Methylation of Fatty Acids (Kropinski Method)脂肪酸甲基化

Hancock Laboratory Methods,Department of Microbiology and Immunology,
University of British Columbia, British Columbia, Canada

http://www.cmdr.ubc.ca/bobh/showmethod.php?methodid=41

OBJECTIVE:

To methylate fatty acids in whole cells or lipopolysaccharide.

REAGENTS :

• Methanol-Hydrochloride Reagent Kit
• >10mg of whole cells or 1 mg of lipopolysaccharide
• 400 nmoles of fatty acid standard (pentadecanoic acids C15)

METHODS:

1. Prepare 1M MeOH-HCl reagent according to the instruction
   given with the kit.
   
2. Add internal standard (C15 fatty acid) to give a final concentration of 400 nmoles/100ml (usually 10mg of C15 in 100ml of reagent.
   
3. Weigh 10mg of whole cells or 1 mg of LPS into a clean screw-cap tube.
   
4. Add 1ml of MeOH-HCl reagent/internal standard into each tube and vortex.
   
5. Heat at 100^oC for 20 minutes. (Note: each tube should be very well sealed with teflon tape and grease to prevent evaporation.)
   
6. Sonicate and heat at 100^oC overnight.
   
7. Neutralize acidity with 0.5N NaOH. Test pH with pH paper.
   
8. Centrifuge in clinical centrifuge for 5 minutes. Save supernatent in clean glass vial.
   
9. Do gas chomatography with programmed REWH method.