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Biomedical subjects

G M Kalmanson

Publications and source records attributed to G M Kalmanson.

At least 73 records · Page 4Linked to original sources
PubMed1968

Penicillin: effect on sodium and potassium transport in bacterial and protoplast forms of Sterptococcus faecalis.

Streptococcus faecalis, incubated in osmotically stabiliz medium in the presence of 1000 units of penicillin per milliliter, accumulated rather than extruded sodium; they accumulated much less potassium than control cells did. These changes were not due to binding of sodium by cell-wall fragments of cells treated with penicillin. Because penicillin had no effect on cation concentrations in stable protoplasts and nongrowing bacterial cells, this effect appeared to be related to the production of the penicillin-induced lesions of the cell wall.

Biological Transport, Active↗
PubMed1968

Production of the Shwartzman reaction with microbial L forms.

Study of potential pathogenicity of microbial L forms was done by the localized Shwartzman reaction. Stable L forms of Proteus mirabilis served as skin preparation in rabbits for induction of Shwartzman reaction by subsequent intravenous injection of either P. mirabilis L forms or Escherichia coli endotoxin. The intensity of the reaction was positively correlated to numbers of L forms in the skin. L forms also served as the intravenous challenge. In vivo multiplication of L forms was not a prerequisite for the reaction, as it could be produced with nonviable, osmotically lysed L forms. The reaction produced with L forms in the skin was more intense than that produced with the parent bacterial form. These latter observations, coupled with the demonstration that L forms disappeared from the skin (lysed?) after 4 hr, in contrast to bacteria which were recoverable for 72 hr (duration of study), suggest release of endotoxin by L forms as a pathogenic mechanism.

Animals↗
PubMed1968

Cores, microbial organelles possibly specific to group D streptococci.

A long, thin, approximately cylindrical core spans the interior of cells of 24-hr cultures of all group D streptococci that were examined, five strains of Streptococcus faecalis, single strains of S. faecalis subsp. zymogenes and S. durans, and three strains of Streptococcus spp. In one strain of S. faecalis, serial section electron microscopy showed that most cells possess a core. The core is 0.10 to 0.16 mum thick and consists of a matrix and an axial array of ribosomelike particles. It resembles one of two types of cores present in a stable protoplast form of one of the S. faecalis strains. Cores were not present in single strains of S. pyogenes (beta-hemolytic group A), S. agalactiae (group B), S. dysgalactiae (group C), S. equisimilis (group C), and S. mitis (viridans group) that were examined; nor were cores observed in single strains of Staphylococcus aureus, Escherichia coli, and Bacillus megaterium. Cores may be useful, therefore, in identification of group D streptococci. For preservation and rapid recognition of cores, a glutaraldehyde-osmium tetroxide sequence of fixation appears superior to the osmium tetroxide method often employed in processing bacteria for electron microscopy.

Bacillus megaterium↗