Topic 2 - Cells Flashcards

1
Q

What do eukaryotic cells contain?

A

-Cell surface membrane
-Nucleus (Including nuclear pores, nuclear envelope, nucleolus, nucleoplasm)
-Mitochondrion
-Cytoplasm
-Rough Endoplasmic reticulum
-Smooth endoplasmic reticulum
-Lysosomes
-Centrioles
-Golgi apparatus (+ vesicles)

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2
Q

What structures are unique to plant cells

A

-Cell wall
-Vacuole
-Chloroplasts

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2
Q

What are plant cell walls made from

A

Cellulose

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3
Q

What are bacteria (Prokaryotic) cell walls made from?

A

Glycoproteins (Murein)

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4
Q

What are fungus cell walls made from

A

Chitin

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4
Q

What is the function of the nucleus

A

Stores hereditary information

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5
Q

What is the function of the nuclear pores

A

Movement of large molecules

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6
Q

What is the function of the nuclear envelope

A

Controls what exits and enters the nucleus

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6
Q

What is the function of the nucleolus

A

Produces ribosomes and ribosomal RNA

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7
Q

What is the function of cell surface membrane

A

Controls what exits and enters the cell

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8
Q

What is the function of the nucleoplasm

A

Makes up the bulk of the nucleus

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9
Q

What is the function of cytoplasm

A

Site of chemical reactions

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10
Q

What is the function of the rough endoplasmic reticulum

A

Produces, stores and transports proteins

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11
Q

What is the function of the smooth endoplasmic reticulum

A

Produces, stores and transports lipids

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12
Q

What is the function of the golgi apparatus ( + vesicles)

A

Packages and modifies molecules

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13
Q

What is the structure and function of the mitochondria

A

Double membrane (cristae and matrix)
Site of aerobic respiration

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14
Q

What is the function of lysosomes

A

Hydrolyses waste material

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14
Q

What is the structure and function of the chloroplasts

A

Grana (discs) and stroma (liquid)
Photosynthesis

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14
Q

What is the function of the vacuole

A

stores unwanted chemicals and maintains the rigidity of the cell

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15
Q

What is the function of centrioles

A

Produces spindle fibers

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16
Q

What is the structure of a prokaryotic cell

A

-Capsule
-Cell wall
-Cell surface membrane
-Pilli
-“Naked” DNA
- Plasmids
-Smaller ribosomes
-Chlorophyll
-Flagellum

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17
Q

What is the structure of viruses

A

-Attachment proteins
-Lipid envelope
-Matrix
-Capsid
-Genetic info (DNA/RNA)
-Reverse transcriptase enzyme

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18
Q

Compare the structure of a eukaryotic and prokaryotic cell

A

-Linear DNA vs naked DNA
-larger ribosomes vs smaller ribosomes
-mitochondria vs no mitochondria
-none vs capsule
- cellulose vs glycoproteins

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19
Q

How is genetic info stored in eukaryotic cells

A

Linear DNA which is associated with histones and stored as chromosomes

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20
Q

What are the types of microscopes

A

-Light/optical
-Scanning electron microscope (SEM)
-Transmission electron microscope (TEM)

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21
Q

How does a SEM work

A

Electrons are fired at a sample and the electrons reflected back are measured

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22
Q

How does a TEM work

A

Fires electrons at a sample and measures the electrons which pass though the specimen

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23
Q

How are electron microscopes focused

A

Using focusing magnets

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24
Q

What are advantages of SEM

A

High magnification and resolution, produces 3d images

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25
Q

What are disadvantages of SEM

A

Expensive, cannot be used on live specimens, heavy metal stains used, black and white image

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26
Q

What are disadvantages of TEM

A

Expensive, cannot be used on live specimens, heavy metal stains used, black and white image

