Inhibition Of Radicle Growth Research Articles

Radicle Growth Regulation of Root Parasitic Plants by Auxin-related Compounds.

Root parasitic plants in the Orobanchaceae, such as Striga and Orobanche, cause significant damage to crop production. The germination step of these root parasitic plants is induced by host-root-derived strigolactones. After germination, the radicles elongate toward the host and invade the host root. We have previously discovered that a simple amino acid, tryptophan (Trp), as well as its metabolite, the plant hormone indole-3-acetic acid (IAA), can inhibit radicle elongation of Orobanche minor. These results suggest that auxin plays a crucial role in the radicle elongation step in root parasitic plants. In this report, we used various auxin chemical probes to dissect the auxin function in the radicle growth of O. minor and Striga hermonthica. We found that synthetic auxins inhibited radicle elongation. In addition, auxin receptor antagonist, auxinole, rescued the inhibition of radicle growth by exogenous IAA. Moreover, a polar transport inhibitor of auxin, N-1-naphthylphthalamic acid, affected radicle bending. We also proved that exogenously applied Trp is converted into IAA in O. minor seeds, and auxinole partly rescued this radicle elongation. Taken together, our data demonstrate a pivotal role for auxin in radicle growth. Thus, manipulation of auxin function in root parasitic plants should offer a useful approach to combat these parasites.

Novel herbicide from an optimized Bacillus altitudinis D30202 solvent extract

AbstractThe herbicidal activity of the fermentation broth, filtrate, and extracts of Bacillus altitudinis D30202 was evaluated against seed germination and seedling growth of wild oat (Avena fatua L.). The bacterial culture filtrate exhibited greater inhibition of the wild oat weed than the fermentation broth. The filtrate was also extracted with organic solvents. The herbicidal potency of the extracts on the growth of wild oat plants was as follows: chloroform (100% inhibition of germination) > n‐butanol (93.8%) > ethyl acetate (66.7%) > petroleum ether (6.3%) > aqueous phase (2.1%); so the chloroform extract was evaluated further. It inhibited wild oat radicle growth by 100%, and plumule growth by 97.9%, while spraying young plants with a 5 mg/mL extract caused severe desiccation of the leaves, stalk wilting, and plant death. IC50 values for inhibition of plumule and radicle growth and germination were 0.64–0.72 mg/mL. Scanning electron microscopy and transmission electron microscopy revealed changes in the microstructure of the leaves and root tips, and degradation of organelles following chloroform extract treatment. The 5 mg/mL extract had no adverse impact on the growth or health of highland barley (Hordeum vulgare L.), corn (Zea mays), and broad bean (Vicia faba L.), indicating that this novel bioherbicide is suitable for control of wild oat weeds in the production of these food crops (while having a minor impact on the health of pea plants and being phytotoxic to wheat plants).

Synthesis of Cyclopeptides Analogues of Natural Products and Evaluation as Herbicides and Inhibitors of Cyanobacteria.

Natural products derived from plants or microorganisms have been considered as eco-friendly herbicides with application in crop protection. Several natural cyclopeptides have been reported as herbicides, while others have been identified as inhibitors of cyanobacteria. In this work, the syntheses of cyclotetrapeptides and cyclopentapeptides analogues of natural products were successfully performed by solid-phase peptide synthesis of their linear precursor and solution-phase macrolactamization. Four of the obtained peptides and cyclopeptides present phytotoxicity with more than 70% of radicle growth inhibition at 67 μg/mL. In addition, evaluation of 20 peptides and cyclopeptides, as inhibitors of cyanobacteria, rendered five active compounds that reduced the concentration of microcystins in the culture medium.

Obtaining New Candidate Peptides for Biological Anticancer Drugs from Enzymatic Hydrolysis of Human and Bovine Hemoglobin.

