Because CGCFinder predicted no CGC for this PUL, the gene cluster depicted below contains dbCAN2 and CGC signature predictions for all genes in the PUL, instead of a predicted CGC.




31275257, Front Microbiol. 2019 Jun 7;10:1286. doi: 10.3389/fmicb.2019.01286. eCollection 2019.

Characterization method

sequence homology analysis

Genomic accession number


Nucelotide position range







Bacteroides vulgatus/821

Degradation or Biosynthesis


Gene Name

Locus Tag

Protein ID

Gene Position

GenBank Contig Range

EC Number

- BVU_4133 ABR41735.1 3 - 1236 (-) CP000139.1:5083183-5084416 -
- BVU_4134 ABR41736.1 1342 - 3847 (-) CP000139.1:5084522-5087027 -
- BVU_4135 ABR41737.1 3849 - 6102 (-) CP000139.1:5087029-5089282 -
- BVU_4136 ABR41738.1 6128 - 8183 (-) CP000139.1:5089308-5091363 -
- BVU_4137 ABR41739.1 8179 - 9307 (-) CP000139.1:5091359-5092487 -
- BVU_4138 ABR41740.1 9493 - 11818 (-) CP000139.1:5092673-5094998 -
- BVU_4139 ABR41741.1 11834 - 14402 (-) CP000139.1:5095014-5097582 -
- BVU_4140 ABR41742.1 14428 - 15265 (-) CP000139.1:5097608-5098445 -

Cluster number


Gene name

Gene position

Gene type

Found by CGCFinder?

- 4 - 1236 (-) CAZyme: CE9 No
- 1343 - 3847 (-) CAZyme: GH2 No
- 3850 - 6102 (-) CAZyme: GH92 No
- 6129 - 8183 (-) CAZyme: GH20 No
- 8180 - 9307 (-) CDS No
- 9494 - 11818 (-) CAZyme: GH20 No
- 11835 - 14402 (-) CAZyme: GH2 No
- 14429 - 15265 (-) CDS No




31275257, Front Microbiol. 2019 Jun 7;10:1286. doi: 10.3389/fmicb.2019.01286. eCollection 2019.


Investigating Host Microbiota Relationships Through Functional Metagenomics.


Laville E, Perrier J, Bejar N, Maresca M, Esque J, Tauzin AS, Bouhajja E, Leclerc M, Drula E, Henrissat B, Berdah S, Di Pasquale E, Robe P, Potocki-Veronese G


The human Intestinal mucus is formed by glycoproteins, the O- and N-linked glycans which constitute a crucial source of carbon for commensal gut bacteria, especially when deprived of dietary glycans of plant origin. In recent years, a dozen carbohydrate-active enzymes from cultivated mucin degraders have been characterized. But yet, considering the fact that uncultured species predominate in the human gut microbiota, these biochemical data are far from exhaustive. In this study, we used functional metagenomics to identify new metabolic pathways in uncultured bacteria involved in harvesting mucin glycans. First, we performed a high-throughput screening of a fosmid metagenomic library constructed from the ileum mucosa microbiota using chromogenic substrates. The screening resulted in the isolation of 124 clones producing activities crucial in the degradation of human O- and N-glycans, namely sialidases, beta-D-N-acetyl-glucosaminidase, beta-D-N-acetyl-galactosaminidase, and/or beta-D-mannosidase. Thirteen of these clones were selected based on their diversified functional profiles and were further analyzed on a secondary screening. This step consisted of lectin binding assays to demonstrate the ability of the clones to degrade human intestinal mucus. In total, the structural modification of several mucin motifs, sialylated mucin ones in particular, was evidenced for nine clones. Sequencing their metagenomic loci highlighted complex catabolic pathways involving the complementary functions of glycan sensing, transport, hydrolysis, deacetylation, and deamination, which were sometimes associated with amino acid metabolism machinery. These loci are assigned to several Bacteroides and Feacalibacterium species highly prevalent and abundant in the gut microbiome and explain the metabolic flexibility of gut bacteria feeding both on dietary and human glycans.