3.2 Cells Flashcards

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1
Q

What is the structure and function of the cell-surface membrane and in which cells can it be found?

A

Structure:
- Phospholipid bilayer.

Function:
● Selectively permeable → enables control of movement of substances in / out of cell
● Molecules / receptors / antigens on surface → allow cell recognition / signalling

Found in: animal, plant, algal and fungal cells

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2
Q

What is the structure and function of the nucleus and in which cells can it be found?

A

Structure:
- Double membrane (nuclear envelope) encloses and protects DNA. Outer membrane of envelope is continuous with rer for easy transportation of substances.
- Nuclear pores allow entry & exit of substances.
- Nucleoplasm contains chromatin (during cell division condenses to form chromosomes) and nucleolus (makes RNA & ribosomes).

Function:
Controls all activities within the cell. Contains DNA required for protein synthesis.

Found in: animal, plant, algal and fungal cells

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3
Q

What is the structure and function of mitochondria and in which cells can they be found?

A

Structure:
- Double membrane isolates respiratory reactions from general cytoplasm (so high conc of enzymes + substrates can be maintained). Inner membrane folds to form cristae (increase SA for attachment of enzymes).
- Matrix.
- Inner membrane spanned with proteins (allows entry of pyrovic acid + oxygen & exit of ATP + carbon dioxide).
- Contains DNA + ribosomes involved in protein synthesis.

Function:
Site of aerobic respiration whereby ATP is produced for energy release.

Found in: animal, plant, algal and fungal cells

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4
Q

What is the structure and function of chloroplasts and in which cells can they be found?

A

Structure:
- Double membrane isolates photosynthetic reactions from general cytoplasm.
- Stroma contains series of flattened sacs (thylakoid membranes) which can be stacked into grana (increased SA for assembly of chlorophyll + attachment of enzymes) - also contains starch granules & lipid droplets.
- Lamella - thylakoid linking grana.
- Contains DNA + ribosomes involved in nucleic acid & protein synthesis.

Function:
Site of photosynthesis. Absorbs light energy.

Found in: plant and algal cells

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5
Q

What is the structure and function of the Golgi apparatus & Golgi vesicles and in which cells can they be found?

A

Structure:
- Stack of membrane bound fluid filled flattened sacs (cisternae).
- Vesicles often seen on the edges of the sacs (small membrane sacs).
- Receives proteins & lipids from the ER & modifies them.
- Proteins/lipids then packaged into vesicles to be transported.

Golgi body function:
Processes & packages new lipids & proteins. Makes lysosomes.
Golgi vesicles function:
Transports lipids & proteins processed by Golgi body.

Found in: animal, plant, algal and fungal cells

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6
Q

What is the structure and function of lysosomes and in which cells can they be found?

A

Structure:
- Type of Golgi vesicle.
- Spherical sacs surrounded by single membrane.
- Contain powerful enzymes which digest and break down materials.

Function:
Releases lysozymes used to digest/break down pathogens or worn out cell components.

Found in: animal, plant, algal and fungal cells

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7
Q

What is the structure and function of ribosomes and in which cells can they be found?

A

Structure:
- Very small organelle that floats freely in cytoplasm or bound to RER.
- Not membrane bound.
- Large & small subunit (ribosomal RNA and protein).

Function:
Site of protein synthesis.

Found in: animal, plant, algal and fungal cells

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8
Q

What is the structure and function of the rough endoplasmic reticulum (rer) and in which cells can it be found?

A

Structure:
- Series of flattened membrane bound sacs (cisternae) continuous with the nucleur membrane.
- Covered in ribosomes (protein synthesis).

Function:
Folds & processes proteins.

Found in: animal, plant, algal and fungal cells

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9
Q

What is the structure and function of the smooth endoplasmic reticulum (ser) and in which cells can it be found?

A

Structure:
- Series of flattened membrane bound sacs (cisternae) continuous with the nucleur membrane.
- No ribosomes (involved in making lipids).

Function:
Synthesises & processes lipids.

