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Weeds, pests, and pathogens are among the pre-harvest constraints in rice farming across rice-growing countries. For weed management, manual weeding and herbicides are widely practiced. Among the herbicides, glyphosate [N-(phosphonomethyl) glycine] is a broad-spectrum systemic chemical extensively used in agriculture. Being a competitive structural analog to phosphoenolpyruvate, it selectively inhibits the conserved 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) enzyme required for the biosynthesis of aromatic amino acids and essential metabolites in eukaryotes and prokaryotes. In the present study, we investigated the antifungal and defense elicitor activity of glyphosate against Magnaporthe oryzae on transgenic-rice overexpressing a glyphosate-resistance OsEPSPS gene (T173I + P177S; TIPS OsmEPSPS) for blast disease management. The glyphosate foliar spray on OsmEPSPS transgenic rice lines showed both prophylactic and curative suppression of blast disease comparable to a blasticide, tricyclazole. The glyphosate displayed direct antifungal activity on Magnaporthe oryzae as well as enhanced the levels of antioxidant enzymes and photosynthetic pigments in rice. However, the genes associated with phytohormones-mediated defense (OsPAD4, OsNPR1.3, and OsFMO) and innate immunity pathway (OsCEBiP and OsCERK1) were found repressed upon glyphosate spray. Altogether, the current study is the first report highlighting the overexpression of a crop-specific TIPS mutation in conjugation with glyphosate application showing potential for blast disease management in rice cultivation.

Plants face a continuous threat of abiotic stresses under the changing environment. Because of climate change, water scarcity has been shown to be a significant environmental constraint on plant productivity. Droughts in particular have been shown to affect plant growth and development, lead to alteration in quality and quantity of crop production, and result in global food insecurity. Phytohormones are known to play critical roles in regulating diverse processes of plant adaption to a drought environment. They regulate cellular functions at molecular levels via various cell signaling. Among various phytohormones, abscisic acid (ABA) is known for its role in drought-stress tolerance in plants. Other phytohormones such as auxins, brassinosteroids (BRs), cytokinins (CK), ethylene (ET), gibberellins (GA), jasmonic acid (JA), and salicylic acid (SA) are also crucial in plant drought tolerance. Several plant growth-promoting microbes have been reported to enhance the phytohormone levels in plants to mitigate the negative effect of drought. However, the transgenic approach appears to be a boon to engineering the genes responsible for regulating phytohormones to develop a drought-tolerant trait. Expression analyses have revealed that genes encoding transcription factors such as bZIP11, DREB2, MYB14, MYB48, WRKY2, WRKY56, WRKY108715, and RD22 play a very crucial role in phytohormone mediated drought response. Furthermore, exogenous applications of phytohormones are shown to enhance endogenous phytohormones. This review highlights the most recent advancements in phytohormone-mediated drought tolerance in major crop plants.

Asparagine is formed by two structurally distinct asparagine synthetases in prokaryotes. One is the ammonia-utilizing asparagine synthetase A (AsnA), and the other is asparagine synthetase B (AsnB) that uses glutamine or ammonia as a nitrogen source. In a previous investigation using sequence-based analysis, we had shown that Leishmania spp. possess asparagine-tRNA synthetase paralog asparagine synthetase A (LdASNA) that is ammonia-dependent. Here, we report the cloning, expression, and kinetic analysis of ASNA from Leishmania donovani. Interestingly, LdASNA was both ammonia- and glutamine-dependent. To study the physiological role of ASNA in Leishmania, gene deletion mutations were attempted via targeted gene replacement. Gene deletion of LdASNA showed a growth delay in mutants. However, chromosomal null mutants of LdASNA could not be obtained as the double transfectant mutants showed aneuploidy. These data suggest that LdASNA is essential for survival of the Leishmania parasite. LdASNA enzyme was recalcitrant toward crystallization so we instead crystallized and solved the atomic structure of its close homolog from Trypanosoma brucei (TbASNA) at 2.2 Å. A very significant conservation in active site residues is observed between TbASNA and Escherichia coli AsnA. It is evident that the absence of an LdASNA homolog from humans and its essentiality for the parasites make LdASNA a novel drug target.