n-Octyl β-D-thioglucopyranoside

From WikiProjectMed
Jump to navigation Jump to search
n-Octyl β-d-thioglucopyranoside
Names
IUPAC name
Octyl 1-thio-β-D-glucopyranoside
Systematic IUPAC name
(2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(octylsulfanyl)oxane-3,4,5-triol
Other names
(1S)-Octyl-β-d-thioglucoside
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.115.951 Edit this at Wikidata
  • InChI=1S/C14H28O5S/c1-2-3-4-5-6-7-8-20-14-13(18)12(17)11(16)10(9-15)19-14/h10-18H,2-9H2,1H3/t10-,11-,12+,13-,14+/m1/s1
    Key: CGVLVOOFCGWBCS-RGDJUOJXSA-N
  • CCCCCCCCS[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)O
Properties
C14H28O5S
Molar mass 308.434 g/mol
Appearance Colourless Waxy Semi-Solid
Melting point 125 to 131 °C (257 to 268 °F; 398 to 404 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

n-Octyl β-d-thioglucopyranoside (octylthioglucoside, OTG) is a mild nonionic detergent that is used for cell lysis or to solubilise membrane proteins without denaturing them.[1][2] This is particularly of use in order to crystallise them or to reconstitute them into lipid bilayers. It has a critical micelle concentration of 9 mM.[3]

It is an analog of the commonly used detergent octyl glucoside, the presence of the thioether linkage making it resistant to degradation by beta-glucosidase enzymes.

Preparation

N-alkyl thioglycosides of the n-octyl-β-d-thioglucopyranoside type are not naturally occurring. However, mustard oil glycosides are common natural S-glycosides.

The synthesis of n-octyl-β-d-thioglucopyranoside[4] starts from D-glucose (I) which is prepared with acetic anhydride and concentrated sulfuric acid to give α-d-glucopyranose pentaacetate (pentaacetylglucose) (II).[5] Pentaacetylglucose is reacted with hydrogen bromide to give 2,3,4,6-tetra-O-acetyl-α-d-glucopyranosyl bromide (acetobromo glucose) (III)[6] which yields with thiourea in acetone almost quantitatively the isothiuronium salt 2,3,4,6-tetra-O-acetyl-β-d-glucopyranosyl-1-isothiuronium bromide (IV).

The nucleophilic thiolate anion formed after neutralization and reduction with sodium sulfite to the thiol in the alkaline reacts again almost quantitatively with 1-bromoctane to n-octyl-2,3,4,6-tetra-O-acetyl-1-thio-β-d-glucopyranoside (peracetylated octylthioglucoside) (V). From V, the target product n-octyl-1-thio-β-d-glucopyranoside (VI) can be obtained in an overall yield of about 80% via the quantitatively proceeding alkaline deacetylation by means of sodium hydroxide in methanol.

Synthese von OTG, ausgehend von α-d-Glucose
Synthese von OTG, ausgehend von α-d-Glucose

In the trichloroacetimidate method of Richard R. Schmidt, the peracetylated O-(α-d-glucopyranyl) trichloroacetimidate forms with 1-octanethiol via boron trifluoride-etherate catalysis upon inversion exclusively n-octyl-1-thio-β-d-glucopyranoside (after deacetylation), while the perbenzylated O-(α-d-glucopyranyl) trichloroacetimidate is converted upon retention to the n-octyl-1-thio-α-d-glucopyranoside (after debenzylation).[7]

Synthese von n-Octyl-thioglucopyranosid nach R.R. Schmidt
Synthese von n-Octyl-thioglucopyranosid nach R.R. Schmidt

The reaction of d-glucose with 1-octanethiol and Olah's reagent[8] (70% hydrogen fluoride HF in pyridine) produces an anomeric mixture of n-octyl-1-thio-α,β-d-glucopyranoside in 95% yield which contains 44% α-anomeres and 56% β-anomers.[9]

Synthese von n-Octyl-α, β-thioglucopyranosid mit Olah’s Reagenz
Synthese von n-Octyl-α, β-thioglucopyranosid mit Olah’s Reagenz

The pure α-octylthioglucoside is accessible by reaction of pentacetyl-β-d-glucose (from d-glucose, acetic anhydride and sodium acetate) in organic solvents at elevated temperatures with 1-octanethiol and boron trifluoride etherate and subsequent deacetylation.[10][11]

Synthese von n-Octyl-α-thioglucopyranosid aus Pentaacetyl-β-glucose
Synthese von n-Octyl-α-thioglucopyranosid aus Pentaacetyl-β-glucose

Properties

n-octyl-β-d-1-thioglucopyranoside is a colorless, odorless, hygroscopic, crystalline solid which readily dissolves in water and short-chain alcohols. Compared with the O-glucoside n-octyl-β-d-glucopyranoside, which has already been introduced earlier as detergent for biochemical applications, the analogous S-glucoside OTG appears to be particularly suitable due to its higher stability, especially against degradation by β-glucosidases.

