Alm:Protoplasting

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(Procedure: outlined)
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==Procedure==
==Procedure==
 +
===Strip outer membrane===
 +
#Step 1
 +
#Step 2
 +
#*Step 2 has some additional information that goes with it.  i.e. Keep at 4°C.
 +
#Step 3
 +
##Step 3 has multiple sub-steps within it.
 +
##Enumerate each of those.
 +
 +
===Permeabilize cell wall===
 +
#Step 1
 +
#Step 2
 +
#*Step 2 has some additional information that goes with it.  i.e. Keep at 4°C.
 +
#Step 3
 +
##Step 3 has multiple sub-steps within it.
 +
##Enumerate each of those.
 +
 +
===Optional: Fuse protoplasts===
 +
#Mix aliquots of protoplasts of each parent strain
 +
#Add PEG
 +
#Step 3
 +
 +
===Regenerate protoplasts===
#Step 1
#Step 1
#Step 2
#Step 2

Revision as of 16:04, 2 April 2007

Contents

Materials for 1 round

  • sucrose, 0.5M
  • SMM, divided
    • SMM + lysozyme

Regeneration:

soft agar (0.8%) plates containing

In some cases, protoplasts were resus- pended in LB medium containing 0.5 M sucrose and spread onto soft agar plates containing LB medium and 0.5 M sucrose with autoclaved plastic spreaders. The plates were subsequently incubated at either 25 or 37 1C.

In other cases, the protoplasts were diluted into molten soft agar at 45 1C containing either LB medium and 0.5 M sucrose or M9 medium, 0.5 M sucrose, and either Leu (100 mg/ml) or Arg (100 mg/ml), depending on the nutritional requirements of the auxotrophic strains used, and then poured onto soft agar plates of the same composition.


Overview

Replace this sentence with a brief description of the protocol and its goal.

Materials

List reagents, supplies and equipment necessary to perform the protocol here. For those materials which have their own OWW pages, link to that page. Alternatively, links to the suppliers' page on that material are also appropriate.

  • supply 1 (i.e. tubes of a certain size? spreaders?)
  • reagent 1
  • X μL reagent 2
    • component A (reagent 2 is made up of multiple components)
    • component B
  • equipment 1
  • equipment 2

Procedure

Strip outer membrane

  1. Step 1
  2. Step 2
    • Step 2 has some additional information that goes with it. i.e. Keep at 4°C.
  3. Step 3
    1. Step 3 has multiple sub-steps within it.
    2. Enumerate each of those.

Permeabilize cell wall

  1. Step 1
  2. Step 2
    • Step 2 has some additional information that goes with it. i.e. Keep at 4°C.
  3. Step 3
    1. Step 3 has multiple sub-steps within it.
    2. Enumerate each of those.

Optional: Fuse protoplasts

  1. Mix aliquots of protoplasts of each parent strain
  2. Add PEG
  3. Step 3

Regenerate protoplasts

  1. Step 1
  2. Step 2
    • Step 2 has some additional information that goes with it. i.e. Keep at 4°C.
  3. Step 3
    1. Step 3 has multiple sub-steps within it.
    2. Enumerate each of those.

Notes

  1. List troubleshooting tips here.
  2. You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
  3. Anecdotal observations that might be of use to others can also be posted here.

Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.

References

Relevant papers and books

  1. [--]
  2. Goldbeter A and Koshland DE Jr. . pmid:6947258. PubMed HubMed [Goldbeter-PNAS-1981]
  3. JACOB F and MONOD J. . pmid:13718526. PubMed HubMed [Jacob-JMB-1961]
  4. Mark Ptashne. A genetic switch. Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press, 2004. isbn:0879697164. [Ptashne-Genetic-Switch]
All Medline abstracts: PubMed HubMed

Contact

or instead, discuss this protocol.

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