Question

You are measuring the growth and competition of Ps. fluorescence and B. megaterium. They are mixed...

You are measuring the growth and competition of Ps. fluorescence and B. megaterium. They are mixed in a culture together. The culture is then added to a PEA plate and to a EMB plate. What is the expected hypothesis?

0 0
Add a comment Improve this question Transcribed image text
Answer #1

Pseudomonas fluorescence is a gram negative bacteria and Bacillus megaterium is a gram postive bacteria. When they are mixed in a culture together and added to PEA plate which is a selective medium for the growth of Gram postive baterias and the active ingredient phenylethyl alcohal reduces the growth of gram negative bacteria thus helps in distinguishing the Ps. fluroscence from B. megaterium while EMB plate helps in inhibiting the growth of gram postive bacteria and promotes the growth of gram negative bacteria Ps. fluroscence . The mechanism behind the process is that when the cultures are mixed together and are plated on different agar mediums we are able to distinguish between different strains of bacteria as PEA allows Gram positive bacteria and EMB allows Gram Negative bacteria. Moreover, their formation of colony patterns also hepls in differentiate between them. As Bacillus megaterium forms dark purple complexes and  Pseudomonas fluorescence and appear red in colour.

Add a comment
Know the answer?
Add Answer to:
You are measuring the growth and competition of Ps. fluorescence and B. megaterium. They are mixed...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • 2. You are given a mixed broth culture of Pseudomonas fluorescence (Gram-negative) and Clostridium sporogenes (Gram-positive)....

    2. You are given a mixed broth culture of Pseudomonas fluorescence (Gram-negative) and Clostridium sporogenes (Gram-positive). You are instructed to isolate and purify each bacterial species. How are you going to do it? Your goal is to have a plate of pure P. fluorescence with isolated colonies and a plate of pure C. sporogenes with isolated colonies. Explain in detail how you are going to perform the exercise. You can use any media you like such as nutrient agar plate,...

  • 3. You are measuring the growth of bacterium using cfu mL·You collect samples at various times an...

    3. You are measuring the growth of bacterium using cfu mL·You collect samples at various times and dilute them in 10-fold series (as shown in the 2 row of the table) and plate 0.1 ml of each of these dilutions on five standard lab agar plates. The average number of colonies per plate are below Time of Colonies on plate at each dilution ars 45 290 TNTC TNTC 195 20 TNTC TNTC 200 TNTC too numerous to count ADB MO...

  • 3. You are measuring the growth of bacterium using cfu mL·You collect samples at various times...

    3. You are measuring the growth of bacterium using cfu mL·You collect samples at various times and dilute them in 10-fold series (as shown in the 2 row of the table) and plate 0.1 ml of each of these dilutions on five standard lab agar plates. The average number of colonies per plate are below Time of Colonies on plate at each dilution ars 45 290 TNTC TNTC 195 20 TNTC TNTC 200 TNTC too numerous to count ADB MO...

  • Consider the three graphs below, which show the quantity of DNA in cells measured by fluorescence...

    Consider the three graphs below, which show the quantity of DNA in cells measured by fluorescence in flow cytometry. The x-axis represents the relative amount of DNA per cell, and the relative intensity of the florescence on the y-axis represents the number of cells with that amount of DNA in the cell. Look at the experiment shown on page 248 of your textbook. 1) A B C 2) 20-40,一60一助100 20-40 60一負100 40, 60 N 100 Amount of fluorescence per cell...

  • You are given a mixed culture of two organisms in a small tube of TSB.

    You are given a mixed culture of two organisms in a small tube of TSB. These two organisms include a Gram-negative strain (your bacterial strain to identify) and a Gram-positive strain (a contaminant). Your first task is to isolate these organisms which will help you identify which Gram-negative strain you are working with. 1) You inoculate two streak plates on TSA media and MacConkey Agar using aseptic technique. For each medium, state whether the medium is selective, differential, or neither and...

  • Think about the results you recorded. a. Growth on the PEA and NA plates was recorded...

    Think about the results you recorded. a. Growth on the PEA and NA plates was recorded as "good growth," "p oor growth," or “no are qualitative and, at least for the first two, subjective terms. What did you use to establish what These constituted "good growth?" bhy wouldn't it be advisable to compare growth of the organisms on each plate to each other? There are at least two answers to this question!

  • Lab Report-Carbohydrates 1. Purpose 2. Special Media for Isolating Bacteria (Lab #12) a. Why are dyes...

    Lab Report-Carbohydrates 1. Purpose 2. Special Media for Isolating Bacteria (Lab #12) a. Why are dyes such as phenol red, eosin or methylene blue added to the media? b. How does the bacterium change the media (i.e color of agar or colonies) after incubation? C. In this experiment, which media are selective, and which are differential? d. How did the results observe on the mannitol salt agar and EMB agar correlate to the Gram reaction of the bacteria? e. What...

  • I counted 25 colonies and I think that it is within an accurate range. I feel...

    I counted 25 colonies and I think that it is within an accurate range. I feel like it is a selective plate because the organism appears to be isolation. 2. You received a mixed culture and know that contains a specific blue/black forming bacterial colony. You decided to plate 0.1ml of the original culture on a specific plate that only allows for the growth of that particular microbe. You got the following plate. A Is this an example of a...

  • Multiple Choice. Highlight the single correct answer choice. 1. Streak plates are useful in microbiology to...

    Multiple Choice. Highlight the single correct answer choice. 1. Streak plates are useful in microbiology to __________. quantify the number of bacteria measure turbidity identify bacteria determine cell shape 2. In the streak-plate technique, the intent is to isolate bacteria by dilution in theory by __________. dilution on a solid surface separating cells within the solid surface using a pipette dilution in water blanks 3. A pure culture consists of which of the following? one genus of microbe one species...

  • Hello, just wanted to check my answers. Answer as many as you like/can. Thankyou. 1) Four...

    Hello, just wanted to check my answers. Answer as many as you like/can. Thankyou. 1) Four grams of soil are added to 36 ml sterile water and mixed well. 0.1 ml of this mix was added to 9.9 ml sterile water. This was diluted by 4 successive 1/10 dilutions. 1.0 ml from the last dilution was used to prepare a pour plate. After incubation 289 colonies were counted. Calculate the # CFU/g soil. 2) A 0.1 ml aliquot of a...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT