Silicon alleviated manganese toxicity in cucumber by cell wall compartmentation

Author(s):  
Jelena Dragisic Maksimovic ◽  
Vuk Maksimovic

<p>As a consequence of normal root growth and development, a considerable range of organic and inorganic substances are exchanged between the root and soil, which causes changes in the biochemical and physical properties of the rhizosphere. Plants modify their rhizosphere in response to various environmental signals and stresses. Low-molecular-weight metabolites are commonly detected in this region and their exudation from plant roots has been associated with abiotic stress, such as inorganic form of manganese (Mn). In this study we investigated the root exudate constituents (phenolics and enzymes) of cucumber (<em>Cucumis sativus</em> L.) plants grown in Mn-free and Mn-contaminated nutrient solutions (0.5 and 100 μM, respectively) with (+Si) or without silicon (–Si) supplied as 1.5 mM silicic acid. High external Mn supply induced both growth inhibition of the whole plant and the appearance of Mn-toxicity symptoms in the leaves, while the simultaneous application of Si alleviated toxicity symptoms. At high Mn supply, concentration of phenolic compounds, as plant-borne substrates for peroxidase (POD) and polyphenol oxidases (PPO), depended on Si application. The increased concentrations of phenolic compounds (e.g., coniferyl alcohol, <em>p</em>-coumaric and isoferulic acid) in –Si plants were in agreement with enhanced POD and PPO activities. The activities of both enzymes were kept at a lower level in +Si plants grown at higher Mn concentrations. These results suggest that Si nutrition modulates the metabolism and utilization of phenolic compounds most probably as a consequence of the formation of Si-polyphenol complexes and their subsequent cross-linking with cell wall polymers. In –Si plants increased activity of the PPO and POD/H<sub>2</sub>O<sub>2</sub> systems lead to the formation of highly reactive compounds, while in +Si plants, lignin biosynthesis is favored. H<sub>2</sub>O<sub>2</sub> in the presence of elevated Mn concentrations produced potentially toxic •OH and Mn<sup>3+</sup> in the Fenton reaction, which was efficiently suppressed by Si application. Silicon thus prevented the formation of toxic intermediates (•OH and Mn<sup>3+</sup>) and accumulation/oxidation of free phenolics leading to oxidative browning, the initial indicator of Mn-toxicity symptoms. In summary, we presented the knowledge about how cucumber can overcome hyperaccumulation of Mn by means of Si-complexation suggesting ways of improving future phytoremediation strategies.</p>

2021 ◽  
Vol 22 (7) ◽  
pp. 3560
Author(s):  
Ruixue Xiao ◽  
Chong Zhang ◽  
Xiaorui Guo ◽  
Hui Li ◽  
Hai Lu

The secondary wall is the main part of wood and is composed of cellulose, xylan, lignin, and small amounts of structural proteins and enzymes. Lignin molecules can interact directly or indirectly with cellulose, xylan and other polysaccharide molecules in the cell wall, increasing the mechanical strength and hydrophobicity of plant cells and tissues and facilitating the long-distance transportation of water in plants. MYBs (v-myb avian myeloblastosis viral oncogene homolog) belong to one of the largest superfamilies of transcription factors, the members of which regulate secondary cell-wall formation by promoting/inhibiting the biosynthesis of lignin, cellulose, and xylan. Among them, MYB46 and MYB83, which comprise the second layer of the main switch of secondary cell-wall biosynthesis, coordinate upstream and downstream secondary wall synthesis-related transcription factors. In addition, MYB transcription factors other than MYB46/83, as well as noncoding RNAs, hormones, and other factors, interact with one another to regulate the biosynthesis of the secondary wall. Here, we discuss the biosynthesis of secondary wall, classification and functions of MYB transcription factors and their regulation of lignin polymerization and secondary cell-wall formation during wood formation.


