Crassulacean acid metabolism
Crassulacean acid metabolism, also known as CAM photosynthesis, is an elaborate carbon fixation pathway in some plants. These plants fix carbon dioxide (CO2) during the night, storing it as the four carbon sugar malate. The CO2 is released during the day, where it is concentrated around the enzyme RuBisCO, increasing the efficiency of photosynthesis. The CAM pathway allows stomata to remain shut during the day; therefore it is especially common in plants adapted to arid conditions.
- 1 Historical background
- 2 Overview of CAM: a two-part cycle
- 3 The benefits of CAM
- 4 Comparison with Template:C4 metabolism
- 5 How to spot a CAM plant
- 6 Biochemistry of Crassulacean Acid Metabolism
- 7 Ecological and Taxonomic Distribution of CAM Plants
- 8 See also
- 9 References
CAM was first discovered in the late 1940s. It was observed by the botanists Ransom and Thomas, in the Crassulaceae family of succulents (which includes jade plants and sedums). Its name refers to acid metabolism in Crassulaceae, not the metabolism of Crassulacean acid.
Overview of CAM: a two-part cycle
CAM is a mechanism whereby CO2 is concentrated around RuBisCO by day, while the enzyme is operating at peak capacity. This concentration of CO2 increases RuBisCO's efficiency, as it is prone to operate in the "reverse" direction via photorespiration - utilising oxygen to break down the reaction products the plant would rather it was producing. It differs from [[C4 carbon fixation|Template:C4 metabolism]], which spatially concentrates CO2 around RuBisCO.
During the night
CAM plants open their stomata during the cooler and more humid night-time hours, permitting the uptake of carbon dioxide with the minimum water loss.
The carbon dioxide is converted to soluble[verification needed] molecules, which can be readily stored by the plant at a sensible concentration.
The precise chemical pathway involves a three-carbon compound phosphoenolpyruvate (PEP), to which a CO2 molecule is added via carboxylation - forming a new molecule, oxaloacetate. This is then reduced, forming malate. Oxaloacetate and malate are built around a skeleton of four carbons - hence the term Template:C4. Malate can be readily stored by the plant in vacuoles within individual cells.
The next day...
Malate can be broken down on demand, releasing a molecule of CO2 as it is converted to pyruvate. The pyruvate can be phosphorylated (i.e. have a phosphate group added by the "energy carrier" ATP) to regenerate the PEP with which we started, ready to be spurred into action the next night. But it is the release of CO2 that makes the cycle worth the plant's while. It is directed to the stroma of chloroplasts: the sites at which photosynthesis is most active. There, it is provided to RuBisCO in great concentrations, increasing the efficiency of the molecule, and therefore producing more sugars per unit photosynthesis.
The benefits of CAM
A great deal of energy is expended during CAM by the production and subsequent destruction of malate. This is in part countered by the increased efficiency of RuBisCO, but the more important benefit to the plant is the ability to leave leaf stomata closed during the day.[verification needed] CAM plants are most common in Template:Wict environments, where water comes at a premium. Being able to keep stomata closed during the hottest and driest part of the day reduces the loss of water through evapotranspiration, allowing CAM plants to grow in environments that would otherwise be far too dry. Template:C3 plants, for example, lose 97% of the water they uptake through the roots to transpiration - a high cost avoided by CAM plants.
Comparison with Template:C4 metabolism
The [[C4 carbon fixation|Template:C4 pathway]] bears resemblance to CAM; both act to concentrate CO2 around RuBisCO, thereby increasing its efficiency. CAM concentrates it in time, providing CO2 during the day, and not at night, when respiration is the dominant reaction.[verification needed] Template:C4 plants, on the contrary, concentrate CO2 spatially, with a RuBisCO reaction centre in a "bundle sheath cell" being innundated with CO2.
How to spot a CAM plant
CAM can be considered an adaptation to arid conditions. CAM plants often display other xerophytic characters, such as thick, reduced leaves with a low surface-area-to-volume ratio; thick cuticle; and stomata sunken into pits. Some shed their leaves during the dry season; others (the succulents[verification needed]) store water in vacuoles.
CAM plants are not only good at retaining water, but use nitrogen very efficiently. However, due to their stomata being closed by day, they are less efficient at CO2 absorption. This limits the amount of carbon they have available for growth.
Biochemistry of Crassulacean Acid Metabolism
At low temperatures (frequently at night), when CAM plants open their guard cells, carbon dioxide molecules diffuse into the spongy mesophyll's intracellular spaces and finally get into the cytoplasm. Here, they can meet phosphoenolpyruvate (PEP), which is a phosphorylated triosephosphate. During this time, CAM plants are synthesizing a protein called PEP carboxylase kinase (PEP-C kinase), which expression can be inhibited by high temperatures (frequently at daylight) and the presence of malate. PEP-C kinase phosphorylates its target enzyme PEP carboxylase (PEP-C). Phosphorylation dramatically enhanced the enzyme‘s capability to catalyze the formation of oxalacetate that can be subsequently transformed into malate by NAD malate dehydrogenase. Malate is then transported via malate shuttles into the vacuole, where it is converted into the storage form maleic acid. In contrast to PEP-C kinase, PEP-C is synthesized all the time but almost inhibited at daylight either by dephosphorylation via PEP-C phosphatase or directly by binding malate. The latter is not possible at low temperatures, since malate is efficiently transported into the vacuole whereas PEP-C kinase readily inverts dephosphorylation.
