Selective Utilization of Polyguluronate by the Human Gut Bacteroides Species.

IF 5.4 2区 医学 Q1 CHEMISTRY, MEDICINAL
Marine Drugs Pub Date : 2025-08-29 DOI:10.3390/md23090348
Nuo Liu, Ming Li, Xiangting Yuan, Tianyu Fu, Youjing Lv, Qingsen Shang
{"title":"Selective Utilization of Polyguluronate by the Human Gut <i>Bacteroides</i> Species.","authors":"Nuo Liu, Ming Li, Xiangting Yuan, Tianyu Fu, Youjing Lv, Qingsen Shang","doi":"10.3390/md23090348","DOIUrl":null,"url":null,"abstract":"<p><p>Human gut <i>Bacteroides</i> species play crucial roles in the metabolism of dietary polysaccharides. Polyguluronate (PG), a major component of alginate, has been widely used in the food and medical industries. However, how PG is utilized by human gut <i>Bacteroides</i> species has not been fully elucidated. Here, using a combination of culturomics, genomics, and state-of-the-art analytical techniques, we elucidated in detail the utilization profiles of PG by 17 different human gut <i>Bacteroides</i> species. Our results indicated that each <i>Bacteroides</i> species exhibited a unique capability for PG utilization. Among all species tested, <i>Bacteroides xylanisolvens</i> consumed the highest amount of PG and produced the greatest quantity of short-chain fatty acids, suggesting that it may be a keystone bacterium in PG utilization. Mass spectrometry showed that PG was degraded by <i>B. xylanisolvens</i> into a series of oligosaccharides. Genomic analyses confirmed that <i>B. xylanisolvens</i> possesses a large and divergent repertoire of carbohydrate-active enzymes. Moreover, genomic annotation identified two enzymes, PL17_2 and PL6_1, in <i>B. xylanisolvens</i> that are potentially responsible for PG degradation. Altogether, our study provides novel insights into PG utilization by human gut <i>Bacteroides</i> species, which has important implications for the development of carbohydrate-based drugs from marine resources.</p>","PeriodicalId":18222,"journal":{"name":"Marine Drugs","volume":"23 9","pages":""},"PeriodicalIF":5.4000,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12471419/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Marine Drugs","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3390/md23090348","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Human gut Bacteroides species play crucial roles in the metabolism of dietary polysaccharides. Polyguluronate (PG), a major component of alginate, has been widely used in the food and medical industries. However, how PG is utilized by human gut Bacteroides species has not been fully elucidated. Here, using a combination of culturomics, genomics, and state-of-the-art analytical techniques, we elucidated in detail the utilization profiles of PG by 17 different human gut Bacteroides species. Our results indicated that each Bacteroides species exhibited a unique capability for PG utilization. Among all species tested, Bacteroides xylanisolvens consumed the highest amount of PG and produced the greatest quantity of short-chain fatty acids, suggesting that it may be a keystone bacterium in PG utilization. Mass spectrometry showed that PG was degraded by B. xylanisolvens into a series of oligosaccharides. Genomic analyses confirmed that B. xylanisolvens possesses a large and divergent repertoire of carbohydrate-active enzymes. Moreover, genomic annotation identified two enzymes, PL17_2 and PL6_1, in B. xylanisolvens that are potentially responsible for PG degradation. Altogether, our study provides novel insights into PG utilization by human gut Bacteroides species, which has important implications for the development of carbohydrate-based drugs from marine resources.

人肠道拟杆菌对聚谷醛酸盐的选择性利用。
人体肠道拟杆菌在膳食多糖的代谢中起着至关重要的作用。聚gulurate (PG)是海藻酸盐的主要成分,在食品和医疗工业中有着广泛的应用。然而,PG是如何被人类肠道拟杆菌利用的还没有完全阐明。在这里,我们结合了培养组学、基因组学和最先进的分析技术,详细阐明了17种不同的人类肠道拟杆菌对PG的利用概况。我们的结果表明,每个拟杆菌种类都表现出独特的PG利用能力。在所有被试菌种中,溶木拟杆菌消耗的PG量最高,产生的短链脂肪酸量最多,表明它可能是利用PG的关键菌。质谱分析结果表明,PG被木聚糖酵母菌降解为一系列低聚糖。基因组分析证实,B.木聚糖溶菌具有大量不同的碳水化合物活性酶。此外,基因组注释还鉴定出了两种酶,PL17_2和PL6_1,它们可能与PG降解有关。总之,我们的研究为人类肠道拟杆菌对PG的利用提供了新的见解,这对从海洋资源中开发碳水化合物为基础的药物具有重要意义。
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
Marine Drugs
Marine Drugs 医学-医药化学
CiteScore
9.60
自引率
14.80%
发文量
671
审稿时长
1 months
期刊介绍: Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.
×
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