2.1.1: Cell structure Flashcards

1
Q

Outline how a student could prepare a temporary mount of tissue for a light microscope.

A
  1. Obtain thin section of tissue e.g. using ultratome or by maceration.
  2. Place plant tissue in a drop of water.
  3. Stain tissue on a slide to make structures visible.
  4. Add coverslip using mounted needle at 45° to avoid trapping air bubbles.
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2
Q

Describe how light microscopes work.

A
  1. Lenses focus rays of light and magnify the view of a thin slice of specimen.
  2. Different structures absorb different amounts and wavelengths of light.
  3. Reflected light is transmitted to the observer via the objective lens and eyepiece.
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3
Q

Describe how a transmission electron microscope (TEM) works.

A
  1. Pass a high energy beam of electrons through a thin slice of specimen.
  2. More dense structures appear darker since they absorb more electrons.
  3. Focus image onto fluorescent screen or photographic plate using magnetic lenses.
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4
Q

Describe how a scanning electron microscope (SEM) works.

A
  1. Focus a beam of electrons onto a specimen’s surface using electromagnetic lenses.
  2. Reflected electrons hit a collecting device and are amplified to produce an image on a photographic plate.
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5
Q

Describe how a laser scanning confocal microscope

works.

A
  1. Focus a laser beam onto a small area on a sample’s surface using objective lenses.
  2. Fluorophores in the sample emit photons.
  3. Photomultiplier tube amplifies the signal onto a detector. An image is produced pixel by pixel in the correct order.
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6
Q

How should the field of view in microscopy be

recorded?

A

Draw a diagram with a sharp pencil. Do not use sketchy lines or shading.

Include a scale bar.

Annotate visible structures.

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7
Q

State an equation to calculate the actual size of a

structure from microscopy.

A

actual size = image size/magnification

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8
Q

Define magnification and resolution.

A

Magnification: factor by which the image is larger than the actual specimen.

Resolution: smallest separation distance at which 2 separate structures can be distinguished from one another.

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9
Q

Why do samples need to be stained for light

microscopes?

A

Coloured dye binds to the structures.
Facilitates absorption of wavelengths of light to produce image.
Differential staining: contrast between heavily & lightly stained areas distinguishes structures.

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10
Q

State the magnification and resolution of a compound optical microscope.

A

magnification: x 2000
resolution: 200 nm

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11
Q

State the magnification and resolution of a TEM.

A

magnification: x 500 000
resolution: 0.5 nm

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12
Q

State the magnification and resolution of an SEM.

A

magnification: x 500 000
resolution: 3 - 10 nm

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13
Q

Explain how to use an eyepiece graticule and stage micrometer to measure the size of a structure.

A
  1. Place micrometer on stage to calibrate eyepiece graticule.
  2. Line up scales on graticule and micrometer. Count how many graticule divisions are in 100μm on the micrometer.
  3. Length of 1 eyepiece division = 100μm / number of divisions.
  4. Use calibrated values to calculate actual length of structures.
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14
Q

Describe the structure of the nucleus.

A

● Surrounded by a nuclear envelope, a semipermeable double membrane.
● Nuclear pores allow substances to enter/exit.
● Dense nucleolus made of RNA & proteins assembles ribosomes.

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15
Q

Describe the function of the nucleus.

A

● Contains DNA coiled around chromatin into chromosomes.
● Controls cellular processes: gene expression determines specialisation & site of mRNA transcription, mitosis, semiconservative replication.

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16
Q

Describe the structure and function of the endoplasmic reticulum (ER).

A

Cisternae: network of tubules & flattened sacs
extends from cell membrane & connects to nuclear envelope:
● Rough ER: many ribosomes attached for protein synthesis & transport.
● Smooth ER: lipid synthesis.

17
Q

Describe the structure and function of the Golgi

apparatus.

A

Planar stack of membrane-bound, flattened sacs, cis face aligns with rER. Molecules are processed in cisternae. Vesicles bud off trans face via exocytosis
● Modifies & packages proteins for export.
● Synthesises glycoproteins.

