Abstract
The cyclopentane ring of calditol, a characteristic lipid molecule of Sulfolobus, a major thermophilic Archaea, was biosynthesized from glucose directly, and galactose was converted to calditol with a similar extent to glucose. This finding indicates the possibility of the "cyclase" enzyme of the calditol carbocycle and the involvement of catalytic oxidoreduction at the C-4 of glucose with broad specificity.
| Original language | English |
|---|---|
| Pages (from-to) | 1230-1231 |
| Number of pages | 2 |
| Journal | Chemistry Letters |
| Volume | 35 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - Nov 5 2006 |
All Science Journal Classification (ASJC) codes
- General Chemistry
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