Cloned (Comment) | Organism |
---|---|
gene LUS1, semi-quantitative RT-PCR enzyme expression analysis | Glycyrrhiza glabra |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Glycyrrhiza glabra | Q764T8 | - |
- |
Source Tissue | Comment | Organism | Textmining |
---|---|---|---|
root | - |
Glycyrrhiza glabra | - |
seedling | - |
Glycyrrhiza glabra | - |
stolon | - |
Glycyrrhiza glabra | - |
Synonyms | Comment | Organism |
---|---|---|
LUS | - |
Glycyrrhiza glabra |
Organism | Comment | Expression |
---|---|---|
Glycyrrhiza glabra | semi-quantitative RT-PCR assays to evaluate the gene expression levels of sequalene synthase (SQS), beta-amyrin synthase (bAS), lupeol synthase (LUS) and cycloartenol synthase (CAS) during stress of seedlings. The expression of the LUS gene is not detectable. Due to osmotic stress, the gene expression levels of SQS and bAS are increased, whereas those of CAS are relatively unchanged at the seedling stage. At the adult plant stage, the expression levels of SQS and bAS are increased under drought stress conditions, whereas the gene expression level of CAS remain relatively constant. controlled drought stress up-regulates the expression of key genes involved in the biosynthesis of triterpenoid saponins and directly enhances the production of secondary metabolites, including glycyrrhizin, in liquorice plant | additional information |
General Information | Comment | Organism |
---|---|---|
metabolism | the enzyme is involved in the glycyrrhizin biosynthetic pathway. Controlled drought stress up-regulates the expression of key genes involved in the biosynthesis of triterpenoid saponins and directly enhances the production of secondary metabolites, including glycyrrhizin, in liquorice plants | Glycyrrhiza glabra |