Manual of Methods for General Bacteriology |
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Page 104
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 , L - phenylalanine , L -
proline ...
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 , L - phenylalanine , L -
proline ...
Page 106
... L - hydroxyproline , L - phenylalanine , L - tyrosine , DL - methionine , L -
cysteine . 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
.
... L - hydroxyproline , L - phenylalanine , L - tyrosine , DL - methionine , L -
cysteine . 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
.
Page 424
A flame ionization ( FI ) detector may be used ; how ever , it will not detect formic
acid . Use a column 6 ft ( 1 . ... or with 5 % FFAP on Chromosorb - G . Both volatile
and methylated fatty acids are detected with the same column . Set the column ...
A flame ionization ( FI ) detector may be used ; how ever , it will not detect formic
acid . Use a column 6 ft ( 1 . ... or with 5 % FFAP on Chromosorb - G . Both volatile
and methylated fatty acids are detected with the same column . Set the column ...
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Contents
Electron Microscopy ROGER M COLE AND TERRY J POPKIN | 34 |
Cell Fractionation CARL A SCHNAITMAN | 52 |
GROWTH RALPH N COSTILOW Editor | 63 |
Copyright | |
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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 example extract filter flask fraction give glass glucose grow growth heat Incubate inoculated isolation laboratory light liquid liter material measure medium membrane method mg/liter Microbiol microscopy mixture mutants needed obtained organisms oxygen plasmid plates positive prepared present Press procedure protein reaction reagent references remove salts 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