Development of nutritionally enhanced sourdough bread through Tritordeum bran incorporation and assessment in an in vitro gut simulation

IF 6.6 Q1 FOOD SCIENCE & TECHNOLOGY
Future Foods Pub Date : 2026-06-01 Epub Date: 2025-12-11 DOI:10.1016/j.fufo.2025.100874
Bilal Sajid Mushtaq , Olga Nikoloudaki , Martina Ben , Kashika Arora , Ali Zein Alabiden Tlais , Andrea Polo , Raffaella Di Cagno , Marco Gobbetti
{"title":"Development of nutritionally enhanced sourdough bread through Tritordeum bran incorporation and assessment in an in vitro gut simulation","authors":"Bilal Sajid Mushtaq ,&nbsp;Olga Nikoloudaki ,&nbsp;Martina Ben ,&nbsp;Kashika Arora ,&nbsp;Ali Zein Alabiden Tlais ,&nbsp;Andrea Polo ,&nbsp;Raffaella Di Cagno ,&nbsp;Marco Gobbetti","doi":"10.1016/j.fufo.2025.100874","DOIUrl":null,"url":null,"abstract":"<div><div>This study for the first time investigated how <em>Tritordeum</em> bran incorporation and starter-assisted sourdough fermentation influence bread nutritional features and gut microbiota, using a defined starter composed of <em>Lactiplantibacillus plantarum</em> LM108.5, <em>Pediococcus pentosaceus</em> TLD10–13, <em>Latilactobacillus curvatus</em> TLD10–17, and <em>Saccharomyces cerevisiae</em> TYD10–5. The bran-based sourdough bread (BSD-B3) showed higher total phenolic compounds (1185 mg GAE/kg), DPPH radical scavenging activity (10.83 mM BHT/100 g), β-glucans (0.39 %), arabinoxylans (3.22 %), and total free amino acids (1758 mg/kg), together with a reduced predicted glycemic index (8.83 %) and improved in vitro protein digestibility (up to 77.2 %) compared to the control (baker’s yeast bread (BYB). Targeted phenolic profiling revealed increased levels of protocatechuic, ferulic, and vanillic acids in BSD-B3, highlighting the contribution of bran and sourdough fermentation to phenolic bioavailability. The impact of <em>Tritordeum</em> sourdough breads with or without bran (TSD-B1 and BSD-B3) on colonic microbiota was evaluated in vitro using the Simulator of the Human Intestinal Microbial Ecosystem (SHIME<sup>Ⓡ</sup>). Application of sourdough bread digesta in the SHIME<sup>Ⓡ</sup> model enhanced short-chain fatty acid production, with BSD-B3 sustaining higher butyrate levels, while TSD-B1 and BYB favored acetate- and propionate-linked bifidogenic activity. Amplicon sequencing (16S rRNA gene) indicated that these metabolic shifts were accompanied by distinct changes in microbial composition and diversity. Our findings suggest that sourdough fermentation, particularly when combined with <em>Tritordeum</em> bran incorporation, produced nutritionally superior bread that selectively alters the gut microbiota.</div></div>","PeriodicalId":34474,"journal":{"name":"Future Foods","volume":"13 ","pages":"Article 100874"},"PeriodicalIF":6.6000,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future Foods","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666833525003338","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/12/11 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"FOOD SCIENCE & TECHNOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

This study for the first time investigated how Tritordeum bran incorporation and starter-assisted sourdough fermentation influence bread nutritional features and gut microbiota, using a defined starter composed of Lactiplantibacillus plantarum LM108.5, Pediococcus pentosaceus TLD10–13, Latilactobacillus curvatus TLD10–17, and Saccharomyces cerevisiae TYD10–5. The bran-based sourdough bread (BSD-B3) showed higher total phenolic compounds (1185 mg GAE/kg), DPPH radical scavenging activity (10.83 mM BHT/100 g), β-glucans (0.39 %), arabinoxylans (3.22 %), and total free amino acids (1758 mg/kg), together with a reduced predicted glycemic index (8.83 %) and improved in vitro protein digestibility (up to 77.2 %) compared to the control (baker’s yeast bread (BYB). Targeted phenolic profiling revealed increased levels of protocatechuic, ferulic, and vanillic acids in BSD-B3, highlighting the contribution of bran and sourdough fermentation to phenolic bioavailability. The impact of Tritordeum sourdough breads with or without bran (TSD-B1 and BSD-B3) on colonic microbiota was evaluated in vitro using the Simulator of the Human Intestinal Microbial Ecosystem (SHIMEⓇ). Application of sourdough bread digesta in the SHIMEⓇ model enhanced short-chain fatty acid production, with BSD-B3 sustaining higher butyrate levels, while TSD-B1 and BYB favored acetate- and propionate-linked bifidogenic activity. Amplicon sequencing (16S rRNA gene) indicated that these metabolic shifts were accompanied by distinct changes in microbial composition and diversity. Our findings suggest that sourdough fermentation, particularly when combined with Tritordeum bran incorporation, produced nutritionally superior bread that selectively alters the gut microbiota.

Abstract Image

利用三曲酵母麸皮制备营养增强酵母面包并在体外肠道模拟中进行评估
本研究首次使用由植物乳杆菌LM108.5、五香Pediococcus pentosaceus TLD10-13、弯曲乳杆菌TLD10-17和酿酒酵母TYD10-5组成的确定的发酵剂,研究了酵母麸皮加入和发酵剂辅助酵母发酵对面包营养特性和肠道微生物群的影响。与对照面包酵母(BYB)相比,麸皮酸面包(BSD-B3)具有更高的总酚类化合物(1185 mg GAE/kg)、DPPH自由基清除活性(10.83 mM BHT/100 g)、β-葡聚糖(0.39%)、阿拉伯木聚糖(3.22%)和总游离氨基酸(1758 mg/kg),同时预测血糖指数降低(8.83%),体外蛋白质消化率提高(77.2%)。靶向酚类分析显示,BSD-B3中原儿茶酸、阿魏酸和香草酸水平增加,突出了麸皮和酵母发酵对酚类生物利用度的贡献。利用人体肠道微生物生态系统模拟器(SHIMEⓇ)体外研究了加麸和不加麸的Tritordeum酵母面包(TSD-B1和BSD-B3)对结肠微生物群的影响。在SHIMEⓇ模型中应用酵母食糜可以促进短链脂肪酸的产生,其中BSD-B3维持较高的丁酸水平,而TSD-B1和BYB则有利于醋酸和丙酸联的双歧性活性。扩增子测序(16S rRNA基因)表明,这些代谢变化伴随着微生物组成和多样性的明显变化。我们的研究结果表明,酵母发酵,特别是当与Tritordeum麸皮结合时,生产出营养丰富的面包,选择性地改变肠道微生物群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Future Foods
Future Foods Agricultural and Biological Sciences-Food Science
CiteScore
8.60
自引率
0.00%
发文量
97
审稿时长
15 weeks
期刊介绍: Future Foods is a specialized journal that is dedicated to tackling the challenges posed by climate change and the need for sustainability in the realm of food production. The journal recognizes the imperative to transform current food manufacturing and consumption practices to meet the dietary needs of a burgeoning global population while simultaneously curbing environmental degradation. The mission of Future Foods is to disseminate research that aligns with the goal of fostering the development of innovative technologies and alternative food sources to establish more sustainable food systems. The journal is committed to publishing high-quality, peer-reviewed articles that contribute to the advancement of sustainable food practices. Abstracting and indexing: Scopus Directory of Open Access Journals (DOAJ) Emerging Sources Citation Index (ESCI) SCImago Journal Rank (SJR) SNIP
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书