This finding is corroborated by the fact that the genome of A. niger contains a locus (An16g04160; galE) with obvious similarity to other fungal galactokinases (Flipphi et al., 2009). Northern analysis performed with the respective gene as a probe showed that the gene was transcribed on all carbon sources investigated. Expression on d-galactose was higher than on d-glucose or glycerol, however, lower than on l-arabinose or d-xylose (Fig. 3a). The finding that galactokinase was active prompted us to study whether a full Leloir pathway is operating

in A. niger. In silico data revealed that the A. niger genome contains orthologs for each gene of this pathway (Flipphi et al., 2009). Expression studies showed that they are all expressed selleck screening library in a fashion similar to galactokinase, for example, transcripts Y-27632 mw were formed on all carbon sources studied, but their transcript levels were higher on pentoses (l-arabinose, d-xylose) and on d-galactose (Fig. 3a). The reason for the higher expression of Leloir pathway genes on l-arabinose and d-xylose than on d-galactose remains unclear at this point and will require further study. Most

notably, however, results obtained from conidiospores formed on glycerol or d-glucose showed that while all transcripts of the Leloir pathway genes were also present in conidiospores, galE (encoding a galactokinase) and galD (encoding an UTP-galactose-1-phosphate uridylyltransferase) were very poorly expressed (Fig. 3b), indicating that the potential to convert d-galactose into an intermediate of the EMP pathway may be dependent on the growth stage of the fungus. Aspergillus niger

has a prominent position amongst microorganisms employed in industrial biotechnology, thus it is not surprising that numerous studies have been devoted to its biology (Andersen et al., 2011). However, its metabolic relationship with d-galactose remained obscure, although this hexose is a major component of hemicelluloses and pectin, whose enzymatic hydrolysis is subject to considerable industrial interest. In this article, we have provided evidence that the d-galactose-negative Digestive enzyme phenotype of A. niger is growth stage dependent, being complete in the conidiospores but only partial in mycelia germinated on any other carbon source. This result required that a d-galactose transporter system needs to be present in A. niger. In the yeast Kluyveromyces lactis, d-galactose and lactose transport are mediated by the same protein (Baruffini et al., 2006), while in the related species A. nidulans, transport of these two sugars are independent (E. Fekete, M. Flipphi and L. Karaffa, unpublished data). Galactose permeases from A.