Increased Cell Wall Thickness Research Articles

Alginate Oligosaccharides Alleviate Salt Stress in Rice Seedlings by Regulating Cell Wall Metabolism to Maintain Cell Wall Structure and Improve Lodging Resistance.

Salt stress is one of the major abiotic stresses that damage the structure and composition of cell walls. Alginate oligosaccharides (AOS) have been advocated to significantly improve plant stress tolerance. The metabolic mechanism by which AOS induces salt tolerance in rice cell walls remains unclear. Here, we report the impact of AOS foliar application on the cell wall composition of rice seedlings using the salt-tolerant rice variety FL478 and the salt-sensitive variety IR29. Data revealed that salt stress decreased biomass, stem basal width, stem breaking strength, and lodging resistance; however, it increased cell wall thickness. In leaves, exogenous AOS up-regulated the expression level of OSCESA8, increased abscisic acid (ABA) and brassinosteroids (BR) content, and increased β-galacturonic activity, polygalacturonase activity, xylanase activity, laccase activity, biomass, and cellulose content. Moreover, AOS down-regulated the expression levels of OSMYB46 and OSIRX10 and decreased cell wall hemicellulose, pectin, and lignin content to maintain cell wall stability under salt stress. In stems, AOS increased phenylalamine ammonia-lyase and tyrosine ammonia-lyase activities, while decreasing cellulase, laccase, and β-glucanase activities. Furthermore, AOS improved the biomass and stem basal width and also enhanced the cellulose, pectin, and lignin content of the stem, As a result, increased resistance to stem breakage strength and alleviated salt stress-induced damage, thus enhancing the lodging resistance. Under salt stress, AOS regulates phytohormones and modifies cellulose, hemicellulose, lignin, and pectin metabolism to maintain cell wall structure and improve stem resistance to lodging. This study aims to alleviate salt stress damage to rice cell walls, enhance resistance to lodging, and improve salt tolerance in rice by exogenous application of AOS.

Cell wall metabolism during the growth of peach fruit: Association of hardness with cell wall pectins

In this study, molecular composition of cell wall polysaccharides of peach during growth was investigated to elucidate influencing mechanism of hardness which regulated fruit quality. Results revealed that as fruit grew stage I to V (almost 36 to 103 day after flowering), hardness firstly increased and then decreased, reaching its peak in stage II. Microstructure indicated an increase in cell wall thickness and a transition from compact to loose adhesion between cell walls from stage Ⅰ to Ⅱ. Moreover, molecular weight (Mw), monosaccharide composition and fourier transform infrared spectra (FTIR) of peach polysaccharides extracted by water (WPP), chelating agent (CPP) and alkali (APP) indicated Mw of WPP and APP showed a downward trend and reaching the highest in stage II for CPP. Similar tendency appeared in the galacturonic acid (GalA) content. Content of galactose and arabinose in all polysaccharide decreased. Degree of esterificationa (DE) of CPP was the lowest in stage II. An increasing trend appeared in WPP. Finally, β-Galactosidase, α-l-arabinofuranosidase, pectin methyl esterase, polygalacturonase and their associated genes were analyzed to be evidence of the change of molecular composition. Above results implied Mw, GalA content and DE of CPP related with hardness during growth.

Impact of Oil Addition on Physicochemical Properties and In Vitro Digestibility of Extruded Pineapple Stem Starch.

