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Hydroxylation

From Wikipedia, the free encyclopedia
Hydroxylation and hydroxylases are not to be confused with hydrolysis and hydrolases.

In chemistry, hydroxylation can refer to:

  • (i) most commonly, hydroxylation describes a chemical process that introduces a hydroxyl group (−OH) into an organic compound.
  • (ii) the degree of hydroxylation refers to the number of OH groups in a molecule. The pattern of hydroxylation refers to the location of hydroxy groups on a molecule or material.[1]

Biological hydroxylation

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In biochemistry, hydroxylation reactions are often facilitated by enzymes called hydroxylases. A C−H bond is converted to an alcohol by insertion of an oxygen atom into a C−H bond. Typical stoichiometries for the hydroxylation of a generic hydrocarbon are these:

2R3C−H + O2 → 2 R3C−OH
R3C−H + O2 + 2e− + 2H+ → R3C−OH + H2O

Since O2 itself is a slow and unselective hydroxylating agent, catalysts are required to accelerate the pace of the process and to introduce selectivity.[2]

Hydroxylation is often the first step in the degradation of organic compounds in air. Hydroxylation is important in detoxification since it converts lipophilic compounds into water-soluble (hydrophilic) products that are more readily removed by the kidneys or liver and excreted. Some drugs (for example, steroids) are activated or deactivated by hydroxylation.[3]

The principal hydroxylation catalyst in nature is cytochrome P-450, hundreds of variations of which are known. Other hydroxylating agents include flavins, alpha-ketoglutarate-dependent hydroxylases (2-oxoglutarate-dependent dioxygenases), and some diiron hydroxylases.[4]

Steps in an oxygen rebound mechanism that explains many iron-catalyzed hydroxylations: H-atom abstraction, oxygen rebound, alcohol decomplexation.[2]

Of proteins

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The hydroxylation of proteins occurs as a post-translational modification and is catalyzed by 2-oxoglutarate-dependent dioxygenases.[5] Hydroxylation improves water‐solubility, as well as affecting their structure and function.

The most frequently hydroxylated amino acid residue in human proteins is proline. This is because collagen makes up about 25–35% of the protein in our bodies and contains a hydroxyproline at almost every 3rd residue in its amino acid sequence. Collagen consists of both 3‐hydroxyproline and 4‐hydroxyproline residues.[6] Hydroxylation occurs at the γ-C atom, forming hydroxyproline (Hyp), which stabilizes the secondary structure of collagen due to the strong electronegative effects of oxygen.[7] Proline hydroxylation is also a vital component of hypoxia response via hypoxia inducible factors. In some cases, proline may be hydroxylated instead on its β-C atom. These three reactions are catalyzed by large, multi-subunit enzymes prolyl 4-hydroxylase, prolyl 3-hydroxylase, and lysyl 5-hydroxylase, respectively. These enzymes require iron (as well as molecular oxygen and α-ketoglutarate). They consume oxygen (the oxidant) and ascorbic acid (vitamin C, the reductant). Deprivation of ascorbate leads to deficiencies in proline hydroxylation, which leads to less stable collagen, which can manifest itself as the disease scurvy. Since citrus fruits are rich in vitamin C, British sailors were given limes to combat scurvy on long ocean voyages; hence, they were called "limeys".[8]

Several other amino acids aside from proline are susceptible to hydroxylation, especially lysine, asparagine, aspartate and histidine. Lysine may be hydroxylated on its δ-C atom, forming hydroxylysine (Hyl).[9] Several endogenous proteins contain hydroxyphenylalanine and hydroxytyrosine residues. These residues are formed are formed by hydroxylation of phenylalanine and tyrosine, a process in which the hydroxylation converts phenylalanine residues into tyrosine residues.[6] Hydroxylation at C-3 of tyrosine gives 3,4- dihydroxyphenylalanine (DOPA), which is a precursor to hormones and can be converted into dopamine.

