as snab biology core practicals

7/21/2019 AS SNAB Biology Core Practicals

1/35

Compiled by Stafford Valentine Redden 1

CORE PRACTICAL ONEDescribe how the effect of caffeine on heart rate in Daphnia can be investigated practically, anddiscuss whether there are ethical issues in the use of invertebrates.

Daphnia, the water flea, is a small freshwater crustacean which lacks physiological methods ofmaintaining a constant body temperature. This means that if the environmental temperature changes, itsbody temperature does so too and its metabolic rate will be expected to rise or fall accordingly. So thetemperature of the organism must be kept constant during the procedure.

In this investigation we shall test the hypothesis that as the concentration of caffeine changes, theheartbeat rate (cardiac frequency) of Daphnia also changes. Fortunately Daphnia is relativelytransparent and its heart can be seen quite easily under the low Power of the microscope.

Setting up the experiment1. Select a large specimen and, with a pipette, transfer it to the centre of a small, dry Petri dish. With filterpaper remove excess water from around the specimen so that itis completely stranded.2. With a seeker place a small blob of silicone grease onto the floor of the Petri dish. Then wipe theneedle clean and use it to gently push the posterior end of the animal into the grease so that it is firmlyanchored. Now fill the Petri dish with water at 300C.3. Place the Petri dish on the stage of a microscope and observe the animal under low Power. The figureabove shows the position of the heart, watch itbeating. Don't confuse the beating of the heart with theflapping of the legs.4. Surround the animal with a circular heating coil and fix it in position as shown in the figure below. Also

clamp a small mercury thermometer, or the temperature probe of a digital thermometer, into position.

Estimating thecardiac frequency

A convenient way of doing this is to time how long it takes for the heart to beat 50 times. If it is beatingtoo frequently for every beat to be counted, make a mark on a piece ofpaper every tenth beat. Doseveral practice runs to get used to the technique when you feel ready, proceed as follows:Replace the distilled water in the Petri dish with caffeine solutions of concentration 1mol dm -3at 30C.Estimate the cardiac frequency.

Switch on the heater so that the water gradually warms up. If the temperature of the water rises toorapidly, switch off the heater and, if necessary, add a few ice chippings. Estimate the cardiacfrequency at caffeine concentrations of 2 mol dm-3, 3 mol dm-3, 4 mol dm-3, 5 mol dm-3and 6 mol dm-3,noting the temperature each time.


2/35


Present your results in a table and. if you have sufficient readings, draw a graph of the cardiacfrequency as a function of the caffeine concentration.

Ethical issues in the use of invertebratesAnimals are often used for research to enhance scientific knowledge. Monkeys are commonly used forbrain research, dogs are used in behavioural experiments, rabbits and mice are often dissected inlaboratories, mice and fruit flies are used in genetic research, etc. Is it cruel and unfair to utilise theseorganisms for research? The issue is very controversial and the ethical guidelines vary from country tocountry and person to person. In the UK it is considered ethical to use invertebrates, such as Daphniain

scientific studies, for the following reasons: Daphnia has reduced awareness of painbecause of the lackof a well developed nervous system. It is transparent and its heart is visible without the need fordissection. Daphnia is abundant in nature and there is no threat to it or its dependent species (foodchains). Some people also feel that it is bred for fish food and will thus die anyway. Daphnia canreproduce asexually and may be clones, therefore there is no loss of genetic variation.

Factors to be controlled- Size of daphnia- Habitat from which daphnia is obtained- Temperature of the surrounding- Oxygen concentration of the water surrounding the daphnia

If daphnia is treated with a chemical,- The volume and concentration of the chemical should be controlled- The duration of exposure to the chemical should be controlled- Time should be allowed for acclimatisation

SAQ1.Sam studied the effect of varying the concentration of the stimulant drug caffeine on heart rate.She chose to use the water flea, Daphnia, for ethical reasons. In her study, Sam attempted to keep thetemperature of the various caffeine solutions constant. As an extension of this work, she decided toinvestigate the effect of temperature on heart rate in more detail. In this new investigation Sam used asmall glass chamber which could hold the Daphnia and water at a set temperature. The whole apparatuscould be placed under a microscope so that the Daphnia heart could be seen. She videoed four Daphnia

at each of five different temperatures for 30 seconds. She used a slow motion replay of the video to countthe number of heart beats in 30 seconds for each Daphnia at each temperature. Her data are summarisedin the table below:

(a) (i) State and explain one ethical reason why Sam chose to use Daphnia for this investigation.(ii) Suggest one reason for her choice of maximum temperature (30 C) and one reason for her choice ofminimum temperature (5 C) used. (2)(iii) In her investigation, how did Sam try to ensure the reliability of her data? (1)(iv) Which aspect of her investigation was improved when Sam decided to video the Daphnia? (1)(b) (i) Calculate the mean heart rate in beats per minute for each temperature. Write your answers in the

spaces provided in the table. Show your working in the space below. (3)


3/35


4/35


Daphnia has a heart which pumps fluid around its body. This fluid has a higher solute concentration thanthe freshwater that Daphnia lives in.The table below gives four statements concerning transport in Daphnia. If a statement is correct, place atick (J) in the box to the right of that statement and if a statement is incorrect, place a cross ( x ) in the box.

(b) A student investigated the effect of caffeine on the heart rate of Daphnia. Three different Daphnia wereused,A, B and C. The table below shows her results at the end of the investigation.

Daphnia Caffeineconcentration/

arbitrary units

Duration ofobservation/ seconds

Number ofheart beats counted

A 5 10 50

A 5 10 53

A 5 10 47

B 10 10 73

B 10 10 76

B 10 10 76

C 15 10 101

C 15 10 99

C 15 10 100

(i) Calculate the mean number of heart beats per 10 seconds for each DaphniaDaphnia A .............................. heart beats per 10 secondsDaphnia B .............................. heart beats per 10 seconds

Daphnia C .............................. heart beats per 10 seconds

(ii) Use your answers from (i) above to predict the mean number of heart beats in 10 seconds for anotherDaphnia placed in a caffeine concentration of 35 arbitrary units. (1)

Statements about transport in Daphnia Tick or cross

(i) The movement of fluid through the heart is an example of mass transport

(ii) Daphnia uses diffusion to transport oxygen into muscle cells

(iii) Daphnia tends to lose water to the freshwater by osmosis

(iv) Daphnia can use active transport to move ions from the freshwater into its body


5/35


(iii) Suggest three reasons why the prediction you made for (ii) above may not be very reliable. (3)(Total 9 marks) SNAB Unit 1 Jan 2008

SAQ4.(a) Daphnia heart rate increases when Daphnia are given the stimulant, caffeine. A student usedthis knowledge to estimate the caffeine content of three drinks. To do this she set up a calibration curve.Initially, she placed one Daphnia in pond water with no caffeine and counted the number of its heart beatsin one minute. She found this to be 180. She then placed the Daphnia in pond water with 10 mg ofcaffeine per 100 cm3of pond water and recorded the time taken for 180 heart beats. This was repeatedfor several different caffeine concentrations and the results are shown in the calibration curve below. Allmeasurements were taken at 15 0C.

