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Mannans

From Wikipedia, the free encyclopedia
Polysaccharides formed from mannose
For other uses, seeMannan.
Subunit of a typical mannan showing four 1,4-linked beta-D-mannose units, one with a galactose side chain.

Mannans arepolymers containing the sugarmannose as a principal component.[1][2]They are a type ofpolysaccharide found inhemicellulose, a major source of biomass found in higher plants such as softwoods. These polymers also typically contain two other sugars,galactose andglucose. They are often branched (unlike cellulose).

Structural diversity

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Plant mannans have β(1-4) linkages, occasionally with α(1-6)galactose branches, forminggalactomannans. They are insoluble and a form of storage polysaccharide.Ivory nut is a source of mannans. An additional type isgalactoglucomannan found in soft wood with a mixed mannose/glucose β(1-4) backbone.[citation needed]Conjac andsalep haveglucomannans with β(1-4) linkages.[3][4] Many mannans areacetylated and some from marine sources, havesulfate esters side chains.

Yeast have a different type of glucomannan in their cell wall, with a α(1-6) linked backbone and α(1-2) and α(1-3) linkedglucose branches, which may also containphosphodiester bonds.[5] Enzymatic digestion or acid catalysis can help solubilize the glucomannan.[6] It is serologically similar to structures found on mammalian glycoproteins. Detection of mannan leads to lysis in themannan-binding lectin pathway.[citation needed]

Synthesis and degradation

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Guanosine diphosphate mannose is the precursor to mannans.[7] As a simplification, the diphosphate group is shown in its protonated form.

GDP-mannose is a substrate forglycosyltransferase for enzymes calledmannosyltransferases.[8]

Biosynthesis

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GDP-mannose is produced fromGTP andmannose-6-phosphate by the enzymemannose-1-phosphate guanylyltransferase.

The degradation of mannans (and many related forms of hemicellulose) has been well studied. The hydrolysis of the main mannan backbone is catalyzed by various enzymes including β-mannosidase, β-glucosidase, and β-mannase. The side chains are degraded byesterases and α-galactosidase.[1]

When a long chain of mannan ishydrolyzed into shorter chains, these smaller molecules are known asmannanoligosaccharide (MOS). MOS by definition can be produced from either insoluble galactomannan or soluble glucomannan, although the latter type is more widely marketed.[9]

Glucomannan MOS is used as prebiotics in animal husbandry and nutritional supplements due to its bioactivity.[citation needed]

Etymology

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From 'manna', produced by several species of tree and shrub e.g.Fraxinus ornus from whose secretionsmannitol was originally isolated.

See also

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References

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  1. ^abMoreira, L. R. S.; Filho, E. X. F. (2008). "An overview of mannan structure and mannan-degrading enzyme systems".Applied Microbiology and Biotechnology.79 (2):165–178.doi:10.1007/s00253-008-1423-4.PMID 18385995.S2CID 9746196.
  2. ^Mannan at the U.S. National Library of MedicineMedical Subject Headings (MeSH)
  3. ^Ye S, Zongo AW, Shah BR, Li J, Li B (2021). "Konjac Glucomannan (KGM), Deacetylated KGM (Da-KGM), and Degraded KGM Derivatives: A Special Focus on Colloidal Nutrition".Journal of Agricultural and Food Chemistry.69 (44):12921–12932.doi:10.1021/acs.jafc.1c03647.
  4. ^Kurt A, Kahyaoglu T (2017). "Purification of glucomannan from salep: Part 1. Detailed rheological characteristics".Carbohydrate Polymers.168:138–146.doi:10.1016/j.carbpol.2017.03.060.
  5. ^Baek KR, Ramakrishnan SR, Kim SJ, Seo SO (2024)."Yeast cell wall mannan structural features, biological activities, and production strategies".Heliyon.10 (6).doi:10.1016/j.heliyon.2024.e27896.PMC 10958358.PMID 38524613. Art. No. e27896.
  6. ^de Souza Theodoro S, Putarov TC, Tiemi C, Volpe LM, de Oliveira CA, de Abreu Glória MB, Carciofi AC."Effects of the solubility of yeast cell wall preparations on their potential prebiotic properties in dogs".PLoS One.14 (11).doi:10.1371/journal.pone.0225659.PMC 6878821.PMID 31765439. Art. No. e0225659.
  7. ^Samuel G, Reeves P (2003). "Biosynthesis of O-antigens: genes and pathways involved in nucleotide sugar precursor synthesis and O-antigen assembly".Carbohydrate Research.338 (23):2503–19.doi:10.1016/j.carres.2003.07.009.PMID 14670712.
  8. ^Pauly, Markus; Gille, Sascha; Liu, Lifeng; Mansoori, Nasim; De Souza, Amancio; Schultink, Alex; Xiong, Guangyan (2013). "Hemicellulose biosynthesis".Planta.238 (4):627–642.Bibcode:2013Plant.238..627P.doi:10.1007/s00425-013-1921-1.PMID 23801299.S2CID 17501948.
  9. ^Nopvichai, C; Charoenwongpaiboon, T; Luengluepunya, N; Ito, K; Muanprasat, C; Pichyangkura, R (2019)."Production and purification of mannan oligosaccharide with epithelial tight junction enhancing activity".PeerJ.7 e7206.doi:10.7717/peerj.7206.PMC 6611449.PMID 31304065.MOS is often prepared by hydrolysis reaction of a mannose-contained glucan polymer, mainly glucomannan and galactomannan.

Further reading

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  • Stewart, James; Curtis, Joan; Spurck, Timothy P.; Ilg, Thomas; Garami, Attila; Baldwin, Tracey; Courret, Nathalie; McFadden, Geoffrey I.; Davis, Antony; Handman, Emanuela (July 2005). "Characterisation of a Leishmania mexicana knockout lacking guanosine diphosphate-mannose pyrophosphorylase".International Journal for Parasitology.35 (8):861–873.doi:10.1016/j.ijpara.2005.03.008.PMID 15936761.
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