Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 82
Page 89
C. halobacteroides requires the addition of 2 % NaCl to all growth media . * The vitamin requirement of C. vibrioides is satisfied by riboflavin ( 100 ug / liter ) . ° Microaerophilic . p Carbon dioxide serves as carbon source .
C. halobacteroides requires the addition of 2 % NaCl to all growth media . * The vitamin requirement of C. vibrioides is satisfied by riboflavin ( 100 ug / liter ) . ° Microaerophilic . p Carbon dioxide serves as carbon source .
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 . cc At least one L. delbrueckii strain ( namely , L. delbrueckii ...
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 . cc At least one L. delbrueckii strain ( namely , L. delbrueckii ...
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 fermentation 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 fermentation system is the maintenance of pH at a constant ...
What people are saying - Write a review
We haven't found any reviews in the usual places.
Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
Copyright | |
7 other sections not shown
Other editions - View all
Common terms and phrases
absorbance acid activity added addition Adjust agar allow amino amount anaerobic applications appropriate assay autoclaving bacteria base broth buffer cells centrifuge chemical colonies column components concentration containing counting cover culture cytoplasmic described determine dilution Dissolve distilled water drop effective electron enzyme examination example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method microscopy mixture mutants needed objective obtained organisms oxygen plasmid plate positive possible prepared present Press procedure protein reaction reagent references remove sample selection separation slide sodium solution specific specimen staining standard sterile surface suspension Table techniques temperature tion transfer tube usually volume Wash York