Studying Cells Flashcards

1
Q

Define Homogenisation

A

Homogenisation
Breaking of cells

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2
Q

What happens after Homogenisation of cells in ‘ Cell Fractionation ‘

A

Placed in cold , isotonic , buffered solution

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3
Q

Why are samples of cells placed in a cold solution ?

A

To stop/ prevent enzyme activity

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4
Q

Why are samples of cells placed in a buffered solution ?

A

To prevent denaturing of enzymes / proteins

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5
Q

Define the term ‘ Isotonic ‘

A

Water potential inside cell is equal to the water potential outside the cell

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6
Q

Why are samples of cells placed in an isotonic solution ?

A

Prevent osmotic damage to organelles

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7
Q

What might happen to cells as a result of not being placed in an isotonic solution ?

A

Hypertonic solution - Water moves out of cell, shrivelling cell
Hypotonic Solution - Cell swells, Bursts (Animal cells) or becomes Turgid ( Plant Cells )

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8
Q

Where must you blend / homogenise the cells ?

A

In the cold, isotonic , buffered solution

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9
Q

Why is the solution of homogenised cells filtered before ultracentrifugation ?

A

Separate large debris that hadn’t been separated in homogenisation

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10
Q

What happens in the first step of ultracentrifugation ?

A

Centrifuge is spun at a slower speed
Most dense organelles gather as a ‘ pellet ‘ at the bottom

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11
Q

What is the solution inside the centrifuge known as ?

A

The supernatant

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12
Q

Why are optical microscopes unable to view sub-cellular structures ?

A

Resolution is too low
Due to longer wavelength of light

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13
Q

Describe how to test for a non-reducing sugar ?

A

Boil with acid
Neutralise
Heat with benedicts solution
Form brick red colour in high quantities of sugar

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