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27
Q

What are advantages of TEM

A

Very high magnification and resolution, can see organelles

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28
Q

What are advantages of a light microscope

A

Easy to use, cheap can magnify live samples

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29
Q

What are disadvantages of light microscopes

A

Relatively low magnification and resolution, cant see organelles

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30
Q

How do you focus a light microscope

A

Using the fine and coarse focusing wheels

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31
Q

What is the order of magnitude

A

m, mm, micrometers, nano meters (X1000 going right, /1000 goinjg left)

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32
Q

What are the four stages of mitosis

A

Prophase, metaphase, anaphase, telophase. (PMAT)

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33
Q

Describe what happens at the metaphase

A

1.Spindle fibres attach to the centromere
2.Chromosomes align at the equator

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33
Q

Describe what happens in the prophase

A

1.Chromatin condenses to form chromosomes
2.Centriole attach at the poles
3.Centrioles produce spindle fibres
4.Nucleolus disappears
5.Nuclear envelope disappears

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34
Q

Describe what happens in the telophase

A

1.Chromosomes are unattached from the spindle fibres
2. Spindle fibres disappear
3. Chromosomes uncoil to form chromatin
4.Nucleolus reappears
5. Nuclear envelope reappears

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35
Q

Describe what happens in the anaphase

A
  1. Sister chromatids are split at the centromere by the spindle fibres
  2. Chromosomes pulled to opposite poles of the cell
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36
Q

What are the 3 stages of the cell cycle

A
  1. Interphase
  2. Mitosis
  3. Cytokinesis
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36
Q

What is interphase split into

A

G1, S, G2

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37
Q

What happen in G1

A

The organelles are duplicated

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38
Q

What happens in S

A

The chromosome is duplicated

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39
Q

What happens in G2

A

The cell “double checks” for mutations in the replicated DNA

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40
Q

RP 2 - Garlic root tip experiment
What is the aim of this practical

A

To investigate mitosis and the mitotic index of a sample

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41
Q

What is the mitotic index

A

The ratio of cells undergoing mitosis to the total number of cells in the sample

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42
Q

Why is are the roots rinsed with distilled water

A

To get rid of excess HCl

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42
Q

Why is toluidine blue stain added

A

To make the chromosomes visible

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42
Q

What is the method for investigating mitosis

A
  1. Heat HCl in a water bath at 55 degrees
  2. Rest the roots of the garlic in the HCl for 5 minutes
    3.Rinse excess HCl with distilled water over a beaker
  3. Use filter paper to dry the root tips
  4. Use a scalpel to cut off the tip of the root
    6.Place root tip on the slide and add toluidine blue stain and macerate with a mounted needle
  5. Add a cover slip and using finger pressure press down to break open the cells
  6. Look for stages of mitosis and record data in order to calculate the mitotic index
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43
Q

Why are the roots dipped in warm HCl

A

To hydrolyse the glycosidic bonds in the cellulose surrounding the cells

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44
Q

Why is the sample macerated

A

To get the cells evenly stained and break up the cellulose around it

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45
Q

Why is a mounted needle used to lower the cover slip

A

To avoid are bubbles from forming

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46
Q

What are the hazards of the mitosis practical

A

Glassware,working with chemicals, working with scalpels, hot water bath

47
Q

What are the risks of the mitosis practical

A

Cuts from broken glass, chemicals on skin or eyes, cutting yourself with scalpel, burns

48
Q

What are the controls for the mitosis practical

A

Handle glass with care, wear goggles, use scalpel with care, do not touch hot water bath

49
Q

What are the actions for the mitosis practical

A

Do not touch broken glass + tell member of staff, get member of staff to rinse eye using first aid kit, stop bleeding and go to medical room, hold under cold water for 20 minutes minimum.

