C4 carbon fixation

C4 carbon fixation or the Hatch–Slack pathway is a photosynthetic process in some plants. It is the first step in extracting carbon from carbon dioxide to be able to use it in sugar and other biomolecules. It is one of three known processes for carbon fixation. "C4" refers to the four-carbon molecule that is the first product of this type of carbon fixation.

C4 fixation is an elaboration of the more common C3 carbon fixation and is believed to have evolved more recently. C4 overcomes the tendency of the enzyme RuBisCO to wastefully fix oxygen rather than carbon dioxide in the process of photorespiration. This is achieved by ensuring that RuBisCO works in an environment where there is a lot of carbon dioxide and very little oxygen. CO
is shuttled via malate or aspartate from mesophyll cells to bundle-sheath cells. In these bundle-sheath cells CO
is released by decarboxylation of the malate. C4 plants use PEP carboxylase to capture more CO
in the mesophyll cells. PEP (phosphoenolpyruvate, three carbons) binds to CO
to make oxaloacetic acid (OAA). OAA then makes malate (four carbons). Malate enters bundle sheath cells through plasmodesmata and releases the CO
. These additional steps, however, require more energy in the form of ATP. Using this extra energy, C4 plants are able to more efficiently fix carbon in drought, high temperatures, and limitations of nitrogen or CO
. Since the more common C3 pathway does not require this extra energy, it is more efficient in the other conditions.

The naming Hatch–Slack pathway is in honor of Marshall Davidson Hatch and C. R. Slack, who elucidated it in Australia in 1966.[1]

C4 pathway

The first experiments indicating that some plants do not use C3 carbon fixation but instead produce malate and aspartate in the first step of carbon fixation were done in the 1950s and early 1960s by Hugo P. Kortschak[2] and Yuri Karpilov.[3] The C4 pathway was elucidated by Marshall Davidson Hatch and C. R. Slack, in Australia, in 1966; it is sometimes called the Hatch-Slack pathway.[1]

In C3 plants, the first step in the light-independent reactions of photosynthesis involves the fixation of CO
by the enzyme RuBisCO into 3-phosphoglycerate. However, due to the dual carboxylase and oxygenase activity of RuBisCo, some part of the substrate is oxidized rather than carboxylated, resulting in loss of substrate and consumption of energy, in what is known as photorespiration.

In order to bypass the photorespiration pathway, C4 plants have developed a mechanism to efficiently deliver CO
to the RuBisCO enzyme. They use their specific leaf anatomy where chloroplasts exist not only in the mesophyll cells in the outer part of their leaves but in the bundle sheath cells as well. Instead of direct fixation by RuBisCO into the three-carbon compound 3-phosphoglycerate, CO
is incorporated into a four-carbon organic acid (either malate or aspartate). The organic acid is produced in the mesophyll cells and then transported into the bundle sheath cells, where it is decarboxylated to regenerate CO
. The chloroplasts of the bundle sheath cells can then use this CO
to produce carbohydrates by the conventional C3 pathway.

There are several variants of the C4 pathways, all of which use a four-carbon organic acid to transport CO
from the mesophyll cells to the bundle sheath cells. They achieve this purpose by using different substrates and enzymes. Three examples are provided in the figures on the right. The NADP-ME type C4 pathway is described in detail below.

NADP-ME type

The first step in the NADP-ME type C4 pathway is the conversion of pyruvate (Pyr) to phosphoenolpyruvate (PEP), by the enzyme Pyruvate phosphate dikinase (PPDK). This reaction requires inorganic phosphate and ATP plus pyruvate, producing PEP, AMP, and inorganic pyrophosphate (PPi). The next step is the fixation of CO
into oxaloacetate by the PEP carboxylase enzyme (PEPC). Both of these steps occur in the mesophyll cells:

pyruvate + Pi + ATP → PEP + AMP + PPi
→ oxaloacetate

PEPC has a lower Km for HCO
— and, hence, higher affinity — than RuBisCO. Furthermore, O2 is a very poor substrate for this enzyme. Thus, at relatively low concentrations of CO
, most CO
will be fixed by this pathway.

