Skip to main content

Part of the book series: Methods in Molecular Biology™ ((MIMB,volume 38))

Abstract

Yeast cultures are held in long-term storage in the National Collection of Yeast Cultures (NCYC; Norwich, UK) by two methods: freeze-dried in glass ampules and under liquid nitrogen using glycerol as a cryoprotectant. Freeze-drying is a generally accepted method for yeast storage, having the advantages of conferring longevity and genetic stability, as well as being suitable for easy worldwide postal distribution of the cultures in glass ampules. However, preservation by freeze-drying tends to be much more labor intensive than storage in liquid nitrogen and requires a higher level of skill to produce an acceptable product. Strain viabilities are generally low, typically being between 1 and 30%, as compared to >30% for those of yeast preserved frozen in liquid nitrogen. There are also several yeast genera, including Lipomyces, Leucosporidium, and Rhodosporidium which have particularly low survival levels and frequently cannot be successfully freeze-dried by the standard method. However, some improvements have been made recently using trehalose as a protectant (1, 2). Techniques for freeze-drying yeasts can be found in Chapters 4.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 79.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. Berny, J. F. and Hennebert, G. L. (1991) Viability and stability of yeast cells and filamentous fungus spores during freeze-drying—effects of protectants and cooling rates. Mycologia 83, 805–815.

    Article  CAS  Google Scholar 

  2. Roser, B. (1991) Trehalose drying: a novel replacement for freeze-drying. Biopharm.—Technol. Bus. Blopharm. 4, 47–53.

    CAS  Google Scholar 

  3. Mikata, K. and Banno, I. (1989) Preservation of yeast cultures by L drying: viability after 5 years of storage at 5°C. IF0 Rex Comm. 14, 80–103.

    Google Scholar 

  4. Gilmour, M. N., Turner, G., Berman, R. G., and Krenzer, A. K. (1978) Compact liquid nitrogen storage system yielding high recoveries of gram-negative anaerobes. Appl. Environ. Microbial. 35, 84–88.

    CAS  Google Scholar 

  5. Pearson, B. M., Jackman, P. J. H., Painting, K. A., and Morris, G J. (1990) Stability of genetically manipulated yeasts under different cryopreservation regimes. Ctyo-Lett. 11, 205–210.

    Google Scholar 

  6. Diller, R. R. and Knox, J. M. (1983) Automated computer-analysis of cell-size changes during cryomicroscope freezing—a biased trident convolution mask technique. Cryo-Lett. 4, 77–92.

    Google Scholar 

  7. Morris, G. J., Coulson G. E., and Clarke K. J. (1988) Freezing injury in Saccharo-myces cerevisiae—the effect of growth conditions. Cryobiology 25, 471–482.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1995 Humana Press Inc.

About this protocol

Cite this protocol

Bond, C.J. (1995). Cryopreservation of Yeast Cultures. In: Day, J.G., Pennington, M.W. (eds) Cryopreservation and Freeze-Drying Protocols. Methods in Molecular Biology™, vol 38. Humana Press, Totowa, NJ. https://doi.org/10.1385/0-89603-296-5:39

Download citation

  • DOI: https://doi.org/10.1385/0-89603-296-5:39

  • Publisher Name: Humana Press, Totowa, NJ

  • Print ISBN: 978-0-89603-296-5

  • Online ISBN: 978-1-59259-525-9

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics