Photorespiration

Photorespiration (also known as the oxidative photosynthetic carbon cycle or C2 cycle) refers to a process in plant metabolism where the enzyme RuBisCO oxygenates RuBP, wasting some of the energy produced by photosynthesis. The desired reaction is the addition of carbon dioxide to RuBP (carboxylation), a key step in the Calvin–Benson cycle, but approximately 25% of reactions by RuBisCO instead add oxygen to RuBP (oxygenation), creating a product that cannot be used within the Calvin–Benson cycle. This process lowers the efficiency of photosynthesis, potentially lowering photosynthetic output by 25% in C3 plants.[1] Photorespiration involves a complex network of enzyme reactions that exchange metabolites between chloroplasts, leaf peroxisomes and mitochondria.

Simplified photorespiration cycle
Simplified photorespiration and Calvin cycle

The oxygenation reaction of RuBisCO is a wasteful process because 3-phosphoglycerate is created at a lower rate and higher metabolic cost compared with RuBP carboxylase activity. While photorespiratory carbon cycling results in the formation of G3P eventually, around 25% of carbon fixed by photorespiration is re-released as CO2[2] and nitrogen, as ammonia. Ammonia must then be detoxified at a substantial cost to the cell. Photorespiration also incurs a direct cost of one ATP and one NAD(P)H.

While it is common to refer to the entire process as photorespiration, technically the term refers only to the metabolic network which acts to rescue the products of the oxygenation reaction (phosphoglycolate).

Photorespiratory reactions
PhotorespirationFrom left to right: chloroplast, peroxisome, and mitochondrion

Addition of molecular oxygen to ribulose-1,5-bisphosphate produces 3-phosphoglycerate (PGA) and 2-phosphoglycolate (2PG, or PG). PGA is the normal product of carboxylation, and productively enters the Calvin cycle. Phosphoglycolate, however, inhibits certain enzymes involved in photosynthetic carbon fixation (hence is often said to be an 'inhibitor of photosynthesis').[3] It is also relatively difficult to recycle: in higher plants it is salvaged by a series of reactions in the peroxisome, mitochondria, and again in the peroxisome where it is converted into glycerate. Glycerate reenters the chloroplast and by the same transporter that exports glycolate. A cost of 1 ATP is associated with conversion to 3-phosphoglycerate (PGA) (Phosphorylation), within the chloroplast, which is then free to re-enter the Calvin cycle.

Several costs are associated with this metabolic pathway; the production of hydrogen peroxide in the peroxisome (associated with the conversion of glycolate to glyoxylate). Hydrogen peroxide is a dangerously strong oxidant which must be immediately split into water and oxygen by the enzyme catalase. The conversion of 2× 2Carbon glycine to 1× C3 serine in the mitochondria by the enzyme glycine-decarboxylase is a key step, which releases CO2, NH3, and reduces NAD to NADH. Thus, one CO
2 molecule is produced for every two molecules of O
2 (two deriving from RuBisCO and one from peroxisomal oxidations). The assimilation of NH3 occurs via the GS-GOGAT cycle, at a cost of one ATP and one NADPH.

Cyanobacteria have three possible pathways through which they can metabolise 2-phosphoglycolate. They are unable to grow if all three pathways are knocked out, despite having a carbon concentrating mechanism that should dramatically lower the rate of photorespiration (see below).[4]

Substrate specificity of RuBisCO
Oxygenase activity of RuBisCO

The oxidative photosynthetic carbon cycle reaction is catalyzed by RuBP oxygenase activity:

RuBP + O
2 → Phosphoglycolate + 3-phosphoglycerate + 2H+

During the catalysis by RuBisCO, an 'activated' intermediate is formed (an enediol intermediate) in the RuBisCO active site. This intermediate is able to react with either CO
2 or O
2. It has been demonstrated that the specific shape of the RuBisCO active site acts to encourage reactions with CO
2. Although there is a significant "failure" rate (~25% of reactions are oxygenation rather than carboxylation), this represents significant favouring of CO
2, when the relative abundance of the two gases is taken into account: in the current atmosphere, O
2 is approximately 500 times more abundant, and in solution O
2 is 25 times more abundant than CO
2.[5]