The effects of palm oil (PO) and coconut oil (CO) additions on the physicochemical properties and in vitro starch digestibility of extruded pineapple stem starch (PSS) were studied. The native PSS was adjusted to 15% moisture and blended with PO or CO in amounts of 5 and 10% (w/w of starch), while the control sample without added oil was adjusted to 25% moisture before being extruded with a twin-screw extruder at a maximum barrel temperature of 140 °C. Due to the lubricating effect, the added oils reduced the expansion ratio of the extrudates, which led to an increase in cell wall thickness, bulk density, hardness, and water adsorption index, but to a reduction in the water solubility index, especially with 10% oils. PO had a greater impact on the physicochemical changes in the extrudates than CO. Surprisingly, no amylose-lipid complex was observed in the extrudates with added oil, as shown by XRD, DSC, and FTIR results. The phenolic compounds contained in PSS remained in all extrudates, which could affect the formation of the amylose-lipid complex during extrusion. The addition of 5% oil had no effect on the digestibility of the starch compared to the control extrudates, while the 10% oils, both PO and CO, reduced the rapidly digestible starch content but significantly increased the resistant starch content of the extruded PSS.

Adaptive cell wall thickening in Enterococcus faecalis is associated with decreased vancomycin susceptibility

ObjectivesEnterococcus faecalis can adopt both a commensal and a nosocomial lifestyle, resisting numerous antibiotics. In this study, we aim to investigate the relationship between the cell wall (CW) thickness and decreased susceptibility to vancomycin (VD) in van-gene negative clinical isolates of E. faecalis (nMIC 8 = 2, nMIC 4 = 3, ST30, ST40, and ST59). MethodsThe CW thickness was assessed in VD strains and compared with vancomycin susceptible isolates of the same sequence type (ST) (Vancomycin susceptible [VS]; nMIC 2 = 5). The VD and VS strains were subjected to serial passage (evolved [ev]) with and without vancomycin selection. Subsequent measurements of CW thickness and vancomycin MICs were performed. ResultsThe VD strains exhibited increased CW thickness when compared with ST-related VS strains (ΔCW thickness VD vs. VS ST30 25 nm, ST59 15 nm, and ST40 1 nm). Serial passages without vancomycin selection led to a decrease in CW thickness and vancomycin MIC in VD strains (ΔCW thickness VD vs. evVD ST30 22 nm, ST59 3 nm, and ST40 2 nm). Serial passages with vancomycin selection caused an increase in CW thickness and vancomycin MIC in ST-related VS strains (ΔCW thickness VS vs. evVS ST30 22 nm, ST59 16 nm, and ST40 1 nm). DiscussionAdaptive changes in CW thickness were observed in response to vancomycin exposure. Increased CW thickness correlated with decreased vancomycin susceptibility, whereas decreased CW thickness correlated with increased vancomycin susceptibility. Core single nucleotide polymorphisms in the evolved mutants were mostly found in genes encoding proteins associated with the cytoplasm or the cytoplasmic membrane. The potential relevance of these adaptive changes is underlined by the observed phenotypes in clinical isolates. Our findings emphasize the importance of monitoring adaptive changes, as vancomycin-resistant enterococci infections are a growing concern.

C-di-AMP levels modulate Staphylococcus aureus cell wall thickness, response to oxidative stress, and antibiotic resistance and tolerance.

