Hostname: page-component-77c89778f8-7drxs Total loading time: 0 Render date: 2024-07-19T05:22:10.270Z Has data issue: false hasContentIssue false

High-Pressure Freezing to Study Structure and Function of the Host Parasite Interface

Published online by Cambridge University Press:  02 July 2020

K. Mendgen*
Affiliation:
Lehrstuhl fur Phytopathologie, Universitat Konstanz, D-78457 , Konstanz, Germany
Get access

Extract

The high-pressure freezing instrument exposes a sample to a pressure of 2100 bar, which lowers the freezing point and, as a result, reduces the rate of ice nucleation and ice-crystal growth. The reduced critical cooling rate allows adequate freezing of samples up to 0,3 mm in thickness without using cryoprotectants. Before pressure application, the sample is sandwiched between specimen holders. To optimize heat conductivity and to avoid damage by the high pressure impact, the free space inside the specimen holders and within the sample has to be filled with liquid. This means that plant leaves need to be infiltrated to remove gas from the intercellular space. We have used water, 3-8% methanol in water, 1-hexadecene or heptane as infiltration medium. Subsequently, samples were freeze substituted in unhydrous acetone with 2% Os04 for 24 h at -90°C. Samples were slowly warmed up to 4°C and embedded in Unicryl, or warmed up to room temperature and embedded in epoxide resin.

Type
Light and Electron Microscopic Techniques for the Study of Plant Pathogenic Fungi and Their Interactions with Host Plants
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References:

1.Galweiler, L. et al. Science 282(1977)2226.CrossRefGoogle Scholar
2.Hahn, M. et al. Molecular Plant-Microbe Interactions 10(1997)438.CrossRefGoogle Scholar
3.Rodriguez-Galvez, E. and Mendgen, K.. Planta 197(1995)535.CrossRefGoogle Scholar
4.Rodriguez-Galvez, E. and Mendgen, K.. Protoplasma 189(1995)61.CrossRefGoogle Scholar
5.Thijssen, M. H. et al. Journal of Microscopy 192(1998)228.CrossRefGoogle Scholar