The ability of RuBisCO to specify between the two gases is known as its selectivity factor (or Srel), and it varies between species,[5] with angiosperms more efficient than other plants, but with little variation among the vascular plants.[6]

A suggested explanation of RuBisCO's inability to discriminate completely between CO
2 and O
2 is that it is an evolutionary relic: The early atmosphere in which primitive plants originated contained very little oxygen, the early evolution of RuBisCO was not influenced by its ability to discriminate between O
2 and CO
2.[6]

Conditions which affect photorespiration
Part of a series on the
Carbon cycle
By regions
Carbon dioxide
Forms of carbon
Metabolic pathways
Carbon respiration
Carbon pumps
Carbon sequestration
Methane
Biogeochemical
Other
  •  Category

Photorespiration rates are increased by:

Altered substrate availability: lowered CO2 or increased O2

Factors which influence this include the atmospheric abundance of the two gases, the supply of the gases to the site of fixation (i.e. in land plants: whether the stomata are open or closed), the length of the liquid phase (how far these gases have to diffuse through water in order to reach the reaction site). For example, when the stomata are closed to prevent water loss during drought: this limits the CO2 supply, while O
2 production within the leaf will continue. In algae (and plants which photosynthesise underwater); gases have to diffuse significant distances through water, which results in a decrease in the availability of CO2 relative to O
2. It has been predicted that the increase in ambient CO2 concentrations predicted over the next 100 years may lower the rate of photorespiration in most plants by around 50%. However, at temperatures higher than the photosynthetic thermal optimum, the increases in turnover rate are not translated into increased CO2 assimilation because of the decreased affinity of Rubisco for CO2.[7]

Increased temperature

At higher temperatures RuBisCO is less able to discriminate between CO2 and O
2. This is because the enediol intermediate is less stable. Increasing temperatures also lower the solubility of CO2, thus lowering the concentration of CO2 relative to O
2 in the chloroplast.

Biological adaptation to minimize photorespiration
Maize uses the C4 pathway, minimizing photorespiration

Certain species of plants or algae have mechanisms to lower uptake of molecular oxygen by RuBisCO. These are commonly referred to as Carbon Concentrating Mechanisms (CCMs), as they increase the concentration of CO2 so that RuBisCO is less likely to produce glycolate through reaction with O
2.

Biochemical carbon concentrating mechanisms

Biochemical CCMs concentrate carbon dioxide in one temporal or spatial region, through metabolite exchange. C4 and CAM photosynthesis both use the enzyme Phosphoenolpyruvate carboxylase (PEPC) to add CO
2 to a 4-Carbon sugar. PEPC is faster than RuBisCO, and more selective for CO
2.

C4

C4 plants capture carbon dioxide in their mesophyll cells (using an enzyme called phosphoenolpyruvate carboxylase which catalyzes the combination of carbon dioxide with a compound called phosphoenolpyruvate (PEP)), forming oxaloacetate. This oxaloacetate is then converted to malate and is transported into the bundle sheath cells (site of carbon dioxide fixation by RuBisCO) where oxygen concentration is low to avoid photorespiration. Here, carbon dioxide is removed from the malate and combined with RuBP by RuBisCO in the usual way, and the Calvin Cycle proceeds as normal. The CO
2 concentrations in the Bundle Sheath are approximately 10–20 fold higher than the concentration in the mesophyll cells.[6]

This ability to avoid photorespiration makes these plants more hardy than other plants in dry and hot environments, wherein stomata are closed and internal carbon dioxide levels are low. Under these conditions, photorespiration does occur in C4 plants, but at a much lower level compared with C3 plants in the same conditions. C4 plants include sugar cane, corn (maize), and sorghum.

CAM (Crassulacean acid metabolism)
Overnight graph of CO2 absorbed by a CAM plant

CAM plants, such as cacti and succulent plants, also use the enzyme PEP carboxylase to capture carbon dioxide, but only at night. Crassulacean acid metabolism allows plants to conduct most of their gas exchange in the cooler night-time air, sequestering carbon in 4-carbon sugars which can be released to the photosynthesizing cells during the day. This allows CAM plants to minimize water loss (transpiration) by maintaining closed stomata during the day. CAM plants usually display other water-saving characteristics, such as thick cuticles, stomata with small apertures, and typically lose around 1/3 of the amount of water per CO
2 fixed.[8]


C2
In C2 plants, the mitochondria of mesophyll cells have no glycine decarboxylase (GDC).

