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The strong aggregation of Poly(3-hexylthiophene) (P3HT) severely limits its use as the hole-transport material in emerging quantum dot photodetectors and photovoltaics. Herein, we propose a facile and cost-effective strategy to control the solution-state aggregation of hole transporting layers by designing a dual polythiophene blend based on P3HT and its alkylthio-substituted analogue named Poly(3-hexylthiothiophene) (P3HTT). In our photodetector device, we have used the dual polythiophene as the hole transport layer and achieved a specific detectivity (D*) on the order of 1012 Jones. In particular, by incorporating a small amount of P3HTT into the dual polythiophene mixture, we observed a remarkable 28% performance enhancement. This study provides a comprehensive analysis of the solution structure of the dual polythiophene blend, elucidates the evolution of the condensed matter structure, and ultimately presents a promising avenue for enhancing the performance of low-cost quantum dot photodetectors. [ABSTRACT FROM AUTHOR]

The emerging solution‐based solar cells and photodetectors have gained worldwide research interest over the past decades. Hole transport materials (HTMs) have greatly advanced the progress of these solution‐based electronics. Nevertheless, developing low‐cost and efficient HTMs is far from satisfactory. In this contribution, poly(3‐pentylthiophene) (P3PT) is introduced as a facile, low‐cost, and versatile dopant‐free polymer HTM for both quantum dot (QD) and perovskite electronic devices. Compared to the broadly used poly(3‐hexylthiophene), P3PT presents the reduced molecular aggregation and preferential face‐on orientation, which can markedly enhance the hole‐carrier transport in optoelectronic devices. Accordingly, P3PT can deliver the substantial improvement of photovoltaic performance from ∼8.6% to ∼9.5% for QD/polythiophene solar cells and from ∼16% to ∼18.8% for perovskite/polythiophene solar cells, which are both among the topmost values in the corresponding fields. Furthermore, P3PT HTMs can also significantly enhance the photodetection performance of QD and perovskite photodetectors by a factor of ∼3, indicating its great application potential in a variety of emerging optoelectronics. [ABSTRACT FROM AUTHOR]

Pathogenesis-related proteins (PR proteins) play crucial roles in the plant defense system. A novel PRP gene was isolated from highly resistant soybean infected with Phytophthora sojae (P. sojae) and was named GmPRP (GenBank accession number: KM506762). The amino acid sequences of GmPRP showed identities of 74%, 73%, 72% and 69% with PRP proteins from Vitis vinifera, Populus trichocarpa, Citrus sinensis and Theobroma cacao, respectively. Quantitative real-time reverse transcription PCR (qRT-PCR) data showed that the expression of GmPRP was highest in roots, followed by the stems and leaves. GmPRP expression was upregulated in soybean leaves infected with P. sojae. Similarly, GmPRP expression also responded to defense/stress signaling molecules, including salicylic acid (SA), ethylene (ET), abscisic acid (ABA) and jasmonic acid (JA). GmPRP was localized in the cell plasma membrane and cytoplasm. Recombinant GmPRP protein exhibited ribonuclease activity and significant inhibition of hyphal growth of P. sojae 1 in vitro. Overexpression of the GmPRP gene in T2 transgenic tobacco and T2 soybean plants resulted in enhanced resistance to Phytophthora nicotianae (P. nicotianae) and P. sojae race 1, respectively. These results indicated that the GmPRP protein played an important role in the defense of soybean against P. sojae infection. [ABSTRACT FROM AUTHOR]

Stretchable electrodes are critical to the development of advanced technologies such as human–machine interaction, flexible sensing, and wearable power supply, making them of significant research value. However, the current preparation methods for high‐performance stretchable electrodes are complex and inefficient, posing challenges for their large‐scale application in the realm of flexible wearables. To address this need, a straightforward and efficient embedding strategy is reported for fabricating stretchable silver nanowire/thermoplastic elastomer composite electrodes (referred to as Strem‐AT) utilizing the viscoelasticity and outstanding mechanical properties of polymer elastomers to achieve outstanding extensibility, conductivity, and a smooth surface. These electrodes exhibit excellent tensile behavior, low surface roughness, and stable electrical properties, enabling their successful integration into stretchable sensors and intrinsically stretchable organic photovoltaic cells (IS‐OPV). When applied to human skin joints for motion detection, the sensor demonstrates remarkable stretchability and stable signal output. Importantly, the all‐polymer IS‐OPV exhibits a top‐notch power conversion efficiency (PCE) of >12.5% and a PCE80% strain exceeding 50%. Furthermore, even after subjecting high‐strain stretching at 50% for 1000 cycles, the IS‐OPV can retain 76% of the initial PCE. This study presents a multifunctional stretchable electrode with high repeatability and easy‐to‐scale fabrication in wearable sensors and photovoltaics. [ABSTRACT FROM AUTHOR]

