Cell Wall Layers Research Articles

Unveiling the impact of embedding resins on the physicochemical traits of wood cell walls with subcellular functional probing

As pressing needs for exploring molecular interactions in plants soar, conventional sample preparation methods come into question. Though resins used to embed plant tissues have long been assumed to bear no palpable effect on their properties, discrepancies in recent studies exploiting nanoscale microscopy suggest that their impact could be significant at small scales. By juxtaposing the traits of poplar sections prepared with and without embedding, we evaluate the diffusion (penetration depth) of acrylic and epoxy resins commonly used for embedding. Our results unveil critical quantitative differences when probing mechanical properties with a microscale nanoindentation indenter or a nanoscale tip. The latter resolves significant stiffness variations between the compound middle lamellae, the secondary cell wall layers S1 and S2, and the cell corner, not accessible with nanoindentation. Similar observations are drawn from comparing confocal Raman and nanoscale infrared spectroscopy. Our findings shed light on the effect of resin diffusion suggesting acrylic LR White to be the least diffusive for plant cell wall studies.

Quantitative Visualization of Weak Layers in Bamboo at the Cellular and Subcellular Levels.

Weak layers in bamboo, which are prone to the generation of cracks or are the preferred routes for crack growth, govern the machining processes and applications of bamboo. Weak layers are avoided during storing but are utilized during splitting and slicing. Gaining an understanding of the weak layers is a priority that will allow for the determination of whether to avoid or utilize them. In this study, scanning electron microscopy was used to observe the weak layers at the cellular and subcellular levels. A nanoindentation instrument and a Raman microscope were used to quantitatively characterize the mechanical properties and chemical components of these weak layers. The results show that among the three types of bamboo cells, vessel cells were the most vulnerable to damage, while fiber cells were the least susceptible to damage. The weak layers at the subcellular level were compound middle lamella (CML), thin layers of cell walls, and pits. The average storage modulus values were as follows: 13.7 GPa for CML, 17.0 GPa for pits, 20.6 GPa for thin layers, and 25.3 GPa for thick layers. Compared with the thick layers, the maximum decrement of cellulose content was 51% in CML and 41% in thin layers. With the lowest cellulose content, CML was the likeliest subcellular structure in which cracks propagated. The hardness of the pits was lower than that of the adjacent non-pit areas. The mechanical properties of bamboo increased by targeted modification of the weak layers. This work demonstrates a comprehensive investigation into weak layers of bamboo and quantitatively visualizes their mechanical and chemical properties.

Study on the ultrastructure and properties of gelatinous layer in poplar

As a fast-growing commercial wood species, poplar often produces tension wood because of the leaning stems of logs, which has a great impact on the production and utilization. The gelatinous layer (G-layer) was the unique component of tension wood, almost entirely composed of cellulose, which was the main reason for the special performance of the poplar tension wood. This study used the transmission electron microscopy, Raman spectroscopy and nanoindentation to examine the ultrastructure and mechanical properties of every wall layer of the poplar cell wall in order to figure out the ultrastructure and properties of G-layer. In particular, the nanoindentation mapping was combined with manual screening to obtain the mechanical performance data of each layer. The fibers in the tension wood were gelatinous wood fibers with obvious G-layers, and the thickness was 2.53 μm, which was much larger than that of other wall layers. Compared with the wood fiber in the opposite wood, the S1 layer was thicker and the S2 layer was thinner, and the entire cell wall thickness was increased in tension wood. G-layer in tension wood had a very high cellulose content, and the Raman strength of lignin was weak. In general, the micromechanical properties of poplar tension wood were better, which was consistent with its macromechanical properties. The characteristics of G-layer, including high cellulose content, small microfibril angle and high crystallinity, made G-layer own better elastic modulus (14.08 GPa) and hardness (0.45 GPa) than other wall layers in the tension wood. Moreover, G-layer had a high proportion in the tension wood cell wall, so the average longitudinal elastic modulus and hardness of wood fiber cells in the tension wood were also higher than those in the opposite wood.

