Soybean transcription factor ORFeome associated with drought resistance: a valuable resource to accelerate research on abiotic stress resistance

Tissue/organ expression pattern of TF genes. The expression of soybean TF-ORFeome candidates in seven soybean organs including root, root tip, leaf, shoot apical meristem (SAM), nodule, flower and green pod were based on published RNA-Seq data [26]. The color scale indicates the degree of gene expression levels (yellow, low expression level; red, high expression level)

An Efficient Brome mosaic virus-Based Gene Silencing Protocol for Hexaploid Wheat (Triticum aestivum L.)

Virus-induced gene silencing (VIGS) is a rapid and powerful method to evaluate gene function, especially for species like hexaploid wheat that have large, redundant genomes and are difficult and time-consuming to transform. The Brome mosaic virus (BMV)-based VIGS vector is widely used in monocotyledonous species but not wheat. Here we report the establishment of a simple and effective VIGS procedure in bread wheat using BMVCP5, the most recently improved BMV silencing vector, and wheat genes PHYTOENE DESATURASE (TaPDS) and PHOSPHATE2 (TaPHO2) as targets. Time-course experiments revealed that smaller inserts (~100 nucleotides, nt) were more stable in BMVCP5 and conferred higher silencing efficiency and longer silencing duration, compared with larger inserts. When using a 100-nt insert and a novel coleoptile inoculation method, BMVCP5 induced extensive silencing of TaPDS transcript and a visible bleaching phenotype in the 2nd to 5th systemically-infected leaves from nine to at least 28 days post inoculation (dpi). For TaPHO2, the ability of BMVCP5 to simultaneously silence all three homoeologs was demonstrated. To investigate the feasibility of BMV VIGS in wheat roots, ectopically expressed enhanced GREEN FLUORESCENT PROTEIN (eGFP) in a transgenic wheat line was targeted for silencing. Silencing of eGFP fluorescence was observed in both the maturation and elongation zones of roots. BMVCP5 mediated significant silencing of eGFP and TaPHO2 mRNA expression in roots at 14 and 21 dpi, and TaPHO2 silencing led to the doubling of inorganic phosphate concentration in the 2nd through 4th systemic leaves. All 54 wheat cultivars screened were susceptible to BMV infection. BMVCP5-mediated TaPDS silencing resulted in the expected bleaching phenotype in all eight cultivars examined, and decreased TaPDS transcript was detected in all three cultivars examined. This BMVCP5 VIGS technology may serve as a rapid and effective functional genomics tool for high-throughput gene function studies in aerial and root tissues and in many wheat cultivars

Mutations of genes in synthesis of the carotenoid precursors of ABA lead to pre-harvest sprouting and photo-oxidation in rice

Pre-harvest sprouting (PHS) or vivipary in cereals is an important agronomic trait that results in significant economic loss. A considerable number of mutations that cause PHS have been identified in several species. However, relatively few viviparous mutants in rice (Oryza sativa L.) have been reported. To explore the mechanism of PHS in rice, we carried out an extensive genetic screening and identified 12 PHS mutants (phs). Based on their phenotypes, these phs mutants were classified into three groups. Here we characterize in detail one of these groups, which contains mutations in genes encoding major enzymes of the carotenoid biosynthesis pathway, including phytoene desaturase (OsPDS), ζ-carotene desaturase (OsZDS), carotenoid isomerase (OsCRTISO) and lycopene β-cyclase (β-OsLCY), which are essential for the biosynthesis of carotenoid precursors of ABA. As expected, the amount of ABA was reduced in all four phs mutants compared with that in the wild type. Chlorophyll fluorescence analysis revealed the occurrence of photoinhibition in the photosystem and decreased capacity for eliminating excess energy by thermal dissipation. The greatly increased activities of reactive oxygen species (ROS) scavenging enzymes, and reduced photosystem (PS) II core proteins CP43, CP47 and D1 in leaves of the Oscrtiso/phs3-1 mutant and OsLCY RNAi transgenic rice indicated that photo-oxidative damage occurred in PS II, consistent with the accumulation of ROS in these plants. These results suggest that the impairment of carotenoid biosynthesis causes photo-oxidation and ABA-deficiency phenotypes, of which the latter is a major factor controlling the PHS trait in rice

PgtE Enzyme of Salmonella enterica Shares the Similar Biological Roles to Plasminogen Activator (Pla) in Interacting With DEC-205 (CD205), and Enhancing Host Dissemination and Infectivity by Yersinia pestis

Yersinia pestis, the cause of plague, is a newly evolved Gram-negative bacterium. Through the acquisition of the plasminogen activator (Pla), Y. pestis gained the means to rapidly disseminate throughout its mammalian hosts. It was suggested that Y. pestis utilizes Pla to interact with the DEC-205 (CD205) receptor on antigen-presenting cells (APCs) to initiate host dissemination and infection. However, the evolutionary origin of Pla has not been fully elucidated. The PgtE enzyme of Salmonella enterica, involved in host dissemination, shows sequence similarity with the Y. pestis Pla. In this study, we demonstrated that both Escherichia coli K-12 and Y. pestis bacteria expressing the PgtE-protein were able to interact with primary alveolar macrophages and DEC-205-transfected CHO cells. The interaction between PgtE-expressing bacteria and DEC-205-expressing transfectants could be inhibited by the application of an anti-DEC-205 antibody. Moreover, PgtE-expressing Y. pestis partially re-gained the ability to promote host dissemination and infection. In conclusion, the DEC-205-PgtE interaction plays a role in promoting the dissemination and infection of Y. pestis, suggesting that Pla and the PgtE of S. enterica might share a common evolutionary origin.Peer reviewe

