Green tea polyphenols: Novel irreversible inhibitors of dopa decarboxylase

被引:45
作者
Bertoldi, M [1 ]
Gonsalvi, M [1 ]
Voltattorni, CB [1 ]
机构
[1] Univ Verona, Fac Med & Chirurg, Sez Chim Biol, Dipartimento Sci Neurol & Vis, I-37134 Verona, Italy
关键词
Dopa decarboxylase; pyridoxal 5'-phosphate; inactivation; green tea gallocatechins;
D O I
10.1006/bbrc.2001.4945
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The green tea gallocatechins, (-)-epigallocatechin-3-O-gallate (EGCG), and (-)-epigallocatechin (EGC) were found to be inhibitors of Dopa decarboxylase (DDC). EG;CG; and EGC inactivate the enzyme in both a time- and concentration-dependent manner and exhibit saturation of the rate of inactivation at high concentrations, with efficiency of inactivation values (k(inact)/K-i) of 868 and 1511 M-1 min(-1), respectively. In contrast, gallic acid behaves as a weak inhibitor of DDC. Protection against inactivation by EGCG; and EG;C was observed in the presence of the active site-directed inhibitor D-Dopa. Either EGCG or EGC induce changes in the absorbance and CD bands of the visible spectrum of enzyme-bound PLP. Taken together, these findings indicate the active site nature of the interaction of DDC with both polyphenols. On the basis of the properties of the EGCG-inactivated enzyme, it can be suggested that inactivation could be ascribed to a covalent modification of not yet identified residue(s) of the active site of DDC. (C) 2001 Academic Press.
引用
收藏
页码:90 / 93
页数:4
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