is a wasteful process that occurs when fixes oxygen instead of carbon dioxide. It reduces photosynthetic efficiency, especially in . High temperatures and dry conditions make photorespiration worse, leading to significant carbon loss.
C4 and have evolved special mechanisms to concentrate CO2 around Rubisco. This reduces photorespiration and allows them to thrive in hot, dry environments where C3 plants struggle. These adaptations make photosynthesis more efficient in challenging conditions.
Photorespiration in C3 Plants
The Photorespiration Process
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Photorespiration occurs when Rubisco fixes O2 instead of CO2 due to high O2 concentration or high temperatures
Leads to the production of 2-phosphoglycolate (2-PG) which is toxic and must be recycled
2-PG is converted to glycolate in the chloroplast then transported to peroxisomes and mitochondria for recycling
Recycling process converts glycolate back into 3-PGA which can re-enter the Calvin cycle
Photorespiration is an energy-consuming process that reduces the efficiency of photosynthesis (up to 50% of fixed carbon can be lost)
Factors Affecting Photorespiration
Photorespiration is more prevalent in C3 plants which include most major crops (wheat, rice, soybeans)
High temperatures increase the rate of photorespiration because Rubisco's affinity for CO2 decreases while its affinity for O2 increases
Dry conditions can cause stomata to close, reducing CO2 concentration in the leaf and increasing photorespiration
Photorespiration is less significant in C4 and CAM plants due to their CO2 concentration mechanisms
C4 Photosynthesis
C4 Plant Anatomy and Physiology
have a unique known as Kranz anatomy which consists of two distinct photosynthetic cell types: mesophyll cells and bundle sheath cells
Mesophyll cells form a ring around the bundle sheath cells and contain , an enzyme with high affinity for CO2
Bundle sheath cells contain Rubisco and carry out the Calvin cycle
C4 plants have a CO2 concentration mechanism that allows them to concentrate CO2 in the bundle sheath cells, reducing photorespiration
The C4 Photosynthetic Pathway
In mesophyll cells, CO2 is initially fixed by PEP carboxylase to form a 4-carbon compound (), hence the name
The 4-carbon compound is then converted to or aspartate and transported to the bundle sheath cells
In the bundle sheath cells, the 4-carbon compound is decarboxylated, releasing CO2 which is then fixed by Rubisco in the Calvin cycle
The remaining 3-carbon compound is transported back to the mesophyll cells to regenerate PEP
This CO2 concentration mechanism allows C4 plants to maintain high rates of photosynthesis even in hot, dry conditions (examples: corn, sugarcane, sorghum)
Crassulacean Acid Metabolism (CAM)
CAM Plant Adaptations
CAM plants are adapted to hot, dry environments and include many succulents (cacti, aloe, jade plant)
CAM plants have a unique CO2 concentration mechanism that allows them to open their stomata at night and close them during the day to conserve water
At night, CAM plants fix CO2 using PEP carboxylase to form malic acid which is stored in the vacuole
During the day, the stomata close and the stored malic acid is decarboxylated, releasing CO2 which is then fixed by Rubisco in the Calvin cycle
The CAM Photosynthetic Pathway
The CAM pathway is divided into four phases that occur over a 24-hour period
Phase I (night): Stomata open, CO2 is fixed by PEP carboxylase to form malic acid which is stored in the vacuole
Phase II (early morning): Stomata close, malic acid continues to be stored
Phase III (day): Malic acid is decarboxylated, releasing CO2 which is fixed by Rubisco in the Calvin cycle
Phase IV (late afternoon/evening): Malic acid reserves are depleted, stomata may reopen to fix more CO2 if conditions allow
The temporal separation of CO2 fixation and the Calvin cycle in CAM plants allows them to conserve water while still maintaining photosynthesis