The student now repeated the study, using the same Daphnia and keeping the temperature at 15 0Cthroughout, but with instant coffee as the source of caffeine. She recorded the time taken for 180 heartbeats to occur. She then repeated this using the two other drinks. The results are shown in the tablebelow. Use the calibration curve to complete the third column of the table.

(b) By using the same Daphnia throughout the investigation, the student was able to control certainvariables that could have affected her results. Give three variables that the student controlled by using thesame Daphnia. (3)(c) At the end of the investigation the student removed the Daphnia from the tea and placed it in pondwater. She then recorded its heart rate and found it to be 190 beats per minute. Suggest two reasons why

the Daphnia heart rate was higher at the end of the investigation compared to the 180 beats per minute atthe start. (2) (Total 8 marks) SNAB Unit one


6/35


CORE PRACTICAL TWO

Describe how to investigate the vitamin C content of food and drink.PROCEDUREAdd Vitamin C solution of a known concentration (CONCA), drop by drop, with a pipette, to 2 cm

3of theDCPIP (blue) solution in a test tube. Shake the tube gently after the addition of each drop and continue toadd drops until the DCPIP solution is decolourised. Record the exact volume of vitamin C (VOLA) youadded. Repeat the procedure and calculate the mean volume.

Repeat the procedure with the fruit juice, containing vitamin C at unknown concentration (CONCB).Record the volume of juice (VOLB) required to decolourise 2 cm

3of the same concentration of DCPIP

solution.Note:If only one or two drops of fruit juice are required to decolourise DCPIP, dilute the juice five timesand try again.Using the same technique, compare the vitamin C contents of different food and drinks.Use the equation below to estimate the concentration of vitamin C in the fruit juices.

CONCB= (VOLAX CONCA) / VOLB

VOLA = Volume of vitamin C solution in mlCONCA= Concentration of vitamin C solution in mg ml

-1VOLB= Volume of fruit juice in mlCONCB= Concentration of vitamin C in fruit juice in mg ml

-1

SAQ5Vitamin C is a water-soluble vitamin which is found in foods of plant origin. It is unstable andeasily destroyed.An investigation was carried out into the effects of boiling on the vitamin C content of somevegetables. The vitamin C content of each of the vegetables was determined in their raw state andafter boiling.The results are shown in the table below.

(a) Complete the table below to make a reliable comparison of the effect of boiling on the vitamin Ccontent on each vegetable. (2)(b)(i) Describe how the vitamin C content of the fresh vegetables could be determined. (4)(ii) State threeprecautions which would need to be taken when carrying out the investigation yourdescribed in (b) (i) (3)(c) Suggest two ways, other than boiling, in which vitamin C may be lost from fresh fruit andvegetables. (2) [Total 11 marks]

SAQ6. Give an account of an experiment you could carry out to investigate the effect of storage timeon the ascorbic acid (vitamin C) content of fresh orange juice. [Total 10 marks]


7/35


SAQ 7 Some students carried out an investigation into the effect or temperature on the vitamin C contentof orange juice. They extracted 600 cm3of orange juice from a batch of fresh oranges and divided it into100 cm3samples. Three samples were kept at 4 C and three samples were kept at 30 C. The vitamin Ccontent of each sample was measured immediately after extraction and then each day for the next fivedays.A copy of the entries in their laboratory notebook is shown below.

(a) (i) Prepare a table and organise the data in a suitable way so that the effect or temperature on thevitamin C content of orange juice can be displayed. (4 marks)(ii) Use the information in your table to present the information in a suitable graphical form. (4 marks)(b) What conclusions can be drawn from the results of this investigation? (2 marks)

(Total 10 marks)Factors to be controlled- Volume and concentration of DCPIP- Concentration of Vitamin C solution- Extent of shaking of the test tube with DCPIP must be standardised

During extraction of Vitamin C juice from fruits or vegetables,

- The mass of fruit or vegetable tissue and the volume of distilled water used for making a pulpmust be standardised.- The conditions of storage of the fruits and vegetables must be standardised.- The duration of storage (age) must also be standardised.


8/35


Note:A less reliable method would be to count the number of dropsof the vitamin C solution and juiceneeded to decolourise the DCPIP.

This method is less reliable because the size of drops could be highly variable in volume.CORE PRACTICAL THREE

Describe how membrane structure can be investigated practically, eg by the effect of alcoholconcentration or temperature on membrane permeability.

The colour of beetroot is due to the presence of a red pigment, anthocyanin, in the cell sap. You aregoing to investigate the effect of temperature on the selectively permeable membranes of beetroot.

SafetyTAKE CARE WITH CORK BORER AND MOUNTED NEEDLEMIND YOUR FINGERSWEAR GOGGLES ONCE THE BUNSEN BURNER IS LIT1. Use a cork borer to cut cylinders of fresh beetroot tissue. Place on a tile and cut into 3 mm wide discs.2. Place all the discs in a small beaker and wash under a running tap for at least 5 minutes.

3. Meanwhile, label the test tubes - 30C, 40C, 50C, 60C, 70C, 80C and 100C and use a graduatedpipette to add 6 cm3cold water to each.

4. Prepare a water bath using a large beaker, tripod and gauze and Bunsen burner.

5. Heat gently to 30C and remove the Bunsen burner.

6. Gently pick 6 beetroot discs with a forcep, one by one.7. Place the discs in the water bath for exactly 1 minute. Then drop them into the test tube labelled 30C.8. Leave the discs in the test tubes for at least 20 minutes.

9. Repeat the procedure for the other tubes.10. Shake the tubes, hold to the light and compare the colour of the liquids in each.11. If possible, use a colorimeter to compare the colours of each liquid.

SAQ8 Amir decided to investigate the permeability of beetroot cell membranes. Beetroots are rootvegetables. They appear red because their cells contain a water soluble red pigment in their vacuoles,which cannot pass through membranes. He carried out an experiment to investigate the effect oftemperature on the permeability of beetroot membrane. High temperature disrupts the structure of themembranes. Several beetroot discs were cut of equal dimensions. Each disc was rinsed in distilled water

and dried using absorbent tissue. One beetroot discs was then placed in a tube containing 25 cm3

of

distilled water and left for 30 minutes at 200

C. The procedure was repeated for temperatures of 300

C,

400C, 500C, 600C and 700C. After 30 minutes, each beetroot disc was removed from the water. The waterhad become red and the discs were slightly pink. Each coloured solution was stirred and a sampleremoved and placed in a colorimeter. The intensity of red coloration (absorbance) was determined by thecolorimeter. The experiment was repeated three times.The results of Amirs investigation are shown in the table below.

Temperature / oC Intensity of red colouration (absorbance) / Arbitrary units

Trial one Trial two Trial 3 Mean

20 0.2 0 0.1

30 0.4 0.3 0.3

40 0.5 0.6 0.6

50 0.9 1.0 1.160 1.6 1.6 1.7

70 1.8 1.6 1.8


9/35


a) i) Suggest why it was necessary to rinse the beetroot discs before they were added to the distilledwater. (1)ii) Suggest how the choice of temperatures could reduce the sensitivity of the results. (2)iii) Suggest a reason for the appearance of red colour in the distilled water at 20 0C. (1)iv) State how Amir ensured the reliability of his data. (2)v) Give one other way in which the reliability of the data can be increased. (1)b) Calculate the mean Absorbance in arbitrary units after 30 minutes for each temperature. Write youranswers in the spaces provided in the table. Show your working in the space below. (3)

c) Use these data to plot a fully-labelled graph to show the effect of temperature on the permeability of themembrane. (4)d) In order to get some idea of the validity of his data, Amir searched the Internet for similar studies. Hecould found similar studies that had used his method. He compared the results from one such study,shown in the following table, with his own.

