Module 2: Section 1 - Cell Structure Flashcards

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1
Q

Plant cells have the all the same organelles as animals cells, but with a few added extras. What are these extras?

A
  • a cell wall with plasmodesmata (‘channels’ for exchanging substances with adjacent cells)
  • a vacuole (compartment that contains cell sap)
  • and of course good old chloroplasts
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2
Q

What is the function of a plasma membrane?

A

Regulates the movement of substances into and out of the cell. It also has receptor molecules on it, which allow it to respond to chemicals like hormones.

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3
Q

Describe a plasma membrane.

A

The membrane found on the surface of animal cells and just inside the cell wall of plant cells and prokaryotic cells. It’s made of mainly lipids and protein.

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4
Q

What is the function of a cell wall?

A

Supports plant cells

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5
Q

What is the function of the nucleus?

A

The nucleus controls the cell’s activities (by controlling the transcription of DNA). DNA contains instructions to make proteins. The pores allow substances (e.g) RNA to move between the nucleus and the cytoplasm. The nucleolus makes ribosomes.

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6
Q

What is the function of a lysosome?

A

Contains digestive enzymes. These are kept separate from the cytoplasm by the surrounding membrane, and can be used to digest invading cells or to break down worn out components of the cell.

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7
Q

What is the function of a ribosome?

A

The site where proteins are made.

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8
Q

What is the function of RER?

A

Folds and processes proteins that have been made at the ribosomes.

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9
Q

What is the function of SER?

A

Synthesises and processes lipids.

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10
Q

What is the function of a vesicle?

A

Transports substances in and out of the cell (via the plasma membrane) and between organelles. Some are formed by the Golgi apparatus or the endoplasmic reticulum, while others are formed at the cell surface.

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11
Q

What is the function of the Golgi apparatus?

A

It processes and packages new lipids and proteins. It also makes lysosomes.

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12
Q

What is the function of the mitochondrion?

A

The site of aerobic respiration, where ATP is produced. They’re found in large numbers in cells that are very active and require a lot of energy.

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13
Q

What is the function of a chloroplast?

A

The site where photosynthesis takes place. Some parts of photosynthesis happen in the grana, and other parts happen in the stroma (a thick fluid found in chloroplasts).

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14
Q

What is the function of a centriole?

A

Involved with the separation of chromosomes during cell division.

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15
Q

What is the function of cilia?

A

The microtubules allow the cilia to move. The movement is used by the cell to move substances along the cell surface.

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16
Q

What is the function of flagellum?

A

The microtubules contract to make the flagellum move. Flagella are used like outboard motors to propel cells forward. (e.g. when a sperm cell swims)

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17
Q

Describe flagellum

A

Flagella on eukaryotic cells are like cilia but longer. They stick out from the cell surface and are surrounded by the plasma membrane. Inside they’re like cilia too - two microtubules in the centre and nine pairs around the edge.

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18
Q

Describe cilia

A

Small, hair-like structures found on the surface membrane of some animal cells. In cross-section, they have an outer membrane and a ring of nine pairs of protein microtubules inside, with two microtubules in the middle.

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19
Q

Describe centriole

A

Small, hollow cylinders, made of microtubules (tiny protein cylinders). Found in animal cells, but only some plant cells.

20
Q

Describe a chloroplast

A

A small, flattened structure found in plant cells. It’s surrounded by a double membrane, and also has membranes inside called thylakoid membranes. These membranes are stacked up in some parts of the chloroplast to form grana. Grana are linked together by lamellae - thin, flat pieces of thylakoid membrane.

21
Q

Describe a mitochondria

A

They’re usually oval-shaped. They have a double membrane - the inner one is folded to form structures called cristae. Inside is the matrix, which contains enzymes involved in respiration.

22
Q

Describe the Golgi apparatus

A

A group of fluid-filled, membrane-bound, flattened sacs. Vesicles are often seen at the edges of the sacs.

23
Q

Describe a vesicle

A

A small fluid-filled sac in the cytoplasm, surrounded by a membrane.

24
Q

Describe a SER

A

Similar to a RER, but with no ribosomes

25
Q

Describe a RER

A

A system of membranes enclosing a fluid-filled space. The surface is covered with ribosomes

26
Q

Describe a ribosome

A

A very small organelle that either floats free in the cytoplasm or is attached to the RER. It is made up of proteins and RNA. It’s not surrounded by a membrane.

27
Q

Describe a lysosome

A

A round organelle surrounded by a membrane, with no clear internal structure.

28
Q

Describe a nucleus

A

A large organelle surrounded by a nuclear envelope (double membrane), which contains many pores. The nucleus contains chromatin (which is made from DNA and proteins) and a structure called the nucleolus.

29
Q

Describe a cell wall

A

A rigid structure that surrounds plant cells. It’s made mainly of the carbohydrate cellulose.

30
Q

Give six steps of how organelles work together to produce a protein

A

1) proteins are made at the ribosomes
2) the ribosomes on the RER make proteins that are excreted or attached to the cell membrane. The free ribosomes in the cytoplasm make proteins that stay in the cytoplasm.
3) new proteins produced at the rough ER are folded and processed (e.g sugar chains are added) in the rough ER
4) then they’re transported from the ER to the Golgi apparatus in vesicles
5) at the Golgi apparatus, the proteins may undergo further processing (e.g sugar chains are trimmed or more are added)
6) the proteins enter more vesicles to be transported around the cell. e.g. glycoproteins (found in mucus) move to the cell surface and are secreted

31
Q

The organelles in cells are surrounded by the cytoplasm. The cytoplasm is more than just a solution of chemicals though - it’s got a network of protein threads running through it. These protein threads are called the cytoskeleton. How are the protein threads arranged in eukaryotic cells?

