Aspartic acid
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| Names | |
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| IUPAC names
Trivial: Aspartic acid Systematic: Aminobutanedioic acid | |
| Other names
Aminosuccinic acid, asparagic acid, asparaginic acid[1] | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.265 |
| EC Number | 200-291-6 |
| KEGG | |
PubChem CID |
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| UNII | |
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| Properties | |
| C4H7NO4 | |
| Molar mass | 133.10 g·mol−1 |
| Appearance | colourless crystals |
| Density | 1.7 g/cm3 |
| Melting point | 270 °C (518 °F; 543 K) |
| Boiling point | 324 °C (615 °F; 597 K) (decomposes) |
| 4.5 g/L[2] | |
| Acidity (pKa) | 3.9 |
| Conjugate acid | Aspartate |
| -64.2·10−6 cm3/mol | |
| Hazards | |
| Safety data sheet | See: data page |
| NFPA 704 | |
| Supplementary data page | |
| Refractive index (n), Dielectric constant (εr), etc. | |
Thermodynamic data |
Phase behaviour solid–liquid–gas |
| UV, IR, NMR, MS | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Aspartic acid (symbol Asp or D;[3] the ionic form is known as aspartate), is an α-amino acid that is used in the biosynthesis of proteins.[4] Similar to all other amino acids it contains an amino group and a carboxylic acid. Its α-amino group is in the protonated –NH+
3 form under physiological conditions, while its α-carboxylic acid group is deprotonated −COO− under physiological conditions. Aspartic acid has an acidic side chain (CH2COOH) which reacts with other amino acids, enzymes and proteins in the body.[4] Under physiological conditions (pH 7.4) in proteins the side chain usually occurs as the negatively charged aspartate form, −COO−.[4] It is a non-essential amino acid in humans, meaning the body can synthesize it as needed. It is encoded by all the codons GAU and GAC.
D-Aspartate is one of two D-amino acids commonly found in mammals.[3]
In proteins aspartate sidechains are often hydrogen bonded to form asx turns or asx motifs, which frequently occur at the N-termini of alpha helices.
The L-isomer of Asp is one of the 22 proteinogenic amino acids, i.e., the building blocks of proteins. Aspartic acid, like glutamic acid, is classified as an acidic amino acid, with a pKa of 3.9, however in a peptide this is highly dependent on the local environment, and could be as high as 14. Asp is pervasive in biosynthesis.
Discovery
Aspartic acid was first discovered in 1827 by Auguste-Arthur Plisson and Étienne Ossian Henry[5] by hydrolysis of asparagine, which had been isolated from asparagus juice in 1806.[6] Their original method used lead hydroxide, but various other acids or bases are more commonly used instead.
Forms and nomenclature
There are two forms or enantiomers of aspartic acid. The name "aspartic acid" can refer to either enantiomer or a mixture of two.[7] Of these two forms, only one, "L-aspartic acid", is directly incorporated into proteins. The biological roles of its counterpart, "D-aspartic acid" are more limited. Where enzymatic synthesis will produce one or the other, most chemical syntheses will produce both forms, "DL-aspartic acid", known as a racemic mixture.
Biosynthesis
Because Aspartate can be synthesized by the body it is classified as a non-essential amino acid. In the human body, aspartate is most frequently synthesized through the transamination of oxaloacetate. The biosynthesis of aspartate is facilitated by an aminotransferase enzyme: the transfer of an amine group from another molecule such as alanine or glutamine yields aspartate and an alpha-keto acid.[4]
Aspartate also plays an important role in the urea cycle.
Chemical synthesis
Racemic aspartic acid can be synthesized from diethyl sodium phthalimidomalonate, (C6H4(CO)2NC(CO2Et)2).[8]
The major disadvantage of the above technique is that equimolar amounts of each enantiomer are made. Using biotechnology it is now possible to use immobilised enzymes to create just one type of enantiomer owing to their stereospecificity.
Metabolism
In plants and microorganisms, aspartate is the precursor to several amino acids, including four that are essential for humans: methionine, threonine, isoleucine, and lysine. The conversion of aspartate to these other amino acids begins with reduction of aspartate to its "semialdehyde", O2CCH(NH2)CH2CHO.[9] Asparagine is derived from aspartate via transamidation:
- -O2CCH(NH2)CH2CO2- + GC(O)NH3+ O2CCH(NH2)CH2CONH3+ + GC(O)O
(where GC(O)NH2 and GC(O)OH are glutamine and glutamic acid, respectively)
Participation in the urea cycle
In the urea cycle, aspartate and ammonia donate amino groups leading to the formation of urea.
Other biochemical roles
Aspartate has many other biochemical roles. It is a metabolite in the urea cycle and participates in gluconeogenesis. It carries reducing equivalents in the malate-aspartate shuttle, which utilizes the ready interconversion of aspartate and oxaloacetate, which is the oxidized (dehydrogenated) derivative of malic acid. Aspartate donates one nitrogen atom in the biosynthesis of inosine, the precursor to the purine bases. In addition, aspartic acid acts as a hydrogen acceptor in a chain of ATP synthase.
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles. [§ 1]
- ↑ The interactive pathway map can be edited at WikiPathways: "GlycolysisGluconeogenesis_WP534".
Neurotransmitter
Aspartate (the conjugate base of aspartic acid) stimulates NMDA receptors, though not as strongly as the amino acid neurotransmitter L-glutamate does.[10]
Applications & market
As of 2014, the global market for aspartic acid is $117MM annually (50-60K MT/Yr)[11] with potential areas of growth accounting for an addressable market of $8.78BB.[12] The three largest market segments include the U.S., Western Europe, and China. Current applications include biodegradable polymers (polyaspartic acid), low calorie sweeteners (aspartame), scale and corrosion inhibitors, and resins.