Temperature (C) Mean Absorbance (arbitrary units)

20 0.0

25 0.2

30 0.3

35 0.4

40 0.7

45 1.250 1.8

55 1.8

60 1.8

i) State one similarity and one difference in the conclusions Amir could make about the effect oftemperature on permeability of the membrane, based on these two sets of data. (2)ii) Suggest one explanation for the similarity and one explanation for the difference you have given above.

(4)CHSE First Semester 2008

SAQ9 The diagram below shows the fluid mosaic model of the cell membrane. (2)

(a) Name the structures labeled A. B, C and D.(b) Describe two ways in which hydrophilic molecules, such as glucose, are able to pass through intactmembranes. (3)

(c) The graph below shows the results or an experiment to investigate the effect of temperature n thepermeability of beetroot cell membranes. The intensity of the color in the water surrounding the beetrootwas measured at the temperatures indicated oil the graph.


10/35


(i) Outline a procedure that you could have used to produce these results. (4)(ii) Explain the effect or the increase in temperature on the permeability of the membranes of beetroot

cells. (3) Total 12 marks SNAB Jan 2005

SAQ10Beetroots are root vegetables. They appear red because their cells contain a water soluble redpigment in their vacuoles, which cannot pass through membranes. An experiment was carried out toinvestigate the effect of alcohol on the permeability of beetroot membrane. Alcohol disrupt the structure ofthe membranes. Several beetroot discs were cut of equal dimensions. Each disc was rinsed in distilled

water and dried using absorbent tissue. Five beetroot discs were then placed in a tube containing 25 cm3

of 0.2% ethanol and left for 30 minutes at 200

C. The procedure was repeated for different concentrationsof ethanol and one set of discs was left in distilled water. After 30 minutes, each set of beetroot discs wasremoved from the solutions and from the water. The ethanol in each tube had become red and the discs

were slightly pink. There was no change in the colour of the discs in the water and the water remainedcolourless. The ethanol in each tube was stirred and a sample removed and placed in a colorimeter. Theintensity of red coloration (absorbance) was determined by the colorimeter. The results of the investigationare shown in the graph below.

a) Explain why the cell membrane is described as having a fluid mosaic structure. (2)b) Suggest why it was necessary to rinse the beetroot discs before they were added to the bile saltsolution. (1)


11/35


c) Describe the effect of increasing ethanol concentration on the intensity of the red colour (absorbance) ofthe solution. (3)d) Suggest an explanation for these results. (4)e) The experiment was repeated using a second beetroot. Suggest why the readings obtained might beslightly different from those for the first beetroot. (1) SVR CHSE 2009

Working of the colorimeter Cuvette contains pigment solution

Factors to be controlled

- The storage conditions and age of beetroot must be taken into account- The diameter and thickness of the discs must be standardised- The volume of water or ethanol in the test tube must be controlled- The number of discs in the test tube must be the same for all trials- The temperature of the water bath must be controlled- The duration of temperature or ethanol treatment must also be standardised- The volume of red pigment in the cuvette must be standardised- A blue filter must be used in the colorimeter during measurement of absorbance

CORE PRACTICAL FOURDescribe how enzyme concentrations can affect the rates of reactions and how this can beinvestigated practically by measuring the initial rate of reaction.

Investigating an enzyme controlled reaction: catalase and hydrogen peroxide concentration

ProcedureSAFETY: Wear eye protection and protect clothing from hydrogen peroxide. Rinse splashes of peroxide

and pureed potato off the skin as quickly as possible as it is an oxidising agent.

Investigationa Use the large syringe to measure 20 cm3pureed potato (pulp) into the conical flask.b Put the bung securely in the flasktwist and push carefully.

c Half-fill the trough, bowl or sink with water.d Fill the 50 cm3measuring cylinder with water. Invert it over the trough of water, with the open end

under the surface of the water in the bowl and with the end of the rubber tubing in the measuringcylinder. Clamp in place.


12/35


e Measure 2 cm3of hydrogen peroxide into the 2 cm3syringe. Put the syringe in place in the bung of theflask but do not push the plunger straight away.

f Check the rubber tube is safely in the measuring cylinder. Push the plunger on the syringe andimmediately start the stop clock.

g After 30 seconds, note the volume of oxygen in the measuring cylinder in a suitable table of results.h Empty and rinse the conical flask and measure another 20 cm 3pureed potato into it. Reassemble the

apparatus, refill the measuring cylinder, and repeat from dtogwith another concentration of hydrogenperoxide. Use a 100 cm3measuring cylinder for concentrations of hydrogen peroxide over 20 vol.

i Calculate the rate of oxygen production in cm3/ s.j Plot a graph of rate of oxygen production against concentration of hydrogen peroxide.

Enzyme Kinetics

This means measuring the rate of enzyme reactions.1. Firstly you need a signal to measure that shows the progress of the reaction. The signal shouldchange with either substrate (S) or product (P) concentration, and it should preferably be something thatcan be measured continuously. Typical signals include colour changes, pH changes, mass changes, gasproduction, volume changes or turbidity changes. If the reaction has none of these properties, it cansometimes be linked to a second reaction, which does generate one of these changes.

2. If you mix your substrate with enzyme and measure your signal, you will obtain a time-course.Ifthe signal is proportional to substrate concentration it will start high and decrease, while if the signal isproportional to product it will start low and increase. In both cases the time-course will be curved (actuallyan exponential curve).

3. How do you obtain a rate from this time-course? One thing that is not a good idea is to measure thetime taken for the reaction, for as the time-course shows it is very difficult to say when the reaction ends: itjust gradually approaches the end-point. A better method is to measure the initial rate - that is the initialslope of the time-course. This also means you don't need to record the whole time-course, but simply takeone measurement a short time after mixing.

4. Repeat this initial rate measurement under different conditions (such as different substrateconcentrations) and then plot a graph of rate vs.the factor. Each point on this second graph is taken froma separate initial rate measurement (or better still is an average of several initial rate measurementsunder the same conditions). Draw a smooth curve through the points.

Be careful not to confuse the two kinds of graph (the time-course and rate graphs) wheninterpreting your data.

An example oftime course measurement is shown in the SAQ below.

SAQ11 The total amount of product formed in an enzyme - controlled reaction was investigated at twodifferent temperatures, 55 C and 65 C. The results are shown in the graph.


13/35


a) (i) Explain how you would calculate the rate of the reaction at 55C over the first 2 hours of theinvestigation. (1)(ii) Explain why the initial rate of this reaction was faster at 65 C than it was at 55 C. (3)b) Use your knowledge of enzymes to explain the difference in the two curves between 4 and 6 hours. (1)c) In this investigation, the enzyme and its substrate were mixed in a buffer solution. What was thepurpose of the buffer solution? (1) (Total 6 marks)

An example ofinitial rate measurement reaction is shown in theSAQ below.

