Homework Answers
1) It is kept in inverted position to avoid contamination with airborne particles and condensation in creating a barrier in microbial growth
2)The term used to describe them are microbiological culture and cell culture
3)When there is observation of different types of microorganism on a petri dish (virus, bacteria, fungus) it is known as mixed culture
4)Swabbing one plate with sterile stab is dine to implant bacteria on a growth medium.
Add Answer to:
Post lab questions 1.Why are inoculated plates incubated in the inverted position? 2.What term is used...
Micrebes in the Environment QUESTIONS What in the advantage of using Petri plate rather thon tet...
Micrebes in the Environment QUESTIONS What in the advantage of using Petri plate rather thon tet t in mieriogy? 2What are bacteria uaing for nutrienta in satrient agsr What is the perpoe of the agar? CRITICAL THINKING Did all the organiems living in or on the environmente aompled gw on your nutrient agar Briefly explain. 1. 2 How could you determine whether the turbidity in your nutrient broth tube was from a mixture of diferent microbes or from the growth...
Ubiquity of Microorganisms and Quadrant Streaking POST LAB DATE: SECTION: NAME: INSTRUCTOR: OULU Questions 1. in...
Ubiquity of Microorganisms and Quadrant Streaking POST LAB DATE: SECTION: NAME: INSTRUCTOR: OULU Questions 1. in microbiology lab, what is the function of an incubatore 2. Define: A. pure culture B. mixed culture C. Chromogenesis D. Enriched media E. Selective media F. Reducing media 3. What is the purpose of quadront streaking 4. Why should nutrient medium always be sterile before it is inoculated with a microbial specimen for culture and isolation 5. Why can't all microorganisms grow on a...
letters C. & D. 35 EXERCISE 3: MICRORES IN THE ENVIRONMENT remove the stop- fingers of...
letters C. & D.
35 EXERCISE 3: MICRORES IN THE ENVIRONMENT remove the stop- fingers of your oth- the flask by passing ames (FIGURE 2a). the flask at an an- first dish with the Buickly and neatly into the dish until a depth of approx 2b). Keep the flask dish cover, move he agar is poured. gently swirl the empty spaces: do he dish covers. eave the Petri plate + 15 minutes until (a) Remove the stopper, and flame the...
please help me with letter B. Value Ulla ination of Living EXERCISE 3: MICROE b. Holding...
please help me with letter B.
Value Ulla ination of Living EXERCISE 3: MICROE b. Holding the flask at an angle, remove the stop- per with the fourth and fifth fingers of your oth- er hand. Heat the mouth of the flask by passing it through the flame three times (FIGURE 2a). Why is it necessary to keep the flask at an an- gle through this procedure? (a) Remove theflask. c. Remove the cover from the first dish with the...
please type up the answers. Conclusions. Questions for further thought and comprehension: 1. What did you...
please type up the answers.
Conclusions. Questions for further thought and comprehension: 1. What did you determine to be the concentration of the original bacterial culture? Do you think your results are accurate? Explain why or why not. 2. Did you have a countable number of colonies on more than one of your plates? Assume you had two plates that had countable numbers of colonies, one with 124 colonies (and a dilution factor of 1/1.000) and one with 11 colonies...
What would be the composition of the canavanine selection plates (see Lab 9) if we did...
What would be the composition of the canavanine selection plates
(see Lab 9) if we did not chose to select for the presence of the
gRNA plasmid?
Plate counting Last week you transformed the PMD2 plasmid that contains the ORNA sequence. The yeast cells were selected on a YNB + histidine + methionine plate in order to make sure that only the cells that contain the plasmid grow and give a colony. Simply count the number of colonies that grew...
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...
Directions: There are two parts for this lab. The first part is working with the Microscope...
Directions: There are two parts for this lab. The first part is
working with the Microscope slides. The second part is working with
media.
Task 1 – Bacteriology Survey Microscope Slides
Directions: There are eight different bacterium you need to
research.
Below is the following bacterium you need to describe and include
an image for.
• Streptococcus
• Treponema
• Neisseria gonorrhoeae
• Klebisella pneumonia
• Unstained Bacillus
• Bacillus cereus
• Clostridium tetani
• Escherichia coli
Task 2 –...
infectious disease lab summary protocol. Questions that need to be answered are attached, aswell as the...
infectious disease lab summary protocol. Questions that need to be
answered are attached, aswell as the lab manuel
Name: ID: Protocol summary for: (Maximum 2 pages, Total = 10 marks) 1) Describe, in a sentence or two, the main objective(s) of this lab. (1) 2) What techniques will you be using in this lab? (2) 3) How many microorganisms will you be working with in this lab? (1) 4) Over the course of this lab (1", 24, ... week), which...
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...
