Cooked aroma

The quick or competitive procedure for making sweet table wines depends on sweetening a dry table wine with a very sweet blending wine or with sugar or grape concentrate and some procedure of sterilization which ensures that no viable yeast cells are present in the closed bottle. The simplest is pasteurization of the blend after it has been bottled. This technique, however, is not favored as it tends to give the wine a cooked aroma and taste. 

The cooked aroma of E paclfica (Pacific krill) is fishy and relatively unacceptable. Its GC profile is quite different than that of other samples, because N,N-dimethyl-2-phenylethyl amine was a principal volatile component while only small quantity of pyrazine and thialdine were observed (see Table I). This amine was not produced by cooking, it occurs in vivo (27). Volatiles from both raw and boiled (85°C, 90 min) E. pacifica were prepared by steam distillation under reduced pressure (20 Torr). 

The flavor of fish and seafoods is composed of taste-active low molecular-weight extractives and aroma-active compounds. The taste-active compoimds are more abundant in the tissues of mollusks and crustaceans than fish. The most important non-volatile taste components are fi-ee amino acids, nucleotides, inorganic salts and quaternary ammonia bases. Alcohols, aldehydes, ketones, furans, nitrogen-containing compounds, sulfur-containing compounds, hydrocarbons, esters and phenols are the most important volatiles is shellfish. Alkyl pyrazines and sulfur-containing compounds are important contributors to the cooked aroma of crustaceans. Furans pyrazines, and Lactones have been found in heat-treated seafoods. Dimethyl disulfide, dimethyl trisulfide, heterocyclic sulfiir-containing compounds (alkylthiophenes) have been found in most thermally treated crustaceans like prawn, crab, oyster, crayfish and shrimp (52). 

In an attempt to produce sugars directly from barley seeds, these were extracted with superheated water in our laboratory. Unfortunately, at the temperature required for hydrolysis, a dark brown extract was obtained, which smelled of burning. At lower temperature, however, a pleasant cooking aroma was obtained, due to the Maillard reaction. Similar results were obtained with other vegetable material, and superheated water could be used to manufacture food flavors [6]. The most inter-... 

The first mass spectrometric investigation of the thiazole ring was done by Clarke et al. (271). Shortly after, Cooks et al., in a study devoted to bicydic aromatic systems, demonstrated the influence of the benzo ring in benzothiazole (272). Since this time, many studies have been devoted to the influence of various types of substitution upon fragmentation schemes and rearrangements, in the case of alkylthiazoles by Buttery (273) arylthiazoles by Aune et al. (276), Rix et al. (277), Khnulnitskii et al. (278) functional derivatives by Salmona el al. (279) and Entenmann (280) and thiazoles isotopically labeled with deuterium and C by Bojesen et al. (113). More recently, Witzhum et al. have detected the presence of simple derivatives of thiazole in food aromas by mass spectrometry (281). 

Rectified oils have been redistilled to improve a particular property or characteristic, such as flavor or aroma. Eor example, natural oil of peppermint is frequently rectified to remove dimethyl sulfide, which has a powerful and objectionable cooked vegetable note deleterious to the use of the oil in cmme de menthe Hqueurs. Distillation is also used to remove psoralens, which are harmful photosensitizing agents present in natural bergamot oil. Color may be removed, eg, from cassia oil, by vacuum steam distillation. A desirable component, such as 1,8-cineole (eucalyptol) 85% in eucalyptus oil, may be... 

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. 

Caramel color is a dark brown or even black product used for centuries in home cooking to provide color and specific aromas to foods. The first commercial caramel was produced in Europe about 1850. ... 

Moss MC, Cook J, Wesnes KA and Duckett P (2003). Aroma of rosemary and lavender essential oils differentially affect cognition and mood in healthy adults. International Journal of Neuroscience, 113, 1507-1530. 

The impact of MOX upon reductive aromas is being exanained in a further research project at the University of Auckland, using SPME GC-MS (Nguyen et ah, 2010). The wines subject to MOX, or stored in an 02-permeable Flextank, recorded lower concentrations of compoimds such as methanethiol (aroma of cooked cabbage, with a perception threshold of 0.3 pg/L Mestres et al., 2000), and 3-(methylthio)-l-propanol... 

Hhong et ah (2009) described the sensory attributes of morama oil as fresh, thick, creamy, and smooth with a grassy and earthy aroma and raw nutty flavor and aftertaste. Compared to both sunflower and olive oils, potato chips fried in morama oil were rated as more acceptable by consumers (Tlhong et ah, 2009). Therefore, as a cooking oil, morama oil has great potential in terms of consumer acceptability. However, its acceptability as a salad oil remains imexplored. 