It is unclear how elevated CO2 (eCO2) and warming interactively influence soil N mineralization in the rhizosphere of rice (Oryza sativa L.), given that the N mineralization process in anaerobic paddy soils differs from that of aerobic upland soils. In this study, we conducted a rhizobox experiment in open top chambers and used 15N-13C dual-labeling to examine the impacts of eCO2 (700 ppm) and warming (2 °C above the ambient) on N mineralization and associated microbial processes in the rhizosphere of rice plants under anaerobic conditions. Compared to the control, the combination of eCO2 and warming increased rice N uptake by 50% in a no-added-N treatment and 32% under an N-added treatment, with the additional uptake mainly consisting of soil-derived N. Co-elevation of CO2 and temperature increased microbial biomass C and N and increased N mineralization by 41% and 23% in the no-added-N and N-added treatments, respectively. The absolute abundances of the N-mineralization genes chiA, pepA, pepN, and urea hydrolysis gene ureC in the rhizosphere increased by 22–30% under eCO2 and warming, corresponding to the additional N mineralization and photosynthetic C allocation into the soil. However, eCO2 plus warming did not increase the metabolic efficiency of N mineralization (mineralized N per unit microbial N). Our results suggest that the co-elevation of CO2 and temperature stimulated microbially mediated soil N mineralization in the rhizosphere of rice, posing a risk on the acceleration of soil organic matter decomposition. [ABSTRACT FROM AUTHOR]

Phytophthora root rot is a devastating disease of soybean caused by Phytophthora sojae. However, the resistance mechanism is not yet clear. Our previous studies have shown that GmAP2 enhances sensitivity to P. sojae in soybean, and GmMYB78 is downregulated in the transcriptome analysis of GmAP2-overexpressing transgenic hairy roots. Here, GmMYB78 was significantly induced by P. sojae in susceptible soybean, and the overexpressing of GmMYB78 enhanced sensitivity to the pathogen, while silencing GmMYB78 enhances resistance to P. sojae, indicating that GmMYB78 is a negative regulator of P. sojae. Moreover, the jasmonic acid (JA) content and JA synthesis gene GmAOS1 was highly upregulated in GmMYB78-silencing roots and highly downregulated in overexpressing ones, suggesting that GmMYB78 could respond to P. sojae through the JA signaling pathway. Furthermore, the expression of several pathogenesis-related genes was significantly lower in GmMYB78-overexpressing roots and higher in GmMYB78-silencing ones. Additionally, we screened and identified the upstream regulator GmbHLH122 and downstream target gene GmbZIP25 of GmMYB78. GmbHLH122 was highly induced by P. sojae and could inhibit GmMYB78 expression in resistant soybean, and GmMYB78 was highly expressed to activate downstream target gene GmbZIP25 transcription in susceptible soybean. In conclusion, our data reveal that GmMYB78 triggers soybean sensitivity to P. sojae by inhibiting the JA signaling pathway and the expression of pathogenesis-related genes or through the effects of the GmbHLH122-GmMYB78-GmbZIP25 cascade pathway. [ABSTRACT FROM AUTHOR]

Phytophthora root and stem rot of soybean (Glycine max), caused by the oomycete Phytophthora sojae, is an extremely destructive disease worldwide. In this study, we identified GmEIL1, which encodes an ethylene‐insensitive3 (EIN3) transcription factor. GmEIL1 was significantly induced following P. sojae infection of soybean plants. Compared to wild‐type soybean plants, transgenic soybean plants overexpressing GmEIL1 showed enhanced resistance to P. sojae and GmEIL1‐silenced RNA‐interference lines showed more severe symptoms when infected with P. sojae. We screened for target genes of GmEIL1 and confirmed that GmEIL1 bound directly to the GmERF113 promoter and regulated GmERF113 expression. Moreover, GmEIL1 positively regulated the expression of the pathogenesis‐related gene GmPR1. The GmEIL1‐regulated defence response to P. sojae involved both ethylene biosynthesis and the ethylene signalling pathway. These findings suggest that the GmEIL1‐GmERF113 module plays an important role in P. sojae resistance via the ethylene signalling pathway. [ABSTRACT FROM AUTHOR]

