The Elements of Bacteriological Technique: A Laboratory Guide for Medical, Dental, and Technical Students. Second Edition Rewritten and Enlarged.Eyre, J. W. H. (John William Henry)
Science
The Elements of Bacteriological Technique: A Laboratory Guide for Medical, Dental, and Technical Students. Second Edition Rewritten and Enlarged.
Eyre, J. W. H. (John William Henry)
Bacteriology -- Technique
_Media for the Study of the Chemical Composition of Bacteria._
~Asparagin Medium (Uschinsky).~--
1. Weigh out and mix
Asparagin 3.4 grammes
Ammonium lactate 10.0 grammes
Sodium chloride 5.0 grammes
Magnesium sulphate 0.2 gramme
Calcium chloride 0.1 gramme
Acid potassium phosphate (KH_{2}PO_{4}) 1.0 gramme
2. Dissolve the mixture in distilled water 1000 c.c.
3. Add glycerine, 40 c.c.
4. Tube, and sterilise as for nutrient bouillon.
~Asparagin Medium (Frankel and Voges).~--
1. Weigh out and mix
Asparagin 4 grammes
Sodium phosphate, (Na_{2}HPO_{4}) 12OH 2 grammes
Ammonium lactate 6 grammes
Sodium chloride 5 grammes
and dissolve in
Distilled water 1000 c.c.
2. Tube, and sterilise as for nutrient bouillon.
NOTE.--Either of the above asparagin media, after the
addition of 10 per cent. gelatine or 1.5 per cent. agar, may
be advantageously employed in the solid condition.
~Proteid Free Broth (Uschinsky).~--
1. Weigh out and mix
Calcium chloride 0.1 gramme
Magnesium sulphate 0.2 gramme
Acid potassium phosphate (KH_{2}PO_{4}) 2.0 grammes
Potassium aspartate 3.0 grammes
Sodium chloride 5.0 grammes
Ammonium lactate 6.0 grammes
2. Dissolve the mixture in distilled water 1000 c.c.
3. Add glycerine 30 c.c.
4. Tube and sterilise as for nutrient broth.
_Media for the Study of Biochemical Reaction._
~Inosite-free Media--Bouillon (Durham).~--
1. Prepare meat extract, 1000 c.c. (_vide_ page 148), from bullock's
heart which has been "hung" for a couple of days.
2. Prepare nutrient bouillon (+10), 1000 c.c. (_vide_, page 161), from
the meat extract, and store in 1-litre flask.
3. Inoculate the bouillon from a pure cultivation of the B. lactis
aerogenes, and incubate at 37° C. for forty-eight hours.
4. Heat in the steamer at 100° C. for twenty minutes to destroy the
bacilli and some of their products.
5. Estimate the reaction of the medium and if necessary restore to +10.
6. Inoculate the bouillon from a pure cultivation of the B. coli
communis and incubate at 37° C. for forty-eight hours.
7. Heat in the steamer at 100° C. for twenty minutes.
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