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Characteristics of enzymatically-deesterified pectin gels produced in the presence of monovalent ionic salts

Authors
Yoo, Sang-HoLee, Bo-HsunSavary, Brett J.Lee, SuyongLee, Hyeon GyuHotchkiss, Arland T
Issue Date
Oct-2009
Publisher
ELSEVIER SCI LTD
Keywords
Pectin methylesterase; Pectin; Monovalent ionic salts; Gel strength; Syneresis
Citation
FOOD HYDROCOLLOIDS, v.23, no.7, pp.1926 - 1929
Indexed
SCIE
SCOPUS
Journal Title
FOOD HYDROCOLLOIDS
Volume
23
Number
7
Start Page
1926
End Page
1929
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/176117
DOI
10.1016/j.foodhyd.2009.02.006
ISSN
0268-005X
Abstract
Pectin methylesterases (PMEs) from Valencia orange (p-PME) and Aspergillus aculeatus (f-PME) were used to produce pectin gels in the presence of 0.2 M monovalent ionic salts. At pH 5.0, pectin gels were induced following enzymatic deesterification of high methoxy pectin, with greater deesterification observed using p-PME compared to f-PME. Under these conditions, the deesterification limit of f-PME ended up with a pectin of DE 30.5-31.9 which did not gel at the PME reaction completion, while p-PME reduced the pectin's DE to 16.0-17.2, resulting in gel formation. The pectin gel induced by KCl was significantly stronger than the NaCl-induced gel, but LiCl did not induce pectin gelation. The gel strength was influenced by both DE and species of monovalent cation. The KCl-induced gels released less water than NaCl-induced gels. A synergistic effect on gel strength was observed from the pectin treated with a combination of (p + f)-PMEs, producing even more stable gels. These results indicated that the pectin gelation of our system would be enhanced both by using larger monovalent cat ion and by lowering the DE value, which would presumably be attributed to the different action patterns recognized for p- and f-PMEs. This pectin gelation system could provide a useful alternative to acid-sugar or calcium cross-linked gels in food and other industrial applications.
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