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60-517: PEMT may refer to: Phosphatidylethanolamine N -methyltransferase , an enzyme encoded by the PEMT gene which synthesizes phosphatidylcholine Polymorphic epithelial mucin , a mucin encoded by the MUC1 gene in humans Post-edited machine translation , whereby humans amend machine-generated translation to achieve an acceptable final product Topics referred to by
120-409: A liquid or gaseous reaction mixture . Important heterogeneous catalysts include zeolites , alumina , higher-order oxides, graphitic carbon, transition metal oxides , metals such as Raney nickel for hydrogenation, and vanadium(V) oxide for oxidation of sulfur dioxide into sulfur trioxide by the contact process . Diverse mechanisms for reactions on surfaces are known, depending on how
180-494: A 22.3 kDa, 199-amino acid protein. Although the enzymatic structure is unknown, PEMT is proposed to contain four hydrophobic membrane-spanning regions, with both its C and N termini on the cytosolic side of the ER membrane. Kinetic studies indicate a common binding site for PE, PMME, and PDME substrates. SAM binding motifs have been identified on both the third and fourth transmembrane sequences. Site-directed mutagenesis has pinpointed
240-529: A choline-deficient diet, the mice developed severe liver failure. Rapid PC depletion due to biliary PC secretion, as well as protein leakage from loss of membrane integrity due to lowered PC/PE ratios, led to steatosis and steatohepatitis . A Val-to-Met substitution at residue 175, leading to reduced PEMT activity, has been linked to non-alcoholic fatty liver disease . This substitution has also been linked to increased frequency of non-alcoholic steatohepatitis. A single-nucleotide polymorphism (G to C) in
300-594: A facet (edge, surface, step, etc.) of a solid. Most of the volume but also most of the surface of a heterogeneous catalyst may be catalytically inactive. Finding out the nature of the active site is technically challenging. For example, the catalyst for the Haber process for the synthesis of ammonia from nitrogen and hydrogen is often described as iron . But detailed studies and many optimizations have led to catalysts that are mixtures of iron-potassium-calcium-aluminum-oxide. The reacting gases adsorb onto active sites on
360-452: A high surface area, most commonly alumina , zeolites or various kinds of activated carbon . Specialized supports include silicon dioxide , titanium dioxide , calcium carbonate , and barium sulfate . In the context of electrochemistry , specifically in fuel cell engineering, various metal-containing catalysts are used to enhance the rates of the half reactions that comprise the fuel cell. One common type of fuel cell electrocatalyst
420-401: A higher specific activity (per gram) on support. Sometimes the support is merely a surface on which the catalyst is spread to increase the surface area. More often, the support and the catalyst interact, affecting the catalytic reaction. Supports can also be used in nanoparticle synthesis by providing sites for individual molecules of catalyst to chemically bind. Supports are porous materials with
480-406: A kinetic barrier. The catalyst may increase the reaction rate or selectivity, or enable the reaction at lower temperatures. This effect can be illustrated with an energy profile diagram. In the catalyzed elementary reaction , catalysts do not change the extent of a reaction: they have no effect on the chemical equilibrium of a reaction. The ratio of the forward and the reverse reaction rates
540-409: A one-pot reaction. In autocatalysis , the catalyst is a product of the overall reaction, in contrast to all other types of catalysis considered in this article. The simplest example of autocatalysis is a reaction of type A + B → 2 B, in one or in several steps. The overall reaction is just A → B, so that B is a product. But since B is also a reactant, it may be present in the rate equation and affect
600-401: A type of catalysis where the catalyst can be toggled between different ground states possessing distinct reactivity, typically by applying an external stimulus. This ability to reversibly switch the catalyst allows for spatiotemporal control over catalytic activity and selectivity. The external stimuli used to switch the catalyst can include changes in temperature, pH, light, electric fields, or
660-618: Is a transferase enzyme ( EC 2.1.1.17 ) which converts phosphatidylethanolamine (PE) to phosphatidylcholine (PC) in the liver . In humans it is encoded by the PEMT gene within the Smith–Magenis syndrome region on chromosome 17 . While the CDP-choline pathway, in which choline obtained either by dietary consumption or by metabolism of choline-containing lipids is converted to PC, accounts for approximately 70% of PC biosynthesis in
