2.1.2 PK Cell & 2.1.3 Methods Of Studying Cells Flashcards

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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
Q

How do you prepare a temporary mount microscope slide?

A

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
Q

What is cell fractionation?

A

The process of separating different organelles of a cell

27
Q

What happens in cell fractionation?

A

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
Q

Why is a cold solution used in cell fractionation?

A

To stops enzymes working effectively

29
Q

Why is an isotonic solution used in cell fractionation?

A

Keeping the concentrations the same prevents osmosis which stops cells bursting

30
Q

Why is a buffered solution used in cell fractionation?

A

Keeps the pH the same

31
Q

What is a homogeniser?

A

Like a blender

To break up the cell wall and the cell membrane

32
Q

What is the supernatant?

A

The liquid left above the solid organelles in a test tube after centrifugation

33
Q

What are the heaviest to lighter organelles?

A
Nucleus 
Mitochondria
Lysosomes 
Endoplasmic reticulum 
Ribosomes
34
Q

How can we measure the size of objects using a light microscope?

A

Using an eyepiece graticule

This is a glass disk placed on the eyepiece of the microscope with a scale etched on

35
Q

How do you calibrate an eyepiece graticule?

A

You use a stage micrometer to line it up and work out the scale