Phytophthora root and stem rot caused by Phytophthora sojae Kaufmann and Gerdemann is a soil-borne disease severely affecting soybean production worldwide. Losses caused by P. sojae can be controlled by both major genes and quantitative trait locus. Here, we tested 112 short-season soybean cultivars from Northeast China for resistance to P. sojae. A total of 58 germplasms were resistant to 7–11 P. sojae strains. Among these, Mengdou 28 and Kejiao 10-262 may harbor either Rps3a or multiple Rps genes conferring resistance to P. sojae. The remaining 110 germplasms produced 91 reaction types and may contain new resistance genes or gene combinations. Partial resistance evaluation using the inoculum layer method revealed that 34 soybean germplasms had high partial resistance, with a mean disease index lower than 30. Combining the results of resistance and partial resistance analyses, we identified 35 excellent germplasm resources as potential elite materials for resistance and tolerance in future breeding programs. In addition, we compared the radicle inoculation method with the inoculum layer method to screen for partial resistance to P. sojae. Our results demonstrate that the radicle inoculation method could potentially replace the inoculum layer method to identify partial resistance against P. sojae, and further verification with larger samples is required in the future. [ABSTRACT FROM AUTHOR]

Phytophthora root rot is a destructive soybean disease worldwide, which is caused by the oomycete pathogen Phytophthora sojae (P. sojae). Wall-associated protein kinase (WAK) genes, a family of the receptor-like protein kinase (RLK) genes, play important roles in the plant signaling pathways that regulate stress responses and pathogen resistance. In our study, we found a putative Glycine max wall-associated protein kinase, GmWAK1, which we identified by soybean GmLHP1 RNA-sequencing. The expression of GmWAK1 was significantly increased by P. sojae and salicylic acid (SA). Overexpression of GmWAK1 in soybean significantly improved resistance to P. sojae, and the levels of phenylalanine ammonia-lyase (PAL), SA, and SA-biosynthesis-related genes were markedly higher than in the wild-type (WT) soybean. The activities of enzymatic superoxide dismutase (SOD) and peroxidase (POD) antioxidants in GmWAK1-overexpressing (OE) plants were significantly higher than those in in WT plants treated with P. sojae; reactive oxygen species (ROS) and hydrogen peroxide (H2O2) accumulation was considerably lower in GmWAK1-OE after P. sojae infection. GmWAK1 interacted with annexin-like protein RJ, GmANNRJ4, which improved resistance to P. sojae and increased intracellular free-calcium accumulation. In GmANNRJ4-OE transgenic soybean, the calmodulin-dependent kinase gene GmMPK6 and several pathogenesis-related (PR) genes were constitutively activated. Collectively, these results indicated that GmWAK1 interacts with GmANNRJ4, and GmWAK1 plays a positive role in soybean resistance to P. sojae via a process that might be dependent on SA and involved in alleviating damage caused by oxidative stress. [ABSTRACT FROM AUTHOR]

Phytophthora root and stem rot of soybean, caused by Phytophthora sojae (P. sojae), is a destructive disease in many soybean planting regions worldwide. In a previous study, an expressed sequence tag (EST) homolog of the major allergen Pru ar 1 in apricot (Prunus armeniaca) was identified up-regulated in the highly resistant soybean ‘Suinong 10’ infected with P. sojae. Here, the full length of the EST was isolated using rapid amplification of cDNA ends (RACE). It showed the highest homolgy of 53.46% with Gly m 4 after comparison with the eight soybean allergen families reported and was named Gly m 4-like (Gly m 4l, GenBank accession no. HQ913577.1). The cDNA full length of Gly m 4l was 707 bp containing a 474 bp open reading frame encoding a polypeptide of 157 amino acids. Sequence analysis suggests that Gly m 4l contains a conserved ‘P-loop’ (phosphate-binding loop) motif at residues 47–55 aa and a Bet v 1 domain at residues 87–120 aa. The transcript abundance of Gly m 4l was significantly induced by P. sojae, salicylic acid (SA), NaCl, and also responded to methyl jasmonic acid (MeJA) and ethylene (ET). The recombinant Gly m 4l protein showed RNase activity and displayed directly antimicrobial activity that inhibited hyphal growth and reduced zoospore release in P. sojae. Further analyses showed that the RNase activity of the recombinant protein to degrading tRNA was significantly affected in the presence of zeatin. Over-expression of Gly m 4l in susceptible ‘Dongnong 50’ soybean showed enhanced resistance to P. sojae. These results indicated that Gly m 4l protein played an important role in the defense of soybean against P. sojae infection. [ABSTRACT FROM AUTHOR]

