1991
DOI: 10.1007/bf00167916
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A kinetic method for calculating the viability of lactic starter cultures

Abstract: A simple method of assessing the viability of a lactic starter culture is presented. The method is based on the kinetics of growth of a culture during the lag and early exponential phases. The microorganisms used throughout this work were Lactobacillus spp. The method was tested with inocula samples of different ages and with samples taken during chemostat runs, at different dilution rates. The results obtained are similar to ones described in the literature for similar situations. The method is very easy to o… Show more

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Cited by 5 publications
(3 citation statements)
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References 16 publications
(17 reference statements)
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“…In this sense, once the growth phase has been detected, it is reliable to consider the presence of nonviable organisms as negligible, and every organism in the sample can be considered as viable. Therefore, the monitoring of the growth phase may enable the estimation of the initial concentration able to develop the observed growth curve (Barreto et al 1991).…”
Section: Introductionmentioning
confidence: 99%
“…In this sense, once the growth phase has been detected, it is reliable to consider the presence of nonviable organisms as negligible, and every organism in the sample can be considered as viable. Therefore, the monitoring of the growth phase may enable the estimation of the initial concentration able to develop the observed growth curve (Barreto et al 1991).…”
Section: Introductionmentioning
confidence: 99%
“…A few authors demonstrated that the harvesting time has a strong impact on cellular parameters such as viability and acidification activity (3,20,24). Béal et al (6) specified that there is an optimal range of time during which to harvest cells in a good physiological state, i.e., at a high cellular concentration and a high acidification activity.…”
mentioning
confidence: 99%
“…Bis(1,3-dibutylbarbituric acid) trimethine oxonol [DIBAC 4 (3)] was used to assess the depolarization state of the cells (7). Dual staining was performed in order to differentiate dead cells with PI and depolarized cells with DIBAC 4 (3) in a single analysis.…”
mentioning
confidence: 99%