BIOLOGY Bacteria Growth Lab Prokaryotes & Viruses - - PDF document

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BIOLOGY Bacteria Growth Lab Prokaryotes & Viruses - - PDF document

Slide 1 / 61 New Jersey Center for Teaching and Learning Progressive Science Initiative This material is made freely available at www.njctl.org and is intended for the non-commercial use of students and teachers. These materials may not be


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This material is made freely available at www.njctl.org and is intended for the non-commercial use of students and teachers. These materials may not be used for any commercial purpose without the written permission of the owners. NJCTL maintains its website for the convenience of teachers who wish to make their work available to other teachers, participate in a virtual professional learning community, and/or provide access to course materials to parents, students and others.

Click to go to website: www.njctl.org New Jersey Center for Teaching and Learning Progressive Science Initiative

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www.njctl.org

BIOLOGY Bacteria Growth Lab

Prokaryotes & Viruses

Slide 2 / 61 Prokaryotes Unit Topics

· Bacterial Growth

Click on the topic to go to that section

· Analysis & Conclusion · Antibacterial Agents

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Bacterial Growth

Return to Table of Contents

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Bacteria reproduce by binary fission. This proliferation by cell division results in rapid bacterial population growth.

Bacterial Growth

Bacterial Growth Animation

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As previously mentioned, bacteria can live almost anywhere and do live almost everywhere! In the lab, bacteria are grown in a medium that contains the nutrients necessary for growth and survival.

Bacterial Growth Slide 6 / 61

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Bacteria can also be grown on a gelatinous, polysaccharide substance called agar that is spread out on the surface of a petri dish. Bacteria are then "plated" on the agar.

Agar Slide 7 / 61 Agar contains:

Salts: provide essential elements like magnesium, phosphorous, nitrogen, and sulfur needed for making proteins and nucleic acids. Sugar: provides a source of carbon Water: solvent

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Bacterial populations typically form colonies - groups of millions or billions

  • f bacteria that live in a

tightly packed area. An individual bacterium can

  • nly be seen with a

microscope, but a bacterial colony growing on a petri dish is visible to the naked eye.

Bacterial colonies growing on a plate of nutrient agar. Hans Knoll Institute. Jena, Germany

Bacterial Colonies Slide 9 / 61

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Plating bacteria on agar allows one to visualize the different types of bacteria that may be present in a solution and to isolate a particular strain of bacteria for further use.

Plating Bacteria

Different types of bacteria can be distinguished by their distinct morphologies (shapes, structures, colors, or patterns).

Streak Plating Demonstration

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A culture is a solution that is optimal for the growth of a specific type of bacteria. Bacterial cultures are used primarily to grow isolated strains of bacteria in the lab.

Cultures Slide 11 / 61

When bacteria are placed in an environment that provides all of their metabolic needs, bacterial populations grow rapidly until they have depleted all of the nutrients in their environment.

Bacterial Growth Slide 12 / 61

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There are four phases to the bacterial growth cycle: *lag phase *log phase *stationary phase and *death phase.

http://www.ryancshaw.com/Files/micro/Animations/BacterialGrowth/PLAY_bacterial_growth.html

Bacterial Growth Phases Slide 13 / 61

During the lag phase, the bacterial cell grows and prepares for cell division

Lag Phase Slide 14 / 61

During the log phase the bacterial population grows rapidly - doubling in size with each generation.

http://www.ryancshaw.com/Files/micro/Animations/BacterialGrowth/PLAY_bacterial_growth.ht

Log Phase Slide 15 / 61

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watch the number of cells here

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watch the cell number take off!

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The stationary phase is reached when the bacteria start to run

  • ut of nutrients and

the number of bacteria dying is equal to the number of bacteria reproducing.

Stationary Phase Slide 36 / 61

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After nutrients have been used up and waste builds up, bacteria begin to die in large numbers and

  • nly very few

reproduce.

Death Phase Slide 37 / 61 Calculating Bacterial Growth

It is possible to estimate the number of bacteria present in a culture after a period of time using the following formula: (2n )(initial number of bacteria) = total number of bacteria n = the number of generations. This can be determined by using the following formula: total time generation time (time it takes the bacteria to divide)

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At a fourth of July picnic, a bowl of potato salad was left out in the hot sun for 2 hours. If the salad originally contained 250 Salmonella enteritidis bacterial cells and Salmonella divides every 10 minutes, how many bacteria would be present at the end of 2 hours? Givens: Initial number of bacteria = 250 total time = 2hrs generation time = 10 minutes n = total time = 120 min. = 12 generation time 10 min.

