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Reuterin

From Wikipedia, the free encyclopedia
Reuterin
Names
Preferred IUPAC name
3-Hydroxypropanal
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard100.016.696Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C3H6O2/c4-2-1-3-5/h2,5H,1,3H2
    Key: AKXKFZDCRYJKTF-UHFFFAOYSA-N
  • InChI=1/C3H6O2/c4-2-1-3-5/h2,5H,1,3H2
    Key: AKXKFZDCRYJKTF-UHFFFAOYAX
  • C(CO)C=O
Properties
C3H6O2
Molar mass74.079 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Reuterin (3-hydroxypropionaldehyde) is theorganic compound with the formula HOCH2CH2CHO. It is a bifunctional molecule, containing both a hydroxy and aldehydefunctional groups.

The name reuterin is derived fromLactobacillus reuteri, which produces the compound biosynthetically from glycerol as a broad-spectrum antibiotic (bacteriocin).[1]L. reuteri itself is named after the microbiologist Gerhard Reuter, who did early work in distinguishing it as a distinct species.

Solution structure

[edit]

In aqueous solution 3-hydroxypropionaldehyde exists in equilibrium with its hydrate (1,1,3-propanetriol), in which the aldehyde group converts to ageminal diol:

HOCH2CH2CHO + H2O → HOCH2CH2CH(OH)2

The hydrate is also in equilibrium with itsdimer (2-(2-hydroxyethyl)-4-hydroxy-1,3-dioxane), which dominates at high concentrations. These three components - the aldehyde, its dimer, and the hydrate are therefore in a dynamic equilibrium.[2]

Besides, 3-hydroxypropionaldehyde suffers an spontaneous dehydration in aqueous solution, and the resulting molecule is calledacrolein.[3]

In fact, the termreuterin is the name given to the dynamic system formed by 3-hydroxypropionaldehyde, its hydrate, the dimer, and acrolein. This last molecule, acrolein, was recently included in reuterin definition.[3][4]

Structure of the dimer of 3-hydroxypropionaldehyde

Synthesis and reactions

[edit]

3-Hydroxypropionaldehyde is formed by the condensation ofacetaldehyde andformaldehyde. This reaction, when conducted in the gas-phase, was the basis for a now obsolete industrial routeacrolein:[5]

CH3CHO + CH2O → HOCH2CH2CHO
HOCH2CH2CHO → CH2=CHCHO + H2O

Presently 3-hydroxypropionaldehyde is an intermediate in the production ofpentaerythritol. Hydrogenation of reuterin gives1,3-propanediol.

Biological activity

[edit]

Reuterin is an intermediate in the metabolism ofglycerol to1,3-propanediol catalysed by thecoenzyme B12-dependentglycerol dehydratase.

Reuterin is a potentantimicrobial compound produced byLactobacillus reuteri. It inhibits the growth of some harmfulGram-negative andGram-positive bacteria, along withyeasts,molds, andprotozoa.[6]L. reuteri can secrete sufficient amounts of reuterin to inhibit the growth of harmful gut organisms, without killing beneficial gut bacteria, allowingL. reuteri to remove gut invaders while keeping normalgut flora intact.[7]

Reuterin is water-soluble, effective in a wide range ofpH, resistant to proteolytic and lipolytic enzymes, and has been studied as afood preservative or auxiliary therapeutic agent.[8][9][10]

Reuterin as an extracted compound has been shown capable of killingEscherichia coli O157:H7 andListeria monocytogenes, with the addition oflactic acid increasing itsefficacy.[3][10] It has also been demonstrated to killEscherichia coli O157:H7 when produced byL. reuteri.[11]

References

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  1. ^Talarico TL, Casas IA, Chung TC, Dobrogosz WJ (December 1988)."Production and isolation of reuterin, a growth inhibitor produced by Lactobacillus reuteri".Antimicrobial Agents and Chemotherapy.32 (12):1854–8.doi:10.1128/AAC.32.12.1854.PMC 176032.PMID 3245697.
  2. ^Vollenweider S, Grassi G, König I, Puhan Z (May 2003). "Purification and structural characterization of 3-hydroxypropionaldehyde and its derivatives".Journal of Agricultural and Food Chemistry.51 (11):3287–93.doi:10.1021/jf021086d.PMID 12744656.
  3. ^abcEngels C, Schwab C, Zhang J, Stevens MJ, Bieri C, Ebert MO, McNeill K, Sturla SJ, Lacroix C (November 2016)."Acrolein contributes strongly to antimicrobial and heterocyclic amine transformation activities of reuterin".Scientific Reports.6 (1): 36246.Bibcode:2016NatSR...636246E.doi:10.1038/srep36246.PMC 5098142.PMID 27819285.
  4. ^Stevens M, Vollenweider S, Lacroix C (2011). "The potential of reuterin produced by Lactobacillus reuteri as a broad spectrum preservative in food".Protective Cultures, Antimicrobial Metabolites and Bacteriophages for Food and Beverage Biopreservation. Elsevier. pp. 129–160.doi:10.1533/9780857090522.1.129.ISBN 978-1-84569-669-6.
  5. ^Dietrich Arntz; Achim Fischer; Mathias Höpp; Sylvia Jacobi; Jörg Sauer; Takashi Ohara; Takahisa Sato; Noboru Shimizu; Helmut Schwind (2012). "Acrolein and Methacrolein".Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH.doi:10.1002/14356007.a01_149.pub2.ISBN 978-3-527-30673-2.
  6. ^Talarico TL, Dobrogosz WJ (May 1989)."Chemical characterization of an antimicrobial substance produced by Lactobacillus reuteri".Antimicrobial Agents and Chemotherapy.33 (5):674–9.doi:10.1128/aac.33.5.674.PMC 172512.PMID 2751282.
  7. ^Casas IA, Dobrogosz WJ (December 1, 2000). "Validation of the Probiotic Concept:Lactobacillus reuteri Confers Broad-spectrum Protection against Disease in Humans and Animals".Microbial Ecology in Health and Disease.12 (4):247–285.doi:10.1080/08910600050216246-1.S2CID 86853703.
  8. ^Vollenweider S, Lacroix C (March 2004)."3-hydroxypropionaldehyde: applications and perspectives of biotechnological production"(PDF).Applied Microbiology and Biotechnology.64 (1):16–27.doi:10.1007/s00253-003-1497-y.hdl:20.500.11850/51119.PMID 14669058.S2CID 27112296.
  9. ^Axelsson LT, Chung TC, Dobrogosz WJ, Lindgren SE (1989)."Production of a Broad Spectrum Antimicrobial Substance by Lactobacillus reuteri".Microbial Ecology in Health and Disease.2 (2):131–136.doi:10.3109/08910608909140210.
  10. ^abEl-Ziney MG, van den Tempel T, Debevere J, Jakobsen M (March 1999)."Application of reuterin produced by Lactobacillus reuteri 12002 for meat decontamination and preservation".Journal of Food Protection.62 (3):257–61.doi:10.4315/0362-028X-62.3.257.PMID 10090245.
  11. ^Muthukumarasamy P, Han JH, Holley RA (November 2003)."Bactericidal effects of Lactobacillus reuteri and allyl isothiocyanate on Escherichia coli O157:H7 in refrigerated ground beef".Journal of Food Protection.66 (11):2038–44.doi:10.4315/0362-028X-66.11.2038.PMID 14627280.
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