FREE BOOKS

Author's List




PREV.   NEXT  
|<   143   144   145   146   147   148   149   150   151   152   153   154   155   156   157   158   159   160   161   162   163   164   165   166   167  
168   169   170   171   172   173   174   175   176   177   178   179   180   181   182   183   184   185   186   187   188   189   190   191   192   >>   >|  
ubes of sterile nutrient media, gelatine (or agar) previously liquefied by heating in the water-bath and cooled to 42 deg. C., otherwise the heat of the medium would destroy many, if not all, of the bacteria introduced. 6. Tube of cultivation to be planted from. 7. Platinum loop. 8. Bunsen burner. 9. Grease pencil. [Illustration: FIG. 121.--Handy form of water-bath for melting tubes of agar and gelatine previous to slanting them; or to making shake cultures or pouring plates.] Method of "Pouring" Plates.-- 1. Place the glass dish on the levelling tripod (Figs. 122, 123); if gelatine plates are to be poured fill the dish with ice water--gelatine solidifies so slowly that it is necessary to hasten the process; if agar is to be used fill with water at 50 deg. C.--agar sets almost immediately at the room temperature and by slightly retarding the process lumpiness is avoided; cover the dish with the square sheet of glass. 2. Place the spirit level on the sheet of glass and by means of the levelling screws adjust the surface of the glass to the horizontal. This leveling is an important matter since the development of a colony is to some extent proportionate to the supply of medium available for its nutrition. Thus in a "smear" on sloped tube culture, the colonies at the upper part of the medium are stunted and small but increase in size and luxuriance of growth the nearer they approach to the bottom of the tube, where there is the greatest depth of medium. [Illustration: FIG. 122.--Plate-levelling stand.] 3. Place three sterile Petri dishes in a row on the surface of the glass plate and number them 1, 2, and 3, from left to right. [Illustration: FIG. 123.--Plate-levelling stand, side view.] 4. Number the previously liquefied tubes of nutrient media 1, 2, and 3. Flame the plugs and see that each plug can be readily removed from the mouth of its tube. 5. Add one loopful of the inoculum to tube No. 1, treating the liquefied medium as bouillon. After replugging, grasp the tube near its mouth by the thumb and first finger of the right hand, and with an even circular movement of the whole arm, diffuse the inoculum throughout the medium; avoid jerky movements, as these cause bubbles of air to form in the medium. [Illustration: FIG. 124.--Mixing emulsion for plates.] The knack of mixing evenly without producing air bubbles, is not always easily acquired, by this
PREV.   NEXT  
|<   143   144   145   146   147   148   149   150   151   152   153   154   155   156   157   158   159   160   161   162   163   164   165   166   167  
168   169   170   171   172   173   174   175   176   177   178   179   180   181   182   183   184   185   186   187   188   189   190   191   192   >>   >|  



Top keywords:
medium
 

gelatine

 

Illustration

 
levelling
 

plates

 

liquefied

 

process

 

surface

 

inoculum

 

bubbles


nutrient

 
previously
 

sterile

 
stunted
 
dishes
 

number

 

Number

 

easily

 

bottom

 

approach


growth

 

nearer

 

greatest

 

acquired

 

increase

 
luxuriance
 

producing

 

replugging

 

bouillon

 

movements


movement

 

diffuse

 
finger
 

removed

 

evenly

 

mixing

 

readily

 

circular

 

treating

 

Mixing


emulsion
 
loopful
 

melting

 

previous

 

slanting

 
pencil
 

burner

 
Grease
 
making
 

tripod