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10.13: Plant Photorespiration

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    Learning Objectives
    • Differentiate between C3, C4, and CAM plant approaches to photorespiration

    High crop yields are pretty important—for keeping people fed, and also for keeping economies running. If you heard there was a single factor that reduced the yield of wheat by 20 percent and the yield of soybeans by 36 percent in the United States, for instance, you might be curious to know what it was[1].

    As it turns out, the factor behind those (real-life) numbers is photorespiration. This wasteful metabolic pathway begins when rubisco, the carbon-fixing enzyme of the Calvin cycle, grabs O2 rather than CO2. It uses up fixed carbon, wastes energy, and tends to happens when plants close their stomata (leaf pores) to reduce water loss. High temperatures make it even worse.

    Some plants, unlike wheat and soybean, can escape the worst effects of photorespiration. The C4 and CAM pathways are two adaptations—beneficial features arising by natural selection—that allow certain species to minimize photorespiration. These pathways work by ensuring that Rubisco always encounters high concentrations of CO2 making it unlikely to bind to O2.

    Now, let’s take a closer look at the C3, C4 and CAM pathways and see how they do (or don’t!) reduce photorespiration.

    C3 plants

    A “normal” plant—one that doesn’t have photosynthetic adaptations to reduce photorespiration—is called a C3 plant. The first step of the Calvin cycle is the fixation of carbon dioxide by rubisco, and plants that use only this “standard” mechanism of carbon fixation are called C3 plants, for the three-carbon compound (3-PGA) the reaction produces[2]. About 85 percent of the plant species on the planet are C3 plants, including rice, wheat, soybeans and all trees.

    Image of the c3 pathway. Carbon dioxide enters a mesophyll cell and is fixed immediately by rubisco, leading to the formation of three PGA molecules, which contain three carbons.
    Figure 1. The C3 Pathway

    C4 plants

    In C4 plants, the light-dependent reactions and the Calvin cycle are physically separated, with the light-dependent reactions occurring in the mesophyll cells (spongy tissue in the middle of the leaf) and the Calvin cycle occurring in special cells around the leaf veins. These cells are called bundle-sheath cells.

    To see how this division helps, let’s look at an example of C4 photosynthesis in action. First, atmospheric CO2 is fixed in the mesophyll cells to form a simple, 4-carbon organic acid (oxaloacetate). This step is carried out by a non-rubisco enzyme, PEP carboxylase, that has no tendency to bind O2. Oxaloacetate is then converted to a similar molecule, malate, that can be transported in to the bundle-sheath cells. Inside the bundle sheath, malate breaks down, releasing a molecule of CO2. The CO2 is then fixed by rubisco and made into sugars via the Calvin cycle, exactly as in C3 photosynthesis.

    Image of the c4 pathway. Initial carbon fixation takes place in mesophyll cells and the Calvin cycle takes place in bundle-sheath cells. PEP carboxylase attaches an incoming carbon dioxide molecule to the three carbon-molecule PEP producing oxaloacetate, a four-carbon molecule. The oxaloacetate is converted to malate, which travels out of the mesophyll cell and into a neighboring bundle-sheath cell. Inside the bundle-sheath cell, the malate is broken down to release carbon dioxide, which then enters the Calvin cycle. Pyruvate is also produced in this step and moves back into the mesophyll cell, where it is converted into PEP, a reaction that converts ATP and Pi into AMP and PPi.
    Figure 2. The C4 Pathway

    This process isn’t without its energetic price: ATP must be expended to return the three-carbon “ferry” molecule from the bundle sheath cell and get it ready to pick up another molecule of atmospheric CO2. However, because the mesophyll cells constantly pump CO2 into neighboring bundle-sheath cells in the form of malate, there’s always a high concentration of CO2 relative to O2 right around rubisco. This strategy minimizes photorespiration.

    The C4 pathway is used in about 3 percent of all vascular plants; some examples are crabgrass, sugarcane and corn. C4 plants are common in habitats that are hot, but are less abundant in areas that are cooler. In hot conditions, the benefits of reduced photorespiration likely exceed the ATP cost of moving CO2 from the mesophyll cell to the bundle-sheath cell.

