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
5. Measure out and add to the medium
Sodium sulphite, 10 per cent. aqueous solution 25 c.c.
6. Tube and sterilise as for nutrient agar.
~Brilliant Green Agar (Conradi).~--
1. Liquefy and measure out into a sterile flask
Nutrient agar 1000 c.c.
2. Adjust reaction to +30 by the addition of normal phosphoric acid; and
filter.
3. Measure out and mix thoroughly with the fluid medium
Brilliant green (Hoechst) 1 per thousand aqueous solution 6.5 c.c.
4. Measure out and add to the medium
Picric acid (Gruebler), 1 per cent. aqueous solution 6.5 c.c.
5. Tube and sterilise as for nutrient agar.
~Brilliant Green Bile Salt Agar (Fawcus).~--
1. Weigh out agar 20 grammes and emulsify in 100 c.c. cold distilled
water.
2. Wash the emulsion into a "tared" 2-litre flask with 500 c.c.
distilled water.
3. Dissolve the agar by bubbling live steam through the flask.
4. Cool, clarify with egg and filter.
5. Weigh out
Sodium taurocholate 5 grammes
Peptone 20 grammes
and add to the medium in the flask.
6. Weigh out
Lactose 5 grammes
and add to the medium in the flask.
7. Adjust reaction to +15 and filter if necessary.
8. Measure out
Brilliant green, 1 per thousand aqueous solution 20 c.c.
and mix thoroughly with the fluid agar.
9. Measure out and add to the medium
Picric acid, 1 per cent. aqueous solution 20 c.c.
10. Tube and sterilise as for nutrient agar.
~China Green Agar (Werbitski).~--
1. Liquefy and measure out into a sterile flask
Nutrient agar 1000 c.c.
2. Adjust the reaction accurately to +13 and filter.
3. Measure out and mix thoroughly with the fluid agar
China green 0.2 per cent. aqueous solution 15 c.c.
4. Tube and sterilise as for nutrient agar.
~Malachite Green Agar (Loeffler).~--
1. Liquefy and measure out into a sterile flask
Nutrient agar 1000 c.c.
2. Weigh out
Dextrose 10 grammes.
and dissolve in nutrient agar.
3. Adjust the reaction to +3, and filter.
4. Measure out and mix thoroughly in the fluid agar
Malachite green, 0.1 per cent. aqueous solution 16 c.c.
for ~"weak"~ medium.
_4a._ To the filtered agar add
Malachite green, 2 per cent. aqueous solution 25 c.c.
for ~"strong"~ medium.
5. Tube and sterilise as for nutrient agar.
~Double Sugar Agar (Russell).~--
1. Liquefy and measure out into a sterile flask
Nutrient agar 1000 c.c.
2. Add 100 c.c. litmus solution to the fluid agar.
3. Weigh out and dissolve in the fluid agar.
Lactose 10 grammes
Dextrose 10 grammes.
4. Render the reaction of the medium neutral to litmus paper by the
cautious addition of normal caustic soda.
5. Tube in quantities of 10 c.c. and sterilise in the steamer at 100° C.
for twenty minutes on each of three successive days.
6. Store for use in a cool dark place.
_B. Diphtheriæ._
~Glycerine Blood-serum.~--
Public-domain text, read in full here on John Shaqi.
Reviews
Reviews
No reviews yet
Be the first to share your thoughts on this work.
Elsewhere in the archive
Join the Discussion
Join the discussion
Sign in to leave a comment or review.
Sign InorCreate an account