M2GSC Medium: Difference between revisions

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== Description ==
== Description ==
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M2GSC medium is based on a modified M2 medium [1] supplemented with glucose, soluble starch, cellobiose, and rumen fluid in an anaerobic broth.


== Recipe ==
== Recipe ==
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'''M2GSC medium composition'''
{| class="wikitable"
|Bacto casitone
| align="right" |10 g
|-
|Bacto yeast extract
| align="right" |2.5 g
|-
|NaHCO<sub>3</sub>
| align="right" |4 g
|-
|Glucose
| align="right" |2 g
|-
|Soluble starch
| align="right" |2 g
|-
|Cellobiose
| align="right" |2 g
|-
|Rumen fluid (spun)
| align="right" |300 ml
|-
|Mineral solution 1
| align="right" |150 ml
|-
|Mineral solution 2
| align="right" |150 ml
|-
|Resazurin (0.1%)
| align="right" |1 ml
|-
|Cysteine HCl
| align="right" |1 g
|-
| colspan="2" |Add distilled H<sub>2</sub>O to 1 L
|}
 
 
'''Mineral solution 1'''
{| class="wikitable"
|K<sub>2</sub>HPO4
| align="right" |3 g
|-
| colspan="2" |Add distilled H<sub>2</sub>O to 1 L
|}
 
 
'''Mineral solution 2'''
{| class="wikitable"
|NaCl
| align="right" |6 g
|-
|KH<sub>2</sub>PO<sub>4</sub>
| align="right" |3 g
|-
|(NH<sub>4</sub>)<sub>2</sub>SO<sub>4</sub>
| align="right" |6 g
|-
|CaCl<sub>2.</sub>2H<sub>2</sub>O
| align="right" |0.6 g
|-
|MgSO<sub>4.</sub>7H<sub>2</sub>O
| align="right" |0.6 g
|-
| colspan="2" |Add distilled H<sub>2</sub>O to 1 L
|}


== Direction ==
== Direction ==
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* Weigh all ingredients as listed into a Pyrex conical glass flask, with the exception of cysteine.
* Add mineral solutions, rumen fluid, resazurin and water.
* Microwave flask on high until rapidly boiling.
* Remove flask from microwave and bubble with a gentle stream of CO<sub>2</sub> until cool. Slowly add cysteine and then flush headspace only as bubble can change pH.
* Dispense M2GSC medium in 9.5 ml volumes into CO<sub>2</sub> flushed Hungate tubes.
* Butyl rubber stoppers should be placed in the neck of tubes while withdrawing the CO<sub>2</sub> sparger and the tubes sealed with screw caps.
* Autoclave tubes at 121ºC for 15 min. on same day as prepared.


== Notes ==
== Notes ==
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Note: for rumen fluid
 
# Thaw once-spun (10,000 g for 20 min) rumen fluid and bubble with N<sub>2</sub> (100%) for 20 minutes.
# Autoclave under N<sub>2</sub> at 121⁰C for 20 minutes in a high pressure Schott bottle to inactivate viruses, etc. The anoxic conditions are to limit the formation of unwanted          oxidation products. Allow to cool.
# Freeze at -80⁰C for 2 hours or -20⁰C overnight.
# Spin at 10,000 G for 20 minutes.


== Sources ==
== Sources ==
[1] Hobson PN. (1969). Rumen bacteria. In: Methods in Microbiology, vol 3B. Academic Press, pp. 133–149.

Latest revision as of 17:11, 30 October 2026

Description

M2GSC medium is based on a modified M2 medium [1] supplemented with glucose, soluble starch, cellobiose, and rumen fluid in an anaerobic broth.

Recipe

M2GSC medium composition

Bacto casitone 10 g
Bacto yeast extract 2.5 g
NaHCO3 4 g
Glucose 2 g
Soluble starch 2 g
Cellobiose 2 g
Rumen fluid (spun) 300 ml
Mineral solution 1 150 ml
Mineral solution 2 150 ml
Resazurin (0.1%) 1 ml
Cysteine HCl 1 g
Add distilled H2O to 1 L


Mineral solution 1

K2HPO4 3 g
Add distilled H2O to 1 L


Mineral solution 2

NaCl 6 g
KH2PO4 3 g
(NH4)2SO4 6 g
CaCl2.2H2O 0.6 g
MgSO4.7H2O 0.6 g
Add distilled H2O to 1 L

Direction

  • Weigh all ingredients as listed into a Pyrex conical glass flask, with the exception of cysteine.
  • Add mineral solutions, rumen fluid, resazurin and water.
  • Microwave flask on high until rapidly boiling.
  • Remove flask from microwave and bubble with a gentle stream of CO2 until cool. Slowly add cysteine and then flush headspace only as bubble can change pH.
  • Dispense M2GSC medium in 9.5 ml volumes into CO2 flushed Hungate tubes.
  • Butyl rubber stoppers should be placed in the neck of tubes while withdrawing the CO2 sparger and the tubes sealed with screw caps.
  • Autoclave tubes at 121ºC for 15 min. on same day as prepared.

Notes

Note: for rumen fluid

  1. Thaw once-spun (10,000 g for 20 min) rumen fluid and bubble with N2 (100%) for 20 minutes.
  2. Autoclave under N2 at 121⁰C for 20 minutes in a high pressure Schott bottle to inactivate viruses, etc. The anoxic conditions are to limit the formation of unwanted oxidation products. Allow to cool.
  3. Freeze at -80⁰C for 2 hours or -20⁰C overnight.
  4. Spin at 10,000 G for 20 minutes.

Sources

[1] Hobson PN. (1969). Rumen bacteria. In: Methods in Microbiology, vol 3B. Academic Press, pp. 133–149.