SB1. Key Concepts - Microscopes and Enzymes Flashcards

1
Q

SB1a - How do you calculate Actual Size?

A

Image Size / Magnification

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2
Q

SB1a - How do you calculate total magnification in a light microscope?

A

Objective Lens x Eyepiece Lens

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3
Q

SB1a - List 3 differences between Light and Electron Microscopes

A
  • Electron microscopes produce a much higher resolution image due to the shorter wavelength of electrons
  • Light Microscopes can show a true colour whereas electron microscopes will show a black and white image since electrons don’t have a colour spectrum
  • Light microscopes can use a live specimen whereas electron microscopes have to use dead specimens due to electrons having to pass through a vacuum
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4
Q

SB1a - Draw SI Units Table

A
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5
Q

SB1a - What 2 things determine how good a microscope is at showing small details?

A
  • Magnification: How much it can zoom in
  • Resolution: The smallest distance between two distinctly different points
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6
Q

SB1a - What has the development of the electron microscope allowed us to do?

A

It has allowed us to see sub-cellular structures as they have a much more powerful resolution and magnifcation

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7
Q

SB1b CP - How do you use use a microscope?

A
  • Put a thin sample of tissue (e.g. onion epidermis) onto a microscope slide
  • Add a few drops of a suitable stain/dye (e.g. iodine), so that the sample can be seen
  • Place a coverslip on top of the tissue and place the slide onto the microscope stage.
  • Use the objective lens with the lowest magnification, and focus on the sample.
  • Increase the magnification and refocus to see different features of the cell.
  • If you record the image you see, note down the magnification it was taken at

Option 2: You microhope you’re doing it right

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8
Q

SB1e - What are enzymes and what are they made up of made up of?

A
  • Enzymes are biological catalysts that speed up reactions.
  • They break down proteins/substances called substrates.
  • Enzymes are made up of amino acids and they are proteins.
  • They are needed to speed up reactions we cannot live without
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9
Q

SB1e - What are the three main nutrient based enzymes? Where are they found and what do they do?

A
  • Amylase: Found in saliva. breaks down starch into Sugar
  • Protease: Found in the stomach, breaks down proteins into amino acids
  • Lipase: Found in the stomach and pancreas, breaks down lipids into fatty acids and glycerol
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10
Q

SB1e - What is a polymer?

A
  • A polymer is a chain of single substances called monomers.
  • The formation of a polymer is called synthesis.
  • Enzymes often break down polymers into monomers
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11
Q

SB1f CP - What tests are used to identify main components in food?

  • Starch
  • Proteins
  • Lipids
  • Sugars
A
  • Starch: Iodine will go from yellow to blue-black
  • Proteins: Biruet’s solution will go from blue to purple
  • Lipids: Add ethanol and shake - a white emulsion-fatty layer should form if it is present
  • Sugars: Benedict’s solution while heating which will turn anywhere from green to yellow to red, indicating how much sugar is present This is a semi-quantitative test. It mostly gives non-measurable values
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12
Q

SB1f- How can we use a calorimeter?

A
  • Burn a known mass of the food under a boiling tube filled with a known volume of water.
  • Calculate the change in temperature of the water.
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13
Q

SB1g - How do enzymes work?

A
  • Each type of enzyme is in a shape that is specific to their substrate.
  • They can be re-used as long as they don’t become denatured
  • The idea that an enzyme bonds with a specific substrate is the lock-and-key mechanism
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14
Q

SB1g - What is the function of the active site of an enzyme?

A

The active site is unique to an enzyme so each enzyme can only work on specific substrates and is where the substrate must be for anything to take place

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15
Q

SB1g - What is the lock and key model?

A
  • The lock and key model is a model of how enzymes work - it compares enzyme action to a lock and key because of how the substrate and active site fit together
  • When the substrate binds to the active site, it forms the Enzyme-Substrate complex.
  • After the enzyme catalyses the reaction, the products are released because they no longer fits tightly into the active site
  • The enzyme is free to be used again
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16
Q

SB1g- How are enzymes denatured?

A
  • Changes in pH and temperature can affect the shape of an enzymes active site.
  • When the active site can no longer accept any substrates, it is said to have become denatured.