ABSTRACT
The differential effects of cellular and ultrastructural characteristics on the optical properties of adaxial and abaxial leaf surfaces in the genus Tradescantia highlight the intricate relationships between cellular arrangement and pigment distribution in the plant cells. We examined hyperspectral and chlorophyll a fluorescence (ChlF) kinetics using spectroradiometers and optical and electron microscopy techniques. The leaves were analysed for their spectral properties and cellular makeup. The biochemical compounds were measured and correlated with the biophysical and ultrastructural features. The main findings showed that the top and bottom leaf surfaces had different amounts and patterns of pigments, especially anthocyanins, flavonoids, total phenolics, chlorophyll-carotenoids, and cell and organelle structures, as revealed by the hyperspectral vegetation index (HVI). These differences were further elucidated by the correlation coefficients, which influence the optical signatures of the leaves. Additionally, ChlF kinetics varied between leaf surfaces, correlating with VIS-NIR-SWIR bands through distinct cellular structures and pigment concentrations in the hypodermis cells. We confirmed that the unique optical properties of each leaf surface arise not only from pigmentation but also from complex cellular arrangements and structural adaptations. Some of the factors that affect how leaves reflect light are the arrangement of chloroplasts, thylakoid membranes, vacuoles, and the relative size of the cells themselves. These findings improve our knowledge of the biophysical and biochemical reasons for leaf optical diversity, and indicate possible implications for photosynthetic efficiency and stress adaptation under different environmental conditions in the mesophyll cells of Tradescantia plants.
Subject(s)
Plant Leaves , Tradescantia , Tradescantia/metabolism , Plant Leaves/metabolism , Plant Leaves/ultrastructure , Fluorescence , Chlorophyll/metabolism , Chlorophyll A/metabolismABSTRACT
We present an approach to the noninvasive determination of the electron capacity of the intersystem pool of electron carriers in chloroplasts in situ. As apt experimental models, we used the leaves of Hibiscus rosa-sinensis and Tradescantia species. Electron paramagnetic resonance and optical response of P700 (the primary electron donor in Photosystem I) were applied to measuring electron transport in chloroplasts. Electron capacities of the intersystem electron transport chain (ETC) were determined from redox transients of P700 upon chromatic transitions (white light â far-red light). During the induction period, we observed the nonmonotonic changes in the number of electron equivalents in the intersystem ETC per P700 (parameter Q). In Hibiscus rosa-sinensis, the light-induced rise of Q from ≈2.5 (in the dark) to Q ≈ 12 was followed by its decrease to Q ≈ 6. The data obtained are discussed in the context of pH-dependent regulation of electron transport in chloroplasts, which provides the well-balanced operation of the intersystem ETC. The decay of Q is explained by the attenuation of Photosystem II activity due to the lumen acidification and the acceleration of plastoquinol re-oxidation as a result of the Calvin-Benson cycle activation. Our computer model of electron and proton transport coupled to ATP synthesis in chloroplasts was used to analyze the up and down feedbacks responsible for pH-dependent regulation of electron transport in chloroplasts. The procedures introduced here may be important for subsequent works aimed at defining the plastoquinone participation in regulation of photosynthetic processes in chloroplasts in situ.
Subject(s)
Chloroplasts/metabolism , Hibiscus/metabolism , Photosynthesis/physiology , Tradescantia/metabolism , Electron Spin Resonance Spectroscopy , Electron Transport , Light , Oxidation-Reduction , Photosystem I Protein Complex/metabolism , Plant Leaves/metabolismABSTRACT
Tradescantia spathacea Sw. (Commelinaceae) is widely cultivated as an ornamental and medicinal plant in Southeast Asia, and its pharmacological properties are well known. On the other hand, this plant species is classified as an invasive weed in some countries. As a noxious weed, T. spathacea has been reported to disrupt the growth of native plants. However, no study has reported on its allelopathic activity. Thus, we investigated the allelopathic property and inhibitory substance of T. spathacea. The extracts of T. spathacea significantly inhibited the shoots and roots of alfalfa (Medicago sativa L.), cress (Lepidium sativum L.), lettuce (Lactuca sativa L.), barnyard grass (Echinochloa crus-galli (L.) P. Beauv.), Italian ryegrass (Lolium multiflorum Lam.), and timothy (Phleum pratense L.) at concentrations ≥ 3 mg dry weight (D.W.) equivalent extract/mL. As the extract concentration increased, the growth of the shoots and roots decreased. The I50 values of the test plant shoots and roots were 11.6-72.4 and 5.4-19.5 mg D.W. equivalent extract/mL, respectively. The extracts were purified by column chromatography, and an inhibitory substance was separated, which inhibited the shoots and roots of cress to 18.8 and 11.6% of control growth, respectively. The results of present findings indicate that T. spathacea extracts possess an allelopathic property, and its inhibitory substance may contribute this activity.
