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Biomedical subjects

D Schlessinger

Publications and source records attributed to D Schlessinger.

280 records · Page 16Linked to original sources

Selection of sucrose-dependent Escherichia coli to obtain envelope mutants and fragile cultures.

Mutants isolated as sucrose-dependent include many with apparent envelope defects, which fact often leads to filamentous growth or lysis in the absence of sucrose. One mutant can grow exponentially in 4 percent sucrose, but is very fragile: it releases all of its RNA and soluble protein when treated with 0.5 percent sodium deoxycholate. These characteristics permit the study of unstable structures and rapid processes in actively growing cells.

Bile Acids and Salts↗

Stability of beta-galactosidase messenger ribonucleic acid in Escherichia coli.

Ben-Hamida, Fakher (Washington University School of Medicine, St. Louis, Mo.), and David Schlessinger. Stability of beta-galactosidase messenger ribonucleic acid in Escherichia coli. J. Bacteriol. 90:1611-1616. 1965.-Synthesis of beta-galactosidase stops within several minutes when preinduced, permeaseless cultures are diluted into medium containing 40 mug/ml of 5-fluorouracil (5-FU) but no inducer. However, if inducer (isopropylthiogalactoside) is left in the medium, enzyme formation in the presence of 5-FU continues for at least 11 min. Thus, inducer may increase the differential metabolic stability of the corresponding messenger ribonucleic acid (RNA; defined as the capacity to produce measurable enzyme) in inducible strains. However, such an interpretation requires that 5-FU rapidly arrest the further synthesis of messenger RNA competent to form active enzyme. C(14)-5-FU, like uracil, does appear to enter cells without measurable lag, saturating the pool of uracil nucleotides, and thereby the messenger RNA being formed, within several minutes. That 5-FU acts very quickly is also supported by the similar continuation of enzyme synthesis in the presence of inducer and antibiotics (actinomycin D and proflavine) which shut off all RNA synthesis, as well as by the response to 5-FU of enzyme synthesis in various constitutive mutants.

Acridines↗

The assessment of antimicrobial combinations.

The traditional approach to the study of the interaction between antimicrobial agents relies on the assumption that inhibition of growth by antimicrobial agents follows a linear dose-response curve. Because this assumption is invalid, we propose that antimicrobial combinations should be assessed by empiric dose-response curves that would distinguish synergistic, additive, and antagonistic effects on the rate of cell growth. This approach predicts synergy for the model combination of trimethoprim and sulfamethoxazole and should also be applicable to other combinations of antimicrobial agents nd to combinations of antitumor agents.

Anti-Bacterial Agents↗