Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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- The table below shows the response of our ESKAPE safe relatives to 4 bacteria isolated from a master grid. We do not know the identity or any characteristics of the unknown bacteria. Each safe relative was spread onto a petri dish using aseptic technique. A grid pattern was taped to each plate and the unknown bacteria were patched into one of the squares. If there was no inhibition visible, including with a magnifying lens, the result was listed as -. If there was an inhibition zone between 1 and 10mm in diameter, the result is listed as +. If the inhibition zone was 10mm or greater, the result is listed as ++. In the lab, the MGC instructors plated all 6 of the ESKAPE pathogen safe relatives on LB agar plates. Then we patched Unknown Bacteria 5 from a Master plate onto the safe relative. The results are shown here: METRIC METRIC METRIC 1 B. subtilis S. epidermidis E. coli Complete the final column (Unknown Bacteria 5) of the table by selecting -, +, or ++ using the criteria in the…arrow_forwardGiven that antibiotic-resistant strains of bacteria are a concern to the general health of a population, what can be done to prevent their development?arrow_forwardYou infect bacteria with two phages during a cis test. This produces a lysate that contains phage particles. Before you can count outcomes, you need to work out the amount of phage to use in subsequent experiments. You start by making two ten- fold serial dilutions of the lysate and then add 1mL of the final diluted lysate to a plate of permissive strain e.coli. You observe 10 plaques. How many phage per mL were present in the original lysate? a. 10 phage/mL o b. 3,300 phage/mL c. 10,000 phage/mL o d. 1,000 phage/mL e. 33 phage/mLarrow_forward
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