Micrebes in the Environment QUESTIONS What in the advantage of using Petri plate rather thon tet t in mieriogy? 2What are bacteria uaing for nutrienta in satrient agsr What is the perpoe of the agar? CRITICAL THINKING Did all the organiems living in or on the environmente aompled gw on your nutrient agar Briefly explain. 1. 2 How could you determine whether the turbidity in your nutrient broth tube was from a mixture of diferent microbes or from the growth...
Ubiquity of Microorganisms and Quadrant Streaking POST LAB DATE: SECTION: NAME: INSTRUCTOR: OULU Questions 1. in microbiology lab, what is the function of an incubatore 2. Define: A. pure culture B. mixed culture C. Chromogenesis D. Enriched media E. Selective media F. Reducing media 3. What is the purpose of quadront streaking 4. Why should nutrient medium always be sterile before it is inoculated with a microbial specimen for culture and isolation 5. Why can't all microorganisms grow on a...
letters C. & D.
35 EXERCISE 3: MICRORES IN THE ENVIRONMENT remove the stop- fingers of your oth- the flask by passing ames (FIGURE 2a). the flask at an an- first dish with the Buickly and neatly into the dish until a depth of approx 2b). Keep the flask dish cover, move he agar is poured. gently swirl the empty spaces: do he dish covers. eave the Petri plate + 15 minutes until (a) Remove the stopper, and flame the...
please help me with letter B.
Value Ulla ination of Living EXERCISE 3: MICROE b. Holding the flask at an angle, remove the stop- per with the fourth and fifth fingers of your oth- er hand. Heat the mouth of the flask by passing it through the flame three times (FIGURE 2a). Why is it necessary to keep the flask at an an- gle through this procedure? (a) Remove theflask. c. Remove the cover from the first dish with the...
please type up the answers.
Conclusions. Questions for further thought and comprehension: 1. What did you determine to be the concentration of the original bacterial culture? Do you think your results are accurate? Explain why or why not. 2. Did you have a countable number of colonies on more than one of your plates? Assume you had two plates that had countable numbers of colonies, one with 124 colonies (and a dilution factor of 1/1.000) and one with 11 colonies...
What would be the composition of the canavanine selection plates
(see Lab 9) if we did not chose to select for the presence of the
gRNA plasmid?
Plate counting Last week you transformed the PMD2 plasmid that contains the ORNA sequence. The yeast cells were selected on a YNB + histidine + methionine plate in order to make sure that only the cells that contain the plasmid grow and give a colony. Simply count the number of colonies that grew...
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...
Directions: There are two parts for this lab. The first part is
working with the Microscope slides. The second part is working with
media.
Task 1 – Bacteriology Survey Microscope Slides
Directions: There are eight different bacterium you need to
research.
Below is the following bacterium you need to describe and include
an image for.
• Streptococcus
• Treponema
• Neisseria gonorrhoeae
• Klebisella pneumonia
• Unstained Bacillus
• Bacillus cereus
• Clostridium tetani
• Escherichia coli
Task 2 –...
infectious disease lab summary protocol. Questions that need to be
answered are attached, aswell as the lab manuel
Name: ID: Protocol summary for: (Maximum 2 pages, Total = 10 marks) 1) Describe, in a sentence or two, the main objective(s) of this lab. (1) 2) What techniques will you be using in this lab? (2) 3) How many microorganisms will you be working with in this lab? (1) 4) Over the course of this lab (1", 24, ... week), which...
Most questions answered within 3 hours.
-
Please show calculations/work
Marcello is filing as single and has 2018 taxable income of
$730,000 which...
asked 13 minutes ago -
"Mini Case Study - Haley Roberts "
Haley Roberts is quite proud that she has grown...
asked 11 minutes ago -
do the following on a UNIX command line, if applicable vi editor
may be used
Consider...
asked 21 minutes ago -
My App is a small but growing start-up
that sees demand for several of its apps...
asked 27 minutes ago -
1. The catabolic Activation Protein (CAP) is a regulatory
protein associated with several carbohydrate metabolism operons...
asked 41 minutes ago -
A car company was preparing their marketing materials for the
2020 version of their popular SUV....
asked 51 minutes ago -
7.13 LAB: Word frequencies (lists)
Write a program that first reads in the name of an...
asked 55 minutes ago -
how
much is the energy of co2 per mole increased when it absorbs
infrared radiation with...
asked 1 hour ago -
which reagent CAN convert the glucose ring into a linear
chain?
a) HCl (aq)
b) H2CrO4...
asked 1 hour ago -
USING MATLAB.
Design a program which uses a for…end loop to add 10 to
a variable...
asked 1 hour ago -
The raft is made up of
ten 18 cm diameter logs, each with a length of...
asked 1 hour ago -
Batteries are one of the major imports of the US from China.
Batteries cost 10 Yuan...
asked 1 hour ago