Applied and Environmental Microbiology, Volume 54, Pages 851-1642American Society for Microbiology, 1988 - Microbial ecology |
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Page 1005
... give 50 % displacement from zero by the mass of M. mazei required to give 50 % displacement from zero . Cross - reac- tions in the two - site assays were calculated by dividing the absorbance value for the 50 - μg ml1 standard ( minus ...
... give 50 % displacement from zero by the mass of M. mazei required to give 50 % displacement from zero . Cross - reac- tions in the two - site assays were calculated by dividing the absorbance value for the 50 - μg ml1 standard ( minus ...
Page 1319
... give a final concentration of 55.6 mM , and the resulting drop in pH was determined with a glass electrode . The final pH was considered to be the minimum for gly- colysis , because glucose was in excess and neutralization of the ...
... give a final concentration of 55.6 mM , and the resulting drop in pH was determined with a glass electrode . The final pH was considered to be the minimum for gly- colysis , because glucose was in excess and neutralization of the ...
Page 1474
ml ) was diluted with particle - free medium to give a final volume of 2 ml . A particle - free acridine orange solution ( 0.2 ml ) was added to give a final acridine orange concentration of 0.01 % . After 2 min , the sample was ...
ml ) was diluted with particle - free medium to give a final volume of 2 ml . A particle - free acridine orange solution ( 0.2 ml ) was added to give a final acridine orange concentration of 0.01 % . After 2 min , the sample was ...
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acenaphthene acetate activity aerobic agar alghumin amino acids anaerobic analysis antibiotic Appl arginine aromatic assay ATCC bacteria Bacteriol bacteriophage bacterium Bacteroides Biol biomass broth buffer carbon carotovora cell wall cellulose chemical chromatography cloned coli colonies compounds concentration containing cremoris culture degradation denitrification detected determined digestion dilution effect Environ enzyme Escherichia coli ethanol fermentation ferulic acid filter fragment gene genetic glucose growth H₂ hybridization incubated infection inhibition inoculated inoculum isolated laboratory lactis lignin lividans medium metabolism metabolites methanogenic method methylcellulose microbial Microbiol microorganisms molecular mutant naphthalene nitrate obtained organic oxide phage phenanthrene phenol plasmid plates present production protein protoplast Pseudomonas resistance rhizobia Rhizobium rumen ruminal samples sediments Society for Microbiology soil solution species spores sterile strains Streptococcus Streptomyces substrate subtilis Table temperature tetracycline tion toxin transfer transformation xylanase yeast extract µg/ml