Isolation and structural characterization of mannanoligosaccharides from aqueous palm kernel cake extract
Palm kernel cake (PKC) is the most valuable by-product obtained from the palm kernel oil extraction process. It has been used widely as an animal feed owing to its high protein content. PKC also contains about 81% of non-starch polysaccharides, mainly in the form of mannan-based polymers. Hydr...
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Format: | Thesis |
Language: | English |
Published: |
2016
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Online Access: | http://psasir.upm.edu.my/id/eprint/66764/1/IB%202016%2021%20IR.pdf http://psasir.upm.edu.my/id/eprint/66764/ |
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Summary: | Palm kernel cake (PKC) is the most valuable by-product obtained from the palm kernel
oil extraction process. It has been used widely as an animal feed owing to its high
protein content. PKC also contains about 81% of non-starch polysaccharides, mainly in
the form of mannan-based polymers. Hydrolysis of mannan into low molecular weight
mannanoligosaccharides (MOS) has been claimed to have prebiotic properties. The
biological mechanism and activities of the MOS are associated with its structure and
molecular weight. However, very little information was available on the structural
characteristics of MOS of different molecular weights from PKC. Therefore, the
objectives of the present study were to isolate MOS of different degree of
polymerization (DP) from the crude PKC extract and structurally characterize the MOS
using chemical derivatization and spectroscopic methods. The crude PKC extract was
obtained by hot water extraction method, followed by delipidation and deproteinization
step. The deproteinized PKC extract containing mixtures of MOS were then separated
into individual compounds based on their molecular weights using refractive index
high performance liquid chromatography (RI-HPLC). The molecular weights of the
MOS were determined using electrospray ionization mass spectrometry (ESI-MS/MS).
The structures of the isolated MOS were investigated using a combination of chemical
analyses such as sugar composition analysis and methylation analysis followed by gas
chromatography mass spectrometry (GC-MS), and other spectroscopic methods such as
nuclear magnetic resonance spectroscopy (NMR). The MOS mixtures were separated
into four individual major compounds with different DP, designated as MOS-III,
MOS-IV, MOS-V and MOS-VI. The molecular weights of the isolated MOS as
determined by ESI-MS/MS were 689, 851, 1013 and 1151 Dalton (Da) corresponding
to tetra-, penta-, hexa- and heptasaccharide of the MOS-III, MOS-IV, MOS-V and
MOS-VI, respectively. Sugar analysis of the isolated MOS indicated the presence of
mannose in each of the oligomers. Methylation and 1D/2D NMR analysis showed that
the MOS have a linear structure consisting of (1→4)-β-D-mannopyranosyl residues
with DP ranging from 4 to 7. They were identified as: a) β-D-Manp-(1→4)-β-D-Manp-
(1→4)-β-D-Manp-(1→4)-β-D-Manp, b) β-D-Manp-(1→4)-β-D-Manp-(1→4)-β-D Manp-(1→4)-β-D-Manp-(1→4)-β-D-Manp, c) β-D-Manp-(1→4)-β-D-Manp-(1→4)-β-
D-Manp-(1→4)-β-D-Manp-(1→4)-β-D-Manp-(1→4)-β-D-Manp, d) β-D-Manp-
(1→4)-β-D-Manp-(1→4)-β-D-Manp-(1→4)-β-D-Manp-(1→4)-β-D-Manp-(1→4)-β-DManp-(
1→4)-β-D-Manp. In conclusion, the present study revealed a successful
application of chromatography, chemical analysis, ESI-MS/MS and NMR to the
isolation and characterization of MOS fraction from PKC. |
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