The Halomonas species isolated from the rhizosphere of the true mangrove Avicennia marina of Indian Sundarbans showed enhanced rice growth promotion under combined stress of salt and arsenic in pot assay. Interestingly, under abiotic stress conditions, Halomonas sp. Exo1 was observed as an efficient producer of exopolysaccharide. The study revealed that salt triggered exopolysaccharide production, which in turn, increased osmotic tolerance of the strain. Again, like salt, presence of arsenic also caused increased exopolysaccharide production that in turn sequestered arsenic showing a positive feedback mechanism. To understand the role of exopolysaccharide in salt and arsenic biosorption, purified exopolysaccharide mediated salt and arsenic sequestration were studied both under in vivo and in vitro conditions and the substrate binding properties were characterized through FT-IR and SEM-EDX analyses. Finally, observation of enhanced plant growth in pot assay in the presence of the strain and pure exopolysaccharide separately, confirmed direct role of exopolysaccharide in plant growth promotion.

The synaptonemal complex (SC) is a widely conserved structure that mediates the intimate alignment of homologous chromosomes during meiotic prophase and is required for proper homolog segregation at meiosis I. However, fundamental details of SC architecture and assembly remain poorly understood. The coiled-coil protein, Zip1, is the only component whose arrangement within the mature SC of budding yeast has been extensively characterized. It has been proposed that the Small Ubiquitin-like MOdifier, SUMO, plays a role in SC assembly by linking chromosome axes with Zip1's C termini. The role of SUMO in SC structure has not been directly tested, however, because cells lacking SUMO are inviable. Here, we provide direct evidence for SUMO's function in SC assembly. A meiotic smt3 reduction-of-function strain displays reduced sporulation, abnormal levels of crossover recombination, and diminished SC assembly. SC structures are nearly absent when induced at later meiotic time points in the smt3 reduction-of-function background. Using Structured Illumination Microscopy we furthermore determine the position of SUMO within budding yeast SC structure. In contrast to previous models that positioned SUMO near Zip1's C termini, we demonstrate that SUMO lies at the midline of SC central region proximal to Zip1's N termini, within a subdomain called the “central element”. The recently identified SUMOylated SC component, Ecm11, also localizes to the SC central element. Finally, we show that SUMO, Ecm11, and even unSUMOylatable Ecm11 exhibit Zip1-like ongoing incorporation into previously established SCs during meiotic prophase and that the relative abundance of SUMO and Ecm11 correlates with Zip1's abundance within SCs of varying Zip1 content. We discuss a model in which central element proteins are core building blocks that stabilize the architecture of SC near Zip1's N termini, and where SUMOylation may occur subsequent to the incorporation of components like Ecm11 into an SC precursor structure. The meiotic cell cycle enables sexually reproducing organisms to generate reproductive cells with half their chromosome complement. Chromosome ploidy is reduced during meiosis by virtue of prior associations established between homologous chromosomes (homologs). Such associations, which are ultimately secured by crossover recombination events, allow homologs to achieve an opposing orientation and segregate from one another at meiosis I. A multimeric protein structure, the synaptonemal complex (SC), mediates the intimate, lengthwise alignment of homologs during meiotic prophase and forms the context in which crossovers mature. The SC's tripartite structure is widely conserved but its composition and architecture remain incompletely understood in any organism. The Small Ubiquitin-like MOdifier (SUMO) localizes to SC in budding yeast. We show that SUMO is required for assembling mature SC and we furthermore demonstrate that SUMO and the recently identified SUMOylated protein, Ecm11, are components of the central element substructure of the budding yeast SC. Our findings suggest that SUMO and Ecm11 are core building blocks of SC, yet our data also suggest that SUMOylation may occur subsequent to Ecm11's incorporation into the SC structure. Finally, our study highlights Structured Illumination as a powerful tool for mapping the fine structure of budding yeast SC.

Macrophytes have the potential to withstand pollutant-induced stress and can be used to clean contaminated water using phyto-extraction, phyto-degradation, phyto-filtration, phyto-stimulation, and phyto-volatilization technique(s). Phytoremediation through constructed wetlands (CWs) for eliminating inorganic and organic pollutants from household sewage and wastewater has attracted scientific attention. CWs are artificially engineered treatment systems that utilize natural cycles or processes involving soils, wetland vegetation, and plant and soil-associated microbial assemblages to remediate contaminated water and improve its quality. Herein, we present a detailed assessment of contaminant removal effectiveness in different CW systems, i.e., free-water surface or surface-flow constructed wetlands (FWSCWs/SFCWs), subsurface-flow constructed wetlands (SSFCWs), and hybrid constructed wetlands (HCWs). Several wetland floral species have been reported as potential phytoremediators, effectively reducing aquatic contamination through biodegrading, biotransforming, and bioaccumulating contaminants. Water hyacinth (Pontederia crassipes) is one of the most resistant macrophytes, capable of tolerating high nitrate (NO₃⁻) and phosphate (PO₄²⁻) concentrations. Other aquatic weeds also effectively alleviate biological oxygen demand (BOD), chemical oxygen demand (COD), total dissolved solids (TDS), and pathogen levels and ameliorate the impact of different ionic forms of nitrogen (N), phosphorus (P), and trace elements (TEs). The review primarily focuses on using hydrophyte(s)-microbe(s) associations in different CWs as an essential phytoremediation tool for sustainable management of freshwater ecosystems, ecorestoration, and prospective resource recovery, favoring a circular bioeconomy (CBE).