Enzymatic hydrolysis of bovine and human hemoglobin generates a diversity of bioactive peptides, mainly recognized for their antimicrobial properties. However, antimicrobial peptides stand out for their ability to specifically target cancer cells while preserving rapidly proliferating healthy cells. This study focuses on the production of bioactive peptides from hemoglobin and evaluates their anticancer potential using two distinct approaches. The first approach is based on the use of a rapid screening method aimed at blocking host cell protein synthesis to evaluate candidate anticancer peptides, using Lepidium sativum seed germination as an indicator. The results show that: (1) The degree of hydrolysis (DH) significantly influences the production of bioactive peptides. DH levels of 3 to 10% produce a considerably stronger inhibition of radicle growth than DH 0 (the native form of hemoglobin), with an intensity three to four times greater. (2) Certain peptide fractions of bovine hemoglobin have a higher activity than those of human hemoglobin. (3) The structural characteristics of peptides (random coil or alpha helix) play a crucial role in the biological effects observed. (4) The α137-141 peptide, the target of the study, was the most active of the fractions obtained from bovine hemoglobin (IC50 = 29 ± 1 µg/mL) and human hemoglobin (IC50 = 48 ± 2 µg/mL), proving to be 10 to 15 times more potent than the other hemoglobin fractions, attributed to its strong antimicrobial potential. The second approach to assessing anticancer activity is based on the preliminary in vitro analysis of hydrolysates and their peptide fractions, with a focus on the eL42 protein. This protein is of major interest due to its overexpression in all cancer cells, making it an attractive potential target for the development of anticancer molecules. With this in mind, astudy was undertaken using a method for labeling formylase (formyl-methionyl-tRNA transformylase (FMTS)) with oxidized tRNA. This approach was chosen because of the similarities in the interaction between formylase and the eL42 protein with oxidized tRNA. The results obtained not only confirmed the previous conclusions but also reinforced the hypothesis that the inhibition of protein synthesis plays a key role in the anticancer mechanism of these peptides. Indeed, the data suggest that samples containing α137-141 peptide (NKT) and total hydrolysates may have modulatory effects on the interaction between FMTS and oxidized tRNA. This observation highlights the possibility that the latter could influence molecular binding mechanisms, potentially resulting in a competitive situation where the ability of substrate tRNA to bind efficiently to ribosomal protein is compromised in their presence. Ultimately, these results suggest the feasibility of obtaining candidate peptides for biological anticancer drugs from both human and bovine hemoglobin sources. These scientific advances show new hope in the fight against cancer, which affects a large number of people around the world.

Evaluation of Propiophenone, 4-Methylacetophenone and 2',4'-Dimethylacetophenone as Phytotoxic Compounds of Labdanum Oil from Cistus ladanifer L.

This is the first study to evaluate the phytotoxic activity of three phenolic compounds present in the essential oil of the labdanum of Cistus ladanifer, an allelopathic species of the Mediterranean ecosystem. Propiophenone, 4'-methylacetophenone, and 2',4'-dimethylacetophenone slightly inhibit total germination and radicle growth of Lactuca sativa, and they strongly delay germination and reduce hypocotyl size. On the other hand, the inhibition effect of these compounds on Allium cepa was stronger on total germination than on germination rate, and radicle length compared to hypocotyl size. The position and number of methyl groups will affect the efficacy of the derivative. 2',4'-dimethylacetophenone was the most phytotoxic compound. The activity of the compounds depended on their concentration and presented hormetic effects. In L. sativa, on paper, propiophenone presented greater inhibition of hypocotyl size at greater concentrations, with IC50 = 0.1 mM, whereas 4'-methylacetophenone obtained IC50 = 0.4 mM for germination rate. When the mixture of the three compounds was applied, in L. sativa, on paper, the inhibition effect on total germination and the germination rate was significantly greater compared to the effect of the compounds when they were applied separately; moreover, the mixture inhibited radicle growth, whereas propiophenone and 4'-methylacetophenone did not exert such effect when applied separately. The activity of the pure compounds and that of the mixture also changed based on the substrate used. When the trial was conducted in soil, the separate compounds delayed the germination of the A. cepa to a greater extent compared to the trial on paper, although they stimulated seedling growth. In soil, L. sativa against 4'-methylacetophenone also showed the opposite effect at low concentrations (0.1 mM), with stimulation of germination rate, whereas propiophenone and 4'-methylacetophenone presented a slightly increased effect.