SAQ 12The graph below shows the results of an investigation into the effect of substrate concentrationon the initial rate of enzyme controlled reaction.

0.20

0.15

0.10

0.05

0

0 10 20 30 40 50 60

Substrate concentration / mg cm

Initialrate ofreaction/ mg ofproducts s1

3

A

B C

a) Suggest two conditions apart from temperature that should be kept constant in this investigation. (2)b) Explain why changes in the substrate concentration cause an increase in the rate of reaction betweenpoints A and B on the graph. (2)c) Suggest why the curve levels off between points B and C. (2)


14/35


d) On the graph, sketch a curve to show how the results for the investigation would change if it wererepeated at a lower temperature. Explain any difference between the two curves. (3)

(Total 9 marks) January 2002 Unit 1, Edexcel

SAQ13A student carried out an experiment to test the hypothesis that an increased concentration of thesubstrate increases the initial rate of an enzyme-controlled reaction.For this investigation, hydrogen peroxide was used as the substrate, and liver tissue was used as the

source of the enzyme catalase. The enzyme was extracted by breaking up 3.0g or liver in 250cm3of water

in a blender for 45 seconds. At the start. 20cm

3

of 31.7 mmol dm

-3

hydrogen peroxide was placed in abeaker. One 6mm diameter disc of filter paper. previously soaked in Iiver extract. was then put at thebottom of the beaker and a stop watch as started. Oxygen bubbles, produced as a result of the reaction,caused the disc to rise to the surface of the liquid in the beaker. The time in seconds for the disc to reachthe surface was recorded. This procedure vas repeated for two more discs and the mean time wasrecorded. The experiment was then continued using increasing concentrations of hydrogen peroxide.A copy of the student's laboratory notes showing the mean times for the discs to rise to the surface ateach concentration is given below.

(a) The initial rate or reaction can be calculated using the formula below.Initial rate = 1 / Mean time

Prepare a table and present the data to show the initial rate of reaction at each concentration of hydrogenperoxide. (4)(b) Use the data in your table to present the information in a suitable graphical form. (4)(c) Describe the trends and patterns shown by these data. (2)(d) What conclusions regarding the hypothesis can be drawn from this investigation? (2)(e) Describe two limitations of this technique that could give rise to unreliable results. (2)(f) Compare the reliability of this method with the method describes in the core practical describedabove and give reasons for your answer.

(g) Describe how a solution containing 160 mmol of hydrogen peroxide per dm3would be dilutedto prepare a solution containing 80 mmol of hydrogen peroxide per dm3. (2 ) SVR


15/35


CORE PRACTICAL FIVE

Describe the stages of mitosis and how to prepare and stain a root tip squash in order to observethem practically.

MethodPROCEDURE:1. Place some 1 molar Hydrochloric acid in the watch glass. Be careful not to get the acid on your skin or

clothing.2. In to this acid place the terminal 3 or 4 mm of the 1 cm long onion root.3. In a short time (a few minutes) the root tip will feel soft when touched with a dissecting needle.4. Now, using forceps or a needle, pick up the softened root tip and transfer it in to a drop of acetocarminestain on a clean slide.5. Using a razor blade or a sharp scalpel, shop the root tip in to tiny pieces. Note: Iron in the scalpel ordissecting needle reacts with the acetocarmine stain to give a better staining reaction.6. Once this procedure is complete, apply a clean cover slip to the slide and heat it gently over an alcohollamp or slide warmer. Do not boil. Then invert the slide on a blotting paper and push down ward firmly,applying pressure with your thumb over the cover glass. This should flatten the cells and disperse them sothey can be observed under the microscope.

SAQ14 (a) The table below describes some of the key events that occur during mitosis Complete thetable by writing the name of the stage of mitosis next to its description.

Key events Stage

Chromatids separate and move to opposite poles of the dividing cell.

Chromosomes shorten and thicken. The nuclear envelope breaks down and the spindle forms.

The spindle fibres break down, the nuclear membrane re-forms and the chromosomeselongate.

Chromosomes line up on the equator of the cell, attached to spindle fibres by theircentromeres.

(4)

(b) The graph below illustrates the change in DNA content during the cell cycle

6

5

4

3

2

1

0

0 2 4 6 8 10 12 14 16 18 20 22 24 26

Time / hours

Mass of DNA /arbitrary units

C D

1G

A B

(i) Calculate the percentage of the cell cycle time spent in G1. (3)

(ii) At which point, A, B, C or D, does chromosome replication (the S phase) begin? Explain your answer.

(Total 9 marks)SAQ 15 The diagram below shows cells from a root tip, prepared by the root tip squash method.


16/35


(a) Describe how you would prepare a root tip squash so that mitosis can be studied. (4)(b) State which of the cells labelled AE is in:(i) metaphase ...................(ii) anaphase ..................... (2)(c) State twoevents that take place during interphase. (2) (Total 8 marks)

SAQ 16 The photograph shows a cell in mitosis as viewed using a transmission electron microscope.

(a) The actual diameter of the cell between points X and Y is 50 m. Calculate the magnification of thisphotograph. Show your working. (3)(b) In the space below make an accurate drawing of the cell. Label the chromosomes, spindle fibres andcentrioles. (5)(c) State the stage of mitosis that this cell is in. (1)(d) State one function of each of the following.Spindle fibresCentrioles (2) (Total 11 marks)

SAQ 17 The diagrams below show four stages of mitosis.


17/35


A

C

B

D (a) (i) Write the letters of the stages in the sequence in which they occur during mitosis. (1)

(ii) Name stage D. (1)(b) The graph below shows how the quantity of DNA varies with time in a cell cycle.

4

3

2

1

00 5 10 15 20 25

Time/hours

Quantity of DNA/ arbitrary units

(i) Explain the changes in the quantity of DNA that take place:between 10 to 15 hoursat 20 hours (2)

(ii) What is happening - in the cell between 15 and 20 hours? (1)(iii) What is the minimum length of time that interphase would occupy in this cell cycle? (1)

(Total 6 marks)

SAQ 18 The flow diagram below shows a method for preparing and staining cells in order to study stagesof mitosis.


18/35


Treat plant material with hydrochloric acid

Place in stain and warm

Break open plant material

Mount on slide

Squash gently

(a) Name a suitable part of a plant to use, giving a reason for your choice. (2)(b) (i) Explain why staining is necessary in this preparation. (1)(ii) Name a suitable stain for this technique. (1)(c) Explain why it is necessary to squash the preparation. (1)

(Total 5 marks)

SAQ19 An investigation was performed to determine the length of time that a cell in an onion root tipspends in each stage of mitosis.

A growing root from an onion was selected and a root tip squash was made. This was examined under a

light microscope and the percentage of cells in each stage of mitosis was determined.

The results are shown in the table below.

Stage of mitosisPercentage of cells in this

stage

Prophase 2.43

Metaphase 1.40

Anaphase 0.70

Telophase 2.78

(a) Describe how you would prepare a root tip squash so that mitosis could be studied. (4)

(b) The percentage of cells in a stage of mitosis is proportional to the duration of that stage. Use thisinformation to compare the duration of each stage of mitosis in these root tip cells by drawing a suitablegraph. (3)

(c) The duration of each stage of mitosis can be calculated using the equation below.

