Increasing human population and changing climate, which have given rise to frequent drought spells, pose a serious threat to global food security, while identification of high yielding drought tolerant genotypes remains a proficient approach to cope with these challenges. To offer a methodology for the evaluation of the drought-tolerant wheat genotypes based on the pheno-physiological traits, a field experiment was executed, entailing four wheat genotypes viz. BARI Gom 26, BAW 1158, BAW 1167, and BAW 1169 and two water conditions viz. control treatment (three times irrigation at 20, 50, and 70 DAS, i.e., 100% field capacity) and stressed treatment (no irrigation during the entire growing season). The results revealed that drought stress drastically reduced the days to booting, heading, anthesis and physiological maturity, relative water content (RWC), chlorophyll content, canopy temperature depression (CTD), and photo-assimilates-spike dry matter (SDM), grains spike⁻¹ and grain yield of all wheat genotypes. In addition, the genotypes BAW 1167 and BARI Gom 26 remained more prone to adverse effects of drought as compared to BAW 1169 and BAW 1158. Furthermore, DS induced biosynthesis of compatible solutes such as proline, especially in BAW 1169, which enabled plants to defend against oxidative stress. It was inferred that BAW 1169 remained superior by exhibiting the best adaptation as indicated by the maximum relative values of RWC, total chlorophyll, CTD, proline content, SDM, grains spike⁻¹, and grain yield of wheat. Thus, based on our findings, BAW 1169 may be recommended for general adoption and utilization in future wheat breeding programs aimed at developing potent drought-tolerant wheat genotypes to ensure food security on a sustainable basis.

Sugarcane, not only fulfills 70% of world sugar needs but is also a prime potential source of bioethanol. It is majorly grown in tropical and subtropical regions. Researchers have improved this grass to great extent and have developed energy cane with ability to accumulate up to 18% sucrose in its Culm. Improvement of this crop is impeded by its complex genome, low fertility, long production cycle and susceptibility to various biotic and abiotic stresses. Biotechnological interventions hold great promise to address these impediments paving way to get improved sugarcane crop. Further, being vegetatively propagated in most of the agroecological regions, it has become more attractive plant to work with. This chapter highlights, how advanced knowledge of omics (genomics, transcriptomics, proteomics and metabolomics) can be employed to improve sugarcane crop. In addition, potential role of in vitro techniques and transgenic technology has also been discussed for developing improved sugarcane clones with enhanced sugar recovery.

Sugarcane holds considerable commercial significance due to its role as the primary source of sugar and its potential as a global biofuel resource. Fungal pathogens and insect pests present significant challenges to the cultivation of this crop, leading to substantial reductions in crop yield and sugar recovery. In response to pathogen infection, plants initiate their defense mechanisms, which involve the upregulation of pathogenesis-related proteins such as chitinase, glucanase, and chitosanase. SUGARWINs refer to a group of PR-4 proteins that are associated with the defense mechanisms of sugarcane against phytopathogens. Their gene expression is induced in response to wounds caused by Diatraea saccharalis larvae and diseases caused by fungal pathogens such Colletothricum falcatum and Fusarium verticillioides. We report the finding of some other proteins that interact with SUGARWINs and may also have a role in the defense against fungal diseases. The sugarcane cDNA library was screened against SUGARWIN1 and SUGARWIN2 proteins to find possible interactors. A strong interaction of both SUGARWIN1 and SUGARWIN2 was observed with oxygen evolving enhancer protein 1 and synaptotagmin 1. These interactions were further validated by BiFC (biomolecular fluorescence complementation) assay. For further molecular characterization, subcellular localization studies of SUGARWINs and interactor proteins were conducted by translational fusion with green fluorescent protein.