Nearly all aspartic acid is manufactured in China.
Superabsorbent polymers
One area of aspartic acid market growth is biodegradable superabsorbent polymers (SAP). The superabsorbent polymers market is anticipated to grow at a CAGR of 5.5% from 2014 to 2019 to reach a value of $8.78BB globally.[12] Around 75% of superabsorbent polymers are used in disposable diapers and an additional 20% is used for adult incontinence and feminine hygiene products. Polyaspartic acid, the polymerization product of aspartic acid, is a biodegradable substitute to polyacrylate.[13] The polyaspartate market comprises a small fraction (est. < 1%) of the total SAP market.
Additional uses
In addition to SAP, aspartic acid has applications in the $19B fertilizer industry, where polyaspartate improves water retention and nitrogen uptake;[14] the $1.1B (2020) concrete floor coatings market, where polyaspartic is a low VOC, low energy alternative to traditional epoxy resins;[15] and lastly the >$5B scale and corrosion inhibitors market.[16]
Sources
Dietary sources
Aspartic acid is not an essential amino acid, which means that it can be synthesized from central metabolic pathway intermediates in humans. However, aspartic acid is found in:
- Animal sources: oysters, luncheon meats, sausage meat, wild game
- Vegetable sources: sprouting seeds, oat flakes, avocado,[17] asparagus,[18] young sugarcane, and molasses from sugar beets.[1]
- Dietary supplements, either as aspartic acid itself or salts (such as magnesium aspartate)
- The sweetener aspartame, an aspartic acid, phenylalanine, formaldehyde trimer (brands: NutraSweet, Equal, Canderel, etc.)
See also
References
- 1 2 "862. Aspartic acid". The Merck Index (11th ed.). 1989. p. 132. ISBN 978-0-911910-28-5.
- ↑ "ICSC 1439 - L-ASPARTIC ACID". inchem.org.
- ↑ "Nomenclature and Symbolism for Amino Acids and Peptides". IUPAC-IUB Joint Commission on Biochemical Nomenclature. 1983. Archived from the original on 9 October 2008. Retrieved 5 March 2018.
- 1 2 3 4 G.,, Voet, Judith; W.,, Pratt, Charlotte (2016-02-29). Fundamentals of biochemistry : life at the molecular level. ISBN 9781118918401. OCLC 910538334.
- ↑ Berzelius JJ, Öngren OG (1839). Traité de chimie (in French). 3. Brussels: A. Wahlen et Cie. p. 81. Retrieved 25 August 2015.
- ↑ Plimmer R (1912) [1908]. Plimmer R, Hopkins F, eds. The chemical composition of the proteins. Monographs on Biochemistry. Part I. Analysis (2nd ed.). London: Longmans, Green and Co. p. 112. Retrieved January 18, 2010.
- ↑ "Nomenclature and symbolism for amino acids and peptides (IUPAC-IUB Recommendations 1983)", Pure Appl. Chem., 56 (5): 595–624, 1984, doi:10.1351/pac198456050595 .
- ↑ Dunn MS, Smart BW (1950). "DL-Aspartic Acid". Organic Syntheses. 30: 7. ; Collective Volume, 4, p. 55 .
- ↑ Lehninger AL, Nelson DL, Cox MM (2000). Principles of Biochemistry (3rd ed.). New York: W. H. Freeman. ISBN 1-57259-153-6.
- ↑ Chen PE, Geballe MT, Stansfeld PJ, Johnston AR, Yuan H, Jacob AL, Snyder JP, Traynelis SF, Wyllie DJ (May 2005). "Structural features of the glutamate binding site in recombinant NR1/NR2A N-methyl-D-aspartate receptors determined by site-directed mutagenesis and molecular modeling". Molecular Pharmacology. 67 (5): 1470–84. doi:10.1124/mol.104.008185. PMID 15703381.
- ↑ Evans J (2014). Commercial Amino Acids. BCC Research. pp. 101–103.
- 1 2 Transparency Market Research. Superabsorbent polymers market - global industry analysis, size, share, growth, trends and forecase, 2014-2020. (2014).
- ↑ Alford DD, Wheeler AP, Pettigrew CA (1994). "Biodegradation of thermally synthesized polyaspartate". J Environ Polym Degr. 2: 225–236.
- ↑ Kelling K (2001). Crop Responses to Amisorb in the North Central Region. University of Wisconsin-Madison.
- ↑ Global concrete floor coatings market will be worth US$1.1 bn by 2020. Transparency Market Research (2015).
- ↑ Corrosion inhibitors market analysis by product, by application, by end-use industry, and segment forecasts to 2020. Grand View Research (2014)
- ↑ Salunkhe DK, Kadam S (18 August 1995). Handbook of Fruit Science and Technology: Production, Composition, Storage, and Processing. CRC Press. pp. 368–. ISBN 978-0-8247-9643-3.
- ↑ Considine DM (6 December 2012). Foods and Food Production Encyclopedia. Springer Science & Business Media. pp. 114–. ISBN 978-1-4684-8511-0.
External links
- GMD MS Spectrum
- American Chemical Society (21 April 2010). "Ancestral Eve' Crystal May Explain Origin of Life's Left-Handedness". ScienceDaily. Archived from the original on 23 April 2010. Retrieved 2010-04-21.
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