Top-Rated Free Essay
Preview

Lab Report

Good Essays
794 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Lab Report
LAB Report #3

Introduction:
In this lab we have focus on Isolation of bacteria from environment.
Microorganisms are found throughout the environment: in the air and water; on the surface of any object such as clothes, walls, furniture; in soil and dust; and on and in our own bodies (skin and mucous membranes). In order to demonstrate the ubiquity and diversity of microbes in the environment, samples from immediate areas of the environment and/or from your body will be obtained and cultured.

Materials:
4 sterile cotton swab, sterile water in test tube, 4 agar plates and 2 blood agar plates, wax pencil and labels.

Procedure:
Appropriately label the cover of each plate as indicated in lab.

1. Determine 2 sampling sources, one from your body and one from the surrounding environment.
2. For the first agar plate, for sampling from air, remove the lids from the plate and allow it to sit uncovered for 15 minutes.
1. For second agar plate, open the “stick” end of the sterile cotton swabs to avoid contamination of the swab. Deep the swab in to the sterile water and collect a dust form the corner of the table by swab and rub the swab over the entire surface of the Petri dish without going back over areas you have already swabbed.
3. For the third agar plate, divide the plate in two different parts like washed and unwashed finger tip and swipe on each side of plate, see the difference between them.
4. For the forth agar plate, divide it into the four equal part and tested four different place for bacterial grow. In first part, remove the sterile cotton swab from the package and immerse it in the sterile water and take the bacteria from forearm and swipe the swab on first part.
For second part, again take the sterile cotton swab and immerse it in sterile water, and take the bacteria from back of ear and rub on the second part.
For third part, again take the sterile cotton swab and immerse it in sterile water, and take the bacteria from handle of microscope and swipe on the third part.
For last part, again take the sterile cotton swab and deep in to the sterile water, and take the bacteria from toilet sit and swipe on the forth part. 5. For the fifth slide, we take blood agar plate and drawing line in central part of the plate. For one part used for kiss on that part and second part used for licked on that part for bacteria grow.
6. For last, we take another blood agar plate and we had to cough on this agar plate.

Leave all agar plates in the incubator for 1 week to grow bacteria.

Discussion:
After one week, I was able to observe my Petri plates, which were filled with bacteria.

The first plate had few yellow color colonies. That shows bacterial growth. Air was contaminant.

For second plate, it had huge yellowish and few brownish color colonies and clear halos around them. Dust also had bactria.

For third plate, on unwashed part had more yellowish color tiny spots and on washed part had few whitish color tiny spot. Washed had few bacteria that may be from the water while unwashed hand had more bacterial contamination.

For forth agar plate, first part had more yellowish color spots, second part had more brownish color spot, third part had no bacterial colonies and forth part had only three yellowish color colonies. That show microscope handle is not bacterial contaminant while all other object is contaminant with bacteria.

For the first blood agar plate, for the side that was kissed had huge brownish color spot and there were clear halos around it, and on other side that was licked had brownish color line. Bacteria also present in both sample.

For the second blood agar plate, there is no discoloration in the plate so I think there have not bacterial growth in the Petri dish.

Conclusion:
In this lab we have focus on mainly “ Isolation of bacteria from environment “ and to observe the growth of bacteria in favorable condition and observation of the color and shape of the bacterial colony.
Bacteria are found in a wide variety of environments---in or on animals and plants, in water, in soil, in air, or on rock. Generally, they are contributors to the environment, decaying nutrients and recycling the minerals (for use by plants and other organisms). Bacteria are both metabolically diverse as well as structurally diverse. As I have learned we carry bacteria when we are in perfect health as well when we are sick. From this lab we have learned that bacteria are present everywhere but we can achieve healthy life by hygiene.

You May Also Find These Documents Helpful

  • Better Essays

    I donned a fresh pair of Nitrile gloves prior to each sample. Using unopened sterile cotton applicators, I moistened swabs with the distilled water. I then swab the area indicated on the package description. Furthermore, I then place the swabs in its original packaging, making sure no contact with any outside element is made.…

    • 746 Words
    • 3 Pages
    Better Essays
  • Good Essays

    Once agar plate is prepared and cooled, label the plate on the backside using the permanent marker, divided in half. On the first plate write one half side “Milk Fresh” and on the other half “Milk Opened.” Then, divide the other agar plate in half. On the one half label “Lettuce Washed” and on the other half label “Lettuce…

    • 630 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    lab4

    • 1760 Words
    • 7 Pages

    The streak-plate method is an example of a solid dilution technique. Bacteria are obtained from a mixed culture with a sterile loop or wire and diluted within three sectors on a petri dish containing appropriate growth medium. After incubation, as a result of this dilution technique, individual colonies of microbes can be obtained. Each individual colony represents…

    • 1760 Words
    • 7 Pages
    Powerful Essays
  • Satisfactory Essays

    Lab 2

    • 559 Words
    • 3 Pages

    2. Label each test tube by the tested material (deionized water, 1% starch solution, onion juice,…

    • 559 Words
    • 3 Pages
    Satisfactory Essays
  • Powerful Essays

    Sterile the loop/or use a sterile loop and obtain culture of the bacteria from the petri dish or tube. Harvest just enough culture. (only use a tiny amount of culture preparing a smear)…

