Evaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymers

Because the use of bacteria for biotechnological processes requires maintaining their viability and geneticstability, preserving them becomes essential. Here, we evaluated three preservation methods for A.chroococcum C26 and A. vinelandii C27; preservation methods: cryopreservation and immobilizatio...

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Main Authors: Daniel Fernando Rojas Tapias, Mabel Patricia Ortiz Vera, Diego Rivera Botia, Joseph Kloepper, Ruth Rebeca Bonilla Buitrago
Format: Article
Language:English
Published: Pontificia Universidad Javeriana 2013-04-01
Series:Universitas Scientiarum
Subjects:
Online Access:http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4404
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author Daniel Fernando Rojas Tapias
Mabel Patricia Ortiz Vera
Diego Rivera Botia
Joseph Kloepper
Ruth Rebeca Bonilla Buitrago
author_facet Daniel Fernando Rojas Tapias
Mabel Patricia Ortiz Vera
Diego Rivera Botia
Joseph Kloepper
Ruth Rebeca Bonilla Buitrago
author_sort Daniel Fernando Rojas Tapias
collection DOAJ
description Because the use of bacteria for biotechnological processes requires maintaining their viability and geneticstability, preserving them becomes essential. Here, we evaluated three preservation methods for A.chroococcum C26 and A. vinelandii C27; preservation methods: cryopreservation and immobilization in drypolymers for 60 days, and freeze-drying for 30. We evaluated their efficiency by counting viable cells andmeasuring nitrogen fixation activity. Additionally, we assessed the effect of three protective agents forfreeze-drying, three for cryopreservation, and four polymers. Freeze-drying proved the best technique tomaintain viability and activity, followed by immobilization and cryopreservation. Bacterial nitrogen fixingability remained unchanged using the freeze-drying method, and bacterial survival exceeded 80%; S/BSAwas the best protective agent. Immobilization maintained bacterial survival over 80%, but nitrogen fixationwas decreased by 20%. Lastly, cryopreservation resulted in a dramatic loss of viability for C26 (BSRapprox. 70%), whereas C27 was well preserved. Nitrogen fixation for both strains decreased regardless ofthe cryoprotective agent used (P < 0.05). In conclusion, the success of Azotobacter preservation methodsdepend on the technique, the protective agent, and the strain used. Our results also indicated that freezedryingusing S/BSA is the best technique to preserve bacteria of this genus.
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spelling doaj.art-be8de11c9f2b45efa0d33278143e552a2022-12-21T17:31:01ZengPontificia Universidad JaverianaUniversitas Scientiarum0122-74832027-13522013-04-0118212913910.11144/Javeriana.SC18-2.etmpEvaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymersDaniel Fernando Rojas TapiasMabel Patricia Ortiz VeraDiego Rivera BotiaJoseph KloepperRuth Rebeca Bonilla BuitragoBecause the use of bacteria for biotechnological processes requires maintaining their viability and geneticstability, preserving them becomes essential. Here, we evaluated three preservation methods for A.chroococcum C26 and A. vinelandii C27; preservation methods: cryopreservation and immobilization in drypolymers for 60 days, and freeze-drying for 30. We evaluated their efficiency by counting viable cells andmeasuring nitrogen fixation activity. Additionally, we assessed the effect of three protective agents forfreeze-drying, three for cryopreservation, and four polymers. Freeze-drying proved the best technique tomaintain viability and activity, followed by immobilization and cryopreservation. Bacterial nitrogen fixingability remained unchanged using the freeze-drying method, and bacterial survival exceeded 80%; S/BSAwas the best protective agent. Immobilization maintained bacterial survival over 80%, but nitrogen fixationwas decreased by 20%. Lastly, cryopreservation resulted in a dramatic loss of viability for C26 (BSRapprox. 70%), whereas C27 was well preserved. Nitrogen fixation for both strains decreased regardless ofthe cryoprotective agent used (P < 0.05). In conclusion, the success of Azotobacter preservation methodsdepend on the technique, the protective agent, and the strain used. Our results also indicated that freezedryingusing S/BSA is the best technique to preserve bacteria of this genus.http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4404Azotobacterbacterial preservationcryopreservationfreeze-dryingimmobilization in polymersbacterial nitrogen fixation.
spellingShingle Daniel Fernando Rojas Tapias
Mabel Patricia Ortiz Vera
Diego Rivera Botia
Joseph Kloepper
Ruth Rebeca Bonilla Buitrago
Evaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymers
Universitas Scientiarum
Azotobacter
bacterial preservation
cryopreservation
freeze-drying
immobilization in polymers
bacterial nitrogen fixation.
title Evaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymers
title_full Evaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymers
title_fullStr Evaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymers
title_full_unstemmed Evaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymers
title_short Evaluation of three methods for preservation of Azotobacter: freeze-drying, cryopreservation, and immobilization in dry polymers
title_sort evaluation of three methods for preservation of azotobacter freeze drying cryopreservation and immobilization in dry polymers
topic Azotobacter
bacterial preservation
cryopreservation
freeze-drying
immobilization in polymers
bacterial nitrogen fixation.
url http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4404
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