2) Cells Flashcards

1
Q

Eukaryotic (eg human) cells
compared with Prokaryotic
(bacterium)

A
  1. Bacterial cell is much smaller than a human cell; (or human cell is much larger than a bacterial cell)
  2. Bacterial cell has a cell wall but human cell does not;
  3. Bacterial cell lacks a nucleus but human cell has a nucleus;
  4. Bacterial cell lacks membrane-bound organelles but human cell has membrane-bound organelles;
  5. Bacterial ribosomes smaller than human ribosomes / bacteria have 70S ribosomes whereas humans have 80S
  6. Bacterial DNA is circular but human DNA is linear
  7. Bacterial DNA is ‘naked’ whereas human DNA is bound to histones/proteins;
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2
Q

How to measure
objects using an eyepiece graticule

A
  1. Use eyepiece graticule to measure the object e.g. nucleus or capillary
  2. Calibrate eyepiece graticule against stage micrometer
  3. Take a number of measurements and calculate the mean
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3
Q

Advantages and
Limitations of Transmission Electron
Microscope

A

Advantages -

  1. Small objects can be seen;
  2. TEM has high resolution as wavelength of electrons shorter;

Limitations -

  1. Cannot look at living cells as cells must be in a vacuum;
  2. Must be thin specimen;
  3. Preparation may create artefact;
  4. Does not produce colour image;
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4
Q

Comparison of TEM
and optical microscope

A
  1. TEM use electrons and optical use light;
  2. TEM allows a greater resolution;
  3. (So with TEM) smaller organelles/named cell structure can be observed
  4. TEM view only dead/dehydrated specimens and optical (can) view live specimens;
  5. TEM does not show colour and optical (can);
  6. TEM requires thinner specimens;
  7. TEM requires a more complex/time consuming preparation;
  8. TEM focuses using magnets and optical uses (glass) lenses;
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5
Q

Advantage of
electron microscope over optical
microscope

A
  1. High resolution;
  2. Can see internal structure of organelles
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6
Q

Conditions required for cell homogenisation

A
  1. Ice-cold – Slows/stops enzyme activity to prevent digestion of organelles/mitochondria;
  2. Buffered – Maintains pH so that enzymes/proteins are not denatured;
  3. Same water potential – Prevents osmosis so no lysis/shrinkage of organelles/mitochondria;
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7
Q

How is mitochondria separated

A
  1. Break open cells/homogenise/produce homogenate;
  2. Remove unbroken cells/larger debris by filtration;
  3. Centrifuge highest density organelle nuclei obtained as pellet at slowest speed
  4. Mitochondria in 2nd pellet as less dense than nucleus/organelle in first pellet;
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8
Q

Stages of mitosis - chromosome behavior in each stage ?

A

Prophase - chromosomes become visible, appear as two sister chromatids joined at centromere

Metaphase - chromosomes line up on the equator, chromosomes attached to spindle fibers by their centromere

Anaphase - centromere splits, sister chromatids pulled to opposite ends of the cell.

Telophase - chromatids unwind an become longer.

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9
Q

How does bacteria replicate

A
  1. Replication of (circular) DNA;
  2. Division of cytoplasm to form 2 daughter cells
  3. Each with a single copy of (circular) DNA;
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10
Q

Mitosis practical - preparing root tip squash techniques

A

1.Push hard – spread/squash tissue;
2 Not push sideways – avoid rolling cells together/breaking chromosomes;

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11
Q

Mitosis Practical – How do we
identify anaphase?

A
  1. Chromosomes/chromatids are (in two groups) at poles of spindle/at ends of spindle;
  2. V-shape shows that (sister) chromatids have been pulled apart at their centromeres
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12
Q

Describe all types of membrane
transports

A
  1. (Simple / facilitated) diffusion from high to low concentration / down concentration gradient;
  2. Small / non-polar / lipid-soluble molecules pass via phospholipids / bilayer; OR Large / polar / water-soluble
  3. molecules go through proteins;
  4. Water moves by osmosis / from high water potential to low water potential / from less to more negative water potential;
  5. Active transport is movement from low to high concentration / against concentration gradient. Active transport/ facilitated diffusion involves proteins/carriers;
  6. Active transport requires energy / ATP;
  7. Ref. to Na+ / glucose co-transport;
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13
Q

Active Transport – mitochondria

A
  1. Mitochondria site of respiration;
  2. Release energy / produce ATP; (Reject make energy in context of this point)
  3. Energy / ATP necessary for active transport;
  4. To move substances against concentration gradient;
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14
Q

Active Transport compared with
facilitated diffusion

A
  1. Facilitated diffusion involves channel or carrier proteins whereas active transport only involves carrier proteins;
  2. Facilitated diffusion does not use ATP / is passive whereas active transport uses ATP;
  3. Facilitated diffusion takes place down a concentration gradient whereas active transport can occur against a concentration gradient
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15
Q

Disruption to respiration to co-
transport of glucose from ileum to
the blood

A
  1. Less ATP / no ATP
  2. For active transport
  3. So sodium ions cannot be pumped into blood
  4. Sodium ion concentration in cell becomes too high
  5. Can’t maintain a concentration gradient for sodium ions so sodium ions cannot diffuse into cells
  6. So glucose cannot be taken into cells from lumen
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16
Q

Why does inhibiting
respiration/using cyanide prevent
active transport?

