required practical 1(enzyme reaction rates)

Questions from the examier

Graphical skills

Could be asked to plot a graph

Sharp pencil for accurate plotting

Dependant variable of the y-axis (The rate of reaction) Quantity of product made or substrate hydrolysed / time

Straight line and ruler to join up points

Indipendant variable on the x-axis (The pH) no units of measure becuase it is pH

The scale would have to be linear.

Scale: s-1 if measuring in seconds

y=mx+c

y= y-axis read off, m is the gradient, x is the x-axis read off, c is the y intersect

rate= change in volume / change in time (cm3s-1)

AT= A Tangent which means you draw a tangent from whatever point is said in the question

Plotting a graph needs to cover more than half the paper

Tables

Look for significant figures and make sure they are all the same

Don't put units in the table they will already be in the header

C.S.M.R

C= Change

S= Same

The pH

Temperature

Things we change- The independant variable

Enzyme

Substrate

Control variable- Things we keep the same

Constant temperature water bath leave in water bath unitl an equilibrium is reached

M= Meaure

Things we measure- The dependant variable

R= Repeat

Relaible accurate mean value

Uncertainties

Resolution (precision)

Is the smallest unit you can measure to or that the intrement can make

  1. eg. Ruler- 23mm is 23+- 0.5 mm (+- half of the smallest unit)
  1. measuring error at the start + error at the end = 23+-1mm

percentage uncertainty

(uncertainty / measurement) x 100

23+-1mm = (1 / 23) x 100

Reapeat readings

(Look on VLE)

Statistical tests and the null hypothesis

Spearman's rank correlation coefficent

t- test

chi2 test

Compares 2 mean values

Catergories. Eg. bule eyes green eyes, Brown hair, Black hair

Bar Charts are related to catergories

Association

null hypothesis

Null = no difference between or no corrolation

Compare calculated value to critical value

If the caluclated is larger than the critical then there is a significant difference and you reject the null hypothesis as there is a significant difference or corrolation

If there is a significant difference

There is a less than 5% probability that the difference or corrolation is due to chance

If the caluculated is less than the critical then there is not a significant difference and you accept the null hypothesis as there is no significant difference or corrolation

If there isnt a significant difference

There is a more than 5% probability that the difference or corrolation is due to chance

Topic links

Digestion

Lipid digestion- Glycerol and 2 fatty acids

Dipeptidases

Endodipeptidases

Amalase

Maltase

Lipase

DNA

DNA and protein sythesis

Proteins and enzymes

Enzyme substrate complexes

The active site of the enzyme has a specific 3D teritiary structure

ATP

Enzymes in membranes

Channel protein acts as an enzyme to join beta gluecose molecules to form cellulose

Proteins in membranes

Ribosomes and organelles

Exocytosis

DNA helicase

DNA polymerase

Inhibitors

Competitve and non competitive inhibitors

Channel proteins

Golgi Apparatus packages proteins