At daylight, CAM plants close their guard cells and discharged malate that is subsequently transported into chloroplasts. There, depending on plant species, it is cleaved into pyruvate and carbon dioxide either by malic enzyme or PEP carboxykinase. Carbon dioxide is then introduced into the Calvin cycle, a coupled and self-recovering enzyme system, which is used to build branched carbohydrates. The by-product pyruvate can be further degraded in the mitochondrial citric acid cycle and therefore, provides additional carbon dioxide molecules for the calvin cycle. Alternatively, pyruvate can be also used to recover PEP via pyruvate phosphate dikinase, a high energy step, which requires ATP and an additional phosphate. In the following cold night, PEP is finally exported into the cytoplasm, where it is involved in fixing carbon dioxide via malate.
Ecological and Taxonomic Distribution of CAM Plants
The majority of plants possessing Crassulacean Acid Metabolism are either epiphytes (e.g. orchids, bromeliads) or succulent xerophytes (e.g. cacti, cactoid Euphorbias), but it is also found in hemiepiphytes (e.g. Clusia), lithophytes (e.g. Sedum, Sempervivum), terrestrial bromeliads, hydrophytes (e.g. Isoetes, Crassula (Tillaea), and from a halophyte (Mesembryanthemum crystallinum), a non-succulent terrestrial plant (Dodonaea viscosa) and a mangrove associate (Sesuvium portulacastrum). Portulacaria afra is the only plant known to display both CAM and C4 pathways.
Crassulacean Acid Metabolism has evolved convergently many times. It occurs in 16,000 species (about 7% of plants), belonging to over 300 genera and around 40 families. It is found in quillworts (relatives of club mosses), in ferns, and in gymnosperms, but the great majority of CAM plants are angiosperms (flowering plants).
The following list summarises the taxonomic distribution of CAM plants.
|Division||Class/Angiosperm group||Order||Family||Plant Type||Clade involved||Type of CAM|
|Lycopodiophyta||Isoetopsida||Isoetales||Isoetaceae||hydrophyte||Isoetes (the sole genus of class Isoetopsida) - I. howellii (seasonally submerged), I. macrospora, I. bolanderi, I. engelmanni, I. lacustris, I. sinensis, I. storkii, I. kirkii|
|Pteridophyta||Polypodiopsida||Polypodiales||Polypodiaceae||epiphyte, lithophyte||CAM is recorded from Microsorium, Platycerium and Polypodium, Pyrrosia and Drymoglossum and Microgramma|
|Pinophyta||Gnetopsida||Welwitschiales||Welwitschiaceae||xerophyte||Welwitschia mirabilis (the sole species of the order Welwitschiales)|
|Aizoaceae||xerophyte||widespread in the family; Mesembryanthemum crystallinum is a rare instance of an halophyte which displays CAM|
|Cactaceae||xerophyte||all cacti have obligate Crassulacean Acid Metabolism in their stems; those few cacti with leaves have C3 Metabolism in those leaves; seedlings have C3 Metabolism.|
|Portulacaceae||xerophyte||recorded in approximately half of the genera (note: Portulacaceae is paraphyletic with respect to Cactaceae and Didieraceae)|
|Saxifragales||Crassulaceae||hydrophyte, xerophyte, lithophyte||CAM is widespread in the family|
|eudicots (rosids)||Vitales||Vitaceae||Cissus, Cyphostemma|
|Euphorbiaceae||CAM is found is some species of Euphorbia  including some formerly placed in the sunk genera Monadenium, Pedilanthus and Synadenium. C4 photosynthesis is also found in Euphorbia (subgenus Chamaesyce).|
|Geraniales||Geraniaceae||CAM is found in some succulent species of Pelargonium, and is also reported from Geranium pratense|
|Cucurbitales||Cucurbitaceae||Xerosicyos danguyi, Dendrosicyos socotrana, Momordica|
|Gentianales||Rubiaceae||epiphyte||Hydnophytum and Myrmecodia|
|Apocynaceae||CAM is found in subfamily Asclepidioideae (Hoya, Dischidia, Ceropegia, Stapelia, Caralluma negevensis, Frerea indica, Adenium, Huernia), and also in Carissa and Akocanthera|
|Lamiales||Gesneriaceae||epiphyte||CAM was found Codonanthe crassifolia, but not in 3 other genera|
|Lamiaceae||Plectranthus marrubioides, Coleus|
|Asterales||Asteraceae||some species of Senecio|
