This strain uses the standard medium without modifications.
Compound | Amount | Unit | |||
---|---|---|---|---|---|
|
NH4Cl | 1.00 | g | ||
|
K2HPO4 | 0.30 | g | ||
|
KH2PO4 | 0.30 | g | ||
|
MgCl2 x 6 H2O | 0.50 | g | ||
|
CaCl2 x 2 H2O | 0.10 | g | ||
|
KCl | 0.10 | g | ||
|
NaCl | 3.00 | g | ||
|
Yeast extract
(OXOID) |
1.00 | g | ||
|
Trypticase peptone
(BD BBL) |
1.00 | g | ||
|
Modified Wolin's mineral solution | 10.00 | ml | ||
|
Sodium resazurin
(0.1% w/v) |
0.50 | ml | ||
|
Na2S2O3 x 5 H2O | 3.16 | g | ||
|
L-Cysteine HCl x H2O | 0.50 | g | ||
|
Na2CO3 | 1.50 | g | ||
|
D-Glucose | 3.60 | g | ||
|
Na2S x 9 H2O | 0.30 | g | ||
|
Distilled water | 1000.00 | ml | ||
1 Dissolve ingredients, except thiosulfate, cysteine, carbonate, glucose, and sulfide, then sparge medium for 30 - 45 min with 80% N2 and 20% CO2 gas mixture to make it anoxic. Add thiosulfate and cysteine, then adjust pH to 7.0 and dispense medium under 80% N2 and 20% CO2 gas atmosphere into anoxic Hungate-type tubes or serum vials to 30% of their volume and autoclave. After autoclaving, add glucose and sulfide from sterile anoxic stock solutions prepared under 100% N2 gas and carbonate from a sterile anoxic stock solution prepared under 80% N2 and 20% CO2 gas atmosphere. Adjust the pH of the complete medium to 7.2 - 7.4, if necessary. |
Compound | Amount | Unit | |||
---|---|---|---|---|---|
|
Nitrilotriacetic acid | 1.50 | g | ||
|
MgSO4 x 7 H2O | 3.00 | g | ||
|
MnSO4 x H2O | 0.50 | g | ||
|
NaCl | 1.00 | g | ||
|
FeSO4 x 7 H2O | 0.10 | g | ||
|
CoSO4 x 7 H2O | 0.18 | g | ||
|
CaCl2 x 2 H2O | 0.10 | g | ||
|
ZnSO4 x 7 H2O | 0.18 | g | ||
|
CuSO4 x 5 H2O | 0.01 | g | ||
|
AlK(SO4)2 x 12 H2O | 0.02 | g | ||
|
H3BO3 | 0.01 | g | ||
|
Na2MoO4 x 2 H2O | 0.01 | g | ||
|
NiCl2 x 6 H2O | 0.03 | g | ||
|
Na2SeO3 x 5 H2O | 0.30 | mg | ||
|
Na2WO4 x 2 H2O | 0.40 | mg | ||
|
Distilled water | 1000.00 | ml | ||
1 First dissolve nitrilotriacetic acid and adjust pH to 6.5 with KOH, then add minerals. Adjust final to pH 7.0 with KOH. |