Ono Kazutoshi, Yanagida Kazuki, Oikawa Tadao, Ogawa Tadashi, Soda Kenji
Department of Biotechnology, Faculty of Engineering, Kansai University, Suita-Shi, Osaka-Fu, Japan.
Phytochemistry. 2006 May;67(9):856-60. doi: 10.1016/j.phytochem.2006.02.017. Epub 2006 Apr 17.
We demonstrated several kinds of D-amino acids in plant seedlings, and moreover alanine racemase (E.C.5.1.1.1) in alfalfa (Medicago sativa L.) seedlings. This is the first evidence for the presence of amino acid racemase in plant. The enzyme was effectively induced by the addition of L- or D-alanine, and we highly purified the enzyme to show enzymological properties. The enzyme exclusively catalyzed racemization of L- and D-alanine. The K(m) and V(max) values of enzyme for L-alanine were 29.6 x 10(-3) M and 1.02 mol/s/kg, and those for D-alanine are 12.0 x 10(-3) M and 0.44 mol/s/kg, respectively. The K(eq) value was estimated to be about 1 and indicated that the enzyme catalyzes a typical racemization of both enantiomers of alanine. The enzyme was inactivated by hydroxylamine, phenylhydrazine and some other pyridoxal 5'-phosphate enzyme inhibitors. Accordingly, the enzyme required pyridoxal 5'-phosphate as a coenzyme, and enzymologically resembled bacterial alanine racemases studied so far.
我们在植物幼苗中发现了几种D-氨基酸,此外还在苜蓿(Medicago sativa L.)幼苗中发现了丙氨酸消旋酶(E.C.5.1.1.1)。这是植物中存在氨基酸消旋酶的首个证据。该酶可通过添加L-或D-丙氨酸有效诱导产生,我们对其进行了高度纯化以展示其酶学性质。该酶仅催化L-和D-丙氨酸的消旋作用。该酶对L-丙氨酸的K(m)和V(max)值分别为29.6×10(-3) M和1.02 mol/s/kg,对D-丙氨酸的K(m)和V(max)值分别为12.0×10(-3) M和0.44 mol/s/kg。K(eq)值估计约为1,表明该酶催化丙氨酸两种对映体的典型消旋作用。该酶可被羟胺、苯肼和其他一些磷酸吡哆醛酶抑制剂灭活。因此,该酶需要磷酸吡哆醛作为辅酶,在酶学性质上与迄今为止研究的细菌丙氨酸消旋酶相似。