Subject(s)
Allelopathy/physiology , Tradescantia/metabolism , Weed Control/standards , Plant Extracts/analysis , Tradescantia/enzymology , Weed Control/methodsABSTRACT
A spectacular but poorly recognized nuclear repatterning is the association of heterochromatic domains during interphase. Using base-specific fluorescence and extended-depth-of-focus imaging, we show that the association of heterochromatic pericentromeres composed of AT- and GC-rich chromatin occurs on a large scale in cycling meiotic and somatic cells and during development in ring- and bivalent-forming Tradescantia spathacea (section Rhoeo) varieties. The mean number of pericentromere AT-rich domains per root meristem nucleus was ca. half the expected diploid number in both varieties, suggesting chromosome pairing via (peri)centromeric regions. Indeed, regular pairing of AT-rich domains was observed. The AT- and GC-rich associations in differentiated cells contributed to a significant reduction of the mean number of the corresponding foci per nucleus in relation to root meristem. Within the first 10 mm of the root, the pericentromere attraction was in progress, as if it was an active process and involved both AT- and GC-rich associations. Complying with Rabl arrangement, the pericentromeres preferentially located on one nuclear pole, clustered into diverse configurations. Among them, a strikingly regular one with 5-7 ring-arranged pericentromeric AT-rich domains may be potentially engaged in chromosome positioning during mitosis. The fluorescent pattern of pachytene meiocytes and somatic nuclei suggests the existence of a highly prescribed ring/chain type of chromocenter architecture with side-by-side arranged pericentromeric regions. The dynamics of pericentromere associations together with their non-random location within nuclei was compared with nuclear architecture in other organisms, including the widely explored Arabidopsis model.
Subject(s)
Base Composition , Cell Differentiation/genetics , Gene Expression Regulation, Developmental , Gene Expression Regulation, Plant , Heterochromatin/genetics , Plant Development/genetics , Tradescantia/genetics , Centromere , Genome, Plant , Heterochromatin/metabolism , In Situ Hybridization, Fluorescence , Meiosis , Tradescantia/metabolismABSTRACT
Using thermoluminescence, PAM-fluorometry, and electron paramagnetic resonance (EPR) for assaying electron transport processes in chloroplasts in situ, we have compared photosynthetic characteristics in Tradescantia fluminensis leaves grown under low light (LL, 50-125 µmol photons m-2 s-1) or high light (HL, 875-1000 µmol photons m-2 s-1) condition. We found differences in the thermoluminescence (TL) spectra of LL- and HL-acclimated leaves. The LL and HL leaves show different proportions of the Q (~ 0 °C) and B (~ 25-30 °C) bands in their TL spectra; the ratios of the "light sums" of the Q and B bands being SQ/SB ≈ 1/1 (LL) and SQ/SB ≈ 1/3 (HL). This suggests the existence of different redox states of electron carriers on the acceptor side of PSII in LL and HL leaves, which may be affected, in particular, by different capacities of their photo-reducible PQ pools. Enhanced content of PQ in chloroplasts of LL leaves may be the reason for an efficient performance of photosynthesis at low irradiance. Kinetic studies of slow induction of Chl a fluorescence and measurements of P700 photooxidation by EPR demonstrate that HL leaves have faster (about 2 times) response to switching on actinic light as compared to LL leaves grown at moderate irradiation. HL leaves also show higher non-photochemical quenching (NPQ) of Chl a fluorescence. These properties of HL leaves (faster response to light and generation of enhanced NPQ) reflect the flexibility of their photosynthetic apparatus, providing sustainability and rapid response to fluctuations of environmental light intensity and solar stress resistance. Analysis of time-courses of the EPR signals of [Formula: see text] induced by far-red (λmax = 707 nm), exciting predominantly PSI, and white light, exciting both PSI and PSII, suggests that there is a contribution of cyclic electron flow around PSI to electron flow through PSI in HL leaves. The data obtained are discussed in terms of photosynthetic apparatus sustainability of HL and LL leaves under variable irradiation conditions.