    CAM plants

    Image of a succulent plant
    Figure 3. Crassulaceae

    Some plants that are adapted to dry environments, such as cacti and pineapples, use the crassulacean acid metabolism (CAM) pathway to minimize photorespiration. This name comes from the family of plants, the Crassulaceae, in which scientists first discovered the pathway.

    Instead of separating the light-dependent reactions and the use of CO2 in the Calvin cycle in space, CAM plants separate these processes in time. At night, CAM plants open their stomata, allowing CO2 to diffuse into the leaves. This CO2 is fixed into oxaloacetate by PEP carboxylase (the same step used by C4 plants), then converted to malate or another type of organic acid[3].

    The organic acid is stored inside vacuoles until the next day. In the daylight, the CAM plants do not open their stomata, but they can still photosynthesis. That’s because the organic acids are transported out of the vacuole and broken down to release CO2, which enters the Calvin cycle. This controlled release maintains a high concentration of CO2 around rubisco[4].

    Image of the C A M pathway. C A M plants temporally separate carbon fixation and the Calvin cycle. Carbon dioxide diffuses into leaves in the night when the stomata are open and is fixed into oxaloacetate by PEP carboxylase which attaches the carbon dioxide to the three-carbon molecule PEP. The oxaloacetate is converted into another organic acid, such as malate. The organic acid is stored until the next day and is then broken down releasing carbon dioxide that can be fixed by rubisco and enter the Calvin cycle to make sugars.
    Figure 4. The CAM Pathway

    The CAM pathway requires ATP at multiple steps (not shown above), so like C4 photosynthesis, it is not an energetic “freebie.”[5] However, plant species that use CAM photosynthesis not only avoid photorespiration, but are also very water-efficient. Their stomata only open at night, when humidity tends to be higher and temperatures are cooler, both factors that reduce water loss from leaves. CAM plants are typically dominant in very hot, dry areas, like deserts.

    Comparisons of C3, C4, and CAM plants

    C3, C4, and CAM plants all use the Calvin cycle to make sugars from CO2. These pathways for fixing CO2 have different advantages and disadvantages and make plants suited for different habitats. The C3 mechanism works well in cool environments, while C4 and CAM plants are adapted to hot, dry areas.

    Both the C4 and CAM pathways have evolved independently over two dozen times, which suggests they may give plant species in hot climates a significant evolutionary advantage[6].

    Type Separation of initial CO2 fixation and Calvin cycle Stomata open Best adapted to
    C3 No separation Day Cool, wet environments
    C4 Between mesophyll and bundle-sheath cells (in space) Day Hot, sunny environments
    CAM Between night and day (in time) Night Very hot, dry environments

    1. Walker, Berkeley J., VanLoocke, Andy, Bernacchi, Carl J., and Ort, Donald R. (2016). The cost of photorespiration to food production now and in the future. Annual Review of Plant Biology 67, 107. ://dx.doi.org/10.1146/annurev-arplant-043015-111709. ↵
    2. Reece, J. B., Urry, L. A., Cain, M. L., Wasserman, S. A., Minorsky, P. V., and Jackson, R. B. (2011). Alternative mechanisms of carbon fixation have evolved in hot, arid climates. In Campbell biology (10th ed.) San Francisco, CA: Pearson, 201. ↵
    3. Crassulacean acid metabolism. (2016, May 29). Retrieved July 22, 2016 from Wikipedia: https://en.Wikipedia.org/wiki/Crassulacean_acid_metabolism#Biochemistry. ↵
    4. Raven, Peter H., Johnson, George B., Losos, Mason, Kenneth A., Losos, Jonathan B., and Singer, Susan R. (2014). Photorespiration. In Biology (10th ed., AP ed.). New York, NY: McGraw-Hill, 165. ↵
    5. Crassulacean acid metabolism. (2016, May 29). ↵
    6. Guralnick, Lonnie J., Amanda Cline, Monica Smith, and Rowan F. Sage. (2008). Evolutionary physiology: the extent of C4 and CAM photosynthesis in the genera Anacampseros and Grahamia of the Portulacaceae. Journal of Experimental Botany, 59(7), 1735–1742. http://dx.doi.org/10.1093/jxb/ern081. ↵

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