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#1733093266749720-427: Is a good reagent for dihydroxylation, but it is highly toxic and expensive. In Upjohn dihydroxylation , the sacrificial catalyst N-methylmorpholine N-oxide (NMMO) regenerates OsO 4 , and only catalytic quantities of OsO 4 are needed. Catalysis may be classified as either homogeneous or heterogeneous . A homogeneous catalysis is one whose components are dispersed in the same phase (usually gaseous or liquid) as
780-631: Is a negative regulator of PEMT transcription, yet is it is a positive regulator of choline-phosphate cytidylyltransferase (CT) transcription. This is one of several examples of the reciprocal regulation of PEMT and CT in the PEMT and CDP-choline pathways. Estrogen has also been shown to be a positive regulator of hepatocyte PEMT transcription. Ablation of the estrogen binding site in the PEMT promoter region may increase risk of hepatic steatosis from choline deficiency. PEMT deficiency in mice, genetically induced by PEMT gene knockout , produced minimal effect on PE and PC levels. However, upon being fed
840-466: Is a stable molecule that resembles the transition state of a chemical reaction can function as weak catalysts for that chemical reaction by lowering its activation energy. Such catalytic antibodies are sometimes called " abzymes ". Estimates are that 90% of all commercially produced chemical products involve catalysts at some stage in the process of their manufacture. In 2005, catalytic processes generated about $ 900 billion in products worldwide. Catalysis
900-476: Is applied is in the oxidation of sulfur dioxide on vanadium(V) oxide for the production of sulfuric acid . Many heterogeneous catalysts are in fact nanomaterials. Heterogeneous catalysts are typically " supported ", which means that the catalyst is dispersed on a second material that enhances the effectiveness or minimizes its cost. Supports prevent or minimize agglomeration and sintering of small catalyst particles, exposing more surface area, thus catalysts have
960-408: Is based upon nanoparticles of platinum that are supported on slightly larger carbon particles. When in contact with one of the electrodes in a fuel cell, this platinum increases the rate of oxygen reduction either to water or to hydroxide or hydrogen peroxide . Homogeneous catalysts function in the same phase as the reactants. Typically homogeneous catalysts are dissolved in a solvent with
1020-417: Is derived from Greek καταλύειν , kataluein , meaning "loosen" or "untie". The concept of catalysis was invented by chemist Elizabeth Fulhame , based on her novel work in oxidation-reduction experiments. An illustrative example is the effect of catalysts to speed the decomposition of hydrogen peroxide into water and oxygen : This reaction proceeds because the reaction products are more stable than
1080-622: Is different from Wikidata All article disambiguation pages All disambiguation pages Phosphatidylethanolamine N-methyltransferase 18618 ENSG00000133027 ENSMUSG00000000301 Q9UBM1 Q61907 NM_001267551 NM_001267552 NM_007169 NM_148172 NM_148173 NM_001290011 NM_001290012 NM_001290013 NM_001290014 NM_008819 NP_001254480 NP_001254481 NP_009100 NP_680477 NP_680478 NP_001276940 NP_001276941 NP_001276942 NP_001276943 NP_032845 Phosphatidylethanolamine N-methyltransferase (abbreviated PEMT )
1140-446: Is found in endoplasmic reticulum and mitochondria-associated membranes. It accounts for ~30% of PC biosynthesis, with the CDP-choline, or Kennedy, pathway making ~70%. PC, typically the most abundant phospholipid in animals and plants, accounts for more than half of cell membrane phospholipids and approximately 30% of all cellular lipid content. The PEMT pathway is therefore crucial for maintaining membrane integrity. PC made via
1200-518: Is largely a result of lower levels of VLDL lipids in the PEMT-deficient mice. Furthermore, the decreased lipid (PC) content in VLDLs causes changes in lipoprotein structure which allow them to be cleared more rapidly in the PEMT-deficient mice. PEMT-deficient mice fed high-fat diets have been shown to resist weight gain and be protected from insulin resistance . One potential reason for this phenomenon
1260-513: Is one of the largest-scale and most energy-intensive processes. In the Haber process nitrogen is combined with hydrogen over an iron oxide catalyst. Methanol is prepared from carbon monoxide or carbon dioxide but using copper-zinc catalysts. Bulk polymers derived from ethylene and propylene are often prepared via Ziegler-Natta catalysis . Polyesters, polyamides, and isocyanates are derived via acid-base catalysis . Most carbonylation processes require metal catalysts, examples include
