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Tracking Permeation of Dimethyl Sulfoxide (DMSO) in Mentha × piperita Shoot Tips Using Coherent Raman Microscopy.
Heidi D Kreckel1, Fionna M D Samuels1, Remi Bonnart2
1Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Dimethyl sulfoxide (DMSO) fully penetrates peppermint shoot tips within 10 minutes, aiding cryopreservation. Its varied signal intensity suggests specific interactions with cellular components during this process.
Area of Science:
- Plant Science
- Cryobiology
- Microscopy
Background:
- Cryopreservation offers cost-effective, long-term storage for vegetatively propagated crops.
- Vitrification, a common cryopreservation technique, uses concentrated cryoprotectants, but their protective mechanisms remain unclear.
- Understanding cryoprotectant localization is crucial for optimizing plant tissue preservation.
Purpose of the Study:
- To visualize the localization of dimethyl sulfoxide (DMSO) within *Mentha × piperita* (peppermint) shoot tips during cryopreservation.
- To investigate the interaction of DMSO with cellular components at the tissue level.
Main Methods:
- Utilized coherent anti-Stokes Raman scattering (CARS) microscopy for direct visualization.
- Applied CARS microscopy to *Mentha × piperita* shoot tips exposed to DMSO.
Main Results:
- Dimethyl sulfoxide (DMSO) demonstrated full penetration into the peppermint shoot tip tissue within 10 minutes of exposure.
- Observed variations in CARS signal intensities indicated potential interactions and accumulation of DMSO in specific cellular regions.
Conclusions:
- DMSO rapidly infiltrates peppermint shoot tips, a key step in vitrification-based cryopreservation.
- The observed DMSO accumulation suggests targeted interactions with cellular components, potentially explaining its cryoprotective role.
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