Calculating Bacterial Growth

(2n )( initial number of bacteria) = final number of bacteria 212 x 250 = 1,024,000 bacteria

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1 Bacillus cereus divides every 30 minutes. You inoculate a

culture with exactly 100 bacterial cells. After 3 hours, how many bacteria are present?

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2 Staph. aureus, a disease causing bacteria, divides every 15

minutes at body temperature. A student gets a cut on her hand, is infected with 10 Staph. aureus bacterial cells, and does not clean the wound. After 1 hour, how many bacteria are present?

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Antibacterial Agents

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Antibacterial Agents

Antibacterial agents are chemical substances that either kill bacteria or inhibit growth. There are 3 main types: antiseptics disinfectants antibiotics

Slide 43 / 61 Antibacterial Agents

antiseptics: chemicals used to kill or inhibit growth on living tissues (examples - hydrogen peroxide, soap, mouthwash) disinfectants: used to kill or inhibit growth on nonliving

  • bjects (examples - bleach and boiling water)

antibiotics: chemicals produced by living organisms (fungi or bacteria) that inhibit growth of bacteria (examples - penicillin and tetracycline) NOTE: some antiseptics are also disinfectants and vice versa

Slide 44 / 61 How do we know they work?

An experiment was done to test the effectiveness of various disinfectants and antibiotics. The experiment had 5 steps.

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How do we know they work? Step 1

A sterile cotton swab was inserted into a culture of E. Coli bacteria.

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The tip of the cotton swab was then placed on the agar plate, streaking the sample of bacterial culture across the plate as show below to inoculate the plate with bacteria.

How do we know they work? Step 2 Slide 47 / 61

3 filter paper disks were dipped in 3 different types of disinfectants and placed in the middle of each quadrant of the first petri dish. Distilled water was placed in the 4th quadrant as a control Disinfectant 1: bleach Disinfectant 2: hydrogen peroxide Disinfectant 3: window cleaner

How do we know they work? Step 3 Slide 48 / 61

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3 disks coated in 3 different antibiotics were placed in the middle of each quadrant of the second petri dish. Distilled water was placed in the 4th quadrant as a control. Antibiotic 1: ampicillin Antibiotic 2: penicillin Antibiotic 3: tetracycline

How do we know they work? Step 4 Slide 49 / 61

Both petri dishes were then taped shut, flipped upside down to prevent condensation from dripping onto the bacteria, and placed inside a 37 degree incubator for 48 hours.

How do we know they work? Step 5 Slide 50 / 61 Predictions and Results

Make your prediction about whether bacteria is killed...

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1 3 2 4 1 3 2 4

Results Dish 2 The clearer areas surrounding the disks are called zones of inhibition and indicate that bacterial growth was inhibited.

Predictions and Results

Results Dish 1

Slide 52 / 61 Predictions and Results

CHECK if a zone of inhibition is present on the plate

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Another mechanism of inhibiting bacterial growth is to infect the bacteria with a virus. A drop of solution containing bacteriophage viruses was added to the bacterial culture below resulting in several clear zones. These clear zones are called plaques. Viral plaques indicate that bacteriophages have infected and killed bacterial cells. Plaques may be counted and used to determine the number of viruses present in a bacterial culture.

Fighting Bacteria with Viruses Slide 54 / 61

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Analysis & Conclusions

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1). Which disinfectant most effectively inhibited the growth of E. coli?

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2). Which antibiotic was most effective in preventing the growth of E. coli?

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3). How do you know that any inhibition you have observed is due to the disinfectants and antibiotics on the disk?

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4). If the same experiment was repeated using a different strain

  • f bacteria and a zone of inhibition was observed around the

disk soaked in window cleaner, what could account for the different results?

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5). You wake up one morning with a severe sore throat and notice white dots lining your tonsils. You quickly visit the doctor, who diagnoses you with a Streptococcus infection (strep throat) and prescribes a 10-day antibiotic treatment. After 3 days, you begin to feel better. Why should you continue taking the antibiotic for the full 10 days?

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  • 6. What causes a zone of inhibition?

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