Wheat is the main staple food in the world, so it is the backbone of food security. Drought not only affects growth and development but also ultimately has a severe impact on the overall productivity of crop plants. Some bacteria are capable of producing exopolysaccharides (EPS) as a survival mechanism, along with other metabolites, which help them survive in stressful conditions. The present study was conducted with the aim of inducing drought stress tolerance in wheat through EPS-producing plant growth-promoting rhizobacteria (PGPR). In this regard, a series of laboratory bioassays were conducted with the aim to isolating, characterizing, and screening the EPS-producing PGPR capable of improving wheat growth under limited water conditions. Thirty rhizobacterial strains (LEW1–LEW30) were isolated from the rhizosphere of wheat. Ten isolates with EPS-producing ability were quantitatively tested for EPS production and IAA production ability. Four of the most efficient EPS-producing strains (LEW3, LEW9, LEW16, and LEW28) were evaluated for their drought tolerance ability along with quantitative production of EPS and IAA under polyethylene glycol (PEG-6000)-induced drought stress. The jar experiment was conducted under gnotobiotic conditions to examine the drought-tolerant wheat genotypes, and two wheat varieties (Johar-16, and Gold-16) were selected for further experiments. The selected varieties were inoculated with EPS-producing rhizobacterial strains and grown under control conditions at different stress levels (0, 2, 4, and 6% PEG-6000). The strain LEW16 showed better results for improving root morphology and seedling growth in both varieties. The maximum increase in germination, growth parameters, percentage, root diameter, root surface area, and root colonization was recorded in Johar-16 by inoculating LEW16 at 6% PEG-6000. Plant growth-promoting traits were tested on the top-performing strains (LEW3, LEW9, and LEW16). Through 16S rRNA sequencing, these strains were identified as Chryseobacterium sp. (LEW3), Acinetobacter sp. (LEW9), and Klebsiella sp. (LEW16), and they showed positive results for phosphorous and zinc solubilization as well as hydrogen cyanide (HCN) production. The partial sequencing results were submitted to the National Center for Biotechnology Information (NCBI) under the accession numbers MW829776, MW829777, and MW829778. These strains are recommended for their evaluation as potential bioinoculants for inducing drought stress tolerance in wheat.

Drought is an important factor which limits growth of sugarcane. To elucidate the physiological and biochemical mechanisms of tolerance, a pot experiment was conducted at Sugarcane Research Institute, Kaiyuan, China. Two genotypes (Yuetang 93-159-sensitive and Yunzhe 05-51-tolerant), were subjected to three treatments; 70±5% (control), 50±5% (moderate drought) and 30±5% (severe drought) of soil field capacity. The results demonstrated that drought induced considerable decline in morpho-physiological, biochemical and anatomical parameters of both genotypes, with more pronounced detrimental effects on Yuetang 93–159 than on Yunzhe 05–51. Yunzhe 05–51 exhibited more tolerance by showing higher dry biomass, photosynthesis and antioxidant enzyme activities. Compared with Yuetang 93–159, Yunzhe 05–51 exhibited higher soluble sugar, soluble protein and proline contents under stress. Yunzhe 05–51 illustrated comparatively well-composed chloroplast structure under drought stress. It is concluded that the tolerance of Yunzhe 05–51 was attributed to improved antioxidant activities, osmolyte accumulation and enhanced photosynthesis. These findings may provide valuable information for future studies on molecular mechanism of tolerance.

Heavy metals are rapidly polluting the environment as a result of growing industrialization and urbanization. The presence of high concentrations of chromium (Cr), along with other pollutants, is widespread in tannery wastewater. In Pakistan, as a result of a severe shortage of irrigation water, farmers use tannery wastewater to grow various crops with a consequent decline in plants’ yield. This experiment was performed to assess growth revival in sunflower plants irrigated with 0%, 25%, 50%, 75%, and 100% tannery wastewater, by foliar application of 0, 2.5, and 5.0 mM citric acid (CA). The wastewater treatment curtailed biomass accumulation, the growth rate, and chlorophyll contents by exacerbating the oxidative stress in sunflowers. Foliar application of CA considerably alleviated the outcomes of Cr toxicity by curbing the Cr absorption and oxidative damage, leading to improvements in plant growth, biological yield, and chlorophyll contents. It is concluded that foliar application of CA can successfully mitigate the Cr toxicity in sunflower plants irrigated with tannery wastewater.

Two oilseed rape genotypes (Jiu-Er-13XI and Zheyou-50), differing in seed oil contents, were subjected to Cd stress in hydroponic experiment. Genotypic differences were observed in terms of tolerance behavior towards Cd exposure. Cd treatment negatively affected both genotypes but the effects were more prominent in Jiu-Er-13XI (low seed oil content) as compared to the Zheyou-50 (high seed oil content). Jiu-Er-13XI accumulated more reactive oxygen species (ROS), which destroyed chloroplast structure and decreased photosynthetic pigments. Total fatty acids, especially 18:2 and 18:3, were severely decreased as suggested by increase in MDA contents. Jiu-Er-13XI accumulated more Cd in its roots and shoots while less amount of tocopherol was observed under Cd stress. In contrast, Zheyou-50 was less affected by Cd stress than its counterpart. It accumulated comparatively less amount of Cd in roots and shoots, along with reduced accumulation of malondialdehyde (MDA) and ROS under Cd stress, than Jiu-Er-13XI. In addition the level of tocopherol, especially the α-Tocopherol, was much higher than Jiu-Er-13XI, which was also supported by high expression of tocopherol biosynthesis genes in Zheyou-50 during early hours. Tocopherol not only restricted the absorption of Cd by roots and its translocation to shoot, but also scavenged the ROS, generated during oxidative stresses. The low level of MDA shows that polyunsaturated fatty acids in chloroplast membranes were intact. In present study the tolerance behavior of Zheyou-50 over Jiu-Er-13XI is attributed to the activities of tocopherol under Cd stress. This study shows that plants with high seed oil are tolerant to Cd stress due to high production of tocopherol.

Hexokinase (HK) is a key enzyme in chitin biosynthesis in insects and plays an important role in development and energy regulation. It also performs a crucial role in the synthesis of Glucose-6-phosphate and its putative functions are studied via injection of dsRNA corresponding to the hexokinase gene from Cnaphalocrocis medinalis (CmHK). This study was designed to analyze the characteristics and expression patterns of HK-related genes in various tissues of C. medinalis at different developmental stages. The CmHK ORF is a 1359 bp in length, encoding a protein of 452 amino acids, with homology and cluster analysis showing that CmHK shares an 85.11% sequence similarity with hexokinase from Ostrinia furnacalis.CmHK was highly expressed in the ovary and in the fifth instar larvae. Injection of dsCmHK significantly suppressed mRNA expression (73.6%) 120 h post-dsRNA injection as compared to a control group. The results demonstrated an increased incidence of larval and pupal mortality of 80% and 78%, respectively, with significant variation in the sex ratio between males (68.33%) and females (35%), overt larval deformities, and a reduction in average weight gain observed 120 h post-dsRNA injection. In addition, dsCmHK-injected C. medinalis showed a significant reduction in ovulation per female and larval hatching rate, along with increased larval and pupal mortality and variation in male and female emergence over three generations (G1, G2, and G3). Taken together, the outcomes of the study provide a foundation to study gene function and a new dimension to control C. medinalis by transgenic RNAi technology.