Cell Structure, Cell Cycle and Microscopy Flashcards

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1
Q

Which organelles are found in an animal cell?

A

A typical animal cell has:
- cell surface (plasma) membrane
- rough endoplasmkc reticulum
- smooth endoplasmkc reticulum
- nucleus
- mitochondria
- cytoplasm
- ribosomes
- Golgi apparatus
- lysosomes

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2
Q

Which organelles are found in a plant cell?

A

A typical plant cell has:
- cell surface membrane
- cellulose cell wall
- chloroplasts
- rough endoplasmic reticulum
- smooth endoplasmic reticulum
- plasmodesmata
- mitochondria
- Golgi apparatus
- permanent vacuole
- ribosomes
- nucleus
- cytoplasm

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3
Q

What is the structural difference between a plant cell and an algal cell?

A

Algal cells have all the same organelles as plant cells and have cellulose cell walls, but they often have one large chloroplast instead of many smaller chloroplasts. Algal cells also tend to be more circular in shape compared to a plant cell.

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4
Q

What is the structural difference between a fungal cell and a plant cell?

A

Fungal cells are similar to plant cells, except that their cell walls are made of chitin, not cellulose and they don’t have chloroplasts because they don’t photosynthesise.

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5
Q

What is the difference between eukaryotic and prokaryotic cells?

A

Eukaryotic cells have a nucleus, whereas prokaryotic cells do not have a nucleus.

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6
Q

What is the ultrastructure of a cell?

A

It is the detailed structure of the cell that can only be seen at high magnification (it can only be viewed with an electron microscope).

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7
Q

What are the main components of a mitochondrion?

A
  • outer membrane
  • inner membrane
  • inter-membrane space
  • cristae
  • matrix
  • ribosomes
  • DNA
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8
Q

What is the function of the double membrane and the inter-membrane space?

A

The double membrane controls the entry and exit of substances into and out of the mitochondrion. The inner membrane is folded to form cristae (extensions). The double membrane forms two aqueous compartments called the inter-membrane space and the matrix.

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9
Q

What is the function of cristae?

A

Cristae are extensions of the inner membrane, which provide a large surface area for the attachment of enzymes and other proteins involved in respiration.

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10
Q

What is the function of the matrix?

A

The matrix is the inner aqueous compartment of the mitochondrion, which contains proteins, lipids, ribosomes and DNA that allows the mitochondria to control the production of their own proteins. Many enzymes involved in respiration are found in the matrix.

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11
Q

What is the function of mitochondria?

A

Mitochondria are the sites of the aerobic stages of respiration (Krebs cycle and the oxidative phosphorylation pathway). They are responsible for the production of ATP, from respiratory substances such as glucose. Therefore, there is a high number of mitochondria in metabolically active cells, which require lots of ATP, such as muscle cells.

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12
Q

What is the structure of a ribosome?

A

Ribosomes are small organelles which consist of a large and a small subunit. They are made up of proteins and RNA and are not surrounded by a membrane.

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13
Q

What is the function of ribosomes?

A

Ribosomes may float freely in the cytoplasm or be associated with the RER. There are two types (80S - found in eukaryotic cells and 70S - found in prokaryotic cells, mitochondria and chloroplasts). 70S are smaller. Ribosomes are the site of protein synthesis.

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14
Q

What is the structure and function of the rough endoplasmic reticulum?

A

The RER is a system of membranes enclosing a fluid-filled space, which has ribosomes on the surface. Its functions are to provide a large surface area for the synthesis of proteins and glycoproteins and to provide a pathway for the transport of materials, especially proteins, throughout the cell.

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15
Q

What is the structure and functions of the smooth endoplasmic reticulum?

A

The SER is a system of membranes enclosing a fluid- filled space (similar to RER but without ribosomes). The functions of the SER are to synthesise, store, and transport lipids and carbohydrates.

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16
Q

What is the structure and function of the Golgi apparatus?

