Threonine Explained

Threonine (symbol Thr or T)[1] is an amino acid that is used in the biosynthesis of proteins. It contains an α-amino group (which is in the protonated −NH form when dissolved in water), a carboxyl group (which is in the deprotonated −COO form when dissolved in water), and a side chain containing a hydroxyl group, making it a polar, uncharged amino acid. It is essential in humans, meaning the body cannot synthesize it: it must be obtained from the diet. Threonine is synthesized from aspartate in bacteria such as E. coli.[2] It is encoded by all the codons starting AC (ACU, ACC, ACA, and ACG).

Threonine sidechains are often hydrogen bonded; the most common small motifs formed are based on interactions with serine: ST turns, ST motifs (often at the beginning of alpha helices) and ST staples (usually at the middle of alpha helices).

Modifications

The threonine residue is susceptible to numerous posttranslational modifications. The hydroxyl side-chain can undergo O-linked glycosylation. In addition, threonine residues undergo phosphorylation through the action of a threonine kinase. In its phosphorylated form, it can be referred to as phosphothreonine. Phosphothreonine has three potential coordination sites (carboxyl, amine and phosphate group) and determination of the mode of coordination between phosphorylated ligands and metal ions occurring in an organism is important to explain the function of the phosphothreonine in biological processes.[3]

History

Threonine was the last of the 20 common proteinogenic amino acids to be discovered. It was discovered in 1936 by William Cumming Rose,[4] collaborating with Curtis Meyer. The amino acid was named threonine because it was similar in structure to threonic acid, a four-carbon monosaccharide with molecular formula C4H8O5[5]

Stereoisomers

Threonine is one of two proteinogenic amino acids with two stereogenic centers, the other being isoleucine. Threonine can exist in four possible stereoisomers with the following configurations: (2S,3R), (2R,3S), (2S,3S) and (2R,3R). However, the name L-threonine is used for one single stereoisomer, (2S,3R)-2-amino-3-hydroxybutanoic acid. The stereoisomer (2S,3S), which is rarely present in nature, is called L-allothreonine.[6]

Biosynthesis

As an essential amino acid, threonine is not synthesized in humans, and needs to be present in proteins in the diet. Adult humans require about 20 mg/kg body weight/day.[7] In plants and microorganisms, threonine is synthesized from aspartic acid via α-aspartyl-semialdehyde and homoserine. Homoserine undergoes O-phosphorylation; this phosphate ester undergoes hydrolysis concomitant with relocation of the OH group.[8] Enzymes involved in a typical biosynthesis of threonine include:

  1. aspartokinase
  2. β-aspartate semialdehyde dehydrogenase
  3. homoserine dehydrogenase
  4. homoserine kinase
  5. threonine synthase.

Metabolism

Threonine is metabolized in at least three ways:

Metabolic diseases

The degradation of threonine is impaired in the following metabolic diseases:

Research of Threonine as a Dietary Supplement in Animals

Effects of threonine dietary supplementation have been researched in broilers.[14]

An essential amino acid, threonine is involved in the metabolism of fats, the creation of proteins, the proliferation and differentiation of embryonic stem cells, and the health and function of the intestines. Animal health and illness are strongly correlated with the need for and metabolism of threonine. Intestinal inflammation and energy metabolism disorders in animals may be alleviated by appropriate amounts of dietary threonine. Nevertheless, because these effects pertain to the control of nutrition metabolism, more research is required to confirm the results in various animal models. Furthermore, more research is needed to understand how threonine controls the dynamic equilibrium of the intestinal barrier function, immunological response and gut flora.[15]

Sources

Foods high in threonine include cottage cheese, poultry, fish, meat, lentils, black turtle bean[16] and sesame seeds.[17]

Racemic threonine can be prepared from crotonic acid by alpha-functionalization using mercury(II) acetate.[18]

