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 |
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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
- Chemistry(all)