Rubisco and Crop Output
From Proteopedia
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== Function == | == Function == | ||
| - | Rubisco or ribulose- 1,5- bisphosphate carboxylase oxygenase is an enzyme that is involved in photosynthesis in plants and is specifically found in chloroplasts. (Harel, et. al) Rubisco is used in the light dependent part of the Calvin cycle. In this cycle, it catalyzes the most important step of carbon fixation. It converts atmospheric carbon dioxide into useable sugar. It does this by using carbon dioxide to make an intermediate, and then finally, 3-Phosphoglycerate. Most all of this 3-Phosphoglycerate is recycled and able to use again. It adds carbons to ribulose bisphosphate and then cleaves the 6 carbons into 2 chains with 3 carbons. Rubisco can also help to oxidize RuBP, a sugar. | + | '''Rubisco''' or ribulose- 1,5- bisphosphate carboxylase oxygenase is an enzyme that is involved in photosynthesis in plants and is specifically found in chloroplasts. (Harel, et. al) Rubisco is used in the light dependent part of the Calvin cycle. In this cycle, it catalyzes the most important step of carbon fixation. It converts atmospheric carbon dioxide into useable sugar. It does this by using carbon dioxide to make an intermediate, and then finally, 3-Phosphoglycerate. Most all of this 3-Phosphoglycerate is recycled and able to use again. It adds carbons to ribulose bisphosphate and then cleaves the 6 carbons into 2 chains with 3 carbons. Rubisco can also help to oxidize RuBP, a sugar. |
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Rubisco is composed of 8 large subunits and 8 small subunits. The large subunits house the binding/active sites. In Rubisco, the active site of bonding is centered around a magnesium ion. However, depending on the organism, Rubisco can also have a different shape. The magnesium ion in the center binds with the lysine on the large subunit. This, in turn, further helps with the Calvin cycle. (Harel, et. al) “The types of residues involved are acidic residues that interact with Mg2+, basic residues and histidines that interact with phosphate and hydroxyl groups, polar residues that interact with hydroxyl groups, one hydrophobic residue, and backbone atoms of several residues.” (Harel, et. al) | Rubisco is composed of 8 large subunits and 8 small subunits. The large subunits house the binding/active sites. In Rubisco, the active site of bonding is centered around a magnesium ion. However, depending on the organism, Rubisco can also have a different shape. The magnesium ion in the center binds with the lysine on the large subunit. This, in turn, further helps with the Calvin cycle. (Harel, et. al) “The types of residues involved are acidic residues that interact with Mg2+, basic residues and histidines that interact with phosphate and hydroxyl groups, polar residues that interact with hydroxyl groups, one hydrophobic residue, and backbone atoms of several residues.” (Harel, et. al) | ||
This enzyme, Rubisco, only works during the day, or when there is a light source, and is turned off at night when it is dark. Carbon dioxide is attached to the binding site which turns it off and then back on again. | This enzyme, Rubisco, only works during the day, or when there is a light source, and is turned off at night when it is dark. Carbon dioxide is attached to the binding site which turns it off and then back on again. | ||
| - | Rubisco activase is Rubisco’s “chaperone” or “regulator”. It turns Rubisco on and off based off of the amount of carbon intake. ATP is used by rubisco activase to change rubisco structurally, which turns it on and off. “The activase is now recognized to be a member of the AAA(+) family, whose members participate in macromolecular complexes that perform diverse chaperone-like functions. The conserved nucleotide-binding domain of AAA(+) family members appears to have a common fold that when applied to the activase is generally consistent with previous site-directed mutagenesis studies of the activase.” (Portis Jr.) | + | '''Rubisco activase''' is Rubisco’s “chaperone” or “regulator”. It turns Rubisco on and off based off of the amount of carbon intake. ATP is used by rubisco activase to change rubisco structurally, which turns it on and off. “The activase is now recognized to be a member of the AAA(+) family, whose members participate in macromolecular complexes that perform diverse chaperone-like functions. The conserved nucleotide-binding domain of AAA(+) family members appears to have a common fold that when applied to the activase is generally consistent with previous site-directed mutagenesis studies of the activase.” (Portis Jr.) |
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== Problems == | == Problems == | ||
Rubisco is the most common protein in the world! Although this is true, just because it is the most abundant doesn’t mean it’s the most useful. Rubisco has some problems working correctly. Compared to other enzymes, the rate of the carboxylation reaction with Rubisco is 3 s-1. This is extremely slow. Another problem with Rubisco is that oxygen, as well as carbon dioxide, can fit into the binding site. This is because they both are similar in size and shape. It is difficult for Rubisco to distinguish which is which. (Goodsell) If this happens, and it does, phosphoglycolate can be made, and this is very toxic. This is Rubisco’s wasteful side chain reaction. To fix these mistakes, it is very costly to the plant, meaning, it costs ATP to fix this. Now the plant has to transport the glycolate across multiple membranes, losing Co2 and making more reactions occur. Depending on varying temperatures Rubisco is working with, its error rate can range from 20- 40%! (Alber, et. Al) | Rubisco is the most common protein in the world! Although this is true, just because it is the most