Proline enhances antioxidative enzyme activity, photosynthesis and yield of Cicer arietinum L. exposed to cadmium stress

Seeds of chickpea inoculated with Rhizobium were sown in pots supplemented with different doses of cadmium (0, 25, 50 or 100 mg per kg of soil). At the stage of 30 days after sowing (DAS), the plants were sprayed with 20 mM solution of proline and were sampled at 90 DAS to assess the various parameters. The foliar treatment of proline resulted in the alleviation of the adverse effects generated by metal exposure, which wasexpressed in terms of the increase in plant growth. The activity of carbonic anhydrase in the cadmium-fed plants sprayed with proline was higher than that of control. The proline applied as foliar spray increased the photosynthetic attributes and yield characteristics in the cadmium-stressed plants. The activity of antioxidative enzymes increased with increasing concentration of cadmium. Maximum values were recorded in the plants exposed to 100 mg cadmium per kg of soil

Perspective of Melatonin-Mediated Stress Resilience and Cu Remediation Efficiency of Brassica juncea in Cu-Contaminated Soils

The present study evaluated the influence of melatonin (MEL) on copper toxicity in terms of morphophysiological, microscopic, histochemical, and stress resilience responses in Brassica juncea. Different levels of Cu (0, 30, and 60 mg kg–1) were given in air-dried soil, and 25 days after sowing (DAS), plants were sprayed with 30, 40, or 50 μM of MEL. The results demonstrated that under Cu stress, a significant amount of Cu accumulated in plant tissues, particularly in roots than in upper ground tissues, thereby suppressing the overall growth as evidenced by decrease in tolerance index and photosynthesis and increase in oxidative stress biomarkers (reactive oxygen species, malondialdehyde, and electrolyte leakage content) and cell death. Interestingly, the follow-up treatment of MEL, mainly 40 μM, efficiently improved the physio-biochemical and growth parameters, sugar accumulation, and metabolism. The potential of MEL in modulating Cu stress is attributed to its involvement in enriching the level of nutrient and improving chloroplast and stomatal organization besides lowering oxidative stress via enhanced levels of antioxidants. MEL improved the Cu reclamation potential in plants by enhancing Cu uptake and its translocation to aerial tissues. Principal component analysis showed that most of the morphophysiological and growth attributes were positively linked with MEL and negatively related to Cu levels, whereas all the stress-enhancing attributes showed a strong relationship with excessive Cu levels in soils. The present study suggested that MEL has the potential to improve growth and photosynthesis resulting in improved stress resilience under Cu stress along with increased remediation capability of mustard for remediation of Cu-contaminated soils

Role of strigolactones : Signalling and crosstalk with other phytohormones

Plant hormones play important roles in controlling how plants grow and develop. While metabolism provides the energy needed for plant survival, hormones regulate the pace of plant growth. Strigolactones (SLs) were recently defined as new phytohormones that regulate plant metabolism and, in turn, plant growth and development. This group of phytohormones is derived from carotenoids and has been implicated in a wide range of physiological functions including regulation of plant architecture (inhibition of bud outgrowth and shoot branching), photomorphogenesis, seed germination, nodulation, and physiological reactions to abiotic factors. SLs also induce hyphal branching in germinating spores of arbuscular mycorrhizal fungi (AMF), a process that is important for initiating the connection between host plant roots and AMF. This review outlines the physiological roles of SLs and discusses the significance of interactions between SLs and other phytohormones to plant metabolic responses

Editorial : An update on brassinosteroids : homeostasis, crosstalk, and adaptation to environmental stress

Over the last three decades, there have been significant advances in the understanding of brassinosteroid (BR) biosynthesis and signaling, particularly in the model plant species Arabidopsis thaliana. BRs regulate a variety of morphogenetic and physiological processes throughout plant life. Notably, BR biosynthesis and signaling are interconnected with the signaling pathways of other phytohormones and environmental stresses. Gathering knowledge about these aspects in monocot and dicot crops is of particular importance as it may allow modulation of these processes and enable the development cultivars better adapted to ongoing climate change. This Research Topic, providing An Update on Brassinosteroids: Homeostasis, Crosstalk, and Adaptation to Environmental Stress is aimed at introducing the latest findings in the regulation of BR metabolism, the interconnection of the BR signalosome with phytohormonal and stress signaling pathways, and the BR-mediated adaptation of plants to environmental conditions. The Research Topic includes five reviews and one original research article. [fragm. tekstu

Effect of Salicylic Acid on the Growth, Photosynthetic Efficiency and Enzyme Activities of Leguminous Plant under Cadmium Stress

The present study was designed with an objective to elucidate the effect of the exogenous application of 10-5 M of salicylic acid (SA) to the foliage of the chickpea plants exposed to 0, 25, 50 or 100 mg cadmium (Cd) per kg of soil. The foliage of the plants grown in soil amended with varying doses of Cd was sprayed with 10-5 M of SA at 30 days after sowing (DAS). The plant samples were collected at 60 and 90 DAS to assess various parameters. The damage caused due to the Cd exposure was partially overcome by the exogenous application of SA. The SA treatment resulted in a significant increase of growth, photosynthesis, yield and the activity of antioxidative enzymes viz. catalase, peroxidase and superoxide dismutase in the plants exposed to 0, 25 or 50 mg Cd per kg of soil. However, the treatment did not prove to be fruitful in alleviating completely the stress generated by 100 mg Cd per kg of soil