Topochemical and light microscopic investigations of non-enzymatic oxidative changes at the initial decay stage of furfuryl alcohol-modified radiata pine (Pinus radiata) degraded by the brown rot fungus Rhodonia placenta

The aim of this study was to visualize non-enzymatic oxidative degradation damages in the initial decay stage of the brown rot fungus Rhodonia placenta degradation in furfuryl alcohol (FA) modified wood cell walls and untreated wood cell walls of radiata pine (Pinus radiata) sapwood. A decay test with small wood blocks (1.5 × 1.5 × 5 mm³) of untreated and furfurylated radiata pine selected from two different furfurylation processes was performed until the first mass loss occurred. The samples were exposed to the brown rot fungus R. placenta, monitored by light microscopy and analyzed topochemically by cellular UV microspectrophotometry (UMSP). The results showed that the FA modification process directly influenced: i) the fungal colonization and hyphal growth, ii) the spectral UV behavior, and iii) degradation patterns of the entire cell wall layers. For the first time, UMSP area scans and selective line scans of individual cell wall regions provide topochemical insights into oxidative degradation at the initial decay stage of furfuryl alcohol-modified P. radiata visualizing oxidative degradation in situ. Knowledge of the initial decay stage of brown rot degradation in FA-modified wood compared to untreated wood extends our understanding of the brown rot decay processes of cell wall compounds.

EgPHI-1, a PHOSPHATE-INDUCED-1 gene from Eucalyptus globulus, is involved in shoot growth, xylem fiber length and secondary cell wall properties.

EgPHI-1 is a member of PHI-1/EXO/EXL protein family. Its overexpression in tobacco resulted in changes in biomass partitioning, xylem fiber length, secondary cell wall thickening and composition, and lignification. Here, we report the functional characterization of a PHOSPHATE-INDUCED PROTEIN 1 homologue showing differential expression in xylem cells from Eucalyptus species of contrasting phenotypes for wood quality and growth traits. Our results indicated that this gene is a member of the PHI-1/EXO/EXL family. Analysis of the promoter cis-acting regulatory elements and expression responses to different treatments revealed that the Eucalyptus globulus PHI-1 (EgPHI-1) is transcriptionally regulated by auxin, cytokinin, wounding and drought. EgPHI-1 overexpression in transgenic tobacco changed the partitioning of biomass, favoring its allocation to shoots in detriment of roots. The stem of the transgenic plants showed longer xylem fibers and reduced cellulose content, while the leaf xylem had enhanced secondary cell wall thickness. UV microspectrophotometry of individual cell wall layers of fibers and vessels has shown that the transgenic plants exhibit differences in the lignification of S2 layer in both cell types. Taken together, the results suggest that EgPHI-1 mediates the elongation of secondary xylem fibers, secondary cell wall thickening and composition, and lignification, making it an attractive target for biotechnological applications in forestry and biofuel crops.

Nanoscale Chemical Features of the Natural Fibrous Material Wood.

Peak force infrared (PFIR) microscopy is a recently developed approach to acquire multiple chemical and physical material properties simultaneously and with nanometer resolution: topographical features, infrared (IR)-sensitive maps, adhesion, stiffness, and locally resolved IR spectra. This multifunctional mapping is enabled by the ability of an atomic force microscope tip in the peak force tapping mode to detect photothermal expansion of the sample. We report the use of the PFIR to characterize the chemical modification of bio-based native and intact wooden matrices, which has evolved into an increasingly active research field. The distribution of functional groups of wood cellulose aggregates, either in native or carboxylated states, was detected with a remarkable spatial resolution of 16 nm. Furthermore, mechanical and chemical maps of the distinct cell wall layers were obtained on polymerized wooden matrices to localize the exact position of the modified regions. These findings shall support the development and understanding of functionalized wood materials.

Molecular characterization and expression analysis of the chicken-type and goose-type lysozymes from totoaba (Totoaba macdonaldi)

Lysozymes play a key role in innate immune response to bacterial pathogens, catalyzing the hydrolysis of the peptidoglycan layer of bacterial cell walls. In this study, the genes encoding the c-type (TmLyzc) and g-type (TmLyzg) lysozymes from Totoaba macdonaldi were cloned and characterized. The cDNA sequences of TmLyzg and TmLyzc were 582 and 432 bp, encoding polypeptides of 193 and 143 amino acids, respectively. Amino acid sequences of these lysozymes shared high identity (60–90%) with their counterparts of other teleosts and showed conserved functional-structural signatures of the lysozyme superfamily. Phylogenetic analysis indicated a close relationship with their vertebrate homologues but distinct evolutionary paths for each lysozyme. Expression analysis by qRT-PCR revealed that TmLyzc was expressed in stomach and pyloric caeca, while TmLyzg was highly expressed in stomach and heart. These results suggest that both lysozymes play important roles in defense of totoaba against bacterial infections or as digestive enzyme.