Duration of a stage =100

timecyclecellstagein thatcellsofPercentage


19/35


The cell cycle time for these cells is 1200 minutes.Determine the duration of each stage of mitosis and present the data in a suitable table. (2)

(Total 9 marks)

SAQ 20 The diagrams below show some cells in different stages of mitosis.

A

B

C

D

(a) Name the stages of mitosis shown by the cells labelled A, B and C. (3)(b) Describe the events that occur in the stage of mitosis shown by cell D. (2)(c) Explain the significance of the stage shown by cell D. (1) (Total 6 marks)

SAQ21 The diagram below shows the stages in the cell cycle of a plant root cell.

Cytokinesis

Telophase

Anaphase

Metaphase

Prophase

Interphase

(a) The cell had 2 arbitrary units of DNA at the start of interphase. State the number of arbitrary units of

DNA in this cell in each of the following stages.(i) at the end of prophase (1)(ii) during anaphase (1)(b) Describe how you would prepare a root tip squash to observe the stages of mitosis. (5)


20/35


(c) Two onion bulbs were grown to obtain some roots. One onion bulb was grown in water, the other in asolution of a drug called vincristine, as shown below.

Onion bulb

Roots

Solution of

vincristine

Water

Vincristine is a drug used in the treatment of cancer. It prevents spindle formation during mitosis. Theresult of a root tip squash on the roots grown in a solution of vincristine showed an increase in thepercentage of cells found in one of the phases compared with roots grown in water.(i) Suggest in which phase of mitosis this increase occurs. (1)(ii) Give an explanation for your answer. (2)(iii) State the precautions that must be taken for the results of the comparison to be reliable. (4)

iv) Use the information in the pie chart to draw a bar graph, showing the relative length of each stage inthe cell cycle. (4) SVR (Total 18 marks)

CORE PRACTICAL SIXDescribe how totipotency can be demonstrated practically using plant tissue culture techniques.Tissue culture techniques for the vegetative propagation of plants (micropropagation) have a number ofadvantages over other methods.

Growth is very rapid.

Growth is independent of seasons.

The technique can be applied to a number of species that are otherwise difficult to propagate.

Apical meristems in infected plants often remain virus-free. Their use for tissue culture has, therefore,permitted the elimination of viruses from infected stocks of a range of species.

Certain types of callus culture give rise to clones that have inheritable characteristics different fromthose of the parent plant. Improved varieties arising in this way can be propagated and usedcommercially.

In the future, it is likely that new varieties and hybrids produced using other modern techniques will becommercially propagated by tissue culture methods.

A recent development has been the commercial use of callus cultures of the shikon plant to producelarge quantities of shikonin, a medically valuable product found, in a lower concentration, in the shikonroot. Plants are valuable sources of many such products, and the application of tissue culture techniquesin this way may, therefore, become more economically important.ProcedureCollect all the apparatus that you will need and prepare any solutions that are required. Set up and

sterilize your work-bench as suggested in the notes on aseptic handling techniques.1. Select a clean floret from a fresh cauliflower head. Place it on a tile and. holding it with forceps.Carefully trim off mini-fIorets' from the curd to produce 20 cuboids of curd tissue,approximately 3 mm x5mm x 5 mm. These will be your explants.


21/35


The next stage of the procedure is to steriiize the surface of the explants with a chlorate (I) solution(Bleach).Caution: You wil l be ushig a fair ly strong bleach solut ion s o take extreme care. From now on y ou

mu st use aseptic handl ing techn iques (p. 17), so return you r forceps to the ethanol beaker.2. Quickly transfer your explants to a clean (preferably sterile) screw-top jar and add chlorate (l) solution toleave a small head space. Reseal the jar and shake the contents for five seconds.3. Shake the jar for five seconds every minute for exactly 10 minutes.4. After exactly 10 minutes. pour off the hypochlorite solution into the 'waste beaker, using the Jar lid to

trap the sterilized explants.5. wash the explants four times as follows. Add approximately 100cm

3sterile water to the jar. Reseal it,

shake for five seconds and pour off the liquid into the 'waste' beaker as in Step 4. The explants may be leftin the last wash until they are required.6. Using sterile forceps (cooled in the wash water) transfer six explants to each of the three petri dishescontaining growth medium. The explants should be widely spaced and pressed gently onto the agar.Flame sterilize and cool your forceps when each dish is complete.7. Seal each dish with Parafilm or insulating tape to reduce dehydration.8. Label each dish clearly on its base and incubate them in the light at 200C to 280C.9. Examine each culture weekly. record and sketch any changes you observe, If some of the explantsshow signs of contamination, the remainder should be aseptically transferred to fresh medium (Steps 6

8).

Aseptic techniques the systematic precautions taken to keep cultures pure and free from

contamination.

All apparatus (Petri dishes, pipettes, flasks, etc) must be sterilised by autoclaving at 121 0C for 15 minutes at

103 kPa. Or by irradiating with ultraviolet rays (Wavelength - 254nm).

Sterile the culture medium by autoclaving.

Wipe the bench / work surfaces with 70% ethanol before and after work.

Flame the necks of bottles to prevent air-borne contamination.

Flame wire loops and forceps before and after use or sterilise by dipping in ethanol.

Lids of containers should not left on benches.

Petri dishes opened slightly during operation to avoid contamination. Cultures after study and contaminated equipment must be autoclaved / sterilised before disposal or reuse.

The composition of the medium used for growth is shown in the table below.

Growth substances used in tissue cultureexperimentsPhytochromes Photosensitive pigments..Caution: Some phytohormones are toxic, socare must be taken when preparing stocksolutions, e.g. protective gloves should beworn. Students should not, of course, comeinto direct physical contact with media.Auxins (Stimulate root development)

e.g Indol 3-yl acetic acid (IAA)1-Naphthyl acetic acid (NAA)2,4-dichlorophenoxy acetic acid (2,4-D)

Cytokinin s (Stimu late cel l divis ion )

6-furfurylaminopurine (Kinetin)6-benzylaminopurine (BAP)


22/35


Outline of plant tissue culture


23/35


SAQ 22 Plant tissue culture is a method used to propagate plants. The flow diagram shows one method ofplant tissue culture.

(a) Name the type of reproduction involved in plant tissue culture. (1 mark)(b) Give two advantages of producing plants using this method rather than from seeds. (2 marks)(c) Why is a viral infection more likely to destroy a complete batch of plants grown by plant tissue culture

than a batch of plants grown from seeds? (1 mark)(d) Callus tissue develops into either shoots or roots depending on the relative concentration of the plantgrowth regulators used. Use your knowledge of genes to suggest how these plant growth regulatorsdetermine the type of plant tissue formed. (1 mark)


24/35


(e) The data below shows the growth of five callus grown atdifferent concentrations of sucrose in theculture medium.

