S. Richardson et al., Characterisation of the substituent distribution in hydroxypropylated potato amylopectin starch, CARBOHY RES, 328(3), 2000, pp. 365-373
The distribution of substituents in hydroxypropylated potato amylopectin st
arch (amylose deficient) modified in a slurry of granular starch (HPPAPg) o
r in a polymer 'solution' of dissolved starch (HPPAPs), was investigated. T
he molar substitution (MS) was determined by three different methods: proto
n nuclear magnetic resonance (H-1 NMR) spectroscopy, gas-liquid chromatogra
phy (GLC) with mass spectrometry, and a colourimetric method. The MS values
obtained by H-1 NMR spectroscopy were higher than those obtained by GLC-ma
ss spectrometry analysis and colourimetry. The relative ratio of 2-, 3-, an
d B-substitution, as well as un-, mono-, and disubstitution in the anhydrog
lucose unit (AGU) were determined by GLC-mass spectrometry analysis. Result
s obtained showed no significant difference in molar distribution of hydrox
ypropyl groups in the AGU between the two derivatives. For analysis of the
distribution pattern along the polymer chain, the starch derivatives were h
ydrolysed by enzymes with different selectivities. Debranching of the polym
ers indicated that more substituents were located in close vicinity to bran
ching points in HPPAPg than in HPPAPs. Simultaneous alpha-amylase and amylo
glucosidase hydrolysis of HPPAPg liberated more unsubstituted glucose units
than the hydrolysis of HPPAPs, indicating a more heterogeneous distributio
n of substituents in HPPAPg. (C) 2000 Elsevier Science Ltd. All rights rese
rved.