Effect of Culture Conditions on Ergosterol as an Indicator of Biomass in the Aquatic Hyphomycetes

ABSTRACT Ergosterol is a membrane component specific to fungi that can be used to estimate fungal biomass using appropriate factors of conversion. Our objectives were to determine the limits of use of ergosterol content as a measure of biomass for aquatic hyphomycetes, and to evaluate a previously established ergosterol-to-biomass conversion factor. We varied inoculum quality, growth medium, and degree of shaking of four aquatic hyphomycete species. In cultures inoculated with homogenized mycelium, we found a significant effect of shaking condition and culture age on ergosterol content. In liquid cultures with defined medium, ergosterol content reached 10 to 11 μg/mg of mycelium (dry mass) and varied by factors of 2.2 during exponential growth and 1.3 during stationary phase. The increase in ergosterol content during exponential phase could be attributed, at least in part, to rapid depletion of glucose. Oxygen availability to internal hyphae within the mycelial mass is also responsible for the differences found between culture conditions. Ergosterol concentration ranged from 0.8 to 1.6 μg/mg in static cultures inoculated with agar plugs. Ergosterol content varied by a factor of 4 in two media of different richnesses. For different combinations of these parameters, strong (r2 = 0.83 to 0.98) and highly significant (P ≪ 0.001) linear relationships between ergosterol and mycelial dry mass (up to 110 mg) were observed. Overall, the ergosterol content varied by a factor of 14 (0.8 to 11 mg/g). These results suggest that care must be taken when the ergosterol content is used to compare data generated in different field environments.

[1]  Karl Esser,et al.  The Mycota : a comprehensive treatise on fungi as experimental systems for basic and applied research , 1994 .

[2]  M. Gardes,et al.  Infraspecific genetic diversity and substrate preference in the aquatic hyphomycete Tetrachaetum elegans , 1999 .

[3]  S. Y. Newell Estimating fungal biomass and productivity in decomposing litter , 1992 .

[4]  J. Weete Lipid Biochemistry of Fungi and Other Organisms , 1980, Springer US.

[5]  H. Bossche Importance and Role of Sterols in Fungal Membranes , 1990 .

[6]  M. Gessner,et al.  Ergosterol-to-Biomass Conversion Factors for Aquatic Hyphomycetes , 1993, Applied and environmental microbiology.

[7]  S. Y. Newell,et al.  Biochemical and Molecular Methods for the Study of Marine Fungi , 1998 .

[8]  Alf Ekblad,et al.  Chitin and ergosterol combined to measure total and living fungal biomass in ectomycorrhizas , 1998 .

[9]  M. Gessner,et al.  Comparison of ATP and Ergosterol as Indicators of Fungal Biomass Associated with Decomposing Leaves in Streams , 1993, Applied and environmental microbiology.

[10]  S. Safe The effect of environment on the free and hydrosoluble sterols of Mucor rouxii. , 1973, Biochimica et biophysica acta.

[11]  K. Cooksey Molecular Approaches to the Study of the Ocean , 1998, Springer Netherlands.

[12]  R. Cooke,et al.  A critical assessment of the validity of ergosterol as an indicator of fungal biomass , 1995 .

[13]  W. D. Grant,et al.  Use of ergosterol, diaminopimelic acid and glucosamine contents of soils to monitor changes in microbial populations , 1987 .

[14]  P. Kuhn Biochemistry of Cell Walls and Membranes in Fungi , 1990, Springer Berlin Heidelberg.

[15]  D. Wicklow,et al.  The fungal community : its organization and role in the ecosystem , 1995 .

[16]  M. Gessner,et al.  Growth and production of aquatic hyphomycetes in decomposing leaf litter , 1997 .

[17]  W. McGill,et al.  Ontological and environmental influences on ergosterol content and activities of polyamine biosynthesis enzymes in Hebeloma crustuliniforme mycelia. , 1990 .

[18]  K. Suberkropp The influence of nutrients on fungal growth, productivity, and sporulation during leaf breakdown in streams , 1995 .