Planta ◽  
2021 ◽  
Vol 253 (5) ◽  
Author(s):  
Peilei Chen ◽  
Valentino Giarola ◽  
Dorothea Bartels

Abstract Main conclusion The cell wall protein CpWAK1 interacts with pectin, participates in decoding cell wall signals, and induces different downstream responses. Abstract Cell wall-associated protein kinases (WAKs) are transmembrane receptor kinases. In the desiccation-tolerant resurrection plant Craterostigma plantagineum, CpWAK1 has been shown to be involved in stress responses and cell expansion by forming a complex with the C. plantagineum glycine-rich protein1 (CpGRP1). This prompted us to extend the studies of WAK genes in C. plantagineum. The phylogenetic analyses of WAKs from C. plantagineum and from other species suggest that these genes have been duplicated after species divergence. Expression profiles indicate that CpWAKs are involved in various biological processes, including dehydration-induced responses and SA- and JA-related reactions to pathogens and wounding. CpWAK1 shows a high affinity for “egg-box” pectin structures. ELISA assays revealed that the binding of CpWAKs to pectins is modulated by CpGRP1 and it depends on the apoplastic pH. The formation of CpWAK multimers is the prerequisite for the CpWAK–pectin binding. Different pectin extracts lead to opposite trends of CpWAK–pectin binding in the presence of Ca2+ at pH 8. These observations demonstrate that CpWAKs can potentially discriminate and integrate cell wall signals generated by diverse stimuli, in concert with other elements, such as CpGRP1, pHapo, Ca2+[apo], and via the formation of CpWAK multimers.


2011 ◽  
Vol 156 (3) ◽  
pp. 1364-1374 ◽  
Author(s):  
Lucinda Denness ◽  
Joseph Francis McKenna ◽  
Cecile Segonzac ◽  
Alexandra Wormit ◽  
Priya Madhou ◽  
...  

2019 ◽  
Author(s):  
Philippe Golfier ◽  
Faride Unda ◽  
Emily K. Murphy ◽  
Jianbo Xie ◽  
Feng He ◽  
...  

AbstractCell wall recalcitrance is a major constraint for the exploitation of lignocellulosic biomass as renewable resource for energy and bio-based products. Transcriptional regulators of the lignin biosynthetic pathway represent promising targets for tailoring lignin content and composition in plant secondary cell walls. A wealth of research in model organisms has revealed that transcriptional regulation of secondary cell wall formation is orchestrated by a hierarchical transcription factor (TF) network with NAC TFs as master regulators and MYB factors in the lower tier regulators. However, knowledge about the transcriptional regulation of lignin biosynthesis in lignocellulosic feedstocks, such as Miscanthus, is limited. Here, we characterized two Miscanthus MYB TFs, MsSCM1 and MsMYB103, and compared their transcriptional impact with that of the master regulator MsSND1. In Miscanthus leaves MsSCM1 and MsMYB103 are expressed at growth stages associated with lignification. Ectopic expression of MsSCM1 and MsMYB103 in tobacco leaves was sufficient to trigger secondary cell wall deposition with distinct sugar and lignin composition. Moreover, RNA-seq analysis revealed that the transcriptional responses to MsSCM1 and MsMYB103 overexpression showed extensive overlap with the response to MsSND1, but were distinct from each other, underscoring the inherent complexity of secondary cell wall formation. Together, MsSCM1 and MsMYB103 represent interesting targets for manipulations of lignin content and composition in Miscanthus towards tailored biomass.


2020 ◽  
Vol 40 (9) ◽  
pp. 1277-1291 ◽  
Author(s):  
Xin Ye ◽  
Xu-Feng Chen ◽  
Li-Ya Cai ◽  
Ning-Wei Lai ◽  
Chong-Ling Deng ◽  
...  

