2012
DOI: 10.1007/s10811-012-9927-9
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Comparative evaluation of different preservation methods for cyanobacterial strains

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Cited by 15 publications
(3 citation statements)
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“…After 28 days of growth, filaments were re-suspended in the culture via pipette mixing and 1 ml of culture was sampled. This aliquot was preserved in 10% v/v glycerol, based on previously described protocols (60)(61)(62). The 1 ml culture aliquot was centrifuged at 10,000g for five minutes until the culture was sufficiently pelleted, followed by removal of supernatant.…”
Section: Discussionmentioning
confidence: 99%
“…After 28 days of growth, filaments were re-suspended in the culture via pipette mixing and 1 ml of culture was sampled. This aliquot was preserved in 10% v/v glycerol, based on previously described protocols (60)(61)(62). The 1 ml culture aliquot was centrifuged at 10,000g for five minutes until the culture was sufficiently pelleted, followed by removal of supernatant.…”
Section: Discussionmentioning
confidence: 99%
“…In our study, 5% DMSO (except for the CB0101 strain), along with the EPS, also worked well for most of the strains. In another study, Esteves-Ferreira et al (2013) used five microalgae and cyanobacterial strains for cryopreservation and found 10% glycerol to be the most efficient CPA [ 36 ]. Some studies have demonstrated the effectiveness of CPAs when used in combination rather than alone.…”
Section: Discussionmentioning
confidence: 99%
“…Maintaining pure cultures using preservation methods is of high importance for biotechnological purposes [46]. The first step toward successful isolation is understanding and mimicking the naturally occurring environmental conditions [47].…”
Section: Isolation Of Cyanobacteria and Microalgaementioning
confidence: 99%