1974
DOI: 10.1128/aem.27.4.793-796.1974
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Relationship of Cellular Components to the Stability of Concentrated Lactic Streptococcus Cultures at -17 C1

Abstract: Concentrated cultures of lactic streptococci varied with respect to survival at-17 C. Cells of each strain grown at pH 6.0 were more stable to freezing than were those grown statically. The lipid fraction of the cells from static cultures was important in preventing death during freezing. As the percentage of octadecenoic acid in the cellular lipids from different cultures increased, the percentage of survivors decreased. Capsular material associated with cells from cultures grown both statically and at pH 6.0… Show more

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Cited by 20 publications
(14 citation statements)
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“…Concentrated frozen cultures of lactobacilli and lactic streptococci are used routinely in the manufacture of various fermented products. However, certain lactobacilli (22, 23) and individual strains of lactic streptococci (1,5,7,13,16,24) are not sufficiently stable to freezing. The instability of frozen cultures of these bacteria presents a difficulty with regard to their use for fermentation processes, especially for the direct inoculation of the food with these cultures.…”
mentioning
confidence: 99%
“…Concentrated frozen cultures of lactobacilli and lactic streptococci are used routinely in the manufacture of various fermented products. However, certain lactobacilli (22, 23) and individual strains of lactic streptococci (1,5,7,13,16,24) are not sufficiently stable to freezing. The instability of frozen cultures of these bacteria presents a difficulty with regard to their use for fermentation processes, especially for the direct inoculation of the food with these cultures.…”
mentioning
confidence: 99%
“…Test strain cultures, grown on various carbon sources as described above, were harvested and washed three times with distilled water and then resuspended in the same solution. The cell suspensions were used to analyze the glucose content by means of the anthrone method (Gilliland & Speck 1974;Ekwunife et al 1991;Khoo et al 2005) and to measure the dry weight of the cells. The milligrams of glucose per milligram of dry cell weight were then calculated, and the results were expressed as a percentage of the glucose content.…”
Section: Effect Of Carbon Source On Cellular Hydrophobicity Fatty Acmentioning
confidence: 99%
“…The measurement of capsular EPS material is complicated by its close association with the bacterial cells (Sutherland, 1972). The concentrations were measured based on the amount of carbohydrate expressed as glucose present in washed cell suspensions (Gilliland and Speck, 1974). The carbohydrate concentrations were determined by either a variation of the anthrone method (Gilliland and Speck, 1974) or the phenol-sulfuric method (Dubois et al, 1956), with glucose as the standard and the amount of EPS expressed as μg of glucose/ml of culture.…”
Section: Measurement Of Capsular Epsmentioning
confidence: 99%
“…bulgaricus were initially tested to determine the level of capsular EPS produced in 10% reconstituted NDM. Volumes of 10 ml of freshly pasteurized 10% NDM were inoculated with each of the eight cultures using 1% inocula and incubated at 45°C for 8 h. The capsular EPS content was based on sugar content of the cells and was determined in a manner similar to that of Gilliland and Speck (1974). The milk proteins were solubilized by adding 1.1 ml of 20% (wt/vol) sodium citrate to 5.5 ml volumes of each culture, and then 4.4 ml of deionized water was added, bringing the final concentration to 2% sodium citrate.…”
Section: Initial Screening Of Cultures For Capsular Eps Productionmentioning
confidence: 99%