Main Page/BPHS 4090/Choloplast Translocation

Required Components

1. Stock culture of Eremosphaera viridis
2. Glass slides, cover slips and micropipette
3. Nikon Optiphot Microscope
4. Radiometric Probe (Model S471 Portable Optometer, UDT Instruments)
5. Cool Snap CCD Camera and MicroManager software
6. Blue and red band-pass filters

Objective

To observe the wavelength dependence of light on chloroplast translocation in the acidophile green algae Eremosphaera viridis as well as describing a mechanism behind this response.

Introduction

Electromagnetic radiation is the driving force for photosynthesis. Plants and other autotrophs convert the energy of light into chemical energy used for synthesizing carbohydrates and other organic compounds, which heterotrophic organisms use for energy and other nutritional requirements. Photosynthesis is a unique process performed by plants, algae, and some species of bacteria. It consists of a series of oxidation and reduction reactions; the basic chemical formula is shown below:

Photosynthesis would not be possible without the energy derived from light. Electromagnetic radiation enters the earth’s atmosphere from the sun where it is harvested by photosynthetic organisms. Wavelengths between 400 and 800 nm are used by photosynthetic organisms. The sun can be approximated as a near perfect blackbody with a surface temperature of 5800 K described by Planck’s Black Body Radiation Law, shown in Equation 1.1

Where U (λ, T) has units of J m^-2 s^-1, h is Planck’s constant, K is Boltzmann’s Constant and c is the speed of light. The color temperature of the sun corresponds to a peak wavelength emission of about 500nm according to Wien’s Displacement Law (Equation 1.2)

Where b = 2.898 x 10^-3 in units of m*K.

The first step in the conversion of the energy of photons to chemical energy is absorption by photosynthetic pigments, principally chlorophyll. The absorption spectrum of chlorophyll a is shown in Figure 1 .

Absorption Spectrum of Chlorophyll a: Chlorophyll a strongly absorbs light at 465nm and 665nm. There is minimal absorption of UV light as well as green/yellow light which appears in the range of 500nm-600nm. These absorbances are for chloroplasts isolated in a solvent of a well-defined dielectric. In the cell, additional pigments and heterogeneous dielectric causes much broader peaks.

Chlorophyll is located inside the thylakoid vesicles in the inner membrane of the chloroplast. After absorbing a photon, an electron in chlorophyll transitions to an excited state. The excited state electron (exciton) is transferred to a photosynthetic reaction center to begin the flow of electrons through the electron transport chain, eventually to produce ATP (from a transmembrane H⁺ gradient) and reducing equivalents (NADP + 2e^– + 2H⁺ —> NADPH + H⁺). Chlorophyll, now with one less electron, is chemically unstable and receives an electron from a water molecule (H₂O). With the loss of 4 electrons from two molecules of water, molecular oxygen (O₂) is produced, as well as 4H⁺ used for ATP synthesis. Oxygen, the waste product of photosynthesis, is vital for heterotrophs in the process of cellular respiration.

As light intensity increases, so do absorption events and the generation of excited state chlorophylls, and downstream electron transport. At a high enough light intensity, these can cause the formation of a variety of undesirable oxidative products that can damage the photosynthetic apparatus. Examples include triplet state chlorophyll, and various reactive oxygen species (through direct reduction of O₂ to O₂^–, and subsequent formation of H₂O₂). The general term photo-oxidation is used to describe this damaging process. There are protective mechanisms to avoid oxidative damage ; one of these may be to decrease the absorptive cross-sectional area of chloroplasts by changing their location in the cell . The phenomenon known as systrophe is described as the accumulation of cytoplasmic organelles around the nucleus . Systrophe of the chloroplasts is observed in the unicellular green algae Eremosphaera viridis when the cell is exposed to intensities of light greater than it would experience in its natural environment.

During this experiment we will be examining chloroplast translocation in the unicellular green algae Eremosphaera viridis, in particular we will be looking at the wavelength dependence of light on systrophe. A typical cell of E. viridis is shown in Figure 2 during the course of a light treatment protocol.

Figure 2: Examples of incipient and Complete Systrophe in Eremosphaera viridis This particular cell was illuminated with a photon flux of 200 μmol m-2 s-1 using a blue bandpass filter with a peak wavelength of 441nm ± 10nm.

From Figure 2, it can be seen that the systrophe effect is quite dramatic! At 0 minutes is how the cell would appear in its resting state, at 20 minutes into the light treatment protocol there are signs of chloroplast translocation, this cell would be classified as incipient systrophe since it is in the process of undergoing systrophe. Lastly at 60 minutes into the light treatment the cell would be classified as complete systrophe. Notice at 60 minutes the cytoplasmic strands which chloroplasts migrate along during light treatments are clearly visible!