18
Q

Describe the structure and function of ribosomes.

A

Formed of protein & rRNA.

Have large subunit which joins amino acids & small subunit with mRNA binding site.

19
Q

Describe the relationship between the organelles

involved in the production and secretion of proteins.

A

The ribosomes that synthesise proteins are attached to the rER. The Golgi apparatus, which modifies proteins for secretion, aligns with the rER.

20
Q

Describe the structure of a mitochondrion.

A

● Surrounded by double membrane.
● Folded inner membrane forms cristae: site of electron transport chain.
● Fluid matrix: contains mitochondrial DNA, respiratory enzymes, lipids, proteins.

21
Q

Describe the structure of a chloroplast.

A

● Vesicular plastid with double membrane.
● Thylakoids: flattened discs stack to form grana; contain photosystems with chlorophyll.
● Intergranal lamellae: tubes attach thylakoids in adjacent grana.
● Stroma: fluid-filled matrix.

22
Q

State the function of mitochondria and chloroplasts.

A

● Mitochondria: site of aerobic respiration to produce ATP.

● Chloroplasts: site of photosynthesis to convert solar energy to chemical energy.

23
Q

Describe the structure and function of a lysosome.

A

Sac surrounded by single membrane embedded H+ pump maintains acidic conditions contains digestive hydrolase enzymes.
Glycoprotein coat protects cell interior:
● digests contents of phagosome
● exocytosis of digestive enzymes

24
Q

Describe the structure and function of a plant cell wall.

A

● Made of cellulose microfibrils for mechanical support.
● Plasmodesmata form part of apoplast pathway to allow molecules to pass between cells.
● Middle lamella separates adjacent cell walls.

25
Q

What are bacterial and fungal cell walls made of?

A

bacteria: peptidoglycan (murein)
fungi: chitin

26
Q

Describe the structure and function of centrioles.

A

● Spherical group of 9 microtubules arranged in triples.
● Located in centrosomes.
● Migrate to opposite poles of cell during prophase & spindle fibres form between them.

27
Q

Describe the structure and function of the

cell-surface plasma membrane.

A

‘Fluid mosaic’ phospholipid bilayer with extrinsic & intrinsic proteins embedded.
● Isolates cytoplasm from extracellular environment.
● Selectively permeable to regulate transport of substances.
● Involved in cell signalling / cell recognition.

28
Q

Explain the role of cholesterol, glycoproteins & glycolipids in the cell- surface membrane.

A

● Cholesterol: steroid molecule connects phospholipids & reduces fluidity.
● Glycoproteins: cell signalling, cell recognition (antigens) & binding cells together.
● Glycolipids: cell signalling & cell recognition.

29
Q

Describe the structure and function of flagella.

A

● Hollow helical tube made of the protein flagellin.

● Rotates to propel (usually unicellular) organism.

30
Q

Describe the structure and function of cilia.

A

● Hairlike protrusions on eukaryotic cells.

● Move back and forth rhythmically to sweep foreign substances e.g. dust or pathogens away / to enable the cell to move.

31
Q

Why is the cytoskeleton important?

A

● Provides mechanical strength.
● Aids transport within cells.
● Enables cell movement.

32
Q

Compare eukaryotic and prokaryotic cells.

A

Both have:
● cell membrane
● cytoplasm
● ribosomes

33
Q

Contrast eukaryotic and prokaryotic cells.

A

Prokaryotic:

  • small cells & always unicellular
  • no membrane-bound organelles & no nucleus
  • circular DNA not associated with proteins
  • small ribosomes (70S)
  • binary fission - always asexual reproduction
  • cellulose cell wall (plants)/ chitin (fungi)
  • capsule, sometimes plasmids & cytoskeleton

Eukaryotic:

  • larger cells & often multicellular
  • always have organelles & nucleus
  • linear chromosomes associated with histones
  • larger ribosomes (80S)
  • mitosis & meiosis - sexual and/or asexual
  • absent in animal cells, in plants they are made of murein (also known as peptidoglycan)
  • no capsule, no plasmids, always cytoskeleton