Table 1.
Examples of engineered cellular/subcellular localization of phytochemical production in Nicotiana sp.
| Host plant | Localization | Engineering strategy | Compound class | Compound accumulation | References |
|---|---|---|---|---|---|
| N. benthamiana | Synthetic hydrophobic organelles | Transient expression; fusing terpenoid enzymes to a microalgal lipid droplet surface protein | Diterpenoids | 2.5 fold increase of target diterpenoids/diterpenoids acids | Sadre et al., 2019 |
| N. benthamiana | Lipid bodies | Transient expression; Co-expression of α-bisabolol synthase with fatty acids biosynthesis regulators | Sesquiterpenoids | 2–4 fold increase of; α-bisabolol, (E)-β -caryophyllene and α-barbatene. | Delatte et al., 2018 |
| N. tabacum | Plastids | Stable transformation; plastome and nuclear transformation with artemisinic acid biosynthetic genes and other enzymes known to affect the metabolic flux | Sesquiterpenoids (artemisinic acid) | Accumulation of more than 120 mg/kg FW of Artemisinic acid. | Fuentes et al., 2016 |
| N. tabacum | Glandular trichomes | Stable transformation; Casbene synthase/Trichome-specific promoters | Diterpenoids (casbene) | Accumulation of 1 mg/g FW of casbene | Tissier et al., 2012 |
| N. sylvestris | Glandular trichomes | Stable transformation; taxadiene synthase/Trichome-specific promoters | Diterpenoids (Taxadiene) | Accumulation of 100 μg/g FW of taxadiene | Tissier et al., 2012 |