Mingxing Zhang

Mingxing Zhang

*This is an algorithmically generated author record based on publicly available information.

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Previous Organizations / Institutes

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Mingxing Zhang has a total of 21 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    OsWRKY76 positively regulates drought stress via OsbHLH148-mediated jasmonate signaling in rice

    by Mingxing Zhang, Ranran Zhao, Kai Huang, Zhiqi Wei, Boya Guo, Shuangzhan Huang, Zhao Li, Wenzhu Jiang, Tao Wu, Xinglin Du

    Drought stress is a major environmental threat that limits plant growth and crop productivity. Therefore, it is necessary to uncover the molecular mechanisms behind drought tolerance in crops. Here, OsWRKY76 positively regulated drought stress in rice. OsWRKY76 expression was induced by PEG treatment, dehydration stress, and exogenous MeJA rather than by no treatment. Notably, OsWRKY76 knockout weakened drought tolerance at the seedling stage and decreased MeJA sensitivity. OsJAZ12 was significantly induced by drought stress, and its expression was significantly higher in OsWRKY76-knockout mutants than in wild-type ZH11 under drought stress. Yeast two-hybrid and bimolecular fluorescence complementation assays showed that OsWRKY76 interacted with OsJAZ12. OsWRKY76 weakened the interaction between OsbHLH148 and OsJAZ12 in yeast cells. The OsJAZ12 protein repressed the transactivation activity of OsbHLH148, and this repression was partly restored by OsWRKY76 in rice protoplasts. Moreover, OsDREB1E expression was lower in OsWRKY76-knockout mutants than in wild-type ZH11 under drought stress, but it was upregulated under normal growth conditions. Yeast one-hybrid, electrophoretic mobility shift, and dual-luciferase assays showed that OsWRKY76 and OsbHLH148 bound directly to the OsDREB1E promoter and activated OsDREB1E expression in response to drought stress. These results suggest that OsWRKY76 confers drought tolerance through OsbHLH148-mediated jasmonate signaling in rice, offering a new clue to uncover the mechanisms behind drought tolerance.


  • Open Access

    Antioxidant, Antimicrobial, Cytotoxic, and Protein Kinase Inhibition Potential inAloe veraL.

    by Huma Tariq, Muhammad Zia, Ihsan- Ul- Haq, Syed Aun Muhammad, Shujaat Ali Khan, Nighat Fatima, Abdul Mannan, Arshad Mehmood Abbasi, Mingxing Zhang

    Aloe verais a multifunctional plant that has gained acceptance as an excellent home remedy source in Asia and the world. The present study was intended to evaluate the phytochemical contents andin vitroantioxidant, antimicrobial, antileishmanial, and protein kinase inhibition activities in different fractions ofA. veraleaf. Methanolic extract ofA. veraleaves was fractionated using column chromatography and ten fractions (AV1-AV10) were obtained. Phenolics composition, antioxidant, antimicrobial, antileishmanial, and protein kinase inhibition activities were evaluated using standard protocols. Well-known compounds ofA. verawere used for in silico study against enzymes involved in brine shrimp and antileishmanial and hyphae formation inhibition assay on the basis of results. Five fractions (AV3 to AV7) possess potential total phenolics and flavonoids contents along with significant biological activities. AV4 fraction exhibited the highest total phenolics content 332.4 ± 32.6μg GAE/mg and total antioxidant activity 150.4 ± 25.815μg AAE/mg determined by phosphomolybdenum complex assay. Fraction AV6 showed 95% antileishmanial effect as well as the lowest LD50value of 0.5305μg/mL in brine shrimp lethality assay. The Protein Kinase inhibition potential inA. veraleaves was determined for the first time and three fractions AV1, AV6, and AV7 depicted activity with the highest zone of inhibition up to 21±0.5mm (AV7). Docking analysis showed thatA. veracontains anthraquinones, anthrones, chromones, and polysaccharides responsible for synergistic cytotoxic, antileishmanial, antibacterial, and antioxidant potential of this plant. Therefore, with more studies,A. veracould probably have the potential to be used for drug development against leishmaniasis.


  • Open Access

    Synthesis and Bioactivity of Novel Coumarin Derivatives

    by Ai-Ying Guan, Chang-Ling Liu, Zhi-Nian Li Miao Li, Ming-Xing Zhang, Hong Zhang

    A series of coumarin derivatives (6-8) containing ( E)-methyl 2-(methoxyimino)-2-phenylacetate, ( E)-2-(methoxyimino )-N-methyl-2-phenylacetamide and methyl methoxy(phenyl)carbamate were synthesized from substituted resorcinols (1) and substituted β-keto esters (2) as starting material via cyclization and condensation reactions. The test results indicated that ( E)-methyl 2-{2-[(3-hexyl-4-methyl-coumarin-7-yloxy)methyl]phenyl}-2-(methoxyimino)acetate (6f) was the optimal structure with good fungicidal activity against cucumber grey mold (CGM) giving 100% control at 100 mg L−1 concentration, much higher than that of coumoxystrobin. Methyl 2-[(3,4-dimethyl-coumarin -7-yloxy)methyl]phenyl(methoxy)carbamate (8a) was another optimal structure with good fungicidal activity against wheat powdery mildew (WPM) showing 100% control at 50 mg L−1 concentration, at the same level as that of the commercial kresoxim-methyl, and very significantly higher than that of coumoxystrobin (no control against WPM at 400 mg L−1).