The product is usually converted to malate (M), a simple organic compound, which is transported to the bundle-sheath cells surrounding a nearby vein. Here, it is decarboxylated by the NADP-malic enzyme (NADP-ME) to produce CO
and pyruvate. The CO
now enters the Calvin cycle and the pyruvate is transported back to the mesophyll cell.

Other types

There are several variants of this pathway, in which different substrates and enzymes are used to transport CO
from the mesophyll cells to the bundle sheath cells:

  1. The four-carbon acid transported from mesophyll cells may be malate (M), as above, or aspartate (Asp), or both (see the PEPC type C4 pathway).
  2. The three-carbon acid transported back from bundle-sheath cells may be pyruvate (Pyr), as above, or alanine (Ala).
  3. The enzyme that catalyses decarboxylation in bundle-sheath cells differs:


Since every CO
molecule has to be fixed twice, first in the mesphyll cells (by the PEPC enzyme) and second in the bundle sheath cells (by RuBisCO), the C4 pathway uses more energy than the C3 pathway. For instance, the C3 pathway requires 18 molecules of ATP for the synthesis of one molecule of glucose, whereas the NADP-ME type C4 pathway used by maize and sugarcane requires 30 molecules of ATP. This energy debt is more than paid for by avoiding losing more than half of photosynthetic carbon in photorespiration as occurs in some tropical plants, making it an adaptive mechanism for minimizing the loss.

C4 Kranz leaf anatomy

The C4 plants often possess a characteristic leaf anatomy called kranz anatomy, from the German word for wreath. Their vascular bundles are surrounded by two rings of cells; the inner ring, called bundle sheath cells, contains starch-rich chloroplasts lacking grana, which differ from those in mesophyll cells present as the outer ring. Hence, the chloroplasts are called dimorphic. The primary function of kranz anatomy is to provide a site in which CO
can be concentrated around RuBisCO, thereby avoiding photorespiration. In order to maintain a significantly higher CO
concentration in the bundle sheath compared to the mesophyll, the boundary layer of the kranz has a low conductance to CO
, a property that may be enhanced by the presence of suberin.[4] The carbon concentration mechanism in C4 plants distinguishes their isotopic signature from other photosynthetic organisms.

Although most C4 plants exhibit kranz anatomy, there are, however, a few species that operate a limited C4 cycle without any distinct bundle sheath tissue. Suaeda aralocaspica, Bienertia cycloptera, Bienertia sinuspersici and Bienertia kavirense (all chenopods) are terrestrial plants that inhabit dry, salty depressions in the deserts of the Middle East. These plants have been shown to operate single-cell C4 CO
-concentrating mechanisms, which are unique among the known C4 mechanisms.[5][6][7][8] Although the cytology of both genera differs slightly, the basic principle is that fluid-filled vacuoles are employed to divide the cell into two separate areas. Carboxylation enzymes in the cytosol can, therefore, be kept separate from decarboxylase enzymes and RuBisCO in the chloroplasts, and a diffusive barrier can be established between the chloroplasts (which contain RuBisCO) and the cytosol. This enables a bundle-sheath-type area and a mesophyll-type area to be established within a single cell. Although this does allow a limited C4 cycle to operate, it is relatively inefficient, with the occurrence of much leakage of CO
from around RuBisCO. There is also evidence for the exhibiting of inducible C4 photosynthesis by non-kranz aquatic macrophyte Hydrilla verticillata under warm conditions, although the mechanism by which CO
leakage from around RuBisCO is minimised is currently uncertain.[9]

The evolution and advantages of the C4 pathway

C4 plants have a competitive advantage over plants possessing the more common C3 carbon fixation pathway under conditions of drought, high temperatures, and nitrogen or CO
limitation. When grown in the same environment, at 30 °C, C3 grasses lose approximately 833 molecules of water per CO
molecule that is fixed, whereas C4 grasses lose only 277. This increased water use efficiency of C4 grasses means that soil moisture is conserved, allowing them to grow for longer in arid environments.[10]

