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Mutagenicity of Maillard reaction products from D-glucose-amino acid mixtures and possible roles of active oxygens in the mutagenicity.

The mutagenicity for Salmonella typhimurium TA100 without S9 mix of Maillard reaction products (MRP) obtained from equimolar amounts of glucose and amino acids under different pHs was investigated. MRP derived from arginine and lysine exhibited the strongest mutagenicity, and weaker mutagenicity was shown by the mixtures with alanine, serine, threonine and monosodium glutamate. MRP from proline and cysteine had no detectable mutagenicity. Furthermore, glucose-arginine and glucose-lysine reaction mixtures, which presented a marked mutagenicity, showed pH- and browning intensity-dependent expression of their mutagenic activities. The mutagenicity of MRP, especially glucose-arginine and glucose-lysine mixtures, was significantly suppressed by active oxygen scavengers such as cysteine, mannitol, alpha-tocopherol, catalase and superoxide dismutase (SOD) and reducing agents such as sodium bisulfite and glutathione. Among these desmutagenic factors tested, cysteine, catalase, sodium bisulfite and glutathione had higher desmutagenic activities than the others. Accordingly, it is assumed that the mutagenicity of MRP is due to the direct action of low-molecular-weight compounds such as carbonyls and heterocyclics produced by the Maillard reaction and is enhanced by active oxygens, especially singlet oxygen and hydrogen peroxide derived from their autoxidation.

Amino Acids↗

Apparent and true amino acid digestibility of a crystalline amino acid mixture and of casein: comparison of values obtained with ileal-cannulated pigs and cecectomized cockerels.

Six ileal-cannulated pigs that averaged 100 kg BW and 16 adult cecectomized cockerels that averaged 2.35 kg BW were used to determine apparent and true digestibilities of amino acids (AA) in a complete crystalline AA mixture and in casein. A protein-free (PF) diet was included as a treatment to estimate endogenous AA losses. Fasted cockerels were compared to cockerels fed PF diets for calculation of true digestibility of AA in cockerels. For the AA diet, true digestibility of indispensable AA in the pig ranged from a low of 97.2% for leucine to a high of 100.5% for arginine (Arg). True digestibility of indispensable AA in casein ranged from a low of 93.5% for isoleucine (Ile) to a high of 99.9% for Arg. Correcting for endogenous losses increased digestibilities of lysine (Lys) and threonine (Thr) in pigs fed the AA diet by 2.4 and 7.1%, respectively, and increased Lys and Thr digestibility in pigs fed the casein diet by 1.8 and 6.1%, respectively. Feeding a PF diet to chickens to correct for endogenous losses resulted in higher true digestibility values for all AA with the exception of tryptophan, methionine, and Arg than those obtained using fasted animals. True digestibilities of Thr were 88.3 and 86.6% for AA and casein diets, respectively, using fasted controls but were 97.5 and 94.5% when the PF control was used. Proline digestibility was increased (P < .05) substantially in both pigs and cockerels when the PF control was used to correct for endogenous AA losses. Regardless of species, Ile in casein had a lower true digestibility value than any other indispensable AA. The results of this study indicated that true digestibilities of AA in a mixture of crystalline AA and in casein are essentially 100% in both pigs and cockerels.

Amino Acids↗