50
Q

What five types of molecules make up the cell membrane

A

-Phospholipids
-glycolipids
-glycoproteins
-proteins
-cholesterol

51
Q

when in water how does a phospholipid behave

A

The head will be attracted to the water and the fatty acid tales would be sticking out the water

52
Q

what does the phospholipid bi layer consist of

A

A hydrophilic phosphate head and a hydrophobic fatty acid tail

53
Q

When submerged in water how would the phospholipids behave

A

They would form a micelle, a 3d structure where all the heads would for a ball like structure and the tails would remain inside

54
Q

what are glycolipids used for in the cell membrane

A

cell recognition, receptors

55
Q

what are glycoproteins used for in cell membranes

A

cell recognition, receptors

56
Q

what are proteins used for in cell membranes

A

Let through larger substances

57
Q

What are the two types of proteins in the cell membrane

A

channel and carrier proteins

58
Q

How do channel proteins work

A

they form a passage for ions to travel

59
Q

How do carrier proteins work

A

They allow larger molecules to diffuse through binding to the complementary receptor which causes a conformational change and pushes the molecules through

60
Q

what is used in facilliated diffusion

A

carrier and channel proteins

61
Q

what type of substances can travel through simple diffusion

A

small, uncharged molecules such as O2 and C02

62
Q

Define diffusion

A

The net movement of molecules form a region of higher concentration t a region of lower concentration until they are evenly distributed

63
Q

What factors affect diffusion

A

-Temperature
-Concentration gradient
-Surface Area
-Thickness of the diffusion pathway

64
Q

Explain how temperature impacts the rate of diffusion

A

Increased temp means increased KE so more collisions

65
Q

Explain how concentration gradient impacts the rate of diffusion

A

Increased concentration gradient so increased molecule to collide

66
Q

Explain how Surface area impacts the rate of diffusion

A

Increased SA means increased rate since there Is more spaces for molecules to diffuse

67
Q

Explain how thickness of diffusion pathway impacts the rate of diffusion

A

Small diffusion pathway means increased rate since less time taken to diffuse

68
Q

Define osmosis

A

The net movement of water from a region of high water potential to a region of lower water potential through a selectively permeable membrane

69
Q

what is water potnetial

A

the tendency of water molecules to move

70
Q

what does a high water potential have

A

a great proportion of water molecules compared to the solute

71
Q

what is water potential measured in

72
Q

What is active transport?

A

The movement of ions or molecules in or out of a cell from a region of lower concentration to a region of higher concentration using ATP and carrier proteins

73
Q

Describe the process of active transport for a Na+ ion

A

1)Firstly the shape of the Na+ ion is complementary to the receptor on the carrier protein and they bind together
2) Then ATP attaches to the opposite side of the carrier protein
3) As a phophate breaks off the ATP energy is released and consequently ADP and a phosphate are produced
4) The energy released changes the shape f the carrier portion so the ion goes through
5) The shape returns to normal and the ADP and phosphate come back together to form ATP

74
Q

What is co-transport

A

The transport of one substance coupled with another through a plasma membrane

75
Q

What is one example of where co-transport occurs

A

The ileum of the small intestine

76
Q

Explain how sodium ions aid the absorption of glucose in the ileum
(First half)

A
  • Sodium ions are actively transported out of the epithelial cell into the capillary
    -Therefore there is a greater concentration of sodium in the lumen compared to the epithelial cell
77
Q

Explain how sodium ions aid the absorption of glucose in the ileum
(Second half)

A

-Sodium ions under go facilitated diffusion from the lumen to the epithelial cell and simultaneously a glucose is also transported through the use of a co-transport protein
-The glucose can diffuse into the capillary from the epithelial cell through facilitated diffusion

78
Q

What are the different types of defence mechanisms

A

Specific and non specific

79
Q

What is a type of non specific defence

A

skin and stomach acid

80
Q

What is a type of specific defence

A

Lymphocytes

81
Q

What are the two types go lymphocytes

A

B and T lymphocytes

82
Q

What 4 types of non self cells can the immune system identify

A

Pathogens, non self material from other organisms, toxins, abnormal body cells such as cancer

83
Q

How many types of lymphocytes are there

A

10 million

84
Q

What process occurs when pathogens are engulfed and destroyed

A

Phagocytosis

85
Q

Is phagocytosis specific or non specific

A

Non specific

86
Q

What is stage 1 of phagocytosis

A

The phagocyte is attracted to the chemicals secretes by the pathogen (moves towards the pathogen using the concentration gradient)