Sucrose

concentration 0.1 mmol dm-30.2 mmol dm-30.3 mmol dm-30.4 mmol dm-30.5 mmol dm-3Initial massof callus 2.1 g 2.6g 2.3g 2.1g 2.7gFinal massof callus 2.6g 3.8g 4.6g 4.2g 5.4g(After one week)

i) Prepare a table and organise the data in a suitable way, so that the growth of the callus at differentsucrose concentrations can be compared. (4)ii) Present your data in a suitable graphical form. (4)iii) Suggest why the reliability of the data may be low. (3)iv) List the factors that must be controlled to get reliable results. (4)

SVR

SAQ 23 Take-all is a disease of wheat caused by a fungus. It can cause serious damage to the crop.There is no gene for resistance to this fungus in wheat. There is, however, a gene for resistance to thisfungus present in oats.The diagram shows how this gene might be transferred to wheat.

(a) (i) The wheat plant with the resistance gene contains recombinant DNA. What is recombinant DNA?(1)(ii) The plasmids act as vectors for the resistance gene. What is a vector? (1)(iii) Suggest how cells with the resistance gene might be selected. (2)b)i) Suggest which tissue would be most suitable for the explants. (1)ii) Explain why explants containing large quantities of xylem do not usually grow into a callus. (2)c) State what is meant by the term totipotency. (2)

d) Distinguish between differentiation and dedifferentiation. (2)e) Suggest why adult animal cells usually do not develop into complete organisms, but plant tissues do.(2)

SVR


25/35


CORE PRACTICAL SEVENDescribe how to determine the tensile strength of plant fibres practically.Extracting fibres from plantsThe objectives of this procedure are:

to extract fibres with possible commercial use from plants

to develop investigative and experimental skills: devise a hypothesis, plan an experiment to produceappropriate results to test that hypothesis, use apparatus and a procedure that is suitable to producevalid results.

Introduction

Fibres have been extracted from plant stems for centuries and used in the commercial manufacture of awide range of textiles and paper. The term fibres is used to describe a range of fibre -like structures, notjust the sclerenchyma. The use of different fibres depends on their properties.

Strength can be defined as the maximum stress a material can withstand without failing (breaking).Tensile strength is the maximum stress caused by a pulling force that a material can stand without failing.Concrete has a tensile strength of 2 x 106N m-2. Compression strength is the maximum strength causedby a pushing force that a material can stand without crushing.

Plant stems must not only be strong. Often they must be able to bend in the wind and return to theiroriginal shape without any permanent distortion. They must not be too stiff.

Fibre Useful part of the plant Applications

Flax Stem of flax plant Linen for clothing

Cotton Hairs on the seeds of a plant belonging to themallow family

Cotton for clothing

Hemp Fibres from stem/ leaves of the hemp plant Used for ropes and carpet-backing

Coir Fibre from the husks of the fruit of the coconut Floor coverings, ropes

Jute Fibre from the stem of the jute plant Hessiansacking and carpets

Manila Hard fibres from the leaves of a type of

banana

Marine cables and other ropes, nets

and mattingPulp Softwood trunks Paper, cardboard

Fibres can be removed from the plant stems by retting. In field retting, the plant stems are cut or pulled upand left to rot in the field where microbial action breaks down the stalks. In water retting, stems areimmersed in water. During soaking, bacteria and fungi break down the soft tissues of the stems leavingthe cellulose intact. This produces more uniform, higher quality fibres, but is more expensive andproduces nitrogen-rich waste water that must be treated before discharge. It is relatively easy to removethe cellulose-rich fibres, as described below.ProcedureSAFETY: Wear eye protection and gloves when handling the plant material.Wash your hands after handling the soaked material.When testing fibres to breaking point, make sure the loads on the material can fall without causing injury.

Preparation of plant fibres

Remove the stems from the water. Wash the stems to remove the softened tissue and then dry theremaining fibres on a paper towel. The outside cuticle and epidermal layer will rub away and the centralpith will be left when you peel away the fibres. These fibres are made up of vascular tissue; they containboth the xylem vessels and sclerenchyma fibres.


26/35


SAQ24 Sisal is a material used to make rope. It is made from the sclerenchyma fibres found in the leavesof the plant,Agave sisalana.After extraction of the fibres, the waste leaf material can be used in the production of organic fertiliser.The four countries that produce most of the worlds sisal are Brazil, Kenya, Tanzaniaand Madagascar.The table below shows the annual harvest of freshly-cut Agave sisalana leaves together with the totalannual production of sisal.

(a) (i) Complete the table to show the total annual production of sisal. (1)(ii) Calculate the total percentage of sisal produced from freshly-cut leaves. Show your working. (2)(b) Nylon is a synthetic (man-made) fibre which can be used to make ropes. Nylon ropes are lighter andstronger than those made using sisal. Suggest two advantages of using sisal rather than nylon to makeropes. (2)(c) (i) Explain what is meant by the term tensile strength of a fibre. (1)(ii) Suggest how you could carry out a practical investigation to compare the tensile strength of sisal andnylon fibres. (4)1. idea of suspending {fibres / bundles of fibres} with weights on / pulling them with aforcemeter/eq;2. { fibres / bundles of fibres} of same diameter used / different diameters accounted for;3. { fibres / bundles of fibres} of same initial length used;4. detail of how {weights added / forcemeter pulled};5. description of measurable endpoint eg {breaking point / stretched to standard length};6. repeated readings taken at each {weight / forcemeter reading} (using different fibre NOT justchecking the reading with same fibre);7. reference to a safety procedure eg {goggles in case fibre snaps / precaution against falling

weights};8. ref to control of {temperature / humidity / other relevant factor};

(d) Describe two ways in which the structure of xylem vessels is similar to that of sclerenchyma fibres. (2)


27/35


CORE PRACTICAL EIGHTDescribe how to investigate plant mineral deficiencies practically.The aim of this practical is to investigate the effects of mineral deficiency on the growth of plants.Seedlings are grown in solutions containing a range of mineral salts, including those which lackphosphate, nitrate, calcium, potassium, magnesium, iron and sulphate, plus the complete medium.

Suitable seedlings which can be used for this experiment include: maize (Zea mays), castor beans(Ricinus communis), tomato (Lycopersicon esculentum) and cabbage (Brassica oleracea). Seeds are

germinated in moist vermiculite (a nutrient free medium that retains moisture and anchors roots at thesame time), then transferred to the nutrient solution, as shown in the Figure. At weekly intervals, the plantsare measured and any deficiency symptoms noted.Method

1. Make up the culture media and set up eight tubes containing the following: Complete (normal) medium Medium lacking phosphate Medium lacking nitrate Medium lacking calcium Medium lacking potassium Medium lacking magnesium Medium lacking iron

Medium lacking sulphate2. Wrap each tube in aluminium foil.3. Select eight seedlings and set up the cultures as shown in Figure.4. Leave the experiment at room temperature and each week record the following:

Shoot and root length Leaf number and size Internode number and length Deficiency symptoms, such as changes in shape or yellowing of leaves.

SAQ 25 The apparatus shown below can be used to study mineral nutrition in flowering plants.

(a) Suggest the function of each of the following.(i) The stream of air (2)(ii) The black paper cover (2)

(b) The nutrient solution contains various mineral ions including magnesium and phosphate. Giveonereason why each of these ions is essential to the plant.MagnesiumPhosphate (2) (Total 6 marks)


28/35


SAQ26An investigation was carried out into the absorption of mineral ions by beech tree seedlings.The absorption of phosphate ions by beech roots was measured in moist air, and in an atmosphereof moist nitrogen.

The results are shown in the graph below.