An Eremosphaera viridis cell has about 400 chloroplasts, based on counting of medial sections of fluorescence images. In a normal chloroplast, there is about 9•10^–13 g of chlorophyll and about 6.7 • 10⁸ chlorophyll molecules per chloroplast. The molecular weight of chlorophyll a is about 894; its extinction coefficient is 1.2 • 10⁵ M^–1 cm^–1 at 430nm .

Materials and Methods

The procedure is divided into four sections:

1. Preparing a sample slide
2. Microscope Set-Up and Kohler Illumination
3. Light Treatments
4. Image Processing

Please follow them in order; each section has its own set of step by step instructions.

Preparing a Sample Slide

1. Take a new glass slide and trace the outline of the cover slip using a permanent black marker as shown in Figure 3A.
2. Spread a thin layer of Vaseline as shown in Figure 3C & D along the outline you just traced using the syringe (Figure 3B), this will prevent your cell sample from drying out under high light tensities
3. Aliquot 10μL of E. viridis in the outline you just traced using a micropipette as shown in Figure 3E
4. Gently place the cover slip on top of the Vaseline layer, being careful not to crush your cell sample
5. Now the slide is ready to be used for light treatments (Figure 3F).

Figure 3

Microscope Set-up and Kohler Illumination:

1. This experiment will be performed using bright-field microscopy. Ensure the ring on the condenser diaphragm is set at 0 (not PH 1 or PH 2), because the phase ring at the PH1 or PH2 setting attenuates the light.
2. Once your specimen slide is prepared, bring it to the microscope and focus on the specimen under the x10 objective.
3. Next close the field diaphragm all the way shut so you can see the edges, they may appear blurry.
4. Use the condenser focus knob to bring the edges of the field diaphragm into the best possible focus.
5. Next use the condenser-centering screws to bring the closed field diaphragm into the center of the field of view.
6. Then open the field diaphragm such that it is slightly larger than the field of view.
7. You are now set up for Kohler illumination.

Light Treatments

The wavelength dependence of light on chloroplast translocation will be investigated. From the absorption spectrum of chlorophyll shown in Figure 1, it is known the chlorophyll strongly absorbs both blue and red light, thus for the wavelength experiments we will be using blue and red filters band-pass filters, their transmissions are shown in Figure 4. The blue band-pass filter emits light at a peak wavelength of 441nm ± 10nm. The red filter is a band-pass filter with a tail at longer wavelengths. This filter has a peak wavelength of 623nm ± 45nm.

Figure 4: Emission Spectra of Band-pass Filters:The blue bandpass filter was fit to a Gaussian function and the red band-pass filter was fit to a Lorentzian Function to account for the long tail end. Both fit functions are shown in black.

The cells will be illuminated with both blue and red light to determine the wavelength dependence of light on chloroplast translocation as described in the following outline:

1. Take the blue band-pass filter labelled 441nm and place it above the light source under the condenser diaphragm.
2. Double click on the Desktop folder called BPHS_4090_Viridis_Systrophe, and then open the Excel spreadsheet called “Photon_Flux_Calculator.xls”. This spreadsheet is already programmed to do all the difficult calculations for you to save you time in the lab!
3. With the blue filter in place turn on the radiometer, use the probe to measure the output power from the light source; this is done by removing the sample slide and placing the probe in the light path where the objective is. You may have to remove one of the eyepieces to get the probe in the light path, do this carefully and ensure you leave the x10 objective (labelled Fluor 10) in place, since this will be used for the light treatments. Ensure the probe is collecting all the light. You should measure a power reading in microwatts; enter this into the spreadsheet to get a photon flux as an output in units of μmol m^-2 s^-1 as shown in Figure 5.

Figure 5: The flux calculator has separate sections for the red and blue bandpass filters. The cells will feel different energies corresponding to the different wavelengths of light according to the Planck relationship E = hc/λ .

4. For the wavelength experiment a photon flux of around 200μmol m^-2 s^-1 is ideal to observe the effect of chloroplast translocation. Adjust the voltage dial knob on the microscope until you get a power reading which gives you a photon flux close to this value,once you do so, record your input power.
5. Next place the cell sample back in the field of view, drop the neutral density filter labelled ND 2 in the light path to avoid pre-treating the cells with light. You’ll have to adjust the microscope again for Kohler Illumination, but it shouldn’t take much adjusting at this point.
6. Move the microscope stage to capture as large of a cell population as possible, try to aim for 20 or more cells if possible by looking through the eyepiece as you move the stage.
7. Ensure your cell sample is in good focus, you’re now ready to make a movie of chloroplast translocation.

Making a Movie of Chloroplast Translocation:

1. Turn on the CoolSnap CCD camera.
2. Open MicroManager 1.3 by double clicking the icon on the desktop, you’ll notice the program ImageJ (Figure 6) opens as well, this will be used later for image processing. Figure 6 – MicroManager Software

Figure 6: MicroManager Software.