Beta-lactam antibiotics are widely used to treat infections caused by the important human pathogen Staphylococcus aureus. Resistance to beta-lactams, as found in methicillin-resistant S. aureus, renders effective treatment difficult. The second messenger cyclic di-3',5'-adenosine monophosphate (c-di-AMP) promotes beta-lactam resistance in clinical S. aureus isolates. C-di-AMP plays a crucial role in the regulation of cellular processes such as virulence, cell wall homeostasis, and resistance to beta-lactams in many bacterial species. In S. aureus, c-di-AMP synthesis is mediated by the diadenylate cyclase DacA, while its degradation is carried out by the phosphodiesterases GdpP and Pde2. In this work, we assessed the effect of altered c-di-AMP levels due to mutations in dacA, gdpP, or gdpP/pde2 on virulence determinants. We report that a previously described growth defect in bacteria producing high c-di-AMP levels is mainly attributable to smaller cell size. High c-di-AMP levels also led to decreased survival upon oxidative stress, reduced production of the antioxidant staphyloxanthin, increased oxacillin and fosfomycin resistance, and increased cell wall thickness. While resistance to ceftaroline was not affected, high c-di-AMP levels promoted tolerance to this antibiotic. In response to cell wall stress induced by antibiotics, the three-component regulatory system VraTSR mediates an increase in cell wall synthesis via the cell wall stress stimulon (CWSS). Increased c-di-AMP levels led to an activation of the CWSS. Upon deletion of vraR, resistance to oxacillin and fosfomycin as well as cell wall thickness diminished in the ΔgdpP mutant, indicating a contribution of the VraTSR system to the cell wall related phenotypes.IMPORTANCEAntibiotic resistance and tolerance are substantial healthcare-related problems, hampering effective treatment of bacterial infections. Mutations in the phosphodiesterase GdpP, which degrades cyclic di-3', 5'-adenosine monophosphate (c-di-AMP), have recently been associated with resistance to beta-lactam antibiotics in clinical Staphylococcus aureus isolates. In this study, we show that high c-di-AMP levels decreased the cell size and increased the cell wall thickness in S. aureus mutant strains. As a consequence, an increase in resistance to cell wall targeting antibiotics, such as oxacillin and fosfomycin as well as in tolerance to ceftaroline, a cephalosporine used to treat methicillin-resistant S. aureus infections, was observed. These findings underline the importance of investigating the role of c-di-AMP in the development of tolerance and resistance to antibiotics in order to optimize treatment in the clinical setting.

Effect of cell size and wall thickness on the compression performance of triply periodic minimal surface based AlSi10Mg lattice structures

Triply periodic minimal surface (TPMS) are mathematical surfaces with zero mean curvature and are spatially invariant. Recently, these surfaces are investigated for potential application in the manufacturing of cellular materials or lattice structures for a variety of purposes. However, designing such structures is a difficult task as the dedicated design platforms impose higher costs. Therefore, in this study, lattice structures have been designed using an in-house developed opensource tool for different cell sizes and cell wall thicknesses. The lattice structures have been additively manufactured through laser powder bed fusion (LPBF) and their design compliance and manufacturing defects have been investigated through optical micrography and SEM. The lattice structures have been subjected to quasistatic uniaxial compression test in as-manufactured and heat-treated conditions and the resulting compressive stress-strain curves have been analyzed in detail to draw a relationship between the two varying quantities and the mechanical properties of the lattice structure. The results show that there has been small but visible differences between the as-designed and as-manufactured lattice structures. The mechanical properties of lattice structures deteriorated with increasing cell size at constant wall thickness and improved with increasing cell wall thickness at constant unit cell size. The heat treatment procedures homogenized and increased plastic deformation while decreasing the strength and modulus values. Overall the study outlined a significant effect of cell geometry, size, and cell wall thickness on the mechanical properties of the TPMS lattice structures.

Development of Echinocandin Resistance in Candida haemulonii: An Emergent, Widespread, and Opportunistic Fungal Pathogen.

Echinocandins, used for the prevention and treatment of invasive fungal infections, have led to a rise in breakthrough infections caused by resistant Candida species. Among these species, those belonging to the Candida haemulonii complex are rare multidrug-resistant (MDR) yeasts that are frequently misidentified but have emerged as significant healthcare-associated pathogens causing invasive infections. The objectives of this study were to investigate the evolutionary pathways of echinocandin resistance in C. haemulonii by identifying mutations in the FKS1 gene and evaluating the impact of resistance on fitness. After subjecting a MDR clinical isolate of C. haemulonii (named Ch4) to direct selection using increasing caspofungin concentrations, we successfully obtained an isolate (designated Ch4'r) that exhibited a high level of resistance, with MIC values exceeding 16 mg/L for all tested echinocandin drugs (caspofungin, micafungin, and anidulafungin). Sequence analysis revealed a specific mutation in the resistant Ch4'r strain, leading to an arginine-histidine amino acid substitution (R1354H), occurring at the G4061A position of the HS2 region of the FKS1 gene. Compared to the wild-type strain, Ch4'r exhibited significantly reduced growth proliferation, biofilm formation capability, and phagocytosis ratio, indicating a decrease in fitness. Transmission electron microscopy analysis revealed alterations in cell wall components, with a notable increase in cell wall thickness. The resistant strain also exhibited higher amounts (2.5-fold) of chitin, a cell wall-located molecule, compared to the wild-type strain. Furthermore, the resistant strain demonstrated attenuated virulence in the Galleria mellonella larval model. The evolved strain Ch4'r maintained its resistance profile in vivo since the treatment with either caspofungin or micafungin did not improve larval survival or reduce the fungal load. Taken together, our findings suggest that the acquisition of pan-echinocandin resistance occurred rapidly after drug exposure and was associated with a significant fitness cost in C. haemulonii. This is particularly concerning as echinocandins are often the first-line treatment option for MDR Candida species.