abundant doesn’t mean it’s the most useful. Rubisco has some problems working correctly. Compared to other enzymes, the rate of the carboxylation reaction with Rubisco is 3 s-1. This is extremely slow. Another problem with Rubisco is that oxygen, as well as carbon dioxide, can fit into the binding site. This is because they both are similar in size and shape. It is difficult for Rubisco to distinguish which is which. (Goodsell) If this happens, and it does, phosphoglycolate can be made, and this is very toxic. This is Rubisco’s wasteful side chain reaction. To fix these mistakes, it is very costly to the plant, meaning, it costs ATP to fix this. Now the plant has to transport the glycolate across multiple membranes, losing Co2 and making more reactions occur. Depending on varying temperatures Rubisco is working with, its error rate can range from 20- 40%! (Alber, et. Al) | ||
| - | Most plants are categorized into C3 and C4 plants. This is based off of the climate they are found in. C3 plants are more accustomed to cooler temperatures, as opposed to C4 plants that are found in warmer temperatures. Photorespiration is more likely to occur in C4 plants than C3 plants, because C4 plants are more accustomed to warmer temps. As temperatures begin to increase, so does photorespiration. Plants are more likely to dehydrate in the warm weather. This forces them to close the stomata in order to conserve water. When the plant closes the stomata, CO2 is prevented from entering the leaf. Photorespiration is when Rubisco binds O2 instead of CO2. This is contrary to the general pattern of photosynthesis, where Rubisco binds to CO2 instead of O2. Rubisco acts differently in C4 than C3 plants. To reduce photorespiration, C4 plants can “harvest” CO2 in bundle sheath cells. They also are useful at collecting carbon and using less water in warmer climates. | + | Most plants are categorized into C3 and C4 plants. This is based off of the climate they are found in. C3 plants are more accustomed to cooler temperatures, as opposed to C4 plants that are found in warmer temperatures. '''Photorespiration''' is more likely to occur in C4 plants than C3 plants, because C4 plants are more accustomed to warmer temps. As temperatures begin to increase, so does photorespiration. Plants are more likely to dehydrate in the warm weather. This forces them to close the stomata in order to conserve water. When the plant closes the stomata, CO2 is prevented from entering the leaf. Photorespiration is when Rubisco binds O2 instead of CO2. This is contrary to the general pattern of photosynthesis, where Rubisco binds to CO2 instead of O2. Rubisco acts differently in C4 than C3 plants. To reduce photorespiration, C4 plants can “harvest” CO2 in bundle sheath cells. They also are useful at collecting carbon and using less water in warmer climates. |
The major problem researchers have been working to change with Rubisco is the oxygenation instead of the carboxylation. The reason this is a problem is because the plant has to fix this, making this issue energetically unfavorable, by losing around 30% of the plants ATP in that step. When Rubisco binds oxygen instead, crop yield becomes lower, this is because it only makes half the product amount of 3-Phosphoglycerate. This limits how many times a plant can undergo the Calvin Cycle to make sugar. When temperatures begin to increase it is even more of an inconvenience and much more difficult for a plant to fix this problem. If we can fix this issue, Rubisco can not only be more successful with photosynthesis, but extremely successful with changing crop growth and quantity. <ref>PMID: 27935049</ref> | The major problem researchers have been working to change with Rubisco is the oxygenation instead of the carboxylation. The reason this is a problem is because the plant has to fix this, making this issue energetically unfavorable, by losing around 30% of the plants ATP in that step. When Rubisco binds oxygen instead, crop yield becomes lower, this is because it only makes half the product amount of 3-Phosphoglycerate. This limits how many times a plant can undergo the Calvin Cycle to make sugar. When temperatures begin to increase it is even more of an inconvenience and much more difficult for a plant to fix this problem. If we can fix this issue, Rubisco can not only be more successful with photosynthesis, but extremely successful with changing crop growth and quantity. <ref>PMID: 27935049</ref> | ||
Revision as of 15:02, 24 April 2019
==Your Heading Here (maybe something like 'Structure')== Modifying Rubisco to Improve Crop Output
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References
- ↑ Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
- ↑ Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644
- ↑ Sharwood RE. Engineering chloroplasts to improve Rubisco catalysis: prospects for translating improvements into food and fiber crops. New Phytol. 2017 Jan;213(2):494-510. doi: 10.1111/nph.14351. Epub 2016 Dec 9. PMID:27935049 doi:http://dx.doi.org/10.1111/nph.14351
- ↑ Sharwood RE. Engineering chloroplasts to improve Rubisco catalysis: prospects for translating improvements into food and fiber crops. New Phytol. 2017 Jan;213(2):494-510. doi: 10.1111/nph.14351. Epub 2016 Dec 9. PMID:27935049 doi:http://dx.doi.org/10.1111/nph.14351
- ↑ Sharwood RE. Engineering chloroplasts to improve Rubisco catalysis: prospects for translating improvements into food and fiber crops. New Phytol. 2017 Jan;213(2):494-510. doi: 10.1111/nph.14351. Epub 2016 Dec 9. PMID:27935049 doi:http://dx.doi.org/10.1111/nph.14351
- ↑ Sharwood RE. Engineering chloroplasts to improve Rubisco catalysis: prospects for translating improvements into food and fiber crops. New Phytol. 2017 Jan;213(2):494-510. doi: 10.1111/nph.14351. Epub 2016 Dec 9. PMID:27935049 doi:http://dx.doi.org/10.1111/nph.14351