Subject(s)
Electron Transport/radiation effects , Tradescantia/metabolism , Chlorophyll/metabolism , Chloroplasts/metabolism , Electron Spin Resonance Spectroscopy , Kinetics , Light , Photosynthesis , Plant Leaves/metabolism , Tradescantia/radiation effectsABSTRACT
In this work, over the course of four seasons (12â¯months), we have monitored the fluorescence quantum efficiency (η) from two sets (S1 and S2) of fresh natural dye extracts from the leaves of Tradescantia pallida purpurea. The natural dye was extracted in aqueous solutions from leaves collected from regions with a predominance of shade (S1) and sun (S2) during the day. The thermo-optical parameter fractional thermal load (φ) was measured using conical diffraction (CD) patterns caused by thermally driven self-phase modulation, for η determination in both sets of solutions. Fluorescence measurements corroborate the CD results, and the η values are, on average, slightly higher (~ 11%) in the summer than in the other seasons for both sets of samples (S1 and S2). In addition, the experimental results are presented using natural dye extracted from Tradescantia pallida purpurea as a fungicide probe in Fusarium solani, Sclerotinia sclerotiorum, and Colletotrichum gloeosporioides fungi. The promising fungicide results obtained for the aqueous natural dye extract were compared with those obtained for other natural dyes and fungi. The fungi tested are of the necrotrophic group and constitute important pathosystems in Brazil, causing diseases in several crops that synthetic fungicides often cannot control or do so with low efficiency.
Subject(s)
Antifungal Agents/chemistry , Coloring Agents/chemistry , Plant Extracts/chemistry , Tradescantia/chemistry , Antifungal Agents/isolation & purification , Antifungal Agents/pharmacology , Coloring Agents/isolation & purification , Coloring Agents/pharmacology , Fungi/drug effects , Plant Leaves/chemistry , Plant Leaves/metabolism , Refractometry , Seasons , Tradescantia/metabolismABSTRACT
Tradescantia fluminensis is an invasive plant species in New Zealand, Australia and parts of the USA. It reproduces vegetatively and can grow to form dense mats up to 60 cm deep. Growth is limited by available light, and shading is one of the few effective methods of control. In this paper, we develop a dynamic model of a vertical cross section of a T. fluminensis mat, capturing vertical variation in its biomass and internal light intensity. We measure both variables at different heights in experimental mats of the species and use these data to parameterize the model. The model produces realistic vertical biomass and light intensity profiles. We show that the mat grows to a steady-state biomass that depends only on: (i) the light absorption coefficient, which we estimate from experimental data and (ii) the ratio of photosynthesis to respiration rate. This steady state undergoes a transcritical bifurcation; when the ambient light intensity falls below a critical level, the biomass shrinks to zero and the mat cannot survive.
Subject(s)
Introduced Species , Models, Biological , Tradescantia/growth & development , Animals , Biomass , Computer Simulation , Conservation of Natural Resources , Darkness , Ecosystem , Introduced Species/statistics & numerical data , Light , Mathematical Concepts , New Zealand , Photosynthesis , Plant Leaves/growth & development , Plant Leaves/metabolism , Plant Leaves/radiation effects , Tradescantia/metabolism , Tradescantia/radiation effectsABSTRACT
Here, we summarize diverse evidence from species that belong to the genus Tradescantia, which we propose as handy and versatile models for studies of the ecology of photosynthesis and the mechanisms of photoacclimation in higher plants. A valuable feature of this genus is the amazingly broad range of ecological niches occupied by its species: from shady understory of tropical rainforest to deserts and semideserts. The former habitats demand shade tolerance (e.g. that featured by Tradescantia fluminensis), whereas the latter requires succulence and/or high light stress tolerance (evident in e.g. Tradescantia navicularis). At the same time, the acclimative traits of Tradescantia species seem quite moderate at first glance. Certainly, their basic principles of acclimation seem to differ in some aspects from the ones typical for most of other higher plants. This review presents a systematic analysis of irradiance responses of Tradescantia species studied on different timescales. The specifics of Tradescantia responses to irradiance make the plants of this genus a 'multitool' for studies in this field. Similarity of irradiance acclimation patterns is a characteristic feature in the ecologically contrasting Tradescantia species, which may inspire further insights into physiology and evolution of plants.
