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棉子糖家族低聚糖在物种中利用的决定因素。

Determinants of raffinose family oligosaccharide use in species.

作者信息

Basu Anubhav, Adams Amanda N D, Degnan Patrick H, Vanderpool Carin K

机构信息

Department of Microbiology, University of Illinois Urbana-Champaign, Urbana, Illinois, USA.

Department of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.

出版信息

bioRxiv. 2024 Jun 7:2024.06.07.597959. doi: 10.1101/2024.06.07.597959.

DOI:10.1101/2024.06.07.597959
PMID:38895307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11185731/
Abstract

species are successful colonizers of the human gut 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 use of some polysaccharides, how 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 . Here, we identify two different types of mutations that increase mRNA levels and improve growth on RFOs. First, a novel spontaneous duplication of and places these genes under control of a ribosomal promoter, driving high transcription. Second, nonsense mutations in a gene encoding the PUL24 anti-sigma factor likewise increase 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 . Examining the genomes of other species, we found homologs of BT1871 in subset and show that representative strains of species containing 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.

摘要

某些物种是人类肠道的成功定植者,能够利用宿主无法消化的多种复杂多糖和寡糖。为此,它们使用多糖利用位点(PULs)中编码的酶。虽然最近的研究揭示了利用某些多糖所需的PULs,但对其如何利用较小的寡糖的研究较少。棉子糖家族寡糖(RFOs)在植物中含量丰富,尤其是豆类,由通过α-1,6键连接到蔗糖(葡萄糖α-1-β-2果糖)部分的可变半乳糖单元组成。先前的研究表明,α-半乳糖苷酶BT1871是利用RFOs所必需的。在这里,我们鉴定出两种不同类型的突变,它们可提高mRNA水平并改善在RFOs上的生长。首先,一个新的自发复制将这些基因置于核糖体启动子的控制之下,驱动高转录。其次,编码PUL24抗σ因子的基因中的无义突变同样增加了转录。然后,我们表明来自PUL22的水解酶与BT1871共同作用以分解RFOs的蔗糖部分,并确定碳水化合物利用的主调节因子(BT4338)在利用RFOs中发挥作用。检查其他物种的基因组,我们在一个子集中发现了BT1871的同源物,并表明含有BT1871同源物的物种的代表性菌株在蜜二糖上的生长比缺乏BT1871同源物的物种更好。总之,我们的研究结果揭示了一种重要的肠道共生菌如何利用丰富的膳食寡糖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/f03e9791f8fd/nihpp-2024.06.07.597959v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/62705eea67be/nihpp-2024.06.07.597959v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/35c049e7cd9b/nihpp-2024.06.07.597959v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/9da67db1c64e/nihpp-2024.06.07.597959v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/8d9aa073ff01/nihpp-2024.06.07.597959v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/2a2e3f4f535f/nihpp-2024.06.07.597959v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/05757bdc73c0/nihpp-2024.06.07.597959v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/f03e9791f8fd/nihpp-2024.06.07.597959v1-f0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/62705eea67be/nihpp-2024.06.07.597959v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/35c049e7cd9b/nihpp-2024.06.07.597959v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/9da67db1c64e/nihpp-2024.06.07.597959v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/8d9aa073ff01/nihpp-2024.06.07.597959v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/2a2e3f4f535f/nihpp-2024.06.07.597959v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/05757bdc73c0/nihpp-2024.06.07.597959v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b4/11185731/f03e9791f8fd/nihpp-2024.06.07.597959v1-f0007.jpg

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