Effects of low temperature and highlight stress on lipid accumulation and cell structure of Tropidoneis maxima.

Tropidoneis maxima is a marine diatom with a rapid growth rate that produces high levels of lipids. To explore whether the lipid content could be further enhanced, cultures were first incubated under optimal conditions and then stressed under low temperature (10°C), a high light intensity level (80 μmol/m2 ·s), and the two factors together (interaction treatment). The results indicated that high light intensity and the temperature-light interaction exhibited greater impacts on lipid synthesis of T. maxima than low temperature. The two stress treatments increased lipid content by 17.16% and 16.6% compared to the control. In particular, higher biomass concentration was obtained with high light intensity (1.082 g L-1 ) and low temperature (1.026 g L-1 ). Moreover, high light intensity (9.06%) and interaction (10.3%) treatments yielded lower starch content compared to low temperature (14.27%) at the end of the stress culture. After 3 days of stress culture, the high light intensity treatment resulted in a 97.01% increase in cell wall thickness and an 18.46% decrease in cell diameter. The results suggest that high light intensity stress on T. maxima would open a new approach to cost-effective biolipid production.

Two monolignoid biosynthetic genes 4-coumarate:coenzyme A ligase (4CL) and p-coumaric acid 3-hdroxylase (C3H) involved in lignin accumulation in pear fruits.

One of the most important factors impacting the quality of pear fruit is the presence of stone cells and lignin. Lignin is the main component of stone cells in pear fruits. Two monolignoid biosynthetic genes 4-coumarate:coenzyme A ligase (4CL) and p-coumaric acid 3-hdroxylase (C3H) are involved in lignin accumulation in pear fruits. However, the functions of these genes in lignin biosynthesis were excluded in pear. In our study, we isolated and cloned Pb4CL11 (GenBank: KM455955.1) and PbC3H1 (GenBank: KM373790.1) from pear, which contained 1644bp encoded 54 amino acids (AA), and 1539bp encoded 513 AA, respectively. The expression of Pb4CL11 and PbC3H1 in Arabidopsis thaliana led to an increase in cell wall thickness for intervascular fibers and xylem cells and lignin content. Overexpression of Pb4CL11 and PbC3H1 in A. thaliana can significantly increase the expression of AtPAL, AtC4H, AtHCT, AtC3H, AtCCOMT, AtCCR, AtF5H, AtCOMT, AtCAD4 and AtCAD5 with promotion of lignin biosynthesis. Taken together, our study's findings not only demonstrated the probable function of Pb4CL11 and PbC3H1 in lignin biosynthesis but also laid the groundwork for future studies using molecular biological methods to control lignin production and the formation of stone cells in pear fruits.