Impacts of Leading Edge Pitting and Delamination on Aerodynamic Characteristics of Wind Turbine Blades under Shear Inflow

Undesirable performance degradation occurs when wind turbine operates in harsh environment, thus investigation of the impact of various degrees of leading edge erosion on the aerodynamic characteristics of wind turbine is significant and highly desirable. In this study, significant research efforts were made to explore the effects of leading edge pitting and delamination on blade surface streamlines, flow structures, pressure coefficients, and aerodynamic forces of horizontal wind turbine under shear inflow. The k-ω shear-stress transport turbulence model was adopted to close the three-dimensional incompressible Reynolds-averaged Navier-Stokes. The results indicate the existence of significant differences on surface streamlines between the smooth and eroded blade. The leading edge of the entire blade gets covered with the attached flow, while just a small area for the eroded blade is covered when it is at the lowest position. Moreover, small separation bubble appears at the suction surface of the section near the blade root, which grows bigger and induces a second vortex when the section moves to the middle of the blade and then the size gets smaller when the section is near the blade tip. With the increase of erosion, the pressure difference of blade surface decreases, indicating a severe decrease in performance of eroded blade. Furthermore, leading edge erosion causes a decrease in average torque coefficients by 19.75, 29.01, 41.82, and 42.54% for various leading edge erosion cases at the inflow wind speed of 10 ms-1, and 25.0, 49.6, 51.3, and 54.6% at the speed of 20 ms-1

Effect of Different Hydrothermal Parameters on Calorific Value and Pyrolysis Characteristics of Hydrochar of Kitchen Waste

Kitchen waste (KW) has high water content and organic matter, which has great potential for energy application, but how to treat it effectively has always been a difficult problem. In this study, the feasibility of transforming kitchen waste into hydrochar as a solid fuel to replace the primary energy by hydrothermal carbonization (HTC) is put forward. An experimental study of proportioned KW under HTC conditions (reaction temperature, residence time, liquid–solid ratio) is carried out by elemental analysis, industrial analysis, energy density calculation, and calorific value measurement. The results show that a proper extension of the residence time to 3.5 h at a liquid–solid ratio of 10 and a reaction temperature of 265 °C for the kitchen waste after HTC would result in a maximum calorific value of 30.933 MJ/Kg for the prepared hydrochar. The maximum ash content of hydrochar at a 265 °C reaction temperature is 3.94% < 10%, which is much lower than the standard of extra-low-ash coal, and the study shows that the hydrochar prepared from kitchen waste by HTC for combustion will greatly improve the combustion efficiency. The three types of kitchen waste under HTC conditions are compared with the three typical types of coal in China by the van Krevelen diagram. The results show that the combustion properties of hydrochar from kitchen waste prepared by the HTC method are better than those of lignite close to bituminous coal and can provide a theoretical basis for replacing primary energy in the future. Finally, by combining thermogravimetric analysis with mathematical modeling, it is calculated that the hydrochar of kitchen waste has a lower activation energy than those of other biomass, which can better facilitate the reaction. The experimental results further determine the feasibility of hydrochar as an alternative primary energy source and provide a theoretical basis for the future conversion of kitchen waste into hydrochar as a solid fuel through HTC

Expression of flavonoid 3’-hydroxylase is controlled by P1, the regulator of 3-deoxyflavonoid biosynthesis in maize

Abstract Background The maize (Zea mays) red aleurone1 (pr1) encodes a CYP450-dependent flavonoid 3’-hydroxylase (ZmF3’H1) required for the biosynthesis of purple and red anthocyanin pigments. We previously showed that Zmf3’h1 is regulated by C1 (Colorless1) and R1 (Red1) transcription factors. The current study demonstrates that, in addition to its role in anthocyanin biosynthesis, the Zmf3’h1 gene also participates in the biosynthesis of 3-deoxyflavonoids and phlobaphenes that accumulate in maize pericarps, cob glumes, and silks. Biosynthesis of 3-deoxyflavonoids is regulated by P1 (Pericarp color1) and is independent from the action of C1 and R1 transcription factors. Results In maize, apiforol and luteoforol are the precursors of condensed phlobaphenes. Maize lines with functional alleles of pr1 and p1 (Pr1;P1) accumulate luteoforol, while null pr1 lines with a functional or non-functional p1 allele (pr1;P1 or pr1;p1) accumulate apiforol. Apiforol lacks a hydroxyl group at the 3’-position of the flavylium B-ring, while luteoforol has this hydroxyl group. Our biochemical analysis of accumulated compounds in different pr1 genotypes showed that the pr1 encoded ZmF3’H1 has a role in the conversion of mono-hydroxylated to bi-hydroxylated compounds in the B-ring. Steady state RNA analyses demonstrated that Zmf3’h1 mRNA accumulation requires a functional p1 allele. Using a combination of EMSA and ChIP experiments, we established that the Zmf3’h1 gene is a direct target of P1. Highlighting the significance of the Zmf3’h1 gene for resistance against biotic stress, we also show here that the p1 controlled 3-deoxyanthocyanidin and C-glycosyl flavone (maysin) defence compounds accumulate at significantly higher levels in Pr1 silks as compared to pr1 silks. By virtue of increased maysin synthesis in Pr1 plants, corn ear worm larvae fed on Pr1; P1 silks showed slower growth as compared to pr1; P1 silks. Conclusions Our results show that the Zmf3’h1 gene participates in the biosynthesis of phlobaphenes and agronomically important 3-deoxyflavonoid compounds under the regulatory control of P1.</p