Search Results (140)

Glyphosate [N-(phosphonomethyl)glycine] is the most widely used herbicide worldwide, and its environmental persistence has prompted increasing interest in microbial processes that may contribute to its dissipation. This study evaluated a collection of 15 soil-derived actinobacterial strains for plant growth-promoting traits, extracellular enzymatic activities, glyphosate tolerance, and glyphosate removal under nutrient-sufficient and phosphate-starved conditions. Herbicide tolerance evaluated on agar plates was widespread across the collection, with all strains sustaining growth at 10 and 50 g L⁻¹ of glyphosate. Under nutrient-sufficient conditions glyphosate removal remained limited, with maximum values of 16.15 ± 2.08% (Streptomyces sp. Con7.16) and 15.34 ± 2.89% (Streptomyces sp. Z38). In contrast, prior phosphate starvation markedly enhanced removal efficiency, reaching 42.21 ± 3.59% in Streptomyces sp. Z38 and 39.46 ± 1.94% in Streptomyces sp. Con7.16. Transmission electron microscopy coupled with X-ray microanalysis in the selected Streptomyces sp. Z38 revealed starvation-associated depletion of intracellular polyphosphate granules, followed by partial replenishment when glyphosate was supplied as the sole phosphorus source, consistent with indirect evidence of glyphosate-derived phosphorus acquisition. Genome mining of Streptomyces sp. Z38 identified candidate genes potentially consistent with a non-canonical, C-P lyase-independent phosphonate utilization route; however, these assignments are based exclusively on bioinformatic evidence and require experimental validation. Collectively, these findings indicate that phosphate limitation enhances glyphosate removal in the selected actinobacteria, and the physiological and genomic data are consistent with a starvation-triggered shift toward alternative phosphorus scavenging strategies. Because this strain is intended for future phytoremediation applications in glyphosate-contaminated agricultural soils, elucidating the underlying phosphorus dynamics is essential for anticipating its functional behavior and environmental relevance. Full article

Phosphorus deficiency in the environment induces phosphate (Pi) starvation responses of plants, in which the phosphate transporter is one of the most critical functional genes in this response mechanism. As a prevalent green manure crop in China, Vicia villosa plays a critical role in sustainable agricultural systems, and the expression of its phosphate transporter gene (VvPHT1) is modulated by soil phosphorus availability, highlighting its key adaptive function in nutrient acquisition and utilization under low-Pi conditions. Functional studies of this gene and its promoter contribute to exploring the molecular mechanisms of the tolerance of green manure crops to low phosphorus stress and to improving phosphorus-efficient V. villosa varieties. In this study, analysis of the VvPHT1 promoter sequence revealed a 1524 bp region containing multiple root-specific cis-regulatory elements, including five NODCON2GM, one NODCON1GM, six OSE2ROOTNODULE, one OSE1ROOTNODULE, and fifteen ROOTMOTIFTAPOX1 motifs. Histochemical GUS staining of transgenic Arabidopsis (Arabidopsis thaliana (L.) Heynh.) showed that the VvPHT1 promoter directed root-specific expression of the GUS reporter gene. A fusion expression vector pCAMBIA1300-VvPHT1--GFP was constructed and transformed into tobacco (Nicotiana tabacum L.) cells for subcellular localization analysis, indicating that the protein encoded by VvPHT1 was localized to the plasma membrane. To quantify its expression, VvPHT1 transcript levels in VvPHT1-overexpressing Arabidopsis (OEPHT1) lines were analyzed by quantitative real-time PCR (qRT-PCR) under different phosphorus supply conditions. The results demonstrated that under low-Pi conditions, the expression of VvPHT1 was significantly upregulated in the OEPHT1 lines compared to those of normal-Pi conditions. Furthermore, under low-Pi treatment, the OEPHT1 lines showed significantly increased fresh weight, primary root length, phosphorus content, and chlorophyll content compared to the wild-type Arabidopsis (WT), while no such differences were observed under normal-Pi conditions. In conclusion, the VvPHT1 promoter exhibits root-specific activity, and the VvPHT1 gene encodes a plasma-membrane-localized phosphate transporter that is strongly induced by phosphorus deficiency. Its overexpression enhances phosphorus uptake and plant growth under low-Pi conditions, suggesting that VvPHT1 likely functions as a high-affinity phosphate transporter involved in the adaptation to phosphorus starvation. Full article