Found in: animal, plant, algal and fungal cells

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10
Q

What is the structure and function of the cell wall and in which cells can it be found?

A

Structure:
- Rigid structure.
- Made of cellulose (in plants).
- Made of chitin (in fungi).

Function:
Strengthens & supports cell, prevents them from changing shape or bursting under pressure due to osmosis.

Found in: plant, algal and fungal cells

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11
Q

What is the structure and function of the cell vacuole and in which cells can it be found?

A

Structure:
- Surrounding membrane called the tonoplast.

Function:
Contains cell sap to keep cell turgid (maintains pressure inside cell).

Found in: plant cells

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12
Q

How do prokaryotic cells differ from eukaryotic cells?

A
  • They are much smaller
  • They have no membrane-bound organelles
  • They have smaller ribosomes
  • They have no nucleus - instead they have a single circular DNA molecule that is free in the cytoplasm
  • They have a cell wall that contains murein (a glycoprotein)
  • Some may have one or more plasmids (small loops of DNA)
  • Some may have a capsule surrounding the cell (secreted layer to protect against attacking immune cells)
  • Some may have one or more flagella (for mobility)
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13
Q

What is the structure of viruses?

A
  • They are are acellular & non-living - invade & reproduce inside host
  • They contain genetic material (DNA or RNA)
  • They are surrounded by a capsid (protein coat which encloses genome (nucleic acids))
  • They have attachment proteins (allow virus to attach to host cell)
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14
Q

What is magnification?
What is resolution?

A

● Magnification = number of times greater image is than size of the real (actual) object.
- Magnification = size of image / size of real object
● Resolution = minimum distance apart 2 objects can be to be distinguished as separate objects

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15
Q

What are the differences between optical microscopes & electron microscopes?

A

Optical:
- Uses light to form image.
- Low resolution (wavelength of light is long).
- Max magnification of x1500.

Electron:
- Uses electrons to form image.
- High resolution.
- Max magnification of x1000000.

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16
Q

What is a condenser (found in an optical microscope)?

A

Gather light from the microscopes light source & concentrate it onto the specimen being viewed.

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17
Q

What are the 2 types of electron microscope?

A
  • Transmission electron microscope (TEM)
  • Scanning electron microscope (SEM)
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18
Q

What are the features of TEMs & SEMs?

A

TEMs:
Work by: Using electromagnets to focus a beam of electrons which is transmitted through the specimen. (Denser parts of the specimen absorb more electrons, making them look darker in the image).
+ Give high resolution images.
+ Can see internal structures of organelles & ribosomes.
- Image viewed is 2D.
- Have to view specimen in vacuum (only non-living specimens can be viewed).
- Can only view very thin specimens.
- Does not show colour.
- Complex preparation so artefacts often present.

SEMs
Work by: Using electromagnets to deflect/bounce electrons off the specimens surface. These can then be detected in cathode ray tube to form image.
- Produces lower resolution images than TEMs.
+ Image viewed is 3D.
- Have to view specimen in vacuum (only non-living specimens can be viewed).
+ Can view thicker specimens.
- Complex preparation so artefacts often present.
- Does not show colour.

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19
Q

What are microscope artefacts and how did the first scientists distinguish between artefacts & organelles?

A

Things you can see down the microscope that aren’t part of the cell/ specimen you’re looking at. Usually made during the preparation of the specimen and shouldn’t be there.
(Common in electron micrographs as specimens need lots of preparation before viewing).

The first scientists could only distinguish by repeatedly preparing specimens in different ways. If an object could be seen with 1 prep technique & not another it was likely to be an artefact.

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20
Q

What is cell fractionation and what are the steps?