Multi-omics analysis provides insight into the phytotoxicity of chicken manure and cornstalk on seed germination

To minimize environmental risks and the phytotoxic influence of organic materials on crop growth, it is necessary to test their phytotoxicity and maturity when they were used in farmland. However, the stress response of seed germination to chicken manure and cornstalks is not clear. This study used multi-omics analysis to investigate the inhibition mechanism of seed germination by chicken manure and cornstalk. Chicken manure caused destructive inhibition of seed germination with higher phytotoxicity (GI = 0). Cornstalk also had a low GI (8.81 %), while it mainly inhibited radicle growth (RL = 9.39 %) rather than seed germination (GR = 93.33 %). The response of radish seed germination to chicken manure and cornstalk phytotoxic stresses was accompanied by metabolic adjustments of storage substance accumulation, antioxidant enzyme activity change, phytohormone induction, and expression of specific proteins and gene regulation. Combined transcriptomic and proteomic analysis revealed that differential expression of 13,090 (5944 upregulated/7146 downregulated) and 3850 (2389 upregulated/1461 downregulated) genes (DEGs), and 1041 (82 upregulated/932 downregulated) and 575 (111 upregulated/464 downregulated) proteins (DEPs) at chicken manure and cornstalk treatment, respectively. Most down-regulated genes and proteins were involved in phenylpropanoid biosynthesis under chicken manure stress, which caused irreversible inhibition of seed germination. Down-regulation of phytohormone signal transduction-related genes under cornstalk stress resulted in inhibition of radicle growth, but the inhibitory stress was restorable. These findings provide new insight into the phytotoxicity of livestock manure and cornstalk on seed germination.

Iridoid Glycosides Isolated from Bellardia trixago Identified as Inhibitors of Orobanche cumana Radicle Growth.

Orobanche cumana is an obligate holoparasitic plant with noxious effects in sunflower crops. Bellardia trixago is a facultative hemiparasitic plant that infects ruderal plants without noxious significance in agriculture and is known to produce a wide spectrum of bioactive metabolites. The objective of this study was to evaluate the allelopathic effects of B. trixago on the growth of O. cumana seedlings. Three different extracts using solvents of increasing polarity (n-hexane, dichloromethane and ethyl acetate) were prepared from the flowers, aerial green organs and roots of two populations, a white-flowered and a yellow-flowered population of B. trixago, both collected in southern Spain. Each extract was studied using allelopathic screenings on O. cumana which resulted in the identification of allelopathic activity of the ethyl acetate extracts against Orobanche radicles. Five iridoid glycosides were isolated together with benzoic acid from the ethyl acetate extract of aerial green organs by bio-guided purification. These compounds were identified as bartsioside, melampyroside, mussaenoside, gardoside methyl ester and aucubin. Among them, melampyroside was found to be the most abundant constituent in the extract (44.3% w/w), as well as the most phytotoxic iridoid on O. cumana radicle, showing a 72.6% inhibition of radicle growth. This activity of melampyroside was significantly high when compared with the inhibitory activity of benzoic acid (25.9%), a phenolic acid with known allelopathic activity against weeds. The ecotoxicological profile of melampyroside was evaluated using organisms representing different trophic levels of the aquatic and terrestrial ecosystems, namely producers (green freshwater algae Raphidocelis subcapitata and macrophyte Lepidium sativum), consumers (water flea Daphnia magna and nematode Caenorhabditis elegans) and decomposers (bacterium Aliivibrio fischeri). The ecotoxicity of melampyroside differed significantly depending on the test organism showing the highest toxicity to daphnia, nematodes and bacteria, and a lower toxicity to algae and macrophytes. The findings of the present study may provide useful information for the generation of green alternatives to synthetic herbicides for the control of O. cumana.

Specialized Metabolites from the Allelopathic Plant Retama raetam as Potential Biopesticides.

