Ap Biology Photosynthesis Lab Report

AP Biology Lab Four: Plant Pigments and Photosynthesis The purpose of this lab is to separate and identify pigments and other molecules within plant cells by a process called chromatography. We will also be measuring the rate of photosynthesis in isolated chloroplasts. Beta carotene, the most abundant carotene in plants, is carried along near the solvent front because it is very soluble in the solvent being used and because it forms no hydrogen bonds with cellulose. Xanthophyll is found further from the solvent font because it is less soluble in the solvent and has been slowed down by hydrogen bonding to the cellulose. Chlorophylls contain oxygen and nitrogen and are bound more tightly to the paper than the other pigments. Chlorophyll a is the primary photosynthetic pigment in plants. A molecule of chlorophyll a is located at the reaction center of the photo systems. The pigments collect light energy and send it to the reaction center. Carotenoids also protect the photosynthetic systems from damaging effects of ultraviolet light. Procedure: 1) Obtain a 50 ml graduated cylinder which has about 1 cm of solvent at the bottom. 2) Cut a piece of filter paper which will be long enough to reach the solvent. Draw a line about 1.5 cm from the bottom of the paper. 3) Use a quarter to extract the pigments from spinach leaf cells. Place a small section of leaf on the top of the pencil line. Use the ribbed edge of the coin to crush the leaf cells. Be sure the pigment line is on top of the pencil line. 4) Place the chromatography paper in the cylinder. 5) Cover the cylinder. When the solvent is about 1 cm from the top of the paper, remove the paper and immediately mark the location of the solvent front before it evaporates. 6) Mark the bottom of each pigment band. Measure the distance each pigment migrated from the bottom of the pigment origin to the bottom of the separated pigment band. Record the distances. 7) Turn on the spectrophotometer to warm up the instrument and set the wavelength to 605 nm. 8) Set up an incubation area that includes a light, water flask, and test tube rack. 9) Your teacher will provide you with two beakers, one containing unboiled chloroplasts and the other containing a solution of boiled chloroplasts. Be sure to keep these on ice at all times. 10) At the top rim, label the cuvettes 1,2,3,4, and 5, respectively. Using lens tissue, wipe the outside walls of each cuvette. Using foil paper, cover the walls and bottom of cuvette 2. Light should not be permitted inside cuvette 2 because it is a control for this experiment. 11) Refer to Table 4.3 to prepare each cuvette. Add 4 ml of distilled water to cuvette 1. To 2,3, and 4, add 3 ml of distilled water and 1 ml of DPIP. To 5, add 3 ml plus 3 drops of distilled water and 1 ml of DPIP. 12) Bring the spectrophotometer to zero by adjusting the amplifier control knob until the meter reads 0% transmittance. Add 3 drops of unboiled chloroplasts and cover the top of cuvette 1 with Parafilm and invert to mix. Insert cuvette 1 into the sample holder and adjust the instrument to 100% transmittance. For each reading, make sure that the cuvettes are inserted into the sample holder so that they face the same way as in the previous reading. 13) Obtain the unboiled chloroplast suspension, stir to mix, and transfer 3 drops to cuvette 2. Immediately cover and mix cuvette 2. Then remove it from the foil sleeve and insert it into the spectrophotometer's sample holder, read the percentage transmittance, and record it as the time 0 reading in Table 4.4. Replace cuvette 2 into the foil sleeve, and place it into the incubation test tube rack. Turn on the flood light. Take and record additional readings at 5,10,and 15 minutes. Mix the cuvette's contents just prior to each readings. Remember to use cuvette 1 occasionally to check and adjust the spectrophotometer to 100% transmittance. 14) Obtain the unboiled chloroplast suspension, mix, and transfer 3 drops to cuvette 3. Immediately cover and mix cuvette 3. Insert it into the spectrophotometer's sample holder, read the percentage transmittance, and record it in Table 4.4. Replace cuvette 3 into the incubation test tube rack.

Take and record additional readings at 5, 10, and 15 minutes. Mix the cuvette's contents just prior to each readings. Remember to use cuvtte 1 occasionally to check and adjust the spectrophotometer to 100% transmittance. 15) Obtain the boiled chloroplast suspension, mix, and transfer 3 drops to cuvette 4. Immediately cover and mix cuvette 4. Insert it into the spectrophotometer's sample holder, read the percentage transmittance, and record it in Table 4.4. Replace cuvette 4 into the incubation test tube rack. Take and record additional readings at 5, 10, and 15 minutes. Mix the cuvette's contents just prior to each readings. Remember to use cuvtte 1 occasionally to check and adjust the spectrophotometer to 100% transmittance. 16) Cover and mix the contents of cuvette 5. Insert it into the spectrophotometer's sample holder, read the percentage transmittance, and record it in Table 4.4. Replace cuvette 5 into the incubation test tube rack. Take and record additional readings at 5, 10, and 15 minutes. Mix the cuvette's contents just prior to each readings. Remember to use cuvtte 1 occasionally to check and adjust the spectrophotometer to 100% transmittance. Results: Table 4.1 Distance Moved by Pigment Band Band Number

Distance (mm)

Band Color

1.

61 mm

Dark Green

2.

54 mm

Light green

3.

59 mm

Faint Yellow

Distance Solvent Front Moved 66 mm.

Table 4.2 Rf Values .89 = Rf for carotene (faint yellow to yellow-orange) - = Rf for xanthophyll (yellow) .81 = Rf for chlorophyll a (bright green to blue green) .92 = Rf for chlorophyll b (yellow green to olive green)

Table 4.4 Transmittance (%)

Cuvette

0

5

10

15

2 Unboiled/Dark

46.8

38.3

41.3

42

3 Unboiled/Light

42.6

46.4

24

22

4 Boiled/Light

56.5

84.8

8.5

7.3

5 No Chloroplasts

25.5

26

50.2

48.2

Analysis: The solubility, size of particles, and their level of attraction to the paper are all involved in the separation of pigments.The different solubilities of the pigments would change the Rf values. DPIP is the electron acceptor in this experiment. DPIP substitutes for the NADP molecules. The electrons that reduce DPIP

come from the photolysis of water. The spectrophotometer measures the percentage of light transmittance through the cuvette due to DPIP reduction. Darkness prevents the reduction of DPIP from occurring. Boiling denatures the protein molecules and stops the reduction. In the dark cuvette, there was no light energy available, so there was no flow of electrons and no photolysis of water, while in the lighted cuvette these processes were allowed to continue. Conclusion: We discovered that the many pigments found in chloroplasts are all involved in gathering energy from sunlight. The spectrum of color displayed on the filter paper showed the pigments and the solubility of each. In lab 4b, the spectrophotometer measured the light transmittance through the various cuvettes and the chloroplast solutions in each. This indicated whether photosynthesis was occurring and at what rate. The cuvette with the unboiled chloroplasts that had been exposed to light showed the biggest change in percent transmittance, which indicates that the amount of light available has a very big effect on the rate at which the light reactions of photosynthesis occur. Errors could have occurred because of damaged spinach, inaccurate reading, fingerprints on the cuvettes, or erroneous measurements.