Manual of Methods for General Bacteriology |
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Page 119
Subject a portion of this culture fined liquid media , and one can select for specific
mc to sonic oscillation , and then use the pour - plate sulfur phototrophs by
varying the cultural conmethod to obtain isolated colonies as described ditions
with ...
Subject a portion of this culture fined liquid media , and one can select for specific
mc to sonic oscillation , and then use the pour - plate sulfur phototrophs by
varying the cultural conmethod to obtain isolated colonies as described ditions
with ...
Page 124
Prepare a secondary enrichment cul ture ; then purify by obtaining isolated
colonies on nitrogen - free agar medium ( Azotobacter me - dium ... For isolation
of cytophagas that are not obligate cellulose decomposers , streak onto tryptone
agar .
Prepare a secondary enrichment cul ture ; then purify by obtaining isolated
colonies on nitrogen - free agar medium ( Azotobacter me - dium ... For isolation
of cytophagas that are not obligate cellulose decomposers , streak onto tryptone
agar .
Page 142
Isolation of Gallionella ferruginea by use of formalin . Can . ... Isolation ,
cultivation and maintenance of the myxobacteria , p . ... Vibrio fetus var .
intestinalis isolated from fecal and intestinal contents of clinically normal sheep :
isolation of ...
Isolation of Gallionella ferruginea by use of formalin . Can . ... Isolation ,
cultivation and maintenance of the myxobacteria , p . ... Vibrio fetus var .
intestinalis isolated from fecal and intestinal contents of clinically normal sheep :
isolation of ...
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Contents
55 | 32 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
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 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