Determinants of raffinose family oligosaccharide use in Bacteroides species.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY Journal of Bacteriology Pub Date : 2024-09-27 DOI:10.1128/jb.00235-24
Anubhav Basu, Amanda N D Adams, Patrick H Degnan, Carin K Vanderpool
{"title":"Determinants of raffinose family oligosaccharide use in <i>Bacteroides</i> species.","authors":"Anubhav Basu, Amanda N D Adams, Patrick H Degnan, Carin K Vanderpool","doi":"10.1128/jb.00235-24","DOIUrl":null,"url":null,"abstract":"<p><p><i>Bacteroides</i> species are successful colonizers of the human colon and can utilize a wide variety of complex polysaccharides and oligosaccharides that are indigestible by the host. To do this, they use enzymes encoded in polysaccharide utilization loci (PULs). While recent work has uncovered the PULs required for the use of some polysaccharides, how <i>Bacteroides</i> utilize smaller oligosaccharides is less well studied. Raffinose family oligosaccharides (RFOs) are abundant in plants, especially legumes, and consist of variable units of galactose linked by α-1,6 bonds to a sucrose (glucose α-1-β-2 fructose) moiety. Previous work showed that an α-galactosidase, BT1871, is required for RFO utilization in <i>Bacteroides thetaiotaomicron</i>. Here, we identify two different types of mutations that increase <i>BT1871</i> mRNA levels and improve <i>B. thetaiotaomicron</i> growth on RFOs. First, a novel spontaneous duplication of <i>BT1872</i> and <i>BT1871</i> places these genes under the control of a ribosomal promoter, driving high <i>BT1871</i> transcription. Second, nonsense mutations in a gene encoding the PUL24 anti-sigma factor likewise increase <i>BT1871</i> transcription. We then show that hydrolases from PUL22 work together with BT1871 to break down the sucrose moiety of RFOs and determine that the master regulator of carbohydrate utilization (BT4338) plays a role in RFO utilization in <i>B. thetaiotaomicron</i>. Examining the genomes of other <i>Bacteroides</i> species, we found homologs of BT1871 in a subset and showed that representative strains of species with a BT1871 homolog grew better on melibiose than species that lack a BT1871 homolog. Altogether, our findings shed light on how an important gut commensal utilizes an abundant dietary oligosaccharide.</p><p><strong>Importance: </strong>The gut microbiome is important in health and disease. The diverse and densely populated environment of the gut makes competition for resources fierce. Hence, it is important to study the strategies employed by microbes for resource usage. Raffinose family oligosaccharides are abundant in plants and are a major source of nutrition for the microbiota in the colon since they remain undigested by the host. Here, we study how the model commensal organism, <i>Bacteroides thetaiotaomicron</i> utilizes raffinose family oligosaccharides. This work highlights how an important member of the microbiota uses an abundant dietary resource.</p>","PeriodicalId":15107,"journal":{"name":"Journal of Bacteriology","volume":null,"pages":null},"PeriodicalIF":2.7000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bacteriology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/jb.00235-24","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Bacteroides species are successful colonizers of the human colon and can utilize a wide variety of complex polysaccharides and oligosaccharides that are indigestible by the host. To do this, they use enzymes encoded in polysaccharide utilization loci (PULs). While recent work has uncovered the PULs required for the use of some polysaccharides, how Bacteroides utilize smaller oligosaccharides is less well studied. Raffinose family oligosaccharides (RFOs) are abundant in plants, especially legumes, and consist of variable units of galactose linked by α-1,6 bonds to a sucrose (glucose α-1-β-2 fructose) moiety. Previous work showed that an α-galactosidase, BT1871, is required for RFO utilization in Bacteroides thetaiotaomicron. Here, we identify two different types of mutations that increase BT1871 mRNA levels and improve B. thetaiotaomicron growth on RFOs. First, a novel spontaneous duplication of BT1872 and BT1871 places these genes under the control of a ribosomal promoter, driving high BT1871 transcription. Second, nonsense mutations in a gene encoding the PUL24 anti-sigma factor likewise increase BT1871 transcription. We then show that hydrolases from PUL22 work together with BT1871 to break down the sucrose moiety of RFOs and determine that the master regulator of carbohydrate utilization (BT4338) plays a role in RFO utilization in B. thetaiotaomicron. Examining the genomes of other Bacteroides species, we found homologs of BT1871 in a subset and showed that representative strains of species with a BT1871 homolog grew better on melibiose than species that lack a BT1871 homolog. Altogether, our findings shed light on how an important gut commensal utilizes an abundant dietary oligosaccharide.

