Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Volatiles from meat

Mottram, D.S., F.B. Whitfield, Aroma volatiles from meat-like Maillard systems, in Thermally Generated Flavors, T.H. Parliment, R.J. McGorrin, C.-T. Ho, Eds., Amer. Chem. Soc., Washington, D.C., 1994, p. 180. [Pg.133]

J. J. Balboni and W. W. Nawar, Apparatus for direct collection of volatiles from meat, J. Agric. Food Chem. 18 746 (1970). [Pg.23]

A review by Bailey and Swain ( ) cited several references which indicated nitrite was responsible for cured meat flavor. These same authors presented chromatograms of volatiles from cured and uncured hams and while the chromatograms were similar, some quantitative differences led to the conclusion that the major difference due to nitrite was its reactivity to retard lipid oxidation. Greene and Price ( ) suggested, however, that sodium chloride was the major factor responsible for cured meat flavor rather than sodium nitrite or an absence of lipid oxidation. It has been concluded from other recent work (2) that nitrite was necessary to produce a typical ham aroma and flavor as well as to retard the development of off-odors and flavors during storage of cooked cured meat. [Pg.293]

Mottram DS, Edwards RA, MacFie HJH. 1982. A comparison of the flavour volatiles from cooked beef and pork meat systems. J Sci Food Agric 33 934-944. [Pg.256]

Four aspects of research involving the use of SFE for the improvement of quality of muscle food products are briefly discussed. These include supercritical CO2 extraction of lipids fi om fresh ground beef and from dried muscle foods the extraction and separation of lipid and cholesterol from beef tallow supercritical CO2 extraction of flavor volatiles from beef and pork lipids for use as additives in synthetic meat flavors and identification and quantitation of flavor volatiles extracted with SC-CO2. [Pg.119]

Analysis of the volatiles from irradiated ground beef, pork, mutton, lamb, and veal showed that the compounds formed are essentially the same in all the meats. All of the samples were irradiated at a dose of 6 megarads, and the volatiles produced show the presence of more than 80 compounds,... [Pg.33]

It is now well established (6,10) that the hydrocarbons, except possibly those having three or four carbon atoms, found in the irradiated meats can come only from the lipid. This hypothesis has been verified in earlier studies, when the volatiles from irradiated methyl oleate (10) were found to contain appreciable quantities of alkanes and alkenes, and now in more detail from studies of both triglycerides and fatty acid esters. [Pg.34]

In meats, of course, there are components which arise from the protein which cannot be present in the products from pure fat. Table III shows some of the sulfur compounds and aromatic compounds which are also found in irradiated meats. Many of these can be postulated as arising from direct bond cleavage of amino acid moieties. Benzene and toluene may come from phenylalanine and phenol and p-cresol from tyrosine. Recent studies have been directed to considering the origin of some of the compounds from proteinaceous substances. Some of the sulfides, disulfides, and mercaptans can derive directly from cysteine or methionine, but those containing more than two carbon atoms in a chain require more than a superficial explanation. In order to evaluate the contribution of the volatiles from the protein as well as the lipid constituents of meat, volatile components produced in various protein substances have also been analyzed. [Pg.37]

Table V. Volatile Compounds Isolated from Meat Substances... Table V. Volatile Compounds Isolated from Meat Substances...
Meat aroma is not the result of one chemical constituent but the sum of the sensory effects of many of these volatiles. Over 90% of the volume of volatile constituents from freshly roasted beef is from lipid, but approximately 40 percent of the volatiles from the aqueous fraction are thought to be heterocyclic compounds, many resulting from Maillard reaction products or their interactions with other ingredients. [Pg.171]

Various kinds of heterocycles and two unsaturated methylketones were identified as characteristic components in the volatiles from cooked small shrimps. Without exception, they were all thermally generated compounds. Some volatile components from cooked small shrimps were in common with those of other animal protein foodstuffs like meat however, various types of compounds found in another foodstuffs were composed of the volatiles from specific shrimp species. Both the precursors and the formation pathways for the typical aroma compounds have already been elucidated, even though it is difficult to explain the different constituents of the volatile components among shrimp species. In future, it will be necessary to investigate the key factors which define the possible pathway to form characteristic volatiles in each foodstuff. [Pg.384]

Volatile Precursors. Investigations involving model systems for meat aromas have been revieved (31-34). More than 600 volatiles have been identified from meat or simulated meat precursors. [Pg.410]

Further evidence of the importance of the Halliard reaction in the formation of volatile flavorants from meat precursors is gleaned by examining ingredients in reaction mixtures patented as synthetic meat constituents. Ching (31), examined 128 patents of meat flavor and found that 55 specified use of both amino acids and sugars. Cysteine, cystine, and glutamic acid were used in 39 such mixtures. Over 80 patents describe meat flavor "reaction products" (32). [Pg.413]

The flavor of raw fresh meat is bland, metallic and slightly salty, whereas desirable meaty flavor is apparent only after heating. The precursors of brothy-desirable meat flavor have been studied extensively. More than 700 volatile components have been identified from meat reaction systems and undoubtedly many others are formed. Despite these efforts, the elucidation of the precise compounds responsible for "meaty" flavor remains an attractive endeavor for food chemical researchers. [Pg.421]

The volatiles from cooked meat contain large numbers of aliphatic compounds including aldehydes, alcohols, ketones, hydrocarbons and acids. These are derived from lipids by thermal degradation and oxidation (J7) and many may contribute to desirable flavor. In addition, the aldehydes, unsaturated alcohols and ketones produced in these reactions, as well as the parent unsaturated fatty acids, are reactive species and under cooking conditions could be expected to interact with intermediates of the Maillard reaction to produce other flavor compounds. [Pg.443]

