Microscopy and cells Flashcards

(46 cards)

1
Q

What is the equation for magnification?

A

Maginfcation=size of image/actual size of object

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2
Q

Define magnification

A

The magnification of a microscope refers to how many times larger the image is compared to the object

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3
Q

Define resolution

A

The resolution of a microscope is the minimum distant between two objects which they can still be viewed as seperate.

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4
Q

Light microscope resolution

A

Limited to 0.2um and 200nm

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5
Q

Light microscope advantages

A

Can see living specimens.
Easier specimen preparation.
Variety of coloured stains.

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6
Q

Light microscope disadvantages

A

Low resolution so organelle detail / smaller components not visible.

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7
Q

TEM electron microscope resolution

A

0.1 nm but not always achieved as difficult specimen prep. / high energy beam can destroy specimen.

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8
Q

TEM electron microscope advantages

A

Very high resolution at high magnification.

Detailed organelle / sub-organelle structure.

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9
Q

TEM electron microscope disadvantages

A

Specimens are not alive i.e. in a vacuum.
Difficult prep. e.g. very thin specimens / complex staining.
Black and white image.
Artefacts can spoil image.

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10
Q

SES microscope resolution

A

20nm

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11
Q

SES microscope advantages

A

3D images show structural formation.

Totally sic pics.

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12
Q

SES microscopes disadvantages

A

Specimens are not alive.
Difficult prep.
Vacuum.
Black and white image.

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13
Q

Describe the structure of a nucleus

A

Surrounded by a nuclear envelope, a semi-permeable double membrane
nuclear pores allow substance to exit/entry
Dense nucelous made of RNA and proteins assemble ribosomones

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14
Q

Functions of the nucleus

A

Acts as the control centre of the cell - controls the cell’s activities
Controls synthesis of proteins
Contains the organism’s genetic material (in the form of DNA)
Manufactures ribosomes from ribosomal RNA

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15
Q

Structure of a mitochondria

A

Double membrane - controls the entry and exit of material
Inner membrane is highly folded to form cristae - this is where respiration (oxidative phosphorylation) takes place and the folds provide a large surface area for increased respirations
Fluid matrix contains mitochondrial DNA, enzymes, lipid and proteins
Usually rod-shaped and around 1-10 micrometers long

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16
Q

Function of mitochondria

A

Site of aerobic respiration
Produce the energy-carrier molecule ATP during respiration
Therefore, cells with a high level of metabolic activity that require a lot of ATP (muscle cells) have lots of large mitochondria with many cristae

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17
Q

Structure of chloroplasts

A

Vesicular plastids with double membrane
Thylakoids flattered discs stack to form grana; contains photosytems with chlorophyll
Intergranal lamellae, tubes attach thlyakoids in adjacent grana
stroma- fulid-filled matrix

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18
Q

Functions of chloroplast

A

Functions:
Carries out photosynthesis (converts light energy to chemical energy)

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19
Q

Structure of Endoplasmic Reticulum (ER)

A

A 3D system of membranes that spreads throughout the cytoplasm of a cell
The membranes form a network of tubules and flattened sacs called cisternae
It is continuous (attached to) the outer nuclear membrane
There are two types of ER:
Rough ER (RER)
SmoothER (SER)

20
Q

Functions of ER

A

Rough ER - has ribosomes on its surface
Provides a large surface area for the synthesis of proteins
Provides a pathway for the transport of proteins throughout the cell
Smooth ER- lipid synthesis

21
Q

Structure of Gogi apparatus

A

A stack of membranes that form flattened sacs, called cisternae
Cis face - where vesicles from the ER fuse
Trans face - where golgi vesicles pinch off regularly from the cisternae

22
Q

Function of Gogi apparatus

A

Collects, modifies and transports molecules around or out of the cell
Proteins, lipids and carbohydrates produced in the ER enter and are passed through the golgi apparatus
Proteins are modified
The proteins are also ‘labelled’, allowing them to be sorted and then sent to their correct destination
Once sorted, the modified proteins and lipids are transported in golgi vesicles to their destination