Ethylene response factors (ERFs) are involved in biotic and abiotic stress; however, the drought resistance mechanisms of many ERFs in soybeans have not been resolved. Previously, we proved that GmERF113 enhances resistance to the pathogen Phytophthora sojae in soybean. Here, we determined that GmERF113 is induced by 20% PEG-6000. Compared to the wild-type plants, soybean plants overexpressing GmERF113 (GmERF113-OE) displayed increased drought tolerance which was characterized by milder leaf wilting, less water loss from detached leaves, smaller stomatal aperture, lower Malondialdehyde (MDA) content, increased proline accumulation, and higher Superoxide dismutase (SOD) and Peroxidase (POD) activities under drought stress, whereas plants with GmERF113 silenced through RNA interference were the opposite. Chromatin immunoprecipitation and dual effector-reporter assays showed that GmERF113 binds to the GCC-box in the GmPR10-1 promoter, activating GmPR10-1 expression directly. Overexpressing GmPR10-1 improved drought resistance in the composite soybean plants with transgenic hairy roots. RNA-seq analysis revealed that GmERF113 downregulates abscisic acid 8′-hydroxylase 3 (GmABA8'-OH 3) and upregulates various drought-related genes. Overexpressing GmERF113 and GmPR10-1 increased the abscisic acid (ABA) content and reduced the expression of GmABA8'-OH3 in transgenic soybean plants and hairy roots, respectively. These results reveal that the GmERF113-GmPR10-1 pathway improves drought resistance and affects the ABA content in soybean, providing a theoretical basis for the molecular breeding of drought-tolerant soybean. [ABSTRACT FROM AUTHOR]

SUMMARY: Phytophthora root and stem rot is a worldwide soybean (Glycine max) disease caused by the soil‐borne pathogen Phytophthora sojae. This disease is devastating to soybean production, so improvement of resistance to P. sojae is a major target in soybean breeding. Mitogen‐activated protein kinase (MAPK) cascades are important signaling modules that convert environmental stimuli into cellular responses. Compared with extensive studies in Arabidopsis, the molecular mechanism of MAPK cascades in soybean disease resistance is barely elucidated. In this work, we found that the gene expression of mitogen‐activated protein kinase 6 (GmMPK6) was potently induced by P. sojae infection in the disease‐resistant soybean cultivar 'Suinong 10'. Overexpression of GmMPK6 in soybean resulted in enhanced resistance to P. sojae and silencing of GmMPK6 led to the opposite phenotype. In our attempt to dissect the role of GmMPK6 in soybean resistance to phytophthora disease, we found that MAPK kinase 4 (GmMKK4) and the ERF transcription factor GmERF113 physically interact with GmMPK6, and we determined that GmMKK4 could phosphorylate and activate GmMPK6, which could subsequently phosphorylate GmERF113 upon P. sojae infection, suggesting that P. sojae can stimulate the GmMKK4–GmMPK6–GmERF113 signaling pathway in soybean. Moreover, phosphorylation of GmERF113 by the GmMKK4–GmMPK6 module promoted GmERF113 stability, nuclear localization and transcriptional activity, which significantly enhanced expression of the defense‐related genes GmPR1 and GmPR10‐1 and hence improved disease resistance of the transgenic soybean seedlings. In all, our data reveal that the GmMKK4–GmMPK6–GmERF113 cascade triggers resistance to P. sojae in soybean and shed light on functions of MAPK kinases in plant disease resistance. Significance Statement: The GmMKK4–GmMPK6–GmERF113 cascade enhances resistance to soybean (Glycine max) phytophthora disease by successive phosphorylation events triggered by Phytophthora sojae. Our work provides new perspectives to develop strategies to improve plant disease resistance and insights into the roles of MAPK cascades in resistance against root and stem rot diseases. [ABSTRACT FROM AUTHOR]

Phytophthora root and stem rot in soybean (Glycine max) is a destructive disease worldwide, and hence improving crop resistance to the causal pathogen, P. sojae , is a major target for breeders. However, it remains largely unclear how the pathogen regulates the various affected signaling pathways in the host, which consist of complex networks including key transcription factors and their targets. We have previously demonstrated that GmBTB/POZ enhances soybean resistance to P. sojae and the associated defense response. Here, we demonstrate that GmBTB/POZ interacts with the transcription factor GmAP2 and promotes its ubiquitination. GmAP2 -RNAi transgenic soybean hairy roots exhibited enhanced resistance to P. sojae , whereas roots overexpressing GmAP2 showed hypersensitivity. GmWRKY33 was identified as a target of GmAP2, which represses its expression by directly binding to the promoter. GmWRKY33 acts as a positive regulator in the response of soybean to P. sojae. Overexpression of GmBTB/POZ released the GmAP2-regulated suppression of GmWRKY33 in hairy roots overexpressing GmAP2 and increased their resistance to P. sojae. Taken together, our results indicate that GmBTB/POZ-GmAP2 modulation of the P. sojae resistance response forms a novel regulatory mechanism, which putatively regulates the downstream target gene GmWRKY33 in soybean. [ABSTRACT FROM AUTHOR]