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#17330932667491320-407: Is produced, and if there is no energy barrier, there is no need for a catalyst. Then, removing the catalyst would also result in a reaction, producing energy; i.e. the addition and its reverse process, removal, would both produce energy. Thus, a catalyst that could change the equilibrium would be a perpetual motion machine , a contradiction to the laws of thermodynamics. Thus, catalysts do not alter
1380-475: Is regenerated. The overall rate is the rate of the slow step An example of heterogeneous catalysis is the reaction of oxygen and hydrogen on the surface of titanium dioxide (TiO 2 , or titania ) to produce water. Scanning tunneling microscopy showed that the molecules undergo adsorption and dissociation . The dissociated, surface-bound O and H atoms diffuse together. The intermediate reaction states are: HO 2 , H 2 O 2 , then H 3 O 2 and
1440-572: Is said to catalyze this reaction. In living organisms, this reaction is catalyzed by enzymes (proteins that serve as catalysts) such as catalase . Another example is the effect of catalysts on air pollution and reducing the amount of carbon monoxide. Development of active and selective catalysts for the conversion of carbon monoxide into desirable products is one of the most important roles of catalysts. Using catalysts for hydrogenation of carbon monoxide helps to remove this toxic gas and also attain useful materials. The SI derived unit for measuring
1500-412: Is so pervasive that subareas are not readily classified. Some areas of particular concentration are surveyed below. Petroleum refining makes intensive use of catalysis for alkylation , catalytic cracking (breaking long-chain hydrocarbons into smaller pieces), naphtha reforming and steam reforming (conversion of hydrocarbons into synthesis gas ). Even the exhaust from the burning of fossil fuels
1560-515: Is that lack of PEMT in adipose tissue may affect normal fat deposition. This article incorporates text from the United States National Library of Medicine , which is in the public domain . Catalysis Catalysis ( / k ə ˈ t æ l ə s ɪ s / ) is the increase in rate of a chemical reaction due to an added substance known as a catalyst ( / ˈ k æ t əl ɪ s t / ). Catalysts are not consumed by
1620-696: Is that these mice, which exhibit hypermetabolic behavior, rely more on glucose than on fats for energy. It was concluded that insufficient choline resulted in the lack of weight gain, supported by the fact that PC produced via the PEMT pathway can be used to form choline. The PEMT deficient mice showed elevated plasma glucagon levels, increased hepatic expression of glucagon receptor , phosphorylated AMP-activated protein kinase (AMPK), and serine-307-phosphorylated insulin receptor substrate 1 (IRS1-s307), which blocks insulin-mediated signal transduction; together, these contribute to enhanced gluconeogenesis and ultimately insulin resistance. Another possibility
1680-652: Is treated via catalysis: Catalytic converters , typically composed of platinum and rhodium , break down some of the more harmful byproducts of automobile exhaust. With regard to synthetic fuels, an old but still important process is the Fischer-Tropsch synthesis of hydrocarbons from synthesis gas , which itself is processed via water-gas shift reactions , catalyzed by iron. The Sabatier reaction produces methane from carbon dioxide and hydrogen. Biodiesel and related biofuels require processing via both inorganic and biocatalysts. Fuel cells rely on catalysts for both
1740-439: Is unaffected (see also thermodynamics ). The second law of thermodynamics describes why a catalyst does not change the chemical equilibrium of a reaction. Suppose there was such a catalyst that shifted an equilibrium. Introducing the catalyst to the system would result in a reaction to move to the new equilibrium, producing energy. Production of energy is a necessary result since reactions are spontaneous only if Gibbs free energy
1800-577: The Monsanto acetic acid process and hydroformylation . Many fine chemicals are prepared via catalysis; methods include those of heavy industry as well as more specialized processes that would be prohibitively expensive on a large scale. Examples include the Heck reaction , and Friedel–Crafts reactions . Because most bioactive compounds are chiral , many pharmaceuticals are produced by enantioselective catalysis (catalytic asymmetric synthesis ). (R)-1,2-Propandiol,
1860-511: The catalytic activity of a catalyst is the katal , which is quantified in moles per second. The productivity of a catalyst can be described by the turnover number (or TON) and the catalytic activity by the turn over frequency (TOF), which is the TON per time unit. The biochemical equivalent is the enzyme unit . For more information on the efficiency of enzymatic catalysis, see the article on enzymes . In general, chemical reactions occur faster in
