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Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT

Determination of metabolically active cell count is an important step in designing, operating and controlling fermentation processes. It’s particularly relevant in processes involving mixed cultures, where multiple species contribute to the total growth. The motivation for the current study is to de...

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Autores principales: Nandy, Subir Kumar, Venkatesh, KV
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052774/
https://www.ncbi.nlm.nih.gov/pubmed/24949271
http://dx.doi.org/10.1186/s13568-014-0038-7
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author Nandy, Subir Kumar
Venkatesh, KV
author_facet Nandy, Subir Kumar
Venkatesh, KV
author_sort Nandy, Subir Kumar
collection PubMed
description Determination of metabolically active cell count is an important step in designing, operating and controlling fermentation processes. It’s particularly relevant in processes involving mixed cultures, where multiple species contribute to the total growth. The motivation for the current study is to develop a methodology to estimate metabolically active cell counts for the individual species in a mixed culture with approximate equal numbers. Further, the methodology should indicate the presence of a contaminant in short time periods since in the agar plate methods used frequently it takes about 24 h. We present a methodology based on the rate of Methylene blue (MB) reduction to evaluate total count of metabolically active cells. The standard curve relating the slope of MB reduction and CFU of the individual species could be used to measure the metabolic activity of each species in the mixed culture. The slope of MB reduction could also be used to obtain the growth rate of individual species in a mixed culture and that of the total cell count. These measurements were achieved in less than 6 minutes during the growth of the cells. Evaluating the metabolic activity of individual species in a mixed culture is tedious, difficult and time consuming. The Methylene Blue dye Reduction Test (MBRT) presented here is capable of quickly estimating colony forming units (CFU) of individual species in a mixed culture if the ratio of the numbers of cells is known. The method was used to dynamically detect the occurrence of a contaminating microorganism during fermentation. The protocol developed here can be adapted to applications in processes involving mixed cultures.
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spelling pubmed-40527742014-06-19 Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT Nandy, Subir Kumar Venkatesh, KV AMB Express Original Article Determination of metabolically active cell count is an important step in designing, operating and controlling fermentation processes. It’s particularly relevant in processes involving mixed cultures, where multiple species contribute to the total growth. The motivation for the current study is to develop a methodology to estimate metabolically active cell counts for the individual species in a mixed culture with approximate equal numbers. Further, the methodology should indicate the presence of a contaminant in short time periods since in the agar plate methods used frequently it takes about 24 h. We present a methodology based on the rate of Methylene blue (MB) reduction to evaluate total count of metabolically active cells. The standard curve relating the slope of MB reduction and CFU of the individual species could be used to measure the metabolic activity of each species in the mixed culture. The slope of MB reduction could also be used to obtain the growth rate of individual species in a mixed culture and that of the total cell count. These measurements were achieved in less than 6 minutes during the growth of the cells. Evaluating the metabolic activity of individual species in a mixed culture is tedious, difficult and time consuming. The Methylene Blue dye Reduction Test (MBRT) presented here is capable of quickly estimating colony forming units (CFU) of individual species in a mixed culture if the ratio of the numbers of cells is known. The method was used to dynamically detect the occurrence of a contaminating microorganism during fermentation. The protocol developed here can be adapted to applications in processes involving mixed cultures. Springer 2014-04-05 /pmc/articles/PMC4052774/ /pubmed/24949271 http://dx.doi.org/10.1186/s13568-014-0038-7 Text en Copyright © 2014 Nandy and Venkatesh; licensee Springer http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Original Article
Nandy, Subir Kumar
Venkatesh, KV
Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT
title Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT
title_full Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT
title_fullStr Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT
title_full_unstemmed Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT
title_short Study of CFU for individual microorganisms in mixed cultures with a known ratio using MBRT
title_sort study of cfu for individual microorganisms in mixed cultures with a known ratio using mbrt
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4052774/
https://www.ncbi.nlm.nih.gov/pubmed/24949271
http://dx.doi.org/10.1186/s13568-014-0038-7
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