Development of the Al12SiCuFe Alloy Foam Composites with ZrSiO4 Reinforcements at Different Foaming Temperatures

Lightweight aluminum composite is a class of foam material that finds many applications. These properties make it suitable for many industries, such as the transportation, aerospace and sports industries. In the present work, closed-cell foams of an Al-Si12CuFe alloy and its composite are developed by a stir casting process. The optimization of the foaming temperature for the alloy and composite foams was conducted in terms of the ligament and node size of the alloy and also the volatility of the zircon with the melt, to provide strength to the cell walls. CaCO3 as a blowing agent was homogeneously distributed in the molten metal without adding any thickener to develop the metal foam. The decomposition rate of CaCO3 is temperature-dependent, which is attributed to the formation of gas bubbles in the molten alloy. Cell structure, such as cell size and cell wall thickness, is controlled by manufacturing process parameters, and both the physical and mechanical properties are dependent on the foam cell structure, with cell size being the major variable. The results show that the increase in cell wall thickness with higher temperature leads to a decrease in cell size. By adding the zircon to the melt, the cell size of the composite foam first increases, and then the thickening of the wall occurs as the temperature is increased. The uniform distribution of the blowing agent in molten metal helps in the formation of a uniform cell structure. In this work, a comparative structural study of alloy foam and composite foam is presented regarding cell size, cell shape and foam stability at different temperatures.

Understanding the Impact of High-Pressure Treatment on Physico-Chemical, Microstructural, and Microbiological Aspects of Pumpkin Cubes.

In this study color, texture, starch-pectin, total antioxidant capacity, microbial count, and microstructure of HPP-treated Violina pumpkin cubes were evaluated. Samples were treated at six different pressures (100 to 600 MPa-HPP100 to HPP600) for 3 min. Moisture, total soluble solids, and pH showed no significant differences between untreated (UNTR) and treated samples. Pumpkin tissue showed great structural modifications as changes in cell size and shape, cell wall damage, increased cell wall thickness, cell detachment and dehydration, and calcium ions deposition mainly from HPP300 to 600. UNTR samples showed the highest value of maximum and minimum cell elongation, perimeter segment, and a more regular cell wall thickness whereas HPP600 showed the lowest values for all these parameters. A noticeable difference was observed in HPP600 samples, with a difference in terms of color (ΔE 11.3 ± 1.9) and hardness (87.4 ± 27.8 N) compared to the UNTR ones (194.9 ± 37.9 N) whereas treatments at other pressures changed less markedly the color and texture. HPP200 could ensure a higher amount of starch and pectin availability while HPP200 and HPP400 showed the highest total antioxidants capacity. High-pressure treatment from HPP400 to 600 gave the highest destruction of microorganisms but negatively influenced the structural quality as well as texture and microstructure.

Different Silicon Application Sources and Factors Influencing Mandibular Wear in Sugarcane Early Shoot Borer, Chilo infuscatellus Walker

Silicon (Si) can improve plant resistance to herbivorous insect attack. Early shoot borer (ESB), is one of the most solemn lepidopterans borers on sugarcane in India. Even with insecticide application, management of this pest is difficult. The management requires a fresh new approach. As a result, the current study aims to determine the effect of silicon on the early shoot borer, Chilo infuscatellus Walker, through biophysical factor analysis and mandibular wear documentation. When sugarcane leaves were treated with calcium silicate at 1000 kg/ha, scanning electron microscopy revealed the presence of silicified cells and trichomes, as well as increased cell wall thickness, silicon content, and waxes content. Furthermore, larvae of an early shoot borer fed silica-treated plants showed a complete wearing of mandibles as compared to untreated check.

