Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 95
Page 180
Once balanced growth has been arise both for growth limited by the rate of
achieved , if the conditions remain the same , the nutrient addition under
chemostat conditions culture will remain in balanced growth indefi and for
unlimited growth ...
Once balanced growth has been arise both for growth limited by the rate of
achieved , if the conditions remain the same , the nutrient addition under
chemostat conditions culture will remain in balanced growth indefi and for
unlimited growth ...
Page 181
This observation can largely erable macromolecular growth has ensued does be
explained by the shorter time available for cell division take place . During this
phase , the the drug to penetrate relative to the growth rate average size of cells ...
This observation can largely erable macromolecular growth has ensued does be
explained by the shorter time available for cell division take place . During this
phase , the the drug to penetrate relative to the growth rate average size of cells ...
Page 206
ST , siln 2 growth to remeasure the specific growth rate . 22 This procedure
isolates the treatment as the sole variable between the two halves of the growth
In our laboratory , we have programmed a run . Run control experiments in which
the ...
ST , siln 2 growth to remeasure the specific growth rate . 22 This procedure
isolates the treatment as the sole variable between the two halves of the growth
In our laboratory , we have programmed a run . Run control experiments in which
the ...
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
MORPHOLOGY | 5 |
NOW | 17 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Copyright | |
7 other sections not shown
Other editions - View all
Common terms and phrases
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 examine example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plate positive prepared present Press procedure protein reaction reagent references remove 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