IGEM:MIT/2008/Notebook/Yogurt/lbulgaricus

Lactobacillus delbrueckii subsp. bulgaricus- Information and Protocols

Transformation methods for each L. delbrueckii strains vary – we are using the optimized method described in the paper on the brainstorming page (Serror et al)

L. bulgaricus Bacterial Strain and its Compatible Plasmid(s)(# transformants produced (µg) for Electrotransformation

• VI104 strain- pLEM415 plasmd (derived from E. coli-L. reuteri) (10^3-10^4)
  • - pX3 plasmid (from L. delbrueckii) (10^3)
  • - pJK650 plasmid (from L. delbrueckii) (10^3)
  • - pULP8 plasmid (heterologous plasmid) (10^2) (low copy plasmid)
  • - pNZ12 plasmid (heterologous plasmid) (10^2) (low copy plasmid)
  • - pG+ host 4 plasmid (heterologous plasmid) (10^2) (low copy plasmid)
  • - pGB305 plasmid (heterologous plasmid) (10^2) (low copy plasmid)
  • - pGT633 plasmid(from L. reuteri) (10) (low copy plasmid)
  • - pCU1882 plasmid(from L. curvatus) (10) (low copy plasmid)
• ATCC 11842 strain – pJK650 plasmid (2 x 10^3)

Optimized Electrotransformation Procedure

1. CELL CULTURE
   1. Inoculate serial dilutions of fresh bacterial culture into 100 ml of MRS containing 0.1% glycine and incubate at 42°C overnight.
   2. Harvest culture at beginning of stationary phase (optical density at 600 nm, 1.7) by centrifugation
2. WASH BUFFER
   1. `Wash bacteria once with 100 ml of cold electroporation buffer (EB) (0.4 M sucrose, 1 mM MgCl2, 5 mM Kh2PO4; PH 6)
   2. Wash bacteria twice with 30 ml of cold EB
3. THERMAL SHOCK
   1. Resuspend cells in EB to an optical density at 600 nm of about 50
   2. Incubate cell suspension at 45°C for 20 min then keep on ice for 10 min
4. ELECTRICAL PULSE
   1. Mix 80 µl of cell suspension with 0.3 to 2 µg of plasmid DNA
   2. Subject sample to a 1-kV, 800-Ω, 25-µF electric pulse in a 0.2-cm cuvette by using a Gene Pulser and a Pulse Controller apparatus.
5. EXPRESSION
   1. Immediately add 2 milliliters of milk medium (0.2 M sucrose, 5% skim milk, 0.1% yeast extract, 1% Casamino Acids, 25mM MgCl2)
6. PLATING, SELECTION
   1. Incubate cells for 3h at 37°C before plating on MRS agar supplemented with antibiotics. Add antibiotic erythromycin at concentration 7.5 µg/ml and chloramphenicol at concentration 7.5 µg/ml
   2. Incubate plates at 37°C for 2 to 3 days under anaerobic conditions in jars containing GasPak

Materials

• MRS + glycine
• Sucrose, MgCl2, Kh2PO4 for the EB
• Gene Pulser and Pulse Controller apparatus for electrophoration
• Sucrose, skim milk, yeast extract, casamino acids for the milk medium
• Erythromycin, chloramphenicol antibiotics
• Jars containing gaspak