Involvement of lignin deposition and cell wall degradation in stem senescence of Chinese flowering cabbage during storage

Chinese flowering cabbage is susceptible to leaf yellowing, however, little is known about stem senescence after harvest. Herein, changes in the microstructures, lignin and cell wall polysaccharide contents, and expression of their corresponding genes during the stem senescence of Chinese flowering cabbage were investigated. Anatomical and chemical analyses revealed that an increase in cell wall thickness was accompanied by lignin deposition around the vascular cells in the stem. Concurrently, the collapse of parenchyma cells developed gradually, which was probably related to the degradation of cell wall polysaccharides including pectin, hemicellulose, and cellulose, among others. The outer stem tissues, including epidermal cells to vascular cells, could be directly peeled, and the middle of the stem was found to contain prominent parenchyma cells as pith tissues. Activity of lignin biosynthesis-related enzymes of phenylalanine ammonia lyase (PAL), cinnamyl alcohol dehydrogenase (CAD), and peroxidase (POD), and the expression of their corresponding genes BrPAL2/3/6, Br4CL1/4, BrCAD2/4/5/11, and BrPOD31/37 were higher in outer peeled tissues than in pith tissues. The enzyme activity of polygalacturonase and pectin methylesterase, and expression levels of the polysaccharide degradation-related genes BrXET2/3, BrCEL3, and BrMAN1/5 were higher in pith than in outer peeled tissues. These results suggest that lignin deposition around the vascular tissue, and cell wall degradation in pith tissues are involved in the stem senescence of Chinese flowering cabbage after harvest.

Changes in the cell walls on fruit skin of Beurré D´Anjou pears (Pyrus communis L.) associated with sunburn injury

• Sunburn reduced cuticular microcrack area and skin thickness, and increased cell wall thickness. • Neutral sugars (NS) content increased in two pectin fractions (WSP and CSP) in sunburn skin. • Hemicellulose and lignin contents increased in sunburn skin. • The expression of Exp and XTH genes increased in response to sunburn. The purpose of this work was to evaluate the effects of sunburn on pear fruit skin at the structural, biochemical, and molecular levels. Pears ( Pyrus communis L.) cv. Beurré D'Anjou were collected at the official commercial harvest time and classified into three groups based on levels of sublethal sunburn: no sunburn (S0), mild sunburn (S1), and moderate sunburn (S2). Skin anatomy was characterized by SEM imaging, cell wall components were quantified by spectrophotometric techniques, and the expression of different genes related to cell wall remodeling was measured in S0, S1, and S2 tissues. Sun-damaged skin cells had reduced size and thickened walls. In the cuticular surface, a reduction of microcracking area, correlated with the intensity of the damage, was further noted. Cell wall fractionation revealed changes in the distribution of neutral sugars (NS) following sunburn, although no differences in uronic acid (UA) content were observed in the different pectin fractions. Hemicellulose and lignin contents were significantly ( P <0.05) increased in sun-damaged tissues. Expression levels of genes encoding polygalacturonase (PcPG2), β-galactosidase (PcGAL2 and PcGAL4), xyloglucan endotransglycosylase (PcXET), and expansin (PCExp1) were increased in the skin of sun-damaged (S1 and S2) fruit. These results indicate that sunburn alters the anatomy and cell wall structure and composition of pear fruit skin, and stimulates different mechanisms involved in the acquisition of stress tolerance.

Effects of antimony stress on growth, structure, enzyme activity and metabolism of Nipponbare rice (Oryza sativa L.) roots

