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AGf~ICULTURAL RESEARCH, PUSA.

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CULTIVATION OF lIfICRO-ORGANISlI18 125<br />

an all-glass syringe of 15 c.c. capacity. The syringe is of the<br />

three-piece type, but without the nozzle, and thc plunger is<br />

hollow, as the head of liquid will not lift a solid glass pistoIl.<br />

The barrel is graduated to 15 c.e. by 0'5 e.e., and the numbers<br />

are engraved so as to be readable when the syringe is vertical.<br />

'l'he syringe is connected to the stopcock by means of a metal<br />

screw fitting. A clamp on a swivel mount securcs the lower<br />

end of the syringe. The amount of fluid delivered is determined<br />

by the adjustable screw. A very thin film of liquid paraffin well<br />

rubbed on the surface of the plunger and barrel will make for<br />

smoother working. The action of the filler is simple. 'rhe head<br />

of medium in the funnel forces up the plunger until it is stopped<br />

by the adjuHtablc screw. The handle of the stopcock is then<br />

turned and the syringe empties itself under the weight of<br />

the plunger. Air bubbles in the syringe are removed by fIrst<br />

filling the apparatus and then turning the syringe by means<br />

of the swivel mount. This brings the nozzle of the syringe<br />

uppermost, and when the plunger is pressed home the ail'<br />

passes through the rubber tube and liquid in the funnel. If a<br />

smoothly working syringe is used, very little head of pressure is<br />

necessary, and the height need not be greater than 18 inches.<br />

Once set, thc accuracy of the filler is much greater than that<br />

of an ordinary pipette, while media can be tubed with greater<br />

rapidity. It works equally well with melted agar m gelatin,<br />

provided that fresh hot supplies are available, and the syringe<br />

and stopcock are washed out immediately after use.<br />

When tubing agar or broth with the filler, the medium is<br />

run into clean but not sterilised test-tubes. These are then<br />

plugged with cotton-wool and sterilised in the steamer 01' in<br />

the autoclavc as indicated under the description of thc various<br />

merlia.<br />

Alternatively the agar or broth is distributed into small<br />

bottles (p. 120), the rap is screwed tightly on, and the whole<br />

container suitably steriliscd.<br />

Depending on the method of inoculation to be used,<br />

solid media are solidified in tubes as follows :-<br />

(a) Upright, for "puncture" or "stab" culiU1·e.­<br />

The test-tube or small screw-capped bottle<br />

is half filled with the medium (about 12 c.c.)<br />

which is allowed to solidify in the upright<br />

position. It is inoculated by plunging a<br />

long straight wire (vide p. 128), charged with<br />

the material, vertically down the centre of<br />

the tube. This method is used for anaerobic

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