Record Display for the EPA National Library Catalog


Main Title Nonselective Biochemical Methods for the Determination of Fungal Mass and Community Structure in Estuarine Detrital Microflora.
Author White, D. C. ; Bobbie, R. J. ; Nickels, J. S. ; Fazio, S. D. ; Davis, W. M. ;
CORP Author Florida State Univ., Tallahassee. Dept. of Biological Science.;Environmental Research Lab., Gulf Breeze, FL.;National Oceanic and Atmospheric Administration, Rockville, MD. Office of Sea Grant.;National Science Foundation, Washington, DC.
Year Published 1979
Report Number EPA-R-080614-30-10 ;NOAA-04-7-158-4406; EPA-600/J-80-084;
Stock Number PB81-126591
Additional Subjects Bacteria ; Fungi ; Lipids ; Cells(Biology) ; Morphology ; Plants(Botany) ; Biochemistry ; Estuaries ; Escherichia coli ; Cultures(Biology) ; Reprints ; Spartina alterniflora ; Neurospora crassa
Library Call Number Additional Info Location Last
NTIS  PB81-126591 Some EPA libraries have a fiche copy filed under the call number shown. 07/26/2022
Collation 15p
Assay of lipid and cell wall components can readily provide differentiation in reciprocal mixtures of bacteria and fungal monocultures. To test natural microbial assemblies, small plastic sheets were exposed in a subtropical estuary. The sheets were then transferred to a laboratory where estuarine environments that inhibit prokaryotic growth and stimulated fungal growth were compared with and environment where eukaryotic growth was inhibited and prokaryotic growth was stimulated. The morphology determined by scanning electron microscopy showed typical mycelial networks where eukaryotic growth was stimulated and none were inhibited. The stimulation of eukaryotic growth produced a greater biomass measured in terms of lipid phosphate, respiratory activity or extractable adenosine nucleotides, but with a slower synthesis of phospholipids and DNA and a smaller concentration of muramaic acid (a unique prokaryote wall component). The stimulation of eukaryotic growth increased the rate of sulpholipid synthesis relative to DNA or phospholipid synthesis.