Manual of Methods for General Bacteriology |
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Page 81
growth factor , but many more require pantothenic acid or pantetheine for growth . The interrelationship of these compounds is shown in the following diagram : Pantoic acid + B - alanine pantothenate → 4 ' - phosphopantothenate ' → 4 ...
growth factor , but many more require pantothenic acid or pantetheine for growth . The interrelationship of these compounds is shown in the following diagram : Pantoic acid + B - alanine pantothenate → 4 ' - phosphopantothenate ' → 4 ...
Page 104
bb dd Table 12 - continued " Add the following at 0.1 g / liter : L - alanine , L - arginine , L - aspartic acid , L - asparagine , L - hydroxyproline , L - isoleucine , L - leucine , L - lysine . HCI , L - methionine , L - norleucine ...
bb dd Table 12 - continued " Add the following at 0.1 g / liter : L - alanine , L - arginine , L - aspartic acid , L - asparagine , L - hydroxyproline , L - isoleucine , L - leucine , L - lysine . HCI , L - methionine , L - norleucine ...
Page 106
HCI , 100 mg each ; L - tryptophan , 40 mg ; and L - glutamic acid , 500 mg . Casein hydrolysate ( 4 g / liter ) can be substituted for the amino acid mixture . ? Add 0.1 each of L - cystine and L - tryptophan per liter .
HCI , 100 mg each ; L - tryptophan , 40 mg ; and L - glutamic acid , 500 mg . Casein hydrolysate ( 4 g / liter ) can be substituted for the amino acid mixture . ? Add 0.1 each of L - cystine and L - tryptophan per liter .
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Contents
1 | 22 |
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
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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