Cell Structure And Microscopy Flashcards

You may prefer our related Brainscape-certified flashcards:
1
Q

Cell membrane

A

Semi-permeable barrier that controls the entry and exit of substances.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Cytosol

A

Fluid portion of the cytoplasm (doesn’t include the organelles or other soluble materials)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Nucleus

A

Contains hereditary material so controls cell activity (via transcription) and mitosis (via DNA replication)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Nucleolus

A

Site of production and assembly of ribosome components.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Ribosome

A

Complexes of RNA and protein that are responsible for polypeptide synthesis (80s in eukaryotic)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Mitochondria

A

Site of aerobic respiration. Produces ATP from organic compounds.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Golgi apparatus

A

An assembly of vesicles and folded membranes involved in the sorting, storing and modification of secretory products.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Lysosome

A

Site of hydrolysis/ digestion/ breakdown of macromolecules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Peroxisome

A

Catalyses breakdown of toxic substances like hydrogen peroxide and other metabolites.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Centrioles

A

Microtubule-organising centres involved in cell division (mitosis/meiosis and cytokinesis)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Endoplasmic reticulum
Rough
Smooth

A

A system of membranes involved in the transport of materials between organelles.
R-studded with ribosomes and involved in the synthesis and transport of proteins destined for secretion.
S- involved in the synthesis and transport of lipids and steroids, as well as metabolism of carbohydrates.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

The cellular levels of organisation in a multicellular organism

A
Stem cells (undifferentiated)
Specialised cells (differentiated- certain genes on/ off)
Tissues- a group of different cells working together to perform a specific function
Organ- groups of tissues aggregated together to perform a function
Organ system- organs working together as a single unit to perform a function.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Prokaryotic vs eukaryotic cells

A
Prokaryotes:
No true nucleus, only a spread out area of nuclear material with no nuclear membrane.
DNA not associated with histones.
Circular strands of DNA (plasmids) but no chromosomes.
No membrane bound organelles
No chloroplast 
70s ribosomes 
No ER, Golgi apparatus and lysosomes
Murein cell wall

Eukaryotes:
Distinct nucleus with a nuclear envelope.
Nucleolus present
Chromosomes present in which DNA is located
Membrane bound organelles
Chloroplasts present in plants and algae
80s ribosomes
ER Golgi apparatus and lysosomes
Cell wall made mostly of cellulose (chitin in fungi)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Additional features of prokaryotic cells and their functions.

A

Murein cell wall- protecting against osmotic lysis
External capsule - protection and helps bacteria stick together
Plasmids- small circular pieces of DNA which have additional genes e.g. antibiotic resistance
Flagella- motile ‘tail’
Pili- microscopic tube extensions to allow transfer of plasmid DNA between individual bacteria (transjugation)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Key features of viruses

A
Acellular 
Non-living 
20-300nm
Contain DNA or RNA nucleic acids (genome)
Enclosed within a capsid 
Sometimes enveloped (e.g.HIV)
Has surface attachment proteins
Require a specific host cell to enter and replicate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Advantages and disadvantages of the light microscope and resolving power

A

Advantages:
Can see living specimens
Easier specimen preparation
Variety of coloured stains

Disadvantages:
Low resolution so organelle detain/ smaller components not visible.

Resolving power: limited 0.2 micrometres/ 200nm

17
Q

Transmission electron microscope (TEM) advantages, disadvantages and resolving power.

A

Advantages:
very high resolution at high magnification.
Detailed organelle/ sub-organelle structure (inside)

Disadvantages:
Specimens are not alive (are in a vacuum)
Difficult preparation because very thin specimens/ complex staining process.
Black and white image.
Artefacts caused by staining process can ruin image.

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

18
Q

Scanning electron microscope advantages, disadvantages and resolving power.

A

Advantages:
3D images show structural formation

Disadvantages:
Specimens are not alive because the system is in a vacuum
Difficult prep
Black and white image.

