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In mutation breeding, mutagenic effectiveness and efficiency are the base parameters to predict the mutagenic potency of any mutagen. Studies on mutagenic effectiveness and mutagenic efficiency of physical mutagen (gamma rays) and chemical mutagen (hydrazine hydrates; HZ) on two cultivars of lentil (Lens culinaris Medik.), viz. DPL 62 (macrosperma) and Pant L 406 (microsperma) have been reported. Dry and healthy seeds were treated with four doses of each gamma rays (100-400 Gy), HZ (0.1-0.4 %) and their combinations. Frequencies of the induced agro-morphological variations into different phenotypic categories were estimated in M2 population that resulted into identification and isolation of wide range of mutants with altered phenotypes. Data on effectiveness and efficiency of various mutagenic treatments calculated on the basis of the frequency of chlorophyll mutations, which showed effectiveness and efficiency were higher at the moderate doses of gamma rays and HZ, while in case of combination treatments; lower doses were most effective and efficient with few inter-varietal exceptions. Phenotyping of the mutants revealed that growth habits was the most sensitive category to which most of the mutant belongs, followed by leaf and flower/pod/seed in both the cultivars studied. Overall, the screened and isolated mutants with economically important agronomic traits can be further propagated in the subsequent generation for development of elite lentil mutant cultivars.
In the current scenario of sky high population and widespread food insecurity, there is an urgent need for productivity improvement of major crops like pulses, one of the most climate friendly and accessible foods for the large poor population of the world. Chickpea is an important pulse crop, having high percentage of nutritional content and is widely used as food across the world. Induced mutagenesis has proved over time as a coherent tool for modern plant breeders to improve the productivity for combating the food insecurity and malnutrition across the globe. Dry and healthy seeds of Cicer arietinum L. var. C-235 were treated with individual and combination doses of gamma rays, sodium azide and hydrazine hydrate to raise the M₁ generation. M₂ seeds harvested from M₁ plants were sown in the nest season. Bio-physiological study in M1 generation showed growth inhibition in the order viz. combination treatment>hydrazine hydrate>gamma rays>sodium azide. In M₂ generation, comparative observations were recorded for morphological variation and quantitative traits to assess the genetic response of the chickpea variety C-235 toward the different concentrations of mutagens. Observations on isolated mutants in M₂ generation revealed that 0.3% HZ + 0.02% SA was most mutagenic while 200 Gy, 0.03% SA and 0.2% HZ were highest in their individual treatment groups. In context to the frequency of morphological mutants studied in M₂ generation, dwarf mutants were found to be highest followed by tall and branching pattern mutants. Highly significant correlation coefficient between yield and other traits showed that the selection for high yielding mutants can be done on the basis of these traits undoubtedly.
Locally available bentonite clay has been modified by magnesium and used to eliminate acid blue 129 from aqueous solutions. The adsorption was studied under different experimental conditions such as dye concentrations, temperature, and shaking time. The adsorption of the dye increased with time and followed the pseudo-first-order kinetic with rate constant “k” 0.126 min-1 at 283 K. Thermodynamic parameters such as ΔH°, ΔS°, and ΔG° were calculated from the slope and intercept of the linear plots of ln K against1/T. Analysis of adsorption results obtained at temperatures of 283, 293, 303, and 313 K showed that the adsorption pattern on bentonite seems to follow Langmuir and Freundlih. The increase in temperature reduces adsorption capacity by magnesium-modified bentonite due to the enhancement of the desorption step in the mechanism. The activation energy of the adsorption process was found to be 3.55 kJ mol-1. The Mg-bentonite showed better adsorption than Ba and Al-bentonite. Our study reveals that abundantly available local clay may be used to eliminate dyes from aqueous solutions.
