Applied and Environmental Microbiology, Volume 54, Pages 851-1642American Society for Microbiology, 1988 - Microbial ecology |
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Page 967
Amplification and extraction of the plasmid were performed as described by
Maniatis et al . ... recipient yeast strains KK1 - R1 and KK2 - R1 , as described
above , was by standard genetic procedures as described by Mortimer and
Hawthorne ...
Amplification and extraction of the plasmid were performed as described by
Maniatis et al . ... recipient yeast strains KK1 - R1 and KK2 - R1 , as described
above , was by standard genetic procedures as described by Mortimer and
Hawthorne ...
Page 1225
Ecc14 was nonmarked , and only Ecc7a population densities were determined in
singleand mixed - strain infections as described above . Virulence and disease
severity were evaluated as described above . RESULTS corresponding mixed ...
Ecc14 was nonmarked , and only Ecc7a population densities were determined in
singleand mixed - strain infections as described above . Virulence and disease
severity were evaluated as described above . RESULTS corresponding mixed ...
Page 1489
Chromatography of the periplasmic cellodextrinase activity on DEAE - Sepharose
CL - 6B , hydroxylapatite HTP , and Bio - Gel P - 150 was conducted in this order
as described previously ( 10 ) . The sample from the Bio - Gel P - 150 column ...
Chromatography of the periplasmic cellodextrinase activity on DEAE - Sepharose
CL - 6B , hydroxylapatite HTP , and Bio - Gel P - 150 was conducted in this order
as described previously ( 10 ) . The sample from the Bio - Gel P - 150 column ...
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acetate acid activity added addition agar amount anaerobic analysis antibiotic appeared Appl assay bacteria bacteriophage buffer carbon cells cellulose chemical chromatography coli colonies compared compounds concentration containing culture degradation described detected determined digestion dilution effect Environ enzyme ethanol experiments extract fermentation filter formed fraction fragment gene glucose grown growth hybridization increase incubated indicated infection inhibition initial inoculated isolated laboratory levels material measured medium methanogenic method microbial Microbiol Microbiology mixed mutant natural nitrate observed obtained occurred organic oxide period phase plant plasmid plates prepared present previously production protein range ratio reaction reduction relative removed reported resistance respectively samples sediments selected showed shown similar soil solution species spores standard strains substrate suggest Table temperature tion transfer transformation treatment University values various yeast