Measurement of Glycogen in Microbiota
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Contents
- 1 Authors:
- 2 This method is also called:
- 3 This method is adapted from: "Optimisation of glycogen quantification in mixed microbial cultures" 2012[1]
- 4 This method was used for: Quantifying Glycogen in Solids at Full-Scale Enhanced Biological Phosphorous Removal Wastewater Facilities, 2018[2]
- 5 Discussion
- 6 Materials and Equipment
- 7 Reagents
- 8 Procedure
- 9 Common Mistakes
- 10 Precision and Interference
Authors:
This method is also called:
This method is adapted from: "Optimisation of glycogen quantification in mixed microbial cultures" 2012[1]
This method was used for: Quantifying Glycogen in Solids at Full-Scale Enhanced Biological Phosphorous Removal Wastewater Facilities, 2018[2]
Discussion
Samples can be prepped by preserving with formaldehyde prior to lyophilizing the same as methods measuring PHA.
Materials and Equipment
- Fume Hood
- Lyophilizer
- 50ml centrifuge tubes (e.g. Falcon Tubes)
Reagents
| Reagent | Concentration | Units | CAS Number |
|---|---|---|---|
| Formaldehyde | 37 | % | 50-00-0 |
| PBS Solution | |||
| HCl | 0.9 | Molar | 7647-01-0 |
Procedure
- Label Tubes;
- While in a fume hood, add 4 to 5 drops (0.25 ml) of 37% formaldehyde to the 50ml centrifuge tube. This will act as a sample preserving agent.
- Place aliquots of 40 ml per sample in 50 ml centrifuge tubes.
- Collect sludge in a 15 ml centrifuge tube (should be about 20 mg solids worth) through one of the following methods;
- Store at 4°C for 2 hours
- Wash the sample as follows to remove paraformaldehyde or formaldehyde.
- Centrifuge at 3000 RCF for 5 min, and carefully decant the supernatant
- b. Add 10 ml of PBS solution and vortex sample to suspend pellet
- c. Centrifuge at 3000 RCF for 5 min, and carefully decant the supernatant
- d. Add 10 ml of PBS solution and vortex sample to suspend pellet
- e. Centrifuge at 3000 RCF for 5 min, and carefully decant the supernatant
- 8. Centrifuge Sample at 5000 rcf for 5min, decant supernatant
- 9. Cover with parafilm and poke holes in the parafilm. Place cap on over parafilm. Freeze sample in -80°C Freezer.
- 10. Start the lyophlizer cooling unit and run for 10 min prior to running.
- 11. Remove cap from sample. Place sample in lyophilizer and start the vacuum pump. Ensure vacuum is being supplied to lyophlilizer container, which contains the sample. Lyophlize overnight.
- 12. When removing from lyophilizer, make sure the lyophilizer lid is off in order to let lyophilizer dry out.
- 13. Place 45 mg of lyophilized matter into a 50ml centrifuge tube. Label the tube.
- 14. Place 45ml of 0.9 M HCl (or load to 1mg/ml if less than 45 mg lyophilized biosolids)
- 15. Place in oven for 3h at 100°C
- 16. Cool Sample in an ice bath prior to HPLC analysis
Common Mistakes
| Mistake | Evidence of the Mistake | Cause | Effect on Results |
|---|---|---|---|
Precision and Interference
- ↑ "Optimisation of glycogen quantification in mixed microbial cultures". Bioresource Technology. 118. 2012-08-01. doi:10.1016/j.biortech.2012.05.087. ISSN 0960-8524.
- ↑ RedCorn, Engelberth (2018). "Quantifying Glycogen in Solids at Full-Scale Enhanced Biological Phosphorous Removal Wastewater Facilities". Journal of Environmental Engineering. 144: Issue 9.