Phosphorus (P) deficiency severely limits maize growth and yield, yet early detection remains challenging, as visible symptoms appear only after prolonged starvation. This study evaluated the capability of hyperspectral imaging (HSI) combined with machine learning to detect P deficiency in maize seedlings at both symptomatic and pre-symptomatic stages. Two greenhouse experiments were conducted: a long-term pot system under high and low P conditions and a short-term hydroponic experiment with three P concentrations of 500, 100, and 0 μmol/L phosphate (Pi). After long-term P deficiency, significant reductions in shoot biomass and Pi content were observed, while root biomass increased and nutrient profiles were altered. Hyperspectral signatures revealed distinct wavelength-specific differences across visible, red-edge, and near-infrared (NIR) regions, with P-deficient leaves showing lower reflectance in green and NIR regions but higher reflectance in the red band. A multilayer perceptron machine learning model achieved 99.65% accuracy in discriminating between P treatments. In the short-term experiment, P deficiency significantly reduced tissue Pi content within one week without affecting pigment composition or photosynthetic parameters. Despite the absence of visible symptoms, hyperspectral measurements detected subtle spectral changes, particularly in older leaves, enabling classification accuracies of 80.71–84.56% in the first week and 85.88–90.98% in the second week of P treatment. Conventional vegetation indices showed weak correlations with Pi content and failed to detect early P deficiency. These findings demonstrate that HSI combined with machine learning can effectively detect P deficiency before visible symptoms emerge, offering a non-destructive, rapid diagnostic tool for precision nutrient management in maize production systems. Full article

Members of the genus Streptomyces are prominent inhabitants of the plant rhizosphere and endosphere and are increasingly recognized for their roles in plant growth promotion and disease suppression. In this study, we isolated genetically distinct Streptomyces from the tomato (Solanum lycopersicum L.) rhizosphere, designated as TOM isolates, and assembled them into a defined 12-member TOM consortium. Application of the TOM consortium significantly promoted root and shoot growth in tomato. RNA-seq analysis revealed coordinated local and systemic transcriptional responses characterized by a predominance of down-regulated genes in both roots and leaves. In roots, differential gene expression reflected selective attenuation of defense- and cell wall-related processes, alongside increased expression of genes associated with phytoalexin biosynthesis, phosphate starvation responses, and hormonal regulation. In leaves, transcriptional reprogramming was dominated by reduced stress-related responses together with activation of metabolic and growth-associated functions. The TOM consortium also reduced disease severity caused by Fusarium oxysporum f. sp. radicis-lycopersici by approximately 60% compared to infected controls. To further characterize functional traits of individual consortium members, isolates were evaluated in vitro for antifungal activity and five strains displaying inhibition were selected for hybrid whole-genome sequencing. Genome analyses revealed diverse taxonomic affiliations and a rich repertoire of biosynthetic gene clusters, including clusters associated with known antimicrobial metabolites as well as numerous low-similarity clusters indicative of substantial unexplored biosynthetic potential. Collectively, this study provides new insights into plant interactions with beneficial Streptomyces, while revealing molecular signatures involved in Streptomyces-mediated plant growth promotion and pathogen suppression. Full article

Mediator is a central transcriptional coactivator that connects sequence-specific transcription factors with RNA polymerase II to control inducible gene expression in plants. MED16 is a Mediator tail module subunit that functions as a context-dependent integrator, helping coordinate developmental programs with environmental adaptation. This review summarizes current evidence for MED16 function from structural and evolutionary perspectives to physiological outputs, with emphasis on how MED16 interacts with transcription factors and other Mediator subunits to shape RNA polymerase II engagement at target loci. In terms of development, MED16 contributes to organ growth and root system architecture, and comparative studies have revealed that it plays conserved roles in lineage-specific wiring. Under abiotic stress, MED16 supports the efficient activation of stress-inducible transcription, including cold acclimation and nutrient stress responses such as phosphate starvation-dependent root remodeling. In immunity, MED16 modulates salicylic acid- and jasmonate/ethylene-associated defence outputs and can be targeted by plant viruses, which is consistent with its role in antiviral transcriptional responses. Mechanistically, MED16 participates in cooperative and competitive interactions within the Mediator complex that tune hormone-responsive outputs, exemplified by MED25-related competition in abscisic acid signalling. We highlight key limitations and future directions, including the need for mechanistic validation beyond Arabidopsis, clearer models of dosage control in crops, improved understanding of context-dependent tail configurations, and high-resolution mapping of MED16 interaction interfaces. Full article