A
  1. Homogenisation (breaking up the cells)
    - vibrating the cells or grinding them up in a blender
    - breaks open plasma membrane & releases organelles into solution
    - must be ice-cold (to reduce lytic enzyme activity (produced by bacteria/ viruses - enzymes that would break down cell wall/membrane)), isotonic (same concentration to prevent damage to organelles by osmosis (lysis/bursting)), buffer (maintain pH to reduce denature of enzymes)
  2. Filtration (getting rid of the big bits)
    - Homogenised cell solution is filtered through a gauze to separate any large cell debris/tissue debris from the organelles
  3. Ultracentrifugation (separating the organelles)
    - cell fragments poured into tube
    - put in centrifuge & is spun at low speed
    - heaviest organelles (like nuclei) get flung to bottom of tube & form thick sediment at bottom (the pellet)
    - the rest stay suspended in fluid above (the supernatant)
    - supernatant drained off, poured into another tube & spun at higher speed
    - process repeats at higher & higher speeds until all organelles are separated in order of mass (nuclei, mitochondria, lysosomes, E.R, ribosomes) (plant cells: chloroplasts in between nuclei & mitochondria)
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21
Q

How do you calculate total magnification of a microscope?

A

Magnification of objective lens x Magnification of eyepiece lens

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22
Q

How do you calculate the magnification of an image?

A

Image size / Actual size

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23
Q

Describe how the size of an object viewed with an optical microscope can be measured.

A

Once calibrated with the stage micrometer 1 division is:
25µm at x400
100µm at x100

  1. Line up (scale of) eyepiece graticule with (scale of) stage micrometre
  2. Calibrate eyepiece graticule - use stage micrometre to calculate size of divisions on eyepiece graticule
  3. Take micrometre away and use graticule to measure how many divisions make up the object
  4. Calculate size of object by multiplying number of divisions by size of division
  5. Recalibrate eyepiece graticule at different magnifications
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24
Q

How do eukaryotic cells divide/replicate?

A

The cell cycle.
- interphase
- mitosis
- cytokinesis

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25
Q

Describe the stages of the cell cycle in eukaryotic cells.

A
  1. Interphase
    ● (S phase) DNA replicates semi-conservatively
    - Leading to 2 chromatids (identical copies) joined at a centromere
    ● (G1/G2) number of organelles & volume of cytoplasm increases, protein synthesis
  2. Mitosis
    ● Nucleus divides
    ● To produce 2 nuclei with identical copies of DNA produced by parent cell
  3. Cytokinesis
    ● Cytoplasm and cell membrane (normally) divide
    ● To form 2 new genetically identical daughter cells
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26
Q

What division stages are there in mitosis?

A

Prophase, Metaphase, Anaphase, Telophase
(PMAT)

27
Q

What is the structure of the chromosomes of a cell at the beginning of mitosis?

A

Chromosomes made of 2 strands joined in the middle by a centromere. The separate strands = chromatids.

The are 2 strands because each chromosome has already made an identical copy during interphase.
When mitosis is over they are 1 strand.

> < - chromosome < - 1 chromatid

28
Q

Describe the behaviour of chromosomes & role of spindle fibres during prophase.

A

● Chromosomes condense, becoming shorter / thicker (so visible)
- Appear as 2 sister chromatids joined by a centromere
● Nuclear envelope breaks down
● Centrioles move to opposite poles forming spindle network

29
Q

Describe the behaviour of chromosomes & role of spindle fibres during metaphase.

A

● Spindle fibres attach to chromosomes by their centromeres
● Chromosomes align along equator

30
Q

Describe the behaviour of chromosomes & role of spindle fibres during anaphase.

A

● Spindle fibres shorten / contract
● Centromere divides
● Pulling chromatids (from each pair) to opposite poles of cell

31
Q

Describe the behaviour of chromosomes & role of spindle fibres during telophase.

A

● Chromosomes uncoil, becoming longer / thinner
● Nuclear envelopes reform = 2 nuclei
● Spindle fibres / centrioles break down

32
Q

What causes cancer?

A

Mitosis is a controlled process.
● Mutations in DNA / genes controlling mitosis can lead to uncontrolled cell division
● Tumour formed if this results in mass of abnormal cells
- Malignant tumour = cancerous, can spread (metastasis)
- Benign tumour = non-cancerous

33
Q

What do most cancer treatments do?

A

Many are directed at controlling the rate of cell division.
This kills the tumour cells but also kills normal cells.