A

The Golgi apparatus consists of a stack of membranes that make up flattened sacs called cisternae, with small, hollow, rounded structures called vesicles. Proteins and lipids produced by the ER are passed through the Golgi apparatus in sequence. The Golgi modifies the proteins, often adding non-protein components, such as carbohydrates, to them. Proteins and lipids are also sorted and transported to vesicles which are pinched off from the ends of the Golgi cisternae.

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17
Q

What are the functions of the Golgi apparatus and vesicles?

A
  • add carbohydrate to proteins to form glycoproteins
  • produce secretory enzymes, such as those secreted by the pancreas
  • secrete carbohydrates, such as those used to make call walls
  • transport, modify and store lipids
  • form lysosomes
    Main function of apparatus is to process and package lipids and proteins. Main function of vesicles of to store proteins and lipids modified by the Golgi apparatus and transport them out of the cell.
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18
Q

How are lysosomes formed?

A

Lysosomes are formed from the budding off of the Golgi body, and as such, contains proteases and lipases found in the Golgi, which were originally made in the endoplasmic reticulum. They also contain lysozymes, which are enzymes which hydrolyse the cell walls of certain bacteria.

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19
Q

What are the functions of lysosomes?

A

Lysosomes are responsible for:
- hydrolysing material ingested by phagocytic cells, such as white blood cells and bacteria
- releasing enzymes to the outside of the cell (exocytosis), in order to destroy material around the cell.
- digest worn-out organelles so that the useful chemicals they are made out of can be reused.
- completely break down cells after they have died (autolysis)

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20
Q

What are centrioles?

A

Centrioles are paired barrel-shaped organelles located in the cytoplasm of animal cells near the nuclear envelope. Most animal cells have two centrioles, which can only be seen with an electron microscope.

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21
Q

What is the function of centrioles?

A

The functions of centrioles are to:
- play a role in facilitating the reproduction of cells
- engage in the arrangement of mitotic spindles during cell division (ensuring equal separation of chromosomes between daughter cells)
- aids in cytokinesis
- organises microtubules in the cell’s cytoplasm (which acts as a part of the cytoskeleton and keeps all organelles in place).

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22
Q

What are the main components of chloroplasts?

A

The components of chloroplasts include:
- chloroplast envelope
- grana and thylakoids (lamellae)
- stroma
- 70S ribosomes and circular DNA

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23
Q

What is the structure and function of the chloroplast envelope?

A

The chloroplast envelope is a double plasma membrane that surrounds the organelle. It is highly selective about what it allows to enter and leave the chloroplast, and as such, controls the movement of substances.

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24
Q

What is the structure and function of grana and lamellae?

A

Grana are stacks of disc-like structures called thylakoids, within which is the photosynthetic pigment chlorophyll. Some grana have tubular extensions called lamellae (singular lamella), which join up with adjacent grana. The grana is where light absorption for photosynthesis occurs.

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25
Q

What is the structure and function of the stroma?

A

The stroma is a fluid-filled matrix within which the second stage of photosynthesis takes place (synthesis of sugars). A number of other structures can be found within the stroma, such as starch grains.

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26
Q

What is the function of 70S ribosomes and circular DNA within chloroplasts?

A

The circular DNA within chloroplasts contains the basic genes for producing chloroplasts (thus allowing their replication). 70S ribosomes produce rubisco (important in the light-independent part of photosynthesis) and thylakoids (which contain chlorophyll).

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27
Q

What is the tonoplast and what are its functions?

A

The tonoplast is the membrane surrounding the permanent vacuole in plant cells. It separates the vacuolar components from the cell’s cytoplasm, which allows for the isolation of potential harmful materials within the vacuole. The tonoplast also regulates the movement of ions within the cell.

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28
Q

What is the vacuole and what are its functions?

