Manual of Methods for General Bacteriology |
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Page 55
The suspension is tegrator . gently agitated during dilution , and conversion to
spheroplasts is monitored by phase micros5 . 1 . 5 . Muramidase Digestion copy .
Egg white lysozyme may be used to prepare Protoplast and spheroplast
formation ...
The suspension is tegrator . gently agitated during dilution , and conversion to
spheroplasts is monitored by phase micros5 . 1 . 5 . Muramidase Digestion copy .
Egg white lysozyme may be used to prepare Protoplast and spheroplast
formation ...
Page 175
GROWTH - YIELD CALCULATIONS 175 grams of dry cells formed Yx / ATP =
moles of ATP formed grams of dry cells formed Yx / 0 , = moles of oxygen
consumed Under many conditions , the yield with respect to ATP synthesis or
oxygen ...
GROWTH - YIELD CALCULATIONS 175 grams of dry cells formed Yx / ATP =
moles of ATP formed grams of dry cells formed Yx / 0 , = moles of oxygen
consumed Under many conditions , the yield with respect to ATP synthesis or
oxygen ...
Page 176
If the data form a straight - line relationship , the intercept will be the value of 1 /
Yg and the slope of the line will be the value of m . Although yields are
conventionally expressed in terms of mass of cells formed per mass or moles of
substrate ...
If the data form a straight - line relationship , the intercept will be the value of 1 /
Yg and the slope of the line will be the value of m . Although yields are
conventionally expressed in terms of mass of cells formed per mass or moles of
substrate ...
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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