Phosphate-solubilizing bacteria (PSB) are pivotal in the cycling of phosphorus within terrestrial ecosystems and hold great promise for sustainable agriculture. In this study, we report the isolation of HRY1—a highly efficient phosphate-solubilizing strain—identified as Escherichia coli, a bacterium not traditionally recognized for plant-beneficial traits. Under optimized conditions (glucose as carbon source, (NH₄)₂SO₄ as nitrogen source, pH 7.0, 1% inoculum, and 5 g/L Ca₃(PO₄)₂), HRY1 consistently solubilized ~16% of inorganic phosphorus, with peak activity coinciding with its stationary growth phase (14 h). Whole-genome sequencing revealed a comprehensive genetic toolkit for phosphorus mobilization, including eight genes implicated in organic acid-mediated mineral dissolution, five high-affinity phosphate transporter genes (pit and pst gene cluster), and three two-component regulatory systems responsive to phosphate starvation (e.g., phoBR). The functional integration of these systems suggests a multifaceted strategy combining acidification, active uptake, and adaptive regulation to thrive under phosphorus limitation. Our findings redefine the ecological scope of E. coli and uncover an unconventional yet potent PSB candidate with significant potential for biofertilizer development and soil phosphorus activation. This discovery reveals E. coli’s untapped potential for phosphorus solubilization, with HRY1’s novelty residing in its high efficiency under optimized conditions and its practical promise as a biofertilizer. Full article

Improving phosphorus use efficiency (PUE) in crops is critical for sustainable agriculture. Although the transcriptional regulation of phosphate starvation responses, centered on regulators such as the PHR1 and SPX proteins, is well established, the post-transcriptional mechanisms remain incompletely understood. This gap hinders a comprehensive view of how plants adapt to low-P conditions. This review synthesizes current knowledge on the gene regulatory networks involved in low-P adaptation in barley, with a specific focus on the emerging role of RNA processing. It highlights the limited knowledge of how alternative splicing contributes to this response. AS provides a rapid and energy-efficient means of fine-tuning gene expression, expanding proteome diversity and enabling more sophisticated adaptation mechanisms than the relatively binary “on/off” mode of transcriptional control. Several core regulators of AS, including serine–arginine-rich proteins and hnRNPs, have been identified, with the former discussed in detail and illustrated with key examples. Building on the advanced mechanistic insights into AS gained from model crops such as rice, this review proposes a predictive framework to prioritize research targets and experimental strategies. Such an approach can accelerate the discovery of analogous mechanisms in barley, thereby bridging a critical knowledge gap and advancing strategies to improve PUE in this important cereal crop. Full article

Cotton is an important cash crop globally. Cotton fiber is the main economic product of cotton plants. Phosphorus, as one of the essential nutrients, plays an important role in plant growth and development. However, few studies focus on phosphorus regulating fiber elongation. In this study, we used the cotton ovule culture system in vitro to explore the effects of various phosphorus levels on fiber and ovule growth, and screened for phosphorus-responsive factor, as well as revealed its action mechanism. The results indicated that fiber elongation was more sensitive than ovule growth to phosphorus deficiency. GhPHR1, a homolog of phosphate starvation response 1 (PHR1) in upland cotton, was significantly upregulated in fibers and ovules under phosphorus-deficient conditions. GhPHR1 directly binds to the promoter of the glucosylceramide synthase gene in cotton (GhGCS1) and positively regulates its expression. Overexpressing GhGCS1 enhanced phosphorus uptake and transport in cotton, increased phosphorus content in fiber cells, and promoted fiber cell elongation. Conversely, downregulating GhGCS1 reduced phosphorus content in fiber cells and suppressed fiber elongation. These findings demonstrate the importance of the GhPHR1-GhGCS1 molecular module in regulating fiber cell elongation and elucidate the molecular mechanism by which phosphorus influences fiber elongation. Full article

