Response of two lines of Medicago ciliaris to Fe deficiency under saline conditions

The aim of this research was to study the responses of two lines of Medicago ciliaris: TN11.11 and TN8.7 to iron deficiency under saline conditions. However; the paper showed also the results of a preliminary study which report the contrastive responses of the two lines to salinity. We found that plant growth and chlorophyll content of TN11.11 line were more affected by salinity than TN8.7. The severity of symptoms was linked to the sodium accumulation in shoots as well as a limitation of potassium uptake. Our data allowed us to note that TN8.7 line is less sensitive and can better cope with the salinity. Concerning the effect of salinity on iron deficiency responses, we noted that root PM H +-ATPase and FCR activities were reduced when iron deficiency was associated with salinity. This probably explained the decrease of Fe uptake. On the contrary, PEPC activity was not affected

Variability of metabolic responses and antioxidant defence in two lines of Medicago ciliaris to Fe deficiency

The aim of this work was to evaluate the effects of Fe deficiency on the activity of several metabolic enzymes (PEPC, PK, PFK, G6PDH and G3PDH), along with the function of the antioxidant enzymes (SK, SDH and PAL) in two lines of Medicago ciliaris, TN11.11 and TN8.7. Plants were grown in a greenhouse under controlled conditions. After germination and pre-treatment, plants were transferred for hydroponic culture. Three treatments were used: 30 \u3bcM Fe (+Fe), 0 \u3bcM Fe (-Fe) and 30 \u3bcM Fe + 10 mM NaHCO3 (+Bic.). Our results showed that all the enzymatic activities increased in extracts of Fe-deficient roots when compared to the control. The above increases in the activity were particularly evident for the bicarbonate-treated roots of TN11.11. PEPC activity was increased by 277% in TN11.11 plants with the addition of bicarbonate to the nutrient solution. Our results indicate also that, in the two lines of Medic, the activity of SK, SDH and PAL in leaves and roots were increased under Fe deficiency (either direct or induced by bicarbonate), to a greater extent in TN11.11 plants. Furthermore, a considerable increase in lipid peroxidation of roots and leaves of Fe-deficient plants was observed in TN8.7 when compared to TN11.11 plants. Our data suggest that the TN11.11 line is more effective in overcoming Fe deficiency than TN8.7. The tolerance of TN11.11 to Fe deficiency is related to its ability to modulate the carbohydrate metabolism and to increase secondary metabolism pathways

Responses of two ecotypes of Medicago ciliaris to direct and bicarbonate-induced iron deficiency conditions

Our study investigates the effect of iron deficiency on morpho-physiological and biochemical parameters of two Medicago ciliaris ecotypes (Mateur TN11.11 and Soliman TN8.7). Iron deficiency was imposed by making plants grow, either in an iron free or by the addition of CaCO 3/NaHCO3 to the Hoagland nutrient solution. Our results showed that both true and bicarbonate Fe-deficiency induced the characteristic iron-chlorosis symptoms, although the intensity of the symptoms was ecotype-dependent. This variability in tolerance to iron deficiency was also displayed by other morphological parameters such as root biomass and chlorophyll concentration. Besides, iron chlorosis induced an increase in biochemical parameters: the iron reducing capacity (measured in vivo on root segments and in vitro on plasma membrane enriched vesicles) and rhizosphere acidification by enhancement of H+-ATPase activity were more pronounced in Mateur ecotype. These findings suggest that Soliman ecotype was more sensitive than Mateur one to iron chlorosis

Root exudation and rhizosphere acidification by two lines of Medicago ciliaris in response to lime-induced iron deficiency

The main objective of this work was to compare the tolerance to lime-induced Fe deficiency of two lines of Medicago ciliaris (TN11.11 and TN8.7). We studied the effects of Fe deficiency on: (1) root biomass and rhizosphere acidification, (2) accumulation in the roots and the exudation into the rhizosphere of organic compounds (citric acid, malic acid and phenols), (3) changes under Fe deficient conditions in the activities of two enzymes, the first related to organic acid metabolism (malate dehydrogenase: MDH) and the other to proton extrusion (H +-ATPase activity). After a pre-treatment of one week, plants were transferred into hydroponic culture under three treatments: +Fe, -Fe and +Fe +lime. Iron deficiency led to 40% increase in root biomass in TN11.11 line in the presence of lime. Both the omission of Fe and the addition of lime to the nutrient solution increased the H +-ATPase activity more in TN11.11 than in TN8.7. In addition, Fe deficiency increased accumulation of organic acids as well as phenols in roots, and stimulated the MDH activity more in TN11.11 than in TN8.7 (+75% and +41% in TN11.11 and TN8.7, respectively). Iron deficiency also increased the amounts of citrate, malate and phenols in root exudates. Our data allowed us to note that the TN11.11 line is more effective in overcoming Fe deficiency than TN8.7