A

The vacuole is a membrane-bound organelle, which contains a solution of mineral salts, sugars, amino acids, wastes and pigments like anthocyanins. The functions of the vacuole include the storage of the listed materials, the isolation of metabolic waste that might be harmful to the cell, the maintenance of turgor pressure (keeping the cell turgid), which helps maintain the rigidity of the cell and the plant. The sugars and amino acids may act as a temporary food store, while the pigments may colour petals to attract pollinating insects.

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29
Q

What are the components of a plant cell wall?

A

Plant cell walls consist of microfibrils of cellulose, embedded in a matrix. There is a thin layer, called the middle lamella, which marks the boundary between adjacent cell walls and joins them together.

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30
Q

What are the functions of the cell wall in plants?

A

The cell wall:
- provides mechanical strength to prevent the cell bursting under the pressure created by the osmotic entry of water
- gives mechanical strength to the plant as a whole
- allows water to pass along it so contributes to the movement of water throughout the plant

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31
Q

Which materials make up the cell walls of plants, algae and fungi?

A
  • plants - cellulose
  • algae - either cellulose, glycoproteins, or a mixture of both
  • fungi - chitin (nitrogen-containing polysaccharide), glycan (polysaccharide) and glycoproteins.
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32
Q

What are the main components of the nucleus?

A

The components of the nucleus include:
- nuclear envelope
- nuclear pore
- nucleoplasm
- chromosomes
- chromatin
- nucleolus

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33
Q

What is the structure and function of the nuclear envelope?

A

The nuclear envelope is a double membrane surrounding the nucleus. Its outer membrane is continuous with the ER of the cell and often has ribosomes on its surface. It controls the entry and exit of materials into and out of the nucleus and contains the reactions taking place within it.

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34
Q

What are nuclear pores and what is their function?

A

Nuclear pores are channels in the nuclear envelope, which allow the passage of large molecules, such as mRNA, out of the nucleus. There are around 3000 pores per nucleus, each around 40-100 nm in diameter.

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35
Q

What is the nucleoplasm and what is its function?

A

The nucleoplasm is the granular, jelly-like substance which makes up the bulk of the nucleus. It is a suspension substance for the organelles inside the nucleus and helps to maintain the shape and structure of the nucleus. It plays an important role in the transportation of materials which are vital to cell metabolism and function. It also helps facilitate processes such as DNA replication and transcription.

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36
Q

What are chromosomes and what is their function?

A

Chromosomes are thread- like structures found in the nucleus of plant and animal cells, consisting of a DNA molecule and its associated proteins. Chromosomes carry hereditary genetic information from one generation of cells to the next (ensuring accurate cell replication), and carry the DNA that codes for proteins.

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37
Q

What is the structure and function of chromatin?

A

Chromatin is a complex of DNA and protein found in the nucleus of eukaryotic cells (it is a chain of nucleosomes), and is responsible for the packaging and condensing of long sections of DNA into more compact, denser structures, which are able to fit into the tight space of the nucleus. Chromatin also facilitates DNA replication, repair and transcription.

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38
Q

What is the structure and function of the nucleolus?

A

The nucleolus is a spherical structure found in the cell’s nucleus, which manufactures ribosomal RNA and assembles ribosomes. There may be more than one nucleolus within a nucleus.

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39
Q

What are the functions of the nucleus as a whole?

A

The nucleus:
- acts as a control centre of the cell through the processes of mRNA and tRNA production, and hence, protein synthesis
- retains the genetic material of the cell in the form of DNA and chromosomes
- manufacture ribosomal RNA and ribosomes

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40
Q

How do you prepare a temporary mount (optical microscope slide)?

