Table 1.
Role of ascorbate in plant growth and development and abiotic stress tolerance
| Enzyme/protein | Target plant | Gene | Gene source | Type of genetic manipulation | Ascorbate content | Phenotypic changes | Reference |
|---|---|---|---|---|---|---|---|
| GDP-mannose pyrophosphorylase | Tobacco | GMPase | Tomato | Overexpression | 2.0–4.0-fold increase | Increased tolerance to temperature stress | Wang et al. 2011 |
| Phosphomannose Isomerase | Arabidopsis | PMI1 | Arabidopsis | RNAi | 0.47–0.65-fold decrease | No phenotypic changes under normal growth conditions in both mutants | Maruta et al. 2008 |
| PMI2 | – | T-DNA knockout | No change | ||||
| Phosphomannomutase | Tobacco | NbPMM | Tobacco | VIGS | Up to 3.0-fold decrease | – | Qian et al. 2007 |
| Arabidopsis | NbPMM | Tobacco | VVMEE | 0.2–0.5-fold increase | – | ||
| AtPMM | Arabidopsis | Overexpression | 0.25–0.33-fold increase | Increased tolerance to MV stress | |||
| Tobacco | PMM | Acerola | Overexpression | 2.0-fold increase | – | Badejo et al. 2009 | |
| VTC4/Myoinositol monophosphatase (IMP) | Arabidopsis | VTC4 | – | T-DNA knockout | 0.61–0.75-fold decrease | 22.4% –34% decreases in myoinositol content | Torabinejad et al. 2009 |
| Slow seed germination under control conditions | |||||||
| Slightly hypersensitive to ABA and NaCl during seed germination | |||||||
| GDP-L-galactose phosphorylase | Arabidopsis | vtc5-1 and vtc5-2 | Arabidopsis | T-DNA knockout | 0.2-fold decrease | Plant growth retardation and bleaching of the cotyledons | Dowdle et al. 2007 |
| L-Galactose dehydrogenase | Tobacco (BY–2 cells) | L–GalLDH | Tobacco | Overexpression | 1.5–2.0-fold increase | Higher mitotic index in cells | Tokunaga et al. 2005 |
| Reduced browning and cells death of cultures | |||||||
| Increased tolerance to MV | |||||||
| L-galactono-1,4-lactone dehydrogenase | Tobacco (BY–2 cells) | GLDH | Tobacco | Antisense downregulation | 0.30-fold decrease | Adversely effected plant cell division, growth and structure of plant cell | Tabata et al. 2001 |
| Tobacco | RrGalLDH | Rosa roxburghii | Overexpression | 2.1-fold increase | Enhanced tolerance to salt stress | Liu et al. 2013a | |
| Monodehydroascorbate reductase | Tobacco | AtMDAR1 | Arabidopsis | Overexpression | Up to 2.2-fold increase | Enhanced tolerance to ozone, salt and PEG stresses | Eltayeb et al. 2007 |
| Tobacco | Am-MDAR | Avicennia marina | Overexpression | Up to 2.0-fold increase | Increased tolerance to salt stress | Kavitha et al. 2010 | |
| Tobacco | MDAR-OX | Arabidopsis | Overexpression | Up to 1.1-fold increase | No change in Aluminium tolerance | Yin et al. 2010 | |
| Dehydroascorbate reductase | Tobacco | DHAR-OX | Arabidopsis | Overexpression | Up to 1.3-fold increase | Increased tolerance to Al stress | Yin et al. 2010 |
| Tobacco | DHAR | Arabidopsis | Overexpression | 1.9–2.1-fold increase | Enhanced tolerance to ozone, drought and salinity | Eltayeb et al. 2006 | |
| Tobacco | DHAR | Wheat | Overexpression | 2.1-fold increase | Increased ozone tolerance and NPR | Chen and Gallie 2005 | |
| Tobacco | Antisense downregulation | 0. 29-fold decrease | Substantially reduced stomatal area and low NPR | ||||
| Tobacco | DHAR | Human | Overexpression | No significant change | Enhanced tolerance to low temperature and NaCl | Kwon et al. 2003 | |
| Ascorbate peroxidase | Tobacco | tAPx | Tobacco | Overexpression | No change | Increased tolerance to MV and chilling stresses under light conditions | Yabuta et al. 2002 |