Adaptive Virtual Impedance Control with MPC’s Cost Function for DG Inverters in a Microgrid with Mismatched Feeder Impedances for Future Energy Communities

More and more distributed generations (DGs), such as wind, PV or battery bank sources, are connected to electric systems or customer loads. However, the locations of these DGs are based on the highest energy that can be potentially harvested for electric power generation. Therefore, these locations create different line impedances based on the distance from the DGs to the loads or the point of common coupling (PCC). This paper presents an adaptive virtual impedance (AVI) in the predictive control scheme in order to ensure power sharing accuracy and voltage stability at the PCC in a microgrid network. The reference voltage from mismatched feeder impedances was modified by utilizing the suggested AVI-based predictive control for creating equal power sharing between the DGs in order to avoid overburdening any individual DG with low-rated power. The AVI strategy used droop control as the input control for generating equal power sharing, while the AVI output was used as the reference voltage for the finite control set–model predictive control (FCS-MPC) for creating a minimum voltage error deviation for the cost function (CF) for the inverter’s vector switching pattern in order to improve voltage stability at the PCC. The proposed AVI-based controller was tested using two DG inverter circuits in a decentralized control mode with different values of line impedance and rated power. The performance of the suggested controller was compared via MATLAB/Simulink with that of a controller based on static virtual impedance (SVI) in terms of efficiency of power sharing and voltage stability at the PCC. From the results, it was found that (1) the voltage transient magnitude for the AVI-based controller was reduced within less than 0.02 s, and the voltage at the PCC was maintained with about 0.9% error which is the least as compared with those for the SVI-based controller and (2) equal power sharing between the DGs increased during the change in the load demand when using the AVI-based controller as compared with using the SVI-based controller. The proposed controller was capable of giving more accurate power sharing between the DGs, as well as maintaining the voltage at the PCC, which makes it suitable for the power generation of consumer loads based on DG locations for future energy communities

Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones

Phytoecdysteroids (PEs) are naturally occurring polyhydroxylated compounds with a structure similar to that of insect molting hormone and the plant hormone brassinosteroids. PEs have a four-ringed skeleton composed of 27, 28, 29, or 30 carbon atoms (derived from plant sterols). The carbon skeleton of ecdysteroid is known as cyclopentanoperhydrophenanthrene and has a β-sidechain on C-17. Plants produce PEs via the mevalonate pathway with the help of the precursor acetyl-CoA. PEs are found in algae, fungi, ferns, gymnosperms, and angiosperms; more than 500 different PEs are found in over 100 terrestrial plants. 20-hydroxyecdysone is the most common PE. PEs exhibit versatile biological roles in plants, invertebrates, and mammals. These compounds contribute to mitigating biotic and abiotic stresses. In plants, PEs play a potent role in enhancing tolerance against insects and nematodes via their allelochemical activity, which increases plant biological and metabolic responses. PEs promote enzymatic and non-enzymatic antioxidant defense systems, which decrease reactive oxygen species in the form of superoxide radicals and hydroxyl radicals and reduce malondialdehyde content. PEs also induce protein biosynthesis and modulate carbohydrate and lipid synthesis. In humans, PEs display biological, pharmacological, and medicinal properties, such as anti-diabetic, antioxidant, anti-microbial, hepatoprotective, hypoglycemic, anti-cancer, anti-inflammatory, antidepressant, and tissue differentiation activity

Foliar application of 28-homobrassinolide mitigates salinity stress by increasing the efficiency of photosynthesis in Brassica juncea

Prior to sowing, seeds of Brassica juncea Czern and Coss cv. Varuna were soaked in water (controls) or in 50, 100 or 150 mM of sodium chloride (NaCl) for 6 h. The resulting plants, at 15, 30 and 45 days after sowing (DAS) were either not treated (controls) or were treated with aqueous solutions of the hormone 28-homobrassinolide (HBL), which was applied to their foliage in concentrations of 10-10, 10-8 or 10-6 M. The concentration of NaCl showed an inverse correlation with the activity of nitrate reductase (EC 1.6.6.1), the activity of carbonic anhydrase (EC 4.2.1.1), chlorophyll content at 60 DAS, the rate of photosynthesis at 60 DAS, and seed yield at 140 DAS (at harvest), all of which decreased in parallel with increases in NaCl concentration. However, treatment with HBL attenuated those decreases and neutralized the ill effects of salinity stress, completely at the lowest NaCl concentration and partially at the higher NaCl concentrations. The seed yield of the crop can be increased by the foliar application of HBL, even under conditions of salinity stress

Specific Roles of Lipoxygenases in Development and Responses to Stress in Plants

Lipoxygenases (LOXs), naturally occurring enzymes, are widely distributed in plants and animals. LOXs can be non-sulfur iron, non-heme iron, or manganese-containing dioxygenase redox enzymes. LOXs catalyze the oxidation of polyunsaturated fatty acids into fatty acid hydroperoxides. Linolenic acid, a precursor in the jasmonic acid (JA) biosynthesis, is converted to 12-oxo-phytodienoic acid through oxygenation with LOX, allene oxide synthase, and allene oxide cyclase. Moreover, JA participates in seed germination, fruit ripening, senescence, and many other physio-biochemical processes. LOXs also play crucial roles in defense responses against biotic stress, i.e., insects, pests, pathogenic attacks, and abiotic stress, such as wounding, UV-rays, extreme temperature, oxidative stress, and drought