A
  1. pipette a small drop of water onto the centre of the glass slide (suspends the specimen between the slide and the coverslip and makes the image clearer)
  2. use forceps to place a thin section of specimen on top of the water (must be thin to let light through)
  3. add a drop of a stain to highlight certain organelles/substances (e.g. eosin stains cytoplasm, iodine in potassium iodide stains starch grains)
  4. use a mounted needle to lower a coverslip onto the specimen slowly (this ensures no air bubbles form, which would obstruct the view of the specimen). The coverslip ensures the specimen doesn’t move and protects it from contamination from the environment. It also protects the lens of the microscope, to stop it coming into contact with the specimen.
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41
Q

How do you prepare a slide for an electron microscope?

A

To prepare a slide for an electron microscope, a sample must undergo primary and secondary fixation, dehydration, resin infiltration and embedding and sectioning and mounting sections on specimen grids. Glass or diamond knives are needed to cut the specimen thin enough. Don’t need to know specific detail, just that electron microscopy is much more time-consuming and difficult to prepare for, due to the necessity for much thinner specimens.

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42
Q

What are microscope artefacts?

A

Artefacts are things that you can see looking down a microscope that aren’t part of the cell or specimen you’re looking at. They can be dust, air bubbles or fingerprints etc. and are created during the preparation of the slide.

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43
Q

Which type of microscopy produces the most artefacts?

A

Electron microscopy produces more artefacts than light microscopy as the slide preparation is so much more complex, which is a limitation of its use.

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44
Q

What are the two types of electron microscope?

A

Transmission electron microscopes (TEM) and scanning electron microscopes (SEM)

45
Q

How do light (optical) microscopes work?

A

Optical microscopes use light to form an image. A light source emits light, which is passed through a condenser. This creates a thin but concentrated ray of light which passes through the specimen. The light spreads out again but is focused by the glass objective lens ad again by the ocular lens, which produces an image for the viewer to see.

46
Q

How do electron microscopes (TEM) work?

A

An electron gun emits pulses of electrons, which are focused by electromagnets onto the specimen. In TEM, the electrons are passed through the specimen and focused by more electromagnets through a glass objective lens, allowing the viewer to see the image. Denser parts of the specimen absorb more electrons, so appear darker.

47
Q

How do electron microscopes (SEM) work?

A

SEM is similar to TEM except that the electrons don’t pass through the specimen, they scan the surface of the specimen. The way SEM works is that a beam of electrons is scanned across the specimen, which knocks off electrons from the specimen, which are gathered in a cathode ray tube to form an image.

48
Q

What is magnification?

A

Magnification is the number of times larger an image appears compared to its actual size.

49
Q

What is resolution?

A

Resolution is the ability to distinguish between two points (smallest distance between two points that can still be viewed as two separate points).

50
Q

What are the differences between TEM and SEM?

A
  • TEM transmits electrons through the specimen, while SEM scans the surface of the specimen with electrons.
  • TEM forms an image by focusing the beam of electrons using electromagnets, while SEM collects electrons which have been knocked off the specimen in a cathode ray tube to form an image
  • In TEM, denser parts of the specimen appear darker as they absorb more electrons, while in SEM, the density of various parts of the specimen is not shown
  • TEM gives 2D images while SEM gives 3D images
  • TEM shows the ultrastructure of cells and organelles but SEM shows the overall 3D shape
  • TEM has a higher resolution than SEM, so shows smaller objects.
  • TEM requires thinner specimens than SEM
  • TEM images are black and white, while SEM can show colour (it may be false colour)
51
Q

What are the differences between light and electron microscopes?

A
  • optical uses light to form an image, electron uses electrons to form an image
  • optical uses glass lenses to focus light, electron uses electromagnets to focus electrons
  • it is easier to prepare slides for optical microscopy than electron microscopy, and as such electron microscope images are more likely to contain artefacts.
  • electron requires much thinner specimens than optical
  • optical microscopes have a maximum resolution of 0.2 micrometers, while electron has 0.0002 micrometres.
  • maximum useful magnification of optical is x1500, electron is x1500000
  • therefore, electron microscopes can be used to view smaller organelles in greater detail, such as ribosomes, centrioles and lysosomes
  • optical shows colour while electron usually doesn’t (if it does it is often false colour)
  • optical can be used on living specimens, while electron can only be used on dead/dehydrated specimens due to the use of a vacuum.
52
Q

What is the equation for magnification?

