Interactions in starch co-gelatinized with phenolic compound systems: Effect of complexity of phenolic compounds and amylose content of starch.

Carbohydr Polym

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi 214122, China; School of Food Science and Technology, Jiangnan University, Wuxi 214122, China. Electronic address:

Published: November 2020

AI Article Synopsis

  • Different types of maize starches were gelatinized with various phenolic compounds (caffeic acid, quercetin, EGCG) to study their effects on thermal properties and structure.
  • In blends with waxy maize starch, caffeic acid increased the decomposition temperature, while it decreased in normal and high amylose starches, indicating complex interactions.
  • Spectroscopic analyses (FTIR and NMR) showed that caffeic acid enhanced the ordered structure in waxy maize starch but reduced it in other starch types, with specific hydrogen bonding patterns influencing the gelatinization process.

Article Abstract

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.

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Source
http://dx.doi.org/10.1016/j.carbpol.2020.116667DOI Listing

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