Lactobacillus transformation (Speer 2012): Difference between revisions

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Back to [[Richard Lab:protocols]]<br>
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==Overview==
==Overview==
This is basically a modified version of the Mason (2005 protocol) for use with ''Lactobacillus plantarum'' and an Eppendorf 2510 electroporator.
This is basically a modified version of the Mason (2005 protocol) for use with ''Lactobacillus plantarum'' and an Eppendorf 2510 electroporator.  For other protocols check out the [[Electro-transformation of Lactobacillus spp.|Lactobacillus transformation archive]].  


==Materials==
==Materials==

Revision as of 13:03, 14 September 2011

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Overview

This is basically a modified version of the Mason (2005 protocol) for use with Lactobacillus plantarum and an Eppendorf 2510 electroporator. For other protocols check out the Lactobacillus transformation archive.

Materials

  • MRS media
  • Glycine
  • Milipore water
  • 50mM EDTA solution
  • 0.5M Sucrose, 10% glycerol solution

Procedure

  1. Grow L. plantarum
    1. Inoculate 5ml MRS medium with L. plantarum freezer stock.
    2. Grow overnight at 30°C without shaking.
  2. Make 100ml 2% glycine:
    1. Add 1g glycine to two flasks of 50ml MRS medium.
    2. Shake to dissolve.
  3. Grow cells:
    1. Add 1ml overnight culture to each flask (1:50 dlution).
    2. Culture for ~3 hours at 37°C with shaking.
  4. Wash 2x with ice-cold DI water:
    1. Centrifuge culture for 5min at 4000g
    2. Resuspend in 25ml ice-cold DI water.
    3. Repeat.
  5. Treat with ice-cold EDTA:
    1. Centrifuge for 5min at 4000g
    2. Resuspend in 10ml 50mM EDTA.
    3. Incubate on ice for 5 minutes
  6. Wash with ice-cold DI water:
    1. Centrifuge culture for 5min at 4000g
    2. Resuspend in 25ml ice-cold DI water.
  7. Wash 2x with Electroporation Buffer:
    1. Centrifuge culture for 5min at 4000g
    2. Resuspend in 25ml ice-cold 0.5M Sucrose, 10% glycerol.
    3. Repeat.
  8. Concentrate cells:
    1. Centrifuge culture for 5min at 4000g
    2. Resuspend in 0.8ml ice-cold 0.5M Sucrose, 10% glycerol.
  9. Divide cells:
    1. Aliquot 90μL of cell concentrate into ~20 microcentrifuge tubes.
    2. Keep on ice until use (within the next two hours).
  10. Add DNA:
    1. Add 10μL of plasmid DNA to the 90μL of cell concentrate.
    2. Keep on ice for 5 minutes.
    3. Put 1mm cuvettes on ice too.
  11. Electroporate:
    1. Pipette the cell/DNA mixture into the cuvette
    2. Electrporate at 1200 volts
    3. Time constant should be ~5.0
  12. Recovery:
    1. Immediately transfer the electroporated cells to 900μL of MRS medium.
    2. Incubate at 30°C for 2-3 hours.
  13. Select:
    1. Plate on medium with the appropriate antibiotic
    2. Incubate at 30°C for two days.
    3. Pick colony

Notes

All questions, input and feedback are welcome!

References

There will be one here soon.


Contact

  • mas853@psu.edu

or instead, discuss this protocol. -->