PEMT - Misplaced Pages Continue
1920-538: The rate-limiting step in conversion of PE to PC. It is suspected that the structure or specific conformation adopted by PE has a lower affinity for the PEMT active site; consequently, upon methylation, PMME would be immediately converted to PDME and PDME to PC, via a Bi-Bi or ping-pong mechanism before another PE molecule could enter the active site. Purification of PEMT by Neale D. Ridgway and Dennis E. Vance in 1987 produced an 18.3 kDa protein. Subsequent cloning, sequencing, and expression of PEMT cDNA resulted in
1980-423: The reactant 's molecules. A heterogeneous catalysis is one where the reaction components are not in the same phase. Enzymes and other biocatalysts are often considered as a third category. Similar mechanistic principles apply to heterogeneous, homogeneous, and biocatalysis. Heterogeneous catalysts act in a different phase than the reactants . Most heterogeneous catalysts are solids that act on substrates in
2040-458: The CDP-choline pathway are typically composed of medium-length, saturated chains. A major pathway for hepatic PC utilization is secretion of bile into the intestine. PEMT activity also dictates normal very low-density lipoprotein (VLDL) secretion by the liver. PEMT is also a significant source and regulator of plasma homocysteine , which can be secreted or converted to methionine or cysteine . The exact mechanism by which PEMT catalyzes
2100-424: The PEMT pathway can be degraded by phospholipases C / D , resulting in the de novo formation of choline. Thus, the PEMT pathway contributes to maintaining brain and liver function and larger-scale energy metabolism in the body. PC molecules produced by PEMT-catalyzed methylation of PE are more diverse, and tend to contain longer chain, polyunsaturated species and more arachidonate , whereas those produced via
2160-478: The activity of enzymes (and other catalysts) including temperature, pH, the concentration of enzymes, substrate, and products. A particularly important reagent in enzymatic reactions is water, which is the product of many bond-forming reactions and a reactant in many bond-breaking processes. In biocatalysis , enzymes are employed to prepare many commodity chemicals including high-fructose corn syrup and acrylamide . Some monoclonal antibodies whose binding target
2220-421: The addition of chemical agents. A true catalyst can work in tandem with a sacrificial catalyst . The true catalyst is consumed in the elementary reaction and turned into a deactivated form. The sacrificial catalyst regenerates the true catalyst for another cycle. The sacrificial catalyst is consumed in the reaction, and as such, it is not really a catalyst, but a reagent. For example, osmium tetroxide (OsO 4 )
2280-442: The adsorption takes place ( Langmuir-Hinshelwood , Eley-Rideal , and Mars- van Krevelen ). The total surface area of a solid has an important effect on the reaction rate. The smaller the catalyst particle size, the larger the surface area for a given mass of particles. A heterogeneous catalyst has active sites , which are the atoms or crystal faces where the substrate actually binds. Active sites are atoms but are often described as
2340-502: The anodic and cathodic reactions. Catalytic heaters generate flameless heat from a supply of combustible fuel. Some of the largest-scale chemicals are produced via catalytic oxidation, often using oxygen . Examples include nitric acid (from ammonia), sulfuric acid (from sulfur dioxide to sulfur trioxide by the contact process ), terephthalic acid from p-xylene, acrylic acid from propylene or propane and acrylonitrile from propane and ammonia. The production of ammonia
2400-400: The catalyst allows the reaction to occur by an alternative mechanism which may be much faster than the non-catalyzed mechanism. However the non-catalyzed mechanism does remain possible, so that the total rate (catalyzed plus non-catalyzed) can only increase in the presence of the catalyst and never decrease. Catalysis may be classified as either homogeneous , whose components are dispersed in
2460-465: The early 2000s, these organocatalysts were considered "new generation" and are competitive to traditional metal (-ion)-containing catalysts. Organocatalysts are supposed to operate akin to metal-free enzymes utilizing, e.g., non-covalent interactions such as hydrogen bonding . The discipline organocatalysis is divided into the application of covalent (e.g., proline , DMAP ) and non-covalent (e.g., thiourea organocatalysis ) organocatalysts referring to