Global climate change escalates the rise of atmospheric CO2 concentration and temperature, which impact crop production in agricultural ecosystems. As the second important macronutrient, phosphorus (P) fundamentally mediates the crop adaptability to climate change. An overview on previous work on crop P acquisition and soil P dynamics in responses to elevated CO2 and temperature would be critical for further advancing our knowledge on P cycling under climate change and its management to maintain agroecosystem sustainability. This review focuses on the effects of elevated CO2 and temperature on root morphology, root exudation, and associated biochemical properties in the rhizosphere in relevant to crop P acquisition and soil P availability. Studies indicate that elevated CO2 and temperature could increase P uptake of crops, such as rice and soybean when crops are grown within the range of optimal growth temperature. Elevated CO2 and temperature not only alter root exudates and changes the activity of soil enzymes and microbes the in rhizosphere environment, but also directly influence soil chemical and biochemical processes and thus the bioavailability of P. It is worth to focus on P-solubilizing microbial community composition, and microbial function on soil P mobilization in the rhizosphere of crops grown under climate change. [ABSTRACT FROM AUTHOR]

Aims: Crop residue amendment is likely to stimulate symbiotic N2 fixation, and clarifying its effect on N2-fixing bacteria, i.e., diazotrophs in the rhizosphere of legume crops, is important for sustainable N management in legume-cereal cropping systems. Therefore, this study aimed to reveal the diazotrophic community composition in the rhizosphere of soybean in response to maize residue amendment. Methods: Being designed with treatments of maize residue, chemical fertilizer, and non-fertilizer applications, this study deployed the 15N-labeling technology combined with high-throughput sequencing of the nifH gene as a molecular marker for diazotrophs to quantify the symbiotically-fixed N2 in soybean plants and link symbiotically fixed N2 to the diazotrophic community diversity in the rhizosphere. Results: Residue amendment increased the abundance of diazotrophs and fundamentally altered the composition of its community in the rhizosphere. It increased the relative abundances of Bradyrhizobium and Azohydromonas compared to the chemical fertilizer treatment. The copy number of nifH in the rhizosphere was associated with dissolved organic carbon and N2 fixation. Conclusions: Residue-induced increase in dissolved organic carbon may provide sufficient carbon sources for diazotroph enrichment and thus enhance nodulation. The maize residue amendment may enrich N2 fixers to facilitate nodulation and subsequent N2 fixation of soybean, highlighting the eco-functional importance of diazotrophs fixing extra N into the rotation system. [ABSTRACT FROM AUTHOR]

Phytophthora sojae is a pathogen that causes stem and root rot in soybean (Glycine max [L.] Merr.). We previously demonstrated that GmBTB/POZ, a BTB/POZ domain-containing nuclear protein, enhances resistance to P. sojae in soybean, via a process that depends on salicylic acid (SA). Here, we demonstrate that GmBTB/POZ associates directly with soybean LIKE HETEROCHROMATIN PROTEIN1 (GmLHP1) in vitro and in vivo and promotes its ubiquitination and degradation. Both overexpression and RNA interference analysis of transgenic lines demonstrate that GmLHP1 negatively regulates the response of soybean to P. sojae by reducing SA levels and repressing GmPR1 expression. The WRKY transcription factor gene, GmWRKY40, a SA-induced gene in the SA signaling pathway, is targeted by GmLHP1, which represses its expression via at least two mechanisms (directly binding to its promoter and impairing SA accumulation). Furthermore, the nuclear localization of GmLHP1 is required for the GmLHP1-mediated negative regulation of immunity, SA levels and the suppression of GmWRKY40 expression. Finally, GmBTB/POZ releases GmLHP1-regulated GmWRKY40 suppression and increases resistance to P. sojae in GmLHP1-OE hairy roots. These findings uncover a regulatory mechanism by which GmBTB/POZ-GmLHP1 modulates resistance to P. sojae in soybean, likely by regulating the expression of downstream target gene GmWRKY40. Zhang et al characterise the mechanism by which GmBTB/POZ enhances resistance to P. sojae in soybean. They show that GmBTB/POZ directly associates with the heterochromatin protein GmLHP1 and mediates its degradation to regulate the salicylic acid signaling pathway, providing insights into the defence against a common soybean disease. [ABSTRACT FROM AUTHOR]

Phytophthora root and stem rot of soybean (Glycine max (L.) Merr.) caused by Phytophthora sojae is a destructive disease worldwide. The enzyme 4-coumarate: CoA ligase (4CL) has been extensively studied with regard to plant responses to pathogens. However, the molecular mechanism of the response of soybean 4CL to P. sojae remains unclear. In a previous study, a highly upregulated 4CL homologue was characterised through suppressive subtractive hybridisation library and cDNA microarrays, in the resistant soybean cultivar 'Suinong 10' after infection with P. sojae race 1. Here, we isolated the full-length EST, and designated as GmPI4L (P. sojae -inducible 4CL gene) in this study, which is a novel member of the soybean 4CL gene family. GmPI4L has 34–43% over all amino acid sequence identity with other plant 4CLs. Overexpression of GmPI4L enhances resistance to P. sojae in transgenic soybean plants. The GmPI4L is located in the cell membrane when transiently expressed in Arabidopsis protoplasts. Further analyses showed that the contents of daidzein, genistein, and the relative content of glyceollins are significantly increased in overexpression GmPI4L soybeans. Taken together, these results suggested that GmPI4L plays an important role in response to P. sojae infection, possibly by enhancing the content of glyceollins, daidzein, and genistein in soybean. Glyceollins and isoflavones are soybean-derived phytoalexins in response to Phytophthora sojae that causes stem and root rot on soybeans worldwide. To understand the function of Gm4CL, we analysed and found that GmPI4L improves defence against P. sojae by enhancing glyceollins and isoflavones content. This study provides the theoretical foundation for clarifying the mechanism of the phenylpropanoid pathway in disease resistance in soybean. [ABSTRACT FROM AUTHOR]

