Journal of Agricultural and Food Chemistry 2002-02-27

Effect of lipid composition on meat-like model systems containing cysteine, ribose, and polyunsaturated fatty acids.

J Stephen Elmore, Maria M Campo, Michael Enser, Donald S Mottram

Index: J. Agric. Food Chem. 50(5) , 1126-32, (2002)

Full Text: HTML

Abstract

This paper compares the volatile constituents of model systems containing the important meat aroma precursors cysteine and ribose, with and without either methyl linoleate, an n-6 fatty acid, or methyl alpha-linolenate, an n-3 acid, both of which are present in meat. Many of the volatile compounds formed from the reaction between cysteine and ribose were not formed, or formed in lower amounts, when lipid was present. This may be due to the reaction between hydrogen sulfide, formed from the breakdown of cysteine, and lipid degradation products. In addition, cysteine and ribose modified lipid oxidation pathways, so that alcohols and alkylfurans were formed rather than saturated and unsaturated aldehydes. Several volatile compounds, which have been found at elevated levels in cooked meat from animals fed supplements high in n-3 acids, were formed when methyl alpha-linolenate reacted with cysteine and ribose. The possible effects of increasing the n-3 content of meat upon flavor formation during cooking are discussed.


Related Compounds

  • 1,4-Dithiane-2,5-d...

Related Articles:

Phytogrowth-inhibitory and antibacterial activities of 2,5-dihydroxy-1,4-dithiane and its derivatives.

1990-01-01

[Chem. Pharm. Bull. 38(1) , 243-5, (1990)]

Synthesis and antiviral/antitumor evaluation of 2-amino- and 2-carboxamido-3-arylsulfonylthiophenes and related compounds as a new class of diarylsulfones.

2001-05-01

[Bioorg. Med. Chem. 9(5) , 1123-32, (2001)]

Hydrogen-bond-mediated cascade reaction involving chalcones: facile synthesis of enantioenriched trisubstituted tetrahydrothiophenes.

2012-02-17

[Org. Lett. 14(4) , 1090-3, (2012)]

Highly diastereoselective DABCO-catalyzed [3 + 3]-cycloaddition of 1,4-dithiane-2,5-diol with azomethine imines.

2013-11-01

[Org. Lett. 15(21) , 5554-7, (2013)]

1, 4-Dithiane-2, 5-diol as an efficient synthon for a straightforward synthesis of functionalized tetrahydrothiophenes via sulfa-Michael/aldol-type reactions with electrophilic alkenes. Baricordi N, et al.

[Tetrahedron 68(1) , 208-213, (2012)]

More Articles...