To cope with the rising food demand, modern agriculture practices are based on the indiscriminate use of agrochemicals. Although this strategy leads to a temporary solution, it also severely damages the environment, representing a risk to human health. A sustainable alternative to agrochemicals is the use of plant metabolites and plant-based pesticides, known to have minimal environmental impact compared to synthetic pesticides. Retama raetam is a shrub growing in Algeria’s desert areas, where it is commonly used in traditional medicine because of its antiseptic and antipyretic properties. Furthermore, its allelopathic features can be exploited to effectively control phytopathogens in the agricultural field. In this study, six compounds belonging to isoflavones and flavones subgroups have been isolated from the R. raetam dichloromethane extract and identified using spectroscopic and optical methods as alpinumisoflavone, hydroxyalpinumisoflavone, laburnetin, licoflavone C, retamasin B, and ephedroidin. Their antifungal activity was evaluated against the fungal phytopathogen Stemphylium vesicarium using a growth inhibition bioassay on PDA plates. Interestingly, the flavonoid laburnetin, the most active metabolite, displayed an inhibitory activity comparable to that exerted by the synthetic fungicide pentachloronitrobenzene, in a ten-fold lower concentration. The allelopathic activity of R. raetam metabolites against parasitic weeds was also investigated using two independent parasitic weed bioassays to discover potential activities on either suicidal stimulation or radicle growth inhibition of broomrapes. In this latter bioassay, ephedroidin strongly inhibited the growth of Orobanche cumana radicles and, therefore, can be proposed as a natural herbicide.

Selected Phenolic Acids Inhibit the Initial Growth of Ambrosia artemisiifolia L.

Simple SummaryIn the context of international commitments to reduce the environmental impact of herbicides, ecologically more favorable control method approaches must be explored. This is particularly important for allergenic Ambrosia artemisiifolia L., one of the most harmful species in the world. Secondary plant metabolites and, in particular, some phenolic compounds are known to have a strong allelopathic effect on weed growth. In this study we investigated whether phenolic acids (chlorogenic acid, caffeic acid, ferulic acid, gallic acid, protocatechuic acid, p-hydroxybenzoic acid, syringic acid, vanillic acid, and p-coumaric acid) can inhibit the early growth of A. artemisiifolia. Phenolic acids were tested at five different dose levels that were up to 16 times than those naturally occurring in plants. The results show that the suppression of the early growth of A. artemisiifolia is strongly dependent on phenolic acid and its dose. Treating seeds with ferulic acid, vanillic acid, p-coumaric acid, p-hydroxybenzoic acid, or a mixture of all phenolic acids resulted in significantly better inhibition of early growth parameters than other phenolic acids. However, none of the phenolic acids tested were effective as bioherbicides at their naturally occurring doses in plants. Therefore, selected doses of phenolic acids with significantly reduced herbicide doses should be further explored to effectively control A. artemisiifolia.This study aimed to investigate whether different doses of specific phenolic acids (chlorogenic acid, caffeic acid, ferulic acid, gallic acid, protocatechuic acid, p-hydroxybenzoic acid, syringic acid, vanillic acid, and p-coumaric acid), alone or in combination, can inhibit the early growth of the common ragweed (Ambrosia artemisiifolia L., Asterales: Asteraceae). A seed bioassay was performed in Petri dishes and placed in a climate chamber to assess the effects of five dose levels of phenolic acids to radicle and shoot length, as well seedling biomass of A. artemisiifolia. The lowest dose of phenolic acid corresponded to the natural phenolic acid concentration previously reported in dry plant tissue samples from Brassicaceae cover crop plants. Results show that the inhibition of the early growth of A. artemisiifolia depends strongly on phenolic acid. Across different treatments, high doses of phenolic acids significantly shortened shoots and radicles, as well as reduced seedling biomass. Treating seeds with ferulic acid alone, vanillic acid alone, p-hydroxybenzoic acid alone, or a mixture of all phenolic acids significantly reduced all early growth parameters. The estimated effective dose for the 50% inhibition (ED50) of radicle growth in A. artemisiifolia seedlings was 368.39 ± 59.85 × 10−8 mol with ferulic acid, 135.41 ± 17.65 × 10−8 mol with p-coumaric acid, 810.36 ± 134.15 × 10−8 mol with p-hydroxybenzoic acid, and 160.11 ± 12.30 × 10−8 mol with the combination of all phenolic acids.

