore, a homologous region from P. fluorescens Pf0-1 contains two clusters, similar to the hybrid R2/F2 pyocin locus from P. aeruginosa PAO1.The differences in organization of the putative phage tail-like pyocins among these prophages clearly indicate that the corresponding loci are subject to extensive recombination.