EC Number   |
Substrates |
Organism |
Products |
Reversibility |
|---|
  4.2.3.B68 | geranylgeranyl diphosphate |
- |
Allokutzneria albata |
spiroalbatene + diphosphate |
- |
? |
| 4.2.3.B68 | geranylgeranyl diphosphate |
- |
Allokutzneria albata DSM 44149 |
spiroalbatene + diphosphate |
- |
? |
| 4.2.3.B68 | more |
for spiroalbatene synthase, the pH- and Mn2+-dependent formation of the side product thunbergol is observed, which is biosynthetically linked to spiroalbatene |
Allokutzneria albata |
? |
- |
? |
| 4.2.3.B68 | more |
the defined stereochemical anchors at the deuterated carbon atoms are used to solve the absolute configuration of spiroalbatene by determining the relative configurations of the stereospecifically deuterated products. Enzyme SaS can potentially yield ent-(S)-(+)-cembrene A from intermediate A.. Product identification by NMR spectroscopic analysis. Development of a method that uses the stereoselectively deuterated precursors (S)- and (R)-(1-13C,1-2H)FPP and (S)- and (R)-(1-13C,1-2H)GPP to determine the absolute configurations of terpenes |
Allokutzneria albata |
? |
- |
? |
| 4.2.3.B68 | more |
for spiroalbatene synthase, the pH- and Mn2+-dependent formation of the side product thunbergol is observed, which is biosynthetically linked to spiroalbatene |
Allokutzneria albata DSM 44149 |
? |
- |
? |
| 4.2.3.B68 | more |
the defined stereochemical anchors at the deuterated carbon atoms are used to solve the absolute configuration of spiroalbatene by determining the relative configurations of the stereospecifically deuterated products. Enzyme SaS can potentially yield ent-(S)-(+)-cembrene A from intermediate A.. Product identification by NMR spectroscopic analysis. Development of a method that uses the stereoselectively deuterated precursors (S)- and (R)-(1-13C,1-2H)FPP and (S)- and (R)-(1-13C,1-2H)GPP to determine the absolute configurations of terpenes |
Allokutzneria albata DSM 44149 |
? |
- |
? |