The present study aimed to identify biologically active secondary metabolites from the rare plant species, Pulsatilla patens subsp. patens and the cultivated P. vulgaris subsp. vulgaris. Chromatographic fractionation of the ethanolic extract of the roots of P. patens subsp. patens resulted in the isolation of two oleanane-type glycosides identified as hederagenin 3-O-β-d-glucopyranoside (2.7 mg) and hederagenin 3-O-β-d-galactopyranosyl-(1→2)-β-d-glucopyranoside (3.3 mg, patensin). HPLC analysis of the methanolic extract of the crude root of P. patens subsp. patens and P. vulgaris subsp. vulgaris revealed the presence of Pulsatilla saponin D (hederagenin 3-O-α-l-rhamnopyranosyl(1→2)-[β-d-glucopyranosyl(1→4)]-α-l-arabinopyranoside). Chromatographic analysis using GC-MS of the silylated methanolic extracts from the leaves and roots of these species identified the presence of carboxylic acids, such as benzoic, caffeic, malic, and succinic acids. The extracts from Pulsatilla species were tested for their antifungal, antimicrobial, and antimalarial activities, and cytotoxicity to mammalian cell lines. Both P. patens subsp. patens and P. vulgaris subsp. vulgaris were active against the fungus Candida glabrata with the half-maximal inhibitory concentration (IC₅₀) values of 9.37 μg/mL and 11 μg/mL, respectively. The IC₅₀ values for cytotoxicity evaluation were in the range of 32–38 μg/mL for P. patens subsp. patens and 35–57 μg/mL for P. vulgaris subsp. vulgaris for each cell line, indicating general cytotoxic activity throughout the panel of evaluated cancer and noncancer cells.
In vivo modulation of HMG-CoA reductase (HMGR) activity and its impact on artemisinin biosynthesis as well as accumulation were studied through exogenous supply of labeled HMG-CoA (substrate), labeled MVA (the product), and mevinolin (the competitive inhibitor) using twigs of Artemisia annua L. plants collected at the preflowering stage. By increasing the concentration (2–16 µM) of HMG-CoA (3-¹⁴C), incorporation of labeled carbon into artemisinin was enhanced from 7.5 to 17.3 nmol (up to 130%). The incorporation of label (¹⁴C) into MVA and artemisinin was inhibited up to 87.5 and 82.9%, respectively, in the presence of 200 µM mevinolin in incubation medium containing 12 µM HMG-CoA (3-¹⁴C). Interestingly, by increasing the concentration of MVA (2-¹⁴C) from 2 to 18 µM, incorporation of label (¹⁴C) into artemisinin was enhanced from 10.5 to 35 nmol (up to 233%). When HMG-CoA (3-¹⁴C) concentration was increased from 12 to 28 µM in the presence of 150 µM mevinolin, the inhibitions in the incorporation of label (¹⁴C) into MVA and artemisinin were, however, reversed and the labels were found to approach their values in twigs fed with 12 µM HMG-CoA (3-¹⁴C) without mevinolin. In another experiment, 14.2% inhibition in artemisinin accumulation was observed in twigs in the presence of 175 µM fosmidomycin, the competitive inhibitor of 1-deoxy-D-xylulose 5-phosphate reductase (DXR). HMG-CoA reductase activity and artemisinin accumulation were also increased by 18.6 to 24.5% and 30.7 to 38.4%, respectively, after 12 h of treatment, when growth hormones IAA (100 ppm), GA₃ (100 ppm) and IAA + GA₃ (50 + 50 ppm) were sprayed on A. annua plants at the pre-flowering stage. The results obtained in this study, hence, demonstrate that the mevalonate pathway is the major contributor of carbon supply to artemisinin biosynthesis and HMGR limits artemisinin synthesis and its accumulation in A. annua plants.
Low-temperature results in various physiological and metabolic disturbances in cells of plants which are sensitive to low-temperatures. Moringa is getting popularity as a field crop because of its multipurpose usage. There is no information available about effects of low-temperature (14-18℃) on moringa seedlings and its mitigation. The present study was conducted to test the performance of moringa seedling grown in wire house under low-temperature conditions in response to foliar application of moringa leaf extract (3% solution), hydrogen peroxide (5 ml L⁻¹), ascorbic acid (50 mg L⁻¹) and salicylic acid (50 mg L⁻¹). Seeds of six moringa accessions [Local landrace grown at Agronomic Research Area, Z.A Hashmi Hall, Firdous Colony; Exotic landrace grown at Lalazaar Colony, Department of Agronomy and Agronomic Research Area] were collected and grown in polythene bags filled with equal ratio of compost, sand, silt and clay. All foliar treatments were applied twice; the first round at the seedling age one month and the second round at the seedling age two months. Foliar application of moringa leaf extract significantly enhanced number of branches (92%) and leaves (39%), leaf total chlorophyll contents (73%), leaf phenolic contents (53%) and membrane stability index (57%) of moringa seedlings compared to control. Healthy and vigorous growth of moringa seedlings with higher concentration of antioxidants ensured the defensive potential of moringa leaf extract against low-temperature condition.
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