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High‐pressure homogenization induced degradation of amylopectin in a gelatinized state
Author(s) -
Wei Benxi,
Cai Canxin,
Jin Zhengyu,
Tian Yaoqi
Publication year - 2016
Publication title -
starch ‐ stärke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.62
H-Index - 82
eISSN - 1521-379X
pISSN - 0038-9056
DOI - 10.1002/star.201500250
Subject(s) - amylopectin , size exclusion chromatography , radius of gyration , polymer , breakage , molar mass distribution , materials science , cellulose , starch , chemical engineering , light scattering , chemistry , amylose , composite material , organic chemistry , scattering , optics , physics , engineering , enzyme
An investigation of the degradation mechanism of a highly branched polymer during a high‐pressure homogenization (HPH) process was performed using gelatinized waxy maize starch as a substrate. The degradation mechanism was studied using high‐performance size‐exclusion chromatography equipped with multi‐angle laser‐light scattering and refractive index detectors. The HPH induced an exponential molecular degradation trend that was a function of HPH pressure/cycles. The results revealed that HPH preferentially disrupted larger molecules and caused their size distribution (or molecular weight) to a narrow range, resulting in a maximum stable size (or molecular weight). A final z ‐average radius of gyration of about 20 nm for amylopectin was observed after HPH for eight cycles at 100 MPa or two cycles at 150 MPa, which was due to the midpoint scission mechanism during the HPH treatment. The increase in molecular density after HPH verified the breakdown of the α‐1,4‐glycosidic bonds among the clusters of (midpoint scission) amylopectin.