Manual of Methods for General Bacteriology |
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Page 175
GROWTH - YIELD CALCULATIONS 175 grams of dry cells formed cell
concentration in a chemostat will automatYx / ATP = . moles of ATP formed ically
adjust to match the rate of limiting nutrient addition , the ratios of medium
components are ...
GROWTH - YIELD CALCULATIONS 175 grams of dry cells formed cell
concentration in a chemostat will automatYx / ATP = . moles of ATP formed ically
adjust to match the rate of limiting nutrient addition , the ratios of medium
components are ...
Page 176
Wash the collected cells with Although yields are conventionally expressed buffer
or distilled water to remove excess me - in terms of mass of cells formed per mass
or dium . Dry the membrane filter and cells to moles of substrate used , this ...
Wash the collected cells with Although yields are conventionally expressed buffer
or distilled water to remove excess me - in terms of mass of cells formed per mass
or dium . Dry the membrane filter and cells to moles of substrate used , this ...
Page 376
Both enzymes are assayed by a determination of a - ketobutyrate formed as its 2 ,
4lactate + NAD dinitrophenylhydrazone . The biodegradative en The isomerase
can also be assayed by a simple zyme can be assayed in cell extracts or in tolu ...
Both enzymes are assayed by a determination of a - ketobutyrate formed as its 2 ,
4lactate + NAD dinitrophenylhydrazone . The biodegradative en The isomerase
can also be assayed by a simple zyme can be assayed in cell extracts or in tolu ...
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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