The impact of natural and artificial weathering on the anatomy of selected tropical hardwoods

Abstract The effect of natural and artificial weathering on the anatomy of seven tropical hardwoods: Bangkirai (Shorea obtusa Wall.), Cumaru (Dipteryx odorata (Aubl.) Wild.), Cumaru Rosa (Dipteryx magnifica (Ducke) Ducke), Ipé (Tabebuia serratifolia Nichols.), Jatobá (Hymenaea courbaril L.), Kusia (Nauclea diderrichii Merill) and Massaranduba (Manilkara bidentata A. Chev.), was studied. As a result of weathering some characteristic anatomical changes occurred: the weakening of connections between cell elements related to the degradation of the middle lamella; micro-cracks in cell walls; total degradation of parenchyma cells in xylem rays, or significant thinning of parenchyma cell walls and their extreme shrinkage; micro-cracks in the vicinity of xylem rays; significant transversal disruptions in libriform fibres; ablation of pit membranes in vessels and parenchyma cells; changes in the secondary wall of libriform fibres, for example, their defibrillation and weathering-degradation of the S1 layer; and spherical formations on the S3 layer of cell walls produced from condensing compounds of degraded lignin and hemicelluloses as well as thermo-mechanical wrinkling. The highest incidence of micro-cracks after both modes of weathering was found in the densest species; Cumaru, Ipé, and Massaranduba.

Rearrangement of the Cellulose-Enriched Cell Wall in Flax Phloem Fibers over the Course of the Gravitropic Reaction

The plant cell wall is a complex structure consisting of a polysaccharide network. The rearrangements of the cell wall during the various physiological reactions of plants, however, are still not fully characterized. Profound changes in cell wall organization are detected by microscopy in the phloem fibers of flax (Linum usitatissimum) during the restoration of the vertical position of the inclined stems. To characterize the underlying biochemical and structural changes in the major cell wall polysaccharides, we compared the fiber cell walls of non-inclined and gravistimulated plants by focusing mainly on differences in non-cellulosic polysaccharides and the fine cellulose structure. Biochemical analysis revealed a slight increase in the content of pectins in the fiber cell walls of gravistimulated plants as well as an increase in accessibility for labeling non-cellulosic polysaccharides. The presence of galactosylated xyloglucan in the gelatinous cell wall layer of flax fibers was demonstrated, and its labeling was more pronounced in the gravistimulated plants. Using solid state NMR, an increase in the crystallinity of the cellulose in gravistimulated plants, along with a decrease in cellulose mobility, was demonstrated. Thus, gravistimulation may affect the rearrangement of the cell wall, which can enable restoration in a vertical position of the plant stem.

Xylan deposition and lignification in differentiating tension wood fibers in Mallotus japonicus (Euphorbiaceae) with multi-layered structure

Abstract Xylan deposition and lignification processes were examined in tension wood fibers with gelatinous layers (G-layers) in Mallotus japonicus (Euphorbiaceae). The cell walls consisted of a multi-layered structure of S1 + S2 + G + n(L + G), where n indicates the number of repetitions (n = 0–3) and L indicates very thin lignified layers. The formation and lignification processes of the multi-layered structure of tension wood fibers were examined by light microscopy, ultraviolet microscopy, and transmission electron microscopy (TEM) following KMnO4 staining. The deposition of xylan was examined by immunoelectron microscopy with a monoclonal antibody (LM11). Immunolabelling of xylan appeared in lignified cell wall layers, except in the compound middle lamella (CML), i.e., the S1, S2, and L layers but not the G-layers. The density of LM11 xylan immunogold labeling in S2 layers increased during the formation of G-layers. This increase was due to the shrinkage of S2 layers during development rather than intrusive deposition of xylan through G-layers. Lignification of the CML, S1, and S2 layers proceeded during G-layer formation. The shrinkage of S2 layers occurred almost simultaneously with the lignification of the S2 layers during G-layer formation, suggesting that the S2 layers shrank with lignification.

