Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.carbpol.2020.116667
DC FieldValue
dc.titleInteractions in starch co-gelatinized with phenolic compound systems: Effect of complexity of phenolic compounds and amylose content of starch
dc.contributor.authorLiu, B
dc.contributor.authorZhong, F
dc.contributor.authorYokoyama, W
dc.contributor.authorHuang, D
dc.contributor.authorZhu, S
dc.contributor.authorLi, Y
dc.date.accessioned2020-12-01T01:57:09Z
dc.date.available2020-12-01T01:57:09Z
dc.date.issued2020-11-01
dc.identifier.citationLiu, B, Zhong, F, Yokoyama, W, Huang, D, Zhu, S, Li, Y (2020-11-01). Interactions in starch co-gelatinized with phenolic compound systems: Effect of complexity of phenolic compounds and amylose content of starch. Carbohydrate Polymers 247 : 116667-116667. ScholarBank@NUS Repository. https://doi.org/10.1016/j.carbpol.2020.116667
dc.identifier.issn01448617
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/184317
dc.description.abstract© 2020 Elsevier Ltd Maize starches of different amylose contents were co-gelatinized with caffeic acid (CA), quercetin (Qu) and epigallocatechin gallate (EGCG), respectively. The decomposition temperature of waxy maize starch (WS)-CA blends was increased compared to WS, while that of normal maize starch (MS) and high amylose starch (HS) was decreased. The more complex of the phenolic compounds, the lower the decomposition temperature of the MS. The results of Fourier-transform infrared spectroscopy suggested that CA increased short range ordered structure of gelatinized WS but decreased that of gelatinized MS and HS. Hydrogen bonds associated with CA and starch led to the arrangement of ordered structures in different starch. Nuclear magnetic resonance (NMR) indicated that all hydroxyl groups of CA and EGCG formed hydrogen bonds, while hydroxyl group at C-4′ of quercetin had priority to form hydrogen bonds. During co-gelatinization process, more single helixes were induced in MS by CA than Qu or EGCG did.
dc.publisherElsevier BV
dc.sourceElements
dc.typeArticle
dc.date.updated2020-08-23T14:44:59Z
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.carbpol.2020.116667
dc.description.sourcetitleCarbohydrate Polymers
dc.description.volume247
dc.description.page116667-116667
dc.published.statePublished
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