Abstract

Fungal-type galactomannan (FTGM) is a polysaccharide composed of α-(1 → 2)-/α-(1 → 6)-mannosyl and β-(1 → 5)-/β-(1 → 6)-galactofuranosyl residues located at the outer cell wall of the human pathogenic fungus Aspergillus fumigatus. FTGM contains a linear α-mannan structure called core-mannan composed of 9 or 10 α-(1 → 2)-mannotetraose units jointed by α-(1 → 6)-linkages. However, the enzymes involved in core-mannan biosynthesis remain unknown. We speculated that two putative α-1,2-mannosyltransferase genes in A. fumigatus, Afu5g02740/AFUB_051270 (here termed core-mannan synthase A [CmsA]) and Afu5g12160/AFUB_059750 (CmsB) are involved in FTGM core-mannan biosynthesis. We constructed recombinant proteins for CmsA and detected robust mannosyltransferase activity using the chemically synthesized substrate p-nitrophenyl α-d-mannopyranoside as an acceptor. Analyses of CmsA enzymatic product revealed that CmsA possesses the capacity to transfer a mannopyranoside to the C-2 position of α-mannose. CmsA could also transfer a mannose residue to α-(1 → 2)-mannobiose and α-(1 → 6)-mannobiose and showed a 31-fold higher specific activity toward α-(1 → 6)-mannobiose than toward α-(1 → 2)-mannobiose. Proton nuclear magnetic resonance (1H-NMR) spectroscopy and gel filtration chromatography of isolated FTGM revealed that core-mannan structures were drastically altered and shortened in disruptant A. fumigatus strains ∆cmsA, ∆cmsB, and ∆cmsA∆cmsB. Disruption of cmsA or cmsB resulted in severely repressed hyphal extension, abnormal branching hyphae, formation of a balloon structure in hyphae, and decreased conidia formation. The normal wild type core-mannan structure and developmental phenotype were restored by the complementation of cmsA and cmsB in the corresponding disruptant strains. These findings indicate that both CmsA, an α-1,2-mannosyltransferase, and CmsB, a putative mannosyltransferase, are involved in FTGM biosynthesis.

Highlights

  • Galactomannan (GM), consisting of d-mannose (Man) and d-galactofuranose (Galf) residues, is a component of the cell wall surface in filamentous fungi[1,2,3,4,5]

  • 1H-NMR spectroscopy and gel filtration chromatography revealed that core-mannan synthase A (CmsA) and core-mannan synthase B (CmsB) are required for the biosynthesis of Fungal-type galactomannan (FTGM) core-mannan (Figs 9, 10 and S6, S7)

  • It is believed that CmsA and CmsB are involved in the transfer of mannose residues at different positions in FTGM

Read more

Summary

Introduction

Galactomannan (GM), consisting of d-mannose (Man) and d-galactofuranose (Galf) residues, is a component of the cell wall surface in filamentous fungi[1,2,3,4,5]. We reported that GfsA is a β-1,5-galactofuranosyltransferase involved in the biosynthesis of β-(1 → 5)-galactofuranosyl chains, major structures in both FTGM and OMGM9,13. The Afu5g10760/AFUB_058360 gene is reported as afmnt[1], a putative α-1,2-mannosyltransferase involved in cell wall stability and virulence in A. fumigatus[21]. We hypothesized that the latter two putative α-1,2-mannosyltransferase genes Afu5g02740/ AFUB_051270 and Afu5g12160/AFUB_059750 are involved in biosynthesis of the FTGM core-mannan and are tentatively termed CmsA and CmsB, respectively. To verify this hypothesis, we constructed recombinant CmsA protein for expression in Escherichia coli and measured the mannosyltransferase activity. We show that disruptant strains ∆cmsA, ∆cmsB, and ∆cmsA∆cmsB (∆cmsAB) show abnormal growth phenotypes and altered sensitivity to antifungal agents

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call