Manual of Methods for General Bacteriology |
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Page 89
C . halobacteroides requires the addition of 2 % NaCl to all growth media . ... N N
' - bis ( 2 - ethanesulfonic acid ) ( PIPES ) , or N - tris ( hydroxymethyl ) methyl - 2 -
aminoethanesulfonic acid ( TES ) or by intermittent additions of NaHCO3 .
C . halobacteroides requires the addition of 2 % NaCl to all growth media . ... N N
' - bis ( 2 - ethanesulfonic acid ) ( PIPES ) , or N - tris ( hydroxymethyl ) methyl - 2 -
aminoethanesulfonic acid ( TES ) or by intermittent additions of NaHCO3 .
Page 90
66 , 1970 . bbb For good growth , this species requires the addition of the
following components to 1 liter of medium 58A : 300 mg of ascorbic acid and 5 ml
of Tween 80 . coc At least one L . delbrueckii strain ( namely , L . delbrueckii 730 )
...
66 , 1970 . bbb For good growth , this species requires the addition of the
following components to 1 liter of medium 58A : 300 mg of ascorbic acid and 5 ml
of Tween 80 . coc At least one L . delbrueckii strain ( namely , L . delbrueckii 730 )
...
Page 166
rameter and trigger the addition of medium to the fermentor so that the indicator
parameter is maintained at a steady value . An example of environmental
parameter control in a fermen - tation system is the maintenance of pH at a
constant ...
rameter and trigger the addition of medium to the fermentor so that the indicator
parameter is maintained at a steady value . An example of environmental
parameter control in a fermen - tation system is the maintenance of pH at a
constant ...
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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