Murale Plants Research Articles

EXPLORING MORPHOLOGICAL TRAITS VARIATION IN CHENOPODIUM MURALE: A COMPREHENSIVE MULTIVARIATE ANALYSIS

Chenopodium murale, a significant weed in wheat, maize, rice, sugarcane, and cotton fields, poses a substantial threat to crop plants due to its competitive nature for water, minerals, and nutrients, leading to significant yield losses. To address this issue, a prescribed study was conducted to assess the morphological traits of Chenopodium murale under three different environmental locations. The results revealed a positive and significant correlation among several study traits: height, dry weight, fresh weight, inflorescence fresh weight, leaf area, leaf length, leaf width, and root length. Notably, plant leaf width emerged as the most influential trait contributing to the plant's height. Furthermore, the study identified location three as an exceptionally favorable environment for the robust growth and development of Chenopodium murale plants. To mitigate potential yield losses in crop plants, the study recommends the timely removal or control of Chenopodium murale, emphasizing the importance of managing its population effectively.

Modulation of the toxic effects of zinc oxide nanoparticles by exogenous salicylic acid pretreatment in Chenopodium murale L.

Due to many uses of zinc oxide nanoparticles (ZnO NPs) in various industries, the release of these particles in the environment and their effects on living organisms is inevitable. In this study, the role of salicylic acid (SA) pretreatments in modulating the toxicity of ZnO NPs was investigated using a hydroponic system. After pretreatment with different concentrations of SA (0, 25, 75, and 150 μM), Chenopodium murale plants were exposed to ZnO NPs (50 mg L-1). The results showed that exogenous SA increased the length, weight, chlorophyll, proline, starch, and soluble sugars in the plants. Besides, SA pretreatments improved water status in the plants treated with ZnO NPs. In SA-pretreated plants, increased activity of catalase (CAT), guaiacol peroxidase (GPX), and superoxide dismutase (SOD) was associated with a decline in electrolyte leakage (EL %) and membrane peroxidation. Under NPs stress, SA pretreatments increased the content of phenolic compounds by increasing the activity of phenylalanine ammonia-lyase (PAL). Exogenous SA reduced the translocation of larger amounts of Zn to the shoots, with more accumulation in the roots. This result can be used to produce healthy food from plants grown in environments contaminated with nanoparticles. It seems that all concentrations of SA reduced the symptoms of ZnO NPs toxicity in the plant by strengthening the function of the antioxidant system and increasing the content of some metabolites. Findings also suggest that SA pretreatment can compensate for the growth reduction caused by ZnO NPs.

Biomass and metal yield of co-cropped Alyssum murale and Lupinus albus

Combining crops is a potential option to gain more value from ultramafic soils. This work was designed to investigate the co-cropping of a legume, Lupinus albus, and a Ni-hyperaccumulator, Alyssum murale Waldst. & Kit, and determine whether growth and metal uptake would be altered by a companion plant. A pot experiment was conducted in a growth chamber in two serpentine topsoils that were low in P but differed in Ni and Mn concentrations. The soils were a Magnesic Eutric Cambisol (S1) and a Hypermagnesic Hypereutric Cambisol (S2). Pots were split into two compartments along the diagonal by a double-layer nylon mesh, and the space between the meshes was filled with same soil. Each plant was either mono-cropped (sown on both compartments) or co-cropped (one species per compartment). For all combinations, two treatments were prepared: one with no P fertilisation and the other with P addition. L. albus and A. murale plants were grown for 45 and 57 days respectively. Results showed that both plants responded positively to P fertilisation. In co-cropping systems on non-P treatments, L. albus accounted for the majority of the total biomass (higher than 90%), whereas with P addition the contribution of A. murale reached almost 40%. P fertilisation provoked an increase in Ni concentration in A. murale (S1), or no change (S2). Co-cropping significantly reduced Ni concentration in shoots of A. murale and total Ni exportation was slightly lower than when plants were grown individually. L. albus accumulated high concentrations of Mn and co-cropping and P deficiency increased Mn uptake. In this co-cropping system L. albus and A. murale interacted positively, and this association is a feasible means to increase the productivity of phytomining on serpentine soils provided appropriate fertilisation is supplied.

