𝔖 Bobbio Scriptorium
✦   LIBER   ✦

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

✍ Scribed by Silvia Sagner; Wolfgang Eisenreich; Monika Fellermeier; Christoph Latzel; Adelbert Bacher; Meinhart H. Zenk


Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
250 KB
Volume
39
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Direct formation of 2-C-methyl-d-erythri
✍ Tomohisa Kuzuyama; Shunji Takahashi; Hiroyuki Watanabe; Haruo Seto πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 French βš– 260 KB

1-Deoxy-D-xyluiose 5-phosphate is biotransformed to 2-C-methyl-D-erythritol 4-phosphate in a single step in the presence of NADPH by a new recombinant enzyme named l-deoxy-D-xylulose 5-phosphate reductoisomerase purified from Escherichia coli.

Elucidation of the 2-C-methyl-d-erythrit
✍ Jean-FranΓ§ois Hoeffler; Catherine Grosdemange-Billiard; Michel Rohmer πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 65 KB

Optically pure 1-deoxy-D-xylulose, a key metabolite for feeding experiments in the methylerythritol phosphate pathway for isoprenoid biosynthesis, is conveniently synthesised from 1,2-O-isopropylidene-a-D-xylofuranose or from D-arabinose. This renders labelling with hydrogen isotopes possible.