Subject(s)
Tradescantia/metabolism , Tradescantia/physiology , Chlorophyll/metabolism , Ecology , Ecosystem , Photosynthesis/physiologyABSTRACT
In plants, the short-term regulation (STR, seconds to minute time scale) of photosynthetic apparatus is associated with the energy-dependent control in the chloroplast electron transport, the distribution of light energy between photosystems (PS) II and I, activation/deactivation of the Calvin-Benson cycle (CBC) enzymes, and relocation of chloroplasts within the plant cell. In this work, using a dual-PAM technique for measuring the time-courses of P700 photooxidation and Chl a fluorescence, we have investigated the STR events in Tradescantia fluminensis leaves. The comparison of Chl a fluorescence and [Formula: see text] induction allowed us to investigate the contribution of the trans-thylakoid pH difference (ΔpH) to the STR events. Two parameters were used as the indicators of ΔpH generation: pH-dependent component of non-photochemical quenching of Chl a fluorescence, and pHin-dependent rate of electron transfer from plastoquinol (PQH2) to [Formula: see text] (via the Cyt b6f complex and plastocyanin). In dark-adapted leaves, kinetics of [Formula: see text] induction revealed three phases. Initial phase is characterized by rapid electron flow to [Formula: see text] (τ1/2 ~ 5-10 ms), which is likely related to cyclic electron flow around PSI, while the outflow of electrons from PSI is restricted by slow consumption of NADPH in the CBC. The light-induced generation of ΔpH and activation of the CBC promote photooxidation of P700 and concomitant retardation of [Formula: see text] reduction (τ1/2 ~ 20 ms). Prolonged illumination induces additional slowing down of electron transfer to [Formula: see text] (τ1/2 ≥ 30-35 ms). The latter effect is not accompanied by changes in the Chl a fluorescence parameters which are sensitive to ΔpH generation. We suggest the tentative explanation of the latter results by the reversal of Q-cycle, which causes the deceleration of PQH2 oxidation due to the back pressure of stromal reductants.
Subject(s)
Fluorescence , Plant Leaves/metabolism , Tradescantia/metabolism , Photosynthesis/genetics , Photosynthesis/physiology , Plant Leaves/genetics , Tradescantia/geneticsABSTRACT
In this work, we have compared photosynthetic characteristics of photosystem II (PSII) in Tradescantia leaves of two contrasting ecotypes grown under the low light (LL) and high light (HL) regimes during their entire growth period. Plants of the same genus, T. fluminensis (shade-tolerant) and T. sillamontana (sun-resistant), were cultivated at 50-125 µmol photons m-2 s-1 (LL) or at 875-1000 µmol photons m-2 s-1 (HL). Analyses of intrinsic PSII efficiency was based on measurements of fast chlorophyll (Chl) a fluorescence kinetics (the OJIP test). The fluorescence parameters Fv/Fm (variable fluorescence) and F0 (the initial level of fluorescence) in dark-adapted leaves were used to quantify the photochemical properties of PSII. Plants of different ecotypes showed different sustainability with respect to changes in the environmental light intensity and temperature treatment. The sun-resistant species T. sillamontana revealed the tolerance to variations in irradiation intensity, demonstrating constancy of maximum quantum efficiency of PSII upon variations of the growth light. In contrast to T. sillamontana, facultative shade species T. fluminensis demonstrated variability of PSII photochemical activity, depending on the growth light intensity. The susceptibility of T. fluminensis to solar stress was documented by a decrease in Fv/Fm and a rise of F0 during the long-term exposition of T. fluminensis to HL, indicating the loss of photochemical activity of PSII. The short-term (10 min) heat treatment of leaf cuttings caused inactivation of PSII. The temperature-dependent heating effects were different in T. fluminensis and T. sillamontana. Sun-resistant plants T. sillamontana acclimated to LL and HL displayed the same plots of Fv/Fm versus the treatment temperature (t), demonstrating a decrease in Fv/Fm at t ≥ 45 °C. The leaves of shadow-tolerant species T. fluminensis grown under the LL and HL conditions revealed different sensitivities to heat treatment. Plants grown under the solar stress conditions (HL) demonstrated a gradual decline of Fv/Fm at lower heating temperatures (t ≥ 25 °C), indicating the "fragility" of their PSII as compared to T. fluminensis grown at LL. Different responses of sun and shadow species of Tradescantia to growth light and heat treatment are discussed in the context of their biochemical and ecophysiological properties.