Evidence of olive mild mosaic virus transmission by Olpidium brassicae

Transmission of three strains of OMMV by an Olpidium sp. was evaluated and compared. The three strains were 1) an OMMV wild type (WT) recovered from olive trees, 2) an OMMV variant (L11) obtained after 15 serial passages of single local lesions induced in Chenopodium murale plants, and 3) a construct OMMV/OMMVL11 in which the coat protein (CP) gene replaced that of the wild type. A single-sporangial culture derived from Chinese cabbage (Brassica pekinensis) used as a bait plant grown in soil of an olive orchard, was identified as Olpidium brassicae based on the size and sequence of the generated amplicon in PCR specific tests. Each of the three virus strains was soil transmitted to cabbage roots in the absence of the fungus at similar rates of 30 to 40%. Separate plant inoculation by O. brassicae zoospores incubated with each viral strain resulted in enhanced transmission of OMMV, reaching 86% of infection whereas that of the other two strains remained practically unaffected at ca. 34%. Binding assays showed that the amount of virus bound to zoospores, estimated spectrophotometrically, was 7% in the case of OMMV, and practically nil in the case of the other two viral strains. Substitution of the coat protein (CP) gene of OMMV by that of the OMMV L11 strain, drastically reduced viral transmissibility in the presence of zoospores to the level of that observed in their absence. Our data shows that OMMV soil transmission is greatly enhanced by O. brassicae zoospores and that the viral CP plays a significant role in this process, most likely by facilitating virus binding and later entrance into the host plant roots.

Exogenous Cytokinin Treatments of an NI Hyper-Accumulator, Alyssum Murale, Grown in a Serpentine Soil: Implications for Phytoextraction

Application of exogenous plant growth regulators was examined as a viable technique to increase the efficiency of plant metal extraction from contaminated soils. The aim of this study was to investigate the alteration of Ni phytoextraction by Alyssum murale, a Ni hyperaccumulator, following the application of cytokinins. The following parameters were investigated: Ni accumulation, plant growth, gas exchange, stomata behavior and the concentration of nonprotein thiols (glutathione, y-Glu-Cys, and phytochelatins). In a pot experiment, A. murale plants grown in a serpentine soil were treated with a mix of naturally occurring cytokinins. Results showed that Ni accumulation in plants ranged from 4000 to 7000 mg kg−1 confirming the hyper-accumulation ability from the soil used. Cytokinin treatments produced a significant increase in plant biomass and transpiration rate whereas no significant variation in Ni accumulation or the concentration of non-protein thiols was observed. The results suggest that A. murale is a plant species sensitive to cytokinin treatment and that cytokinin treatment is potentially useful in increasing the phytoextraction capability by increasing biomass. Moreover, for first time, evidence was obtained that the Ni hyperaccumulation mechanism is independent of water flux and transpiration rate.

Purification and characterization of thermostable monomeric chloroplastic Cu/Zn superoxide dismutase from Chenopodium murale.

Superoxide dismutase is the first line of defense against oxidative stress and thus helps in maintaining the cellular integrity. Chenopodium murale, a weed species adapted to widely varying climatic conditions faces extremes of temperatures ranging from 4 °C to 45 °C (Tmax) during growth and development. From this plant, we have purified a thermostable chloroplastic Cu/Zn superoxide dismutase (Chl Cu/Zn SOD) to homogeneity using minimal steps. Incubation of lysed chloroplasts at 70 °C for 1h reduced the interference of cytosolic SOD isoforms and reduced the protein content by 75 %. Chloroplastic SOD was purified from the heat stable fraction by gel filtration chromatography. The purified enzyme had a native molecular weight of 24 kDa, a half-life of 47.9 min at 80 °C and showed a single band at 24 kDa on SDS-PAGE. The N-terminus contained the conserved amino acids of chl Cu-Zn SOD. The Chl Cu/Zn SOD protein and its activity were enhanced under very high temperatures, high light intensities and in water stress/recovered C. murale plants under controlled environment conditions. Chl Cu/Zn SOD was also one of the predominant isoforms throughout growing period in field grown plants and declined during senescence. The Chl Cu/Zn SOD activity increased with the increase in ambient temperature and peaked in April with a 45 °C Tmax. These results clearly indicate that the chloroplastic Cu/Zn SOD is stably expressed at extreme environmental conditions. The presence of stable monomeric chloroplastic Cu/Zn SOD might help the plants to maintain the cellular homeostatis against adverse environmental conditions.

