Nitrogen compounds, flavoring from

It appears, then, that there is a general, meaty aroma, common to cooked beef, pork, and lamb (and probably poultry), attributable to the pyrolysis of the mixture of low molecular weight nitrogenous and carbonyl compounds extracted from the lean meat by cold water. But the aromas of roast beef, roast pork, roast lamb, and roast chicken are unmistakably different. The chemical composition of the muscular fat deposits of these animals differ appreciably, and it is to these lipid components that we must look to account for the specific flavor differences. Heating the carefully separated fat alone does not give a meaty aroma at all, much less an animal-specific one. It is the subsequent reactions of pyrolysis products of nonlipid components that give the characteristic aromas and flavors of roasted meats (20). 

The most popular method involves 2-thiobarbituric acid (TBA) two molecules of 2-thiobarbituric acid are condensed with malonaldehyde. The emergent chromogen — the two tautomeric structures of the red TBA-malonaldehyde adduct — is determined at 532 nm, and also often at 450 nm, to determine aUcenals and aUcanals, respectively. The qualitative Kreis test was based on a similar principle it involved detection of the epihydrine aldehyde — a tautomeric malondialdehyde — in a color reaction with resorcine or phloroglucinol. The popularity of the TBA test stems from a correlation between the results and sensory evaluations. Paradoxically, this is related to the most important drawback of the TBA technique — its lack of specificity. In addition to the reaction with malonaldehyde, TBA forms compounds of identical color with other aldehydes and ketones, products of aldehyde interaction with nitrogen compounds, and also with saccharides, ascorbic acid, creatine, creatinine, trimethylamine oxide, trimethylamine, proteins, and amino acids. For this reason, the TBA test may even be treated as a proteolysis indicator (Kolakowska and Deutry, 1983). Recently, TBA-reactive substances (TEARS) were introduced, primarily to stress that the reaction involves hydroperoxides in addition to aldehydes. Due to the nonspecificity of the TEARS test, its results reflect the rancidity of food better than other conventional methods, especially off-flavor, which is caused by volatiles from lipids as well as being affected by products of lipids interaction with nitrogenous compounds. 

Musty or potato-like flavor and aroma have been observed as a defect in milk (Hammer and Babel 1957) and Gruyere de Comte cheese (Dumont et al. 1975). This off-flavor results from the production of nitrogenous cyclic compounds by Pseudomonas taetrolens and P. perolens (Morgan 1976). Musty-flavored compounds produced by these organisms include 2,5-dimethylpyrazine and 2-methoxy-3-isopropyl-pyrazine. The Gruyere de Comte with potato off-flavor contained 3-methoxy-2-propyl pyridine, as well as alkyl pyrazine compounds (Dumont et al. 1975). Murray and Whitfield (1975) postulated that alkyl pyrazines are formed in vegetables by condensation of amino acids such as valine, isoleucine, and leucine with a 2-carbon compound. Details of the synthetic mechanism in pseudomonads are unknown. 

Molasses. A large number of volatile and nonvolatile compounds have been identified in the flavor fractions of various types of molasses (51-621. Compound classes identified include aliphatic and aromatic acids, aldehydes, phenols, lactones, amines, esters, furans, pyrazines, and sulfides. Most of these compounds can arise from carbohydrate degradation through a number of traditional pathways especially because residual nitrogen-containing sources are present. 

Thiazoles are a class of compounds possessing a flve-membered ring with sulfur and nitrogen in the 1 and 3 positions, respectively. The potential for thiazole derivatives as flavorants is evident from the work of Stoll et al. (24) who found the strong nut-like odor of a cocoa extract to be due to a trace amount of 4-methyl-5-vinylthla-zole. Since then, numerous thiazoles have been identified in food flavors. 

Poiishing fiitration Free fatty acids Odor and flavor compounds Bieaching earth Citric acid Carbonaceous materiai tank to deodorizer Pumping from deodorizer to poiish fiiter to oii cooier to storage tank 204-274 (400-525) 50-70 (122-158) 60-66 (140-151) 60-66 (140-151) Nitrogen or air Nitrogen or air... 

The main volatiles in wines are the higher aliphatic alcohols, ethyl esters, and acetates formed from yeasts during fermentation. Acetates are very important flavors characterized by fruity notes, C4-Ci0 fatty acid ethyl esters manly confer fruity scents to the wine. Other wine aroma compounds are C6 alcohols, such as 1-hexanol and cis- and trans-3-hexen-l-ol, 2-phenylethanol, and 2-phenylethyl acetate. Contents of these compounds in wine are linked to the winemaking processes used fermentation temperature, yeast strain type, nitrogen level in must available for yeasts during fermentation, clarification of wine (Rapp and Versini, 1991). Much literature on the wine aroma compounds was reported in reviews by Schreier (1979) and Rapp (1988). 

In addition to lipid oxidation and hydrolysis reactions, the rancid off-flavor results from interactions, particularly those between aldehydes and nitrogen-containing compounds. However, for some of these interactions, it is impossible to evaluate the off-flavor. 

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