Summary: Phytophthora sojae is a destructive pathogen of soybean [Glycine max (L.) Merr.] which causes stem and root rot on soybean plants worldwide. However, the pathogenesis and molecular mechanism of plant defence responses against P. sojae are largely unclear. Herein, we document the underlying mechanisms and function of a novel BTB/POZ protein, GmBTB/POZ, which contains a BTB/POZ domain found in certain animal transcriptional regulators, in host soybean plants in response to P. sojae. It is located in the cell nucleus and is transcriptionally up‐regulated by P. sojae. Overexpression of GmBTB/POZ in soybean resulted in enhanced resistance to P. sojae. The activities and expression levels of enzymatic superoxide dismutase (SOD) and peroxidase (POD) antioxidants were significantly higher in GmBTB/POZ‐overexpressing (GmBTB/POZ‐OE) transgenic soybean plants than in wild‐type (WT) plants treated with sterile water or infected with P. sojae. The transcript levels of defence‐associated genes were also higher in overexpressing plants than in WT on infection. Moreover, salicylic acid (SA) levels and the transcript levels of SA biosynthesis‐related genes were markedly higher in GmBTB/POZ‐OE transgenic soybean than in WT, but there were almost no differences in jasmonic acid (JA) levels or JA biosynthesis‐related gene expression between GmBTB/POZ‐OE and WT soybean lines. Furthermore, exogenous SA application induced the expression of GmBTB/POZ and inhibited the increase in P. sojae biomass in both WT and GmBTB/POZ‐OE transgenic soybean plants. Taken together, these results suggest that GmBTB/POZ plays a positive role in P. sojae resistance and the defence response in soybean via a process that might be dependent on SA. [ABSTRACT FROM AUTHOR]

