Identification of the bioactive components from pH-modified citrus pectin and their inhibitory effects on galectin-3 function

Tao Zhang, Yu Lan, Yi Zheng, Fengjian Liu, Dongyang Zhao, Kevin H. Mayo, Yifa Zhou*, Guihua Tai*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

36 Citations (Web of Science)

Abstract

Citrus pectin is widely used as a gelling/thickening agent and stabilizer in the food and pharmaceutical industries. The usefulness of citrus pectin, however, has been limited due to its large size, an obstacle that can be partially overcome with ph-modified citrus pectin (mcp). In the present study, we fractionated mcp into four fractions (mcp-1, -2, -3, and -4) and then sub-fractions of type-i rhamnogalacturonan-rich pectins (rg-i: mcp-1a, mcp-2a, mcp-3sa and mcp-4a) and homogalacturonan-rich pectins (hg: mcp-2b, mcp-3sb, mcp-3p, mcp-4b). Upon analysis of their chemical structures, we found that the rg-i sub-fractions contain (1 ? 4)-linked ß-d-galactan and (1 ? 5)-linked a-l-arabinans or type-i arabinogalactan side-chains. Because parent mcp is known to inhibit hemagglutination mediated by galectin-3 (a lectin associated with cancer progression and metastasis), we used this assay to define which mcp fraction best promotes anti-galectin-3 activity. Our results demonstrate that mcp-2 was the most inhibitory with a mic of 0.06 µg/ml (ten-fold more potent than parent mcp), and that rg-i-rich pectins with (1 ? 4)-linked ß-d-galactan side-chains were more active than the other rg-i-rich and hg-rich pectins. These findings provide new insight into structure-activity relationships of mcp and provide impetus towards the development of mcp-based food stabilizers and galectin-3 targeted therapeutics for use in the clinical setting.
Original languageEnglish
Pages (from-to)113-119
JournalFood Hydrocolloids
Volume58
DOIs
Publication statusPublished - Jul 2016

Keywords

  • Citrus pectin
  • RG-I
  • HG
  • Chemical analysis
  • Galectin-3
  • Agglutination

Cite this