Subject(s)
Photosystem II Protein Complex/metabolism , Tradescantia/metabolism , Chlorophyll/metabolism , Hot Temperature , Light , Photosynthesis/physiologyABSTRACT
Numerous investigations have demonstrated that even soil in which concentrations of individual elements do not exceed permissible limits can cause harmful effects in living organisms. In the present study, polluted-soil-induced oxidative stress was evaluated using Tradescantia clone 4430, which is widely used for genotoxicity evaluations, employing biochemical (superoxide dismutase (SOD), contents of ascorbic acid (AA), carotenoids (Car), hydrogen peroxide (H2O2), chlorophyll (Chl) a/b ratio), and molecular (RAPD and differential display (DD-PCR)) markers after long-term exposure. The activity (staining intensity) of SOD isoforms in Tradescantia leaves was higher in plants grown in all heavy-metal-polluted test soils compared to the control. No direct link between the soil pollution category and the contents of AA, Car, Chl a/b in Tradescantia leaves was revealed, but the concentration of H2O2 was shown to be a sensitive biochemical indicator that may appropriately reflect the soil contamination level. Both short-term (treatment of cuttings with H2O extracts of soil) and long-term (0.5 and 1.0 year) exposure increased MN frequencies, but the coincidence of the MN induction and the soil pollution level was observed only in some cases of long-term exposure. Soil (geno)toxin-induced polymorphism in the RAPD profile was determined with two primers in plants after long-term exposure to soils of an extremely hazard category. Transcript profiling of plants after long-term cultivation in test soils using DD-PCR showed that the majority of differentially expressed transcript-derived fragments (TDFs) were homologous to genes directly or indirectly participating in photosynthesis, the abiotic stress response, and signal transduction cascades.
Subject(s)
Industry , Metals, Heavy/toxicity , Oxidative Stress , Soil Pollutants/toxicity , Soil/chemistry , Tradescantia/drug effects , DNA Damage , Gene Expression Profiling , Hydrogen Peroxide/metabolism , Metals, Heavy/analysis , Oxidative Stress/drug effects , Oxidative Stress/genetics , Soil Pollutants/analysis , Tradescantia/genetics , Tradescantia/metabolism , Transcriptome/drug effectsABSTRACT
Discharge of wastewater from electroplating and leather industries is a major concern for the environment due to the presence of toxic Cr6+ and other ions, such as sulfate, nitrate, phosphate, etc. This study evaluated the potential of Tradescantia pallida, a plant species known for its Cr bioaccumulation, for the simultaneous removal of Cr6+, SO42-, NO3-, and PO43-. The effect of different co-ions on Cr6+ removal by T. pallida was examined following the Plackett-Burman design of experiments carried out under batch hydroponics conditions. The results revealed a maximum removal of 84% Cr6+, 87% SO42-, 94% NO3- and 100% PO43- without any phytotoxic effect on the plant for an initial Cr6+ concentration in the range 5-20 mg L-1. SO42- and NO3- enhanced Cr uptake at a high initial Cr concentration (20 mg L-1), whereas PO43- did not affect Cr uptake both at high and low initial Cr concentrations. The Cr6+ removal kinetics in the presence of different ions was well described by the pseudo-second-order kinetic model which revealed that both biosorption and bioaccumulation of the metal played an important role in Cr6+ removal. Increase in the total carbohydrate and protein content of the plant following Cr6+ and co-ions exposure indicated a good tolerance of the plant toward Cr6+ toxicity. Furthermore, enhancement in the lipid peroxidation and catalase activity in T. pallida upon Cr6+ exposure revealed a maximum stress-induced condition in the plant. Overall, this study demonstrated a very good potential of the plant T. pallida for Cr6+ removal from wastewater even in the presence of co-ions.