Comparison of S'-Octylglucoside with O-Glucoside[1]
characteristics Critical micelle concentration Solubilization ability dialysability Chem. Stability Β-glucosidase stability Transparency at 280 nm Denaturation tendency Chem. analytics
n-Octyl-β-d-thiogluco-pyranosid 9mM (+) ++ + + + + + +
n-Octyl-β-d-gluco-pyranosid 23-25 mM + ++ ++ (-) – + + +

++ very good + good (+) ok (-) poor – very poor

The cost advantage for octylthioglucoside stated in publications from the 1980s is evidently no longer given because of the recently developed, efficient enzymatic synthesis pathways for O-octylglucoside (directly from D-glucose, 1-octanol by means of β-glucosidase).[12]

The α-anomeric octylthioglucoside exhibits liquid crystalline properties forming a smectic phase A.[11]

Application

Nonionic detergents solubilize membrane proteins gently and (largely) preserving their physiological function by interaction with the hydrophobic membrane regions embedded in the lipid bilayers of cell membranes.[13] Above the so-called critical micelle concentration CMC [OTG: 9 mM, or 0.2772% (w/v)], mixed micelles of membrane proteins and surfactant molecules are formed, with OTG concentrations of 1.1-1.2% (w/v) for the solubilization of membrane proteins from E. coli.[2][4] No denaturation of the membrane proteins was found after solubilization with octylthioglucoside.[1]

For the analysis of the biological activity of membrane proteins, it is often necessary to reconstitute the proteins into the lipid bilayers of liposomes. For this, the solution of the solubilized protein is subject to dialysis or ion exchange chromatography in the presence of phospholipids or membrane lipid mixtures to remove the surfactant. For example, 95% of the OTG can be removed from a 43 mM surfactant solution under standard conditions within 6 hours.[2]

Octylthioglucoside (15 mM) is clearly superior to its O-analog octyl glucoside (OT) in the solubilization and stabilization against thermal and light-induced denaturation of the light-driven proton pump Bacteriorhodopsin from the biomembranes of halobacteria.[14]

References

  1. ^ a b c T. Tsuchiya, S. Saito (1984), "Use of n-Octyl-β-D-thioglucoside, a new nonionic detergent, for solubilization and reconstitution of membrane proteins", J. Biochem., vol. 96, no. 5, pp. 1593–1597, doi:10.1093/oxfordjournals.jbchem.a134989, PMID 6396301
  2. ^ a b c S. Saito, T. Tsuchiya (1984), "Characteristics of n-octyl-β-D-thioglucopyranoside, a new nonionic detergent useful for membrane biochemistry", Biochem. J., vol. 222, no. 3, pp. 829–832, doi:10.1042/bj2220829, PMC 1144249, PMID 6237644
  3. ^ "Products". sigmaaldrich.com. [dead link]
  4. ^ a b S. Saito, T. Tsuchiya (1985), "Synthesis of Alkyl-β-D-thioglucopyranoside, a series of new nonionic detergents", Chem. Pharm. Bull., vol. 33, no. 2, pp. 503–508, doi:10.1248/cpb.33.503
  5. ^ "Acetobromoglucose [2,3,4,6-Tetraacetyl-α-d-glucopyranosyl bromide]". Organic Syntheses. doi:10.15227/orgsyn.022.0001.
  6. ^ Lemieux, R. U. (1963), Whistler, R. L.; Wolfrom, M. L.; BeMiller, J. N. (eds.), Methods in Carbohydrate Chemistry, Vol. 2, Reactions of Carbohydrates, New York: Academic Press Inc., pp. 221–222
  7. ^ R.R. Schmidt, M. Stumpp (1983), "Glycosylimidate. 8. Synthese von 1-Thio-glycosiden", Liebigs Ann. Chem. (in German), vol. 1983, no. 7, pp. 1249–1256, doi:10.1002/jlac.198319830717
  8. ^ G.A. Olah, J.G. Shih, G.K.S. Prakash (1986), "Fluorine-containing reagents in organic synthesis", J. Fluorine Chem., vol. 33, no. 1–4, pp. 377–396, doi:10.1016/S0022-1139(00)85282-3{{citation}}: CS1 maint: multiple names: authors list (link)
  9. ^ US 5118804, J. Defaye, A. Gadelle, C. Pedersen, "Process for preparing alkyl-1-thioglycosides and alkyl-glycosides, anomer mixtures thereof", published 1992-06-02, assigned to Beghin-Say, S.A. 
  10. ^ EP 1041080, M. Tsuji, H. Yamazaki, "Process for the preparation of pentaacetyl-beta-D-glucopyranose", published 2000-10-04, assigned to Nisshin Flour Milling Co., Ltd. 
  11. ^ a b H.A. van Doren, R. van der Geest (1989), "Synthesis and liquid crystalline properties of the n-alkyl-1-thio-α-D-glucopyranosides, a new homologous series of carbohydrate mesogens", Carbohydrate Research, vol. 194, pp. 71–77, doi:10.1016/0008-6215(89)85007-4
  12. ^ A. Ducret, J.-F. Carrière, M. Trani, R. Lortie (2002), "Enzymatic synthesis of octyl glucoside by almond β-gluconidase in organic media", Can. J. Chem., vol. 80, no. 6, pp. 653–656, doi:10.1139/v02-081{{citation}}: CS1 maint: multiple names: authors list (link)
  13. ^ "OTG, 1-S-Octyl-β-D-Thioglucopyranoside (Octylthioglucose) 28351" (PDF). Pierce Chemical Co. January 1998. Archived from the original (PDF; 44 kB) on 2017-03-12. Retrieved 2017-02-26.
  14. ^ A. Asada, M. Sonoyama (2011), "Solubilization and structural stability of bacteriorhodopsin with a mild nonionic detergent, n-octyl-β-thioglucoside", Biosc. Biotechnol. Biochem., vol. 75, no. 2, pp. 376–378, doi:10.1271/bbb.100726, PMID 21307577, S2CID 37825917

External links

Retrieved from "https://mdwiki.org/wiki/N-Octyl_β-D-thioglucopyranoside"