Manual of Methods for General Bacteriology: By Philipp Gerhardt, Editor-in-chief ; R.G.E. Murray, Editor, I. Morphology ... [et Al.].Philipp Gerhardt, American Society for Microbiology |
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Page 83
growth factors. However, there is as yet no known instance of the obligatory
requirement for a preformed peptide for bacterial growth, although peptides are
usually readily utilized (and frequently desirable) sources of essential amino
acids.
growth factors. However, there is as yet no known instance of the obligatory
requirement for a preformed peptide for bacterial growth, although peptides are
usually readily utilized (and frequently desirable) sources of essential amino
acids.
Page 100
TABLE 10–Continued * Any one of the following amino acids at a concentration
of 0.62 or 0.36M can serve as carbon and energy source or nitrogen source:
glutamic acid, aspartic acid, serine, proline, a-alanine, asparagine, glutamine,
and ...
TABLE 10–Continued * Any one of the following amino acids at a concentration
of 0.62 or 0.36M can serve as carbon and energy source or nitrogen source:
glutamic acid, aspartic acid, serine, proline, a-alanine, asparagine, glutamine,
and ...
Page 103
71110 (mg) 10 10 10 10 2.5 2.5 1.0 10 10 10 10 10 10 'I'race elements Yes" Yes'
Yes' Yes' Amino acids Yes' Yes' Yes" Yes" Yes“ Yes' Yes' Yes' Yes“ Yes“ Yes“
Yes“ Casein hydrolysate (acid) (5) 5.0“ 5.0” 5.0" Purines and pyrimidines .
71110 (mg) 10 10 10 10 2.5 2.5 1.0 10 10 10 10 10 10 'I'race elements Yes" Yes'
Yes' Yes' Amino acids Yes' Yes' Yes" Yes" Yes“ Yes' Yes' Yes' Yes“ Yes“ Yes“
Yes“ Casein hydrolysate (acid) (5) 5.0“ 5.0” 5.0" Purines and pyrimidines .
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Contents
MORPHOLOGY | 5 |
Light Microscopy R G E MURRAY AND C F Robinow 2 Specimen Preparation for Light Microscopy R G E MURRAY AND C F Robi | 17 |
Determinative Methods of Light Microscopy R N DoETscH | 21 |
Copyright | |
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acetate Adjust agar allow amino acids anaerobic aqueous assay autoclaving bacteria bacterial cells Bacteriol bacteriology bacterium biotin broth buffer carbon centrifuge chemical coli colonies column components compounds concentration containing cover slip culture described detergents determined dilution Dissolve distilled water electron microscopy endospores enzyme Escherichia coli ethanol film filter final first flask fraction g Distilled genetic glass glucose gradient gram-negative gram-positive grid growth heat hydroxylapatite Incubate inoculated isolation laboratory lipids liquid liter measure medium membrane metabolic method mg/liter Microbiol microbiology mixture mutagens mutants NaCl nitrogen nutrient organisms oxidation oxygen Pasteur pipette pellet phage pipette plasmid plate prepared procedure protein radioactivity reaction reagent remove sample slide sodium solution specific spheroplasts staining standard sterile substrate sucrose surface suspension Table techniques temperature thiamine tion tube vials vitamin vol/vol volume Wash wt/vol yeast extract