Synthetic hydroxylations

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Hydroxylations are well explored but only rarely useful in organic synthesis. Peroxytrifluoroacetic acid converts some arenes to phenols. Salts of peroxydisulfate converts phenols to quinols in the Elbs persulfate oxidation. Mixtures of ferrous sulfate and hydrogen peroxide, the Fenton reagent, behaves similarly.[10]

Installing hydroxyl groups into organic compounds can be effected by biomimetic catalysts, i.e. catalysts whose design is inspired by enzymes such as cytochrome P450.[11]

Whereas many hydroxylations insert O atoms into C−H bonds, some reactions add OH groups to unsaturated substrates. The Sharpless dihydroxylation is such a reaction: it converts alkenes into diols. The hydroxy groups are provided by hydrogen peroxide, which adds across the double bond of alkenes.[12]

Examples

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References

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  1. ^ Middleton, Elliott Jr; Kandaswami, Chithan; Theoharides, Theoharis C. (2000). "The Effects of Plant Flavonoids on Mammalian Cells: Implications for Inflammation, Heart Disease, and Cancer". Pharmacological Reviews. 52 (4): 673–751. PMID 11121513.
  2. ^ a b Huang, X.; Groves, J. T. (2017). "Beyond ferryl-mediated hydroxylation: 40 years of the rebound mechanism and C–H activation". Journal of Biological Inorganic Chemistry. 22 (2–3): 185–207. doi:10.1007/s00775-016-1414-3. PMC 5350257. PMID 27909920.
  3. ^ Cerniglia, Carl E. (1992). "Biodegradation of polycyclic aromatic hydrocarbons". Biodegradation. 3 (2–3): 351–368. doi:10.1007/BF00129093. S2CID 25516145.
  4. ^ Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. ISBN 1-57259-153-6.[page needed]
  5. ^ Zurlo, Giada; Guo, Jianping; Takada, Mamoru; Wei, Wenyi; Zhang, Qing (December 2016). "New Insights into Protein Hydroxylation and Its Important Role in Human Diseases". Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1866 (2): 208–220. doi:10.1016/j.bbcan.2016.09.004. ISSN 0006-3002. PMC 5138100. PMID 27663420.
  6. ^ a b T. Shantha Raju (2019), "Hydroxylation of Proteins", Co- and Post-Translational Modifications of Therapeutic Antibodies and Proteins, John Wiley & Sons, pp. 119–131, doi:10.1002/9781119053354.ch10, ISBN 978-1-119-05335-4, S2CID 243626930
  7. ^ Holmgren, Steven K; Bretscher, Lynn E; Taylor, Kimberly M; Raines, Ronald T (1999). "A hyperstable collagen mimic". Chemistry & Biology. 6 (2): 63–70. doi:10.1016/S1074-5521(99)80003-9. PMID 10021421.
  8. ^ Voet, Donald; Voet, Judith G.; Pratt, Charlotte W. (2016). Principles of Biochemistry. Wiley. p. 143. ISBN 978-1-119-45166-2.
  9. ^ Hausinger RP (January–February 2004). "Fe(II)/α-ketoglutarate-dependent hydroxylases and related enzymes". Crit. Rev. Biochem. Mol. Biol. 39 (1): 21–68. doi:10.1080/10409230490440541. PMID 15121720. S2CID 85784668.
  10. ^ Smith, Michael B.; March, Jerry (2007), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (6th ed.), New York: Wiley-Interscience, p. 964, ISBN 978-0-471-72091-1
  11. ^ Jia, Chengguo; Kitamura, Tsugio; Fujiwara, Yuzo (2001). "Catalytic Functionalization of Arenes and Alkanes via C−H Bond Activation". Accounts of Chemical Research. 34 (8): 633–639. doi:10.1021/ar000209h. PMID 11513570.
  12. ^ Kolb, Hartmuth C.; Vannieuwenhze, Michael S.; Sharpless, K. Barry (1994). "Catalytic Asymmetric Dihydroxylation". Chemical Reviews. 94 (8): 2483–2547. doi:10.1021/cr00032a009.
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