Manual of Methods for General Bacteriology |
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Page 114
High - Temperature Incubation for Thermophiles ( 6 ) The growth of organisms other than thermophiles is inhibited by a high incubation temperature , so incubate enrichments for thermophiles at an appropriately high temperature .
High - Temperature Incubation for Thermophiles ( 6 ) The growth of organisms other than thermophiles is inhibited by a high incubation temperature , so incubate enrichments for thermophiles at an appropriately high temperature .
Page 122
Incubate at 25 ° C for 1 to 2 days . The Formalin will kill contaminating bacteria but not Gallionella . Transfer 1 - ml portions of the Formalintreated culture to fresh bottles of medium without Formalin . Incubate cultures at 25 ° C ...
Incubate at 25 ° C for 1 to 2 days . The Formalin will kill contaminating bacteria but not Gallionella . Transfer 1 - ml portions of the Formalintreated culture to fresh bottles of medium without Formalin . Incubate cultures at 25 ° C ...
Page 124
Incubate at 30 ° C with agitation . Observe the culture microscopically at periodic intervals for the development of large , ovoid cells , 2 um or more in diameter . Prepare a secondary enrichment culture ; then purify by obtaining ...
Incubate at 30 ° C with agitation . Observe the culture microscopically at periodic intervals for the development of large , ovoid cells , 2 um or more in diameter . Prepare a secondary enrichment culture ; then purify by obtaining ...
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Contents
1 | 22 |
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 amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York