Aims: In agricultural systems, residue amendment is an important practice for nutrient management, but the role of microbes in mineralization of crop residue nitrogen (N) is not well known. Therefore, this study aimed to examine how the residue N mineralization was associated with changes of the microbial community composition in crop rhizosphere.A rhizobox system was deployed to separate the rhizosphere zone into the root-growth (central), and 2 mm (proximal) and 4 mm (transitional) zones away from the central zone, and the gradient change of the residue-N mineralization along the zones was assessed. Soybean plants were grown in a Mollisol without or with amendment of 15N-labelled soybean and maize residues. Furthermore, amplicon sequencing was performed to detect the shift of microbial community composition associated with the residue-N mineralization.The residue-N was mineralized faster in the rhizosphere than the bulk soil, and from soybean residue than maize residue. Greater enrichment of taxa against the unit of residue-N mineralization in the soybean than maize residue treatment was correspondent with the enriched ammonification genes, likely contributing to the enhanced mineralization of soybean residue-N in the rhizosphere. A gradual increase in dissolved organic C and a decrease in available N concentration from the central root zone to the bulk soil, might shift bacterial community favoring the residue-N mineralization in the rhizosphere.The spatial changes in chemical properties across the rhizosphere lead to the recruitment of microbiome taxa to enhance the mineralization of N derived from crop residues.Methods: In agricultural systems, residue amendment is an important practice for nutrient management, but the role of microbes in mineralization of crop residue nitrogen (N) is not well known. Therefore, this study aimed to examine how the residue N mineralization was associated with changes of the microbial community composition in crop rhizosphere.A rhizobox system was deployed to separate the rhizosphere zone into the root-growth (central), and 2 mm (proximal) and 4 mm (transitional) zones away from the central zone, and the gradient change of the residue-N mineralization along the zones was assessed. Soybean plants were grown in a Mollisol without or with amendment of 15N-labelled soybean and maize residues. Furthermore, amplicon sequencing was performed to detect the shift of microbial community composition associated with the residue-N mineralization.The residue-N was mineralized faster in the rhizosphere than the bulk soil, and from soybean residue than maize residue. Greater enrichment of taxa against the unit of residue-N mineralization in the soybean than maize residue treatment was correspondent with the enriched ammonification genes, likely contributing to the enhanced mineralization of soybean residue-N in the rhizosphere. A gradual increase in dissolved organic C and a decrease in available N concentration from the central root zone to the bulk soil, might shift bacterial community favoring the residue-N mineralization in the rhizosphere.The spatial changes in chemical properties across the rhizosphere lead to the recruitment of microbiome taxa to enhance the mineralization of N derived from crop residues.Results: In agricultural systems, residue amendment is an important practice for nutrient management, but the role of microbes in mineralization of crop residue nitrogen (N) is not well known. Therefore, this study aimed to examine how the residue N mineralization was associated with changes of the microbial community composition in crop rhizosphere.A rhizobox system was deployed to separate the rhizosphere zone into the root-growth (central), and 2 mm (proximal) and 4 mm (transitional) zones away from the central zone, and the gradient change of the residue-N mineralization along the zones was assessed. Soybean plants were grown in a Mollisol without or with amendment of 15N-labelled soybean and maize residues. Furthermore, amplicon sequencing was performed to detect the shift of microbial community composition associated with the residue-N mineralization.The residue-N was mineralized faster in the rhizosphere than the bulk soil, and from soybean residue than maize residue. Greater enrichment of taxa against the unit of residue-N mineralization in the soybean than maize residue treatment was correspondent with the enriched ammonification genes, likely contributing to the enhanced mineralization of soybean residue-N in the rhizosphere. A gradual increase in dissolved organic C and a decrease in available N concentration from the central root zone to the bulk soil, might shift bacterial community favoring the residue-N mineralization in the rhizosphere.The spatial changes in chemical properties across the rhizosphere lead to the recruitment of microbiome taxa to enhance the mineralization of N derived from crop residues.Conclusions: In agricultural systems, residue amendment is an important practice for nutrient management, but the role of microbes in mineralization of crop residue nitrogen (N) is not well known. Therefore, this study aimed to examine how the residue N mineralization was associated with changes of the microbial community composition in crop rhizosphere.A rhizobox system was deployed to separate the rhizosphere zone into the root-growth (central), and 2 mm (proximal) and 4 mm (transitional) zones away from the central zone, and the gradient change of the residue-N mineralization along the zones was assessed. Soybean plants were grown in a Mollisol without or with amendment of 15N-labelled soybean and maize residues. Furthermore, amplicon sequencing was performed to detect the shift of microbial community composition associated with the residue-N mineralization.The residue-N was mineralized faster in the rhizosphere than the bulk soil, and from soybean residue than maize residue. Greater enrichment of taxa against the unit of residue-N mineralization in the soybean than maize residue treatment was correspondent with the enriched ammonification genes, likely contributing to the enhanced mineralization of soybean residue-N in the rhizosphere. A gradual increase in dissolved organic C and a decrease in available N concentration from the central root zone to the bulk soil, might shift bacterial community favoring the residue-N mineralization in the rhizosphere.The spatial changes in chemical properties across the rhizosphere lead to the recruitment of microbiome taxa to enhance the mineralization of N derived from crop residues. [ABSTRACT FROM AUTHOR]

[Display omitted] • Maize residue amendment altered the N accumulation pattern in soybean. • Residue N was the minimal source of grain N in soybean. • Residue amendment increased the nodule density and N 2 fixation efficiency. • The diazotrophic community abundance was enriched with residue amendment. Crop residue amendment to soil is recommended as an effective management practice to return nutrients, especially in the maize-soybean rotation system where large amounts of maize residues are produced. Quantifying the utilisation of maize-residue N by the subsequent soybean crop is essential for optimising the N fertilisation strategy for sustainable production. However, whether and how maize residue amendment alters N acquisition in soybean plants are largely unknown. It was hypothesised that maize residue would supply N and enhance N 2 fixation to meet the N requirements of subsequent soybeans. Three treatments, namely: 1) chemical fertiliser (55.2, 35.2 and 22.4 kg ha−1 of N, P and K, respectively), 2) maize residue (8 t ha−1), and 3) non-fertiliser were applied in a maize-soybean rotation system in a Mollisol soil. It was demonstrated that soybean seed yield in the maize-residue treatment was the same as that in the chemical fertiliser treatment, with 2.9 vs. 3.2 t ha−1 in 2014, 2.7 vs. 2.6 t ha−1 in 2016, and 3.0 vs. 3.1 t ha−1 in 2018. A follow-up pot experiment using 15N-labelled residue indicated that the residue-derived N accounted for 0.5 % of the total N in soybean seeds and the proportion of symbiotically fixed N reached 82 %. The amount of fixed N during the pod-filling period in the residue treatment was 0.66 g plant-1, which was 49 % and 41 % higher than those in the chemical fertiliser and non-fertiliser treatments, respectively. The stimulation of N 2 fixation was associated with an increase in fixed N per nodule and the enrichment of diazotrophs in the rhizosphere of soybean. With maize residue amendment, the increased N 2 -fixing capability of nodules during the reproductive period, rather than residue-derived N, fulfilled the N demand for maintaining seed yield of soybean. In the maize-soybean rotation system, maize residue amendment would facilitate the N 2 fixation to partly substitute for N fertiliser for soybean production in Mollisols. [ABSTRACT FROM AUTHOR]