    • 1400 Words
    • 6 Pages
    Powerful Essays
  • Good Essays

    Unknown Bacteria

    • 1076 Words
    • 5 Pages

    Materials provided by the instructor, including an agar plate and cotton swab were used to collect…

    • 1076 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Prokaryotes Lab Report

    • 652 Words
    • 3 Pages

    -Obtained a sterile petri dish of nutrient agar,kept led on ,and used the marker to divided the petri dish ,into teo sector.…

    • 652 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Lightly streak 4 quadrants on TSA agar for anaerobic chamber. Make sure you can’t see bacteria…

    • 1019 Words
    • 5 Pages
    Good Essays
  • Satisfactory Essays

    Gram Staining

    • 454 Words
    • 2 Pages

    For this lab we used three cultures; Escherichia Coli, Bacillus Subtilis, and Staphylococcus Epidermidis. Using a different slide for each sample we started by preparing and fixing each slide. Next we covered the slide with crystal violet for 30 seconds then rinsed with water. Next we covered the slide with Grams Iodine for 10 seconds and rinsed with water. The next step is to decolorize the slide with ethanol, using a small amount on the slide for no more than ten seconds, and rinsing with water. The last stain we needed to put on the slide was Safranin for 30 seconds,and rinsed with water again. After blotting the slide dry we began to examine the slides under a microscope. We first began at 10x magnification to find the general area were the sample was on the slide. Then we moved to 100x magnification and used oil immersion.…

    • 454 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    Sterilized Cotton Swabs

    • 258 Words
    • 2 Pages

    2. The sterilized cotton swabs are first made damp using sterilized water. The swabs are rubbed in the following 5 places and then rolled and rubbed in the petri dishes:…

    • 258 Words
    • 2 Pages
    Satisfactory Essays
  • Powerful Essays

    4. Remove the lid of a petri dish (experimental) whilst still inverted as to reduce the likelihood of air borne microbes contaminating the agar by the gravitational settling of particles. Proceed to place either the 10g of blue vein cheese onto the lid (allowing enough to be present so the blue vein cheese touches the surface of the agar once the petri dish is closed) or 10 of yoghurt onto the surface of the agar via the sterile cotton swab.…

    • 1340 Words
    • 5 Pages
    Powerful Essays
  • Good Essays

    To begin the lab, turn the agar plate over and divide the plate into four quadrants and label the agar plate whether you used the E. coli or B. megaterium and number the quadrants 1 through 4. Please keep in mind that one pair will test the E. coli and Environment 1 or 2, and one pair will test B. megaterium and Environment 1 or 2. After, you will need to swab the E. coli and B. megaterium on two different nutrient agar plates using a sterile disposable inoculating loop. Remember not to dig in into the agar or the agar might break. Then, you will choose two environmental samples (rat, turtle or fountain) and do the same steps you used for the E. coli or B. megaterium. When you have swabbed…

    • 718 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Api 20# Lab Report

    • 544 Words
    • 3 Pages

    Methods: The method used for the API (analytical profile index) 20E System was the aseptic technique was used for the inoculating loop to get a unknown colony from the streak plate or pure culture slant. A small amount was smeared over the filter paper and several drops of oxidase reagent were added and the color change was noted. Another loop-full of bacteria was added to the test tube containing 5 ml of sterile saline, recapped and shaken by flicking. 5 ml of water was added to the bottom of the incubation tray to provide a humid atmosphere. A Pasteur pipette was then filled with a bacterial suspension. The incubation tray was tilted and tubes ONPG, TDA, IND, GLU, MAN, INO, SOR, RHA, SAC, MEL, AMY and ARA were filled with the bacterial suspension. The microtubes ADH, LDC, ODC, H2S and URE were slightly underfilled. Both the tube and cupule sections of CIT, VP and GEL tubes were filled. After inoculation, the cupule sections of ADH, LDC, ODC, H2S and URE were filled with mineral oil to create an anaerobic condition. The lid was then placed on the incubation tray and incubated at 37 degrees Celsius for 18-24 hours. An isolation streak was made on the TSA plate with a portion of the bacterial suspension to ascertain the purity of the suspension. After 18-24…

    • 544 Words
    • 3 Pages
    Good Essays
  • Good Essays

    Petri dish

    • 717 Words
    • 3 Pages

    1. Before starting the experiment, make sure you clean your work area with Chlorox and wear gloves at all times. Place your petri dishes on clean paper towels.…

    • 717 Words
    • 3 Pages
    Good Essays
  • Powerful Essays

    7. The repeated washing step was repeated for 5 times. After the final wash cycle, the plate was turned into blotting paper or clean towel and tapped to remove any remainders. The correct washing procedure is critical for successful performance of the test. Also, the well should not be allowed to dry during the assay procedure.…

    • 1005 Words
    • 5 Pages
    Powerful Essays