Subject(s)
Biodegradation, Environmental , Chromium , Tradescantia , Wastewater , Water Pollutants, Chemical , Chromium/metabolism , Electroplating , Ions , Kinetics , Lipid Peroxidation , Oxidation-Reduction , Tradescantia/metabolism , Water Pollutants, Chemical/metabolismABSTRACT
The kinetics of irradiation-induced changes in leaf optical transparence (ΔT) and non-photochemical quenching (NPQ) of chlorophyll fluorescence in Tradescantia fluminensis and T. sillamontana leaves adapted to different irradiance in nature was analyzed. Characteristic times of a photoinduced increase and a dark decline of ΔT in these species were 12 and 20 min, respectively. The ΔT was not confirmed to be the main contributor to the observed middle phase of NPQ relaxation kinetics (τ = 10-28 min). Comparison of rate of photoinduced increase in ΔT and photosystem II quantum yield recovery showed that the former did not affect the tolerance of the photosynthetic apparatus (PSA) to irradiances up to 150 µmol PAR·m-2·s-1. Irradiance tolerance correlated with the rate of "apparent NPQ" induction. Considering that the induction of apparent NPQ involves processes significantly faster than ΔT, we suggest that the photoprotective mechanism induction rate is crucial for tolerance of the PSA to moderate irradiance during the initial stage of light acclimation (first several minutes upon the onset of illumination).
Subject(s)
Chlorophyll/chemistry , Fluorescence , Photosystem II Protein Complex/chemistry , Plant Leaves/chemistry , Tradescantia/chemistry , Chlorophyll/metabolism , Photosystem II Protein Complex/metabolism , Plant Leaves/metabolism , Tradescantia/metabolismABSTRACT
In this work, we have compared photosynthetic performance and expression of the PsbS and Lhcb1 proteins in two contrast ecotypes of Tradescantia species, T. fluminensis (shade-tolerant) and T. sillamontana (light-resistant), grown at two intensities of light: 50-125 µmol photons m-2 s-1 (low light, LL) and 875-1000 µmol photons m-2 s-1 (high light, HL). Using the EPR method for measuring the P700 content, we have found that LL-grown plants of both species have higher (by a factor of ≈1.7-1.8) contents of PSI per fresh weight unit as compared to HL-grown plants. Acclimation of plants to LL or HL irradiation also influences the Chl(a + b) level and expression of the PsbS and Lhcb1 proteins. Immunoblotting analysis showed that acclimation to HL stimulates (by a factor of ≈1.7-1.8) the level of PsbS related to the total number of P700 centers. In light-resistant species T. sillamontana, the ratio PsbS/P700 is about 2-times higher than in shade-tolerant species T. fluminensis grown under the same conditions. This should enhance the capacity of their leaves for protection against the light stress. In agreement with these observations, the capacity of leaves for NPQ induction was enhanced during plant acclimation to HL. Kinetic studies of P700 photooxidation and light-induced changes in the yield of Chl a fluorescence also revealed that the short-term regulation of electron transport processes in chloroplasts, which manifested themselves in the kinetics of [Formula: see text] induction and the rate of Chl a fluorescence quenching, occurred more rapidly in HL-grown plants than in LL-grown plants. Thus, both factors, enhanced expression of PsbS and more rapid response of the photosynthetic electron transport chain to dark-to-light transitions should increase the capacity of HL-grown plants for their resistance to rapid fluctuations of solar light.
Subject(s)
Acclimatization , Chlorophyll/metabolism , Tradescantia/metabolism , Acclimatization/physiology , Chlorophyll/physiology , Chlorophyll A , Fluorescence , Gene Expression Regulation, Plant/radiation effects , Light , Light-Harvesting Protein Complexes/metabolism , Light-Harvesting Protein Complexes/physiology , Oxidation-Reduction , Plant Proteins/metabolism , Tradescantia/physiologyABSTRACT
Phytoremediation is an efficient method for the removal of heavy metals from contaminated systems. A productive disposal of metal accumulating plants is a major concern in current scenario. In this work, Cr(VI) accumulating Tradescantia pallida plant parts were investigated for its reuse as a biosorbent for the removal of Cr(VI) ions. The effect of pH, contact time, sorbent dosage, Cr(VI) concentration and temperature was examined to optimize these process parameters. Results showed that Cr(VI) exposed/unexposed T. pallida leaf biomass could remove 94% of chromium with a sorption capacity of 64.672 mg g(-1). Whereas the kinetics of Cr(VI) biosorption was well explained by the pseudo second-order kinetic model, the Langmuir model better described the data on Cr(VI) sorption isotherm compared with the Freundlich model. The changes in the free energy (ΔG°), entropy (ΔS°) and enthalpy (ΔH°) were found to be -5.276 kJ mol(-1), 0.391 kJ mol(-1) K(-1) and 11.346 kJ mol(-1), respectively, which indicated the process to be spontaneous, feasible and endothermic in nature. FTIR spectra of T. pallida leaf biomass revealed the active participation of ligands, such as -NH, amide, hydroxyl and sulphonate groups present in the biomass for Cr(VI) binding, SEM analysis revealed a porous structure of the biosorbent for an easy uptake of Cr(VI).
