Rubisco and Crop Output
From Proteopedia
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- | <StructureSection load='1aus' size='340' side='right' caption=' | + | <StructureSection load='1aus' size='340' side='right' caption='Spinach RuBisCO (PDB code [[1aus]])' scene=''> |
== 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.Rubisco is used in the light dependent part of the Calvin cycle. In this cycle, it catalyzes the first step of carbon fixation. It converts atmospheric carbon dioxide into useable sugar. It does this by using carbon dioxide to make an intermediate- an Enediolate intermediate, then a unstable 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 (Ribulose 1,5-bisphosphate), a sugar. <ref name="Andersson">PMID:8648644</ref> | + | '''Rubisco''' or '''ribulose- 1,5- bisphosphate carboxylase oxygenase''' is an enzyme that is involved in photosynthesis in plants and is specifically found in chloroplasts. Rubisco is used in the light dependent part of the Calvin cycle. In this cycle, it catalyzes the first step of carbon fixation. It converts atmospheric carbon dioxide into useable sugar. It does this by using carbon dioxide to make an intermediate- an Enediolate intermediate, then a unstable 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 (Ribulose 1,5-bisphosphate), a sugar. <ref name="Andersson">PMID:8648644</ref> |
== Structure == | == Structure == | ||
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Scientists can and have used Rubisco to make advances in plant technology. With the ever-changing problems going on in this world, some plant proteins can help change food scarcity. Some plant proteins, including Rubisco, can be even more useful and sustainable than proteins found in animals. It also has a lot of nutritional value, along with amino acids. For example, lysine is the most common amino acid found. Lysine may reduce anxiety by blocking stress response receptors, and it can also improve the absorption/retention of calcium. “Highly purified Rubisco is a tasteless, odourless white powder with a nutritional value reported to be equal to or superior to that of other food proteins. Rubisco also possesses some desirable functional properties which might enable food processors to successfully incorporate the protein into a number of different food products (desserts, composite meat products, ice cream, beverages). Further developments are to come to test Rubisco into food systems such as desserts / yogurt for texturing and flavouring improvements.” | Scientists can and have used Rubisco to make advances in plant technology. With the ever-changing problems going on in this world, some plant proteins can help change food scarcity. Some plant proteins, including Rubisco, can be even more useful and sustainable than proteins found in animals. It also has a lot of nutritional value, along with amino acids. For example, lysine is the most common amino acid found. Lysine may reduce anxiety by blocking stress response receptors, and it can also improve the absorption/retention of calcium. “Highly purified Rubisco is a tasteless, odourless white powder with a nutritional value reported to be equal to or superior to that of other food proteins. Rubisco also possesses some desirable functional properties which might enable food processors to successfully incorporate the protein into a number of different food products (desserts, composite meat products, ice cream, beverages). Further developments are to come to test Rubisco into food systems such as desserts / yogurt for texturing and flavouring improvements.” | ||
<ref name="van de Velde"> van de Velde, Fred., et. al “From Waste Product to Food Ingredient: The Extraction of Abundant Plant Protein RuBisCo.” New Food Magazine, 13 May 2011, </ref> | <ref name="van de Velde"> van de Velde, Fred., et. al “From Waste Product to Food Ingredient: The Extraction of Abundant Plant Protein RuBisCo.” New Food Magazine, 13 May 2011, </ref> | ||
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== Problems == | == Problems == |
Current revision
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References
- ↑ 1.0 1.1 Andersson I. Large structures at high resolution: the 1.6 A crystal structure of spinach ribulose-1,5-bisphosphate carboxylase/oxygenase complexed with 2-carboxyarabinitol bisphosphate. J Mol Biol. 1996 May 31;259(1):160-74. PMID:8648644 doi:10.1006/jmbi.1996.0310
- ↑ Portis AR Jr. Rubisco activase - Rubisco's catalytic chaperone. Photosynth Res. 2003;75(1):11-27. doi: 10.1023/A:1022458108678. PMID:16245090 doi:http://dx.doi.org/10.1023/A:1022458108678
- ↑ van de Velde, Fred., et. al “From Waste Product to Food Ingredient: The Extraction of Abundant Plant Protein RuBisCo.” New Food Magazine, 13 May 2011,
- ↑ Alber, Birgit., et. al “A Short History of RubisCO: the Rise and Fall (?) of Nature's Predominant CO2 Fixing Enzyme.” Current Opinion in Biotechnology, Elsevier Current Trends, 29 Aug. 2017,
- ↑ 5.0 5.1 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
- ↑ Carmo-Silva E, Scales JC, Madgwick PJ, Parry MA. Optimizing Rubisco and its regulation for greater resource use efficiency. Plant Cell Environ. 2015 Sep;38(9):1817-32. doi: 10.1111/pce.12425. Epub 2014 Sep, 26. PMID:25123951 doi:http://dx.doi.org/10.1111/pce.12425
- ↑ 7.0 7.1 PMID: 23417088