Phytotoxic essential oil from black turmeric (Curcuma caesia Roxb.) rhizome: Screening, efficacy, chemical basis, uptake and mode of transport

Plant-based phytotoxins play an important role in plant-plant interaction and are of great promise for the development of bioherbicide. In this study, screening of essential oils from six different Curcuma rhizomes identified black turmeric (Curcuma caesia Roxb.) oil as an efficient growth inhibitor in wheatgrass coleoptile bioassay (IC50 57.1 µg/mL). The phytotoxic efficacy of this oil was further confirmed through the dose dependent (10.0–300.0 µg/mL) inhibition of germination, coleoptile and radicle growth of wheatgrass seeds in water medium (IC50 176.7, 90.6 and 93.0 µg/mL respectively) and the pre-germinated seeds in agar medium. Activity-guided fractionation and purification of the crude oil identified curzerenone, a major furanosesquiterpene in this oil as the most active phytotoxin (IC50 13.0 µg/mL in coleoptile bioassay; 188.3, 34.7 and 36.7 µg/mL respectively in water medium). Structure-activity relationship study indicated the importance of all the functional groups for its phytotoxicity. A significant contribution by the oxygenated monoterpenes towards oil phytotoxicity was also evidenced. Though inhibitory efficacy of the oil was comparatively weak in soil, a profound activity through aerial diffusion was observed against germination and/or growth of fresh and pre-germinated wheatgrass seeds (IC50 1.4–6.2 mg/L air). The study also confirmed the uptake of active phytotoxins with no detectable transformation by the seeds in water and their persistence in the soil for at least one and half months. Further, its applicability was demonstrated through an efficient post-emergence growth inhibition (IC50 37.0–81.4 µg/mL) of bermudagrass weed in water and agar medium.

Dynamic Changes to Endogenous Germination Inhibitors in Cercis chinensis Seeds during Dormancy Release

The purpose of this study was to determine whether Cercis chinensis seeds contain endogenous germination inhibitors, and if so, to clarify the dynamic changes to the inhibitors during dormancy release. A cabbage seed germination test was conducted to assess the seed extract activities during dormancy release. The endogenous inhibitor components were analyzed by gas chromatography–mass spectrometry and the dynamic changes to the endogenous inhibitors were analyzed by high-performance liquid chromatography. The analyses revealed 1,2,3-benzenetriol (phenolic compound) in the seedcoat is a water-soluble endogenous inhibitor, and the IC50 (the concentration at which 1,2,3-benzenetriol inhibited radicle growth of cabbage seeds by 50%) of 1,2,3-benzenetriol was 51.2 µg⋅mL–1. During dormancy release, the seed 1,2,3-benzenetriol content decreased to 17.7 µg⋅mL–1 (stratified for 60 days) from 561.4 µg⋅mL–1 (control). The abscisic acid (ABA) content exhibited the same tendency, decreasing from 5.6 ng⋅mL–1 to 0.5 ng⋅mL–1 after 60-day stratification. Exogenous ABA was highly inhibitory toward cabbage seed germination, with an IC50 of 1.5 ng⋅mL–1. These results indicate that ABA and 1,2,3-benzenetriol are important endogenous inhibitors in C. chinensis seeds, wherein they regulate seed dormancy, even at low concentrations.

Chemical composition and phytotoxic potential of Eucalyptus globulus essential oil against Lactuca sativa and two herbicide-resistant weeds: Avena fatua and Amaranthus hybridus

Weed control in sustainable agriculture requires new bioherbicidal molecules to replace synthetic herbicides that have damaged the environment and generated resistance in weeds. This study was conducted to investigate the chemical composition of Eucalyptus globulus essential oil and to explore its bioherbicidal potential on the germination and radicle growth inhibition. The phytotoxic effects of E. globulus essential oil (1, 10 and 20 μL mL-1) were tested in comparison to those of the synthetic herbicide Glyphosate (1, 10 and 20 μL mL-1) in bioassays of germination and radicle growth of Lactuca sativa and the resistant weeds Avena fatua and Amaranthus hybridus. Gas Chromatography with Flame Ionization Detector and Gas Chromatography-Mass Spectroscopy analysis showed that major monoterpenes comprised 1,8-Cineole (86.94%), α-pinene (7.71%), d-limonene (2.65%), and p-cymene (1.48%). The seed germination and radicle length exhibited different degrees of inhibition in response to the concentration of E. globulus essential oil. At some concentrations, both the Glyphosate herbicide and the E. globulus essential oil demonstrated the same phytotoxicity against the resistant weeds A. fatua and A. hybridus. Essential oil bioactivity Lethal Concentration (LC50) in the majority of cases was lowest for A. hybridus, followed by A. fatua and L. sativa. Based on the results, it can be concluded that E. globulus essential oil possesses phytotoxic potential and could be explored as a bioherbicide for resistant weeds management programs.

