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picture1_Module Instructions


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File: Module Instructions
module the gram stain procedure click start lab from a liquid culture take a loopful of bacteria emulsify it in a small drop of water or saline on the slide ...

icon picture PDF Filetype PDF | Posted on 14 Sep 2022 | 3 years ago
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        Module: The Gram Stain  
         
        Procedure - click “start lab” 
         
        From a liquid culture, take a loopful of bacteria emulsify it in a small drop of water or 
        saline on the slide. This should be a thin, not milky, suspension or it will not stain 
        properly. Air dry the slide. This is done automatically in the virtual module. 
         
        To begin:  
        1.  Heat fix the slide: click on the Bunsen burner, pass the slide gently two or three times 
         (1-2 seconds) through the flame. Do not overheat - this will cause distortion of the 
         cells.  
        2.  Flood the slide with crystal violet for 1 minute 
        3. Rinse with H20  
        4.  Flood the slide with iodine for 1 minute 
        5. Rinse with H20 
        6. Decolorize with alcohol for 5-10 seconds 
        7. Rinse with H20 
        8.  Flood the slide with safranin for 1 minute 
        9. Rinse with H20 
        10. View slide under the microscope   
         
        The “slide” contains E. coli and Staph. aureus – is that what you see?  
        If not, think about what you might have done incorrectly 
        Then, repeat the exercise. 
         
        When you are finished with the exercise, click on “Examine Examples” to see actual 
        micrographs of several bacteria that have been gram stained. You will recognize the 
        names of many of the bacteria from lecture.    
         
        Some Pitfalls: 
   
        1. Slide not heat-fixed: smear will wash off → what would you expect to see? 
        2. Slide over heat-fixed: cellular morphology may be distorted 
        3.  Slide over-decolorized: gram-positive bacteria will appear gram-negative 
        4. Slide under-decolorized: gram-negative bacteria will appear gram-positive 
        5. Smear too thick: cells in very thick areas will not decolorize properly and gram 
        negative bacteria will appear gram-positive 
        6. Insufficient time for safranin counterstain: gram-negative bacteria may be very faint 
        and difficult to see 
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...Module the gram stain procedure click start lab from a liquid culture take loopful of bacteria emulsify it in small drop water or saline on slide this should be thin not milky suspension will properly air dry is done automatically virtual to begin heat fix bunsen burner pass gently two three times seconds through flame do overheat cause distortion cells flood with crystal violet for minute rinse h iodine decolorize alcohol safranin view under microscope contains e coli and staph aureus that what you see if think about might have incorrectly then repeat exercise when are finished examine examples actual micrographs several been stained recognize names many lecture some pitfalls fixed smear wash off would expect over cellular morphology may distorted decolorized positive appear negative too thick very areas insufficient time counterstain faint difficult...

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