2.1.2 PK Cell & 2.1.3 Methods Of Studying Cells Flashcards

1
Q

What is a prokaryotic cell?

A

A cell without a nucleus

They are smaller

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2
Q

What is in a bacterial cell that isn’t in a normal eukaryotic cell?

A

Plasmid
Genetic DNA
Flagellum
Slime capsule

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3
Q

What is the function of a slime capsule?

A

Protects the bacterial cell

Allows the cell to adhere to smooth surfaces

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4
Q

What is the function of the flagellum?

A

Uses a propeller like motion to move

A sensory organelle - sensitive to chemical and temperature

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5
Q

What is the cell wall made from in a bacterial cell?

A

Peptidoglycan / murein

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6
Q

What are common features of a virus?

A

Protein coat/ capsid
Genetic material
Glycoproteins

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7
Q

What is the function of the capsid/protein coat?

A

Protects the nucleic acid from being digested by enzymes

Provides site and proteins on the surface to allow viron penetration

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8
Q

What is the role of viral attachment proteins?

A

Binds to cell membranes, to then allow the DNA to be inserted into the cell

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9
Q

What is the size of a prokaryotic ribosome?

A

70S

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10
Q

What are the types of microscopes?

A

Light/Optical
Scanning Electron
Transmission Electron

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11
Q

How does a light/optical microscope work?

A

Uses visible light and magnifying lens to enlarge them
Can only see organelles larger than 0.2 μm
Can magnify up to 2000x

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12
Q

What is resolution?

A

The minimum distance apart that two objects can be distinguished as separate objects in an image

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13
Q

What are the advantages of light/optical microscope?

A
Cheap
Living samples can be viewed
Preparation is quick
Unaffected by magnetic fields 
No vacuum required
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14
Q

What are the disadvantages of light/optical microscope?

A

Poor resolution
Only magnifies up to 2000x
Preparation may distort specimen

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15
Q

How does a scanning electron microscope work?

A

It scans the surface with a broad static beam of electrons producing various signals containing information about the topography (shape and features of the surface)

Done in a vacuum chamber

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16
Q

What are the advantages of using a scanning electron microscope?

A

Easy to use
Sample can be seen as a 3D image
Fairly high resolution
Works fast

17
Q

What are the disadvantages of a scanning electron microscope?

A

Specimen must be conductive
Preparation could produce artefacts
Images are black and white
Living specimens can’t be observed as it is done in a vacuum

18
Q

How does a transmission electron microscope work?

A

A focused beam of electrons, using electromagnetic lenses, travels through a vacuum to the sample
Parts of the specimen absorb the electrons and appear darker

19
Q

What are the advantages of transmission electron microscope?

A

Very powerful magnification
Images are high quality/resolution
Provides information on element and compound structure

20
Q

What are the disadvantages of transmission electron microscope?

A

High energy beam may destroy the sample
Living specimens can’t be observed as it is done in a vacuum
Potential for artefacts
Complex staining process and images are still in black and white

21
Q
Conversions of: 
Millimetres
Micrometers 
Nanometers
Picometres 

From meters

A

10 ^-3
10 ^-6
10 ^-9
10 ^-12

22
Q

What is the equation for magnification?

A

IAM
I / A x M

I am an iams cat😅

23
Q

What is actual size?

A

What is would be in real life

Quite little in micrometers

24
Q

What is image size?

A

Whatever you can see in front of you

25
How do you prepare a temporary mount microscope slide?
Use forceps to handle the sample Smooth out air bubbles/creases Add a stain to colour the sample Add a little water to stick the glass together
26
What is cell fractionation?
The process of separating different organelles of a cell
27
What happens in cell fractionation?
The tissue is cut up and put in a cold, isotonic, buffered solution Further broken up in a homogeniser forming homogenate The homogenate is spun in a ultracentrifuge at a low speed for 10mins to force the heaviest organelles to the bottom The supernatant is transferred to another tube and spun at a higher speed This is repeated
28
Why is a cold solution used in cell fractionation?
To stops enzymes working effectively
29
Why is an isotonic solution used in cell fractionation?
Keeping the concentrations the same prevents osmosis which stops cells bursting
30
Why is a buffered solution used in cell fractionation?
Keeps the pH the same
31
What is a homogeniser?
Like a blender | To break up the cell wall and the cell membrane
32
What is the supernatant?
The liquid left above the solid organelles in a test tube after centrifugation
33
What are the heaviest to lighter organelles?
``` Nucleus Mitochondria Lysosomes Endoplasmic reticulum Ribosomes ```
34
How can we measure the size of objects using a light microscope?
Using an eyepiece graticule This is a glass disk placed on the eyepiece of the microscope with a scale etched on
35
How do you calibrate an eyepiece graticule?
You use a stage micrometer to line it up and work out the scale