87
Q

What is stage 2 of phagocytosis

A

The phagocyte receptor cells bind to the pathogen

88
Q

What is stage 3 of phagocytosis

A

The phagocyte undergoes endocystosis and forms a phagosome

89
Q

What is stage 4 of phagocytosis

A

The phagosome fuses with the lysosome and the lysozymes hydrolase the pathogen

90
Q

What is stage 5 of phagocytosis

A

The soluble products dissolve into the phagocyte and the antigen is displayed on the surface of the phagocyte

91
Q

What type of cells are responsible for cell mediated immunity

92
Q

Where are t cells produces

A

bone marrow `

93
Q

Where do t cells mature

A

the thymus

94
Q

What type of cells can t cells work on

A

body cells only (phagocytes, host body cells, b cells)

95
Q

Whats the first step of t cell action

A

Clonal selection

96
Q

What happens in the clonal selecction of t cells

A

The t cell with the complementary receptor is identified

97
Q

What happens in the proliferation of t cells

A

the chosen t cell is replicated during mitosis

98
Q

What three types of cells can t cells differentiate into

A

t memory, t helper, t cytotoxic

99
Q

What is the role of a t memory cell

A

secondary immune response

100
Q

What is the role of a t helper cell

A

stimulates phagocytosis and b cell proliferation

101
Q

What is the role of a t cytotoxic cells

A

destroys infected cells

102
Q

What types of cells are used in humoral immunity

103
Q

what type of cells do b cells interact with

104
Q

What happens in the clonal selection of b cells

A

the b cell with the complementary antibody to the antigen of the pathogen is identified

105
Q

What happens in the proliferation of b cells

A

the antigen is processed and displayed by the help of t helper cells

106
Q

What can b cells differentiate into

A

b memory and b plasma cells

107
Q

What do b memory cells do

A

Help with immunity during future infection by producing b plasma cells

108
Q

What do b plasma cells do

A

produce antibodies

109
Q

What 2 regions are found in an antibody

A

Variable (where the antigen binds) and constant

110
Q

What two types of chains are found in antibodies

A

Heavy and light chain

111
Q

What does the hinge region allow

A

the binding of more than one antigen at once

112
Q

What type of bonds are found within the antibody

A

disulfide bridges

113
Q

Why are disulfide bridges important in the antibody

A

They are in the tertiary structure so determine the shape if the protein and make them complementary to a specific antigen

114
Q

What is agglutination

A

where multiple antibodies bind to multiple antigens to form a clump

115
Q

Why is agglutination important

A

It makes a structure that is too large to enter the cell and makes it easier for phagocytes to engulf and destroy pathogens

116
Q

What is neutralisation

A

When an antibody-antigen complex is formed to prevent the cell from entering

117
Q

What occur when there is a secondary exposure to a pathogen

A

Antibodies are produced faster and in greater numbers

118
Q

What is a vaccine

A

A substance containing one or more antigens of a pathogen to stimulate an immune response

119
Q

What are the two types of immunity

A

active and passive

120
Q

What is passive immunity

A

Uses only antibodies and is a short term response

121
Q

What is active immunity

A

Where the person is exposed to the pathogen or antigen directly (long term response)

122
Q

What are the two types of active immunity

A

Natural and artificial

123
Q

What is natural immunity

A

when a person is exposed to the pathogen in normal circumstances

124
Q

What is artificial immunity

A

The basis of vaccination

125
Q

What does a successful vaccination programme need

A
  1. Economical sustainability
  2. Little side effects
  3. means of production and transport
  4. Means of administration`
126
Q

What are the ethical implications of vaccination

A
  1. use of animals
    2.side effects
  2. not everyone wants to be vaccinated
127
Q

What is herd immunity

A

Vast majority being vaccinated to reduce the spread of a pathogen