2007
DOI: 10.1080/14620316.2007.11512299
|View full text |Cite
|
Sign up to set email alerts
|

Proline metabolism in cherry tomato exocarp in relation to temperature and solar radiation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

3
12
0

Year Published

2009
2009
2020
2020

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 19 publications
(15 citation statements)
references
References 38 publications
3
12
0
Order By: Relevance
“…The insoluble and soluble fractions were washed twice with 960 and 700 mL L −1 ethanol respectively. Both fractions were centrifuged at 3500 × g for 10 min and the supernatants were stored at 4 °C for subsequent determination of free proline30 according to the method proposed by Paquin and Lechasseur 31…”
Section: Methodsmentioning
confidence: 81%
See 1 more Smart Citation
“…The insoluble and soluble fractions were washed twice with 960 and 700 mL L −1 ethanol respectively. Both fractions were centrifuged at 3500 × g for 10 min and the supernatants were stored at 4 °C for subsequent determination of free proline30 according to the method proposed by Paquin and Lechasseur 31…”
Section: Methodsmentioning
confidence: 81%
“…Table 4 shows higher proline contents in cherry tomato fruits at the third sampling in both greenhouses, again suggesting stress in the plant tissue,16, 40 and more specifically under heat and light stress 41, 42. These results agree with those of a previous study in which high temperature and intensified solar radiation provoked a large accumulation of proline in the exocarp of cherry tomato fruits 30. Furthermore, the proline content was greater in the parral greenhouse over the entire production cycle (Table 4), coinciding with higher temperature, solar radiation and VPD values (Fig 1).…”
Section: Resultsmentioning
confidence: 99%
“…This appears to be supported by Jiménez-Bremont et al (2006) who reported that exogenous PAs decreased Pro accumulation in salinity-exposed Phaseolus vulgaris L. The Pro degradation seems to be beneficial in the response to stress, given that the degradation of Pro to glutamate generates reducing equivalents that support mitochondrial oxidative phosphorylation (Hare and Cress 1997). Furthermore, the proline dehydrogenase activity is capable of consuming O2 •- (Hare and Cress 1997), and perhaps could reduce the oxidizing power of the cell and in turn possibly generate ROS (Rosales et al 2007, López-Carrión et al 2008. On the other hand, SNP appears to be capable of mitigating damage associated with salinity stress by reducing oxidative stress and inducing Pro degradation, mechanisms that permit the plant to adapt under these conditions (López-Carrión et al 2008).…”
Section: Resultsmentioning
confidence: 99%
“…For the extraction and assay of PDH, fresh leaves or roots (0.5 g) were homogenized in 50 mM Tris-HCl buffer containing 7 mM MgCl 2 , 0.6 M KCl, 3 mM EDTA, 1 mM dithiothreitol, and 5% (w/v) polyvinylpolypyrrolidone, crosslinked, and adjusted to a pH of 7.4. The homogenate was filtered and centrifuged at 39,000 g n for 20 min at 4°C (Rosales et al, 2007). The supernatant was used to determine PDH activity.…”
Section: Methodsmentioning
confidence: 99%