Springer Lab: Random Spore Analysis: Difference between revisions
(New page: Adapted from Growth and Manipulation of Yeast, Douglas by A. Treco and Fred Winston. Curr. Protoc. Mol. Biol. 82:13.2.1-13.2.12. C 2008 by John Wiley & Sons, Inc '''Materials''' Spores (...) |
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Adapted from Growth and Manipulation of Yeast, Douglas by A. Treco and Fred Winston. Curr. Protoc. Mol. Biol. 82:13.2.1-13.2.12. C 2008 by John Wiley & Sons, Inc | Adapted from Growth and Manipulation of Yeast, Douglas by A. Treco and Fred Winston. Curr. Protoc. Mol. Biol. 82:13.2.1-13.2.12. C 2008 by John Wiley & Sons, Inc | ||
Revision as of 05:22, 23 May 2012
Adapted from Growth and Manipulation of Yeast, Douglas by A. Treco and Fred Winston. Curr. Protoc. Mol. Biol. 82:13.2.1-13.2.12. C 2008 by John Wiley & Sons, Inc
Materials
Spores (see Sporularion protocol) 10mg/mL Zymolyase-100T (zymo research, us biologicals) 2-Mercaptoethanol (2-ME) 1.5% (v/v) Nonidet P-40 (NP-40) Ethanol
Prepare the tetrads 1. Microcentrifuge 0.5 ml sporulation culture for 30 seconds to 1 min until a pellet is formed. Pour off supernatant, and resuspend pellet in 5 ml water, vortex and centrifuge again. Resuspend in 0.5 mL of water.
2. Mix the following components:
0.5 mL of spores resuspended in water 25 microL of zymolyase 5 microL of 2-ME
Lyse unsporulated cells 3. Incubate overnight at 30C with gentle shaking.
Treatment of the sporulated culture with Zymolyase in a hypotonic solution results in lysis of unsporulated diploid cells. The preparation should be examined microscopically after the Zymolyase treatment to evaluate its effectiveness. A higher concentration of the enzyme or the more concentrated preparation of Zymolyase (Zymolyase-100T) can be used
4. Add 0.2 mL of 1.5% Nonidet P-40 (NP-40). Vortex tubes until most tetrads are disrupted (as observed by microscopy).
The spores should be examined after the last sonication step to ensure that no spores remain stuck together. More vortexing steps (or even sonication) at higher power settings will release the more tenacious spores. If spores remain stuck to each other, add 2 ml glass beads (Type I,Sigma) and shake 30 min at 300 rpm in an Erlenmyer flask at 30◦C. Let the beads settle and remove the supernatant containing the spores.
5. Centrifuge spores10 min at 1200×g. Aspirate or pour off supernatant and resuspend in 0.5 ml water. Vortex vigorously. Repeat.
6. Dilute the spores with water 1:1000 or get 10^3 spores/ml. Plate 100 μl on several YPD plates and incubate 1-2 days at 30C.
7. Screen spore colonies for markers of interest by replica plating
