Cell Biology Flashcards

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1
Q

What was the importance of the electron microscope in cytology?

A

-Electrons have a much shorter wavelength than light. -Therefore produces images with a better resolution.

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2
Q

What is the resolution (resolving power) of a microscope?

A

-Ability to discern detail. -Can be expressed as the smallest distance between 2 objects that can be distinguished as separate.

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3
Q

What is the magnification (linear mag) of a microscope?

A

-size of an image compared to the size of the object.

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4
Q

what is the equation of magnification?

A

MAG = length of image/length of object

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5
Q

What can a light microscope do?

A

-can magnify to an unlimited extent -image becomes bigger and more blurred, without showing extra detail (poor resolution).

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6
Q

What does an electron microscope use?

A
  • beam of electrons instead of light. - e(-) have shorter wavelength (0.004nm) -Can achieve useful magnifications of up to x500,000
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7
Q

What are the limitations of electron microscope?

A
  • prep procedures - strength of the lenses.
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8
Q

What is TEM, and how does it work?

A

-Transmission electron microscope -work by sending a beam of e(-) through a very thin slice of material, creating a 2D image -to produce constrast, the material is stained by heavy metals that will scatter the e(-).

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9
Q

What is SEM, and how does it work?

A

-Scanning e(-) microscopes -creates 3D images by bouncing e(-) off the surface of a material that has been coated with a heavy metal. -magnification is less compared to TEM (x20,000)

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10
Q

1 micrometer …

A

= 0.001mm =10 to the power of -3 mm (1 mm = 1000 micrometers)

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11
Q

1 nanometer…

A

= 0.001 micrometer = 10 to the power of -3 micrometers (1 micrometer = 1000 nanometer)

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12
Q

what is the average animal cell diameter?

A

15 micrometer

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13
Q

what is the average red blood cell diameter?

A

7 micrometers 7000 nanometers 7 to the power of -6 metres

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14
Q

what is the cell ultrastructure?

A

refers to the structure as seen with the e(-) microscope.

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15
Q

where are organelles visible?

A

in the cytoplasm of the cell

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16
Q

what is structure and function of nucleus

A

-contains the chromosomes, is surrounded by a nucleus envelope with pores. -Also contains the nucleolus. -The DNA on the chromosomes controls the cell by controlling protein synthesis.

17
Q

what is structure and function of nucleolus

A

-Darker stained (denser) area within the nucleus. - site of synthesis of rRNA

18
Q

what is structure and function of cell membrane

A
  • A phospholipid bilayer, which associated proteins etc. - It surrounds the whole cell. -controls movement of substances in and out of the cell.
19
Q

what is structure and function of ribosomes

A
  • small particles containing proteins and RNA. -protein synthesis
20
Q

what is structure and function of rough endoplasmic rectiumulm (RER)

A
  • membrane systems with associated ribosomes. -they run through the cytoplasm and form flatterned sacs. -synthesis (on the ribsosmes) and transport of proteins within the cell.
21
Q

what is structure and function of smooth endoplasmic recticulum (SER)

A
  • Membrane systems without ribosomes, forming sacs and tubules. - synthesis and transport of lipids and steroids.
22
Q

what is structure and function of Glogi appartus?

A

-dense systems of membranes and sacs, with associated vesicles. -site of modification of proteins (e.g. synthesis of glycoproteins) and packaging them into vesicles (e.g. secretion from the cell) or formation of lysosomes.

23
Q

what is structure and function of Lysosomes

A

-membrane bound compartments, containing hydrolytic enzymes. - digestion and destruction of worn out organelles or particles taken into cell by phagocytosis.

24
Q

what is structure and function of mitochondria

A

-rod shaped structures, surrounded by a double membrane: inner membrane is founded into cristae. -site of aerobic respiration: Krebs’ cycle (in the matrix) and oxidative phosphorylation (on cristae).

25
Q

what is structure and function of centrioles

A

-cylindrical structures formed from nine groups of protein microtubules. NOT PRESENT IN PLANT CELLS. -concerned in the organisation of the spindle during cell division.

26
Q

what is structure and function of cytoplasmic matrix

A
  • the background material of the cell cytoplasm. - mostly water, containing proteins, ions (Na+, K+, Cl-) and other solutes. - many chem reactions occur here. (e.g. the glycolytic pathways of anaerobic respiration).
27
Q

what are eukaryotic cells

A

-animal and plant cells are relatively large with complex internal structures and a TRUE MEMBRANE BOUND NUCLEUS.

28
Q

what are prokaryotic cells

A

bacterial cells, they are simpler.

29
Q

what are the main differences in prokaryotic cells

A

-no true nucleus or nuclear envelope. The genetic material is free in the cytoplasm= nucleoid. -fewer organelles, no membranous organelles such as endoplasmic reticulum or Golgi. -ribosomes are present, but they are smaller. -genetic material is in the form of a single circular strand of DNA (NOT A TRUE CHROMOSOME), plus smaller rings of DNA in the cytoplasm= PLASMIDS. -Cell wall, but not made of cellulose- made of peptidoglcans. Sometimes the cell wall is surrounded by a protective capsule. -the whole cell is SMALLER (around 1 micrometer) -some bacteria have pili (for attachments) and a flagellum (for movement), but these are not always present.

30
Q

what is cell fractionation and the benefits

A

-cells are broken up and the different types of organelles are separated from each other. -we can get a suspension containing a single type of organelle, which can be further investigated by e.g. chemical analysis.

31
Q

what is homogenisation

A

-the process of breaking up cellular material e.g. in a blender. -this is done in a with the material immersed in 1. An ice cold (so enzymes stop working), 2. Isotonic (so organelles don’t swell or shrink due to osmotic effects), 3. Buffer (to maintain pH at the correct level) solution.

32
Q

what is differential centrifugation

A
  • the homogenate (mixture) is filtered and spun at progressively higher and higher speeds. -the larger/denser organelles sediment first (forming a pellet at the bottom). -the supernatant (liquid part) is then poured off, and centrifuged at a higher speed. -the next largest organelles then sediment out as a new pellet. -this can be repeated at higher and higher speeds, to give different fractions containing different cell components. -the different fractions can then be subjected to analysis: e.g. identifying chem composition, or looking for tracer chemicals.
33
Q

what is the order of cell components separated during the differential centrifugation process

A
  1. nuclei= 500rpm, force of 600g 2. mitochondria, lysosomes= force of 15,000g 3. fragments of ER and cell membrane= 50,000 rpm 4. ribosomes= force of 300,000g 5. cytoplasmic matrix and its soluble components.
34
Q

what are the units svedberg (S)

A

that rate at which the particles sediment out in centrifiguation

35
Q

what is chromatography and the process

A

-separates out the chemicals in a mixture so they can be identified. -A mixture is placed onto a background material (e.g. onto paper or gel). -A solvent moves through this background material, drawing the components of the mixture with it, -the components of the mixture are separated according to their solubility in the solvent and their affinity for a background. Different substances move different distances.