Abstract
We optimized conditions for cryopreservation of a cyanophage (Ma-LMM01) infecting the toxic cyanobacterium Microcystis aeruginosa. The quality of cryopreservation was estimated by comparing the phage titer before and after preservation at 4, -80, or -196°C and with or without a cryoprotectant: glycerol, dimethyl sulfoxide (DMSO), or Cellbanker. Storage at 4°C for 100 days resulted in ~90% loss of infectivity; whereas cryopreservation at -196°C resulted in stable preservation with or without cryoprotectant. Therefore, we established methods to stably preserve the phage, Ma-LMM01, that may be useful in further studies of cyanophages and may be used in isolating new phages. © 2007, Japanese Society of Microbial Ecology & The Japanese Society of Soil Microbiology. All rights reserved.
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Takashima, Y., Yoshida, T., Kashima, A., Hiroishi, S., & Nagasaki, K. (2007). Cryopreservation of a Myovirus Infecting the Toxin-Producing Cyanobacterium Microcystis aeruginosa. Microbes and Environments, 22(3), 297–299. https://doi.org/10.1264/jsme2.22.297
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