Some antimony (Sb) contaminated areas are used for rice cultivation in response to economic demands. However, little is known about the effects of Sb stress on the growth and metabolism of rice roots. Thus, a hydroponic experiment was carried out on the growth, root anatomy, enzyme activity, and metabolism of Nipponbare rice (Oryza sativa L. ssp. japonica cv. Nipponbare) under varying levels of Sb (III) stress (0 mg L−1, 10 mg L−1, and 50 mg L−1). With the increase of Sb concentration, rice root length and root fresh weight declined by 67.8 % and 90.5 % for 10 mg L−1 Sb stress and 94.1 % and 98.4 % for 50 mg L−1 Sb stress, respectively. Anatomical analysis of cross-sections of Sb-treated roots showed an increase in cell wall thickness and an increase in the number of cell mitochondria. The 10 mg L−1 and 50 mg L−1 Sb stress increased the activity of enzyme superoxide dismutase (SOD) in root cells by 1.94 and 2.40 times, respectively. Compared to the control, 10 mg L−1 Sb treatment increased the activity of catalase (CAT) and peroxidase (POD), as well as the concentrations of antioxidant glutathione (GSH) in the root by 1.46, 1.38, and 0.52 times, respectively. However, 50 mg L−1 Sb treatment significantly decreased the activity or content of CAT, POD and GSH by 28.1 %, 13.5 % and 28.2 %, respectively. Nontargeted LC/MS-based metabolomics analysis identified 23 and 13 significantly differential metabolites in rice roots exposed to 10 mg L−1 and 50 mg L−1 Sb, respectively, compared to the control. These differential metabolites were involved in four main metabolic pathways including the tricarboxylic acid cycle (TCA cycle), butanoate metabolism, alanine, aspartate and glutamate metabolism, and alpha-linolenic acid metabolism. Taken together, these findings indicate that Sb stress destroys the structure of rice roots, changes the activity of enzymes, and affects the metabolic pathway, thereby reducing the growth of rice roots and leading to toxicity.

Role of the Global Fitness Regulator Genes on the Osmotic Tolerance Ability and Salinity Hazard Alleviation of Trichoderma asperellum GDFS 1009 for Sustainable Agriculture.

Velvet family proteins are global regulators of fungal growth and development. Here, we reported the role of Vel1 and Lae1 from T. asperellum in osmotic tolerance. Deletion of the Vel1 and Lae1 genes led to the retardation of vegetative mycelial growth under saline conditions. The strain carrying the overexpression locus of the Vel1 and Lae1 genes was highly resistant to oxidative stress by upregulating the enzymes and genes involved in antioxidant activity. Major physiological changes in the cell wall and vacuoles occurred under high saline conditions. The Vel1 and Lae1 overexpression strains increased cell wall thickness and the number of vacuoles, which seems to lead to an increase of the osmolyte content of glycerol and proline. The absorption of Na+ content in the vacuole of the Vel1 and Lae1 overexpression strains was increased, while the absorption of Na+ was impaired in the Vel1 and Lae1 knock out strains, in which the Na+ was localized in the cell wall membrane. This result supported the significant correlation of the expression of genes with the ionic transportation in T. asperellum. Maize root colonization by the Vel1 and Lae1 gene overexpression strain was increased, which would mitigate the stress caused by the absorption of Na+ in the maize roots and increased the plant growth. Our results highlighted the importance of Vel1 and Lae1 proteins to the salinity stress tolerance of T. asperellum and the mitigation of Na+ stress to plants for sustainable agriculture.

Antibacterial activity of novel linear polyamines against Staphylococcus aureus.

New therapeutic options are urgently required for the treatment of Staphylococcus aureus infections. Accordingly, we sought to exploit the vulnerability of S. aureus to naturally occurring polyamines. We have developed and tested the anti-staphylococcal activity of three novel linear polyamines based on spermine and norspermine. Using a panel of genetically distinct and clinically relevant multidrug resistant S. aureus isolates, including the polyamine resistant USA300 strain LAC, compound AHA-1394 showed a greater than 128-fold increase in inhibition against specific S. aureus strains compared to the most active natural polyamine. Furthermore, we show that AHA-1394 has superior biofilm prevention and biofilm dispersal properties compared to natural polyamines while maintaining minimal toxicity toward human HepG2 cells. We examined the potential of S. aureus to gain resistance to AHA-1394 following in vitro serial passage. Whole genome sequencing of two stable resistant mutants identified a gain of function mutation (S337L) in the phosphatidylglycerol lysyltransferase mprF gene. Inactivation of mutant mprF confirmed the importance of this allele to AHA-1394 resistance. Importantly, AHA-1394 resistant mutants showed a marked decrease in relative fitness and increased generation time. Intriguingly, mprF::S337L contributed to altered surface charge only in the USA300 background whereas increased cell wall thickness was observed in both USA300 and SH1000. Lastly, we show that AHA-1394 displays a particular proclivity for antibiotic potentiation, restoring sensitivity of MRSA and VRSA isolates to daptomycin, oxacillin and vancomycin. Together this study shows that polyamine derivatives are impressive drug candidates that warrant further investigation.