Importance: The gut microbiome is important in health and disease. The diverse and densely populated environment of the gut makes competition for resources fierce. Hence, it is important to study the strategies employed by microbes for resource usage. Raffinose family oligosaccharides are abundant in plants and are a major source of nutrition for the microbiota in the colon since they remain undigested by the host. Here, we study how the model commensal organism, Bacteroides thetaiotaomicron utilizes raffinose family oligosaccharides. This work highlights how an important member of the microbiota uses an abundant dietary resource.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Bacteroides 菌类使用棉子糖家族寡糖的决定因素。
嗜酸乳杆菌是人类结肠的成功定植者,可以利用宿主无法消化的各种复杂多糖和寡糖。为此,它们使用多糖利用基因座(PULs)编码的酶。虽然最近的研究发现了利用某些多糖所需的 PULs,但对乳酸菌如何利用较小的低聚糖的研究则较少。棉子糖家族低聚糖(RFO)在植物(尤其是豆科植物)中含量丰富,由通过 α-1,6 键连接到蔗糖(葡萄糖 α-1-β-2 果糖)分子的可变半乳糖单位组成。之前的研究表明,在泰氏乳杆菌(Bacteroides thetaiotaomicron)中,α-半乳糖苷酶 BT1871 是利用 RFO 的必要条件。在这里,我们发现了两种不同类型的突变,它们能提高 BT1871 的 mRNA 水平并改善 B. thetaiotaomicron 在 RFO 上的生长。首先,BT1872 和 BT1871 的新型自发重复将这些基因置于核糖体启动子的控制之下,从而推动了 BT1871 的高转录。其次,编码 PUL24 反σ因子基因的无义突变同样增加了 BT1871 的转录。然后,我们发现 PUL22 的水解酶与 BT1871 一起分解 RFO 的蔗糖分子,并确定碳水化合物利用的主调节因子(BT4338)在 B. thetaiotaomicron 利用 RFO 的过程中发挥作用。在研究其他乳杆菌物种的基因组时,我们在一个子集中发现了 BT1871 的同源物,并表明与缺乏 BT1871 同源物的物种相比,具有 BT1871 同源物的物种的代表性菌株在三聚果糖上生长得更好。总之,我们的发现揭示了一种重要的肠道共生菌如何利用丰富的膳食低聚糖:肠道微生物组对健康和疾病都很重要。肠道微生物群的多样性和密集性使其对资源的竞争十分激烈。因此,研究微生物利用资源的策略非常重要。棉子糖家族低聚糖在植物中含量丰富,是结肠微生物群的主要营养来源,因为它们不被宿主消化。在这里,我们研究了模式共生生物 Bacteroides thetaiotaomicron 如何利用棉子糖家族低聚糖。这项工作强调了微生物群中的一个重要成员如何利用丰富的膳食资源。
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 去求助
来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
期刊最新文献
A flagellar accessory protein links chemotaxis to surface sensing. Vibrio cholerae: a fundamental model system for bacterial genetics and pathogenesis research. Combinatorial control of type IVa pili formation by the four polarized regulators MglA, SgmX, FrzS, and SopA. Corrinoid salvaging and cobamide remodeling in bacteria and archaea. Discovery and synthesis of leaderless bacteriocins from the Actinomycetota.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1