Subject(s)
Chromium/metabolism , Environmental Restoration and Remediation/methods , Tradescantia/metabolism , Waste Disposal, Fluid/methods , Water Pollutants, Chemical/metabolism , Adsorption , Biodegradation, Environmental , Plant Leaves/metabolism , Plant Roots/metabolism , Plant Shoots/metabolismABSTRACT
Tradescantia pallida (Wandering jew)-a succulent perennial herb-was screened to be a potent chromium (Cr) accumulator. Its ability to grow under Cr stress was examined by studying biochemical changes and physiological response of the plant in presence of 5-20 mg L(-1) Cr(VI) concentration in hydroponic environment for up to ca. 90 days. Average Cr(VI) bioaccumulation in plant roots reached about 408 µg g(-1) dry weight (dw) after 30 days and up to 536 µg g(-1)dw after 60 days of culture. Biochemical changes in the plant exposed to Cr(VI) indicated a reduction in the total carbohydrate and protein content. Furthermore, lipid peroxidation, catalase, peroxidase and ascorbate peroxidase activity were measured in different parts of the plant exposed to Cr(VI). Increased activities of these enzymes showed their important role in overcoming the Cr-induced oxidative stress on the plant.
Subject(s)
Antioxidants/metabolism , Chromium/metabolism , Tradescantia/metabolism , Antioxidants/chemistry , Ascorbate Peroxidases/metabolism , Lipid Peroxidation , Oxidation-Reduction , Oxidative Stress , Plant Proteins/metabolism , Plant Roots/chemistry , Plant Roots/metabolism , Superoxide Dismutase/metabolism , Tradescantia/chemistry , Tradescantia/enzymologyABSTRACT
Soil mutagens permanently and directly affect terrestrial plants, soil microorganisms and invertebrates and indirectly impact vertebrate and human populations. However, the dynamic response to soil mutagens under conditions of long-term exposure has been studied insufficiently. The clonal nature of Tradescantia #4430 and the well-developed associated test systems for evaluation of genotoxicity allow investigation of the permanent effects of direct exposure to the soil not only on plants of the same genotype, but even with the same individual plants, as was done in the present study. Twenty soil samples of different origin were studied in Tradescantia after 0.5, 1 and 2 years of direct exposure to the soil, in order to examine the induction of pink cells (PC), colorless cells (CC) and branched hairs (BH). Additionally, after 0.5 years, micronucleus (MN) formation was assessed, and after 1 year, the variation of random amplified polymorphic DNA (RAPD) markers was evaluated. Nine soil samples were of urban origin, and the others came from different soils from former military grounds. The results of the 0.5-year exposure were compared with the effects of aqueous/DMSO extracts tested in previous work. The long-term exposure period allowed not only a better differentiation of the soils within territories, but also permitted detection of differences between soils of urban and military origin. The results also depended on the test used to evaluate genotoxicity. The 'burst' phenomenon, consisting of a sudden increase of BH variation and, especially, of CC, was observed only in tests of samples from several military sites, mainly after a 2-year exposure. MN formation was less frequent after 0.5 years of exposure compared with the results from aqueous extracts, and this difference was highly significant. The variation of the RAPD markers in a significant portion of the soil samples coincided with a higher level of variation according to other tests (PC, CC, BH), but predicting the genotoxicity of the soils based on their elemental soil composition at the end of the experiment was impossible. At several points where a 'burst' was observed, the concentration of a number of elements was lower. A cumulative effect is hypothesized to explain these observations. Tradescantia clone #4430 is the most suitable system for such studies.