● Some disrupt spindle fibre activity / formation
- So chromosomes can’t attach to spindle by their centromere
- So chromatids can’t be separated to opposite poles (no anaphase)
- So prevents / slows mitosis
● Some prevent DNA replication during interphase
- So can’t make 2 copies of each chromosome (chromatids)
- So prevents / slows mitosis

34
Q

How to prokaryotic cells divide/replicate?

A

Binary fission.

35
Q

What are the steps of binary fission?

A
  1. Circular DNA + plasmids replicate (DNA once & plasmids many times).
  2. The cell gets bigger & DNA loops move to opposite poles of cell.
  3. Cytoplasm begins to divide (& new cell walls begin to form).
  4. Cytoplasm divides & 2 daughter cells produced, each with one copy of circular DNA but many plasmid copies.
36
Q

How do viruses replicate if they are acellular?

A

Do not undergo cell division as not alive - invade and reproduce inside host cells.
1. Virus attaches to host cell receptor proteins (using their attachment proteins). *
2. Genetic material is released into host cell.
3. Genetic material & proteins are replicated by host cell ‘machinery’.
4. Viral components assemble.
5. Replicated virus released from host cell.

*(different viruses have different attachment proteins so require different receptor proteins on host cell = some viruses can only affect certain cells)

37
Q

What is the structure of all cell membranes?

A

fluid-mosaic model

38
Q

What are the features of the fluid mosaic model?

A

● Molecules free to move laterally in phospholipid bilayer (fluid)
● Many components:

● Phospholipids form a bilayer- fatty acid tails face inwards, phosphate heads face outwards
● Proteins
- Intrinsic / integral proteins span bilayer eg. channel and carrier proteins
- Extrinsic / peripheral proteins on surface of membrane
● Glycolipids (lipids with polysaccharide chains attached) found on exterior surface
● Glycoproteins (proteins with polysaccharide chains attached) found on exterior surface
● Cholesterol (sometimes present) bonds to phospholipid hydrophobic fatty acid tails

39
Q

What is the arrangement of phospholipids in membranes?

A

● Bilayer, with water present on either side
● Hydrophobic fatty acid tails repelled from water so point away from water / to interior
● Hydrophilic phosphate heads attracted to water so point to water

40
Q

What is the function of cholesterol in membranes?

A

● Restricts movement of other molecules making up membrane
● So decreases fluidity (and permeability) / increases rigidity

41
Q

Explain how temperature affects permeability of cell-surface membranes.

A

● As temperature increases, permeability increases
- Phospholipids gain kinetic energy and fluidity increases
- Transport proteins denature at high temperatures as H bonds break, changing tertiary structure
● At very low temperatures, permeability increases
- Ice crystals can form which pierce the cell membrane and increase permeability

42
Q

Explain how pH affects permeability of cell-surface membranes.

A

● High or low pH increases permeability
- Transport proteins denature as H / ionic bonds break, changing tertiary structure

43
Q

Explain how lipid-soluble solvents eg. alcohol affect permeability of
cell-surface membranes.

A

● As concentration increases, permeability increases
● Ethanol (a lipid-soluble solvent) may dissolve phospholipid bilayer (gaps form)

44
Q

Suggest how cell membranes are adapted for other functions.

A

● Phospholipid bilayer is fluid → membrane can bend for vesicle formation / phagocytosis
● Glycoproteins / glycolipids act as receptors / antigens → involved in cell signalling / recognition

45
Q

Describe how movement across membranes occurs by simple diffusion.

A

● Lipid-soluble (non-polar) or very small substances eg. O2, steroid hormones
● Move from an area of higher conc. to an area of lower conc. down a conc. gradient
● Across phospholipid bilayer
● Passive - doesn’t require energy from ATP / respiration (only kinetic energy of substances)

46
Q

What factors affect rate of diffusion?

A

● Increasing surface area of membrane increases rate of movement
● Increasing concentration gradient increases rate of simple diffusion

47
Q

Explain the limitations imposed by the nature of the phospholipid bilayer.

