Functional analysis of three putative galactofuranosyltransferases with redundant functions in galactofuranosylation in Aspergillus niger

Galactofuranose (Gal f )-containing glycostructures are important to secure the integrity of the fungal cell wall. Golgi-localized Gal f -transferases (Gfs) have been identified in Aspergillus nidulans and Aspergillus fumigatus . BLASTp searches identified three putative Gal f -transferases in Aspergillus niger . Phylogenetic analysis showed that they group in three distinct groups. Characterization of the three Gal f -transferases in A. niger by constructing single, double, and triple mutants revealed that gfsA is most important for Gal f biosynthesis. The growth phenotypes of the ΔgfsA mutant are less severe than that of the ΔgfsAC mutant, indicating that GfsA and GfsC have redundant functions. Deletion of gfsB did not result in any growth defect and combining ΔgfsB with other deletion mutants did not exacerbate the growth phenotype. RT-qPCR experiments showed that induction of the agsA gene was higher in the ΔgfsAC and ΔgfsABC compared to the single mutants, indicating a severe cell wall stress response after multiple gfs gene deletions.