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)
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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
Nutrient agar 750 c.c.
then cool to 55°C.
5. Mix the oleic acid emulsion with the agar.
6. Add 10 c.c. sterile neutral red, 1 per cent. aqueous solution.
7. Tube in quantities of 10 c.c., slant, and allow to set.
8. Incubate for forty-eight hours at 37° C. and reject any contaminated
tubes. Store the sterile tubes for future use.
_Coli-typhoid Group._
~Parietti's Bouillon.~--
1. Measure out pure hydrochloric acid, 4 c.c., and add to it carbolic
acid solution (5 per cent.), 100 c.c. Allow the solution to stand at
least a few days before use.
2. This solution is added in quantities of 0.1, 0.2. and 0.3 c.c.
(delivered by means of a sterile graduated pipette) to tubes each
containing 10 c.c. of previously sterilised nutrient bouillon (_vide_
page 163).
3. Incubate at 37° C. for forty-eight hours to eliminate contaminated
tubes. Store the remainder for future use.
~Carbolised Bouillon.~--
1. Prepare nutrient bouillon (_vide_ page 163, sections 1 to 6). Measure
out 1000 c.c.
2. Weigh out carbolic acid, 1 gramme (2.5 or 5 grammes may be needed for
special purposes), and dissolve it in the medium.
3. Tube, and sterilise as for bouillon.
~Carbolised Gelatine.~--
1. Prepare nutrient gelatine (_vide_ page 164, sections 1 to 7). Measure
out 1000 c.c.
2. Weigh out carbolic acid, 5 grammes (= 0.5 per cent.), and dissolve it
in the gelatine.
3. Filter if necessary through papier Chardin.
4. Tube, and sterilise as for nutrient gelatine.
One or 2.5 grammes of carbolic acid (= 0.1 per cent. or 0.25 per cent.)
are occasionally used in place of the 5 grammes to meet special
requirements.
~Carbolised Agar.~--
1. Prepare nutrient agar (_vide_ page 167, sections 1 to 8). Measure out
1000 c.c.
2. Weigh out 1 gramme pure phenol and dissolve in the medium.
3. Filter if necessary through papier Chardin.
4. Tube, and sterilise as for nutrient agar.
~Litmus Gelatine.~--
1. Prepare nutrient gelatine (_vide_ page 164, sections 1 to 8).
2. Add sterile litmus solution, sufficient to tint the medium a deep
lavender colour.
3. Tube, and sterilise as for nutrient gelatine.
~Lactose Litmus Bouillon (Lakmus Molke).~--
1. Weigh out peptone, 4 grammes, and emulsify it with 200 c.c. meat
extract (_vide_ page 148), previously heated to 60°C.
2. Weigh out salt, 2 grammes, and lactose, 20 grammes, and mix with the
emulsion.
3. Wash the mixture into a sterile litre flask with 200 c.c. meat
extract and add 600 c.c. distilled water.
4. Heat in the steamer at 100° C. for thirty minutes, to completely
dissolve the peptone, etc.
5. _Neutralise carefully to litmus paper_ by the successive additions of
small quantities of decinormal soda solution.
6. Replace in the steamer for twenty minutes to precipitate phosphates,
etc.
7. Filter through two thicknesses of Swedish filter paper.
8. Add sterile litmus solution, sufficient to colour the medium a deep
purple.
9. Tube, and sterilise as for bouillon.
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