|dc.description.abstract||In this thesis atomistic, statistical mechanical and coarse grained simulation techniques
are used to study the properties of biopolymers and in particular the plant
polysaccharide pectin. Spectroscopic aspects, structural and conformational behavior,
and mechanical properties of the molecule in di erent physical states are
After an introduction to the area and the theoretical techniques utilised herein
(chapter 1), chapter 2 deals with the spectroscopic characterisation of pectin.
Spectra were obtained theoretically by undertaking complete energy minimisation
and Hessien calculations using DFT techniques implemented in Gamess (PC &
US) packages. The calculated IR absorptions of di erent pectinic species and
oligomers coupled on di erent surfaces were compared with experimental results.
Herein, it is con rmed that experimental FTIR studies coupled with DFT calculations
can be used as an e ective tool for the characterisation of pectin, and
studying chemical coupling of the biopolymer to surfaces.
In chapter 3, the properties of single chain polymer systems in controlled solvent
conditions were studied using Brownian dynamics simulations, motivated by the
formation of secondary structure architectures in biopolymer systems. We focus
on the conformational properties of the chain in the presence of an additional torsional
potential. New, interesting, and biologically relevant structures were found
at the single molecule scale when a torsional potential was considered in the calculations.
In chapter 4, results from DFT calculations carried out on single pectin sugar
molecules (lengths and the free energies) are incorporated into a statistical mechanical
model of polymer stretching, in order to obtain the force-extension behaviour
of a single molecule pectin. This captures a good deal of the phenomenology of
the single molecule stretching behavior of pectin.
Chapter 5 summarises the conclusions of the work and nally chapter 6 suggests
direction for further work.||en_US