Chapter 5: Plasma Membranes Flashcards

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1
Q

Effect of low temperature on active transport + osmosis + phloem loading?

A
  • Molecules –> little KE (move slowly) –> less respiration/ATP produced.
  • Less active transport of sugars/sucrose into sieve tube elements.
  • Less osmosis of water into sieve tube element.
  • Less hydrostatic pressure (HP) created.
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2
Q

Effect of increasing temperature on active transport + osmosis + phloem loading?

A
  • Molecules –> more KE (move quickly) –> more respiration/ATP produced.
  • More active transport of sugars/sucrose into sieve tube elements.
  • More osmosis of water into sieve tube elements.
  • More HP generated/created.
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3
Q

Effect of VERY HIGH temperature on active transport + osmosis + phloem loading?

A
  • Enzymes denatured.
  • Shape change to precise 3D shape of tertiary structure of enzymes.
  • Carrier/Channel proteins denature.
  • No longer complementary to substrate.
  • No longer bind to substrate.
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4
Q

Roles of proteins in cell surface membranes?

A
  • Glycoproteins –> cell adhesion/recognition/signalling/receptor sites/attach to water molecules.
  • Channel proteins –> transport by facilitated diffusion.
  • Carrier proteins –> transport by active transport.
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5
Q

Roles of different lipid components of plasma membranes?

A
  • Phospholipids –> form bilayer.
  • Non-polar hydrophobic fatty acid tails in bilayer –> hydrophobic core that prevents diffusion of polar molecules/ions.
  • Hydrophobic barrier –> compartmentalisation/isolation of contents of organelles –> separates different areas.
  • Bilayer –> allows diffusion of non-polar molecules (O2) easily through cell surface membrane.
  • Glycolipids –> cell recognition.
  • Cholesterol –> regulates membrane fluidity + stabilises membrane –> dual hydrophilic/hydrophobic properties + waterproofs the skin.
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6
Q

Why is alcohol used in antiseptic wipes?

A
  1. Alcohol disrupts cell surface membrane of bacteria –> pure alcohol dissolves the membrane.
  2. Helps prevent infection.
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7
Q

Define Simple Protein.

A

Protein without prosthetic group.

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8
Q

Describe (using beetroot) how you would use a colorimeter to investigate how cell membrane permeability changes with temperature.

A
  1. Use beetroot –> contains betalain dye.
  2. Cut beetroots into cubes of equal size/area.
  3. Place beetroot cubes in sample of water at different temps.
  4. At least 5 different temps.
  5. Sample water after set time.
  6. Use filter in colorimeter.
  7. Calibrate/zero colorimeter.
  8. Read absorbance.
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9
Q

How do water molecules cross selectively permeable membranes by simple diffusion?

A
  1. Water molecules small.
  2. Moving fast between phospholipid molecules.
  3. Through transient gaps.
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10
Q

Why is the cell surface membrane described as selectively permeable and not semi-permeable?

A
  • Only certain ions/molecules can cross cell surface membranes.
  • Depends on size (larger = slower), charge (partial +ve or -ve (polar) repelled by hydrophobic core of bilayer), presence of transport protein.
  • Semi-permeable does not give the idea of selectivity.
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11
Q

Outline the general process of active transport.

A
  1. Molecule/ion to be transported binds to receptors on channel of carrier proteins on outside of cell.
  2. On inside of cell ATP binds to carrier proteins and is hydrolysed to ADP + phosphate.
  3. Binding of phosphate molecule to carrier protein causes protein to change shape –> opening up to inside of cell.
  4. Molecule/ion released inside cell.
  5. Phosphate molecule released from carrier protein + recombines with ADP to form ATP.
  6. Carrier protein returns to original shape.
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12
Q

Outline the process of exocytosis.

A
  1. Vesicles formed by Golgi apparatus move towards + fuse with cell surface membrane.
  2. Contents of vesicle released outside cell.
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13
Q

Outline process of endocytosis.

A
  1. Cell surface membrane invaginates when it comes into contact with material to be transported.
  2. Membrane enfolds material until it fuses forming a vesicle.
  3. Vesicle pinches off and moves into cytoplasm to transfer material for further processing in cell.
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