Project Number: 6618-41000-015-05
Start Date: Jan 15, 2009
End Date: Aug 31, 2013
Pectin methylesterases (PME) present in commercial papaya fruit (Carica papaya) extracts, used industrially in the formulation of food ingredients for their inherent PME activity, will be purified with a multi-dimensional strategy incorporating affinity chromatography. The hypothesis that these enzymes can be used to rationally design functional polysaccharide food ingredients will be tested. They will be characterized for biochemical, physical and kinetic properties, and their ability to manipulate pectin nano-structure. Mass spectrometry and N-terminal amino acid sequencing will be used to establish identity tags and relatedness of individual PME forms, establishing a basis for subsequent cloning. A recently defined model homogalacturonan will be demethylated with purified papaya PME(s) to pectins with predetermined degrees of methylation. Introduced demethylated block sequence will be characterized by limited digestion with endo polygalacturonase to release demethylated fragments. Released oligomers of galacturonic acid will be visualized and quantified using HPAEC coupled to an evaporative light scattering detector, allowing for the estimation of average demethylated block size and number per pectin molecule. Capillary electrophoresis will be used to probe the intermolecular distribution of introduced demethylated blocks. These data will be used to mathematically model the enzyme mode of action/degree of processivity. Modified homogalacturonans will be submitted to functional testing (rheology, calcium sensitivity and suspension properties) to enable comparison of nano-structure features to functional properties. The relationship between block size/number and influence of reaction conditions on enzyme mode of action and pectin functionality will allow for predictive modeling of food product quality related to the listed variables.