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IntroductionPseudomonas aeruginosa is present throughout nature and is a common opportunistic pathogen in the human body. Carbapenem antibiotics are typically utilized as a last resort in the clinical treatment of multidrug-resistant infections caused by P. aeruginosa. The increase in carbapenem-resistant P. aeruginosa poses an immense challenge for the treatment of these infections. Bacteriophages have the potential to be used as antimicrobial agents for treating antibiotic-resistant bacteria.Methods and ResultsIn this study, a new virulent P. aeruginosa phage, Phage_Pae01, was isolated from hospital sewage and shown to have broad-spectrum antibacterial activity against clinical P. aeruginosa isolates (83.6%). These clinical strains included multidrug-resistant P. aeruginosa and carbapenem-resistant P. aeruginosa. Transmission electron microscopy revealed that the phage possessed an icosahedral head of approximately 80 nm and a long tail about 110 m, indicating that it belongs to the Myoviridae family of the order Caudovirales. Biological characteristic analysis revealed that Phage_Pae01 could maintain stable activity in the temperature range of 4~ 60°C and pH range of 4 ~ 10. According to the in vitro lysis kinetics of the phage, Phage_Pae01 demonstrated strong antibacterial activity. The optimal multiplicity of infection was 0.01. The genome of Phage_Pae01 has a total length of 93,182 bp and contains 176 open reading frames (ORFs). The phage genome does not contain genes related to virulence or antibiotic resistance. In addition, Phage_Pae01 effectively prevented the formation of biofilms and eliminated established biofilms. When Phage_Pae01 was combined with gentamicin, it significantly disrupted established P. aeruginosa biofilms.ConclusionWe identified a novel P. aeruginosa phage and demonstrated its effective antimicrobial properties against P. aeruginosa in both the floating and biofilm states. These findings offer a promising approach for the treatment of drug-resistant bacterial infections in clinical settings.

The type synthesis problem of the spreading tray adjustment mechanism in the rice transplanting machine is analyzed， by the topological design theory and method of parallel mechanism based on Position and orientation characteristics set， 14 types of 3-degree-of-freedom 2T1R parallel mechanisms driven by moving pair are synthesized for the spreading tray adjustment mechanism. Considering the practical application requirements， a mechanism with strong practicality is selected， and the topological feature analysis and kinematic analysis are carried out for this mechanism， which lays the theoretical foundation for the subsequent specific structure design.

The Baima vanadium titanomagnetite deposit, located in the Panzhihua-Xichang (Panxi) metallogenic belt in China, is one of the super-large deposits in the region. The titanomagnetite upgrading process involves grinding the raw ore followed by magnetic separation. To determine the processing characteristics of the ore and assess the upgrading process, this study employs various methods and techniques, including the X-ray fluorescence spectrometer (XRF), chemical element analysis, the electron probe microanalyzer (EPMA), and the advanced mineral identification and characterization system (AMICS). The results show that the Fe grades in the upgraded raw ore, upgraded concentrate, and upgraded tailings are 55.68%, 57.89%, and 15.62%, respectively. After upgrading, the titanomagnetite content increased from 77.41% to 82.10%, and the Fe distribution in titanomagnetite also increased from 91.05% to 93.14%. In the upgraded raw ore, titanomagnetite particles followed a normal distribution, with 50.44% in the 38–74 μm range. In the upgraded concentrate, titanomagnetite was concentrated in the 19–38 μm range. Based on EPMA data, the theoretical Fe grade in titanomagnetite was calculated to be 65.08%, indicating the potential for further improvement through the upgrading process. This study elucidates the mineralogical characteristics during the vanadium titanomagnetite upgrading, providing a theoretical basis to further enhance the Fe recovery rate.

