Practical 1 - effect of temp on enzymes Flashcards

1
Q

what is a buffer solution

A

Solution that resists any change in PH

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2
Q

how to calculate mitotic index

A

number of dividing cells/ Total umber of cells

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3
Q

why was a root tip used in RP2

A

where dividing cells are/growing occurs/ mitosis is

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4
Q

why was a stain used on the root tip cells in RP2

A

To stain the DNA + so we can see the chromosomes clearly and determine what stage there in

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5
Q

why was the root tip firmly squashed in RP2

A

To let light through / thin layer + so optical microscope can work

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6
Q

Why would another investigation on a different garlic root tip provide different results/Mitotic index ?

A

Different time of day

Different type of garlic species

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7
Q

equation for percentage change in mass

A

change in mass / original mass x 100

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8
Q

what is the advantage of giving results as percentage change in RP3

A

Change in mass is comparative despite different starting masses

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9
Q

why does taking additional readings increase reliability of a investigation

A

reduce effect of anomalies / can identify anomalies

find a mean

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10
Q

on a graph of percentage mass change against concentration of salt solution how do you find the water potential of inside the potato - RP3

A

Where the line of best fit meets the x axis/ there is no change in mass at that conc of solution + the water potential inside the potato cells

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11
Q

what is a colorimeter

A

measures absorbance of light in a liquid

the higher the absorbance of the light the more concentrated the solution

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12
Q

what type of graph is used to convert absorbance values into concentration values in RP4

A

calibration curve

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13
Q

describe the aseptic techniques required to transfer bacteria onto agar plate - RP6

A
  • Flame neck of bottle
  • use sterilised pipette
  • open lid of agar plate facing Bunsen burner
  • use Spreader in ethanol to spread round
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14
Q

In RP6 why is the agar plate with bacteria kept at 25 C in incubator and not higher

A

lower temp avoids pathogenic bacteria growing

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15
Q

how to calculate Rf value

A

distance travelled by pigment / distance travelled by solvent

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16
Q

Why does DCIP change colour in RP8

A

Accepts electrons relseased in LDR that would go to reduce NADP

Reduced DCIP goes from blue to colourless

17
Q

why does Methylene Blue turn colourless in RP9

A

Methylene Blue accepts electrons that are transported in aerobic respiration

the reduced form of Methylene blue is colourless

18
Q

how do you use the calibration curve in RP11 to determine glucose concentrations of unknown samples

A
  • using the line of best fit find where the absorbance values of the unknown samples are