Manual of Methods for General Bacteriology |
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Page 79
... the obligately parasitic bacteria energy source by one or another heterotrophic
grow only in the presence of living animal , plant , bacterium . or other bacterial
cells which provide yet uniHeterotrophic bacteria utilize organic com - dentified ...
... the obligately parasitic bacteria energy source by one or another heterotrophic
grow only in the presence of living animal , plant , bacterium . or other bacterial
cells which provide yet uniHeterotrophic bacteria utilize organic com - dentified ...
Page 116
3 mm wide , oval in of mud containing decaying plant materials , as cross section
. Seal the ends of the capillary in a from small ponds , lakes , or streams .
Incubate flame . Break the capillary near one end with the flasks at ca . 25°C for
10 days ...
3 mm wide , oval in of mud containing decaying plant materials , as cross section
. Seal the ends of the capillary in a from small ponds , lakes , or streams .
Incubate flame . Break the capillary near one end with the flasks at ca . 25°C for
10 days ...
Page 520
... 415 Pilimelia terevasa , media and cultural requirements , 88 Pipetting , safety
precautions , 489 - 490 Planobispora longispora , media and cultural
requirements , 88 Plant symbiosis by rhizobia , 127 Plasmid - curing agents , 228
Plasmid ...
... 415 Pilimelia terevasa , media and cultural requirements , 88 Pipetting , safety
precautions , 489 - 490 Planobispora longispora , media and cultural
requirements , 88 Plant symbiosis by rhizobia , 127 Plasmid - curing agents , 228
Plasmid ...
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
Copyright | |
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absorbance acid activity added addition Adjust agar allow amino acids amount anaerobic applications appropriate assay autoclaving bacteria Bacteriol base broth buffer cells centrifuge colonies column components compounds concentration containing counting cover culture described determine dilution Dissolve distilled water effective electron enzyme example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method mg/liter Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts sample selection separation slide sodium solution specific staining standard sterile substrate surface suspension Table techniques temperature tion transfer tube usually values vitamin volume Wash York