A

magnification = image size/actual size (assuming the units are the same for both)

53
Q

What is an eyepiece graticule/eyepiece micrometer?

A

It is a piece of glass with a scale consisting of 100 divisions on it, which can be placed in the eyepiece of a microscope to measure the size of a specimen. Eyepiece units are not a true scale, as they change their value depending on magnification.

54
Q

What is a stage micrometer?

A

A stage micrometer is a microscope slide with an accurate scale on it. It is often 10mm in length, with each division representing 0.1mm. When aligned with the eyepiece graticule, it can be used to calculate the actual value of 1 epu at a certain magnification, which can be used to calculate the actual size of specimens.

55
Q

What is the formula for finding the value of 1 epu (eyepiece unit) at a particular magnification?

A

1 epu = stage micrometer units (smu) / eyepiece units (epu)

56
Q

What is the conversion from mm to micrometres?

A

1mm = 0.001 um

57
Q

How would you calibrate a microscope and calculate an actual size of a specimen using a microscope?

A
  1. place the micrometer eyepiece into the eyepiece of the microscope
  2. place the stage micrometer slide onto the stage of the microscope at the desired objective lens
  3. align the eyepiece graticule and stage micrometer units to calculate the value of 1 epu at that objective lens
  4. remove the stage micrometer from the stage of the microscope and add the specimen slide that you want to measure to the stage
  5. measure epu of the specimen and calculate actual size by multiplying the number of epu by the calculated actual value of 1 epu.
58
Q

How do you calculate actual size of a specimen from an image of it?

A

Measure the scale bar in mm, then convert to um. Divide image size of scale bar (measured length) by actual size of the scale bar (as stated in the image) to get the magnification factor. Measure the length/width of the structure you are asked to measure then divide this image size by the magnification factor to get the actual size of the structure.

59
Q

How do you use an optical microscope?

A
  • clip the slide to the stage
  • select the lowest-power objective lens
  • use the coarse focusing knob to bring the stage up to just below the objective lens
  • use the coarse focusing knob to move the stage downwards until the image is roughly in focus
  • adjust the focus with the fine adjustment knob until you get a clear image
  • to get a greater magnification, swap to a higher power objective lens and refocus
60
Q

How do you do a scientific drawing?

A

Draw what you see in the microscope without using shading, and use continuous lines (no feathering). Include a scale bar and labels, but don’t cross over label lines.

61
Q

What is cell fractionation?

A

Cell fractionation is a technique which separates organelles according to their density, enabling different organelles to be viewed under a microscope and their ultrastructure to be studied.

62
Q

What are the main steps of cell fractionation?

A
  1. Homogenisation (breaking up the cells)
  2. Filtration (removing large pieces of debris)
  3. Ultracentrifugation (separating organelles)
63
Q

What is homogenisation and how can it be achieved?

A

Homogenisation is the process by which cells are broken up. It can be done by vibrating the cells or by grinding them in a blender, which breaks up the plasma membrane and releases the organelles into solution. The solution must be ice cold, to reduce the activity of enzymes that may damage the organelles. The solution should be isotonic (same concentration of chemicals as outside the cell), which prevents damage to the organelles by osmosis. A buffer solution is added to maintain a constant pH.

64
Q

What is filtration (in the context of cell fractionation) and what does it achieve?

A

Filtration is when the homogenised cell solution is filtered through a gauze to separate large cell debris, such as connective tissue, from the organelles. The organelles are much smaller than the debris, so can pass through the gauze.

65
Q

What is ultracentrifugation and what does it achieve?

