Isoprenoid biosynthesis via the methylerythritol phosphate pathway - Mechanistic investigations of the 1-deoxy-D-xylulose 5-phosphate reductoisomerase

被引:81
作者
Hoeffler, JF [1 ]
Tritsch, D [1 ]
Grosdemange-Billiard, C [1 ]
Rohmer, M [1 ]
机构
[1] Univ Strasbourg, CNRS, Inst Le Bel, F-67070 Strasbourg, France
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 2002年 / 269卷 / 18期
关键词
isoprenoid; 2-C-methyl-D-erythritol; 4-phosphate; 1-deoxyxylulose 5-phosphate reductoisomerase; 2-C-methyl-D-erythrose;
D O I
10.1046/j.1432-1033.2002.03150.x
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 1-deoxyxylulose 5-phosphate reductoisomerase (DXR, EC 1.1.1.267) catalyzes the conversion of 1-deoxy-d-xylulose 5-phosphate (DXP) into 2-C -methyl-d-erythritol 4-phosphate (MEP). This transformation is a two-step process involving a rearrangement of DXP into the putative intermediate 2-C -methyl-d-erythrose 4-phosphate followed by a NADPH-dependent reduction of the latter aldehyde. By using [1-(13) C]DXP as a substrate, the rearrangement of DXP into [5-(13) C]2-C -methyl-d-erythrose 4-phosphate was shown to be NADPH dependent, although it does not involve areduction step. The putative aldehyde intermediate, obtained by chemical synthesis, was converted into MEP by the DXR in the presence of NADPH and into DXP in the presence of NADP(+) , indicating the reversibility of the reaction catalyzed by the DXR. This reversibility was confirmed by the conversion of MEP into DXP in the presence of NADP(+) . The equilibrium was, however, largely displaced in favour of the formation of MEP. The reduction step required the presence of a divalent cation such as Mg2+ or Mn2+ .
引用
收藏
页码:4446 / 4457
页数:12
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