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
4. The semicircle now appears as in figure 100, a, the dark lines
indicating the creases already formed.
5. Fold the point 1 over to the point 3, and 1a to 3a, to form the
creases 4 and 4a, indicated in the diagram by the light lines. Fold
point 1 over to 3a, and 1a to 3, to form the creases 5 and 5a.
[Illustration: FIG. 100.--Filter folding: a, Filter folded in half,
showing creases; b, appearance of filter on completion of folding;
c, filter opened out ready for use.]
6. Thus far the creases have all been made on the same side of the
paper. Now subdivide each of the eight sectors by a crease through its
centre on the opposite side of the paper, indicated by the faint broken
lines in the diagram. Fold up the filter gradually as each crease is
made, and when finished the filter has assumed the shape of a wedge, as
in figure 100, b.
When opened out the filter assumes the shape represented in figure 100,
c.
The folded filter is next placed inside a glass funnel supported on a
retort stand, and moistened with hot distilled water before the
filtration of the medium is commenced.
~Liquefiable solid media~ are filtered through a specially made filter
paper--"papier Chardin"--which is sold in boxes of twenty-five
ready-folded filters.
[Illustration: FIG. 101.--Hot-water filter funnel and ring burner.]
Gelatine, when properly made, filters through this paper as quickly as
bouillon does through the Swedish filter paper, and does _not_ require
the use of the hot-water funnel.
Agar, likewise, if properly made, filters readily, although not at so
rapid a rate as gelatine. If badly "egged," and also during the winter
months, it is necessary to surround the glass funnel, in which the
filtration of the agar is carried on, by a hot-water jacket. This is
done by placing the glass funnel inside a double-walled copper
funnel--the space between the walls being filled with water at about
90° C.--and supporting the latter on a ring gas burner fixed to a retort
stand (Fig. 101). The gas is lighted and the water jacket maintained at
a high temperature until filtration is completed. If the steam
steriliser of the laboratory is sufficiently large, it is sometimes more
convenient to place the flask and filtering funnel bodily inside, close
the steriliser and allow filtration to proceed in an atmosphere of live
steam, than to use the gas ring and hot-water funnel.
STORING MEDIA IN BULK.
After filtration fill the medium into sterile litre flasks with
cotton-wool plugs and sterilise in the steamer for twenty minutes on
each of three consecutive days. After the third sterilisation, and when
the flasks and contents are cool, cut off the top of the cotton-wool
plug square with the mouth of the flask; push the plug a short distance
down into the neck of the flask and fill in with melted paraffin wax to
the level of the mouth. When the wax has set the flasks are stored in a
cool dark cupboard for future use.
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