The investigation of a series of model meat systems has demonstrated the important role of volatile sulfur-containing heterocyclic components substituted with sulfur in the 3-position. One of these 3-substituted sulfur compounds, 2-methy1-3-methy1thio-furan was identified recently in the volatiles from cooked beef aroma (5J and from a heated yeast extract composition (6J and is considered a meaty character impact compound. [Pg.461]

Irradiation of the lipid (fet soluble) phase of a meat extract does not produce the characteristic off-odor while irradiation of the aqueous (water soluble) portion of die meat extract results in a typical irradiation odor (20). 3) Irradiation of sulfur-containing amino acids or polypeptides produced a similar off-odor as the irradiation odor (21). 4) The amount of VSCs increased with radiation dose while volatiles from lipids were not always correlated with radiation dose (19). Several earlier researchers suggested that hydrogen sulfide (H2S) and methanethiol (MT) were important for the development of the off-odor (12, 20, 22). Patterson and Stevenson (23), using GC-olfactory analysis, showed that dimethyl trisulfide (DMTS) was the most potent off-odor compound in irradiated raw chicken meats followed by cis-3- and trans-6-nonenals, oct-l-en-3-one and bis(methylthio-)methane. Aim and his colleagues have published extensively on irradiation-induced volatile compounds in raw meats (11). They have identified MT, dimethyl sulfide (DMS), dimethyl disulfide (DMDS) and DMTS in different types of irradiated raw meats using GC-FID and GC-MS. [Pg.211]

Meat flavor is due to a great number of volatiles from different chemical classes. However, most of the odorants described as meaty aroma contain sulfur. The two most important reactions which generate meaty aroma compounds are the reactions between sulfur containing amino acids and reducing sugars (Maillard reaction) and the thermal degradation of thiamin [35], Sulfur-containing furans are the basic chemicals responsible for the aroma of thermally treated meat. [Pg.307]

Phospholipids contribute specific aroma to heated milk, meat and other cooked foods through lipid oxidation derived volatile compounds and interaction with Maillard reaction products. Most of the aroma significant volatiles from soybean lecithin are derived from lipid decomposition and Maillard reaction products including short-chain fatty acids, 2-heptanone, hexanal, and short-chain branched aldehydes formed by Strecker degradation (reactions of a-dicarbonyl compounds with amino acids). The most odor-active volatiles identified from aqueous dispersions of phosphatidylcholine and phos-phatidylethanolamine include fra 5 -4,5-epoxy-c/5-2-decenal, fran5,fran5-2,4-decadienal, hexanal, fra 5, d5, d5 -2,4,7-tridecatrienal (Table 11.9). Upon heating, these phospholipids produced cis- and franj-2-decenal and fra 5-2-undecenal. Besides fatty acid composition, other unknown factors apparently affect the formation of carbonyl compounds from heated phospholipids. [Pg.318]

Pimento Berry Oil. The pimento or allspice tree, Pimenta dioca L. (syn. P. officinalis, Liadl.), a native of the West Indies and Central America, yields two essential oils of commercial importance pimento berry oil and pimenta leaf oil. The leaf oil finds some use ia perfumery for its resemblance to clove leaf and cinnamon leaf oils as a result of its high content of eugenol. Pimento berry oil is an item of commerce with extensive appHcation by the flavor industry ia food products such as meat sauces, sausages, and pickles, and moderate use ia perfumery, where it is used primarily as a modifier ia the modem spicy types of men s fragrances. The oil is steam-distilled from dried, cmshed, fully grown but unripe fmits. It is a pale yellow Hquid with a warm-spicy, sweet odor with a fresh, clean topnote, a tenacious, sweet-balsamic-spicy body, and a tea-like undertone. A comparative analysis of the headspace volatiles of ripe pimento berries and a commercial oil has been performed and differences are shown ia Table 52 (95). [Pg.337]

Lipid hydroperoxides are either formed in an autocatalytic process initiated by hydroxyl radicals or they are formed photochemically. Lipid hydroperoxides, known as the primary lipid oxidation products, are tasteless and odourless, but may be cleaved into the so-called secondary lipid oxidation products by heat or by metal ion catalysis. This transformation of hydroperoxides to secondary lipid oxidation products can thus be seen during chill storage of pork (Nielsen et al, 1997). The secondary lipid oxidation products, like hexanal from linoleic acid, are volatile and provide precooked meats, dried milk products and used frying oil with characteristic off-flavours (Shahidi and Pegg, 1994). They may further react with proteins forming fluorescent protein derivatives derived from initially formed Schiff bases (Tappel, 1956). [Pg.316]

N-Nitrosamines, formed principally from the reaction of naturally occurring secondary amines with nitrites that may be added to foods or produced by bacterial reduction of nitrates, have been identified in many food systems including cured meat products, nonfat dried milk, dried malt and beer. In addition, the presence of less volatile and non-volatile N-nitroso compounds or their precursors in foods have been suggested from a number of model system studies. [Pg.165]


See other pages where Volatiles from meat is mentioned: [Pg.537]    [Pg.537]    [Pg.32]    [Pg.171]    [Pg.171]    [Pg.175]    [Pg.310]    [Pg.377]    [Pg.445]    [Pg.465]    [Pg.191]    [Pg.195]    [Pg.197]    [Pg.312]    [Pg.13]    [Pg.37]    [Pg.657]    [Pg.660]    [Pg.182]    [Pg.81]    [Pg.1019]    [Pg.58]    [Pg.67]    [Pg.24]    [Pg.338]    [Pg.339]    [Pg.166]   
See also in sourсe #XX -- [ Pg.32 ]




SEARCH



© 2024 chempedia.info