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Catalysts · 2021 ·Vol. 11 ·期 10 ·1158 · IF 4.146

Immobilization of Fusarium solani Cutinase onto Magnetic Genipin-Crosslinked Chitosan Beads

Zhanyong Wang,Tingting Su,Jingjing Zhao

Genipin was used as a crosslinking agent to prepare magnetic genipin-crosslinked chitosan beads, which were then used as a carrier for immobilizing recombinant cutinase fromFusarium solani(FSC) to obtain immobilized FSC. The optimal temperature for the immobilized FSC was 55 °C, which was 5 °C higher than that of the free enzyme, whereas its optimal pH was increased from 8.0 to 9.0; this indicates that the immobilized FSC had improved pH and thermal stability. After repeated use for 10 cycles, the activity of the immobilized FSC remained at more than 50%; after being stored at 4 °C for 30 days, its activity was still approximately 88%. We also found that the Km of the immobilized FSC was higher than that of the free enzyme. These results indicate that the performance of FSC was improved after immobilization, which is an important basis for the subsequent application of FSC in industrial production.Keywords:immobilization;cutinase;chitosan;genipin

研究领域: 生物技术 · 酶学 · 材料科学
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PEST MANAGEMENT SCIENCE · 2024 · IF 3.8

Synthesis of paeonol hydrazone derivatives and their anti-oomycete, anti-fungal, and nematicidal activities

Mei Hu,Xiaolong Guo,Yuee Tian,Yan Li,Yibo Liu,Xiaobo Huang,Genqiang Chen,Zhiping Che

BACKGROUND The natural product paeonol is a rich and sustainable natural bioresource, and its derivatives have various unique biological efficacy. As is well known, Schiff bases are a class of organic compounds with a wide range of biological activities, including anti-fungal, insecticidal, anti-viral, and nematicidal. RESULTS To discover biorational natural product-based pesticides, nine intermediates (2–10), 12 sulfonylhydrazones (11a–11c, 12a–12c, 13a–13c, and 14a–14c) and 20 benzylidene hydrazones (18a–18r, 19a, and 20a) were synthesized by structural modification of paeonol, and their structures were characterized by proton nuclear magnetic resonance ( 1 H NMR), carbon-13 ( 13 C) NMR, and high-resolution mass spectrometry (HRMS). The stereochemical configurations of compounds 14a, 18d, and 18r were unambiguously confirmed by single-crystal X-ray diffraction. Furthermore, bioactivities of these compounds as anti-oomycete, anti-fungal, and nematicidal agents against three serious agricultural pests, Phytophthora capsici , Fusarium graminearum , and Heterodera glycines were evaluated. Among all tested compounds: (i) compound 7 exhibited promising anti-oomycete against Phytophthora capsici , with a half maximal effective concentration (EC 50 ) value of 15.81 mg L −1 ; (ii) compounds 2, 7, 10, and 19a displayed promising anti-fungal against F. graminearum , with EC 50 values of 12.22, 14.72, 23.39, and 33.10 mg L −1 , respectively; (iii) ten compounds (12a–12c, 14c, 18g–18j, 18m, and 19a) showed significant nematicidal activity against H. glycines , with median lethal concentration (LC 50 ) values all less than 30.00 mg L −1 . Especially for compound 18g, its LC 50 value is the smallest, at 12.65 mg L −1 . CONCLUSION The research results indicate that introducing nitro groups at the C5 position of paeonol, or introducing halogens at both C5 and C3 positions, can significantly enhance its biological activity against Phytophthora capsici , F. graminearum , and H. glycines . © 2024 Society of Chemical Industry.

研究领域: 植物化学 · 农药科学 · 生物活性研究
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INTERNATIONAL JOURNAL OF PHARMACEUTICS · 2024 · IF 5.3

Encapsulation of thyme essential oil in dendritic mesoporous silica nanoparticles: Enhanced antimycotic properties and ROS-mediated inhibition mechanism

Liyuan Yu,Jianqin Peng,Qun Han,Wanxin Huang,Yijie Jiang,Yongming Ruan,Xia Liu,Gesmi Milcovich,Xuexiang Weng

