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Today you will perform a frequently used procedure called the Kirby-Bauer Antimicrobial Susceptibility test (disc diffusion technique). Each group will inoculate his/her own plate of Mueller-Hinton agar with an assigned culture. To that inoculated plate, you will then aseptically add sterile filter paper discs (using a disc dispenser), which contain a known concentration of antibiotics. As soon as the antibiotic discs touch the agar, the antibiotic will begin to diffuse into the surrounding agar. During incubation the bacteria you inoculated onto the agar…
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First, four quadrants were made with Sharpie on the bottom of the nutrient agar plate, to tell the four disks apart later on. When the agar plate is sectioned, a cotton swab of Serratia marcesans must be carefully swiped gently, all over the top of the nutrient inside the plate. The plate must be evenly swabbed like coloring a coloring book to ensure readable results after the antibiotics are tested. The cotton swab is disposed of carefully in the designated waste bag to avoid contamination after use.…
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–Lewis Thomas Although Fleming didn’t know it at the time, penicillin and other antibiotics preferentially kill bacteria because they target what is unique about bacterial cells. According to the cell theory, all living things are made of cells, and CHAPTER 3: CELL FUNCTION AND STRUCTURE 3620001C03.indd 41 41 1/27/11 10:14 AM INFOGRAPHIC 3.1 How Penicillin Was Discovered A fortuitous observation by Fleming led to the discovery of the first antibiotic.…
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Procedure: Obtained a small Styrofoam cooler placed two small light bulbs in side and observed temperature over 24 hours to ensure temperature could be maintained between 98-100 degrees. Using a 10% bleach solution I then cleaned my work area. Transferring one capsule of L. acidopholis into a tube of MRS broth using the aseptic transfer technique then marked a line on test tube to record sediment. Labeled tube of nutrient broth S. epidermidis, then using a sterile swab obtained sample of bacteria from skin then transferred using the aseptic transfer technique into the sterile media. Incubated both specimens for 48 hours observed and recording results of growth at 24 and 48 hours. After observing final growth pattern at 48 hours prepared both wet mount and direct stain slide for each of the cultures. Viewed under microscope using both the 40X and 100X oil immersion lens. Disinfected work area.…
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The tests performed on the unknown bacteria cultures were all used to determine the identity of the bacteria. Each of the tests performed provided some key information about the bacteria in question and how it functions. Not all of the tests were performed on every culture, however, as some of the tests were used only for gram (+) or gram () bacteria, while others were even more specific and used only for cocci bacteria. The tests performed and what constitutes a positive and negative test are as follows.…
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I would prescribe Sue sulfa drugs. The bacteria is a Gram negative so penicillin would be difficult to infiltrate the cell wall. The others are within the cells. So Sulfa drugs would be best.…
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being tested. Serratia marcescens is usually found in soil and plants, and the accumulation of…
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| Glucose fermented to acid and protein in media was broken down to alkaline end product…
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The unknown bacteria A and bacteria B have to be identified by its genus and species. First both bacteria had to be inoculated into a TSA agar media using the streak plate method. Four quadrants were drawn, so that the bacteria could be isolated as much as possible. Each bacteria was inoculated into two different plates, so that one could be incubated at 37 degrees Celsius and the other at 25 degrees Celsius. Bacteria B, which was incubated at room temperature showed red colonies throughout its media. This identified it as the gram-negative bacteria Serratia marcescens, but further tests had to be conducted to fully confirm. Bacteria A showed a white opaque growth in both of its plates.…
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Five sterile petri-dishes were each labeled with the time that the plate would be exposed to UV radiation (0 seconds or negative control, 15 seconds, 30 seconds, 45 seconds, and 60 seconds). Aseptic technique was critical during each transfer of agars. Plain 50 agar was poured equally to each plate labeled. A cotton end of the applicator stick was wet with the liquid culture of bacteria, Serratia marcescens, and applied on the surface of agar the same way it was carried out to cover the agar gradient in the first part of the experiment. Plates were prepared for the UV exposure.…
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Procedures: This experiment called for prepared agar in a petri dish, smeared s. epidermis on the surface of the prepared agar, and a 3 separate quadrants labeled gentamicin, novobiacin, and penicillin. Once those steps were completed a tablet of the 3 antibiotics were placed in the center of the 3 quadrants with the petri dish lid closed. We then placed the petri dish in the incubator for 24-48 hours at 37 degree for growth.…
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An unknown labeled with number 8 was given out by the lab instructor. The goal at this point was to determine unknown gram positive vacteria. The procedures performed consisted of sterile technique in addition to being followed as stated in the referenced course laboratory manual by Matar (1) , unless otherwise noted.…
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In this laboratory exercise explore the differences of microorganism and continue our use of specialized media and use some biochemical testing.This report discloses the basic laboratory instruments will be used in each of our practices .It is of great importance to recognize and identify the different instruments and laboratory tools, because in this way will we be able to use them properly and also to call them by name and know why.…
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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.…
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There are several antimicrobial agents to treat infections. Beta-lactams are the types ending in “illin” and those beginning with “ceph” or “cef” such as penicillin and the cephalosporin. The mechanism of action is the inhibition of bacterial cell growth by interference with cell wall synthesis, which bind to and inactivate the penicillin-binding proteins (PBPs) (Arcangelo & Peterson, 2013). Another antimicrobial category is aminoglycosides, which usually ends with “mycin” or “cin” such as gentamicin and neomycin. Aminoglycoside are primarily used to combat gram-negative bacteria such as Escherichia coli and Klebsiella. Tetracyclines such as doxycycline are used against gram-positive, gram-negative and atypical organisms and are labeled “broad spectrum” (Arcangelo & Peterson, 2013). These types of antimicrobials are used for urinary tract infections and acne problems. Fluoroquinolones are used to treat illnesses such as respiratory and urinary tract infection. These medicines include ciprofloxacin and levofloxacin. Fluoroquinolones may cause sudden serious, and potentially permanent nerve damage called peripheral neuropathy (Miller, 2013). Macrolides are bacteriostatic antibiotics with a broad spectrum of activity against many gram-positive bacteria (Miller, 2013). Examples are erythromycin and azithromycin, which are used to fight against streptococci and staphylococci.…
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