Somatic embryogenesis in Chenopodium rubrum and Chenopodium murale in vitro

In order to establish an efficient system for in vitro plant regeneration of a short day plant Chenopodium rubrum L. and a long day plant Chenopodium murale L., optimum culture conditions for somatic embryogenesis were investigated. The effects of different growth regulators, their combination and their concentrations on somatic embryos induction in different explant types (root, hypocotyl, cotyledon and leaf) were tested. Somatic embryogenesis was induced in both plants on Murashige and Skoog (MS) medium supplemented with sucrose (3 %), agar (0.7 %) and 1 - 10 μM 2,4-dichlorophenoxyacetic acid (2,4-D) as the sole growth regulator. The largest embryogenic capacity was found in root explants of Chenopodium rubrum on 1 μM 2,4-D and in basal parts of cotyledons in C. murale plants on 10 μM 2,4-D.

The Lettuce infectious yellows virus (LIYV)-encoded P26 is associated with plasmalemma deposits within LIYV-infected cells

Cytological, immunological, and mutagenesis approaches were used to identify the viral factors associated with the formation of plasmalemma deposits (PLDs) in whole plants and protoplasts infected by Lettuce infectious yellows virus (LIYV). Transmission electron microscopy and immunogold labeling using polyclonal antibodies to four of the five LIYV RNA 2-encoded large proteins, capsid protein (CP), minor capsid protein (CPm), HSP70 homolog (HSP70h), and P59, showed specific labeling of LIYV virions or virion aggregates around the vesiculated membranous inclusions, but not PLDs in LIYV-infected Nicotiana benthamiana, Nicotiana clevelandii, Lactuca sativa, and Chenopodium murale plants, and Nicotiana tabacum protoplasts. In contrast, antibodies to the RNA 2-encoded P26 showed specific labeling of PLDs but not virions in both LIYV-infected plants and protoplasts. Virion-like particles (VLPs) were seen in protoplasts infected by all LIYV RNA 2 mutants except for the CP (major capsid protein) mutant. PLDs were more difficult to find in protoplasts, but were seen in protoplasts infected by the CP and CPm mutants, but not in protoplasts infected by the P26, HSP70h, or P59 mutants. Interestingly, although the CPm mutant showed VLPs and PLDs, the PLDs did not show associated virions/virion-like particles as was always observed for PLDs seen in protoplasts infected by wild-type LIYV. Immunoblot analyses performed on purified LIYV virions showed that P26 was not detected with purified virions, but was detected in the cell wall, 1000 g and 30,000 g pellet fractions of LIYV-infected plants. These data suggest that P26 is associated with the LIYV-induced PLDs, and in contrast to the other RNA 2-encoded large proteins, P26 is not a virion protein.

Effect of Darkness on Growth and Flowering of Chenopodium rubrum and C. murale Plants in vitro

Chenopodium rubrum, a short-day plant, and C. murale, a long-day plant, were grown in vitro in continuous darkness. Control C. rubrum plants exposed to continuous darkness for 15 d at cotyledonary phase, did not flower, while 80 % of plants flowered on the medium with 5 % glucose and 10 mg dm-3 GA3. Control C. murale plants exposed to continuous darkness for 10 d at the age of 4th pair of leaves, did not flower, while GA3 (1 - 5 mg dm-3) stimulated flowering up to 65 %.

