# Metabolic pathway analysis reveals hierarchical pentose sugar utilization and metabolic flexibility of Bifidobacterium longum

**Authors:** Lisa Friess, Fionnuala M. McAuliffe, Paul D. Cotter, Anthony L. Shiver, Kerwyn Casey Huang, Anne de Jong, Douwe van Sinderen

PMC · DOI: 10.1080/19490976.2026.2647591 · Gut Microbes · 2026-03-23

## TL;DR

This study explores how Bifidobacterium longum metabolizes plant-derived pentose sugars, revealing shared transport systems and distinct metabolic pathways for arabinose, xylose, and ribose.

## Contribution

The study identifies specific genes and metabolic pathways involved in pentose sugar utilization in B. longum, revealing hierarchical co-metabolism and metabolic flexibility.

## Key findings

- B. longum uses a shared ABC transporter (penABCD) for arabinose, xylose, and ribose uptake.
- Arabinose and xylose are converted to xylulose-5-phosphate via araBDA, xylA, and xylB, while ribose is converted to ribose-5-phosphate via rbsK.
- Xylose is preferentially metabolized over ribose, and arabinose and xylose are co-metabolized.

## Abstract

Plant-derived pentose sugars represent a major nutrient source in the gut, yet their metabolism remains incompletely defined. Strains of the human gut commensal Bifidobacterium longum subsp. longum utilise arabinose- and xylose-containing glycans, which are found in the pectin and hemicellulose layers of plant cell walls. To gain insight into the metabolism of these two pentoses as well as ribose, a naturally occurring sugar and a component of RNA and ATP, we identified and analysed the genes responsible for their uptake and subsequent catabolism. Based on transcriptomic data and mutant phenotype analyses, we show that these three pentoses share a common, ABC-type uptake system encoded by penABCD. Furthermore, we identify a gene cluster, araBDA, and two genes, xylA and xylB, that are required for conversion of arabinose and xylose, respectively, into xylulose-5-phosphate, and rbsK, which converts ribose into ribose-5-phosphate. These intermediate metabolic products enter the bifid shunt, an energy-generating fermentative pathway typical of bifidobacteria. We also show that arabinose and xylose are co-metabolized, while xylose is preferentially utilised before ribose. This study provides molecular insights using a multi-omics approach, including comparative genomics and transcriptomics combined with mutational analysis, into how B. longum subsp. longum metabolizes pentose-containing plant glycans, common yet indigestible components of the adult human diet.

## Linked entities

- **Genes:** xylA (D-xylose isomerase) [NCBI Gene 915615], XYLB (xylulokinase) [NCBI Gene 9942], RBKS (ribokinase) [NCBI Gene 64080]
- **Chemicals:** arabinose (PubChem CID 229), xylose (PubChem CID 135191), ribose (PubChem CID 10975657), xylulose-5-phosphate (PubChem CID 850), ribose-5-phosphate (PubChem CID 77982)
- **Species:** Bifidobacterium longum subsp. longum (taxon 1679)

## Full-text entities

- **Genes:** ABC transporter [NCBI Gene 13877144], XYLB (xylulokinase) [NCBI Gene 9942], ACSL1 (acyl-CoA synthetase long chain family member 1) [NCBI Gene 2180] {aka ACS1, FACL1, FACL2, LACS, LACS1, LACS2}, ATP-binding protein [NCBI Gene 9537996]
- **Chemicals:** nucleosides (MESH:D009705), ADP (MESH:D000244), CaCl2 (MESH:D002122), DTT (MESH:D004229), trichloroacetic acid (MESH:D014238), Hemicellulose (MESH:C007916), Acetyl-phosphate (MESH:C011632), pectin (MESH:D010368), sugar (MESH:D000073893), iron chloride (MESH:C024555), Coomassie Brilliant Blue (MESH:C004692), galactose (MESH:D005690), lacto-N-tetraose (MESH:C013084), NaCl (MESH:D012965), AraU (MESH:D001086), pentose-phosphate (MESH:D010428), Glucose (MESH:D005947), glycan (MESH:D011134), hydroxamic acid (MESH:D006877), ribulose (MESH:C100182), acetate (MESH:D000085), Tris-Base (MESH:D014325), iron (MESH:D007501), MgCl2 (MESH:D015636), SDS (MESH:D012967), Tc (MESH:D013667), Km (MESH:D007612), TPP (MESH:D013835), arabinan (MESH:C030080), oligosaccharide (MESH:D009844), Arabinose (MESH:D001089), arabinoxylan (MESH:C085118), HCl (MESH:D006851), xylan (MESH:D014990), hexose (MESH:D006601), ATP (MESH:D000255), AraA (MESH:D014740), monosaccharide (MESH:D009005), Carbohydrate (MESH:D002241), cytidine (MESH:D003562), tetracycline (MESH:D013752), KOH (MESH:C029943), imidazole (MESH:C029899), ribonucleosides (MESH:D012263), lactate (MESH:D019344), inosine (MESH:D007288), O (MESH:D010100), D-ribose (MESH:D012266), fructose (MESH:D005632), D-xylulose-5-phosphate (MESH:C031625), cysteine-HCl (MESH:D003545), D-ribose 5-phosphate (MESH:C031626), pentose (MESH:D010429), purine (MESH:C030985), uridine (MESH:D014529), AraBDA (-), Ni (MESH:D009532), D-xylose (MESH:D014994), lactose (MESH:D007785), xylulose (MESH:D014996)
- **Species:** Bifidobacterium longum (species) [taxon 216816], Escherichia coli BL21(DE3) (strain) [taxon 469008], Streptococcus thermophilus (species) [taxon 1308], Bifidobacterium longum subsp. longum (subspecies) [taxon 1679], Homo sapiens (human, species) [taxon 9606], Bacteriophage sp. (species) [taxon 38018], Escherichia coli (E. coli, species) [taxon 562], gut metagenome (species) [taxon 749906], Corynebacterium glutamicum (species) [taxon 1718], Bifidobacterium breve (species) [taxon 1685], Bifidobacterium longum NCC2705 (strain) [taxon 206672], Bifidobacterium breve UCC2003 (strain) [taxon 326426]
- **Mutations:** D3024R
- **Cell lines:** E. coli 10-beta — Mus musculus (Mouse), Hybridoma (CVCL_C5CP), EC101 — Mus musculus (Mouse), Hybridoma (CVCL_J815), BL21 (DE3) — Mus musculus (Mouse), Hybridoma (CVCL_B7HM), JCM1217 — Homo sapiens (Human), Transformed cell line (CVCL_1V56), NCIMB 8809 — Homo sapiens (Human), Transformed cell line (CVCL_4H50), DH5alpha — Drosophila hydei (Fruit fly), Spontaneously immortalized cell line (CVCL_Z531)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13011590/full.md

## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC13011590/full.md

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Source: https://tomesphere.com/paper/PMC13011590