C2 photosynthesis (also called glycine shuttle and photorespiratory CO2 pump) is a CCM that works by making use of – as opposed to avoiding – photorespiration. It performs carbon refixation by delaying the breakdown of photorespired glycine, so that the molecule is shuttled from the mesophyll into the bundle sheath. Once there, the glycine is decarboxylated in mitochondria as usual, releasing CO2 and concentrating it to triple the usual concentration.[9]

Although C2 photosynthesis is traditionally understood as an intermediate step between C3 and C4, a wide variety of plant lineages do end up in the C2 stage without further evolving, showing that it's an evolutionary steady state of its own. C2 may be easier to engineer into crops, as the phenotype requires fewer anatomical changes to produce.[9]

Algae

There have been some reports of algae operating a biochemical CCM: shuttling metabolites within single cells to concentrate CO2 in one area. This process is not fully understood.[10]

Biophysical carbon-concentrating mechanisms

This type of carbon-concentrating mechanism (CCM) relies on a contained compartment within the cell into which CO2 is shuttled, and where RuBisCO is highly expressed. In many species, biophysical CCMs are only induced under low carbon dioxide concentrations. Biophysical CCMs are more evolutionary ancient than biochemical CCMs. There is some debate as to when biophysical CCMs first evolved, but it is likely to have been during a period of low carbon dioxide, after the Great Oxygenation Event (2.4 billion years ago). Low CO
2 periods occurred around 750, 650, and 320–270 million years ago.[11]

Eukaryotic algae

In nearly all species of eukaryotic algae (Chloromonas being one notable exception), upon induction of the CCM, ~95% of RuBisCO is densely packed into a single subcellular compartment: the pyrenoid. Carbon dioxide is concentrated in this compartment using a combination of CO2 pumps, bicarbonate pumps, and carbonic anhydrases. The pyrenoid is not a membrane bound compartment, but is found within the chloroplast, often surrounded by a starch sheath (which is not thought to serve a function in the CCM).[12]

Hornworts

Certain species of hornwort are the only land plants which are known to have a biophysical CCM involving concentration of carbon dioxide within pyrenoids in their chloroplasts.

Cyanobacteria

Cyanobacterial CCMs are similar in principle to those found in eukaryotic algae and hornworts, but the compartment into which carbon dioxide is concentrated has several structural differences. Instead of the pyrenoid, cyanobacteria contain carboxysomes, which have a protein shell, and linker proteins packing RuBisCO inside with a very regular structure. Cyanobacterial CCMs are much better understood than those found in eukaryotes, partly due to the ease of genetic manipulation of prokaryotes.

Possible purpose of photorespiration

Lowering photorespiration may not result in increased growth rates for plants. Photorespiration may be necessary for the assimilation of nitrate from soil. Thus, a lowering in photorespiration by genetic engineering or because of increasing atmospheric carbon dioxide (due to fossil fuel burning) may not benefit plants as has been proposed.[13] Several physiological processes may be responsible for linking photorespiration and nitrogen assimilation. Photorespiration increases availability of NADH, which is required for the conversion of nitrate to nitrite. Certain nitrite transporters also transport bicarbonate, and elevated CO2 has been shown to suppress nitrite transport into chloroplasts.[14] However, in an agricultural setting, replacing the native photorespiration pathway with an engineered synthetic pathway to metabolize glycolate in the chloroplast resulted in a 40 percent increase in crop growth.[15][16][17]

Although photorespiration is much lower in C4 species, it is still an essential pathway – mutants without functioning 2-phosphoglycolate metabolism cannot grow in normal conditions. One mutant was shown to rapidly accumulate glycolate.[18]

Although the functions of photorespiration remain controversial,[19] it is widely accepted that this pathway influences a wide range of processes from bioenergetics, photosystem II function, and carbon metabolism to nitrogen assimilation and respiration. The oxygenase reaction of RuBisCO may prevent CO2 depletion near its active sites[20] and contributes to the regulation of CO2. concentration in the atmosphere[21] The photorespiratory pathway is a major source of hydrogen peroxide (H
2O
2) in photosynthetic cells. Through H
2O
2 production and pyrimidine nucleotide interactions, photorespiration makes a key contribution to cellular redox homeostasis. In so doing, it influences multiple signalling pathways, in particular, those that govern plant hormonal responses controlling growth, environmental and defense responses, and programmed cell death.[19]