|Araceae||Zamioculcas zamiifolia is the only CAM plant in Araceae, and the only non-aquatic CAM plant in Alismatales|
|Poales||Bromeliaceae||epiphyte||Bromelioideae (91%), Puya (24%), Dyckia and related genera (all), Hechtia (all), Tillandsia (many)|
|Agavaceae||xerophyte||Agave, Hesperaloe, Yucca|
|Asphodelaceae||xerophyte||Aloe, Gasteria and Haworthia|
|Ruscaceae||Sansevieria, Dracaena|
|Commelinales||Commelinaceae||Callisia, Tradescantia, Tripogandra|
- Ransom S. L. (1960). "Crassulacean acid metabolism". Annual Rev Plant Physiol. 11: 81–110. doi:10.1146/annurev.pp.11.060160.000501. Unknown parameter
- Raven, J.A. (2001). "Roots: evolutionary origins and biogeochemical significance". Journal of Experimental Botany. 52 (90001): 381–401. doi:10.1093/jexbot/52.suppl_1.381. Unknown parameter
- Boston & Adams, Evidence of crassulacean acid metabolism in two North American isoetids, Aquatic Botany 15(4): 381-386 (1983)
- Holtum & Winter, Degrees of crassulacean acid metabolism in tropical epiphytic and lithophytic ferns, Australian Journal of Plant Physiology 26(8): 749-757 (1999)
- Wong & Hew, Diffusive Resistance, Titratable Acidity, and CO2 Fixation in Two Tropical Epiphytic Ferns, American Fern Journal 66(4): 121-124 (1976)
- Crassulacean Acid Metabolism
- abstract to Carter & Martin, The occurrence of Crassulacean acid metabolism among ephiphytes in a high-rainfall region of Costa Rica, Selbyana 15(2): 104-106 (1994)
- abstract to Martin et al., The Occurrence of Crassulacean Acid Metabolism in Epiphytic Ferns, with an Emphasis on the Vittariaceae, International Journal of Plant Sciences 166(4): 623-630 (2005)
- Vovides et al, CAM-cycling in the cycad Dioon edule Lindl. in its natural tropical deciduous forest habitat in central Veracruz, Mexico, Botanical Journal of the Linnean Society 138(2): 155–162 (2002)
- Schultze, Ziegler & Stichler, Environmental control of crassulacean acid metabolism in Welwitschia mirabilis Hook. Fil. in its range of natural distribution in the Namib desert, Oecologia 24(4): 323-334 (1976)
- Sipes & Ting, Crassulacean Acid Metabolism and Crassulacean Acid Metabolism Modifications in Peperomia camptotricha, Plant Physiol. 77(1): 59-63 (1985)
- Chu, Dai, Ku & Edwards, Induction of Crassulacean Acid Metabolism in the Facultative Halophyte Mesembryanthemum crystallinum by Abscisic Acid, Plant Physiol. 93(3): 1253–1260 (1990)
- Guralnick & Jackson, The Occurrence and Phylogenetics of Crassulacean Acid Metabolism in the Portulacaceae, Int. J Plant Sci. 162(2): 257–262 (2001)
- Cockburn, Variation in Photosynthetic Acid Metabolism in Vascular Plants: CAM and Related Phenomena, New Phytologist 101(1): 3-24 (1985)
- Nelson, Sage & Sage, Functional Leaf Anatomy of plants with Crassulacean Acid Metabolism, Functional Plant Biology 32: 409-419 (2005)
- Lüttge, Ecophysiology of Crassulacean Acid Metabolism (CAM), Annals of Botany 93: 629-652 (2004)
- Bender et al, 13C/12C Ratio Changes in Crassulacean Acid Mechanism Plants, Plant Physiology 52: 427-430 (1973)
- Jones, Cardon & Czaja, A phylogenetic view of low-level CAM in Pelargonium (Geraniaceae), American Journal of Botany 90: 135-142 (2003)
- Bastide, Sipes, Hann & Ting, Plant Physiol. 103(4): 1089–1096 (1993)
- abstract to Lange & Zuber, Frerea indica, a stem succulent CAM plant with deciduous C3 leaves, Oecologia 31(1): 67-72 (1977)
- [abstract to http://links.jstor.org/sici?sici=0002-9122(198603)73:3%3C336:CAMITG%3E2.0.CO;2-H Guralnick et al, Crassulacean Acid Metabolism in the Gesneriaceae, American Journal of Botany 73(3): 336-345 (1986)]
- Fioretti & Alfani, Anatomy of Succulence and CAM in 15 Species of Senecio, Botanical Gazette 149(2): 142-152 (1988)
- Holtum, Winter, Weeks and Sexton, Crassulacean acid metabolism in the ZZ plant, Zamioculcas zamiifolia (Araceae), American Journal of Botany 94: 1670-1676 (2007)
- Winter & Smith, Multiple origins of crassulacean acid metabolism and the epiphytic habit in the Neotropical family Bromeliaceae, PNAS 101(10): 3703-3708 (2004)