Methylated derivatives of l-tyrosine in reaction catalyzed by l-amino acid oxidase: isotope and inhibitory effects

L-Amino acid oxidase (LAAO) is widely distributed in nature and shows important biological activity. It induces cell apoptosis and has antibacterial properties. This study was designed to investigate the effect of methyl substituent on its activity as methylated derivatives of L-tyrosine, labelled with short-lived B1 emitters, have been used in oncological diagnostics. To study isotope effects in the oxidative deamination of O-methyl-L-tyrosine, the deuterated sotopomer, i.e. O-methyl-[2-2H]-L-tyrosine, was synthesized by isotope exchange, catalyzed enzymatically by tryptophanase. Isotope effects were determined using the spectrophotometric non-competitive method. The values of isotope effects indicate that the a-C–H bond cleavage occurs in the rate determining step of the investigated reaction and a-hydrogen plays a role in the substrate binding process at the enzyme active site. The inhibitory effect on LAAO activity was studied with a-methyl-L-tyrosine and N-methyl-L-tyrosine. The mode of inhibition was determined based on Lineweavear–Burk plots intersections. a-Methyl-Ltyrosine has been found a mixed type inhibitor of the investigated enzyme, whereas N-methyl-L-tyrosine is a non-competitive inhibitor of LAAO.