| Tobacco/ Spinach | Antisense downregulation | – | Plants failed to grow | ||||
| Arabidopsis | HvAPX1 | Barley | Overexpression | – | Increased tolerance to salt stress | Xu et al. 2008 | |
| Arabidopsis | OsAPXa and OsAPXb | Rice | Overexpression | – | Increased tolerance to salt stress | Lu et al. 2007 | |
| Tobacco | CAPOA1 | Pepper | Overexpression | – | Increased plant growth | Sarowar et al. 2005 | |
| Increased tolerance to MV stress | |||||||
| Tobacco BY-2 cells | cAPX | Arabidopsis | Antisense downregulation | No change | Increased tolerance against heat and salt stresses | Ishikawa et al. 2005 | |
| Tobacco | StAPX | Tomato | Overexpression | – | Improved seed germination | Sun et al. 2010a | |
| Increased tolerance to salt and osmotic stresses | |||||||
| Rice | Apx1/ Apx2 | Rice | RNAi (Apx1+ Apx2) | Up to 1.5-fold decrease | No change in plant growth and development | Rosa et al. 2010 | |
| Increased tolerance to aluminium | |||||||
| RNAi (Apx1 or Apx2) | – | Produced semi-dwarf phenotype | |||||
| Rice | OsAPx-R | Rice | RNAi | – | Delayed plant development | Lazzarotto et al. 2011 | |
| Rice | OsAPXa | Rice | Overexpression | – | Increased spikelet fertility under cold stress | Sato et al. 2011 | |
| Rice | Osapx2 | Rice | Overexpression | – | Enhanced stress tolerance | Zhang et al. 2013 | |
| Sensitive to abiotic stresses | |||||||
| – | T-DNA knockout | – | Semi-dwarf seedlings, yellow-green leaves, leaf lesion-mimic and seed sterility | ||||
| Alfalfa | Osapx2 | Rice | Overexpression | – | Increased salt resistance | Guan et al. 2012 | |
| Tomato | cAPX | Pea | Overexpression | – | Enhanced tolerance to UV-B and heat stresses | Wang et al. 2006 | |
| Tomato | cAPX | Pea | Overexpression | – | Enhanced tolerance to chilling and salt stresses | Wang et al. 2005 | |
| Tomato | LetAPX | Tomato | Antisense downregulation | No significant change | Transgenic plants photosynthetically less efficient and sensitive to chilling stress | Duan et al. 2012b | |
| Ascorbate oxidase | Tobacco | AAO | Cucumber | Overexpression | No change | Plants become susceptible to ozone | Sanmartin et al. 2003 |
| Tobacco | AAO | Cucumber | Overexpression | No change | Increased drought tolerance due to reduced stomatal conductance | Fotopoulos et al. 2008 | |
| Tobacco | AAO | Pumpkin | Overexpression | 2.0-fold increase in apoplastic ASA | Number of smaller flowers significantly increased 6% to 14% reduction of in seed weight | Pignocchi et al. 2003 | |
| Tobacco | Antisense downregulation | 2.0-fold increase in apoplastic ASA | No significant changes | ||||
| Tobacco | AAO | Tobacco | Overexpression | – | Severe inhibition of germination and seed yield under high salinity | Yamamoto et al. 2005 | |
| Tobacco | AAO | Tobacco | Antisense downregulation | – | Increased tolerance to salt stress | Yamamoto et al. 2005 | |
| – | Increased seed yield under salt stress | ||||||
| Arabidopsis | AAO | – | T-DNA knockout | Increased tolerance to salt stress | |||
| Increased seed yield under salt stress | |||||||
| Myoinositol oxygenase | Rice | OsMIOX | Rice | Overexpression | No change | Increased drought tolerance | Duan et al. 2012a |
| ASA mannose pathway regulator 1 | Arabidopsis | AMR1 | – | T-DNA knockout | 2.0–3.0-fold increase | Increased ozone tolerance | Zhang et al. 2009 |
APx-R, APX-related; CAPOA1, Capsicum annuum ascorbate peroxidase-like 1 gene; MV, methyl viologen; NPR, net photosynthetic rate; PEG, polyethylene glycol; RNAi, RNA interference; VIGS, Virus-induced gene silencing; VVMEE, Viral-vector-mediated ectopic- expression.