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Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction

Ultra-low temperature (ULT) storage of microbial biomass is routinely practiced in biological laboratories. However, there is very little insight regarding the effects of biomass storage at ULT and the structure of the cell envelope, on cell viability. Eventually, these aspects influence bacterial c...

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Autores principales: Sarnaik, Aditya, Mhatre, Apurv, Faisal, Muhammad, Smith, Dylan, Davis, Ryan, Varman, Arul M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128238/
https://www.ncbi.nlm.nih.gov/pubmed/33999956
http://dx.doi.org/10.1371/journal.pone.0251640
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author Sarnaik, Aditya
Mhatre, Apurv
Faisal, Muhammad
Smith, Dylan
Davis, Ryan
Varman, Arul M.
author_facet Sarnaik, Aditya
Mhatre, Apurv
Faisal, Muhammad
Smith, Dylan
Davis, Ryan
Varman, Arul M.
author_sort Sarnaik, Aditya
collection PubMed
description Ultra-low temperature (ULT) storage of microbial biomass is routinely practiced in biological laboratories. However, there is very little insight regarding the effects of biomass storage at ULT and the structure of the cell envelope, on cell viability. Eventually, these aspects influence bacterial cell lysis which is one of the critical steps for biomolecular extraction, especially protein extraction. Therefore, we studied the effects of ULT-storage (-80°C) on three different bacterial platforms: Escherichia coli, Bacillus subtilis and the cyanobacterium Synechocystis sp. PCC 6803. By using a propidium iodide assay and a modified MTT assay we determined the impact of ULT storage on cellular viability. Subsequently, the protein extraction efficiency was determined by analyzing the amount of protein released following the storage. The results successfully established that longer the ULT-storage time lower is the cell viability and larger is the protein extraction efficiency. Interestingly, E. coli and B. subtilis exhibited significant reduction in cell viability over Synechocystis 6803. This indicates that the cell membrane structure and composition may play a major role on cell viability in ULT storage. Interestingly, E. coli exhibited concomitant increase in cell lysis efficiency resulting in a 4.5-fold increase (from 109 μg/ml of protein on day 0 to 464 μg/ml of protein on day 2) in the extracted protein titer following ULT storage. Furthermore, our investigations confirmed that the protein function, tested through the extraction of fluorescent proteins from cells stored at ULT, remained unaltered. These results established the plausibility of using ULT storage to improve protein extraction efficiency. Towards this, the impact of shorter ULT storage time was investigated to make the strategy more time efficient to be adopted into protocols. Interestingly, E. coli transformants expressing mCherry yielded 2.7-fold increase (93 μg/mL to 254 μg/mL) after 10 mins, while 4-fold increase (380 μg/mL) after 120 mins of ULT storage in the extracted soluble protein. We thereby substantiate that: (1) the storage time of bacterial cells in -80°C affect cell viability and can alter protein extraction efficiency; and (2) exercising a simple ULT-storage prior to bacterial cell lysis can improve the desired protein yield without impacting its function.
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spelling pubmed-81282382021-05-27 Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction Sarnaik, Aditya Mhatre, Apurv Faisal, Muhammad Smith, Dylan Davis, Ryan Varman, Arul M. PLoS One Research Article Ultra-low temperature (ULT) storage of microbial biomass is routinely practiced in biological laboratories. However, there is very little insight regarding the effects of biomass storage at ULT and the structure of the cell envelope, on cell viability. Eventually, these aspects influence bacterial cell lysis which is one of the critical steps for biomolecular extraction, especially protein extraction. Therefore, we studied the effects of ULT-storage (-80°C) on three different bacterial platforms: Escherichia coli, Bacillus subtilis and the cyanobacterium Synechocystis sp. PCC 6803. By using a propidium iodide assay and a modified MTT assay we determined the impact of ULT storage on cellular viability. Subsequently, the protein extraction efficiency was determined by analyzing the amount of protein released following the storage. The results successfully established that longer the ULT-storage time lower is the cell viability and larger is the protein extraction efficiency. Interestingly, E. coli and B. subtilis exhibited significant reduction in cell viability over Synechocystis 6803. This indicates that the cell membrane structure and composition may play a major role on cell viability in ULT storage. Interestingly, E. coli exhibited concomitant increase in cell lysis efficiency resulting in a 4.5-fold increase (from 109 μg/ml of protein on day 0 to 464 μg/ml of protein on day 2) in the extracted protein titer following ULT storage. Furthermore, our investigations confirmed that the protein function, tested through the extraction of fluorescent proteins from cells stored at ULT, remained unaltered. These results established the plausibility of using ULT storage to improve protein extraction efficiency. Towards this, the impact of shorter ULT storage time was investigated to make the strategy more time efficient to be adopted into protocols. Interestingly, E. coli transformants expressing mCherry yielded 2.7-fold increase (93 μg/mL to 254 μg/mL) after 10 mins, while 4-fold increase (380 μg/mL) after 120 mins of ULT storage in the extracted soluble protein. We thereby substantiate that: (1) the storage time of bacterial cells in -80°C affect cell viability and can alter protein extraction efficiency; and (2) exercising a simple ULT-storage prior to bacterial cell lysis can improve the desired protein yield without impacting its function. Public Library of Science 2021-05-17 /pmc/articles/PMC8128238/ /pubmed/33999956 http://dx.doi.org/10.1371/journal.pone.0251640 Text en © 2021 Sarnaik et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Sarnaik, Aditya
Mhatre, Apurv
Faisal, Muhammad
Smith, Dylan
Davis, Ryan
Varman, Arul M.
Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction
title Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction
title_full Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction
title_fullStr Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction
title_full_unstemmed Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction
title_short Novel perspective on a conventional technique: Impact of ultra-low temperature on bacterial viability and protein extraction
title_sort novel perspective on a conventional technique: impact of ultra-low temperature on bacterial viability and protein extraction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128238/
https://www.ncbi.nlm.nih.gov/pubmed/33999956
http://dx.doi.org/10.1371/journal.pone.0251640
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