M. Carmen Ríos Rodríguez

PLASMID CURING OF OENOCOCCUS OENI

Two strains of Oenococcus oeni, RS1 (which carries the plasmid pRS1) and RS2 (which carries the plasmids pRS2 and pRS3), were grown in the presence of different curing agents and at different temperatures. Sublethal temperature together with acriflavine generated all possible types of cured strains, i.e., lacking pRS1 (from strain RS1), and lacking pRS2, pRS3, or both (from strain RS2). Sublethal temperature together with acridine orange only generated cured strains lacking pRS3. These results suggest that acriflavine is a better curing agent than acridine orange for O. oeni, and that pRS3 is the most sensitive to these curing agents. We also observed spontaneous loss of pRS2 or both pRS2 and pRS3 by electroporation. The ability to cure O. oeni strains of plasmids provides a critical new tool for the genetic analysis and engineering of this commercially important bacterium.

Conformational effects on the photoinduced proton-transfer processes in 1-methyl-2-(3′-hydroxy-2′-pyridyl)benzimidazole

The ground- and excited-state behaviour of 1-methyl-2-(3′-hydroxy-2′-pyridyl)benzimidazole (MeHPyBI) in various solvents has been studied by UV–Vis absorption spectroscopy and by time-resolved and steady-state fluorescence spectroscopy. Three species were detected in the ground state in aqueous solutions of pH near to neutrality: a non-planar enol form, a planar cis-enol form and a planar keto tautomer. Electronic excitation of both the cis-enol form and the keto tautomer yields the excited keto form, the former through an ultrafast excited-state intramolecular proton-transfer (ESIPT). The non-planar enol form cannot undergo ESIPT and partly deprotonates at the hydroxy group to afford the anion. In non-aqueous solvents only the cis-enol form was detected in the ground state, yielding the keto tautomer in the excited state. The first protonation of MeHPyBI takes place at the benzimidazole N(3). Whereas the photoexcited cation shows fluorescence in acidified acetonitrile, it deprotonates at the hydroxy group in acidified ethanol, yielding the keto tautomer. In acidic aqueous solution, the excited cation undergoes a two-step tautomerization by two different routes to afford a keto cation, protonated at the pyridyl N. All the protonated and deprotonated forms of MeHPyBI are non-planar in the ground state both in water and ethanol, but they adopt a planar structure in the excited state. Comparison of the behaviour of MeHPyBI with related molecules reveals that the existence of planar forms and the neutral keto species in the ground state is favoured by the presence of the pyridyl nitrogen. The conformational equilibria in the ground state are crucial for the excited-state behaviour of these types of molecules.

Characterization of pRS5: a theta-type plasmid found in a strain of Pediococcus pentosaceus isolated from wine that can be used to generate cloning vectors for lactic acid bacteria.

The nucleotide sequence of pRS5 (10153bp) is reported. Through sequence analysis, 9 open reading frames (ORFs) were identified and the following features observed: a region likely involved in replication whose structural features indicate that pRS5 belongs to the pUCL287 group of theta-type replicons, and hypothetical proteins putatively involved in plasmid copy number control, restriction-modification system, toxin-antitoxin system and a putative integrase. Shuttle vectors for Escherichia coli and lactic acid bacteria (LAB) as well as a small cloning vector for direct use in LAB were constructed using the replication region of pRS5. The ability of such vectors to accept and express other genes was assessed. All pRS5-derivatives were maintained at a high rate over 200 generations without selective pressure.

The use of the replication region of plasmid pRS7 from Oenococcus oeni as a putative tool to generate cloning vectors for lactic acid bacteria.

A chimeric plasmid, pRS7Rep (6.1 kb), was constructed using the replication region of pRS7, a large plasmid from Oenococcus oeni, and pEM64, a plasmid derived from pIJ2925 and containing a gene for resistance to chloramphenicol. pRS7Rep is a shuttle vector that replicates in Escherichia coli using its pIJ2925 component and in lactic acid bacteria (LAB) using the replication region of pRS7. High levels of transformants per µg of DNA were obtained by electroporation of pRS7Rep into Pediococcus acidilactici (1.5 × 10(7)), Lactobacillus plantarum (5.7 × 10(5)), Lactobacillus casei (2.3 × 10(5)), Leuconostoc citreum (2.7 × 10(5)), and Enterococcus faecalis (2.4 × 10(5)). A preliminary optimisation of the technical conditions of electrotransformation showed that P. acidilactici and L. plantarum are better transformed at a later exponential phase of growth, whereas L. casei requires the early exponential phase for better electrotransformation efficiency. pRS7Rep contains single restriction sites useful for cloning purposes, BamHI, XbaI, SalI, HincII, SphI and PstI, and was maintained at an acceptable rate (>50%) over 100 generations without selective pressure in L. plantarum, but was less stable in L. casei and P. acidilactici. The ability of pRS7Rep to accept and express other genes was assessed. To the best of our knowledge, this is the first time that the replication region of a plasmid from O. oeni has been used to generate a cloning vector.