Resolving power: 20nm

19
Q

Magnification equation

A

Magnification= size of image (divided by) actual size of object

20
Q

Principles of cell fractionation and ultracentrifugation

A
  1. Homogenisation
    - This breaks open the cells
    - Done by vibrating the cells or grinding them up in a blender
    - It is done with a cold, isotonic buffer: cold to slow down and stop organelle activity, particularly the hydrolytic enzymes in lysosomes. Isotonic to prevent movement of water in and out of organelles by osmosis (no net flow) so cells don’t shrink or burst.
    - A buffer solution to prevent changes in PH levels (and enzyme activity)
  2. Filtration
    Filter the solution through a gauze to remove debris e.g. large cell debris or tissue debris
  3. Ultracentrifugation
    - Spin the solution in a centrifuge at low speed
    - The heaviest organelles (nuclei, chloroplast) fall to the bottom (pellets). The rest of the organelles stay suspended in the fluid above the sediment. This is the supernatant.
    - The supernatant is drained off, poured into another tube, and spun again at a higher speed. Mitochondria and lysosomes fall to the bottom.
    - The supernatant is drained off again, poured into another tube and spun at a higher speed so the lightest organelles remain (ribosomes).
21
Q

Stages of mitosis in eukaryotic cells

A

Interphase:
Decondensed chromatin in the nucleus.
Nucleolus visible
Nuclear membrane visible
Centrioles present in animal cells. Centrioles replicate.
DNA replication takes place before mitosis starts

Prophase:
Chromatin condenses and chromosomes become visible
Nucleoli disappear
Nuclear membrane disappears
Centrioles move to poles of the cell and form spindle fibres (spindle apparatus)
Chromosomes attach to the spindle at their centromeres

Metaphase:
Chromosomes (made up of 2 sister chromatids) line up on the equator of the spindle apparatus.

Anaphase:
The centromeres divide and the spindle fibres begin to shorten.
Sister chromatids are pulled to opposite poles by the spindle fibres using energy from ATP,
The separated chromatids are now referred to as separate chromosomes.

Telophase:
The chromosomes reach the poles
The chromosomes decondense and are no longer visible
The spindle breaks down and the centrioles reappear
The nuclear membrane reappears and the nucleoli appear.

Cytokinesis:
Division of the cytoplasm to form 2 genetically identical daughter cells.

22
Q

How would you prepare a slide showing stages of mitosis in plant cells?

A
  • Use a sharp scalpel to remove the last 1mm of an actively growing root tip (cells at tip will be actively going through the cell cycle/ dividing).
  • Place the tip in some 1M hydrochloric acid for 10 minutes- breaks down the plant tissue so it’s easier to separate the cells for viewing.
  • Rinse the root tip in water
  • Crush the root tip on your slide (one cell thick)
  • Add the stain- darkens the chromosomal DNA so phases of mitosis are easier to distinguish
  • Place on a cover slip
  • Cell preparation is to be one cell thick so light can come through and individual cells can be counted.
23
Q

Mitotic index

A

Mitotic index = cells in mitosis (divided by) the total number of cells.
Cells in mitosis can be distinguished by them having visible chromosomes.

24
Q

How may tumours and cancer develop

A

Tumours (cancer) develops when cells lose control over the cell cycle and divide in an uncontrollable manner.
This results in a mass of rapidly dividing, abnormal cells.
Cancers result from mutations of key genes that control the cell cycle.
Treatments involve:
-Preventing DNA from replicating
-Inhibiting the metaphase stage of mitosis by interfering with spindle formation.

25
Q

Cell division in prokaryotic cells

A

Binary fission

  • The circular DNA molecule replicates and both copies attach to the cell membrane.
  • The plasmids also replicate
  • The cell membrane begins to grow between the two DNA molecules and begins to pinch inward, dividing the cytoplasm into two.
  • A new cell wall forms between the two molecules of DNA, dividing the original cells into two identical daughter cells, each with a single copy of the circular DNA and a variable number of copies of the plasmids.
26
Q

Simplified virus replication

A

As viruses are non-living, they can’t undergo cell division. They replicate by attaching to their host cell with the attachment proteins on their surface. They inject their nucleic acids into the host cell. The genetic information on the injected viral nucleic acid (on the mRNA) then provides the instructions for the host cells metabolic processes to start producing the viral components, nucleic acid, enzymes and structural proteins which are assembled into new viruses.