beta-1,6-Glucan is an essential fungal-specific component of the Saccharomy
ces cerevisiae cell wall that interconnects all other wall components into
a lattice. Considerable biochemical and genetic effort has been directed at
the identification and characterization of the steps involved in its biosy
nthesis. Structural studies show that the polymer plays a central role in w
all structure, attaching mannoproteins via their glycosylphosphatidylinosit
ol (GPI) glycan remnant to beta-1,9-glucan and chitin. Genetic approaches h
ave identified genes that upon disruption result in beta-1,6-glucan defects
of varying severity, often with reduced growth or lethality. These gene pr
oducts have been localized throughout the secretory pathway and at the cell
surface, suggesting a possible biosynthetic route. Current structural and
genetic data have therefore allowed the development of models to predict bi
osynthetic events. Based on knowledge of beta-1,3-glucan and chitin synthes
is, it is likely that the bulk of beta-1,6-glucan polymer synthesis occurs
at the cell surface, but requires key prior intracellular events. However,
the activity of most of the identified gene products remain unknown, making
it unclear to what extent and how directly they contribute to the synthesi
s of this polymer. With the recent availability of new tools, reagents and
methods (including genomics), the field is poised for a convergence of bioc
hemical and genetic methods to identify and characterize the biochemical st
eps in the synthesis of this polymer.