Drylands are stressful environment for plants growth and production. Plant growth-promoting rhizobacteria (PGPR) acts as a rampart against the adverse impacts of drought stress in drylands and enhances plant growth and is helpful in agricultural sustainability. PGPR improves drought tolerance by implicating physio-chemical modifications called rhizobacterial-induced drought endurance and resilience (RIDER). The RIDER response includes; alterations of phytohormonal levels, metabolic adjustments, production of bacterial exopolysaccharides (EPS), biofilm formation, and antioxidant resistance, including the accumulation of many suitable organic solutes such as carbohydrates, amino acids, and polyamines. Modulation of moisture status by these PGPRs is one of the primary mechanisms regulating plant growth, but studies on their effect on plant survival are scarce in sandy/desert soil. It was found that inoculated plants showed high tolerance to water-deficient conditions by delaying dehydration and maintaining the plant’s water status at an optimal level. PGPR inoculated plants had a high recovery rate after rewatering interms of similar biomass at flowering compared to non-stressed plants. These rhizobacteria enhance plant tolerance and also elicit induced systemic resistance of plants to water scarcity. PGPR also improves the root growth and root architecture, thereby improving nutrient and water uptake. PGPR promoted accumulation of stress-responsive plant metabolites such as amino acids, sugars, and sugar alcohols. These metabolites play a substantial role in regulating plant growth and development and strengthen the plant’s defensive system against various biotic and abiotic stresses, in particular drought stress.

https://www.mdpi.com/2073-4395/10/11/1683/pdf

Water Conservation and Plant Survival Strategies of Rhizobacteria under Drought Stress

In the process of growth and development, plants are exposed to various abiotic stresses such as salinity, drought, low temperature, which limit crop yield and quality. During evolution, plants acquire series of resistances to these environmental stresses and survive through physiological, biochemical, and molecular responses. These responses are usually originated by regulating the expression of relevant genes. bZIP (basic leucine zipper) transcription factors, as one of the largest transcription factor regulatory families, play very important roles in responses to these abiotic stresses. bZIP TFs could be activated by drought, high salt and chilling damages. By binding specifically to cis-elements in the promoter region of stress related genes, they can regulate the transcriptional expressions of target genes, thereby regulating stress resistance of plants. This article comprehensively reviews the structural characteristics of bZIPs and their regulation mechanisms on target genes under various abiotic stresses.

/pdf/regulation-mechanisms-of-plant-basic-leucine-zippers-to-13szuuq86v.pdf

Regulation Mechanisms of Plant Basic Leucine Zippers to Various Abiotic Stresses

Soybean is one of the most important food crops in the world. However, with the environmental change in recent years, many environmental factors like drought, salinity, heavy metal, and disease seriously affected the growth and development of soybean, causing substantial economic losses. In this study, we screened a bZIP transcription factor gene, GmbZIP152, which is significantly induced by Sclerotinia sclerotiorum (S. sclerotiorum), phytohormones, salt-, drought-, and heavy metal stresses in soybean. We found that overexpression of GmbZIP152 in Arabidopsis (OE-GmbZIP152) enhances the resistance to S. sclerotiorum and the tolerance of salt, drought, and heavy metal stresses compared to wild-type (WT). The antioxidant enzyme related genes (including AtCAT1, AtSOD, and AtPOD1) and their enzyme activities are induced by S. sclerotiorum, salt, drought, and heavy metal stress in OE-GmbZIP152 compared to WT. Furthermore, we also found that the expression level of biotic- and abiotic-related marker genes (AtLOX6, AtACS6, AtERF1, and AtABI2, etc.) were increased in OE-GmbZIP152 compared to WT under S. sclerotiorum and abiotic stresses. Moreover, we performed a Chromatin immunoprecipitation (ChIP) assay and found that GmbZIP152 could directly bind to promoters of ABA-, JA-, ETH-, and SA-induced biotic- and abiotic-related genes in soybean. Altogether, GmbZIP152 plays an essential role in soybean response to biotic and abiotic stresses.

