Bacteria Classification By Gram Staining THE AMERICAN UNIVERSITY IN CAIRO BIOLOGY DEPARTMENT SCIENCE 453: BIOLOGY FOR ENGINEERS REPORT No. 1 Presented By: Karim A. Zak lama 92-1509 Sci. 453-01 24/2/96 Objective: To test a sample of laboratory prepared bacteria and categorise it according to Christians gram negative Bacteria">gram positive and gram negative classes and also by viewing it under a high powered microscope and oil immersions; classify its shape and note any special characteristics. Introduction: Bacteria was categorised into two groups in 1884 by the Danish Bacteriologist Christian, gram positive and gram negative by a staining technique where the ability to avoid de-coloration of Crystal Violet solution by alcohol would render the category of gram positive, and gram negative if the bacteria is de-coloured. This could be noted by the final colour of the bacteria: a violet colour where Gram positive and a pink colour of the Safranin added pending the de-colouring process.
Materials: 1. Bacteria Sample 2. microscope slide 3. Gram Staining Kit and Wash Bottles a. Crystal Violet Solution b.
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... against a dark background. The Gram Staining Method is used as a tool for differentiation of Gram-positive and Gram-negative bacteria, as a first step ... was washed with water and added with decolourizer till crystal violet colour disappeared. The slide the rinsed with water. 5) Safranin was ...
Iodine Solution c. 95% Ethyl Alcohol d. Safranin e. Distilled Water 4.
Bibulous Blotting Paper 5. Microscope 6. Oil Procedure: A. Preparation: 1.
Bacteria is cultivated on agar jelly in an incubator at 25 C for 24 hours. 2. Obtain a microscope slide and with a toothpick, smear a thin coat of the bacteria sample onto the slide 3. Cover the smear with a drop Crystal Violet and leave standing for 20 seconds 4. Wash off the stain with distilled water; drain and blot off the excess with bibulous paper. 5.
Apply Grams Iodine on the smear and leave to stand for 1 minute. 6. Drain the excess iodine and apply 95% Ethyl alcohol for 20 second duration or till the alcohol runs clearly from the slide. 7. The smear should rinsed for a few seconds with distilled water to stop the action of the alcohol. 8.
Drain and blot off the excess with bibulous 9. Introduce Safranin to the smear and leave standing for 20 seconds. 10. Wash off the stain with distilled water; drain and blot off the excess with bibulous paper. 11. Leave the slide to air dry.
B. Examination: 1. Place the slide under microscope on low powered lens. 2.
Move the slide using the apparatus until the sample can be seen as a blur under the microscope. 3. Focus the lens to ensure that there is a sample directly under the lens. 4. Move to higher powered lens, repeat step 3. 5.
Move to higher powered lens, repeat step 3 6. Move microscope aside and add Oil immersion, leave for a few seconds and re-examine the slide. Note Shape and colour and any other observations. Results and Observations: It was evident by visual examination that the alcohol was de-colouring or a least partially de-colouring the bacteria. The sample appeared a dark pink or close to violet by the naked eye; a microscope was needed to ensure results.
Under the low powered microscope shades of pink were noted. Under the medium power, the shades were more clear but no shape could be made out. Under the high powered microscope clumps of pink rod (bacilli) shaped bacteria cells could be observed. Under Oil Immersion and high powered lens the cells could seen more spaced out and thus a clearer indication of the pink colour, bacilli shape and spores could be made out in the individual cells. Conclusion: The Shape was noted as Bacilli (Rod-like) shaped cells; a gram variable shape, distinct in either Gram Negative or Gram positive bacteria.
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The final colour of the cells were stained pink by the Safranin showing the de-coloration of the crystal violet proving the bacteria is of the gram negative class. Under oil immersion the cells became more sparse and under the high powered lens of the microscope spores could be seen, as little bubbles, in the cells. This tells us that the bacteria was in its terminal state. The presence of spores in the bacteria at its terminal state tells us that the bacteria could be an old culture.
Old bacteria cultures which are gram positive tend to de-colour, yet more slowly than gram negative bacteria. The speed of de-coloration was not inspected very clearly thus no further conclusion could be reached, yet it is possible that this an old culture of Bacilli shaped Gram Positive bacteria. Recommendation: It is recommended that the same sample be tested again for de- coloration; focusing on de-coloration speed. If the de-coloration is fast then the sample is definitely gram negative, slow de-coloration would tell us it is gram positive. For future samples it would be recommended to keep the bacteria sample for this specific test for only 16 hours as recommended to avoid the presence of old cultures which are anomalous to this test.
