Biosynthesis of 2-C-methyl-D-erythritol in plants by rearrangement of the terpenoid precursor, 1-deoxy-D-xylulose 5-phosphate

DOI: 10.1016/S0040-4039(98)00296-2

Source and publish data:

Tetrahedron Letters p. 2091 - 2094 (1998)

Update date:2022-08-30

Topics:

Authors:

Sagner, Silvia

Eisenreich, Wolfgang

Fellermeier, Monika

Latzel, Christoph

Bacher, Adelbert

Zenk, Meinhart H.

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Article abstract of DOI:10.1016/S0040-4039(98)00296-2

Leaves of Liriodendron tulipifera convert 1-deoxy-D-xylulose to 2-C- methyI-D-erythritol via: a skeletal-rearrangement reminiscent of the formation of terpene precursors from 1-deoxy-D-xylulose. The data suggest that 2-C-methyl-D-erythritol 4-phosphate is either an intermediate or a side product of the deoxyxylulose 4-phosphate pathway of terpenoid biosynthesis.

Full text of DOI:10.1016/S0040-4039(98)00296-2

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