External links

Notes and References

  1. Web site: Nomenclature and Symbolism for Amino Acids and Peptides . IUPAC-IUB Joint Commission on Biochemical Nomenclature . 1983 . 5 March 2018. https://web.archive.org/web/20081009023202/http://www.chem.qmul.ac.uk/iupac/AminoAcid/AA1n2.html. 9 October 2008 . live.
  2. Threonine synthesis from aspartate in Escherichia coli cell-free extracts: pathway dynamics . Raïs . Badr . Chassagnole . Christophe . Lettelier . Thierry . Fell . David . Mazat . Jean-Pierre . 2001 . Biochem J. 10.1042/bj3560425. 11368769 . 1221853 . 356 . Pt 2 . 425–32.
  3. Jastrzab, Renata (2013). "Studies of new phosphothreonine complexes formed in binary and ternary systems including biogenic amines and copper(II)". Journal of Coordination Chemistry. 66 (1): 98–113.
  4. Book: A Dictionary of scientists.. 1999. Oxford University Press. Daintith, John., Gjertsen, Derek.. 9780192800862. Oxford. 459. 44963215.
  5. Meyer . Curtis . The Spatial Configuation of Alpha-Amino-Beta-Hydroxy-n-Butyric Acid . Journal of Biological Chemistry . 20 July 1936 . 115 . 3 . 721–729 . 10.1016/S0021-9258(18)74711-X . free .
  6. Nomenclature and symbolism for amino acids and peptides (Recommendations 1983) . Pure and Applied Chemistry . 1 January 1984 . 56 . 5 . 601, 603, 608 . 10.1351/pac198456050595. free .
  7. Book: https://www.nap.edu/read/10490/chapter/12. Dietary Reference Intakes for Energy, Carbohydrates, Fiber, Fat, Fatty Acids, Cholesterol, Protein, and Amino Acids. Institute of Medicine. The National Academies Press. 2002. Washington, DC. 589–768. Protein and Amino Acids. 10.17226/10490. 978-0-309-08525-0. Institute of Medicine.
  8. .
  9. Book: Biochemical, Physiological, and Molecular Aspects of Human Nutrition – E-Book. Stipanuk. Martha H.. Caudill. Marie A.. 2013. Elsevier Health Sciences. 9780323266956. en.
  10. Book: Biochemistry for Nurses. Bhardwaj. Uma. Bhardwaj. Ravindra. Pearson Education India. 9788131795286. en.
  11. Fang . H . Kang . J . Zhang . D . Microbial production of vitamin B12: a review and future perspectives. . Microbial Cell Factories . 30 January 2017 . 16 . 1 . 15 . 10.1186/s12934-017-0631-y . 28137297 . 5282855 . free .
  12. Adeva-Andany . M . Souto-Adeva . G . Ameneiros-Rodríguez . E . Fernández-Fernández . C . Donapetry-García . C . Domínguez-Montero . A . Insulin resistance and glycine metabolism in humans. . Amino Acids . January 2018 . 50 . 1 . 11–27 . 10.1007/s00726-017-2508-0 . 29094215. 3708658 .
  13. Dalangin . R . Kim . A . Campbell . RE . The Role of Amino Acids in Neurotransmission and Fluorescent Tools for Their Detection. . International Journal of Molecular Sciences . 27 August 2020 . 21 . 17 . 6197 . 10.3390/ijms21176197 . 32867295 . 7503967 . free .
  14. Qaisrani . Shafqat Nawaz . Ahmed . Ibrar . Azam . Faheem . Bibi . Fehmida . Saima . Pasha . Talat Naseer . Azam . Farooq . 2018-07-01 . Threonine in broiler diets: an updated review . Annals of Animal Science . en . 18 . 3 . 659–674 . 10.2478/aoas-2018-0020 . 2300-8733. free .
  15. Tang . Qi . Peng . Tan . Ning . Ma . Xi . Ma . 2021-07-28 . Physiological Functions of Threonine in Animals: Beyond Nutrition Metabolism . Nutrients . 13 . 8 . 2592 . 10.3390/nu13082592 . free . 34444752 . 8399342 .
  16. Web site: Error. ndb.nal.usda.gov. 2013-05-29. 2018-11-16. https://web.archive.org/web/20181116093022/https://ndb.nal.usda.gov/ndb/foods/show/4632?fg=&man=&lfacet=&count=&max=&sort=&qlookup=&offset=&format=Full&new=. dead.
  17. Web site: SELF Nutrition Data - Food Facts, Information & Calorie Calculator. nutritiondata.self.com. 27 March 2018.
  18. .