PEMT - Misplaced Pages Continue
2520-431: The equilibrium constant. (A catalyst can however change the equilibrium concentrations by reacting in a subsequent step. It is then consumed as the reaction proceeds, and thus it is also a reactant. Illustrative is the base-catalyzed hydrolysis of esters , where the produced carboxylic acid immediately reacts with the base catalyst and thus the reaction equilibrium is shifted towards hydrolysis.) The catalyst stabilizes
2580-414: The iron particles. Once physically adsorbed, the reagents partially or wholly dissociate and form new bonds. In this way the particularly strong triple bond in nitrogen is broken, which would be extremely uncommon in the gas phase due to its high activation energy. Thus, the activation energy of the overall reaction is lowered, and the rate of reaction increases. Another place where a heterogeneous catalyst
2640-761: The liver, the PEMT pathway has been shown to have played a critical evolutionary role in providing PC during times of starvation. Furthermore, PC made via PEMT plays a wide range of physiological roles, utilized in choline synthesis, hepatocyte membrane structure, bile secretion, and very low-density lipoprotein (VLDL) secretion. Phosphatidylethanolamine N-methyltransferase is also known as lipid methyl transferase, LMTase, phosphatidylethanolamine methyltransferase, phosphatidylethanolamine-N-methylase, and phosphatidylethanolamine-S-adenosylmethionine-methyltransferase. The PEMT enzyme converts phosphatidylethanolamine (PE) to phosphatidylcholine (PC) via three sequential methylations by S-adenosyl methionine (SAM). The enzyme
2700-493: The precursor to the antibacterial levofloxacin , can be synthesized efficiently from hydroxyacetone by using catalysts based on BINAP -ruthenium complexes, in Noyori asymmetric hydrogenation : One of the most obvious applications of catalysis is the hydrogenation (reaction with hydrogen gas) of fats using nickel catalyst to produce margarine . Many other foodstuffs are prepared via biocatalysis (see below). Catalysis affects
2760-1076: The preferred catalyst- substrate binding and interaction, respectively. The Nobel Prize in Chemistry 2021 was awarded jointly to Benjamin List and David W.C. MacMillan "for the development of asymmetric organocatalysis." Photocatalysis is the phenomenon where the catalyst can receive light to generate an excited state that effect redox reactions. Singlet oxygen is usually produced by photocatalysis. Photocatalysts are components of dye-sensitized solar cells . In biology, enzymes are protein-based catalysts in metabolism and catabolism . Most biocatalysts are enzymes, but other non-protein-based classes of biomolecules also exhibit catalytic properties including ribozymes , and synthetic deoxyribozymes . Biocatalysts can be thought of as an intermediate between homogeneous and heterogeneous catalysts, although strictly speaking soluble enzymes are homogeneous catalysts and membrane -bound enzymes are heterogeneous. Several factors affect
2820-428: The presence of a catalyst because the catalyst provides an alternative reaction mechanism (reaction pathway) having a lower activation energy than the non-catalyzed mechanism. In catalyzed mechanisms, the catalyst is regenerated. As a simple example occurring in the gas phase, the reaction 2 SO 2 + O 2 → 2 SO 3 can be catalyzed by adding nitric oxide . The reaction occurs in two steps: The NO catalyst
2880-492: The promoter region of the PEMT has been demonstrated to contribute to development of organ dysfunction in conjunction with a low-choline diet. PEMT modulates levels of blood plasma homocysteine , which is either secreted or converted to methionine or cysteine. High levels of homocysteine are linked to cardiovascular disease and atherosclerosis , particularly coronary artery disease . PEMT deficiency prevents atherosclerosis in mice fed high-fat, high-cholesterol diets. This
2940-437: The reaction and remain unchanged after it. If the reaction is rapid and the catalyst recycles quickly, very small amounts of catalyst often suffice; mixing, surface area, and temperature are important factors in reaction rate. Catalysts generally react with one or more reactants to form intermediates that subsequently give the final reaction product, in the process of regenerating the catalyst. The rate increase occurs because
3000-415: The reaction product ( water molecule dimers ), after which the water molecule desorbs from the catalyst surface. Catalysts enable pathways that differ from the uncatalyzed reactions. These pathways have lower activation energy . Consequently, more molecular collisions have the energy needed to reach the transition state . Hence, catalysts can enable reactions that would otherwise be blocked or slowed by
