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R Grüneberg

Publications and source records attributed to R Grüneberg.

5 recordsLinked to original sources

Palindromic sequences and A+T-rich DNA elements promote illegitimate recombination in Nicotiana tabacum.

Illegitimate recombination is the prevailing molecular mechanism for the integration of recombinant DNA into the genome of most eukaryotic systems and the generation of deletions by intrachromosomal recombination. We developed a ?selectable marker system to screen for intrachromosomal illegitimate recombination events in order to assess the sequence and structure-specific requirements for illegitimate recombination in tobacco. In 12 illegitimate recombination products analysed, we found that all deletion termini localise to sites of palindromic structures or to A+T-rich DNA elements. All deletion termini showed microhomologies of two to six nucleotides. In three plants, the recombination products contained filler-DNA or an inversion of an endogenous segment. Our data strongly suggest that illegitimate recombination in plants is mediated by a DNA synthesis-dependent process, and that this mechanism is promoted by DNA regions that can form palindromic structures or facilitate DNA unwinding.

Adenosine↗

The bactericidal activity of vancomycin and teicoplanin against Streptococcus pneumoniae.

The in vitro inhibitory and bactericidal activity of vancomycin and teicoplanin against clinical isolates of Streptococcus pneumoniae was investigated. Minimum inhibitory concentrations (MICs) were determined using an agar incorporation technique. Vancomycin (MIC range 0.12-0.25 mg/l) and teicoplanin (MIC range 0.03-0.12 mg/l) were both very active against the isolates examined. Single-time-point minimum bactericidal concentrations (MBCs) were determined using a macrobroth incorporation technique. Both antimicrobials brought about a 99.9% reduction in viability of the original inocula during 24 hours' exposure at concentrations of 4-8 times the MIC for vancomycin and 2-4 times the MIC for teicoplanin. Time-kill curves of vancomycin, teicoplanin and penicillin against a penicillin-susceptible and a penicillin-resistant strain of S. pneumoniae showed a greater than 3.0 log10 cfu/ml reduction in viability of cultures within 6 hours of exposure to all three of the antimicrobials at a concentration equal to eight times the MIC. The results suggest that clinical trials of the efficacy of teicoplanin in the treatment of infections caused by S. pneumoniae are warranted.

Glycopeptides↗