Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 86
Page 85
QUANTITATIVE GROWTH - RESPONSE ASSAYS 85 30 30 TABLE 1 . Key to
media and cultural requirements for representative groups and species of
bacteria Optimal Group , genus , and speciesa growth Number - letter key to
mediao ...
QUANTITATIVE GROWTH - RESPONSE ASSAYS 85 30 30 TABLE 1 . Key to
media and cultural requirements for representative groups and species of
bacteria Optimal Group , genus , and speciesa growth Number - letter key to
mediao ...
Page 87
Gram - Negative Chemolithotropic Bacteria : Nitrobacter winogradskyi ' 25 - 30
41C ( Table 11 ) Nitrococcus mobilis 25 - 30 42C ( Table 11 ) Nitrosococcus
nitrosus ' , e 20 - 25 41C ( Table 11 ) Nitrosolobus multiformis , m 25 - 30 43C (
Table ...
Gram - Negative Chemolithotropic Bacteria : Nitrobacter winogradskyi ' 25 - 30
41C ( Table 11 ) Nitrococcus mobilis 25 - 30 42C ( Table 11 ) Nitrosococcus
nitrosus ' , e 20 - 25 41C ( Table 11 ) Nitrosolobus multiformis , m 25 - 30 43C (
Table ...
Page 88
37 196 66 87 132 60 125 34 47 83 63 TABLE 1 - continued Optimal Group ,
genus , and species “ growth Number - letter key to media ' References temp ( °C
) Bacterionema matruchotii * x , fff 37 63A , 56C ( Tables 6 , 12 ) 102
Bifidobacterium ...
37 196 66 87 132 60 125 34 47 83 63 TABLE 1 - continued Optimal Group ,
genus , and species “ growth Number - letter key to media ' References temp ( °C
) Bacterionema matruchotii * x , fff 37 63A , 56C ( Tables 6 , 12 ) 102
Bifidobacterium ...
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
55 | 32 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
4 other sections not shown
Other editions - View all
Common terms and phrases
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 enrichment enzyme examine 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 microscopy mixture mutants 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