Serine proteinase inhibitors (IP's) are proteins found naturally in a wide range of plants with a significant role in the natural defense system of plants against herbivores. The question addressed in the present study involves assessing the ability of the serine proteinase inhibitor in combating nematode infestation. The present study involves engineering a plant serine proteinase inhibitor (pin2) gene into T. durum PDW215 by Agrobacterium-mediated transformation to combat cereal cyst nematode (Heterodera avenae) infestation. Putative T(0) transformants were screened and positive segregating lines analysed further for the study of the stable integration, expression and segregation of the genes. PCR, Southern analysis along with bar gene expression studies corroborate the stable integration pattern of the respective genes. The transformation efficiency is 3%, while the frequency of escapes was 35.71%. chi(2) analysis reveals the stable integration and segregation of the genes in both the T(1) and T(2) progeny lines. The PIN2 systemic expression confers satisfactory nematode resistance. The correlation analysis suggests that at p < 0.05 level of significance the relative proteinase inhibitor (PI) values show a direct positive correlation vis-à-vis plant height, plant seed weight and also the seed number.

Water deficit arises as a result of low temperature, salinity and dehydration, thereby affecting plant growth adversely and making it imperative for plants to surmount such situations by acclimatizing/adapting at various levels. Water deficit stress results in significant changes in gene expression, mediated by interconnected signal transduction pathways that may be triggered by calcium, and regulated via ABA dependent and/or independent pathways. Hence, adaptation of plants to such stresses involves maintaining cellular homeostasis, detoxification of harmful elements and also growth alterations. Stress in general cause excess production of reactive oxygen species (ROS) and the plants overcome the same by either preventing the accumulation of ROS or by eliminating the ROS formed. Ion homeostasis includes processes such as cellular uptake, sequestration and export in conjunction with long distance transport. Requisite amounts of osmolytes are hence synthesized under stress to maintain turgor along with maintaining the macromolecular structures and also for scavenging ROS. Another noteworthy response is the accumulation of novel proteins, including enzymes involved in the biosynthesis of osmoprotectants, heat-shock proteins (HSPs), late embryogenesis abundant (LEA) proteins, antifreeze proteins, chaperones, detoxification enzymes, transcription factors, kinases and phosphatases. The LEAs belong to a redundant protein family and are highly hydrophilic, boiling-soluble, non-globular and therefore have been defined and classified accordingly. The precise function of LEAs is still unknown, but substantial evidence indicates their involvement in dessication tolerance as the expression of LEAs confers increased resistance to stress in heterologous yeast system and also significantly improves water deficit tolerance in transgenic plants. Genetic manipulation of plants towards conferring abiotic stress tolerance is a daunting task, as the abiotic stress tolerance mechanism is highly complex and various strategies have been exploited to address and evaluate the stress tolerance mechanism, and the molecular responses to water deficit via complex signaling networks. Genomic technologies have recently been useful in integrating the multigenicity of the plant stress responses through, transcriptomics, proteomics and metabolite profilling and their interactions. This review deals with the recent developments on genetic approaches for water stress tolerance in plants, with special emphasis on LEAs.

No abstract

No abstract

No abstract

Introduction: The shoot-up of antimicrobial resistance leading to the Multidrug Resistance (MDR) phenomenon in clinical pathogens has forced us to develop novel technologies to cease this global threat immediately. Iron oxide nanoparticles can be a breakthrough solution to this dilemma due to its magnetic properties and biocompatibility. Non toxic and biocompatible applications of magnetic nanoparticles can be enriched further by special surface coating with organic or inorganic molecules. Aim: To determine the antibacterial activity of green synthesised iron oxide nanoparticles against various clinical isolates. Materials and Methods: This was a cross-sectional study conducted from June 2021 to April 2022. This study was conducted at the Department of Microbiology, SRM Medical College Hospital and Research Centre (SRMMCH&RC), Kattankulathur, Chengalpattu, Tamil Nadu, India. Nanoparticles underwent surface modifications and characterisation using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDX), Ultraviolet (UV) Visible Absorption Spectra, and Fourier-Transform Infrared Spectroscopy (FT-IR) followed by charge characterisation through Agarose Gel Electrophoresis. Kirby-Bauer Disc Diffusion method was used for screening the sensitivity and resistance pattern of 50 selected isolates and Minimum Inhibitory Concentration (MIC) was assessed using MIC Microbroth Dilution technique with the help of resazurin. Results: Out of the four different concentrations of bare and coated nanoparticles (0.0375 mg/mL, 0.07 mg/mL, 0.15 mg/mL, 0.3 mg/mL), bare nanoparticles inhibited the growth of Methicillin Resistant Staphylococcus aureus (MRSA) at 0.3 mg/mL while citrate-coated nanoparticles inhibited the growth at 0.15 mg/mL, 0.018 mg/mL, 0.0375 mg/mL, 0.07 mg/mL, and 0.15 mg/mL dilutions were used in case of Carbapenem-resistant Klebsiella pneumoniae (CR K. pneumoniae) and MDR Escherichia coli, from which both organisms were inhibited at 0.15 mg/mL of bare and coated nanoparticles. Conclusion: Iron nanoparticles synthesised from the marine algae Chaetomorpha antennina could be used in the future as a drug carrier or as an antimicrobial agent.

No abstract