An unexpected discovery toward argon-rich water amelioration of cadmium toxicity in Medicago sativa L.

Argon has organ-protective effects on animals. However, whether or how argon influences plant responses remains elusive. In this study, we discovered that the growth inhibition of hydroponically cultured alfalfa seedlings under 100 μM CdCl2 condition was significantly ameliorated by 100 % saturated argon-rich water (ARW). Less Cd uptake and accumulation were also observed in both root and shoot parts, which could be explained by the modified root cell walls, including the increased cell wall thickness, lignin content, and demethylation degree of covalently bound and ion-bound pectin, as well as the down-regulated expression of natural-resistance-associated-macrophage protein1 (Nramp1) encoding a heavy metal ion transporter in root tissue. The hindered Cd translocation from root to shoot achieved by ARW addition was validated by the decreased expression of heavy metal ATPase 2/4 (HMA2/4) in roots and decreased Cd content in xylem saps. The reestablished glutathione (GSH) homeostasis and redox balance, two important indicators of plant defense against Cd poisoning, were also observed. Further greenhouse experiments demonstrated that the phenotypic and physiological performances of alfalfa plants cultured in Cd-contaminated soil were significantly improved by irrigating with ARW. Above results implied that ARW confers plants tolerance against cadmium toxicity by impairing Cd uptake and accumulation and restoring GSH and redox homeostasis. These findings might open a new window for understanding argon biology in higher plants.

A Cork Cell Wall Approach to Swelling and Boiling with ESEM Technology

The bark of cork oak (Quercus suber L.) is mostly used for cork stopper production; when bark undergoes a series of industrial procedures, boiling usually leads to changes in the characteristics of its tissue. Trees are traditionally grown under natural conditions; however, irrigation is now being used in plantations. This permanent water availability affects cork oak development, while its effects on industrial procedures are unknown. This study provides the first insight into the behaviour of the cell walls of cork during the process of swelling and boiling when trees have been grown under irrigation, that is, subject to a specific water regime. Cork tissue is analysed using environmental and scanning electron microscopy under three regimes: raw conditions, following immersion in water, and after boiling. Additionally, the radial expansion of samples is determined. The results show greater cell wall expansion in cork from the irrigated site than in cork from the traditional rainfed plot when hydrated for 24 h. After boiling, the cell walls of the cork from the rainfed site are thinner than in the raw stage, which is in contrast to the irrigated cork. This study suggests that irrigation during cork oak growth produces a higher capacity for adsorption, increasing cell wall thickness from the raw stage to the boiling stage.

Flexural and Out-of-Plane Compression Performance of Hexagonal Rubber Wood Core Sandwich with Increasing Cell Wall Thickness

This paper investigates the rubber wood honeycomb core by manipulating its cell wall thickness. Rubber wood honeycomb core was fabricated with cell walls range from 1 mm to 3 mm. The impacts of the cell geometrical parameters on the flexural and out-of-plane compression performance are studied. In the case of solid rubber wood without facesheet, the density is much higher than those rubber wood honeycomb composites. The failure can be disastrous without facesheet under bending. Rubber wood honeycomb sandwiches are able to offer the similar specific flexural strength with lower density. With increasing wall thickness from 1 mm to 3 mm, the specific flexural strength increased by 12.32 %. Meanwhile, specific compressive strength improved by 11 % from 1 mm to 2 mm. However, its specific strength dropped by 3.55 % when the wall thickness at 3 mm. Minimum improvement in the compressive strength per density has caused the decrement.