Skip to main navigation Skip to search Skip to main content

Amylose content modulates lycopene isomerization and anti-oxidative activity of starch-lycopene complexes during small intestinal digestion

  • Zhengming Zhou
  • , Qile Zhang
  • , Lei Li
  • , Dongmei Liu
  • , Xinyi Deng
  • , Yue Ma
  • , Wang Hin Ng
  • , Jian Zhu
  • , Wing Tak Wong
  • , Cheng Li*
  • *Corresponding author for this work

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

Abstract

Starch-lycopene complexes may function as resistant starch, but their structural interactions and effects on digestibility and bioactivity remain poorly characterized. In this study, starch-lycopene complexes were prepared using waxy (WCS), normal (NCS), and high-amylose (G50CS) corn starches, and effects of amylose content on their structure, digestibility, and bioactivity were systematically investigated. Notably, lycopene (LYC) undergoes isomerization during complexation. Although complexes with more amylose released less total lycopene, the proportion of cis-lycopene was higher. Structural and simulation analyses revealed trans-lycopene (predominant) and cis-lycopene formed resistant complexes with amylose, while cis-lycopene formed slowly digestible complexes with amylopectin (DP 12–24). NCS-LYC (medium amylose) achieved an optimal balance in cis-lycopene release and proportion, resulting significantly enhanced antioxidant enzyme activities (SOD 1.32-fold, CAT 2.74-fold, and GSH-Px 1.35-fold) and reduced MDA levels by 60.6 % in H₂O₂-induced Caco-2 cells. These findings highlight amylose's role in modulating digestibility and lycopene isomerization, assisting the design of functional starch-based foods. © 2025 Elsevier Ltd.
Original languageEnglish
Article number146501
Number of pages15
JournalFood Chemistry
Volume495
Issue numberPart 2
Online published23 Sept 2025
DOIs
Publication statusPublished - 15 Dec 2025

Funding

The authors would like to acknowledge the financial support from the NSFC/RGC Joint Research Scheme sponsored by the Research Grants Council of the Hong Kong Special Administrative Region, China and National Natural Science Foundation of China (Project No. N_CUHK464/24), the Direct Grant for Research 2023/2024 and 2024/2025 from The Chinese University of Hong Kong (Project code: 4053622, 4053690), CUHK-Improvement on Competitiveness in Hiring New Faculties Funding Scheme (PI: Ref. 310), CUHK-School of Life Sciences Start-up funding, the CUHK Nissin Foods Scholarship.

Research Keywords

  • In vitro digestion
  • Molecular simulation
  • Oxidative injured Caco-2 cells
  • Starch-lycopene complex

RGC Funding Information

  • RGC-funded

Fingerprint

Dive into the research topics of 'Amylose content modulates lycopene isomerization and anti-oxidative activity of starch-lycopene complexes during small intestinal digestion'. Together they form a unique fingerprint.

Cite this