SUMMARY
About 90% of the hydrogen sulfide (H2S) produced by heated chicken muscle comes from muscle protein. To identify specific H2S precursors, the identity, quantity, and H2Sproducing capability of sulfur compounds in chicken muscle were investigated. The only sulfur compounds found in muscle nonprotein were methionine, taurine, and glutathione. Of these, only glutathione produced H2S. Therefore the principal H2S precursor in chicken muscle nonprotein is sulfur, occurring as eystine and/or cysteine in the tripeptide glutathione. Since the only sulfur compounds reported in chicken muscle protein are methionine, cystine, and/or cysteine, and since methionine does not produce H2S, the sulfur in the H2S produced by muscle protein must also come from cystine and/or cysteine. Glutathione gives off H2S about 180 times as fast as does chicken muscle protein, but, because there is approximately 1 to 2 thousand times as much protein as glutathione in muscle, protein is the principal H2S precursor. Since cystine plus cysteine, sulfur in protein and in glutathione is the only H2S precursor, the rate of H2S evolution from heated chicken muscle can be approximately predicted from its cystine content.
SUMMARY: Fat of raw poultry, separated from solid tissue and washed with water at temperatures not exceeding 40°C does not contain cooked poultry aroma and does not develop it when heated. Hence, cooked poultry aroma cannot be derived from the fat alone. Washed and filtered fat from cooked poultry contains characteristic cooked poultry aroma dissolved in it. The aroma of this fat is caused by compounds which dissolve in it during cooking and which apparently stem from nonfat or lean portions of the meat. The ability of fat to dissolve or acquire substances during cooking was demonstrated by showing that fat of cooked poultry contains more sulfur than does fat of raw poultry. Less than 2% of this sulfur build‐up occurs as hydrogen sulfide. The magnitude of the sulfur build‐up was 8 to 14 times greater in the fat of roasted poultry than it was in the fat of simmered chicken. Authentic amino acids in contact with poultry fat at a typical roasting temperature readily underwent Strecker type degradation. Furthermore, aroma components representing typical amino acid degradation products were found in fat from roasted turkey. These analytical results indicate protein, amino acids and probably also sugars and other water soluble components are invoved in aroma formation. Hence fat contributes to cooked poultry aroma indirectly and passively through its ability to dissolve and retain aroma components formed during cooking. Consequently, the characteristic cooked poultry aroma in fat of cooked poultry is not derived from the fat itself but comes from and is thus dependent on the “lean”.
when injected subcutaneously, but was pathogenic for baby chicks when exposed intracerebrally, intranasally, intramuscularly, subcutaneously, and intraperitoneally. REFERENCE Reagan, R. L., M. G. Lillie, J. E. Hauser and A. L. Brueckner, 1948. Response of the Syrian hamster to the virus of Newcastle disease. Proc. Soc. Exp. Biol. Med. 68: 293-294.
The 35 parts per billion (ppb) H,S in freshly prepared broth and the 180 to 730 ppb H,S in meat of freshly simmered, roasted and fried chicken all substantially exceed the 10 ppb H,S odor threshold in water. Hence, HeS contributes directly to the aroma of these products. Freezing, thawing and reheating can reduce the H,S in broth to subthreshold levels thus indicating the transient nature of its direct contribution to aroma. In a model system, HeS was passed through molten chicken fat containing 5% acetaldehyde. After expulsion of excess HsS and acetaldehyde the residual highly odorous fat exhibited a fixed sulfur content. These exploratory results, together with related results reported in the literature, suggest that a reaction beween HIS and acetaldehyde was involved and that such interactions between H,S and carbonyls in fat could be quite general. Thus HS mav also contribute to cooked chicken flavor and aroma through the 7brmation of such secondary products.
Summary
Groups of turkeys were fed, for eight weeks prior to slaughter, diets varying in the type of animal protein concentrate (fish meal vs. meat scraps) and varying in degree of unsaturation and kind of vegetable oil present (coconut oil vs. linseed oil). Chemical and organoleptic analyses of the fresh and stored carcasses established the following points:
Differences in fatty acid composition of dietary fat of turkeys have a marked effect on the fatty‐acid composition of carcass fat and correspondingly play a decisive role in the storage life of the turkey carcass.
Typically fishy flavors and odors in roasted turkey meat, which can be caused by feeding fish (oil) products, can also be produced in the absence of fish products by a highly unsaturated vegetable oil, linseed oil. The fishy flavor is present in the roasted, freshly slaughtered turkey and apparently increases very little if any in intensity during storage.
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