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Download fileO‑Methylation in Carbohydrates: An NMR and MD Simulation Study with Application to Methylcellulose
journal contribution
posted on 2021-10-27, 11:36 authored by Alessandro Ruda, Göran Widmalm, Jakob WohlertMethylated carbohydrates
are important from both biological and
technical perspectives. Specifically, methylcellulose is an interesting
cellulose derivative that has applications in foods, materials, cosmetics,
and many other fields. While the molecular dynamics simulation technique
has the potential for both advancing the fundamental understanding
of this polymer and aiding in the development of specific applications,
a general drawback is the lack of experimentally validated interaction
potentials for the methylated moieties. In the present study, simulations
using the GROMOS 56 carbohydrate force field are compared to NMR spin–spin
coupling constants related to the conformation of the exocyclic torsion
angle ω in d-glucopyranose and derivatives containing
a 6-O-methyl substituent and a 13C-isotopologue thereof.
A 3JCC Karplus-type relationship
is proposed for the C5–C6–O6–CMe torsion
angle. Moreover, solvation free energies are compared to experimental
data for small model compounds. Alkylation in the form of 6-O-methylation
affects exocyclic torsion only marginally. Computed solvation free
energies between nonmethylated and methylated molecules were internally
consistent, which validates the application of these interaction potentials
for more specialized purposes.
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solvation free energiessmall model compoundsinteresting cellulose derivativemd simulation studycc </ sub13 </ supmethylcellulose methylated carbohydratespresent studyj </</ submethylated moleculesmethylated moieties‑ methylationtype relationshiptorsion angletechnical perspectivesspecialized purposessimulations usingmethyl substituentisotopologue thereofinternally consistentinteraction potentialsgeneral drawbackfundamental understandingexperimental dataderivatives containing>< sub