Induction of extracellular beta-galactosidase (Bga1) formation by D-galactose in Hypocrea jecorina is mediated by galactitol

Microbiology (Reading). 2007 Feb;153(Pt 2):507-512. doi: 10.1099/mic.0.2006/001602-0.

Abstract

The ability of Hypocrea jecorina (Trichoderma reesei) to grow on lactose strongly depends on the formation of an extracellular glycoside hydrolase (GH) family 35 beta-galactosidase, encoded by the bga1 gene. Previous studies, using batch or transfer cultures of pregrown cells, had shown that bga1 is induced by lactose and d-galactose, but to a lesser extent by galactitol. To test whether the induction level is influenced by the different growth rates attainable on these carbon sources, bga1 expression was compared in carbon-limited chemostat cultivations at defined dilution (=specific growth) rates. The data showed that bga1 expression by lactose, d-galactose and galactitol positively correlated with the dilution rate, and that galactitol and d-galactose induced the highest activities of beta-galactosidase at comparable growth rates. To know more about the actual inducer for beta-galactosidase formation, its expression in H. jecorina strains impaired in the first steps of the two d-galactose-degrading pathways was compared. Induction by d-galactose and galactitol was still found in strains deleted in the galactokinase-encoding gene gal1, which is responsible for the first step of the Leloir pathway of d-galactose catabolism. However, in a strain deleted in the aldose/d-xylose reductase gene xyl1, which performs the reduction of d-galactose to galactitol in a recently identified second pathway, induction by d-galactose, but not by galactitol, was impaired. On the other hand, induction by d-galactose and galactitol was not affected in an l-arabinitol 4-dehydrogenase (lad1)-deleted strain which is impaired in the subsequent step of galactitol degradation. These results indicate that galactitol is the actual inducer of Bga1 formation during growth on d-galactose in H. jecorina.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Culture Media
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Galactitol / metabolism*
  • Galactose / metabolism*
  • Gene Expression Regulation, Enzymologic
  • Gene Expression Regulation, Fungal*
  • Glucose / metabolism
  • Hypocrea / enzymology*
  • Hypocrea / genetics
  • Hypocrea / growth & development
  • Hypocrea / metabolism
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism*

Substances

  • Culture Media
  • Fungal Proteins
  • Galactitol
  • beta-Galactosidase
  • Glucose
  • Galactose