CCAP 106 . Waris-H

What is this page?
Equipment needed:

Final pH: 7.0

Select a strain (optional):

ml
Compound Amount Unit
Ca(NO3)2 x 4 H2O
(100 g/l stock solution)
1 ml
MgSO4 x 7 H2O
(20 g/l stock solution)
1 ml
(NH4)2HPO4
(20 g/l stock solution)
1 ml
KNO3
(100 g/l stock solution)
1 ml
HEPES
(238.31 g/l stock solution)
1 ml
Fe-EDTA 1 ml
P-II Metals 1 ml
Vitamin mix 1 ml
SE2 (Soil Extract 2) 10 ml
Deionized water 1000 ml
1 Make up to 1 litre with deionized water and adjust pH to 7.0 with 1M NaOH or 1M HCl. Autoclave at 15 psi for 15 minutes.

Fe-EDTA #

1000
Compound Amount Unit
Na2-EDTA x 2 H2O 5.22 g
FeSO4 x 7 H2O 4.98 g
KOH
(1 N)
54.00 ml
1 1M KOH is heated for 30 min (100°C); once cooled it is added to the mixture. Then heat the solution for 20 mins at 115°C

P-II Metals #

1000
Compound Amount Unit
Na-EDTA x 2 H2O 3.000 g
H3BO3 1.140 g
ZnSO4 x 7 H2O 0.021 g
CoCl2 x 6 H2O 0.004 g
MnCl2 x 4 H2O 0.144 g
Distilled water 1000.000 ml
1 Dissolve EDTA and boric acid in distilled H2O, then add metals one after the other.

Vitamin mix #

1000
Compound Amount Unit
Thiamine HCl 0.1 g
Biotin 1.0 mg
Cyanocobalamin 0.2 mg
Niacinamide 0.1 mg

SE2 (Soil Extract 2) #

1000
Compound Amount Unit
Soil
(air-dried)
trace
Distilled water trace
1 Site selection for a good soil is very important and for most purposes a soil from undisturbed deciduous woodland is best. Sites to avoid are those showing obvious signs of man's activity and particular care should be taken to avoid areas where fertilizers, crop sprays or other toxic chemicals may have been used.
2 A rich loam with good crumb structure should be sought. Stones, roots and larger invertebrates should be removed during an initial sieving through a 1 cm mesh. The sieved soil should be spread to air dry and handpicked for smaller invertebrates and roots. It should be turned periodically and picked over again. When dry sieve through a finer mesh (2-4 mm) and store in an airtight container away from light and heat.
3 Soil is prepared as above. Air-dried soil and twice its volume of supernatant distilled water are autoclaved together at 15 psi for 2 hours and left to cool. The supernatant is then decanted and then distributed to containers in volumes suitable for making up batches of media. The aliquots and their containers are autoclaved for an appropriate length of time (e.g. 1 litre or less for 15 minutes) and are then kept in a cool place (e.g. a refrigerator) until required.