A

Ultracentrifugation is when the solution of organelles is poured into a tube and spun at low speed in a centrifuge. The heaviest organelles, like nuclei, are flung to the sides and form a sediment at the bottom of the pellet. The rest of the organelles stay suspended in the fluid above the sediment - the supernatant. The supernatant is drained off and poured into another tube. It is spun in the centrifuge again at higher speed. The next heaviest organelles form a pellet at the bottom of the tube (chloroplasts, mitochondria). The supernatant is drained again and the process repeated at higher speeds to remove lighter organelles.

66
Q

Which order are organelles removed in during ultracentrifugation?

A

Organelles are removed from heaviest to lightest, which is nuclei, chloroplasts, mitochondria, lysosomes, endoplasmic reticulum, ribosomes.

67
Q

What is the supernatant in ultracentrifugation?

A

The supernatant is the solution above the sediment, containing lighter organelles than those removed.

68
Q

What is the pellet in ultracentrifugation?

A

The pellet is the sediment at the bottom of the centrifuge tube containing heavy organelles removed by the spinning of the tube.

69
Q

What are the biggest differences between eukaryotic and prokaryotic cells?

A

Prokaryotic cells are much smaller than eukaryotic cells (often 10-100 times smaller). Prokaryotic cells have circular DNA which lies free in the cytoplasm and extra plasmids, while eukaryotic cells have linear DNA which is contained in a nucleus. P cells have ‘naked’ DNA (not associated to his tones or RNA to form chromosomes), while E cells have DNA which is associated with histones to form chromosomes. P cells have 70S ribosomes (smaller) while E cells have 80S ribosomes (larger). P cells have few organelles and none which are envelope-bound. E cells have many organelles and many which are envelope-bound (e.g. nucleus, mitochondria, chloroplasts). P cells have rigid cell walls made of murein (a glycoprotein), while E cells have cellulose cell walls (plants), chitin cell walls (fungi). P have mesosomes (extensions of the cell membrane) to provide a surface for respiration, while E have mitochondria for aerobic respiration.

70
Q

What are the main components of a prokaryotic cell?

A

Always present:
- cell wall containing murein
- cell surface membrane
- cytoplasm
- circular DNA
- 70S ribosomes

Sometimes present:
- flagellum
- capsule
- mesosomes
- plasmids
- pili

71
Q

What is the function of the cell wall in prokaryotic cells?

A

The cell wall supports the cell and prevents it from changing shape. It’s made of murein, which is a glycoprotein, which is strong.

72
Q

What is the function of the cell surface membrane in prokaryotic cells?

A

The cell surface membrane is mainly made of lipids and proteins. It controls the movement of substances into and out of the cell.

73
Q

What is the function of the cytoplasm in a prokaryotic cell?

A

The cytoplasm is where many metabolic processes of the cell occur, and maintains cell shape. It also suspends the organelles.

74
Q

What is the function of ribosomes in prokaryotic cells?

A

The ribosomes in prokaryotic cells are 70S ribosomes, so are smaller than those found in eukaryotic cells. They do still carry out protein synthesis.

75
Q

What is the function of the circular DNA in prokaryotic cells?

A

The circular DNA in prokaryotic cells is free in the cytoplasm and not associated to histones, so doesn’t form chromosomes. The circular DNA stores genetic material and ensures continuity between generations of cells through DNA replication and codes for proteins.

76
Q

What is the function of plasmids in prokaryotic cells?

A

Plasmids are small loops of DNA that are separated from the main circular DNA molecule. They contain genes that can be passed between prokaryotes (e.g. genes for antibiotic resistance). They are not always present.

77
Q

What is the function of the capsule in prokaryotic cells?

A

The capsule is made of secreted slime and helps protect bacteria from drying out and from attack by cells of the immune system of the host organism. Not always present.

78
Q

What is the purpose of the flagellum in prokaryotic cells?

A

The flagellum is a long, hair-like structure that rotates, enabling the prokaryote to move. Some have more than one but they are not always present.