• The application of manure and fertilizer increased SOC concentration in the top 40 cm of a Mollisol. • The C concentration in POC was exponentially correlated with soil nitrogen (N), phosphorus (P) and N:P ratio. • Nitrogen, rather than P mainly regulates C storage in POC. Organic matter application significantly influences soil carbon storage and sequestration in cropland. The investigation of C sequestration through soil organic carbon (SOC) fractions in the soil profile and its relation to nutrient stoichiometry are essential for evaluating the effect of farming practice on soil fertility. This study aimed to examine the effect of cattle manure application on nutrient stoichiometry, which would be associated with soil C stock in SOC fractions, such as microbial biomass C (MBC), dissolved organic C (DOC) and water-soluble organic C (WSOC), coarse particulate organic carbon (cPOC), fine particulate organic carbon (fPOC) and the mineral-associated organic carbon (MOC). A four-year manure application experiment was conducted in a Mollisol, in which fertilization treatments comprised (1) NoF: the non-fertilizer control, (2) F: synthetic fertilizer, i.e. 20.3, 21.2 and 12.2 kg ha−1 of nitrogen (N), phosphorus (P) and potassium (K) in soybean, and 69.0, 28.1 and 6.1 kg ha−1 of N, P and K for corn on an annual basis, respectively, (3) F + M: synthetic fertilizer plus 15 Mg ha-1 of cattle manure and (4) F + 2M: synthetic fertilizer plus 30 Mg ha−1 of cattle manure in a soybean-corn rotation. SOC concentration in top 10 cm of soil was 18 % and 19 % higher under F + M than that under NoF and F, respectively. Whereas, F+2 M significantly increased SOC concentration by 32 %, 32 %, 14 %, and 11 % in 0−10, 10−20, 20−30, and 30−40 cm of soil depth compared to that in respective soil depth under NoF. Compared to NoF and F, manure application (F + M and F+2 M) significantly increased MBC in the top 30 cm of soil depth and DOC concentration in the top 20 cm of soil depth, but significantly decreased WSOC concentration in the top 20 cm of soil depth. F+2 M significantly increased cPOC concentration in the top 30 cm of soil depth compared to NoF and F. F + M significantly increased fPOC concentration in the top 50 cm of soil depth, compared to NoF, and F. F+2 M further increased the fPOC concentration in the top 30 cm of soil depth, compared to F + M. There was no difference among fertilization treatments in MOC concentration in any soil depth. There were significant exponential correlations of C concentration in POC fractions with soil N, P and N/P ratio. These results indicate that the combination of manure and synthetic fertilizer increased C accumulation in the POC fraction especially in the top 30 cm of soil depth. The change of nutrient stoichiometry was responsible to the accumulation of soil organic matter, highlighting that N, rather than P mainly regulated C accumulation in POC. Increasing input of N fertilizer combined with manure application would benefit the formation of soil organic matter in agricultural Mollisols. [ABSTRACT FROM AUTHOR]

Excessive nitrogen (N) fertilizer input to agroecosystem fundamentally alters soil microbial properties and subsequent their ecofunctions such as carbon (C) sequestration and nutrient cycling in soil. However, between soils, the rhizobacterial community diversity and structure in response to N addition is not well understood, which is important to make proper N fertilization strategies to alleviate the negative impact of N addition on soil organic C and soil quality and maintain plant health in soils. Thus, a rhizo-box experiment was conducted with soybean grown in two soils, i.e. soil organic C (SOC)-poor and SOC-rich soil, supplied with three N rates in a range from 0 to 100 mg N kg−1. The rhizospheric soil was collected 50 days after sowing and MiSeq sequencing was deployed to analyze the rhizobacterial community structure. The results showed that increasing N addition significantly decreased the number of phylotype of rhizobacteria by 12.3%, and decreased Shannon index from 5.98 to 5.36 irrespective of soils. Compared to the SOC-rich soil, the increases in abundances of Aquincola affiliated to Proteobacteria, and Streptomyces affiliated to Actinobacteria were greater in the SOC-poor soil in response to N addition. An opposite trend was observed for Ramlibacter belong to Proteobacteria. These results suggest that N addition reduced the rhizobacterial diversity and its influence on rhizobacterial community structure was soil-specific. [ABSTRACT FROM AUTHOR]