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Indole-3-acetic acid (IAA) is a gut microbial metabolite of tryptophan that plays a crucial role in gut health. To maximize its bioactivity, colon-targeted delivery using acylated starch was developed. This study aims to investigate the interrelationships among the structural characteristics of starch and the biological functions of acylated starch in vivo. Three starches with distinct native structures (potato starch/POS, pea starch/PES and wheat starch/WHS), were acylated with IAA to produce POSIAA, PESIAA, and WHSIAA. All acylated starches showed substitution degrees of 0.31-0.36. The physicochemical properties of these acylated starches were thoroughly characterized. In vitro digestion demonstrated significant increases in resistant starch content for PESIAA and WHSIAA. In mice, acylated starches elevated IAA levels throughout the gastrointestinal tract, with maximal release in the colon. 16S rRNA sequencing revealed that acylated starches increased beneficial bacteria (Oscillospira and Parabacteroides) and reduced the Firmicutes/Bacteroidetes ratio, which are critical for maintaining intestinal homeostasis. Mice treated with PESIAA showed the highest gut microbiota community richness and diversity, as well as significantly improved colitis. These results provide insights into starch-based delivery systems that target metabolites to the colon, thereby regulating gut microbiota and promoting host health.
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http://dx.doi.org/10.1016/j.carbpol.2025.124031 | DOI Listing |
Int J Biol Macromol
September 2025
School of Chinese Meteria Medica, Beijing University of Chinese Medicine, Beijing 102488, China. Electronic address:
In this study, acylated starch from Canna edulis starch was syntheized by reacting it with short-chain fatty acids (SCFAs) and investigated its fermentation properties using fecal samples from healthy individuals and type 2 diabetes mellitus (T2DM) patients in vitro. Additionally, the correlation was analyzed between intestinal flora and T2DM indicators through in-vivo animal experiments. The in-vitro fermentation results showed that, compared to controls, Canna edulis butyrylated starch (PSB) increased butyric acid concentration by 6.
View Article and Find Full Text PDFCarbohydr Polym
November 2025
Key Laboratory for Natural Active Pharmaceutical Constituents Research in Universities of Shandong Province, School of Pharmaceutical Sciences, Shandong Analysis and Test Center, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250014, China. Electronic address:
Indole-3-acetic acid (IAA) is a gut microbial metabolite of tryptophan that plays a crucial role in gut health. To maximize its bioactivity, colon-targeted delivery using acylated starch was developed. This study aims to investigate the interrelationships among the structural characteristics of starch and the biological functions of acylated starch in vivo.
View Article and Find Full Text PDFFood Res Int
October 2025
Yunnan Key Laboratory of Plateau Food Advanced Manufacturing, Kunming 650500, China. Electronic address:
Propionate-acylated resistant starch has garnered attention for its unique ability to infuse specific SCFAs in the distal colon. Here, MPS with an elevated level of resistant starch was first prepared. Then, the effects of MPS on hepatic steatosis and the gut mycobiome were investigated in mice.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
College of Food Science, Southwest University, Chongqing 400715, China; Chongqing Key Laboratory of Speciality Food Co-Built by Sichuan and Chongqing, Chongqing 400715, China. Electronic address:
This study investigated the influence of deacetylated konjac glucomannan (DKGM) on the quality, retrogradation and digestion properties of instant black highland barley rice (IBHBR). Compared with KGM, DKGM shortened the cooking time of IBHBR by 21.78 %, reduced cooking loss by 47.
View Article and Find Full Text PDFCarbohydr Polym
October 2025
Wageningen University, Biobased Chemistry and Technology, Bornse Weilanden 9, 6708 WG Wageningen, the Netherlands.
Branching enzymes (BEs; EC 2.4.1.
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