Topic 2.1 - Structure of eukaryote and prokaryote cells Flashcards

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1
Q

List three ways eukaryotic cells differ from prokaryotic cells.

A

membrane bound organelles

DNA is enclosed in a nucleus

Have larger ribosomes (80S) than prokaryotic cells

Has a murein cell wall, a capsule and plasmid

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2
Q

Function of nucleus

A

containing chromosomes, consisting of protein-bound(histones) , linear DNA within the nucleoplasm.

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3
Q

Function of nuclear envelope

A

Double membrane surrounding the nucleus with nuclear pores to let molecules in and out

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4
Q

Plasma

Membrane

A

Involved in the transport of substances via diffusion or facilitated diffusion, active transport

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5
Q

Cytoplasm

A

Where chemical reactions take place

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6
Q

Ribosome

A

Where amino acids are joined together to make proteins (i.e. protein synthesis)

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7
Q

Mitochondria

A

Site of AEROBIC respiration

Produces ATP (releases energy)

Contains short, circular DNA (not associated with proteins)

Has a double membrane. The inner membrane is folded forming cristae.

Contains smaller (70S) ribosomes

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8
Q

Rough Endoplasmic Reticulum (RER)

A

Has ribosomes on their surface which are involved in protein synthesis

Proteins are also folded up inside the RER

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9
Q

Smooth endoplasmic reticulum

A

Synthesis and storage of molecules such as lipids, steroids and sterols

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10
Q

Golgi Apparatus and golgi vesicles

A

Modifies proteins (e.g. by adding carbohydrate groups to form a glycoprotein or lipid groups to make a lipoprotein)

Stores proteins

Packages proteins into vesicles

Transport vesicles to cell surface

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11
Q

Lysosomes

A

A vesicle that contains hydrolytic enzymes (lysozymes) which are used to digest molecules

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12
Q

Chloroplast

A

Chlorophyll absorb light for photosynthesis to produce carbohydrates

Has a double membrane. Inside there are thylakoid membranes which can form a stack called a granum (pl. grana). The grana are linked by lamellae.

Contain starch grains

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13
Q

Define resolution

A

Resolution is the minimum distance apart that the two objects can be in order for them to appear as separate items.

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14
Q

Describe the procedure to prepare a slide

A

Add a drop of water to the slide

Remove a thin section of tissue and place it onto the slide (flat as possible)

Add 1 drop of iodine dissolved in potassium iodide to stain the sample (This is only correct if it is plant tissue)

Lower a coverslip on top using a mounting needle

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15
Q

Explain why it was important that the sections of tissue were thin

A

A thin section allows more light through;

allows a single layer of cells to be viewed.

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16
Q

Why are electron microscopes used to view cells?

A

They have a HIGH resolution

because electrons have a shorter wavelength than light.

This allows you to view internal structures/organelles of a cell.

(Remember using this – Light microscope = Low resolution = Longer wavelength)

17
Q

Name two structures in a eukaryotic cell that cannot be identified using an optical microscope.

A

Mitochondrion / ribosome / endoplasmic reticulum / lysosome / cell-surface membrane

18
Q

Describe the limitations of using a transmission electron microscope to investigate cell structure.

A

Cannot look at living material / Must be in a vacuum;

 Specimen must be (very) thin;

Artefacts present;

Complex staining method / complex / long preparation time;

 Image not in 3D / only 2D images produced.

19
Q

Write an equation to calculate magnification

A

Magnification = Image length / Actual Length

20
Q

What is meant by ‘cell fractionation

A

Separating out the contents of a cell into the different ‘fractions’ (i.e. different parts).

This usually means separating out the different organelles by DENSITY.

This is useful for scientists because it allows them to study individual organelles

21
Q

What is homogenisation?

A

Using a blender (or a homogenizer) to break open the cell membrane to release all of the organelles inside

22
Q

Why is the solution filtered?

A

To remove any whole cells or large cell debris

23
Q

Why is it cold?

A

To reduce enzyme activity TO prevent digestion of organelles

24
Q

Why is it isotonic?

A

To prevent osmosis, SO that the ORGANELLES do not shrivel or burst/ lysis

25
Q

Why is it buffered?

A

So that the pH is kept constant, SO that proteins/ enzymes are not denatured

26
Q

What does ultracentrifugation mean?

A

Ultracentrifugation is used to separate very small things – such as different lengths of DNA/RNA

The sample is put into a tube

It is spun at a low speed (low Revolutions Per Minute = RPM)

The most dense organelle forms a sediment/pellet at the bottom of the test tube

The other organelles remain suspended in the supernatant

The supernatant is removed and put into a clean test tube and spun at higher speed

The second most dense organelle forms a sediment at the bottom etc