C4 carbon fixation has evolved on up to 61 independent occasions in 19 different families of plants, making it a prime example of convergent evolution.[11] This convergence may have been facilitated by the fact that many potential evolutionary pathways to a C4 phenotype exist, many of which involve initial evolutionary steps not directly related to photosynthesis.[12] C4 plants arose around 35 million years ago[11] during the Oligocene (precisely when is difficult to determine) and did not become ecologically significant until around 6 to 7 million years ago, in the Miocene.[13] C4 metabolism in grasses originated when their habitat migrated from the shady forest undercanopy to more open environments,[14] where the high sunlight gave it an advantage over the C3 pathway.[15] Drought was not necessary for its innovation; rather, the increased resistance to water stress was a byproduct of the pathway and allowed C4 plants to more readily colonize arid environments.[15]

Today, C4 plants represent about 5% of Earth's plant biomass and 3% of its known plant species.[10][16] Despite this scarcity, they account for about 23% of terrestrial carbon fixation.[13][17] Increasing the proportion of C4 plants on earth could assist biosequestration of CO
and represent an important climate change avoidance strategy. Present-day C4 plants are concentrated in the tropics and subtropics (below latitudes of 45 degrees) where the high air temperature contributes to higher possible levels of oxygenase activity by RuBisCO, which increases rates of photorespiration in C3 plants.

Plants that use C4 carbon fixation

About 8,100 plant species use C4 carbon fixation, which represents about 3% of all terrestrial species of plants.[17][18] All these 8,100 species are angiosperms. C4 carbon fixation is more common in monocots compared with dicots, with 40% of monocots using the C4 pathway, compared with only 4.5% of dicots. Despite this, only three families of monocots use C4 carbon fixation compared to 15 dicot families. Of the monocot clades containing C4 plants, the grass (Poaceae) species use the C4 photosynthetic pathway most. 46% of grasses are C4 and together account for 61% of C4 species. These include the food crops maize, sugar cane, millet, and sorghum.[19][20] Of the dicot clades containing C4 species, the order Caryophyllales contains the most species. Of the families in the Caryophyllales, the Chenopodiaceae use C4 carbon fixation the most, with 550 out of 1,400 species using it. About 250 of the 1,000 species of the related Amaranthaceae also use C4.[10][21]

Members of the sedge family Cyperaceae, and members of numerous families of eudicots – including Asteraceae (the daisy family), Brassicaceae (the cabbage family), and Euphorbiaceae (the spurge family) – also use C4.

There are very few trees which use C4. Only a handful are known: Paulownia, seven Hawaiian Euphorbia species and a few desert shrubs that reach the size and shape of trees with age.[22][23]

Converting C3 plants to C4

Given the advantages of C4, a group of scientists from institutions around the world are working on the C4 Rice Project to produce a strain of rice, naturally a C3 plant, that uses the C4 pathway by studying the C4 plants maize and Brachypodium.[24] As rice is the world's most important human food—it is the staple food for more than half the planet—having rice that is more efficient at converting sunlight into grain could have significant global benefits towards improving food security. The team claim C4 rice could produce up to 50% more grain—and be able to do it with less water and nutrients.[25][26][27]

The researchers have already identified genes needed for C4 photosynthesis in rice and are now looking towards developing a prototype C4 rice plant. In 2012, the Government of the United Kingdom along with the Bill & Melinda Gates Foundation provided US$14 million over three years towards the C4 Rice Project at the International Rice Research Institute.[28]

See also


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  2. Nickell, Louis G. (1993). "A tribute to Hugo P. Kortschak: The man, the scientist and the discoverer of C4 photosynthesis". Photosynthesis Research. 35 (2): 201–204. doi:10.1007/BF00014751. PMID 24318687.
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  6. Voznesenskaya, Elena; Vincent R. Franceschi; Olavi Kiirats; Elena G. Artyusheva; Helmut Freitag; Gerald E. Edwards (2002). "Proof of C4 photosynthesis without Kranz anatomy in Bienertia cycloptera (Chenopodiaceae)". The Plant Journal. 31 (5): 649–662. doi:10.1046/j.1365-313X.2002.01385.x. PMID 12207654.
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  8. Akhani, H.; Chatrenoor, T.; Dehghani, M.; Khoshravesh, R.; Mahdavi, P.; Matinzadeh, Z. (2012). "A new species of Bienertia (Chenopodiaceae) from Iranian salt deserts: a third species of the genus and discovery of a fourth terrestrial C4 plant without Kranz anatomy". Plant Biosystems. 146: 550–559. doi:10.1080/11263504.2012.662921.
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