A

In eukaryotic cells the protein threads are arranged as microfilaments (small solid strands) and microtubules (tiny protein cylinders)

32
Q

What are the four main functions of the cytoskeleton?

A

1) the microtubules and microfilaments support the cell’s organelles, keeping them in position
2) they also help to strengthen the cell and maintain its shape
3) as well as this, they’re responsible for the movement of materials within the cell. For example, the movement of chromosomes when they separate during cell division depends on contraction of microtubules in the spindle
4) the proteins of the cytoskeleton can also cause the cell to move. For example, the movement of cilia and flagella is caused by the cytoskeletal protein filaments that run through them. So in the case of single cells that have a flagellum (e.g sperm cells), the cytoskeleton propels the whole cell

33
Q

How can microtubules and microfilaments be prevented from functioning?

A

The assembly of microtubules and microfilaments, and the movement of materials along them, requires energy from respiration. So microtubules and microfilaments can be prevented from functioning using respiratory inhibitors.

34
Q

How do you view prokaryotic cells and why?

A

Prokaryotes like bacteria are roughly a tenth the size of eukaryotic cells. This means that normal microscopes aren’t really powerful enough to look at their internal structure. So, bacterial cells have to be seen under an electron microscope.

35
Q

What is the formula for calculating magnification?

A

magnification = image size/object size

36
Q

Define magnification

A

Magnification is how much bigger the image is than the specimen

37
Q

Define resolution

A

Resolution is how detailed the image is. More specifically, it’s how well a microscope distinguishes between two points that are close together. If a microscope lens can’t separate two objects, then increasing the magnification won’t help.

38
Q

Tell me three things about light microscopes

A

1) light microscopes use light
2) they have a lower resolution than electron microscopes - they have a maximum resolution of about 0.2 micrometres. So they’re usually used to look at whole cells or tissues
3) the maximum useful magnification of a light microscope is about x 1500

39
Q

Tell me four things about Laser Scanning Confocal Microscopes

A

1) Laser Scanning Confocal Microscopes use laser beams to scan a specimen, which is usually tagged with a fluorescent dye
2) The laser causes the dye to fluoresce - give off light. This light is then focused through a pinhole onto a detector. The detector is hooked up to a computer, which generate an image. The image can be 3D
3) The pinhole means that any out-of-focus light is blocked, so these microscopes produce a much clearer image that a normal light microscope
4) They can be used to look at objects at different depths in thick specimens

40
Q

Electron microscopes use electrons instead of light to form an image. They have a higher resolution than light microscopes so give more detailed images. What are the two kinds of electron microscope and how do they work?

A

1) transmission electron microscope (TEM) - use electromagnets to focus a beam of electrons, which is then transmitted through the specimen. Denser parts of the specimen absorb more electrons, which makes them look darker on the image you end up with. TEMs are good because they provide higher resolution images (so they can be used to look at a range of organelles) but they can only be used on thin specimens.
2) scanning electron microscope (SEM) - scan a beam of electrons across the specimen. This knocks off electrons from the specimen, which are gathered in a cathode ray tube to form an image. The images produced show the surface of the specimen and can be 3D. But they give lower resolution images than TEMs.

41
Q

What is the maximum resolution and maximum magnification of a light microscope/TEM and SEM?

A

light microscope: max r = 0.2 micrometres / max m = x1500

TEM: max r = 0.0002 micrometres / max m = can be more than x1000000

SEM: max r = 0.002 micrometres / max m = usually less than x500000

42
Q

In light microscopes and TEMs, the beam of light (or electrons) passes through the object being viewed. An image is produced because some parts of the object absorb more light (or electrons) than others.

Sometimes the object being viewed is completely transparent. This makes the whole thing look white because the light rays (or electrons) just pass straight through. How would you get past this problem?

A

To get round this, the object can be stained:

  • for the light microscope, this means using some kind of dye. Common stains include methylene blue and eosin.
  • the stain is taken up by some parts of the object more than others - the contrast makes different parts show up.
  • different stains are used to make different things show up. For example, eosin is used to stain cell cytoplasms. Methylene blue stains DNA.
  • more than one stain can be used at once
43
Q

How do you stain a sample for an electron microscope?

A

For the electron microscope, objects are dipped in a solution of heavy metals (like lead). The metal ions scatter the electrons, again creating contrast - some parts of the object show up darker than others.

44
Q

How do you prepare a microscope slide for a dry mount?

A
  • your specimen needs to let light through it for you to be able to see it clearly under the microscope. So if you’ve got a thick specimen, you’ll need to take a thin slice to use on your slide
  • use tweezers to pick up your specimen and put it in the middle of a clean slide
  • pop a cover slip on top
45
Q

How do you prepare a microscope for a wet mount?

A
  • start by pipetting a small drop of water onto the slide. Then use the tweezers to place your specimen on top of the water drop
  • to put the cover slip on, stand the slip upright on the slide, next to the water droplet. Then carefully tilt and lower it so it covers the specimen. Try not to get any air bubbles under there - they’ll obstruct your view of the specimen
  • once the cover slip is in position, you can add a stain. Put a drop of stain next to one edge of the cover slip. Then put a bit of paper towel next to the opposite edge. The stain will get drawn under the slip, across the specimen.

NB: wet mounts are good for looking at tiny organisms that live in water