Manual of Methods for General Bacteriology |
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Page 90
Saprophytic strains grow in simple media ; others require more complex media or
supplements ( e . g . , mycobactin ) , and still others have not been cultivated
outside living cells . Growth is slow on all media . ktk Boil all liquid media for 10
min ...
Saprophytic strains grow in simple media ; others require more complex media or
supplements ( e . g . , mycobactin ) , and still others have not been cultivated
outside living cells . Growth is slow on all media . ktk Boil all liquid media for 10
min ...
Page 148
usually helpful to grow the inoculum for the agar when supplied with a source of
fixed nitrogen in a broth containing a minimum concentration ( such as
ammonium sulfate ) , but can only grow of the particular growth factor to be tested
; this as ...
usually helpful to grow the inoculum for the agar when supplied with a source of
fixed nitrogen in a broth containing a minimum concentration ( such as
ammonium sulfate ) , but can only grow of the particular growth factor to be tested
; this as ...
Page 228
It should be noted that the most effective 1 . Grow a culture of the bacterium to be
concentration of a curing agent may vary as mutagenized to the late logarithmic
phase of growth in L broth ( 13 . 9 . 1 ) or nutrient broth bacterium being treated .
It should be noted that the most effective 1 . Grow a culture of the bacterium to be
concentration of a curing agent may vary as mutagenized to the late logarithmic
phase of growth in L broth ( 13 . 9 . 1 ) or nutrient broth bacterium being treated .
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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