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To keep pace with ever growing global population, progressive and sustained increase in rice production is necessary, especially in areas with extremely variable climatic conditions, where rice crop suffers from numerous abiotic stresses including salinity. Designing an effective phenotyping strategy requires thorough understanding of plant survival under stress. The investigation was carried out with four rice cultivars namely FR13A, IR42, Rashpanjor, and Pokkali that differed in salinity tolerance. The study showed that a genotype with initial vigour had some advantage in preserving shoot biomass under salt stress. Though both FR13A and IR42 showed sensitivity to salinity, FR13A with higher initial biomass maintained greater dry weight under saline condition. Increase of Na+:K+ ratio under salinity, due to accelerated absorption of Na+ and lesser absorption of K+ compared to control, was considerably higher in susceptible (118–200 %) than in tolerant (33–48 %) genotypes. While Na+ concentration in shoot increased significantly in both tolerant and susceptible genotypes, decrease in shoot K+ content was noticed only in susceptible genotypes. The imbalance of Na+ and K+ contents led to increased H2O2 production, causing greater peroxidation of membrane lipids and reduction in chlorophyll content and CO2 photosynthetic rate. Certain chlorophyll fluorescence parameters could distinguish between salinity tolerant and sensitive genotypes. To protect the plant from oxidative damage, several enzymatic and nonenzymatic antioxidants such as ascorbate were involved. The genotypes with capacity to assemble antioxidant enzymes in time could detoxify the reactive oxygen species more efficiently, leading to greater protection and reduced impact of salt stress.
Soluble somatic extract of adult Acanthocheilonema viteae was resolved into three major peaks - Fr. I, Fr. II and Fr. III by gel-filtration on Sephadex G-200 column. Protein rich Fr. I was highly efficient in detecting haemagglutinating and precipitating antibodies while Fr. II, a carbohydrate rich fraction was reactive in detecting hom ocyt otropic antibodies. Fraction II also reacted feebly in precipitation test. Fraction III was though weakly but exclusively reactive in P-K test. On SDS-PAGE analysis Fr. I revealed 33 protein bands with molecular weights ranging from 25 to 100 kD. The 15 bands of Fr. II remained within the molecular weight range of 10 and 28 kD. Fraction III containing 9 protein components mostly within 17 kD when used as immunogen caused significant reduction in microfilaraemia (P<0.001) and lowered adult worm recovery (P<0.05) as compared to other fractions and control groups.
Tolerance limit, kinetics of nitrogen uptake and activity of nitrate reductase (NR), nitrite reductase (NiR) and glutamine synthetase (GS) enzymes of cyanobacterium Desmonostoc muscorum PUPCCC 405.10 were studied under the regime of chloroacetanilide herbicide pretilachlor. The organism was isolated from the paddy field under application of the herbicide and tolerated pretilachlor up to 10 ppm under laboratory conditions. The incubation of the cyanobacterium in 2.5 ppm pretilachlor did not cause significant effect on N uptake while supplementation of 5–10 ppm pretilachlor in medium reduced the rate of nitrate and nitrite uptake by 35–73 % with 50 % decrease in Vmax and no change in Km. These results indicated that herbicide did not affect the affinity of uptake system to nitrate and nitrite. In presence of herbicide, the activity of nitrogen assimilation enzymes was inhibited by 16 % for NR and 18 % for NiR. Unchanged Km and decreased Vmax (50–60 %) in presence of herbicide indicated non-competitive- type inhibition of the enzymes.A50 %decrease in Vmax and Km of ammonium uptake indicated un-competitive type inhibition of the ammonium transport system by the herbicide. GS activity also exhibited non-competitive inhibition in presence of pretilachlor with 21 % decrease in activity with unchanged Km and 40 % decrease in Vmax. Likewise, decreases in nitrogenase activity by 43 % and heterocyst formation by 40 % were recorded in presence of herbicide. Results indicated that pretilachlor affected nitrogen assimilation at uptake level and interacted with nitrogen-assimilating enzymes in a non-competitive manner.
Collar rot (Sclerotium rolfsii) of chickpea (Cicer arietinum) is one of the devastating soil-borne diseases of fungal origin, due to which 10-30% yield loss is recorded annually according to severity of the disease. Management of collar rot of chickpea is not feasible in the absence of effective soil fungicides. However, Trichoderma harzianum and plant growth promoting rhizobacteria (PGPR) have shown high efficacy against this disease in vitro as well as in the field. We used T. harzianum (104, 106 and 108 spore/ml) and two PGPRs (Pseudomonas fluorescens strain 4 and P. aeruginosa) as foliar spray with the fresh and heat inactivated microorganisms. Foliar application of T. harzianum (108 spore/ml) and P. fluorescens strain 4 (108 cfu/ml) showed maximum efficacy in reducing plant mortality as compared to the control. Foliar application of fresh-and heat-inactivated (121°C for 10 min) P. fluorescens strain 4, and T. harzianum reduced 15-25% plant mortality but P. aeruginosa showed very little disease control of 10-15%. However, regarding plant growth promotion, it was observed that fresh-and heat-inactivated P. fluorescens strain 4 showed maximum efficacy followed by fresh and heat inactivated P. aeruginosa and T. harzianum as compared to the control. The disease-controlling efficacy was also associated with the increase in phenolic acid synthesis in chickpea plants. The control of chickpea collar rot by biocontrol agents is safe and ecologically sound and appears to be a healthy approach to the disease control.
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