Surface properties of thermally treated European beech wood studied by PeakForce Tapping atomic force microscopy and Fourier-transform infrared spectroscopy

AbstractNatural constituents of wood cell-wall layers are affected in various ways by thermal treatment. This study investigated the effect of high-temperature treatment on the properties of cell-wall layers. The properties were studied using PeakForce quantitative nanomechanical mapping and Fourier-transform infrared spectroscopy (FTIR). European beech wood was thermally treated at 200 °C for 1, 3, and 5 h in an oxidizing atmosphere. Modulus of elasticity, adhesion force, and roughness of the secondary S2layer and the compound middle lamella (CML) were determined using atomic force microscopy (AFM). Results showed that both the S2layer and CML were affected by thermal treatment. Stiffening of the S2layer was caused by increased crystallinity of the cellulose-dominated component, having peaked after 1 h of treatment. The degradation thereafter resulted in a decrease of the S2as well as the CML stiffness. An increase of CML roughness after 3 h of treatment was associated with the effect of thermal degradation on CML integrity. The analysis suggested that the reduction in syringyl lignin is potentially associated with an increase in adhesion of cell-wall layers.

Cell Wall Reinforcements Accompany Chilling and Freezing Stress in the Streptophyte Green Alga Klebsormidium crenulatum.

Adaptation strategies in freezing resistance were investigated in Klebsormidium crenulatum, an early branching streptophyte green alga related to higher plants. Klebsormidium grows naturally in unfavorable environments like alpine biological soil crusts, exposed to desiccation, high irradiation and cold stress. Here, chilling and freezing induced alterations of the ultrastructure were investigated. Control samples (kept at 20°C) were compared to chilled (4°C) as well as extracellularly frozen algae (−2 and −4°C). A software-controlled laboratory freezer (AFU, automatic freezing unit) was used for algal exposure to various temperatures and freezing was manually induced. Samples were then high pressure frozen and cryo-substituted for electron microscopy. Control cells had a similar appearance in size and ultrastructure as previously reported. While chilling stressed algae only showed minor ultrastructural alterations, such as small inward facing cell wall plugs and minor alterations of organelles, drastic changes of the cell wall and in organelle distribution were found in extracellularly frozen samples (−2°C and −4°C). In frozen samples, the cytoplasm was not retracted from the cell wall, but extensive three-dimensional cell wall layers were formed, most prominently in the corners of the cells, as determined by FIB-SEM and TEM tomography. Similar alterations/adaptations of the cell wall were not reported or visualized in Klebsormidium before, neither in controls, nor during other stress scenarios. This indicates that the cell wall is reinforced by these additional wall layers during freezing stress. Cells allowed to recover from freezing stress (−2°C) for 5 h at 20°C lost these additional cell wall layers, suggesting their dynamic formation. The composition of these cell wall reinforcement areas was investigated by immuno-TEM. In addition, alterations of structure and distribution of mitochondria, dictyosomes and a drastically increased endoplasmic reticulum were observed in frozen cells by TEM and TEM tomography. Measurements of the photosynthetic oxygen production showed an acclimation of Klebsormidium to chilling stress, which correlates with our findings on ultrastructural alterations of morphology and distribution of organelles. The cell wall reinforcement areas, together with the observed changes in organelle structure and distribution, are likely to contribute to maintenance of an undisturbed cell physiology and to adaptation to chilling and freezing stress.

Measurement of moisture-dependent ion diffusion constants in wood cell wall layers using time-lapse micro X-ray fluorescence microscopy

Our future bioeconomy depends on increased utilization of renewable lignocellulosic biomass. Controlling the diffusion of chemicals, such as inorganic ions, within secondary plant cell walls is central to many biomass applications. However, insufficient understanding of intra-cell-wall diffusion within secondary plant cell walls is hindering the advancement of many lignocellulosic biomass applications. In this work, X-ray fluorescence microscopy was used to measure diffusion constants of K+, Cu2+, and Cl− diffusing through loblolly pine (Pinus taeda) cell wall layers under 70%, 75%, or 80% relative humidity (RH). Results revealed that diffusion constants increased with RH, the larger Cu2+ diffused more slowly than the K+, and the Cl− diffusion constant was the same as that for the counter cation, indicating cations and anions diffused together to maintain charge neutrality. Comparison with electrical conductivity measurements showed that conductivity is being controlled by ion mobility over these RH. The results further support that intra-cell-wall diffusion of inorganic ions is a Fickian diffusion process occurring through rubbery amorphous polysaccharides, which contradicts previous assertions that intra-cell-wall diffusion is an aqueous process occurring through water pathways. Researchers can now utilize polymer science approaches to engineer the molecular architecture of lignocellulosic biomass to optimize properties for specific end uses.

