Manual of Methods for General Bacteriology |
From inside the book
Results 1-3 of 70
Page 96
Compositions of undefined media ( A ) 64 through 75 for the bacteria listed in
Table 1 Amt ( in units given in column 1 ) / liter for medium : Component 64A 65A
66A 67A 68A 69A 70A 71A | 72A 73A 74A 75A Glucose® ( g ) 2.0-10 10 10 1.0
10 ...
Compositions of undefined media ( A ) 64 through 75 for the bacteria listed in
Table 1 Amt ( in units given in column 1 ) / liter for medium : Component 64A 65A
66A 67A 68A 69A 70A 71A | 72A 73A 74A 75A Glucose® ( g ) 2.0-10 10 10 1.0
10 ...
Page 294
A popular glucose glucose + H2O + O2 solution to this problem is the Clark
oxygen oxidase electrode ( 13 ) in which the platinum electrode is gluconic acid +
H2O2 covered with a gas - permeable membrane . Whereas the platinum
electrode ...
A popular glucose glucose + H2O + O2 solution to this problem is the Clark
oxygen oxidase electrode ( 13 ) in which the platinum electrode is gluconic acid +
H2O2 covered with a gas - permeable membrane . Whereas the platinum
electrode ...
Page 382
Let the cultures grow with vigorous ing : shaking to approximately 50 ug of cell
dry weight Culture 1 : 0.02 M glucose per ml of culture or longer ( visible turbidity
) , Culture 2 : 0.02 M glucose plus 100 ug of L - argiand then treat as follows .
nine ...
Let the cultures grow with vigorous ing : shaking to approximately 50 ug of cell
dry weight Culture 1 : 0.02 M glucose per ml of culture or longer ( visible turbidity
) , Culture 2 : 0.02 M glucose plus 100 ug of L - argiand then treat as follows .
nine ...
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