3. Click on Live Feed and turn the eyepiece mounting block about 45 degrees to the left, this allows light to pass through to the CCD camera and will project a live image onto the computer monitor.
4. Next lift up the ND2 filter and adjust the exposure time, start by setting it to 1ms, you’ll also notice the cells on the screen are out of focus, use the fine focus adjustment until you get crisp edges along the periphery of the cell.
5. Adjust the exposure until you get a live image that isn’t oversaturated (Figure 7).

Figure 7: MicroManager Live Feed.

6. Due to the limited field of view, you’ll only be able to get about 1 cell in the live feed. Move the microscope stage slowly (since the response from the CCD is slightly delayed) until you get 1 cell in the field of view as shown in Figure 7.
7. Click on “Multi-D acq.” Then set the number to 360 and interval to 10 seconds, and then hit acquire (Figure 8). This tells the program to take an image every 10 seconds; this will eventually give you a movie 60 minutes long, which should allow you to see some significant chloroplast translocation as shown in Figure 2.

Figure 8: Multi-Dimensional Acquisition.

8. Once finished click on the save icon. Save your data in the directory C:\BPHS4090_Viridis_Systrophe, label your data by your name, date and title of work. This will create a file folder with all the images you acquired.

Figure 9: Sequence Options.

9. Next you’ll be using ImageJ. Click “File->Import->Image Sequence”, double click on your file folder and select one of the images and press Open. Another window will open called “Sequence Options” (Figure 9), it will verify the number of images you have and open them as a stack, make sure the box titled “Sort Names Numerically” is checked and click Ok.
10. This may take a little while, once all the images are loaded, use the mouse cursor icon to make a box around your cell and click on “Image->Crop”. Every image you imported will be cropped.
11. Next click on “Image->Adjust->Brightness/Contrast”, another window called “B&C” will open; adjust the settings to ensure your images look the best they can. Once happy with the results click on Set, a new window will open, make sure the “Propagate to all open images” box is checked and click OK (Figure 10). This will adjust the brightness and contrast for every image in your imported stack.

Figure 10: Adjusting Image Brightness and Contrast.

12. Once your image is adjusted for proper brightness and contrast select “File->Save as->AVI”, select a frame rate of about 10fps, this will make a movie 36 seconds long assuming you took 360 frames. A movie at this speed will dramatically show chloroplast translocation assuming the one cell you chose to view undergoes the effect. Save the AVI in the directory C:\BPHS4090_Viridis_Systrophe by your name, date and title of work.
13. Copy your movie and the file called “Viridis_Systrophe_Spectrum.xls” onto a USB Key, this spreadsheet will be used for one of the questions. You can find the file in the desktop folder called “BPHS_4090_Viridis_Systrophe”.
14. Look at your cell sample through the field of view and record how many cells are incipient systrophe and how many are complete systrophe using the criteria in Figure 2.
15. Once this is done discard your cell sample slide in the bin labelled “Sharps”
16. Next prepare a new sample slide and repeat the above procedure using the red filter labelled 623nm. DO NOT make a movie using the red filter; record the total number of cells in the field of view and illuminate the cells for an hour. After the light treatment record the number of incipient and complete systrophe. Be sure to adjust your power to get the desired photon flux of 200 μmol m^-2 s^-1 and ensure your microscope is set up for Kohler illumination.

Questions/Write-up

There is no formal write-up for this experiment, briefly describe the purpose of the experiment, the experimental set-up and the physics behind the biological process we’re observing, this will be your introduction. You should type up your results into a table comparing the illumination trials using red and blue filters. Provide a brief discussion interpreting your results. In addition you need to provide answers to the 9 questions on the next page.

1. The effect of systrophe is thought to be a defence mechanism for the cell by decreasing the absorptive cross sectional area of chloroplasts within the cell. We can test this hypothesis by using a simple mathematical model to represent the cell. Assume each cell of E. viridis in its resting state is a sphere with a shell of chloroplasts along the periphery of the cell. In reality chloroplasts are also distributed radially along the cytoplasmic strands within the cell (analogous to the spokes of a bicycle wheel); however for simplicity we will only consider the outer shell of chloroplasts. After the cell undergoes systrophe, the chloroplasts surround the nucleus in a thicker shell. In the table below some data are provided of cellular dimensions for 3 arbitrary cells before and after systrophe using time lapsed images .
Cell 1Cell 2Cell 3Cell Diameter (μm)122.5108.5130.5Systrophe Diameter (μm)80.164.7103.8Nucleus Diameter (μm)41.845.861.3Thickness of Chloroplast Shell (Before Systrophe) (μm)4.65.55.3Figure 10: Adjusting Image Brightness and Contrast.





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