Palcic M M, Antoun M, Tanizawa K, Soda K, Floss H G
J Biol Chem. 1985 May 10;260(9):5248-51.
The steric course of the replacement of the anthranilyl group of kynurenine by hydrogen was determined by conversion of (2S,3R)- and (2S,3S)-[3-3H]kynurenine into alanine with kynureninase in D2O, followed by chirality analysis of the alanine methyl group. To minimize enolization, the labeled substrates were generated in situ from the corresponding stereospecifically tritiated tryptophan species. The result, replacement in a retention mode, together with the finding that tritium from the alpha-position of the substrate is recycled and appears both at C alpha and C beta of the product suggests a single base mechanism and an active site geometry of the pyridoxal phosphate-substrate complex in which H alpha and the beta-substituent are syn oriented.
通过在重水中用犬尿氨酸酶将(2S,3R)-和(2S,3S)-[3-³H]犬尿氨酸转化为丙氨酸,然后对丙氨酸甲基进行手性分析,确定了犬尿氨酸的邻氨基甲酰基被氢取代的立体过程。为了尽量减少烯醇化,标记的底物由相应的立体特异性氚化色氨酸物种原位生成。结果表明,取代以保留模式进行,同时发现底物α-位的氚被循环利用并出现在产物的Cα和Cβ处,这表明存在单一碱机制以及磷酸吡哆醛-底物复合物的活性位点几何结构,其中Hα和β-取代基呈顺式取向。