3060-419: The reaction rate. As the reaction proceeds, the concentration of B increases and can accelerate the reaction as a catalyst. In effect, the reaction accelerates itself or is autocatalyzed. An example is the hydrolysis of an ester such as aspirin to a carboxylic acid and an alcohol . In the absence of added acid catalysts, the carboxylic acid product catalyzes the hydrolysis. Switchable catalysis refers to
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#17330932667493120-499: The reaction. For example, Wilkinson's catalyst RhCl(PPh 3 ) 3 loses one triphenylphosphine ligand before entering the true catalytic cycle. Precatalysts are easier to store but are easily activated in situ . Because of this preactivation step, many catalytic reactions involve an induction period . In cooperative catalysis , chemical species that improve catalytic activity are called cocatalysts or promoters . In tandem catalysis two or more different catalysts are coupled in
3180-487: The residues Gly98, Gly100, Glu180, and Glu181 to be essential for SAM binding in the active site. PEMT activity is unrelated to enzyme mass, but rather is regulated by supply of substrates including PE, as well as PMME, PDME, and SAM. Low substrate levels inhibit PEMT. The enzyme is further regulated by S-adenosylhomocysteine produced after each methylation. PEMT gene expression is regulated by transcription factors including activator protein 1 (AP-1) and Sp1 . Sp1
3240-423: The same phase (usually gaseous or liquid) as the reactant, or heterogeneous , whose components are not in the same phase. Enzymes and other biocatalysts are often considered as a third category. Catalysis is ubiquitous in chemical industry of all kinds. Estimates are that 90% of all commercially produced chemical products involve catalysts at some stage in the process of their manufacture. The term "catalyst"
3300-405: The same term [REDACTED] This disambiguation page lists articles associated with the title PEMT . If an internal link led you here, you may wish to change the link to point directly to the intended article. Retrieved from " https://en.wikipedia.org/w/index.php?title=PEMT&oldid=1064713055 " Category : Disambiguation pages Hidden categories: Short description
3360-448: The sequential methylation of PE by three molecules of SAM to form PC remains unknown. Kinetic analyses as well as amino acid and gene sequencing have shed some light on how the enzyme works. Studies suggest that a single substrate binding site binds all three phospholipids methylated by PEMT: PE, phosphatidyl-monomethylethanolamine (PMME) and phosphatidyl-dimethylethanolamine. The first methylation, that of PE to PMME, has been shown to be
3420-414: The starting compound, but this decomposition is so slow that hydrogen peroxide solutions are commercially available. In the presence of a catalyst such as manganese dioxide this reaction proceeds much more rapidly. This effect is readily seen by the effervescence of oxygen. The catalyst is not consumed in the reaction, and may be recovered unchanged and re-used indefinitely. Accordingly, manganese dioxide
3480-500: The substrates. One example of homogeneous catalysis involves the influence of H on the esterification of carboxylic acids, such as the formation of methyl acetate from acetic acid and methanol . High-volume processes requiring a homogeneous catalyst include hydroformylation , hydrosilylation , hydrocyanation . For inorganic chemists, homogeneous catalysis is often synonymous with organometallic catalysts . Many homogeneous catalysts are however not organometallic, illustrated by
3540-474: The transition state more than it stabilizes the starting material. It decreases the kinetic barrier by decreasing the difference in energy between starting material and the transition state. It does not change the energy difference between starting materials and products (thermodynamic barrier), or the available energy (this is provided by the environment as heat or light). Some so-called catalysts are really precatalysts . Precatalysts convert to catalysts in
3600-617: The use of cobalt salts that catalyze the oxidation of p-xylene to terephthalic acid . Whereas transition metals sometimes attract most of the attention in the study of catalysis, small organic molecules without metals can also exhibit catalytic properties, as is apparent from the fact that many enzymes lack transition metals. Typically, organic catalysts require a higher loading (amount of catalyst per unit amount of reactant, expressed in mol% amount of substance ) than transition metal(-ion)-based catalysts, but these catalysts are usually commercially available in bulk, helping to lower costs. In
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