Lab 1 Exam - Terminology / Questions Flashcards
__________ : Plastic plate in which Agar is placed
Petri plate
__________ : Food for the organism
Culture Media
__________ : Solid culture media (gel in media)
Agar
__________ : is also a generic term used to describe any food for a microbe
Agar
__________ : grow on the surface of the agar
Microbes
Agar plates are __________ when not in use. and the label goes on the __________
- Upside down
- Backside
__________ : Population of microbes growing on the surface of the agar
Colony
__________ : Liquid culture media
Broth
__________ : Cloudy: broth ________ Indicates microbe are growing in the media
- Turbid
- Turbidity
__________ : Destroy all life (microbes)
Sterilize
__________ : Free of all life (microbes)
Sterile
__________ : A chamber in which steam asunder pressure: used to sterilize material in microbiology
Autoclave
__________ : Chamber set at a specific temperature. This is where the inoculated agar plates and tubes containing broth are placed to grow cultures
Incubator
__________ : Techniques to avoid contamination
Aseptic techniques
__________ : To introduce or transfer microbes into “something” such as culture media
Inoculate
__________ : Ocular Magnification X Objective Magnification
Total Magnification
Total Magnification : __________ Magnification X __________ Magnification
- Ocular
- Objective
Ocular Magnification is __X
10
Objective magnification is the __________
Lens choice
__________ : Automatic focusing
Parfocal
__________ : The area viewed through the ocular lens
Field of view
__________ : The distance between the end of the objective lens and the slide
Working distance
__________ : Ability to see detail: Clarity
Resolution
__________ : Adjustments in the distance between the ocular lenses to fit the eyes of the user
Interpupillary Adjustment
Two ways to control light intensity are:
- On/Off Intensity regulator
- Iris Diaphragm
-Focusing Procedure - Shortcut-
- 2.
- Adjust the light regulator control to as bright as possible
- Move low power objective into position
- Adjust the coarse focus knob so the low power lens is as close as possible to the stage
- Plug the Microscope in and turn it on
2. Close the iris diaphragm
-Focusing Procedure - Shortcut-
- Plug the Microscope in and turn it on
- Close the iris diaphragm
3.
4. - Adjust the coarse focus knob so the low power lens is as close as possible to the stage
- Adjust the light regulator control to as bright as possible
- Move low power objective into position
-Focusing Procedure - Shortcut-
- Plug the Microscope in and turn it on
- Close the iris diaphragm
- Adjust the light regulator control to as bright as possible
- Move low power objective into position
5.
- Adjust the coarse focus knob so the low power lens is as close as possible to the stage
Objective Lens Power:
Scanning Power = __X
4
Objective Lens Power:
Low Power = __X
10
Objective Lens Power:
High Dry Power = __X
40
Objective Lens Power:
Oil Immersion = __X
100
Objective Lens Band Color:
Oil Immersion = __________
White
Objective Lens Band Color:
High Dry Power = __________
Blue
Objective Lens Band Color:
Low Power = __________
Yellow
Objective Lens Band Color:
Scanning Power = __________
Red
4 examples of Aseptic techniques:
- Flaming the mouth of a test tube
- Not completely taking off the top of an agar plate
- Wearing gloves, lab coat, and disinfecting the lab bench
Flaming the loop/needle
4 examples of Aseptic techniques:
- Flaming the loop/needle
- Not completely taking off the top of an agar plate
- Wearing gloves, lab coat, and disinfecting the lab bench
Flaming the mouth of a test tube
4 examples of Aseptic techniques:
- Flaming the loop/needle
- Flaming the mouth of a test tube
- Wearing gloves, lab coat, and disinfecting the lab bench
Not completely taking off the top of an agar plate
4 examples of Aseptic techniques:
- Flaming the loop/needle
- Flaming the mouth of a test tube
- Not completely taking off the top of an agar plate
4.
Wearing gloves, lab coat, and disinfecting the lab bench
Why is it important that petri plates be incubated upside down?
So the condensation does not drip down onto the agar
How many times should the mouth of a test-tube be flamed after the lid is taken off?
3
Why should the mouth of the test-tube be flamed when the lid is taken off?
To prevent contaminants
Why is it important that after being flamed, a loop must be cooled before it is used to perform an inoculation?
- So you don’t kill the bacteria
- Dont create aerosols
How would you determine which area on an agar was the most contaminated?
The area with the most colonies
How can you determine if different types of microbes are growing on the sampled area of an agar?
Different Colony Morphology
What types of microbes are growing on the PDA plate?
Yeast and Mold
What types of microbes are growing on the TSA plate?
Bacteria
Parts of a Dissecting Microscope:
- - -Head -Ocular Lens -Magnification Knob
- Base
- Focusing Knob
Parts of a Dissecting Microscope:
-Base
-Focusing Knob
-
-
-Magnification Knob
- Head
- Ocular Lens
Parts of a Dissecting Microscope:
-Base
-Focusing Knob
-Head
-Ocular Lens
-
-Magnification Knob
Highest total magnification that can be reached with a Dissecting Microscope is ___X
300X
Magnification of the magnification knob on a dissecting microscope is ____X
7-30
The dissecting microscope in Microbiology is used to?
Determine colony morphology