79
Q

What is the function of the pili in prokaryotic cells?

A

The pili are used for the attachment of the cell to other cells or surfaces and can be involved in sexual reproduction. Not always present

80
Q

What is the function of mesosomes in prokaryotic cells?

A

Mesosomes are infoldings of the cell surface membrane which may allow photosynthesis or to carry out nitrogen fixation. Not always present.

81
Q

What is an example of organelles working together within cells?

A

The exocytosis and production of enzymes and the production of cell surface glycoproteins are both examples of organelles working together within the acinar cells of the pancreas.

82
Q

What is exocytosis?

A

Exocytosis is the fusion of the secretory vesicles to the cell surface membrane, to release substances from inside the cell to the outside of the cell.

83
Q

Which organelles have to work together during the production and exocytosis of enzymes in the pancreas?

A
  • RER (ribosomes)
  • Golgi apparatus
  • Golgi vesicles
  • lysosomes
  • cell surface plasma membrane
84
Q

How are enzymes produced and secreted by a cell?

A

Amino acids pass from the blood into the cell via the plasma membrane. The amino acids are transported to ribosomes on the Rough Endoplasmic Reticulum (RER) by transfer RNA (tRNA). In the nucleus, transcription occurs, producing an mRNA strand which codes for the enzyme to be produced. The mRNA binds to ribosomes on the RER, initiating protein synthesis from amino acids. The newly synthesised polypeptide/protein enters the RER. Small transfer vesicles bud off the RER, carrying proteins and fuse with the Golgi apparatus. Proteins may be modified e.g. addition of carbohydrate groups and packaged as they move through the Golgi apparatus. Secretory vesicles e.g. lysosomes or Golgi vesicles bud off the Golgi apparatus. Proteins are now in the final structures e.g. glycoproteins or enzymes. Secretory vesicles move towards the membrane, sometimes they are stored. The secretory vesicles fuse to the plasma membrane to release enzymes into the digestive system (exocytosis).

85
Q

How do bacteria reproduce?

A

Bacteria reproduce via binary fission, which involves the replication of circular DNA and plasmids (if present) and the division of the cytoplasm to produce two daughter cells.

86
Q

Bacteria multiply exponentially - what does this mean?

A

This means that if a culture of bacteria increases by a factor of 2 in one generation, then the formula to find the number of cells (N) after one generation is N=N0 x 2^n, where N0 is the initial number at time zero, and n is the number of divisions or generations.

87
Q

What does it mean that viruses are acellular?

A

It means that viruses are not made up of cells, and as such, do not contain many organelles that cells often have.

88
Q

What does it mean that viruses are non-living?

A

Viruses are non-living because they can’t reproduce on their own, they need to take over the processes of a host cell in order to do this. Therefore, they are not classified as alive.

89
Q

What are the three main structures in a virus particle?

A
  • capsid (protein coat)
  • core of nucleic acids (DNA or RNA)
  • attachment proteins (e.g. glycoproteins)
90
Q

What does the capsid do?

A

Protects the nucleic acids from enzymes when outside host. Binds to host cell surface and assists in penetration of host and introduction of nucleic acid.

91
Q

What does the core of nucleic acids do in a virus particle?

A

The core of nucleic acids carries genetic information for the particle and allows viral proteins and nucleic acids to be replicated, enabling the production of more virus particles.

92
Q

What do virus particles sometimes have?

A

They sometimes have an external envelope derived from host plasma membrane. If it contains glycoproteins, spikes will form, allowing attachment to host. Some viruses also have enzymes within them (e.g. HIV has the enzyme reverse transcriptase within it).

93
Q

What is the classic shape of a bacteriophage?

A

Bacteriophages are viruses which infect bacteria. They have a polyhedral head and helical tail. They work by injecting their DNA into the host cell and getting the host cell to replicate them. The cell lyses (which kills it) and releases more virus particles to infect other cells.