The knee adaptive rehabilitation apparatus is designed， which consists of a swinging guide linkand a crank slider mechanism.According to ergonomics，the size range of the shank in the adaptive rehabilitation apparatus is determined by analyzing the motion characteristics of human knee joint. In order to realize the adaptive adjustment of the rotation angle of human knee joint， the kinematics model of the mechanism is established based on the complex vector method. According to the kinematics equation，the relation between the knee joint extension angle and the height of the movable frame in the mechanism is obtained， thus the size of the mechanism is determined. Through the simulation analysis and comparison between the adaptive rehabilitation apparatus and the traditional rehabilitation apparatus （crank slider mechanism）， the results show that the motion characteristics of the tandem type rehabilitation apparatus and the traditional rehabilitation apparatus （crank slider mechanism） can meet the stretching angle of the knee rehabilitation apparatus， but the motion stability of tandem type knee joint apparatus is better.

According to the physiological characteristics of human ankle and parallel mechanism， several 0T3R parallel mechanisms are synthesized based on the Position and Orientation Characteristics （POC） set by taking the Single-Opened Chain （SOC） as the unit. Then combined with the characteristics of human ankle， one of the 0T3R parallel mechanisms is selected， and its kinematics analysis is carried out. Based on the established inverse displacement solution equation and by using the Matlab， the data solving is carried out. Finally， the obtained data is used as the driving function to simulate the mechanism in Adams. The simulation results verify the feasibility of the parallel mechanism， and a theoretical basis for the subsequent optimization design of mechanism size is provided.

We have previously defined four single-gene mutations, con1, con2, con4, and con7, that control various stages of spore morphogenesis in the rice blast fungus. To delineate the developmental pathway of spore morphogenesis, we investigated the interactions among these morphogenetic genes by generating strains with double mutations via transformation-mediated gene disruption. Plasmids containing portions of the inactivated CON4 and CON7 genes were introduced into strains harboring single mutation to produce double mutants. Interaction between con1 and con4 resulted in reduced vegetative growth and suppression of sporulation. Interaction between con1 and con7 suppressed spore production but not vegetative growth. The con2/con4 and con4/con7 double mutants produced hybrid spore types with characteristic features of both parental mutants. The con2/con7 mutant produced con2 type spores, indicating that con2 is epistatic to con7 in spore morphogenesis. The epistatic relationship, however, reversed when traits related to pathogenesis were considered. Double mutants harboring the con7 mutation could not form appressoria or colonize plant tissue, indicating that con7 is epistatic to con2 and con4 in appressorium formation and pathogenesis. Thus, morphogenetic genes interact at multiple levels leading to different epistatic relationships in the pathways of spore morphogenesis, appressorium formation, and pathogenesis.

Commercial cultivation of the mushroom fungus, Agaricus bisporus, utilizes a substrate consisting of a lower layer of compost and upper layer of peat. Typically, the two layers are seeded with individual mycelial inoculants representing a single genotype of A. bisporus. Studies aimed at examining the potential of this fungal species as a heterologous protein expression system have revealed unexpected contributions of the mycelial inoculants in the morphogenesis of the fruiting body. These contributions were elucidated using a dual-inoculant method whereby the two layers were differientially inoculated with transgenic β-glucuronidase (GUS) and wild-type (WT) lines. Surprisingly, use of a transgenic GUS line in the lower substrate and a WT line in the upper substrate yielded fruiting bodies expressing GUS activity while lacking the GUS transgene. Results of PCR and RT-PCR analyses for the GUS transgene and RNA transcript, respectively, suggested translocation of the GUS protein from the transgenic mycelium colonizing the lower layer into the fruiting body that developed exclusively from WT mycelium colonizing the upper layer. Effective translocation of the GUS protein depended on the use of a transgenic line in the lower layer in which the GUS gene was controlled by a vegetative mycelium-active promoter (laccase 2 and β-actin), rather than a fruiting body-active promoter (hydrophobin A). GUS-expressing fruiting bodies lacking the GUS gene had a bonafide WT genotype, confirmed by the absence of stably inherited GUS and hygromycin phosphotransferase selectable marker activities in their derived basidiospores and mycelial tissue cultures. Differientially inoculating the two substrate layers with individual lines carrying the GUS gene controlled by different tissue-preferred promoters resulted in up to a ∼3.5-fold increase in GUS activity over that obtained with a single inoculant. Our findings support the existence of a previously undescribed phenomenon of long-distance protein translocation in A. bisporus that has potential application in recombinant protein expression and biotechnological approaches for crop improvement.