Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN: 9780134580999
Author: Elaine N. Marieb, Katja N. Hoehn
Publisher: PEARSON
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There are various parameters to assess microbial growth.
What are some microbial growth curve characteristics? Can you explain how microbiologists measure specifically bacteria growth?
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- What information can obtain from observing the growth of bacteria on liquid agar?arrow_forwardcould you please plot the semilog graph of the Growth Curve and calculate the doubling time of the attached data?arrow_forwardWhich of the following is NOT correctly matched? A. Halophile – microbe that can grow in an environment with high osmotic pressure (e.g., salt) B. None of the other four answers (all are correctly matched) C. Agar – complex polysaccharide from seaweed used as a solidifying agent in culture media D. Colony – a population of microbial cells arising from a single cell or spore or from a group of attached cells E. Capnophile – microbe requiring an elevated molecular oxygen (O2) environment for optimal growtharrow_forward
- What is the difference between a bactericidal antibiotic and an antibiotic that is bacteriostatic? Examine the zone of inhibition around each disk for the presence of micro colonies within the zone. What do these micro colonies represent? Why didn't plants evolve anti-microbial agents against all the microbes in their environment?arrow_forward1. Plate count data are used to calculate microbial population density as colony forming units (CFUs) per milliliter of culture. Culture density (CFU/mL) = number of colonies (dilution factor) x (volume plated, in mL) Use these data below to calculate the CFU/mL in this sample of bacteria after 1 hr of growth. **Important to know for these types of questions - only use colony counts that fall between 10 and 300. TNTC = too numerous to count, so many colonies that you can't distinguish them to count. Use the plates with numbers of colonies that can be counted, calculate the CFU on each one, and then calculate the average between all of them. Looking for more assistance? Read section 7.3 in the textbook. Time 1h Dilution (before plating) Volume spread on plate 0.1 mL 0.1 mL 0.1 mL 0.1 mL none 1:10 (1 x 10-¹) 1:100 (1 x 10-²) 1:1,000 (1 x 10-³) Number of colonies observed (replicate plates) TNTC 499 83 10 TNTC 518 87 8 TNTC indicates too numerous to count. *Cell density could not be…arrow_forwardPlease discuss the different environmental factors that influence microbial growth. What would be the basic profile of a microbe pathogenic to humans?arrow_forward
- Compare and contrast bacteriocidal, bacteriostatic and bacteriolytic agents. What are their effects on the optical density (OD) and viable count of a bacterial culture, respectively?arrow_forwardWhat is the difference between selective and differential media? Give one example of each.arrow_forwardWhy do soil microbes naturally produce antibiotics?arrow_forward
- What is the major difference between an enrichment culture and a selective culture? Why are microbial doubling times in nature typically longer than those obtained in the lab? Briefly describe the following mechanisms of measuring bacterial growth: Direct microscopic cell count Plate count Most probable numberarrow_forwardIs nutrient agar (NA) a complex or defined medium? Explained based on its composition. Is NA a differential, selective, neither differential nor selective media? Explaining based on what kind of Organism it allows to grow?arrow_forwardDescribe methods used to grow microbes anaerobically and under high CO2 conditionsarrow_forward
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