Absorption ofphosphate ions/ arbitrary units

10

9

8

7

6

5

4

3

2

1

0

0 5

Time / hours

10 15 20 25 30

Roots in airRoots in nitrogen

(a) Calculate the rate of absorption of phosphate ions by beech roots in air between 10 hours and 20hours. Show your working. (3)(b) (i) Compare the rates of absorption of phosphate ions by roots in air and roots in nitrogen. (2)(ii) Suggest an explanation of the difference in rates of absorption. (2)(c)(i) Suggest tworeasons why the atmosphere in which the roots are kept has to be moist. (2)

(ii) Suggest twofactors that should be kept constant in this experiment. (2) (Total 11 marks)


29/35


SAQ 27An experiment was carried out to investigate the uptake of different mineral ions by barleyplants. A large number of barley seedlings was grown in a nutrient solution containing a range of

mineral ions including potassium (K+), calcium (Ca2+), magnesium (Mg2+) and nitrate (NO3).

The experiment was set up as shown in the diagram below.

The concentration of these ions in the solution were measured at the beginning and at the end of theexperiment.


Mineral ion

NitratePotassiumMagnesiumCalcium

Concentration of ions in nutrient solution / arbitrary units

At start of experiment At end of experiment

7.03.02.05.0

1.80.02.15.6

(a) Calculate the percentage difference between the concentration of nitrate ions at the beginningand at the end of the experiment. Show your working. (3)(b) What do the results suggest about the mechanism of absorption of potassium ions?Explain your answer. (3)(c) Suggest an explanation for the changes in concentrations of magnesium and calcium ions during

the experiment. (2)(d) State two precautions which should have been taken to ensure that results for all the barleyseedlings were comparable. (2)(e) Describe the pathway taken by mineral ions as they pass from the nutrient solution to the xylemin the roots of the seedlings. (3)

(Total 13 marks)


30/35


SAQ 28 Duckweeds are small, green plants that float on the surface of freshwater ponds.Experiments were carried out on the growth of two species of duckweed, Lemna gibbaand Lemnapolyrrhiza. L. gibbaplants contain non-photosynthetic air sacs which enable them to float on thesurface of the water.In these experiments the two species were grown in complete mineral nutrient solutions as follows.

Experiment A Lemna gibbaand Lemna polyrrhizatogetherExperiment B Lemna polyrrhizaonlyExperiment C Lemna gibbaonly

The dry mass of the plants was measured each week for 8 weeks.The results for experiment A are shown in the table below.

WeekDry mass / mg

Lemna polyrrhiza Lemna gibba

0

1

2

3

4

5

6

7

8

25

69

87

106

87

100

87

81

37

22

84

169

197

289

344

344

347

345

(a) Plot the data in suitable graphical form on graph paper. (5)(b) Describe the growth of L. polyrrhizaand L. gibbain experiment A. (4)

(c) The results for experiments B and C are shown in the table below.

Week Experiment BLemna polyrrhiza

Experiment CLemna polyrrhiza

0

1

2

3

4

5

6

78

63

100

188

306

381

448

562

594641

50

119

200

259

291

356

350

369400

(i) Compare the growth of L. polyrrhizain experiments A and B (2)(ii) Suggest a reason for the difference in growth in these two experiments. (1)(d) (i) How does the growth of L. polyrrhizain experiment B differ from L. gibba in experiment C?(ii) Suggest an explanation for this difference. (2) (Total 15 marks)


31/35


CORE PRACTICAL NINEDescribe how to investigate the antimicrobial properties of plants.

Preparation of media and plate pouringIntroductionThere are many different types of media which are used for the culture of micro-organisms. These may beobtained in ready-formulated preparations, or can be made using separate ingredients. In this practical,we look at the method for preparing and sterilizing nutrient agar medium.

Nutrient agar medium can be used for the culture of bacteria. If ready-formulated media are used, then itis made up using distilled water.Materials

Ready-formulated Nutrient agar medium.

Distilled water

50 ml Universal bottle

Petri dishes

Autoclave

Incubator

Gas burner

Glass rods

Electronic weighing balance Measuring cylinders

Conical flasks, sterilized cotton

MethodNutrient agar mediumAdd 28 g of formulated ingredients in 1 litre of distilled water and stir it until it dissolve.Dispense into a suitable containers and autoclave at 121 C for 15 minutes.

Procedure for pouring a plateAllow liquid agar to cool to about 50 C (just cool enough for comfortable handling) after removalfrom autoclave. Unscrew cap of bottle with little finger as shown in Figure (a). It can be held by little

finger during the procedure to avoid placing it on the bench where it could become contaminated.

Flame mouth of bottle for a few seconds. This is done toproduce an upward flow of air from thebottle so that any organisms in the area will not fall into the bottle. (It is not done to kill micro-organisms; the bottle would have to be heated for too long to achieve this effect). Refer Figure (b).

Pour the molten agar (about15-20 cm3) slowly into the base of the sterile Petri dish, lifting the lidonly as much as necessary. Do not spill agar on the edges of the dish (if so, start again). Replacethe lid and allow the agar to set. Refer Figure (c).

If the plate is to be used for streaking or spreading the surface of the agar and lid can be driedonce the agar is set. They are best dried upside down in an incubator at about 37 C, andarranged as shown in Figure (d) to minimize the risk of contamination (slight in thesecircumstances).

Preparation of streak plate of bacteria

Introduction

In this practical, an agar plate will be poured using sterile nutrient agar and inoculated using a culture of asuitable bacterium, such as Bacillus subtilis. Streak plates are useful to isolate pure culture as, individualcolonies will have grown from a single cell. Single colonies can be used to subculture another agar plateto obtain a pure isolate.

Materials Sterile Petri dishes

Sterile nutrient agar

Boiling water bath


32/35


Bacteriological loop

Slope culture of Bacillus subtilis, or other suitable bacterium.

Chinagraph pencil or spirit marker pen

MethodPouring a sterile agar plate1. Before starting, wipe the bench surface using a suitable disinfectant solution2. Melt the agar in a boiling water bath, remove carefully using tongs allow to cool to about 45

C. At this temperature, the agar will be cool enough to handle safely, but will remain molten.Agar starts to set below about 42 C.

3. On the base of sterile Petri dish, write your name, the date and the name of the organism withwhich the plate will be inoculated. Petri dishes should be always be labeled on the base, as it ispossible for lids to be transposed.

4. Working near a Bunsen burner with a blue flame, hold the molten, but cooled, nutrient agar inone hand and using little finger of the other hand, remove the lid of the bottle. Do not place thelid on the bench.

5. Pass the neck of the bottle through the Bunsen flame using the hand in which you are holdingthe lid of the bottle, raise the lid of the Petri dish to an angle of about 45 and carefully pour inthe agar until the dish is nearly half full. Replace the Petri dish lid, flame the neck of the bottleagain and replace the lid.

6. Leave the agar plate to set.

MethodPreparing a streak plate1. Have ready your sterile agar plate and slope culture of the bacterium to be used.2. Sterilize the bacteriological loop by holding it in a blue Bunsen flame until red hot.3. Allow the loop to cool and whilst still holding the loop, remove the lid from the slope culture

using the little finger of the hand in which you are holding the loop. Do not place the lid on thebench.