The symmetrical compounds (17, R = R = R ) are formed from an aldehyde and ammonium sulfide (2,29,35) or hydrogen sulfide and ammonia (33), Thialdine (17, R - R - R = Me) is an important aroma compound found in the volatiles of beef broth (48), pressure-cooked meat (49), and fried chicken (50), It is also obtained from acetaldehyde (2,29,37) or from B-mercaptoacetaldehyde and ammonium sulfide (37), In our experiments, it was synthesized as a white powder from a reaction of acetaldehyde with ammonium sulfide in 60% yield. 

Homstein and Crowe 18) and others (79-27) suggested that, while the fat portion of muscle foods from different species contributes to the unique flavor that characterizes the meat from these species, the lean portion of meat contributes to the basic meaty flavor thought to be identical in beef, pork, and lamb. The major differences in flavor between pork and lamb result from differences in a number of short chain unsaturated fatty acids that are not present in beef. Even though more than 600 volatile compounds have been identified from cooked beef, not one single compound has been identified to date that can be attributed to the aroma of "cooked beef." Therefore, a thorough understanding of the effect of storage on beef flavor and on lipid volatile production would be helpful to maintain or expand that portion of the beef market. 

The most important flavour compound in raw onions is thiopropanal-S-ox-ide, the lachrymatory factor [145,146]. Other important flavour compounds are 3,4-dimethyl-2,5-dioxo-2,5-dihydrothiophene and alkyl alkane thiosulfonates such as propyl methanethiosulfonate and propyl propanethiosulfonate with a distinct odour of freshly cut onions [35, 36, 147]. Various thiosulfinates that have a sharp and pungent odour may also contribute to the flavour of onions. These compounds, however, are rapidly decomposed to a mixture of alkyl and alkenyl monosulfides, disulfides and trisulfides (Scheme 7.3) of which dipropyl disulfide, methyl ( )-propenyl disulfide, propyl ( )-propenyl disulfide, dipropyl trisulfide and methyl propyl trisulfide are the most important contributors to the aroma of raw and cooked onions (Table 7.5, Fig. 7.6) [148-150]. Recently, 3-mercapto-2-methylpentan-l-ol was identified in raw and cooked onions eliciting intense meat broth, sweaty, onion and leek-like odours [142, 151]. 

Products of the LOX pathway or compounds formed by autoxidation of fatty acids (Scheme 7.2) are also important for leek aroma [31, 163]. Volatile compounds of the LOX pathway are not pronounced in the aroma profile of freshly cut leeks owing to a high content of thiosulfinates and thiopropanal-S-oxide [30]. In processed leeks that have been stored for a long time (frozen storage), however, these aliphatic aldehydes and alcohols have a greater impact on the aroma profile owing to volatilisation and transformations of sulfur compounds [31, 165]. The most important volatiles produced from fatty acids and perceived by GC-O of raw or cooked leeks are pentanal, hexanal, decanal and l-octen-3-ol (Table 7.5) [31, 35, 148, 163, 164]. 

The edible portion of broccoli Brassica oleracea var. italica) is the inflorescence, and it is normally eaten cooked, with the main meal. Over 40 volatile compounds have been identified from raw or cooked broccoli. The most influential aroma compounds found in broccoli are sulfides, isothiocyanates, aliphatic aldehydes, alcohols and aromatic compounds [35, 166-169]. Broccoli is mainly characterised by sulfurous aroma compounds, which are formed from gluco-sinolates and amino acid precursors (Sects. 7.2.2, 7.2.3) [170-173]. The strong off-odours produced by broccoli have mainly been associated with volatile sulfur compounds, such as methanethiol, hydrogen sulfide, dimethyl disulfide and trimethyl disulfide [169,171, 174, 175]. Other volatile compounds that also have been reported as important to broccoli aroma and odour are dimethyl sulfide, hexanal, (Z)-3-hexen-l-ol, nonanal, ethanol, methyl thiocyanate, butyl isothiocyanate, 2-methylbutyl isothiocyanate and 3-isopropyl-2-methoxypyrazine... 

The buds and the leaves (less often) of the Brussels sprout plant (Brasska olera-cea var. gemmifera) are eaten cooked with the main meal. In Brussels sprouts, breakdown products from glucosinolates are dominant and represent about 80-90% of the volatiles in headspace samples [176]. The residual volatiles are mostly sulfur compounds [176]. Compounds likely to be associated with the aroma of Brussels sprouts are 2-propenyl isothiocyanate, dimethyl sulfide, dimethyl disulfide and dimethyl trisulfide (Table 7.6) [35,176]. 