94
Q

How are viruses classified?

A

Virus structures are classified as either helical, polyhedral or complex (polyhedral head, helical tail). The nucleic acid type is either DNA or RNA and the plasma membranes of host cells can be enveloped or naked.

95
Q

What are logarithm scales?

A

Logarithm scales show orders of magnitude in a linear fashion in which zero can never be reached. An example of a logarithmic scale would be 1 10 1000 10000 all equally spaced with graduation within them representing either one, ten, 100 or 1000 depending on what the section began with. The graduation get closer together as you move from right to left (towards the higher number).

96
Q

In multicellular organisms, can all cells continue to divide throughout their lifetimes?

A

No, only some cells retain their ability to divide throughout their lifetimes. Those than can divide show a cell cycle.

97
Q

What are the main stages of the cell cycle?

A

The main stages of the cell cycle in the order that they occur are:
- interphase
- mitosis (nuclear division)
- cell division (cytokinesis)

98
Q

What are the stages of interphase and what happens in each one?

A

In the order in which they occur:
- gap phase 1 - cell grows and new organelles and proteins are made
- synthesis - cell replicates its DNA, ready to divide by mitosis
- gap phase 2 - cell keeps growing and proteins needed for cell division are made
During interphase, normal cell activity occurs, but the cell’s DNA is unravelled and replicated, organelles are replicated and the ATP content is increased (as it is needed to provide energy for cell division)

99
Q

What is mitosis?

A

Mitosis is the stage of the cell cycle in which a eukaryotic cell divides to produce two identical daughter cells, each with identical copies of DNA produced by the parent cell during DNA replication.

100
Q

What is the purpose of mitosis?

A

Mitosis is needed for the growth of multicellular organisms and for repairing damaged tissues.

101
Q

Describe the structure of chromosomes.

A

When mitosis begins, the chromosomes are made of two strands of DNA called chromatids held together by a centromere. Two strands on the same chromosome are sister chromatids. Two identical chromosomes which code for the same characteristics are homologous chromosomes.

102
Q

What are the stages of mitosis in order?

A
  • Prophase
  • Metaphase
  • Anaphase
  • Telophase
103
Q

What happens during prophase?

A

Chromosomes shorten and thicken by condensation, becoming visible as a result. Centrioles move to opposite poles of the cell. Protein microtubules radiate from each centriole, making the spindle fibres. Towards the end of prophase, the nuclear envelope disintegrates and the nucleolus disappears. Each chromosome exists as a pair of sister chromatids, joined by a centromere.

104
Q

What happens in metaphase?

A

In metaphase, the chromosomes attach to the spindle fibres at their centromeres and they align on the equator of the cell (spindle equator).

105
Q

What happens in anaphase?

A

The centromeres separate and divide into two. The spindle fibres shorten, due to the contraction of microtubules, which in turn, pull the chromatids to the poles, where the centromere leads first.

106
Q

What happens in telophase?

A

In telophase, the chromatids have reached opposite poles of the cell, so are now referred to as chromosomes. The chromosomes uncoil and lengthen, so are no longer visible. The spindle fibres break down and the nuclear envelope reforms. The nucleolus reappears.

107
Q

What happens during cell division (cytokinesis)?

A

Cytokinesis is the final stage of the cell cycle, in which the cytoplasm of the cell divides, forming two separate, genetically identical daughter cells. In reality, cytokinesis doesn’t happen after mitosis but it actually occurs during anaphase and telophase.

108
Q

What can cause cancer?

A

Cancer can be caused by uncontrolled mitosis. This may be a result of a genetic mutation. Many treatments of cancer focus on disrupting the cell cycle as a result, as this will stop the tumour from growing. Some drugs target G1 phase of interphase, as this prevents the synthesis of enzymes needed for DNA replication, meaning the cell can’t enter S phase and is forced to kill itself. Some drugs and radiation damage DNA, which causes the cell to kill itself.