Dendritic mesoporous silica nanoparticles (DMSNs) have emerged as promising nanocarriers due to their unique three-dimensional structure and tunable pore characteristics. This study investigates the potential of DMSNs to deliver thyme essential oil (TEO) for enhanced antifungal activity against Fusarium oxysporum (F. oxysporum), a major plant pathogen. DMSNs were successfully synthesized and characterized, followed by the encapsulation of TEO within their porous structure. The resulting TEO@DMSNs composites exhibited significant antifungal activity against F. oxysporum, with inhibition rates reaching 70%, indicating an effective crop protection with a dose-dependent effect. The enhanced antifungal efficacy of TEO@DMSNs compared to free TEO is attributed to the sustained release of TEO and the synergistic effect of the nanocarrier itself. In-depth mechanism investigations revealed that TEO@DMSNs likely disrupted the fungal cell membrane, leading to leakage of cellular contents and ultimately cell death. Moreover, DMSNs and TEO@DMSNs were found to be safe for plant growth, demonstrating their potential as environmentally friendly antifungal agents. This study provides valuable insights into the design and development of advanced nanocarriers for targeted drug delivery and disease management in agriculture.

CAS / MDL: 141-78-6 102-71-6
研究领域: 农业科学 · 纳米生物学 · 植物病理学
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Scientific Reports · 2016 ·Vol. 6 ·期 1 ·1-10 · IF 5.228

Regiospecific synthesis of prenylated flavonoids by a prenyltransferase cloned from Fusarium oxysporum

Yang Xiaoman,Yang Jiali,Jiang Yueming,Yang Hongshun,Yun Ze,Rong Weiliang,Yang Bao

Due to their impressive pharmaceutical activities and safety, prenylated flavonoids have a high potent to be applied as medicines and nutraceuticals. Biocatalysis is an effective technique to synthesize prenylated flavonoids. The major concern of this technique is that the microbe-derived prenyltransferases usually have poor regiospecificity and generate multiple prenylated products. In this work, a highly regiospecific prenyltransferase (FoPT1) was found from Fusarium oxysporum . It could recognize apigenin, naringenin, genistein, dihydrogenistein, kampferol, luteolin and hesperetin as substrates and only 6- C -prenylated flavonoids were detected as the products. The catalytic efficiency of FoPT1 on flavonoids was in a decreasing order with hesperetin >naringenin >apigenin >genistein >luteolin >dihydrogenistein >kaempferol. Chalcones, flavanols and stilbenes were not active when acting as the substrates. 5,7-Dihydroxy and 4-carbonyl groups of flavonid were required for the catalysis. 2,3-Alkenyl was beneficial to the catalysis whereas 3-hydroxy impaired the prenylation reaction. Docking studies simulated the prenyl transfer reaction of FoPT1. E186 was involved in the formation of prenyl carbonium ion. E98, F89, F182, Y197 and E246 positioned apigenin for catalysis.

研究领域: 生物化学 · 药理学 · 生物技术
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INDUSTRIAL CROPS AND PRODUCTS · 2025 · IF 6.2

High foliar adhesion carvacrol-chitosan nanoparticles assist cotton against Fusarium oxysporum infection

Jing Zhou,Rourou Wang,Ming Niu,Zhenghua Zhang,Minrui Zhu,Lumei Pu,Weibing Xu,Runtian Ma

The infection caused by Fusarium oxysporum severely threatens cotton production. Herein, carvacrol-chitosan nanoparticles (CS@CAR) are facilely fabricated using tripolyphosphate as a crosslinker. When the initial mass ratio of chitosan to carvacrol is 1:0.4, the nanoparticles show the best stability and drug loading. Morphological analysis reveals that the CS@CAR nanoparticles possesses a uniform spherical structure with an average diameter of approximately 150 nm. About 51.23 % of total CAR is released within the 48 h in the simulated fungal infection environment. The contact angle of drug-loaded particles decreases by 12.2 and 6.6 ° compares with that of pure water and unloaded particles. The fluorescence intensity of leaves before and after rain erosion is 1.3 times and 1.2 times that of the pure water control group by fluorescence imaging analysis. The bacteriostatic activity of drug-loaded nanoparticles is 6–7 times that of non-drug-loaded nanoparticles. The contents of nucleic acid, protein, and malondialdehyde leaked by spores after treatment with drug-loaded particles are 1.4, 1.5 and 2.3 times those in the non-drug-loaded particle treatment group, respectively. The CS@CAR entirely prevents Fusarium oxysporum from infecting cotton leaves in spore inoculation experiments. The CS@CAR nanoparticles are expected to be used to prevent and control the infection of Fusarium oxysporum on cotton.