Cell wall structural changes lead to separation and shedding of biofouled epidermal cell wall layers by the brown alga Ascophyllum nodosum.

Marine plants control the accumulation of biofouling organisms (epibionts) on their surfaces by various chemical and physical means. Ascophyllum nodosum is a perennial multicellular brown alga known to shed patches of epidermal material, thus removing epibionts and exposing unfouled surfaces to another cycle of colonization. While surface shedding is documented in multiple marine macroalgae, the cell and developmental biology of the phenomenon is almost unexplored. A previous investigation of Ascophyllum not only revealed regular cycles of epibiont accumulation and epidermal shedding but also stimulated the development of methods to detect the corresponding changes in epidermal (meristoderm) cells that are reported here. Confocal laser scanning microscopy of cell walls and cytoplasm fluorescently stained with Solophenyl Flavine 7GFE (Direct Yellow 96) and the lipophilic dye Rhodamine B (respectively) was combined with light and electron microscopy of chemically fixed or freeze-substituted tissues. As epibionts accumulated, epidermal cells generated thick, apical cell walls in which differentially stained central layers subsequently developed, marking the site of future cell wall separation. During cell wall separation, the outermost part of the cell wall and its epibionts plus the upper parts of the anticlinal walls between neighboring cells detached in a layer from multiple epidermal cells, exposing the remaining inner part of the cell wall to new colonizing organisms. These findings highlight the dynamic nature of apical cell wall structure and composition in response to colonizing organisms and lay a foundation for further investigations on the periodic removal of biofouling epibionts from the surface of Ascophyllum fronds.

Thickness-dependent stiffness of wood: potential mechanisms and implications

Abstract When wood is split or cut along the grain, a reduction in tensile stiffness has been observed. The averaged mechanical properties of wood samples, veneers or splinters therefore change when their thickness is less than about 1 mm. The loss of stiffness increases as the thickness approaches that of a single cell. The mechanism of the effect depends on whether the longitudinal fission plane is between or through the cells. Isolated single cells are a model for fission between cells. Each cell within bulk wood is prevented from twisting by attachment to its neighbours. Separation of adjacent cells lifts this restriction on twisting and facilitates elongation as the cellulose microfibrils reorientate towards the stretching direction. In contrast when the wood is cut or split along the centre of the cells, it appears that co-operative action by the S1, S2 and S3 cell-wall layers in resisting tensile stress may be disrupted. Since much of what is known about the nanoscale mechanism of wood deformation comes from experiments on thin samples, caution is needed in applying this knowledge to structural-sized timber. The loss of stiffness at longitudinal fracture faces may augment the remarkable capacity of wood to resist fracture by deflecting cracks into the axial plane. These observations also point to mechanisms for enhancing toughness that are unique to wood and have biomimetic potential for the design of composite materials.

Atomic force microscopy imaging of delignified secondary cell walls in liquid conditions facilitates interpretation of wood ultrastructure

Deep understanding of the physicochemical and structural characteristics of wood at the nanoscale is essential for improving wood usage in biorefining and advancing new high performance materials design. Herein, we use in situ atomic force microscopy and a simple delignification treatment to elucidate the nanoscale architecture of individual secondary cell wall layers. Advantages of this approach are: (i) minimal sample preparation that reduces the introduction of potential artifacts; (ii) prevention of structural rearrangements due to dehydration; (iii) increased accessibility to structural details masked by the lignin matrix; and (iv) possibility to complement results with other analytical techniques without sample manipulation. The methodology permits the visualization of parallel and helicoidally arranged microfibril aggregates in the S1 layer and the determination of lignin contribution to microfibril aggregates forming S2 layers. Cellulose and hemicelluloses constitute the core of the aggregates with a mean diameter of approximately 19 nm, and lignin encloses the core forming single structural entities of about 30 nm diameter. Furthermore, we highlight the implications of sample preparation and imaging parameters on the characterization of microfibril aggregates by AFM.

ResNeXt convolution neural network topology-based deep learning model for identification and classification of Pediastrum

For identification of different Pediastrum species in a sample, the determination of microscopic feature and colony morphology are the preliminary steps before sending them to the higher genomic and proteomic level. Great efforts with high expertise are required for the time-consuming manual process. In the present study, the first time an effort has been done to address the problem for identification and classification of Pediastrum species with the help of convolutional neural networks (CNNs). The modified ResNeXt CNN (Convolution Neural Network) model is used for training and validation of the data set consisting of 42,000 algal images. Modified ResNeXt CNN topology differentiates cells based on the formation of coenobia, cell arrangement and feature and particularly the sculptures on the outer sporopollenin cell-wall layers. An experimental result of 98.45% classification accuracy and F1-score more than 0.98 demonstrates the effectiveness of the proposed method. In the future, such time and cost-effective facilities can be used as promising sources for phycological studies.

