3.8 Article

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

Journal

EUROPEAN JOURNAL OF BIOCHEMISTRY
Volume 269, Issue 18, Pages 4446-4457

Publisher

WILEY
DOI: 10.1046/j.1432-1033.2002.03150.x

Keywords

isoprenoid; 2-C-methyl-D-erythritol 4-phosphate; 1-deoxyxylulose 5-phosphate reductoisomerase; 2-C-methyl-D-erythrose 4-phosphate

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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+ .

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