Abstract

Abstract An extensively boiled supernatant2 (S2) fraction from beef round steak contains two major Salmonella frameshift mutagens, designated as HPLC peaks A and B. These same mutagens arise, but in different proportions, when S2 is boiled with creatine phosphate (CP), and they are produced in much greater quantities from a boiled mixture of S2 + L‐tryptophan (Trp) + CP + FeSO4 (S2 ∗). A third mutagen, peak C, is also generated in the S2 ∗ mixture. Mutagen peaks A, B, and C were purified to homogeneity and shown by their absorption spectra, mass fragmentation patterns, and other data to be 2‐amino‐3‐methylimidazo[4,5‐f]quinoline (IQ), 3‐amino‐l‐methyl‐5H‐pyrido[4,3‐b]‐indole (Trp‐P‐2), and 3‐amino‐l,4‐dimethyl‐5H‐pyrido[4,3‐b]indole (Trp‐P‐1), respectively. This is the first demonstration that IQ, Trp‐P‐2, and Trp‐P‐1 can form under aqueous conditions at 100°C from reactions between low molecular wt precursors that are present in meat juice. Further simplification of and studies with the S2 fraction of be...

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