Volatile Compounds Produced in Ground Muscle Tissue of Canary Rockfish (Sebastes pinniger) Stored on Ice

1972 ◽  
Vol 29 (8) ◽  
pp. 1125-1129 ◽  
Author(s):  
A. Miller III ◽  
R. A. Scanlan ◽  
J. S. Lee ◽  
L. M. Libbey

Volatile compounds associated with the progressive degradation of ground muscle tissue of canary rockfish (Sebastes pinniger) stored on ice were determined by combined gas–liquid chromatography and mass spectrometry. Compounds positively identified included dimethyl sulfide, n-propyl alcohol, acetaldehyde, propionaldehyde, acetone, ethyl alcohol, 2- and 3-pentanone, diacetyl, hexanal, 1-pentene-3-ol, 3-methyl-1-butanol, acetoin, trimethylamine, and dimethylamine. The following compounds were tentatively identified: propenal, octenal or octadienal, butyraldehyde, 3-methyl butanal, 2-butanone, and methyl vinyl ketone.

1994 ◽  
Vol 61 (2) ◽  
pp. 241-248 ◽  
Author(s):  
Nathalie Jollivet ◽  
Jean Chataud ◽  
Yves Vayssier ◽  
Maurice Bensoussan ◽  
Jean-Marc Belin

SummaryEight strains of Geotrichum candidum isolated from cheese were compared for aroma production. Twenty-four components, including alcohols, methyl ketones, fatty acids and esters, were identified by gas–liquid chromatography and gas chromatography–mass spectrometry of the volatile compounds produced by G. candidum cultures. Strains could be differentiated by their ability to produce dimethyldisulphide, phenol, phenylethanol and methyl ketones.


1984 ◽  
Vol 30 (2) ◽  
pp. 188-191 ◽  
Author(s):  
S Yoshioka ◽  
S Saitoh ◽  
S Seki ◽  
K Seki

Abstract Six non-glucose polyols--mannose, fructose, 1-deoxyglucose, mannitol, glucitol, and inositol--were identified and evaluated in human serum and cerebrospinal fluid by gas-liquid chromatography and by gas-liquid chromatography/mass spectrometry. Concentrations of fructose, mannose, and inositol in the serum of healthy persons or children without metabolic diseases varied with age, as already reported for 1-deoxyglucose. Fructose, inositol, and glucitol concentrations in cerebrospinal fluid significantly exceeded those in serum. The method described here for determining polyols and for evaluating polyol patterns in serum, as well as the resulting data on children and healthy subjects, should be useful in investigations of the clinical and physiological significance of polyols.


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