Identifying the pathways for foliar water uptake in beech (Fagus sylvatica L.): a major role for trichomes.

Foliar water uptake (FWU), the direct uptake of water into leaves, is a global phenomenon, having been observed in an increasing number of plant species. Despite the growing recognition of its functional relevance, our understanding of how FWU occurs and which foliar surface structures are implicated, is limited. In the present study, fluorescent and ionic tracers, as well as microcomputed tomography, were used to assess potential pathways for water entry in leaves of beech, a widely distributed tree species from European temperate regions. Although none of the tracers entered the leaf through the stomatal pores, small amounts of silver precipitation were observed in some epidermal cells, indicating moderate cuticular uptake. Trichomes, however, were shown to absorb and redistribute considerable amounts of ionic and fluorescent tracers. Moreover, microcomputed tomography indicated that 72% of empty trichomes refilled during leaf surface wetting and microscopic investigations revealed that trichomes do not have a cuticle but are covered with a pectin-rich cell wall layer. Taken together, our findings demonstrate that foliar trichomes, which exhibit strong hygroscopic properties as a result of their structural and chemical design, constitute a major FWU pathway in beech.

The Living Fossil Psilotum nudum Has Cortical Fibers With Mannan-Based Cell Wall Matrix.

Cell wall thickening and development of secondary cell walls was a major step in plant terrestrialization that provided the mechanical support, effective functioning of water-conducting elements and fortification of the surface tissues. Despite its importance, the diversity, emergence and evolution of secondary cell walls in early land plants have been characterized quite poorly. Secondary cell walls can be present in different cell types with fibers being among the major ones. The necessity for mechanical support upon increasing plant height is widely recognized; however, identification of fibers in land plants of early taxa is quite limited. In an effort to partially fill this gap, we studied the fibers and the composition of cell walls in stems of the sporophyte of the living fossil Psilotum nudum. Various types of light microscopy, combined with partial tissue maceration demonstrated that this perennial, rootless, fern-like vascular plant, has abundant fibers located in the middle cortex. Extensive immunodetection of cell wall polymers together with various staining and monosaccharide analysis of cell wall constituents revealed that in P. nudum, the secondary cell wall of its cortical fibers is distinct from that of its tracheids. Primary cell walls of all tissues in P. nudum shoots are based on mannan, which is also common in other extant early land plants. Besides, the primary cell wall contains epitope for LM15 specific for xyloglucan and JIM7 that binds methylesterified homogalacturonans, two polymers common in the primary cell walls of higher plants. Xylan and lignin were detected as the major polymers in the secondary cell walls of P. nudum tracheids. However, the secondary cell wall in its cortical fibers is quite similar to their primary cell walls, i.e., enriched in mannan. The innermost secondary cell wall layer of its fibers but not its tracheids has epitope to bind the LM15, LM6, and LM5 antibodies recognizing, respectively, xyloglucan, arabinan and galactan. Together, our data provide the first description of a mannan-based cell wall in sclerenchyma fibers, and demonstrate in detail that the composition and structure of secondary cell wall in early land plants are not uniform in different tissues.

A mechanistic insight into the bioaccesible herbometallic nanodrug as potential dual therapeutic agent

Vanga Bhasma, a herbometallic mixture compound is used as gastrointestinal digestive medicine in ayurveda. Here, we have studied its bioaccessbility as antibacterial and anti cancer agent. Their characteristic FESEM, XRD, FTIR, UV absorption spectra were determined, which indicates high mineral content in Vanga Bhasma nanoparticles. Biological studies like MIC, MBC evaluate its antibacterial property, bacterial ROS generation enhance the ravages of peptidoglycan layer of bacterial cell wall. Further anti-cancerous potential of synthesized Vanga Bhasma nanoparticles was also studied on breast cancer cell line showing its potential to induce apoptosis through oxidative damage and mitochondrial membrane damage. Our studies thus successfully establish the dual therapeutic attribute of Vanga Bhasma nanoparticles as anticancer and antibacterial agent.