Abstract Little is known about the physiological and molecular mechanisms underlying magnesium (Mg)-deficiency-induced enlargement, cracking and lignification of midribs and main lateral veins of Citrus leaves. Citrus sinensis (L.) Osbeck seedlings were irrigated with nutrient solution at a concentration of 0 (Mg-deficiency) or 2 (Mg-sufficiency) mM Mg(NO3)2 for 16 weeks. Enlargement, cracking and lignification of veins occurred only in lower leaves, but not in upper leaves. Total soluble sugars (glucose + fructose + sucrose), starch and cellulose concentrations were less in Mg-deficiency veins of lower leaves (MDVLL) than those in Mg-sufficiency veins of lower leaves (MSVLL), but lignin concentration was higher in MDVLL than that in MSVLL. However, all four parameters were similar between Mg-deficiency veins of upper leaves (MDVUL) and Mg-sufficiency veins of upper leaves (MSVUL). Using label-free, liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis, we identified 1229 and 492 differentially abundant proteins (DAPs) in MDVLL vs MSVLL and MDVUL vs MSVUL, respectively. Magnesium-deficiency-induced alterations of Mg, nonstructural carbohydrates, cell wall components, and protein profiles were greater in veins of lower leaves than those in veins of upper leaves. The increased concentration of lignin in MDVLL vs MSVLL might be caused by the following factors: (i) repression of cellulose and starch accumulation promoted lignin biosynthesis; (ii) abundances of proteins involved in phenylpropanoid biosynthesis pathway, hormone biosynthesis and glutathione metabolism were increased; and (iii) the abundances of the other DAPs [viz., copper/zinc-superoxide dismutase, ascorbate oxidase (AO) and ABC transporters] involved in lignin biosynthesis were elevated. Also, the abundances of several proteins involved in cell wall metabolism (viz., expansins, Rho GTPase-activating protein gacA, AO, monocopper oxidase-like protein and xyloglucan endotransglucosylase/hydrolase) were increased in MDVLL vs MSVLL, which might be responsible for the enlargement and cracking of leaf veins.


2005 ◽  
Vol 37 (5) ◽  
pp. 409-423 ◽  
Author(s):  
Markus HAUCK ◽  
Alexander PAUL

Decreasing abundance of epiphytic lichens with increasing Mn supply from the substratum or from stemflow was found in several coniferous forests of Europe (Germany) as well as western (Montana, British Columbia) and eastern North America (New York State). Experiments carried out with Hypogymnia physodes and other species of chloro- and cyano-lichens suggest that these correlations are causal. High Mn concentrations e.g. reduce chlorophyll concentrations, chlorophyll fluorescence and degrade the chloroplast in lichen photobionts. Excess Mn inhibits the growth of soredia of H. physodes and causes damage in the fine- and ultra-structure of the soredia. Adult lichen thalli remain structurally unaffected by Mn. Manganese uptake does not result in membrane damage. Calcium, Mg, Fe and perhaps also Si alleviate Mn toxicity symptoms in H. physodes. Lecanora conizaeoides is not sensitive to Mn in laboratory experiments or in the field. The data suggest that high Mn concentrations are an important site factor for epiphytic lichens in coniferous forests that until recently has been overlooked. Manganese reaching the microhabitat of epiphytic lichens is primarily soil-borne and is usually not derived from pollution.


2019 ◽  
Vol 35 (1) ◽  
pp. 309-336 ◽  
Author(s):  
Andrew Muroyama ◽  
Dominique Bergmann

Cell polarity in plants operates across a broad range of spatial and temporal scales to control processes from acute cell growth to systemic hormone distribution. Similar to other eukaryotes, plants generate polarity at both the subcellular and tissue levels, often through polarization of membrane-associated protein complexes. However, likely due to the constraints imposed by the cell wall and their extremely plastic development, plants possess novel polarity molecules and mechanisms highly tuned to environmental inputs. Considerable progress has been made in identifying key plant polarity regulators, but detailed molecular understanding of polarity mechanisms remains incomplete in plants. Here, we emphasize the striking similarities in the conceptual frameworks that generate polarity in both animals and plants. To this end, we highlight how novel, plant-specific proteins engage in common themes of positive feedback, dynamic intracellular trafficking, and posttranslational regulation to establish polarity axes in development. We end with a discussion of how environmental signals control intrinsic polarity to impact postembryonic organogenesis and growth.


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