For the Phenol Red Broth tubes: Glucose tube was yellow with a bubble trapped in the durham tube Lactose tube was Yellow with no bubble trapped in the durham tube Sucrose tube was Yellow with no bubble trapped in the durham tube Mannitol tube was Yellow with no bubble trapped in the durham tube For the MRVP tubes: Methyl red tube was Yellowish Voges-Proskauer tube was Red SIM Tube: Growth along the inoculation stab. No black

For the Phenol Red Broth tubes: Glucose tube was yellow with a bubble trapped in the durham tube Lactose tube was Yellow with no bubble trapped in the durham tube Sucrose tube was Yellow with no bubble trapped in the durham tube Mannitol tube was Yellow with no bubble trapped in the durham tube For the MRVP tubes: Methyl red tube was Yellowish Voges-Proskauer tube was Red SIM Tube: Growth along the inoculation stab. No black

Name: What Organism could this be? For the Phenol Red Broth tubes:Glucose tu
Uploaded: 2024-03-20T06:42:55.000Z
Channel: Bartleby
Description: What Organism could this be? For the Phenol Red Broth tubes:Glucose tube was yellow with a bubble trapped in thedurham tubeLactose tube was Yellow with no bubble trapped in thedurham tubeSucrose tube was Yellow with no bubble trapped in thedurham tub

Comprehensive Medical Assisting: Administrative and Clinical Competencies (MindTap Course List)

6th Edition

ISBN:9781305964792

Author:Wilburta Q. Lindh, Carol D. Tamparo, Barbara M. Dahl, Julie Morris, Cindy Correa

Publisher:Wilburta Q. Lindh, Carol D. Tamparo, Barbara M. Dahl, Julie Morris, Cindy Correa

Chapter42: Basic Microbiology

Section: Chapter Questions

Problem 4CR

See similar textbooks

Similar questions

What kind of method of preparation was done? method of preparation (e.g. decoction, infusion, maceration, percolation, etc.)
Based on the graph below, write a discussion in detail
Laboratory Report Sheet – ENZYMES Procedure: Potato Peroxidase a. Prepare 3 test tubes. Place 1 mL of potato extract to each test tubes. To the first test-tube - add 5 drops of 1% phenol+ 3 drops of H2O2 second test tube – add 5 drops of catechol or pyrogallol + 3 drops H2O2 third test tube - add 5 drops of guiac solution + 3 drops H2O2 b. Shake well and observe change in color. 2. Repeat procedure 1, a, b, and c, but this time use boiled potato extract. QUESTION: WHAT ARE THE OBSERVATIONS FOR EACH TUBE?
From the results shown in figure , determine which drugs couldbe used to treat the yeast infection. Taking into account their adverseside effects, which drug would probably be the best choice?
You just finished plating your electroporatio products on your YPD-Zeocin plate and you think you did everything perfectly but you come back the folloeing week and have zero colonies. Which of the following could be the reason for the absence of colonies? A) You centrifuged your electroporated cells for 30 sec at 16,000 rpm instead of 4,000 rpm before plating them B) You added sorbitol+YPD to your cells thirty minutes after pulsing your cells C) The Zeocin had not been added to the plates when they were made. D) All of the above E) Both a and b only
Pretend you want to test whether a certain bacterium can take iron away from hemoglobin. What is the best media to grow the organism on? O Rabbit serum O Blood agar plate O Mannitol salt agar O Mueller Hinton plate
Using the attached image, explain the observed results on the NA and ECM plates. Be sure to address why each sample is either able or unable to grow on each plate and include the genotype(s) of the cells which are capable of growth.
This is the growth curve for Clostirdium (incubated under optimal growth conditions). Use it to answer the following questions. 3 Cell concentration (million cells/ml) 2.5 2 0.2 1.5 1 0.5 0 2 The growth rate is lag log 0.25 4 0.32 0.5 units 6 million of cells per ml (Image description.: Horizontal axis is time in hours, Vertical is cell concentration in millions of cells per ml. Curve starts at 0,0, increases by 4 hours to 0.5 million cells/ml, goes up steeply over two hours from 0.5 million/ml at 4 hours to 2.5 million cells/ml at 8 hours, 8-12 hour shows an increase of 0.3 to 2,8 million cellls/ml and last 2 hours is flat at 2.8million cells/ml.) From 12 hr to 14 hr is called phase. lunar 2 8 Time (hours) 10 5 stationary 12 cells 14 death 16 million of cells per ml per hour hours million of cells
Why is washing with Hank’s balanced salt solution with 0.5% antibiotic-antimycotic done for Splenocyte Preparation?
In disc diffusion studies, where will the lowest concentration of the tested chemical be in the agar plate? in the agar directly below the disc O in the agar halfway between the disc and the petri dish wall O in the agar furthest away from the disc the cehmical is equally distributed throughout the agar
Describe characteristics of Proteus Vulgaris in the Agar: (How does colonies look like (color) and explain does it grow on that agar. Blood Agar (Aerobic) MacConkey EMB PEA Mannitol Salt Agar Chocolate Agar Nutrient Agar
Describe characteristics of Streptococcus Agalactiae in the Agar: (How does colonies look like (color) and explain does it grow on that agar. Blood Agar (Aerobic) MacConkey EMB PEA Mannitol Salt Agar Chocolate Agar Nutient Agar