A
  1. Oxygen is required for aerobic respiration which releases ATP
  2. ATP is needed to change the shape of the protein carrier
  3. Which would cause the release of the transported ion/molecule
  4. So no ATP, no Active Transport
17
Q

How do we find water potential of
plant tissue practically

A
  1. Plot a graph with concentration on the x-axis and percentage change in mass on the y-axis;
  2. Find concentration where curve crosses the x-axis/where percentage change is zero;
  3. Use (another) resource to find water potential of sucrose concentration (where curve crosses x-axis);
18
Q

What is antigen?

A
  • foreign protein which stimulates an immune response - produces antibodies
19
Q

What is antibody

A
  • a protein which is specific to an antigen
  • produced by B cells or secreted by plasma cells.
20
Q

Antibody specificity

A
  1. Antibody has (specific) tertiary structure
  2. Has binding site/ variable region which only binds to one antigen
  3. Antigen is only found on this particular (pathogen/cell/tissue)
  4. so antibody (only) binds to / forms antigen/antibody complex with these (pathogen/cell/tissue) destroying them
21
Q

What is a monoclonal antibody

A
  1. Antibody specific/complementary to one antigen only
  2. Antibodies all the same and from one original plasma cell
  3. Derived from a hybridoma cell/fused B lymphocyte and cancer cell
22
Q

What is phagocytosis

A
  1. Phagosome/vesicle fuses with lysosome;
  2. (pathogen) destroyed by lysozymes/hydrolytic enzymes;
  3. Antigen (from pathogen) displayed on cell membrane (of phagocyte/antigen presenting cell);
23
Q

HIV treatment with anti-retroviral
drug AZT

A
  1. Person (infected with HIV) has HIV DNA (in their DNA);
  2. New HIV (particles) still made;
  3. (AZT) inhibits reverse transcriptase;
  4. (AZT) stops replication of HIV;
  5. Stops destruction of more / newly infected T cells;
  6. So immune system continues to work (and AIDS does not develop);
24
Q

Immunity – Compare Active and
Passive Immunity

A
  1. Active involves memory cells, passive does not;
  2. Active involves production of antibody by plasma cells/memory cells;
  3. Passive involves antibody introduced into body from outside/named source;
  4. Active long term, because antibody produced in response to antigen;
  5. Passive short term, because antibody (given) is broken down;
  6. Active (can) take time to develop/work, passive fast acting;
25
Q

Antigen-Antibody
complex formation

A
  1. Antibody has 4 polypeptide chains and has a quaternary structure
  2. Antibody has a variable region which has a specific amino acid sequence/primary structure
  3. Shape of the binding site is complementary to the antigen
  4. Forming an antigen-antibody comple
26
Q

Compare Primary and
Secondary Response

A
  1. Before vaccination no antibody released because patients not yet encountered vaccine/antigen/virus;
  2. Primary response/after first dose) activation/clonal selection/expansion of B cells into plasma cells;
  3. Plasma cells release antibodies;
  4. Secondary response/after second dose) memory cells produce more antibodies/produce antibodies more
    quickly;
27
Q

How a vaccine
produces an immune response

A
  1. Vaccine contains antigen from pathogen;
  2. Macrophage presents antigen on its surface;
  3. T cell with complementary receptor protein binds to antigen;
  4. T cell stimulates B cell;
  5. (With) complementary antibody on its surface;
  6. B cell/plasma cell secretes large amounts of antibody;
  7. B cell divides to form clone all secreting/producing same antibody;
28
Q

Humoral Response

A
  1. Antigen on surface of bacterium binds to surface protein / surface receptor on a (specific/single) B cell;
  2. (Activated) B cell divides by mitosis / produces clone;
  3. (Division) stimulated by cytokines / by T cells;
  4. B cells/plasma cells release antibodies;
  5. (Some) B cells become memory cells;
  6. Memory cells produce plasma / antibodies faster;
29
Q

Monoclonal Antibody

A
  1. Antibody specific/complementary to one antigen only
  2. Antibodies all the same/one type only/ from one original plasma cell
  3. Derived from a hybridoma cell/fused B lymphocyte and cancer cell