The Elements of Bacteriological Technique - novelonlinefull.com
You’re read light novel The Elements of Bacteriological Technique Part 44 online at NovelOnlineFull.com. Please use the follow button to get notification about the latest chapter next time when you visit NovelOnlineFull.com. Use F11 button to read novel in full-screen(PC only). Drop by anytime you want to read free – fast – latest novel. It’s great if you could leave a comment, share your opinion about the new chapters, new novel with others on the internet. We’ll do our best to bring you the finest, latest novel everyday. Enjoy
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).
6. Filter through papier Chardin, using the hot-water funnel.
7. Tube, and sterilise as for nutrient agar.
(Leave the reaction unaltered.)
~Serum Sugar Media (Hiss).~--
In these media the fermentation of carbohydrate substance by bacterial action is indicated by the coagulation of the serum proteids in addition to the production of an acid reaction.
~Serum Dextrose Water (Hiss).~--
1. Measure out into a litre flask
Serum water (See page 170) 1000 c.c.
2. Weigh out
Dextrose 10 grammes
and dissolve in the serum water.
3. Filter through Swedish filter paper.
4. Measure out and add to the medium
Litmus solution (Kahlbaum) 50 c.c.
5. Tube in quant.i.ties of 10 c.c. and sterilise in the steamer at 100 C.
for twenty minutes on each of three successive days.
Laevulose, galactose, maltose, lactose, etc., can be subst.i.tuted in similar amounts for dextrose and the medium completed as above.
~Omeliansky's Nutrient Fluid~ (_For Cellulose Fermenters_).--
1. Weigh out and mix
Pota.s.sium phosphate 4.0 grammes Magnesium sulphate 2.0 grammes Ammonium sulphate 4.0 grammes Sodium chloride 0.25 gramme
2. Dissolve in distilled water 4000 c.c.
3. Flask in quant.i.ties of 250 c.c.
4. Weigh out and add 5 grammes precipitated chalk to each flask.
5. Sterilise in the steamer at 100 C. for twenty minutes on each of three successive days.
_Media for the Study of Chromogenic Bacteria._
~Milk Rice (Eisenberg).~--
1. Measure out nutrient bouillon, 70 c.c., and milk, 210 c.c., and mix thoroughly.
2. Weigh out rice powder, 100 grammes, and rub it up in a mortar with the milk and broth mixture.
3. Fill the paste into sterile capsules, spreading it out so as to form a layer about 0.5 cm. thick, over the bottom of each.
4. Heat over a water-bath at 100 C. until the mixture solidifies.
5. Replace the lids of the capsules. Sterilise in the steamer at 100 C.
for thirty minutes on each of three consecutive days.
(A solid medium of the colour of _cafe au lait_ is thus produced.)
~Milk Rice (Soyka).~--
1. Measure out nutrient bouillon, 50 c.c., and milk, 150 c.c., and mix thoroughly.
2. Weigh out rice powder, 100 grammes, and rub it up in a mortar with the milk and broth mixture.
3. Fill the paste into sterile capsules, to form a layer over the bottom of each.
4. Replace the lids of the capsules.
5. Sterilise in the steamer at 100 C. for thirty minutes on each of three consecutive days.
(A pure white, opaque medium is thus formed.)
_Media for the Study of Phosph.o.r.escent and Photogenic Bacteria._
~Fish Bouillon.~--
1. Weigh out herring, mackerel, or cod, 500 grammes, and place in a large porcelain beaker (or enamelled iron pot).