Phytotoxic condensed organic compounds are common in fast but not slow pyrolysis biochars

Biochar chemistry varies with feedstock and pyrolysis parameters: fast pyrolysis may not provide sufficient time for volatile compounds – some phytotoxic – to escape from biochar particles. Lettuce and radish seeds were treated with biochar leachate derived from 100 slow pyrolysis biochars (20 wood species, each pyrolyzed at 300–700 °C for 60 min), and 20 fast pyrolysis biochars (two species pyrolyzed at 500 and 550 °C for 1–5 min). Slow pyrolysis biochar leachates enhanced radicle extension growth by (60% for lettuce; 16% for radish), while fast pyrolysis biochar leachates inhibited radicle growth by (63% for lettuce; 8% for radish). Slow pyrolysis biochars showed higher concentrations of Ca, Mg, K, Fe, Mn, and Zn than fast pyrolysis biochars, whereas fast pyrolysis biochars generally showed higher concentrations of phytotoxic volatile fatty acids, such as acetic and pentanoic acid. These results suggest the importance of extended pyrolysis residence times in producing high-nutrient biochars free from toxicity effects.

Aluminium Rhizotoxicity in Cicer arietinum

The effects of aluminium (Al)-induced alterations on elongating radicles of Cicer arietinum L. were studied in relation to growth and biochemical markers of oxidative stress. Elongating radicles (c. 1 mm) were treated with 0–3 mM aluminium chloride (pH 4.5) for seven days at room temperature (26 ± 2°C). The results indicated that exposure to Al significantly inhibited radicle growth. This growth inhibition was accompanied by excessively high levels of reactive oxygen species (ROS) production. The levels of ROS were significantly positively correlated with Al concentration. Levels of lipid and protein oxidation products increased significantly with an increase in Al concentration, and were significantly positively correlated with ROS levels. On the other hand, Al stress significantly decreased the activities of selected enzymatic antioxidants. Collectively, the results suggest that Al rhizotoxicity in C. arietinum is partially mediated by oxidative stress brought about by excessive ROS production and reduced antioxidant scavenging activity.

Evaluation of Allelopathic Activity of Chinese Medicinal Plants and Identification of Shikimic Acid as an Allelochemical from Illicium verum Hook. f.

This study focused on the potential allelopathy of 50 species of Chinese medicinal plants, which are mainly distributed in the Xinjiang Uyghur Autonomous Region, Inner Mongolia, and Yunnan Province. The “sandwich method” was adopted and used for the screening for allelopathic potential among these plant species. Further phytotoxic evaluation of the candidate species was conducted by applying plant extracts to crops and weed species. The results of this study indicated that among the 50 medicinal plant species evaluated, the fruits of Illicium verum Hook. f. (star anise) showed the most significant allelopathic potential through the leaf leachates. Shikimic acid was identified to be the main bioactive compound (about 7% dry weight) in star anise by reversed-phase High Performance Liquid Chromatography (RP-HPLC) analysis. The phytotoxic bioassay indicated that both the crude extract of the Chinese star anise and the synthetic shikimic acid showed strong inhibitory activity on the radicle and hypocotyl growth of lettuce. The radicle growth inhibition of lettuce caused by the crude extract of star anise could be explained by the contribution of the biological activity of shikimic acid. In conclusion, shikimic acid could be a putative allelochemical in the fruits of Illicium verum and could be utilized in sustainable weed management.

Plant Growth Inhibitory Activities and Volatile Active Compounds of 53 Spices and Herbs.

