Overexpression of Δ1-pyrroline-5-carboxylate synthetase increases proline production and confers salt tolerance in transgenic potato plants
By Aïda Hmida-Sayari, R. Gargouri-Bouzid, Amira Bidani, Leila Jaoua, A. Savouré, S. Jaoua. 2005
297 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/077f59950914d166d174579f05424c375dd55b12
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
In Molecular Biology
- Aditya Banerjee
- B. Campbell
- D. Ahmad
- Margaret C. Jewell
- Vinay Kumar
- L. Romero
- M. S. Khan
- M. A. Rosales
In Plant Science
- V. S. Dagaonkar
- L. P. Aurangabadkar
- M. S. Phalak
- Aditya Banerjee
- B. Campbell
- D. Ahmad
- Margaret C. Jewell
- Vinay Kumar
Citations in the corpus
- Transgenic Plants for Abiotic Stress Resistance (2010, background): “…such as potato, where salt tolerance, measured by comparing tuber yield of transgenic lines cultivated in a greenhouse and watered with saline water to that of plants watered with normal tap water, had a less significant effect on tuber yield of transgenic plants than WT (Hmida-Sayari et al. 2005).”
- Role of nitric oxide under saline stress: implications on proline metabolism (2008, background): “Moreover, different studies with transgenic plants show that an increase in the proline content due to the overexpression of enzymes in charge of its synthesis improve salinity tolerance (Hmida-Sayari et al. 2005).”
- Genetic engineering of chickpea (Cicer arietinum L.) with the P5CSF129A gene for osmoregulation with implications on drought tolerance (2009, methodology): “The concentration of MDA was calculated by using an extinction coefficient of 155 mM -1 cm -1 ( Heath and Packer 1968 ).”
- Metabolic and molecular-genetic regulation of proline signaling and itscross-talk with major effectors mediates abiotic stress tolerance in plants (2015, background): “The Pro content in transgenic plants overexpressing P5CS and subjected to salt stress was much higher than in the control plants (Hmida-Sayari et al., 2005).”
- Utilization of genes encoding osmoprotectants in transgenic plants for enhanced abiotic stress tolerance (2015, background): “Triticum aestivum P5CS Salt [33] of its expression was observed in plant growth, tuber morphology and yield [36].”
- Enhanced proline accumulation and salt stress tolerance of transgenic indica rice by over-expressing P5CSF129A gene (2009, background): “Several researchers have demonstrated that over-expression of P5CS genes increases proline production and confers salt tolerance in transgenics in a number of crop plants including rice (Anoop and Gupta 2003; Su and Wu 2004), wheat (Vendruscolo et al. 2007), potato ( Hmida-Sayari et al. 2005 ) and t”
- Research Advances in Mechanisms of Turfgrass Tolerance to Abiotic Stresses: From Physiology to Molecular Biology (2014, unknown): “…has been used effectively to create new germplasm with improved salinity tolerance and to investigate molecular and genetic mechanisms of salinity tolerance in various plant species (Hmida-Sayari et al., 2005; Hu et al., 2006; Rodrı́guez-Rosales et al., 2008; Yang et al., 2009; Mian et al., 2011).”
- Differential responses of the enzymes involved in proline biosynthesis and degradation in drought tolerant and sensitive cotton genotypes during drought stress and recovery (2008, background): “Several repots have demonstrated that overexpression of proline biosynthetic enzymes such as P5CS, P5CR and OAT increases proline production and confers salt and drought tolerance in transgenic plants (Wu et al. 2003 ;D e Ronde et al. 2004; Hmida-Sayari et al.2005; Simon-Sarkadi et al. 2006; Grusz”