Plants adapt to phosphate starvation by remodeling root architecture and reallocating carbohydrates. Glucose-6-phosphate 1-epimerase (G6PE), a key enzyme in carbon and energy metabolism, is hypothesized to contribute to phosphate starvation responses. Here, we investigated the role of G6PE in rice and Arabidopsis through phenotypic, physiological, and molecular analyses of osg6pe and atg6pe mutants. Under normal-phosphate (NP) conditions, both mutants exhibited significantly reduced biomass and fresh weight compared with the wild-type (WT) plants, indicating growth inhibition caused by the mutations. Under low-phosphate (LP) conditions, the mutants displayed enhanced root growth, suggesting that G6PE functions as a negative regulator of radial root growth under phosphate deficiency. The osg6pe mutant showed elevated phosphate content and increased leaf starch accumulation under LP, whereas it accumulated more phosphate but less starch under NP. Expression analysis revealed that G6PE transcripts were suppressed under NP but remained relatively stable under LP. Notably, among phosphate starvation-induced (PSI) genes, only PHT1;4 showed notable transcriptional changes in both species. These findings indicate that G6PE contributes to phosphate homeostasis by modulating carbohydrate metabolism, restraining radial root growth, and selectively regulating PHT1 expression under phosphate-deficient conditions. Full article

Apyrase (nucleotide triphosphate diphosphohydrolase, NTPDase; EC 3.6.1.5) functions in a variety of plant growth and developmental processes, as well as responses to pathogens, in part, by regulating extracellular ATP (eATP) concentrations. In this study, we investigated potential roles of apyrase in the recruitment of phosphate (Pi) from extracellular nucleotides in Arabidopsis thaliana seedlings that constitutively overexpress apyrase 1 (APY1). Under Pi limitation, both WT and APY1 seedlings had decreased Pi contents and a characteristic remodeling of root system architecture (RSA). This phosphate starvation response (PSR) was prevented by the uptake of Pi released through the metabolism of extracellular NTP, which occurred at a higher rate in APY1 seedlings. APY1 seedlings had higher Pi contents than WT seedlings on Pi-sufficient media supplemented with NTP and exhibited markedly increased LR and root hair (RH) formation. Genome-wide expression profiling revealed that this expanded RSA of APY1 seedlings was correlated with the induction of >100 genes involved in regulation of auxin homeostasis, signaling, and transport, which previous studies have shown to be increased when APY1 is overexpressed. APY1 regulation of [eNTP] and purinergic signaling may thus contribute to modulation of auxin responses, resulting in enhanced uptake of Pi from the medium, including Pi released via eNTP metabolism. Full article

The ABCB subfamily, a subset transporter of the ATP-binding cassette (ABC) superfamily, is vital for various plant life processes, especially in the transport of polar auxin and brassinosteroids. Although ABCB transporters have been characterized in diverse plant species, their specific functions in wheat remain largely unexplored. In this study, we identified 99 TaABCB members in wheat and categorized them into four groups based on their conserved domains and phylogenetic relationships. These members were found to be unevenly distributed across all 21 wheat chromosomes. We conducted a comprehensive genome-wide analysis encompassing gene structure, protein motifs, gene duplication events, collinearity, and cis-acting elements. Transcriptome analysis revealed that different TaABCB members displayed distinct expression patterns under phosphate starvation stress. Notably, we discovered that TaABCB7 might play a role in regulating wheat’s phosphate starvation. Crucially, we pinpointed an elite haplotype, H001, of the candidate gene TaABCB7, which has been progressively selected and employed in wheat breeding improvement programs. Overall, this study enhances our comprehensive understanding of TaABCB members and offers a potential gene resource for molecular marker-assisted selection breeding in wheat. Full article

Phosphorus (P) is a limiting nutrient for plant growth and productivity. Improving P use efficiency is important for crop production. In Lactuca sativa (lettuce), five phosphate starvation response 1 (PHR1) genes were identified and characterized through a bioinformatics approach. The expression patterns of LsaPHR1s were examined using qRT-PCR under various treatments, including devoid phosphorus (DP), low phosphorus (LP), high phosphorus (HP), darkness, ABA, IAA, and MeJA. The results indicate that LsaPHR1s in lettuce responded to phosphorus stress, hormones, and darkness. Furthermore, we engineered LsaPHR1.1 knock-out mutants via CRISPR/Cas9-mediated genome editing. Then, the mutants were subjected to phosphorus stress (DP, LP, and HP). In contrast to WT, the mutants improved nitrate and ammonium contents, increased antioxidant enzyme activity, and elevated antioxidant and chlorophyll contents. Our results offer a potential strategy for improving phosphorus stress tolerance in lettuce, which holds great significance for maintaining yield and quality. Full article