Subject(s)
Biological Assay/methods , DNA Damage , Mutagenesis , Mutagens/chemistry , Soil/chemistry , Tradescantia/metabolism , Humans , Micronuclei, Chromosome-Defective/chemically induced , Pigmentation , Random Amplified Polymorphic DNA Technique , Tradescantia/geneticsABSTRACT
Using the automated cell pressure probe, small and highly reproducible hydrostatic pressure clamp (PC) and pressure relaxation (PR) tests (typically, applied step change in pressure = 0.02 MPa and overall change in volume = 30 pL, respectively) were applied to individual Tradescantia virginiana epidermal cells to determine both exosmotic and endosmotic hydraulic conductivity (L(p)(OUT) and L(p)(IN), respectively). Within-cell reproducibility of measured hydraulic parameters depended on the method used, with the PR method giving a lower average coefficient of variation (15.2%, 5.8%, and 19.0% for half-time, cell volume [V(o)], and hydraulic conductivity [L(p)], respectively) than the PC method (25.4%, 22.0%, and 24.2%, respectively). V(o) as determined from PC and PR tests was 1.1 to 2.7 nL and in the range of optically estimated V(o) values of 1.5 to 4.9 nL. For the same cell, V(o) and L(p) estimates were significantly lower (about 15% and 30%, respectively) when determined by PC compared with PR. Both methods, however, showed significantly higher L(p)(OUT) than L(p)(IN) (L(p)(OUT)/L(p)(IN) â 1.20). Because these results were obtained using small and reversible hydrostatically driven flows in the same cell, the 20% outward biased polarity of water transport is most likely not due to artifacts associated with unstirred layers or to direct effects of externally applied osmotica on the membrane, as has been suggested in previous studies. The rapid reversibility of applied flow direction, particularly for the PR method, and the lack of a clear increase in L(p)(OUT)/L(p)(IN) over a wide range of L(p) values suggest that the observed polarity is an intrinsic biophysical property of the intact membrane/protein complex.
Subject(s)
Cell Membrane/metabolism , Cell Polarity , Plant Epidermis/cytology , Plant Epidermis/metabolism , Tradescantia/cytology , Tradescantia/metabolism , Water/metabolism , Biological Transport , Cell Size , HumidityABSTRACT
Previous studies have suggested that the red light and CO2 responses of stomata are caused by a signal from the mesophyll to the guard cells. Experiments were conducted to test the idea that this signal is a vapour-phase ion. Stomata in isolated epidermes of Tradescantia pallida were found to respond to air ions created by an electrode that was positioned under the epidermes. Anthocyanins in the epidermes of this species were observed to change colour in response to these air ions, and this change in colour was attributed to changes in pH. A similar change in lower epidermal colour was observed in intact leaves upon illumination and with changes in CO2 concentration. Based on the change in epidermal colour, the pH of the epidermis was estimated to be approximately 7.0 in darkness and 6.5 in the light. Stomata in isolated epidermes responded to pH when suspended over (but not in contact with) solutions of different pH. We speculate that stomatal responses to CO2 and light are caused by vapour-phase ions, possibly hydronium ions that change the pH of the epidermis.
Subject(s)
Mesophyll Cells/metabolism , Phase Transition , Plant Stomata/cytology , Tradescantia/metabolism , Anthocyanins/metabolism , Electrodes , Ions , Mesophyll Cells/cytology , Plant Stomata/metabolism , Solutions , Tradescantia/physiology , VolatilizationABSTRACT
Chlorophyll fluorescence analysis is one of the most convenient and widespread techniques used to monitor photosynthesis performance in plants. In this work, after a brief overview of the mechanisms of regulation of photosynthetic electron transport and protection of photosynthetic apparatus against photodamage, we describe results of our study of the effects of actinic light intensity on photosynthetic performance in Tradescantia species of different ecological groups. Using the chlorophyll fluorescence as a probe of photosynthetic activity, we have found that the shade-tolerant species Tradescantia fluminensis shows a higher sensitivity to short-term illumination (≤20min) with low and moderate light (≤200µEm(-2)s(-1)) as compared with the light-resistant species Tradescantia sillamontana. In T. fluminensis, non-photochemical quenching of chlorophyll fluorescence (NPQ) and photosystem II operational efficiency (parameter ΦPSII) saturate as soon as actinic light reaches ≈200µEm(-2)s(-1). Otherwise, T. sillamontana revealed a higher capacity for NPQ at strong light (≥800µEm(-2)s(-1)). The post-illumination adaptation of shade-tolerant plants occurs slower than in the light-resistant species. The data obtained are discussed in terms of reactivity of photosynthetic apparatus to short-term variations of the environment light.