From: Role of L-ascorbate in alleviating abiotic stresses in crop plants
Enzyme | Target plant | Gene | Gene source | Type of genetic manipulation | Ascorbate content | Phenotypic change | Reference |
---|---|---|---|---|---|---|---|
GDP-l-galactose phosphorylases | Tomato | GGP/ VTC2 | Actinidia chinensis | Overexpression | 3.0–6.0-fold increase in fruits | – | Bulley et al. 2012 |
Strawberry |  |  | Overexpression | 2.0-fold increase in fruits | – | ||
Potato |  | Potato/Arabidopsis | Overexpression | Up to 3.0-fold increase in tuber | – | ||
GDP-mannose pyrophosphorylase | Potato | GMPase | Potato | Antisense downregulation | 0.88–1.44-fold reduction in leaves | Dark spots on leaf veins and stems | Keller et al. 1999 |
 |  |  |  | 0.56-fold reduction in tubers | Early senesce | ||
GDP-Mannose 3’,5’-epimerase | Tomato | SlGME1 | Tomato | Overexpression | Up to 1.42-fold increase in leaves | Improved tolerance to various abiotic stresses such as cold, salt and MV | Zhang et al. 2011 |
 |  |  |  | Up to 1.60-fold increase in fruits |  | ||
 | SlGME2 |  | Overexpression | Up to 1.37-fold increase in leaves |  | ||
 |  |  |  | Up to 1.24-fold increase in fruits |  | ||
L-galactose guanyltransferase | Tobacco | GalT | Kiwifruit | Transient expression (leaves) | Up to 3.0-fold increase | – | Laing et al. 2007 |
L-Galactose dehydrogenase | Tobacco | L-GalDH | Arabidopsis | Overexpression | No change | – | Gatzek et al. 2002 |
Arabidopsis |  | Arabidopsis | Antisense downregulation | 0.7-fold decrease | – |  | |
L-galactono-1,4-lactone dehydrogenase | Rice | L-GalLDH | Rice | RNAi | 0.6–0.87-fold decrease | Slow plant growth rate and poor seed set | Liu et al. 2011 |
 |  | Rice | Overexpression | Up to 1.48-fold increase | Increased NPR and higher seed set | ||
Tomato | SlGalLDH | Tomato | RNAi | No change | Slow plant growth rate | Alhagdow et al. 2007 | |
 |  |  |  |  | Strong reduction in leaf and fruit size | ||
Rice | L-GalLDH | Rice | RNAi | 0.3– 0.5-fold decrease | Slow growth rate, reduced tiller number, decreased NPR and premature senescence | Liu et al. 2013b | |
L-gulono-c-lactone oxidase | Arabidopsis | GLOase | Rat | Overexpression | Up to 2.0–3.0-fold increase | – | Radzio et al. 2003 |
Lettuce | GLOase | Rat | Overexpression | 4.0–7.0-fold increase | – | Jain and Nessler 2000 | |
Tobacco |  |  | Overexpression | Up to 7.0-fold increase | – | ||
Tomato | GLOase | Rat | Overexpression | 1.5-fold increase in fruits | Enhanced tolerance to MV, NaCl, and mannitol | Lim et al. 2012 | |
Potato | GLOase | Rat | Overexpression | Up to 1.41-fold increase | Enhanced tolerance to MV, NaCl, and mannitol | Hemavathi et al. 2010 | |
D-galacturonic acid reductase | Arabidopsis | GalUR | Strawberry | Overexpression | 2.0–3.0-fold increase | – | Agius et al. 2003 |
Potato | GalUR | Strawberry | Overexpression | 1.6–2.0-fold increase | Enhanced tolerance to MV, NaCl, and mannitol | Hemavathi et al. 2009 | |
Tomato (Hairy Roots) | GalUR | Strawberry | Overexpression | 2.5-fold increase | High growth rate | Wevar Oller et al. 2009 | |
Monodehydroascorbate reductase | Tomato | LeMDAR | Tomato | Overexpression | Up to 1.18-fold increase | Enhanced tolerance to temperature (low/high) and MV stresses | Li et al. 2010 |
 |  |  |  |  | High NPR | ||
 |  |  | Antisense downregulation | Up to 1.3-fold decrease | Susceptible to various abiotic stresses | ||
Tomato | MDAR | Tomato | Overexpression | 0.7-fold reduced in fruits | – | Haroldsen et al. 2011 | |
 |  |  |  | No change in leaves |  | ||
Dehydroascorbate reductase | Tomato | DHAR | Tomato | Overexpression | 1.6-fold increase in fruits | – | Haroldsen et al. 2011 |
 |  |  |  | No change in leaves |  | ||
Maize (Kernels) | DHAR | Wheat | Overexpression | 6.0-fold increase | – | Naqvi et al. 2009 | |
Maize | DHAR | Wheat | Overexpression | Up to 1.8-fold (leaves) and 1.9–fold (kernels) increase | – | Chen et al. 2003 | |
Tobacco | DHAR | Wheat | Overexpression | 2.2–3.9-fold increase | – | Chen et al. 2003 | |
Tobacco | DHAR | Rice | Overexpression | Up to 1.6-fold increase | Enhanced tolerance to salt and cold stresses | Le Martret et al. 2011 | |
Tobacco | DHAR | Human | Overexpression (chloroplasts) | 1.1-fold increase | Increased SOD and APX activities in conjunction via triple gene construct | Lee et al. 2007 | |
 |  |  |  |  | Increased tolerance to MV and NaCl induced stress | ||
Potato | DHAR | Sesame | Overexpression | 1.1–1.3-fold increase in tuber with patatin promoter | – | Goo et al. 2008 | |
 |  |  | Overexpression | 1.5- and 1.6-fold increase in leaves and tuber respectively, with CaMV35S promoter | 1.5- and 1.6-fold increase in leaves and tuber respectively, with CaMV35S promoter | ||
Potato | StDHAR1 | Potato | Overexpression (Cytosol) | Up to 0.69-fold increase in leaves | – | Qin et al. 2011 | |
 |  |  |  | Up to 0.29-fold increase in tubers |  | ||
 |  |  |  | Up to 0.50-fold increase in leaves | – | ||
 | StDHAR2 |  | Overexpression (Chloroplast) | No significant change in tubers |  | ||
Arabidopsis | DHAR1 | Rice | Overexpression | > 1.4-fold increase | Enhanced tolerance to salt stress | Ushimaru et al. 2006 | |
Arabidopsis | DHAR | Arabidopsis | Overexpression | 2.0–4.25-fold increase | Enhanced tolerance to high–light and high–temperature stress | Wang et al. 2010 | |
Myoinositol oxygenase | Arabidopsis | miox4 | Arabidopsis | Overexpression | 2.0–3.0-fold increase | – | Lorence et al. 2004 |