SPX (SYG1/Pho81/XPR1) family genes play a pivotal role in phosphorus signaling, phosphorus uptake, and phosphorus translocation in plants. However, to date, the SPX family genes have not been systematically investigated in cotton. In this study, we conducted a genome-wide analysis and identified 44 SPX family genes in Gossypium hirsutum, classifying them into four subfamilies (SPX, SPX-MFS, SPX-EXS, and SPX-RING) based on conserved domains. An expression analysis revealed that the majority of SPX family genes were highly expressed in the root and stem. We identified hormone response, stress response, low-temperature response, and PHR1 binding sequence (P1BS) cis-elements in the promoters of the SPX genes. Additionally, the expression of GhPHO1-4, GhSPX1-1/1-2/1-3, and GhSPX-MFS2-1/2-2 was significantly altered under phosphorus-deficient conditions and may be involved in the regulation of Pi response. A Y2H assay suggested that GhSPX1-1 interacts with GhPHR1A and GhSPX1-2 interacts with GhPHL1A. Our findings provide a basis for further cloning and functional verification of genes related to the regulatory network of low phosphorus tolerance in cotton. Full article

The investigation of phosphorus metabolism and regulatory mechanisms is conducive to maintaining stable production of crops within a low-phosphorus environment. In phosphorus signal transduction, a few phosphorus starvation response (PHR) transcription factors were identified to bind to the characteristic cis-element, namely the PHR1 binding sequence (P1BS). While the molecular function of the PHR transcription factor has been intensively elucidated, here, we explore a novel transcription factor, BnaA01.KAN3, that undergoes specific binding to the P1BS by yeast one-hybrid and electrophoretic mobility shift assays, and its expression is induced with low-phosphorus stress. BnaA01.KAN3 possessed transcriptional activation and was located in the nucleus. The spatiotemporal expression pattern of BnaA01.KAN3 exhibited tissue specificity in developmental seed, and its expression level was especially high 25–30 days after pollination. Regarding the phenotype analysis, the independent heterologous overexpression lines of BnaA01.KAN3 in Arabidopsis thaliana exhibited not only significantly longer taproots but also an increased number of lateral roots compared to that of the wild type undergoing low-phosphorus treatment, while no differences were seen under normal phosphorus conditions. Furthermore, these lines showed higher anthocyanin and inorganic phosphorus contents with normal and low-phosphorus treatment, suggesting that BnaA01.KAN3 could enhance phosphorus uptake or remobilization to cope with low-phosphorus stress. In summary, this study characterized the transcription factor BnaA01.KAN3 that modulates low-phosphate adaptation and seed development, providing insights for improving phosphorus use efficiency and yield traits in Brassica napus. Full article

Phosphorus, as an essential nutrient, plays an important role in plant growth and development. Although Phosphate Starvation Response 1 (PHR1) or PHR1-like have been recognized as central regulators of phosphorus (Pi) homeostasis in several plants, they have not been systematically studied in Cucurbitaceae. In this study, 11, 10, 8, 12, 12, and 22 PHR genes were identified in cucumber, melon, bottle gourd, watermelon, wax gourd, and pumpkin, respectively, by genome-wide analysis. Phylogenetic analysis showed that the Cucurbitaceae PHR genes were divided into seven distinct subfamilies. These genes were further phylogenetically analyzed for their chromosomal localization, gene structure, protein structure, and synteny. Genomic homology analysis showed that many PHR genes existed in the corresponding homology blocks of six Cucurbitaceae species. qRT-PCR analysis showed that the CmoPHR genes exhibited differential expression under different concentrations of phosphate treatment. Transcriptional self-activation assays showed that CmoPHR2, CmoPHR9, CmoPHR16, and CmoPHR17 proteins had transcriptional self-activating activity. The results of this study provide a basis for the further cloning and functional validation of genes related to the phosphate regulatory network in pumpkin. Full article