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
and add to contents of flask.
4. Measure out 25 c.c. of the solution and titrate it against decinormal
sodic hydrate, using litmus as the indicator. Control the result and
estimate the amount of sodic hydrate necessary to be added to render the
remainder of the solution neutral to litmus. Add this quantity of sodic
hydrate.
5. Filter.
6. Add litmus solution 47.5 c.c. (= 5 per cent.).
7. Tube, and sterilise as for nutrient bouillon.
~Capaldi-Proskauer Medium No. II.~--
1. Weigh out and mix
Peptone 20 grammes
Mannite 1 gramme
2. Dissolve in water 1000 c.c. in a 2-litre flask.
3. Neutralise to litmus as in No. I (_vide supra_, Step 4).
4. Filter.
5. Add litmus solution 47.5 c.c. (= 5 per cent.).
6. Tube, and sterilise as for nutrient bouillon.
~Urine Media. Bouillon.~--
1. Collect freshly passed urine in sterile flask.
2. Place the flask in the steamer at 100° C. for thirty minutes.
3. Filter through two thicknesses of Swedish filter paper.
4. Tube, and sterilise as for nutrient bouillon. (Leave the reaction
unaltered.)
~Urine Gelatine.~--
1. Collect freshly passed urine in sterile flask.
2. Take the specific gravity, and, if above 1010, dilute with sterile
water until that gravity is reached.
3. Estimate (with control) at the boiling-point, and note the reaction
of the urine.
4. Weigh out gelatine, 10 per cent., and add to the urine in the flask.
5. Heat in the steamer at 100° C. for one hour to dissolve the gelatine.
6. Estimate the reaction and add sufficient caustic soda solution to
restore the reaction of the medium mass to the equivalent of the
original urine.
7. Cool to 60° C. and clarify with egg as for nutrient gelatine (_vide_
page 166).
8. Filter through papier Chardin.
9. Tube, and sterilise as for nutrient gelatine.
~Urine Gelatine (Heller).~--
1. Collect freshly passed urine in sterile flask.
2. Filter through animal charcoal to remove part of the colouring
matter.
3. Take the specific gravity, and if above 1010, dilute with sterile
water till this gravity is reached.
4. Add Witté's peptone, 1 per cent.; salt, 0.5 per cent.; gelatine, 10
per cent.
5. Heat in the steamer at 100° C. for one hour, to dissolve the
gelatine, etc.
6. Add normal caustic soda solution in successive small quantities, and
test the reaction from time to time with litmus paper, until the fluid
reacts faintly alkaline.
7. Cool to 60° C. and clarify with egg as for nutrient gelatine (_vide_
page 166).
8. Filter through papier Chardin.
9. Tube, and sterilise as for nutrient gelatine.
~Urine Agar.~--
1. Collect freshly passed urine in sterile flask.
2. Take the specific gravity and if above 1010, dilute with sterile
water till this gravity is reached.
3. Weigh out 1.5 per cent. or 2 per cent. powdered agar, and add it to
the urine.
4. Heat in the steamer at 100° C. for ninety minutes to dissolve the
agar.
5. Cool to 60° C. and clarify with egg as for nutrient agar (_vide_ page
168).
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