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Biomedical subjects

P Gerhardt

Publications and source records attributed to P Gerhardt.

At least 163 records · Page 9Linked to original sources
PubMed1967

Differential dialysis culture for separation and concentration of a macromolecular product.

A differential dialysis flask, constructed with three chambers and two membranes of different porosity, was used to effect the separation and concentration of enterotoxin B produced extracellularly by a culture of Staphylococcus aureus. Variables were examined that affected the diffusion of glucose, as measured by half-equilibration time and permeability coefficient; the relative chamber volume, type of membrane, membrane masking, and mixing all exerted a substantial influence on diffusion rates. A number of membrane filters were tested for usefulness; one type, made with vinylidene fluoride, had desirable physical and diffusional properties, but neither it nor others consistently withheld the bacteria for more than a marginally useful period of about 50 hr. In ordinary two-chambered dialysis culture, the amount of enterotoxin reached 10 times that in control culture; in differential, three-chambered dialysis culture the comparable factor of increase was about 7, with about two-thirds of this amount being separated from cells in the product chamber of the flask.

Dialysis↗
PubMed1966

Structural details of anthrax spores during stages of transformation into vegetative cells.

Moberly, Betty J. (The University of Michigan, Ann Arbor), F. Shafa, and Philipp Gerhardt. Structural details of anthrax spores during stages of transformation into vegetative cells. J. Bacteriol. 92:220-228. 1966.-Anthrax spores in stages of dormancy, activation, germination, and outgrowth into vegetative cells were examined in an electron microscope. The fine structure proved to be much like that observed in related species of Bacillus, except for a visible alteration after heat activation and clusters of vesicle-like bodies in the cytoplasm of vegetative cells.

Bacillus anthracis↗
PubMed1963

Dialysis Fermentor Systems for Concentrated Culture of Microorganisms.

Cell-mass production of Serratia marcescens was studied in dialysis systems in which growth was managed in a fermentor remote from, but connected by conduits and pumps with, a nutrient reservoir. Dialysis was accomplished with membrane tubing in either the fermentor or the reservoir, or best with membrane sheet in a plate-and-frame dialyzer that was remote from but connected with both vessels. Growth trials with these systems demonstrated their ability to produce virtually unlimited population density in a liquid culture, viable counts in excess of 10 cells/ml and partial cell volume of 50% being attained. The system used for growth also may be used, after the growth cycle, to concentrate cells still further by osmotic dehydration with a hydrophilic colloid. The dialyzer-dialysis system that was evolved permits independent control of the component operations and is believed to be adaptable to any desired scale of size.

Journal Article↗