23
Q

Lysosomes structure

A

Form when vesicles that bud off the golgi apparatus contain hydrolytic enzymes for breaking things down (eg. proteases, lipases or lysozymes)

24
Q

Lysosomes function

A

Hydrolyse material taken up by cells (phagocytic cells)
Release enzymes to the outside of the cell (exocytosis) in order to destroy external material
Digest old, worn out organelles for recycling
Break down of cells that have died

25
Structure of ribosomes
Small granules found in all cells Occur in large numbers (can be almost 25% of the dry mass of the cell) They may either be found in the cytoplasm or be attached to the rough ER 2 types: 80S (found in Eukaryotic cells) - larger 70S (found in Prokaryotic cells, mitochondria and chloroplasts) - smaller
26
Function of a ribosomes
the site of protein synthesis
27
Structure of vacuole
A fluid-filled sac with a single membrane Usually a single large vacuole in plant cells Contains a solution of minerals, sugars, amino acids, wastes and sometimes pigments
28
Function of vacuole
They support herbaceous plants (non-woody/soft) or herbaceous parts of woody plants by making cells turgid/rigid Storage of substances Sugars & amino acids - temporary food stores Pigments - give colour in petals to attract pollinating insects
29
Structure of centroiles
Small hollow cylinders A centrosome = 2 centrioles (oriented at right-angles to each other) Form a network of fine fibres in the cytoplasm called the cytoskeleton made out of microtubules and filaments
30
Function of centrolie
Supports the cell’s shape Organises and moves organelles During cell division the pair separate to opposite ends of the cell and form the spindle
31
Structure of cell wall
Found in plant cells Made of cellulose micro-fibrils - very strong so supports the functions Fungi also have Cell walls (chitin) Algae also have cell walls (cellulose or Glycoproteins or both)
32
Functions of cell wall
Providing the cell with strength to prevent it bursting due to osmosis Providing strength and support to the whole plant
33
Cytoplasm
Contains enzymes, site of many reactions and dissolve solutes and adds supports to the cell
34
plamaisa membrane
bi-layer of lipids and proteins channel it allows certain molecules and charged molecules to enter and exist the cell as it is semi-permeable.
35
Role of plasimds
small ring of DNA that carries non-essential DNA can be exchanged between bacterial cells via conjunction
36
Role of the flagellum
Roating tail propels organism
37
Role of collapse
Prevent desiccation and chemical attack
38
Pilus
Transfer of material between bacteria
39
Describe the first stage of cell fractionation and ultracentrifugation.
Homogenisation: This breaks open the cells to release the organelles. Vibrating the cells, or grinding them up in a blender.
40
Why use a ice-cold solution
cold to slow down and stop organelle activity, particularly the hydrolytic enzymes in lysosomes
41
Why is it buffered
to prevent changes in pH levels so organelle proteins are not damaged.
42
Why use the same water potential or isotonic
isotonic to prevent the movement of water in and out of organelles by osmosis.
43
Describe stage two of cell fractionation and ultracentrifugation.
Filter the solution through a gauze to remove debris e.g. large cell debris or tissue debris.
44
Describe stage three of cell fractionation and ultracentrifugation.
Ultracentrifugation: Spin the solution in a centrifuge at a low speed. The heaviest organelles (nuclei, chloroplasts) fall the to the bottom. The rest of the organelles stay suspended in the fluid above this sediment. This is the supernatant. The supernatant is drained off, poured into another tube, and spun again at a very high speed. This time, organelles like mitochondria and lysosomes fall to the bottom. Again, the supernatant is drained off, poured into another tube and spun at a higher speed. Finally, the lightest organelles remain. Material is separated on the basis of mass / density.
45
Detail viral replication
Requires a host cell Complementary attachment proteins bind to cell surface receptors Viral genetic material injected / enters host cell Viral genes transcribed and viral proteins produced e.g. capsid Viral genome replicated many times New viruses assembled Exit cell via cell surface membrane e.g. budding
46
What are the key features of viruses?
Acellular, non-living (NOT cells!) 20-300 nm Contain DNA or RNA nucleic acids (genome) Enclosed within a protein coat - capsid Surface attachment proteins Require a specific host cell to enter and replicate no metabolism no membrane