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Cite: NAR/gkaa742 2020



PUL General Information

Literature Information

PUL ID

PUL0332

PubMed

28091525, Sci Rep. 2017 Jan 16;7:40248. doi: 10.1038/srep40248.

Characterization method

fosmid library screen,enzyme activity assay,thin-layer chromatography

Genomic accession number

LT674122

Nucelotide position range

387-30039

Substrate

beta-glucan

Loci

SIP56247.1-SIP56265.1

Species

uncultured bacterium/77133

Degradation or Biosynthesis

degradation

Gene Name

Locus Tag

Protein ID

Gene Position

GenBank Contig Range

EC Number

- - SIP56247.1 387 - 1368 (-) LT674122.1:774-1755 3.2.1.4
- - SIP56248.1 1480 - 2773 (-) LT674122.1:1867-3160 -
- - SIP56249.1 2864 - 4148 (-) LT674122.1:3251-4535 3.1.1.-
- - SIP56250.1 4220 - 5114 (-) LT674122.1:4607-5501 -
- - SIP56251.1 5458 - 7903 (-) LT674122.1:5845-8290 3.2.1.23
- - SIP56252.1 8125 - 10612 (+) LT674122.1:8512-10999 2.4.1.280
- - SIP56253.1 10630 - 11635 (+) LT674122.1:11017-12022 1.1.1.-
- - SIP56254.1 11641 - 13657 (+) LT674122.1:12028-14044 3.2.1.22
- - SIP56255.1 13848 - 14487 (+) LT674122.1:14235-14874 -
- - SIP56256.1 14610 - 15240 (+) LT674122.1:14997-15627 -
- - SIP56257.1 15385 - 15619 (-) LT674122.1:15772-16006 -
- - SIP56258.1 15633 - 15810 (-) LT674122.1:16020-16197 -
- - SIP56259.1 16670 - 16808 (-) LT674122.1:17057-17195 -
- - SIP56260.1 16804 - 19300 (-) LT674122.1:17191-19687 -
- - SIP56261.1 19404 - 21144 (-) LT674122.1:19791-21531 -
- - SIP56262.1 21174 - 24246 (-) LT674122.1:21561-24633 -
- - SIP56263.1 24301 - 26392 (-) LT674122.1:24688-26779 3.2.1.185
- - SIP56264.1 26511 - 27642 (-) LT674122.1:26898-28029 5.1.3.3
- - SIP56265.1 27672 - 30039 (-) LT674122.1:28059-30426 3.2.1.185

Cluster number

1

Gene name

Gene position

Gene type

Found by CGCFinder?

- 388 - 1368 (-) CAZyme: GH5_2 Yes
- 1481 - 2773 (-) CAZyme: GH5_7 Yes
- 2865 - 4148 (-) CAZyme: CE7 Yes
- 4221 - 5114 (-) TF: DBD-Pfam|HTH_AraC,DBD-Pfam|HTH_AraC,DBD-SUPERFAMILY|0036286,DBD-SUPERFAMILY|0035607 Yes
- 5459 - 7903 (-) CAZyme: GH2 Yes
- 8126 - 10612 (+) CAZyme: GH94 Yes
- 10631 - 11635 (+) TC: gnl|TC-DB|P63144|8.A.5.1.3 Yes
- 11642 - 13657 (+) CAZyme: GH97 Yes
- 13849 - 14487 (+) other Yes
- 14611 - 15240 (+) other Yes
- 15386 - 15619 (-) other Yes
- 15634 - 15810 (-) STP: STP|NTP_transf_2 Yes
- 16671 - 16808 (-) other Yes
- 16805 - 19300 (-) other Yes
- 19405 - 21144 (-) TC: gnl|TC-DB|Q8A1G2|8.A.46.1.1 Yes
- 21175 - 24246 (-) TC: gnl|TC-DB|Q45780|1.B.14.6.1 Yes
- 24302 - 26392 (-) CAZyme: GH127 Yes
- 26512 - 27642 (-) other Yes
- 27673 - 30039 (-) CAZyme: GH127 Yes

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PUL ID

PUL0332

PubMed

28091525, Sci Rep. 2017 Jan 16;7:40248. doi: 10.1038/srep40248.

Title

A fibrolytic potential in the human ileum mucosal microbiota revealed by functional metagenomic.

Author

Patrascu O, Beguet-Crespel F, Marinelli L, Le Chatelier E, Abraham AL, Leclerc M, Klopp C, Terrapon N, Henrissat B, Blottiere HM, Dore J, Bera-Maillet C

Abstract

The digestion of dietary fibers is a major function of the human intestinal microbiota. So far this function has been attributed to the microorganisms inhabiting the colon, and many studies have focused on this distal part of the gastrointestinal tract using easily accessible fecal material. However, microbial fermentations, supported by the presence of short-chain fatty acids, are suspected to occur in the upper small intestine, particularly in the ileum. Using a fosmid library from the human ileal mucosa, we screened 20,000 clones for their activities against carboxymethylcellulose and xylans chosen as models of the major plant cell wall (PCW) polysaccharides from dietary fibres. Eleven positive clones revealed a broad range of CAZyme encoding genes from Bacteroides and Clostridiales species, as well as Polysaccharide Utilization Loci (PULs). The functional glycoside hydrolase genes were identified, and oligosaccharide break-down products examined from different polysaccharides including mixed-linkage beta-glucans. CAZymes and PULs were also examined for their prevalence in human gut microbiome. Several clusters of genes of low prevalence in fecal microbiome suggested they belong to unidentified strains rather specifically established upstream the colon, in the ileum. Thus, the ileal mucosa-associated microbiota encompasses the enzymatic potential for PCW polysaccharide degradation in the small intestine.