The inhibitory activities of the leachates and volatiles from 53 plant species (spices and herbs) were evaluated against lettuce (Lactuca sativa “Great Lakes 366”) seedling growth using the sandwich and dish pack methods, respectively. With the sandwich method, parsley (Petroselinum sativum) showed the strongest inhibitory effect on lettuce radicle growth (77%), followed by tarragon (Artemisia dracunculus) (72%). However, caraway (Carum carvi), dill (Anethum graveolens) (seed), laurel (Laurus nobilis), rosemary (Rosmarinus officinalis), and sage (Salvia officinalis) were the most inhibitory species (100% inhibition of lettuce radicle and hypocotyl growth inhibition at all distance wells) in the dish pack method. Cardamom (Elettaria cardamomum) and thyme (Thymus vulgaris) also showed strong inhibitory activity (100% for radicle and hypocotyl growth inhibition at all 41 and 58 mm distance wells). The headspace sampling and gas chromatography-mass spectrometry (GC-MS) analysis identified the main inhibitory active compounds as carvone in caraway and dill (seeds), 1,8-cineole in laurel and cardamom, and borneol in thyme. Both camphor and 1,8-cineole were detected in rosemary and sage, and the total activity evaluation showed that camphor was the major inhibitory compound in rosemary, although both compounds played equal roles in sage.

Interspecific variation, antioxidant and allelopathic activity of the essential oil from three Launaea species growing naturally in heterogeneous habitats in Egypt

AbstractEssential oils (EOs) from the aerial parts of three Launaea species collected from two different habitats were extracted [Launaea mucronata collected from coastal desert (LMC) and from inland desert (LMD), Launaea nudicaulis collected from coastal desert (LNC) and from inland desert (LND), Launaea spinosa (LS)]. The EOs were analysed by gas chromatography mass spectrometry (GC‐MS) and tested for antioxidant activity as well for allelopathic activity against purslane. A total of 117 compounds were identified from all samples, including 64 from LS, 50 from LMC, 39 from LMD, 24 from LNC, and 20 from LND, representing 100% of the total oil mass. The oxygenated sesquiterpenes were the major compounds of the EOs from LS, LMC, LMD, LNC, and LND, representing 62.73, 61.02, 58.35, 43.22, and 48.33%, respectively, whereas the monoterpene hydrocarbons were minor compounds in all samples. α‐Acorenol (31.42%), trans‐longipinocarveol (12.04%), and γ‐eudesmol (6.31%) represented the major compounds of the EO from LS, whereas hexahydrofarnesyl acetone and n‐heneicosane represented the major compounds from LMC, LMD, LNC, and LND. Correlations between the EOs of the five samples were studied via principal component analysis and agglomerative hierarchical clustering, based on the chemical composition of the EOs. There was a significant variation between Launaea species regarding both the quality and the quantity of EO composition, whereas no significant difference was observed based on the habitats (coastal and inland deserts). The EOs of the five Launaea samples exhibited meaningful antioxidant activities, as follows: LND > LNC > LMD > LMC > LS. Moreover, the EOs of the five Lanaea samples exhibited significant allelopathic activity against purslane weed in a concentration‐dependent manner. LMD and LMC showed the highest effect, with germination inhibition of 96.1 and 87.9% at 250 μL L−1, and radicle growth inhibition of 92.6 and 89.7%, but LS was the least effective extract. Our results showed that the variation in the quality and quantity of EO composition is mainly species specific, with a slight correlation with habitats.

Allelopathic potential of selected woody species growing on fly-ash deposits

The objective of this study was to determine the allelopathic potential of Robinia pseudoacacia L., Ailanthus altissima (Mill.) Swingle and Amorpha fruticosa L. that grow on the fly-ash deposits at the ?Nikola Tesla ? A? thermoelectric power plant in Obrenovac. The chemical characteristics of fly ash, such as pH, electrical conductivity (EC), content of carbon (C) and nitrogen (N), contents of available phosphorus (P2O5) and potassium (K2O), the contents of total and available Fe, Cu, Mn, Ni and Zn as well as of phenolic acids (3,5 dihydroxybenzoic acid (3,5-DHBA) and ferulic acid) and flavonoids (rutin and quercetin) were analyzed in control fly ash (bare zones without vegetation cover) and plant rhizospheric fly ash. In order to determine the allelopathic activity of phenolic compounds in fly ash, modified soil sandwich allelopathic biotests were performed, and Trifolium pratense L. (red clover) was used as the indicator species. A. fruticosa showed the highest allelopathic activity, followed by A. altissima whereas R. pseudoacacia showed the lowest allelopathic potential. Negative correlation was noted between radicle and hypocotyl growth inhibition of red clover and the pH of fly ash. Positive correlations were found between radicle growth inhibition and the content of C, P2O5, total concentrations of Cu, available concentrations of Mn and Ni, the contents of ferulic acid, 3,5-DHBA, and rutin. Our results indicate that A. fruticosa and A. altissima increased the content of phenolics in fly ash, which can act as allelochemicals leading to radicle growth inhibition of red clover in the pioneer plant community on fly-ash deposits. These woody species that colonized fly-ash deposits can initiate the beginning of pedogenetic processes altering the ecosystem processes at degraded sites.