4. Pass the neck of the culture bottle through the Bunsen flame, then use the loop to remove asmall portion of the culture. Replace the lid on the culture bottle.

5. Now lift the lid of the Petri dish and use the loop to streak out the culture as shown in Figure.Be careful not to Plough up the surface of the agar. When you have finished, flame the loopagain before placing it on the bench.

6. Fasten the lid of the Petri dish using two pieces of adhesive tape. Invert the dish, and incubateat 30 C for 24 hours.

Results and discussion1. Record the appearance of your streak after incubation. Were you successful in obtaining single

colonies of the bacterium?2. List the different methods of sterilization, which have been used in this practical.3. Explain why it is important:(a) to avoid ploughing up the surface of the agar when inoculating

(b) not to seal the dishes all around with adhesive tape(c) to invert the dishes when they are incubated.

SAQ 29 Mutation in bacteria can be investigated by inoculating agar plates containingconcentrations of antibiotic sufficiently high to prevent bacterial growth. Only bacteria thathave mutated and become resistant to the antibiotic will grow and form colonies.

An experiment was carried out to investigate the mutagenic potential of three compounds, A, Band C. Bacteria of a strain known to be sensitive to penicillin were exposed for two minutes tovarying concentrations of compounds A or B or C. Plates containing penicillin were then

inoculated with 107bacteria and incubated for three days.


33/35



010

20304050

100200

23

67

11142440

14

914233470

24

352136

Number of colonies

Compound A Compound B Compound C

Concentration of compound

/ cmg 3

(a) Describe the results obtained with each compound and in each case suggest a reasonfor the result.

Compound ACompound B

Compound C (6)(b) Mutation rate is defined as the chance that a mutation would occur in one generation.

Calculate the mutation rate for the bacteria in compound A at 200 g cm-3concentration. Show your working. (2)

(c) Suggest tworeasons why bacteria are suitable organisms for studies of mutation. (2)(d) Suggest why antibiotics used to treat human disease should not be used to treat disease

in animals reared for food. (2)(e) Draw a graph to compare the effects of the concentration of the compound A,B and C on

the growth of the colonies. (4) (Total 16 marks)

SAQ 30 An experiment was carried out to test the sensitivity of the bacterium Bacillus subtilis todifferent antibiotics. The surface of a nutrient agar plate was flooded with a broth culture of thebacterium. The excess broth was discarded. Five filter paper discs, (A, B, C, D and E), eachcontaining a different antibiotic, were placed on the nutrient agar surface.

The plate was allowed to stand for 30 minutes at room temperature before being incubated at30 C for 24 hours. The appearance of the plate after the incubation is shown in the diagram.

E

D

A

B

C

Clearzones

Bacteria growingon agar

Antibiotics discs

(a) State two ways in which antibiotics may inhibit the growth of bacteria such asBacillussubtilis. (2)

(b) Suggest why the surface of the nutrient agar was flooded with the broth culture ratherthan being inoculated by a streaking technique. (1)


34/35


(c) Suggest why the plate was allowed to stand for 30 minutes at room temperature beforebeing incubated. (1)

(d) Suggest what the results indicate about the sensitivity of B. subtilisto the antibiotics. (1)(Total 5 marks)

SAQ 31. In the culturing of microorganisms in the laboratory it is necessary to use aseptictechniques to prevent contamination.

The diagram below shows how a simple autoclave is used to sterilise laboratory equipmentand culture media.

Heat Heat

Left to cool

Water

Steam

Massadded

Valveclosed

Valveopen

Aluminiumfoil

Cottonwool plug

(a) The pressure of steam builds up to 103 kPa. This raises the boiling point of water to121C. The contents of the autoclave are maintained at this temperature for 15-20

minutes. Explain why these conditions are necessary for effective sterilisation. (2)(b) Suggest why the cotton wool plugs of the flasks are covered with aluminium foil. (1)(c) Describe and explain two precautions, other than the use of sterile equipment, you

would need to take to prevent contamination of cultures of microorganisms. (4)(Total 7 marks)

SAQ 31A suspension of bacteria was spread evenly over solid medium in a petri dish. The culturewas incubated at 25 C for 12 hours.After 12 hours two discs were placed on the surface of the medium. Each disc had beensoaked in a different antibiotic (antibiotic A and antibiotic B).The culture was then incubated for 48 hours to allow the antibiotics to diffuse into the medium.The appearance of the culture before and after incubating with the antibiotic-soaked discs isshown below.

AA

B B

Antibiotic-soaked disc

Bacterialcolonies

Appearence of culture after 12 hours,on adding the antibiotic-soaked discs

Appearence of culture 48 hoursafter adding the discs


35/35

(a) Describe the effect of each antibiotic on the growth of bacteria. Suggest a reason for theeffect of each antibiotic.Antibiotic AAntibiotic B (4)

(b) Suggest why antibiotics such as penicillin affect bacterial cells but not the cells of thepatient they are used to treat. (3) (Total 7 marks)

Reliability:When the variability in replicated results is very high, the reliability is relatively low. This maybe due to certain variables not being controlled of faulty experimental procedures. Range bars or errorbars on the graph will give a fair indication of the reliability. If there is considerable overlap between errorbars, then variability is very high and reliability is low. Students should be able to identify factors that maydecrease the reliability of the results.

Accuracy: accuracy can be defined as the difference between the actual values and the measuredvalues. If the difference is high, then accuracy is low and vice versa. Accuracy can be improved by usingappropriate apparatus and methods for making measurements.

Question one (Core practical) Data organisation.a. Tabulation

The Independent variable comes in thefirst column.Arrange values in ascending order.The independent variableis controlled by the experimenter.The dependent variableis measured to give the results.The dependent factor depends on the independent variable.

Label all columns and rows appropriately and accurately.Include SI units in the headings of the columns and rows.Be consistentwith significant figures / decimal places.You are generally asked to find the mean or the percentage difference.

Mean = sum of readings / number of readings. ( e.g. Mean= 12 + 11.2 + 13.1 / 3 = 12.1)

Percentage Difference = (Difference / Initial reading) x 100

b. GraphAxes: Independent variable onX - axis. Label appropriately withunits.

Dependent variable onY - axis. Label appropriately withunits.

Scale: The curve should cover more than 50 % of the graphpaper.

Plot all points accurately. Mark the plotted point with a dotand a circle or with across.

Line: Join each point with a neat straight line, passing exactly through the point. Do not extrapolate.

c. Describe the trends in the graph. Do NOT make theoretical assumptions. Make conclusions based on theexperimental data. Refer to the hypothesis being investigated, while making conclusions.

d. Limitations are genuine sources of error. Look out for variables like temperature, pH, etc. not beingcontrolled. Also check if the experiment has been replicated.

Every experiment has two main components:

1. Control of variable / factors.Ensure that you control all Variables and factors that can affect your results. State sensible values, with SI units

and describe sensible ways of controlling these variables. Describe the type of apparatusthat could be used.

Controlling factors effectively will improve the reliability of your results.

2. Making quantifiable measurements.

The results of your experiment should have numerical values, so that the data can be analysed and resultscan be drawn.

Using an appropriate method and suitable apparatus can improve the accuracy ofyour results.

as snab biology core practicals

Documents