1970
DOI: 10.1128/jb.103.3.789-792.1970
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Synchronous Growth of Enteric Bacteria

Abstract: Helmstetter and Cummings devised a technique of synchronization in which cells are implanted on a membrane filter and the membrane is subjected to reverse flow of liquid medium. The cells in the effluent stream have predominantly the characteristics of newborn cells. The advantage of this technique is that the population experiences a minimum of physiological stress; hence, the behavior of the synchronous culture should reflect the normal divisional cycle. The disadvantage is that strains other than Escherichi… Show more

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Cited by 36 publications
(12 citation statements)
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“…The Coulter counter may be used to estimate cell multiplication in cultures of M. avium if certain problems are recognized. When the counter is calibrated to count the smallest cells of M. avium, which may be one-fifth the volume of cells of Escherichia coli (14), particulate material that sloughs off the cells during growth will also be counted. Most of this material passes an 0.8-,um filter and few viable cells do.…”
Section: Discussionmentioning
confidence: 99%
“…The Coulter counter may be used to estimate cell multiplication in cultures of M. avium if certain problems are recognized. When the counter is calibrated to count the smallest cells of M. avium, which may be one-fifth the volume of cells of Escherichia coli (14), particulate material that sloughs off the cells during growth will also be counted. Most of this material passes an 0.8-,um filter and few viable cells do.…”
Section: Discussionmentioning
confidence: 99%
“…Experiments for determining specific growth rates were conducted in a G76 gyratory water-bath shaker (New Brunswick Scientific Co., New Brunswick, N.J.) adjusted to predetermined temperatures (5 to 35 C) and an agitation rate of 120 rev/min. A 250-ml Erlenmeyer flask containing 50 ml of TSB was inoculated with 0.2 ml of culture (grown at 10 C for 2 to 3 days in TSB), and the culture was transferred periodically (inoculum, 0.1 ml) until it reached the steadystate of growth (13,14). Growth was determined by periodically measuring optical density at 600 nm with a Beckman spectrophotometer (model DB) with 5-cm cuvettes.…”
Section: Materuils and Methodsmentioning
confidence: 99%
“…This strain was cultivated for 2 months in continuous exponential growth at low density by periodic transfer in glucose minimal medium, after which cultivation a clone was isolated as a colony on a plate of eosinmethylene blue-lactose agar. The isolate (29) which has been designated strain ML30G ("G" denoting long cultivation in glucose minimal medium), was kept on slants of the same medium.…”
mentioning
confidence: 99%