Toxicity evaluation of the landfill leachate after treatment with photo-Fenton, biological and photo-Fenton followed by biological processes

The objective of this study was the toxicity evaluation of landfill leachate samples both raw and after treatment by photo-Fenton (PF), biological (Bio) and photo-Fenton followed by biological (PF-Bio) processes. The organisms Artemia salina and Lactuca sativa were exposed to the leachate in different dilution. In the phytotoxicity evaluation, the inhibition of root (RGI) and radicle (RAGI) growth, and the number of germinated seeds (GR) were evaluated. In the ecotoxicity analysis, the 50% lethal dose (LD50) for each type of treatment was evaluated. The raw leachate, and after treatments PF, Bio and PF-Bio presented COD of 12,797, 1,347, 1,685, 220 mg/L and BOD5 of 4,251, 1,060, 692 and 89 mg/L, respectively. The GR was 0, 95, 25 and 40%, RGI was 100, 83, 100, 93%, whereas RAGI was 100, 72, 100 and 79% in the raw leachate and after treatments PF, Bio and PF-Bio, respectively. LD50 values of 0.25, 0.40, 0.38 and 0.54 were obtained for the raw effluent and after the PF, Bio and PF-Bio treatments, respectively. Smaller values of COD, BOD5, ecotoxicity and phytotoxicity were observed in the effluent after the PF-Bio treatment, indicating that this is the most environmentally suitable system for the treatment of landfill leachate.

Evaluation of the anti-proliferative and cytotoxic potentials of fractions of methanol leaf extract of Cnidoscolus aconitifolius

The partitioned aqueous and chloroform fractions obtained from the methanol extract of the leaf of Cnidoscolus aconitifolius were examined for anti-proliferative (1-30 mg/mL) and cytotoxic activities (20-400 μg/mL) using the seed radicle inhibition and tadpole mortality assays over a period of 24 and 96 h respectively. The vacuum liquid chromatographic sub-fractions of the active chloroform fraction weresimilarly evaluated at 1-10 mg/mL and 5-20 μg/mL concentrations respectively. At 100 μg/mL the chloroform fraction produced 86.67 % mortality which increases to 100 % at 400 μg/mL where the aqueous fraction gave 36.67 %. The potency was further increased as the VLC sub-fractions C4-C6, gave 33 % cytotoxicity at 5 μg/mL and which later increased to 100 % at 10 μg/mL. At the end of 96 h, the control seed had average length of 32.32 ± 2.73 mm compared to 1.92 ± 0.36 and 0.52 ± 0.36 mm observed in the seeds treated with 20 and 30 μg/mL of the chloroform fraction indicating 94.01 and 98.39 % inhibition where as there was total radicle growth inhibition (100 %) of seeds treated with 5 mg/mL of the active VLC sub-fractions (C1-3, C4-C6 and C7). The results showed a significant cytotoxic and growth inhibitory effects of the plant extract, particularly the chloroform fraction and its sub-fractions which further corroborate the folkloric use of the plant in treating cancer. However, further chromatographic analysis of the active VLC sub-fraction and their respective biological studies using cancer cell-lines are needed to support this.Keywords: Cnidoscolus aconitifolius, Sorghum bicolor, anti-proliferative, cytotoxicity, methanol extract, aqueous fraction, chloroform extract , vacuum liquid chromatography,