/pdf/gmbzip152-a-soybean-bzip-transcription-factor-confers-185t1uu2.pdf

GmbZIP152, a Soybean bZIP Transcription Factor, Confers Multiple Biotic and Abiotic Stress Responses in Plant

Osmotic stress caused by drought and high salinity is the key factor limiting plant growth. However, its underlying molecular regulatory mechanism remains unclear. In this study, we found the stress-related gene Zm00001d019704 (ZmSRG7) based on transcriptome sequencing results previously obtained in the laboratory and determined its biological function in maize. We found that ZmSRG7 was significantly expressed in both roots and leaves under 10% PEG6000 or 150 mM NaCl. Subcellular localization showed that the gene was localized in the nucleus. The germination rate and root length of the ZmSRG7 overexpressing lines were significantly increased under drought or salt stress compared with the control. However, after drought stress, the survival rate and relative water content of maize were increased, while the water loss rate was slowed down. Under salt stress, the Na+ concentration and Na+: K+ ratio of maize was increased. In addition, the contents of antioxidant enzymes and proline in maize under drought or salt stress were higher than those in the control, while the contents of MDA, H2O2 and O2− were lower than those in the control. The results showed that the ZmSRG7 gene played its biological function by regulating the ROS signaling pathway. An interaction between ZmSRG7 and the Zmdhn1 protein was found using a yeast two-hybrid experiment. These results suggest that the ZmSRG7 gene can improve maize tolerance to drought or salt by regulating hydrogen peroxide homeostasis.

/pdf/overexpression-of-zmsrg7-improves-drought-and-salt-tolerance-g69kfvob.pdf

Overexpression of ZmSRG7 Improves Drought and Salt Tolerance in Maize (Zea mays L.)

Drought stress adversely influences the crop plants. Herein, present research was designed to elucidate the role of plant growth promoting bacteria for amelioration of water stress in wheat. A pot experiment was conducted for screening the microorganisms on the basis of plant growth, chlorophyll and proline content under water stress. Bacillus sp. BT3 and Klebsiella sp. HA9 were found to be more promising strains that positively influenced the plant growth, chlorophyll and proline status of seedlings under water stress condition. Further, Bacillus sp.BT3 and Klebsiella sp. HA9 along with check strain (BioNPK) were used for elucidating their detailed effect on morphological, biochemical, physiological and molecular traits to mitigate water stress in wheat. Microbial inoculation significantly improved plant height, fresh weight and dry weight of root and shoot, relative water content, chlorophyll content and root morphological parameters over the uninoculated water stressed (30% FC) control. Likewise, sugar content, protein content and antioxidant enzymes were also significantly enhanced due to microbial inoculation under water stress (30% FC). Microbial inoculation significantly decreased proline, glycine betaine, lipid peroxidation, peroxide and superoxide radicals in wheat over the uninoculated water stressed (30%FC) control. Quantitative real-time (qRT) PCR analysis revealed that Bacillus sp. BT3, Klebsiella sp. HA9 and BioNPK inoculation significantly upregulated stress responsive genes (DHN, DREB, L15 and TaABA-8OH) over the uninoculated water stressed (30% F.C.) control. The study reports the potential of Bacillus sp. BT3 and Klebsiella sp. HA9 along with BioNPK in water stress alleviation in wheat which could be recommended as effective bioinoculants. 

/pdf/deciphering-the-mechanisms-of-microbe-mediated-drought-1xfgsrvj.pdf

Deciphering the mechanisms of microbe mediated drought stress alleviation in wheat

NCP1, a NINJA family protein lacking EAR motif, acts as a negative regulator of ABA signaling by interacting with and inhibiting the activity of transcriptional activator ABP9. The phytohormone abscisic acid plays a pivotal role in regulating plant responses to a variety of abiotic stresses including drought and salinity. Maize ABP9 is an ABRE-binding bZIP transcription activator that enhances plant tolerance to multiple stresses by positively regulating ABA signaling, but the molecular mechanism by which ABP9 is regulated in mediating ABA responses remains unknown. Here, we report the identification of an ABP9-interacting protein, named ABP Nine Complex Protein 1 (NCP1) and its functional characterization. NCP1 belongs to the recently identified NINJA family proteins, but lacks the conserved EAR motif, which is a hallmark of this class of transcriptional repressors. In vitro and in vivo assays confirmed that NCP1 physically interacts with ABP9 and that they are co-localized in the nucleus. In addition, NCP1 and ABP9 are similarly induced with similar patterns by ABA treatment and osmotic stress. Interestingly, NCP1 over-expressing Arabidopsis plants exhibited a reduced sensitivity to ABA and decreased drought tolerance. Transient assay in maize protoplasts showed that NCP1 inhibits the activity of ABP9 in activating ABRE-mediated reporter gene expression, a notion further supported by genetic analysis of drought and ABA responses in the transgenic plants over-expressing both ABP9 and NCP1. These data together suggest that NCP1 is a novel negative regulator of ABA signaling via interacting with and inhibiting the activity of ABP9.

Maize NCP1 negatively regulates drought and ABA responses through interacting with and inhibiting the activity of transcription factor ABP9

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Maize NCP1 negatively regulates drought and ABA responses through interacting with and inhibiting the activity of transcription factor ABP9