Plant Pigments and Photosynthesis

Introduction:
Photosynthesis has two main parts, which are the light dependent and the light –independent. In the light-dependent reactions pigments trap energy from light, and this energy is used to split water molecules (photolysis). The light-independent reactions or dark phase of photosynthesis involve the fixing of carbon dioxide. It makes glucose and fructose chains and also releases oxygen , which passes through the stomata of the plant.

Organisms that carry out photosynthesis making their own organic molecules are called autotrophic. Some autotrophic organisms include plants, algae, and blue-green bacteria. Plants have many varieties of pigments, all of which absorb different colors of light. Chlorophyll a is the primary plant pigment and makes up about three-fourths of all the plant pigments. It absorbs red and blue light and is not found in photosynthetic bacteria.

Chlorophyll b is another plant pigment. It absorbs blue-green and orange-red light. Carotenoids are a type of accessory pigment that absorb blue and blue-green light. These pigments are fat soluble and usually masked by chlorophyll a. Anthocyanin is another accessory pigment that absorbs bright red colors. There is also chlorophyll c and d that sometimes take the place of chlorophyll b.

Chromatography is a process used to separate mixtures that can separate plant pigments. This lab uses paper chromatography where a piece of paper is used to wick solvent up to the pigments and separate them according to solubilities. The rate of migration on a chromatogram is the Rf value.

Hypothesis

Plants contain several different pigments, and the rate of photosynthesis in plant cells is directly related to light and temperature.

Materials

Exercise 4A: Plant Pigment Chromatography

This exercise required 1 50-mL graduated cylinder, a small amount of a solvent, a stopper, filter paper, scissors, a pencil, spinach leaves, and a quarter.

Exercise 4B: Photosynthesis/The Light Reaction

The materials needed for this part of the lab were a spectrophotometer, a light, a water flask, a test tube rack, ice, 5 labeled cuvettes, lens tissue, foil, and parafilm. The substances put in the cuvettes were 5 mL of phosphate buffer, approximately 16 mL of distilled water, 9 drops of unboiled chloroplasts, and 3 drops of boiled chloroplasts.

Methods

Exercise 4A: Plant Pigment Chromatography

A 50-mL graduated cylinder was filled with about 1 cm of solvent and then tightly stoppered. The filter paper was then cut to a point on one end, and a line was drawn 1.5 cm above the point. Using the ribbed edge of a quarter, spinach cells were extracted onto the pencil line. This procedure was repeated 8-10 times using a new portion of the leaf each time. The filter paper was then placed in the cylinder with the tip barely touching the solvent and none of the edges touching the sides. When the solvent reached 1 cm below the top of the paper, it was removed from the cylinder. The solvent location was immediately marked, and then the bottom of each pigment band was also marked.

Exercise 4B: Photosynthesis/The Light Reaction

The spectrophotometer was set to 605 nm and allowed to warm up. The chloroplast suspensions were prepared the previous day, part of which were boiled, and stored on ice until they were ready for use. An incubation area was prepared with a flood light, water flask, and test tube rack, by using the flask as a heat sink between the light and the rack. Five cuvettes were numbered respectively and then wiped with lens tissue. The walls and bottom of cuvette 2 were covered with foil and a foil cap was made for the top.

To each cuvette 1 mL of phosphate buffer was added. Then, to cuvette 1 4 mL of distilled water was added, but to cuvettes 2, 3, and 4 3 mL of distilled water was added. Next, 1 mL of DPIP was added to cuvettes 2, 3,and 4. To cuvette 5, 3 mL plus 3 drops of distilled water were added and 1 mL of DPIP. To cuvette 1, 3 drops of unboiled chloroplasts were added.

The spectrophotometer was brought back to zero and the contents of cuvette 1 were mixed by inverting and placed in the sample holder. Cuvette 1 was used periodically through this experiment to recalibrate the spectrophotometer. Three drops of unboiled chloroplasts were added to cuvette 2. After removing the foil sleeve, it was placed in the sample holder and the transmittance was recorded. Additional readings were also taken at 5, 10, and 15 minutes. Next, three drops of unboiled chloroplasts were transferred to cuvette 3. The percent transmittance was recorded at 0, 5, 10, and 15 minutes. Three drops of boiled chloroplasts were added to cuvette 4, and the transmittances were recorded at the same times. Finally, cuvette 5 was mixed and placed in the sample holder. The transmittance readings were recorded.

 

Results

Table 4.1 Distance Moved by Pigment Band

Band Number

Distance (mm)

Band Color

1.

0 mm

Yellow-brown

2.

5 mm

Light green

3.

30 mm

Green

4.

48 mm

Yellow

Distance Solvent Front Moved 60 mm.

Table 4.2 Rf Values

0.8 = Rf for xanthophyll (yellow)

0.5 = Rf for chlorophyll a (bright green to blue green)

0 = Rf for chlorophyll b (yellow green to olive green)

Table 4.4 Transmittance (%)

 

 

Cuvette

0

5

10

15

2 Unboiled/Dark

41%

43%

44%

43%

3 Unboiled/Light

35%

38%

39%

37%

4 Boiled/Light

51%

52%

53%

54%

5 No Chloroplasts

57%

57%

56%

55%

Lab 4B Color Chart

Cuvette

Initial Color

Final Color

1

Clear

Clear

2

Light clear blue

Blue/green

3

Light clear blue

D