A

● Restricts movement of water soluble (polar) & larger substances eg. Na
+ / glucose
● Due to hydrophobic fatty acid tails in interior of bilayer

48
Q

Describe how movement across membranes occurs by facilitated diffusion.

A

● Water-soluble (polar) / slightly larger substances
● Move down a concentration gradient
● Through specific channel / carrier proteins
● Passive - doesn’t require energy from ATP / respiration (only kinetic energy of substances)

49
Q

Explain the role of carrier and channel proteins in facilitated diffusion.

A

● Shape / charge of protein determines which substances move
● Channel proteins facilitate diffusion of water-soluble substances
- Hydrophilic pore filled with water
- May be gated- can open / close
● Carrier proteins facilitate diffusion of (slightly larger) substances
- Complementary substance attaches to binding site
- Protein changes shape to transport substance

50
Q

What factors affect facilitated diffusion?

A

● Increasing surface area of membrane increases rate of movement
● Increasing number of channel / carrier proteins increases rate of facilitated diffusion
● Increasing concentration gradient increases rate of facilitated diffusion
- Until number of channel / carrier proteins becomes a limiting factor as all in use / saturated

51
Q

Describe how movement across membranes occurs by osmosis.

A

● Water diffuses / moves
● From an area of high to low water potential (ψ) / down a water potential gradient
● Through a partially permeable membrane
● Passive - doesn’t require energy from ATP / respiration (only kinetic energy of substances)

52
Q

What is water potential?

A

A measure of how likely water molecules are to move out of a solution. Pure (distilled) water has the maximum possible ψ (0 kPA).
Increasing solute concentration decreases ψ.

53
Q

What is an isotonic solution?
What happens if you put a cell in an isotonic solution?

A
54
Q

What is an hypotonic solution?
What happens if you put a cell in an hypotonic solution?

A
55
Q

What is an hypertonic solution?
What happens if you put a cell in an hypertonic solution?

A
56
Q

What factors affect rate of osmosis?

A

● Increasing surface area of membrane increases rate of movement
● Increasing water potential gradient increases rate of osmosis

57
Q

Why can water diffuse directly across the phospholipid bilayer?

A
58
Q

How else can water travel through cell membranes?

A
59
Q

Describe how movement across membranes occurs by active transport.

A

● Substances move from area of lower to higher concentration / against a concentration gradient
● Requiring hydrolysis of ATP and specific carrier proteins

60
Q

What factors affect active transport?

A

● Increasing surface area of membrane increases rate of movement
● Increasing number of channel / carrier proteins increases rate of active transport

61
Q

Describe the role of carrier proteins and the importance of the hydrolysis of ATP in active transport.

A
  1. Complementary substance binds to specific carrier protein
  2. ATP binds, hydrolysed into ADP + Pi, releasing energy
  3. Carrier protein changes shape, releasing substance on side with higher concentration
  4. Pi released → protein returns to original shape
62
Q

Describe how movement across membranes occurs by co-transport.

A

● Two different substances bind to and move simultaneously via a
co-transporter protein (type of carrier protein)
● Movement of one substance against its concentration gradient is often
coupled with the movement of another down its concentration gradient

63
Q

Describe an example that illustrates co-transport.

A

Absorption of sodium ions and glucose (or amino acids) by cells lining the mammalian ileum:
1. ● Na+ actively transported from epithelial cells to blood (by Na+/K+ pump)
● Establishing a conc. gradient of Na+ (higher in lumen than epithelial cell)
2. ● Na+ enters epithelial cell down its concentration gradient with glucose against its concentration gradient
● Via a co-transporter protein
3. ● Glucose moves down a conc. gradient into blood via facilitated diffusion
(The movement of sodium can be considered indirect / secondary active transport, as it is reliant on a concentration gradient established by active transport.)

64
Q

Explain the adaptations of some specialised cells in relation to the rate of transport across their internal and external membranes.

A

● Membrane folded eg. microvilli in ileum → increase in surface area.
● More protein channels / carriers → for facilitated diffusion (or active transport - carrier proteins only)
● Large number of mitochondria → make more ATP by aerobic respiration for active transport