It has been postulated that photorespiration may function as a "safety valve",[22] preventing the excess of reductive potential coming from an overreduced NADPH-pool from reacting with oxygen and producing free radicals, as these can damage the metabolic functions of the cell by subsequent oxidation of membrane lipids, proteins or nucleotides. The mutants deficient in photorespiratory enzymes are characterized by a high redox level in the cell,[23] impaired stomatal regulation,[24] and accumulation of formate.[25]

See also

References
  1. Sharkey T (1988). "Estimating the rate of photorespiration in leaves". Physiologia Plantarum. 73 (1): 147–152. doi:10.1111/j.1399-3054.1988.tb09205.x.
  2. Leegood RC (May 2007). "A welcome diversion from photorespiration". Nature Biotechnology. 25 (5): 539–40. doi:10.1038/nbt0507-539. PMID 17483837. S2CID 5015366.
  3. Peterhansel C, Krause K, Braun HP, Espie GS, Fernie AR, Hanson DT, Keech O, Maurino VG, Mielewczik M, Sage RF (July 2013). "Engineering photorespiration: current state and future possibilities". Plant Biology. 15 (4): 754–8. doi:10.1111/j.1438-8677.2012.00681.x. PMID 23121076.
  4. Eisenhut M, Ruth W, Haimovich M, Bauwe H, Kaplan A, Hagemann M (November 2008). "The photorespiratory glycolate metabolism is essential for cyanobacteria and might have been conveyed endosymbiontically to plants". Proceedings of the National Academy of Sciences of the United States of America. 105 (44): 17199–204. Bibcode:2008PNAS..10517199E. doi:10.1073/pnas.0807043105. PMC 2579401. PMID 18957552.
  5. Griffiths H (June 2006). "Plant biology: designs on Rubisco". Nature. 441 (7096): 940–1. Bibcode:2006Natur.441..940G. doi:10.1038/441940a. PMID 16791182. S2CID 31190084.
  6. Ehleringer JR, Sage RF, Flanagan LB, Pearcy RW (March 1991). "Climate change and the evolution of C(4) photosynthesis". Trends in Ecology & Evolution. 6 (3): 95–9. doi:10.1016/0169-5347(91)90183-x. PMID 21232434.
  7. Hermida-Carrera, Carmen; Kapralov, Maxim V; Galmés, Jeroni (21 June 2016). "Rubisco catalytic properties and temperature response in crops". Plant Physiology. 171 (4): 2549–61. doi:10.1104/pp.16.01846. PMC 4972260. PMID 27329223.
  8. Taiz L, Zeiger E (2010). "Chapter 8: Photosynthesis: The Carbon Reactions: Inorganic Carbon–Concentrating Mechanisms: Crassulacean Acid Metabolism (CAM)". Plant Physiology (Fifth ed.). Sinauer Associates, Inc. p. 222.
  9. Lundgren, Marjorie R. (December 2020). "C 2 photosynthesis: a promising route towards crop improvement?". New Phytologist. 228 (6): 1734–1740. doi:10.1111/nph.16494. PMID 32080851.
  10. Giordano M, Beardall J, Raven JA (June 2005). "CO2 concentrating mechanisms in algae: mechanisms, environmental modulation, and evolution". Annual Review of Plant Biology. 56 (1): 99–131. doi:10.1146/annurev.arplant.56.032604.144052. PMID 15862091.
  11. Raven JA, Giordano M, Beardall J, Maberly SC (February 2012). "Algal evolution in relation to atmospheric CO2: carboxylases, carbon-concentrating mechanisms and carbon oxidation cycles". Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 367 (1588): 493–507. doi:10.1098/rstb.2011.0212. PMC 3248706. PMID 22232762.
  12. Villarejo A, Martinez F, Pino Plumed M, Ramazanov Z (1996). "The induction of the CO2 concentrating mechanism in a starch-less mutant of Chlamydomonas reinhardtii". Physiologia Plantarum. 98 (4): 798–802. doi:10.1111/j.1399-3054.1996.tb06687.x.
