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Summary: Softening in fruit adversely impacts their edible quality and commercial value, leading to substantial economic losses during fruit ripening, long‐term storage, long‐distance transportation, and marketing. As the apple fruit demonstrates climacteric respiration, its firmness decreases with increasing ethylene release rate during fruit ripening and postharvest storage. However, the molecular mechanisms underlying ethylene‐mediated regulation of fruit softening in apple remain poorly understood. In this study, we identified a WRKY transcription factor (TF) MdWRKY31, which is repressed by ethylene treatment. Using transgenic approaches, we found that overexpression of MdWRKY31 delays softening by negatively regulating xyloglucan endotransglucosylase/hydrolases 2 (MdXTH2) expression. Yeast one‐hybrid (Y1H), electrophoretic mobility shift (EMSA), and dual‐luciferase assays further suggested that MdWRKY31 directly binds to the MdXTH2 promoter via a W‐box element and represses its transcription. Transient overexpression of ethylene‐induced MdNAC7, a NAC TF, in apple fruit promoted softening by decreasing cellulose content and increasing water‐soluble pectin content in fruit. MdNAC7 interacted with MdWRKY31 to form a protein complex, and their interaction decreased the transcriptional repression of MdWRKY31 on MdXTH2. Furthermore, MdNAC7 does not directly regulate MdXTH2 expression, but the protein complex formed with MdWRKY31 hinders MdWRKY31 from binding to the promoter of MdXTH2. Our findings underscore the significance of the regulatory complex NAC7–WRKY31 in ethylene‐responsive signalling, connecting the ethylene signal to XTH2 expression to promote fruit softening. This sheds light on the intricate mechanisms governing apple fruit firmness and opens avenues for enhancing fruit quality and reducing economic losses associated with softening. [ABSTRACT FROM AUTHOR]

Summary: In wireless charging systems for electric vehicles, fluctuations in coil mutual inductance can affect both system output power and efficiency. This paper introduces a coil mutual inductance model that accounts for metal shielding material. The formula for coil mutual inductance is derived using Maxwell's equations and boundary conditions. Additionally, the paper presents a tactic for adapting the mutual inductance with the aid of an intelligent optimization algorithm, which is utilized for steadying the mutual inductance of the transmission coil. Lastly, a model of the transmission coil is developed to authenticate the practicality of the mutual inductance equation and the adaptation scheme. Measurement and calculation results indicate that the difference between the calculated value of the mutual inductance formula and the actual mutual inductance value of the coil, following deflection and offset, is below 5%. Moreover, the algorithm, along with the employed adaptation strategy, consistently demonstrates effectiveness in maintaining the mutual inductance value within a predefined range. The temporal efficiency of the algorithm, as measured by the time taken to determine this coordinate position, is consistently under 1 s. This ensures that the algorithm exhibits a rapid response time, a crucial attribute in ensuring its practical utility. [ABSTRACT FROM AUTHOR]

SUMMARY: Drought stress is one of the dominating challenges to the growth and productivity in crop plants. Elucidating the molecular mechanisms of plants responses to drought stress is fundamental to improve fruit quality. However, such molecular mechanisms are poorly understood in apple (Malus domestica Borkh.). In this study, we explored that the BTB‐BACK‐TAZ protein, MdBT2, negatively modulates the drought tolerance of apple plantlets. Moreover, we identified a novel Homeodomain‐leucine zipper (HD‐Zip) transcription factor, MdHDZ27, using a yeast two‐hybrid (Y2H) screen with MdBT2 as the bait. Overexpression of MdHDZ27 in apple plantlets, calli, and tomato plantlets enhanced their drought tolerance by promoting the expression of drought tolerance‐related genes [responsive to dehydration 29A (MdRD29A) and MdRD29B]. Biochemical analyses demonstrated that MdHDZ27 directly binds to and activates the promoters of MdRD29A and MdRD29B. Furthermore, in vitro and in vivo assays indicate that MdBT2 interacts with and ubiquitinates MdHDZ27, via the ubiquitin/26S proteasome pathway. This ubiquitination results in the degradation of MdHDZ27 and weakens the transcriptional activation of MdHDZ27 on MdRD29A and MdRD29B. Finally, a series of transgenic analyses in apple plantlets further clarified the role of the relationship between MdBT2 and MdHDZ27, as well as the effect of their interaction on drought resistance in apple plantlets. Collectively, our findings reveal a novel mechanism by which the MdBT2‐MdHDZ27 regulatory module controls drought tolerance, which is of great significance for enhancing the drought resistance of apple and other plants. Significance Statement: Collectively, our findings clearly decipher a novel regulatory network for drought tolerance in the apple plant, which centers on the regulatory module MdBT2‐MdHDZ27 and its roles in transcriptional regulation and post‐transcriptional modification, which will be useful for improving the drought tolerances of apple and other economically important plant species. [ABSTRACT FROM AUTHOR]

A systematic density functional theory study, including 17 exchange–correlation functionals, was performed on 22 composite structures consisting of organic molecules, e.g., ethylene, ethane, and benzene, and superhalogen substitutions arising from [MgX3]− and [Mg2X5]− (X = F, Cl). Range-separated hybrid functionals ω B97M-V, ω B97X-D3(BJ), ω B97XD, ω B97X, and CAM-B3LYP, as well as double-hybrid functionals B2PLYP and DSD-PBEP86-D3(BJ), are verified to provide reliable results with accuracy approaching that at the coupled-cluster single double triple [CCSD(T)] level. The basis set effect of density functional theory calculation is usually moderate, and triple-ξ quality, e.g., Def2-TZVP, is enough in most cases. In addition, the average values from HF and MP2 method, indicated as (MP2 + HF)/2, are also quite close to those of CCSD(T). [ABSTRACT FROM AUTHOR]