The roundish flower head, the curd, of the cauliflower plant (Brasska oleracea var. botrytis) is the edible portion of this vegetable. It can be eaten raw in salads or as a pickled condiment in vinegar. More often it is boiled and eaten with the main meal or is converted into sauces and soups. Over 80 volatile compounds have been identified in raw and cooked cauliflower. Among the compounds potentially active in cooked cauliflower, certain sulfides such as methanethiol, dimethyl sulfide and dimethyl trisulflde have often been incriminated in objectionable sulfurous aromas and overcooked off-flavours [169, 177, 178, 181-183]. Additional aldehydes have been found to be the most abundant cauliflower volatiles, with nonanal as a major component [175,177]. A recent study showed that volatiles such as 2-propenyl isothiocyanate, dimethyl trisulflde, di-... 

Raw potato possesses little aroma. Approximately 50 compounds have been reported to contribute to raw potato aroma. Raw potatoes have a high content of LOX, which catalyses the oxidation of unsaturated fatty acids into volatile degradation products (Scheme 7.2) [187]. These reactions occur as the cells are disrupted, e.g. during peeling or cutting. Freshly cut, raw potatoes contain ( ,Z)-2,4-decadienal, ( ,Z)-2,6-nonadienal, ( )-2-octenal and hexanal, which are all products of LOX-initiated reactions of unsaturated fatty acids [188,189]. It is reported that two compounds represent typical potato aroma in raw potato methional and ( ,Z)-2,6-nonadienal [189]. Other important volatiles in raw potatoes produced via the LOX pathway are l-penten-3-one, heptanal, 2-pen-tyl furan, 1-pentanol and ( , )-2,4-heptadienal [189]. Pyrazines such as 3-iso-propyl-2-methoxypyrazine could be responsible for the earthy aroma of potato [35]. Some of the most important character-impact compounds of raw potatoes are summarised in Table 7.8. Aroma compounds from cooked, fried and baked potatoes have previously been reviewed [35]. 

The root of carrot Daucus carota) is eaten raw or cooked. The characteristic aroma and flavour of carrots are mainly due to volatile compounds, although non-volatile polyacetylenes and isocoumarins contribute significantly to the bitterness of carrots [1,2]. More than 90 volatile compounds have been identified from carrots (Table 7.9) [207-215]. The carrot volatiles consist mainly of terpenoids in terms of numbers and amounts and include monoterpenes, sesquiterpenes and irregular terpenes. Monoterpenes and sesquiterpenes account... 

The Maillard reaction is inextricably linked to the desirable flavour and colour characteristics of cooked foods and this review provides an insight into some of the chemistry associated with flavour generation in the reaction and the different aromas which are involved. The chemical pathways associated with the initial and intermediate stages of the Maillard reaction are presented and routes by which the important classes of aroma compounds may be formed from Maillard intermediates are discussed. 

Oxazoles have been found in relatively few cooked foods, although over 30 have been reported in coffee and cocoa, and 9 in cooked meat. Oxazolines have been found in cooked meat and roast peanuts, but not to any extent in other foods. 2,4,5-Trimethyl-3-oxazoline has been regularly detected in cooked meat [26], and when it was first identified in boiled beef [27] it was thought that the compound possessed the characteristic meat aroma however, on synthesis it was shown to have a woody, musty, green flavour with a threshold value of 1 mg/kg [28]. Other 3-oxazolines have nutty, sweet or vegetable-like aromas and the oxazoles also appear to be green and vegetable-like [28]. The contribution of these compounds to the overall aroma of heated foods is probably not as important as the closely related thiazoles and thiazolines. 

A number of furans with thiol, sulphide or disulphide substitution have been reported as aroma volatiles, and these are particularly important in meat and coffee. In the early 1970s, it was shown that furans and thiophenes with a thiol group in the 3-position possess strong meat-like aromas and exceptionally low odour threshold values [50] however, it was over 15 years before such compounds were reported in meat itself In 1986,2-methyl-3-(methylthio)furan was identified in cooked beef and it was reported to have a low odour threshold value (0.05 pg/kg) and a meaty aroma at levels below 1 pg/kg [51]. Gasser and Grosch [52] identified 2-methyl-3-furanthiol and the corresponding disulphide, bis(2-methyl-3-furanyl) disulphide, as major contributors to the meaty aroma of cooked beef. The odour threshold value of this disulphide has been reported as 0.02 ng/kg, one of the lowest known threshold values [53]. Other thiols which may contribute to meaty aromas include mercaptoketones, such as 2-mercapto-pentan-3-one. 2-Furylmethanethiol (2-furfurylmercaptan) has also been found in meat, but is more likely to contribute to roasted rather than meaty aromas. Disulphides have also been found, either as symmetrical disulphides derived from two molecules of the same thiol or as mixed disulphides from two different thiols [54]. 

Pyridine has been isolated in the volatile components from cooked beef ( sukiyaki ) in Japan (Shibamoto etal., 1981), fried chicken in the United States (Tang et al., 1983), fried bacon (Ho et al., 1983), Beaufort cheese (Dumont Adda, 1978), black tea aroma (Vitzthum et al., 1975) and coffee aroma (Aeschbacher et al., 1989). 

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