Nucleolytic activities and appearance of a new DNase in relation to nickel and manganese accumulation in Alyssum murale

Summary Serpentine and non-serpentine plants of Alyssum murale, a nickel (Ni) accumulator plant, from North Greece, were studied in order to examine: (1) The ability of natural plants to accumulate metals; (2) the ability of their seedlings to tolerate increasing concentrations of Ni 2+ or Mn 2+ (0, 0.16, 0.32, 0.5 and 1 mmol/L), when grown in nutrient solution; (3) the activities and electrophoretic patterns of root and shoot DNases and RNases under the above conditions. Measurements of metal concentrations in serpentine and non-serpentine natural plants and the respective soils revealed: (1) Very low calcium (Ca)/magnesium (Mg) (∼0.16) ratio and high concentration of Ni in serpentine soil; (2) very high Ca/Mg (∼17) ratio and high concentration of manganese (Mn) in non-serpentine soil; (3) the ability of serpentine natural plants to accumulate Ni and the inability of plants of both serpentine and non-serpentine populations to accumulate Mn. A. murale plants grown in nutrient solution with increasing Ni 2+ or Mn 2+ concentrations showed a negative correlation between the Ni 2+ or Mn 2+ concentrations in the nutrient solution, and the chlorophyll concentration, shoot and especially root length. The accumulation of Ni 2+ or Mn 2+ in the plant showed a positive correlation with increasing Ni 2+ or Mn 2+ concentrations in the nutrient solution. Application of 0.5 mmol/L Ni 2+ or Mn 2+ resulted in the inhibition of DNase activities and the appearance of a new DNase form, in both root and shoot detected by electrophoresis in active ssDNA polyacrylamide gel. The new gel-extracted DNase showed nicking action against plasmid DNA and has been characterised as an endo-DNase. In contrast, electrophoretic patterns and RNase activities were unaffected. According to our studies on growth, both serpentine and non-serpentine plants of A. murale have a constitutive ability to tolerate and accumulate Ni 2+ or Mn 2+ ; they have similar DNase and RNase electrophoretic patterns and show a new DNase form under Ni 2+ or Mn 2+ stress. This is the first report on the response of nucleolytic enzymes under metallic elements hyperaccumulation.

The Effects of Growth Regulators on Flowering of Chenopodium murale Plants in vitro

In vitro culture of Chenopodium murale L. (ecotype 197) green and herbicide SAN 9789 - treated white plants was established and the effects of benzylaminopurine (BAP), indole-3-acetic acid (IAA) and gibberellic acid (GA3) on growth and flowering were tested. Green plants did not flower on glucose free media, while 17 % of plants flowered on 5 % glucose-containing medium. SAN 9789 (10−5 M) inhibited growth and flowering. BAP and IAA (0.1 – 5 mg dm−3) also inhibited growth and flowering of green and white plants. GA3 (10 mg dm−3) stimulated leaf development in green plants, but had no significant effect on white plants, and stimulated flowering of green (41 %) and white (33 %) plants.

Ethylene production and metabolism of 1-aminocyclopropane-1-carboxylic acid in a long-day plant,Chenopodium murale L., as influenced by photoperiodic flower induction

Chenopodium murale plants, induced to flower by 5 days of continuous light, produced 43% more ethylene than vegetative plants kept under short days (16 h darkness, 8 h light). The 1-aminocyclopropane-1-carboxylic acid (ACC)-induced ethylene production, using saturating ACC concentration (10 mol·m−3) was also 55% higher in induced plants. Their ACC and N-malonyl-ACC (MACC) levels were also higher, the former increasing by 56% in both shoots and roots, the latter by 288% and 108% in shoots and roots, respectively. Administration of labeled [2,3-14C]ACC produced a very similar relative content of ACC and MACC in both treatments. The only process influenced by flower induction was ACC conversion to ethylene. Induced plants converted 66% more ACC than the vegetative ones. The effects of photoperiod on ethylene formation and metabolism in a long-day plant (LDP)C. murale and a short-day plant (SDP)C. rubrum are compared. Ethylene formation seems to be under photoperiodic control in both species, but its role in flower induction remains obscure.