  13. Rachmilevitch S, Cousins AB, Bloom AJ (August 2004). "Nitrate assimilation in plant shoots depends on photorespiration". Proceedings of the National Academy of Sciences of the United States of America. 101 (31): 11506–10. Bibcode:2004PNAS..10111506R. doi:10.1073/pnas.0404388101. PMC 509230. PMID 15272076.
  14. Bloom AJ, Burger M, Rubio Asensio JS, Cousins AB (May 2010). "Carbon dioxide enrichment inhibits nitrate assimilation in wheat and Arabidopsis". Science. 328 (5980): 899–903. Bibcode:2010Sci...328..899B. doi:10.1126/science.1186440. PMID 20466933. S2CID 206525174.
  15. South PF, Cavanagh AP, Liu HW, Ort DR (January 2019). "Synthetic glycolate metabolism pathways stimulate crop growth and productivity in the field". Science. 363 (6422): eaat9077. doi:10.1126/science.aat9077. PMC 7745124. PMID 30606819.
  16. Timmer J (7 December 2017). "We may now be able to engineer the most important lousy enzyme on the planet". Ars Technica. Retrieved 5 January 2019.
  17. Timmer J (3 January 2019). "Fixing photosynthesis by engineering it to recycle a toxic mistake". Ars Technica. Retrieved 5 January 2019.
  18. Zabaleta E, Martin MV, Braun HP (May 2012). "A basal carbon concentrating mechanism in plants?". Plant Science. 187: 97–104. doi:10.1016/j.plantsci.2012.02.001. PMID 22404837.
  19. Foyer CH, Bloom AJ, Queval G, Noctor G (2009). "Photorespiratory metabolism: genes, mutants, energetics, and redox signaling". Annual Review of Plant Biology. 60 (1): 455–84. doi:10.1146/annurev.arplant.043008.091948. PMID 19575589.
  20. Igamberdiev AU (2015). "Control of Rubisco function via homeostatic equilibration of CO2 supply". Frontiers in Plant Science. 6: 106. doi:10.3389/fpls.2015.00106. PMC 4341507. PMID 25767475.
  21. Igamberdiev AU, Lea PJ (February 2006). "Land plants equilibrate O2 and CO2 concentrations in the atmosphere". Photosynthesis Research. 87 (2): 177–94. doi:10.1007/s11120-005-8388-2. PMID 16432665. S2CID 10709679.
  22. Stuhlfauth T, Scheuermann R, Fock HP (April 1990). "Light Energy Dissipation under Water Stress Conditions: Contribution of Reassimilation and Evidence for Additional Processes". Plant Physiology. 92 (4): 1053–61. doi:10.1104/pp.92.4.1053. PMC 1062415. PMID 16667370.
  23. Igamberdiev AU, Bykova NV, Lea PJ, Gardeström P (April 2001). "The role of photorespiration in redox and energy balance of photosynthetic plant cells: A study with a barley mutant deficient in glycine decarboxylase". Physiologia Plantarum. 111 (4): 427–438. doi:10.1034/j.1399-3054.2001.1110402.x. PMID 11299007.
  24. Igamberdiev AU, Mikkelsen TN, Ambus P, Bauwe H, Lea PJ, Gardeström P (2004). "Photorespiration Contributes to Stomatal Regulation and Carbon Isotope Fractionation: A Study with Barley, Potato and Arabidopsis Plants Deficient in Glycine Decarboxylase". Photosynthesis Research. 81 (2): 139–152. doi:10.1023/B:PRES.0000035026.05237.ec. S2CID 9485316.
  25. Wingler A, Lea PJ, Leegood RC (1999). "Photorespiratory metabolism of glyoxylate and formate in glycine-accumulating mutants of barley and Amaranthus edulis 2". Planta. 207 (4): 518–526. doi:10.1007/s004250050512. S2CID 34817815.

Further reading
  • Stern K (2003). Introductory Plant Biology. New York: McGraw-Hill. ISBN 978-0-07-290941-8.
  • Siedow JN, Day D (2000). "Chapter 14: Respiration and Photorespiration". Biochemistry and Molecular Biology of Plants. American Society of Plant Physiologists.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.