CAS / MDL: 499-75-2 9012-76-4
研究领域: 植物病理学 · 纳米生物学
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JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY · 2023 · IF 6.1

Degradation of α-Subunits, Doa1 and Doa4, are Critical for Growth, Development, Programmed Cell Death Events, Stress Responses, and Pathogenicity in the Watermelon Fusarium Wilt Fungus Fusarium oxysporum f. sp. niveum

Muhammad Noman,Azizullah,Temoor Ahmed,Yizhou Gao,Hui Wang,Xiaohui Xiong,Jiajing Wang,Jiajun Lou,Dayong Li,Fengming Song

The ubiquitin–proteasome system (UPS) regulates protein quality or control and plays essential roles in several biological and biochemical processes in fungi. Here, we present the characterization of two UPS components, FonDoa1 and FonDoa4, in watermelon Fusarium wilt fungus, Fusarium oxysporum f. sp. niveum (Fon), and their biological functions. FonDoa1 localizes in both the nucleus and cytoplasm, while FonDoa4 is predominantly present in the cytoplasm. Both genes show higher expression in germinating macroconidia at 12 h. Deletion of FonDoa1 or FonDoa4 affects vegetative growth, conidiation, conidial germination/morphology, apoptosis, and responses to environmental stressors. FonDoa1, but not FonDoa4, positively regulates autophagy. The targeted disruption mutants exhibit significantly attenuated pathogenicity on watermelon due to defects in the infection process and invasive fungal growth. Further results indicate that the WD40, PFU, and PUL domains are essential for the function of FonDoa1 in Fon pathogenicity and environmental stress responses. These findings demonstrate the previously uncharacterized biological functions of FonDoa1 and FonDoa4 in phytopathogenic fungi, providing potential targets for developing strategies to control watermelon Fusarium wilt.

CAS / MDL: 4602-84-0
研究领域: 真菌学 · 植物病理学 · 分子生物学
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PLoS One · 2026 ·Vol. 21 ·期 5 ·e0339014 · IF 2.8

Physiologic and molecular response of Fusarium oxysporum f. sp. zingiberi to ginger autotoxins

Yan Zhang,Hongshen Guo,Yanping Xu,Xiaochuan Chen,Miaomiao Zhang,Naicheng Li,Abdullah Gera

Long-term monoculture of ginger triggers Fusarium wilt, a disease caused by Fusarium oxysporum f. sp. zingiberi ( Foz ). However, the interaction between autotoxins and pathogens remains poorly understood. This study examined the allelopathic effects of four autotoxins, syringic acid, coumarin, ferulic acid, and 7-hydroxycoumarin, on the growth, reproduction, and virulence traits of Foz . These compounds were previously identified as inhibitors of ginger growth and enzyme activity. The results revealed that the responses of Foz varied, likely because of the structural differences among the autotoxins. Syringic acid significantly inhibited mycelial growth, sporulation, and spore germination, while markedly enhancing the activity of cell wall-degrading enzymes and mycotoxin synthesis, as evidenced by the upregulation of FUB3 and FUB9 . Coumarin demonstrated a pronounced inhibitory effect on biomass production while concurrently stimulating sporulation and mycotoxin synthesis, as indicated by the upregulation of FUB6 and FUB9 . Ferulic acid treatment reduced the activity of cell wall-degrading enzymes and spore germination, while upregulating sporulation and mycotoxin synthesis. A similar pattern was observed with 7-hydroxycoumarin, which exerted a strong inhibitory effect on mycelial growth, biomass production, mycotoxin synthesis, and FUB gene cluster expression, except for FUB1 and FUB3 expression. In conclusion, four autotoxins exhibited diverse defensive roles against Fusarium wilt, whereas the pathogen enhanced its pathogenicity to counter host regulations. This study provides the first evidence of an interaction between ginger autotoxins and Foz .

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Microorganisms · 2025 ·Vol. 13 ·期 6 ·1423 · IF 4.2

Cepharanthine Inhibits Fusarium solani via Oxidative Stress and CFEM Domain-Containing Protein Targeting

Yuqing Wang,Zenghui Yang,Jingwen Xue,Yitong Wang,Haibo Li,Zhihong Wu,Yizhou Gao

Cepharanthine (CEP) is a natural bisbenzylisoquinoline alkaloid known for its antibacterial, antiviral, and anti-inflammatory activities. Its antifungal effect, however, has not been well studied. In this work, we used machine learning-based virtual screening with Random Forest, Neural Network, and Support Vector Machine models to identify potential inhibitors ofFusarium solani. CEP was selected as a candidate and tested experimentally. The results showed that it inhibited the growth ofFusarium solani,Fusarium proliferatum,Fusarium oxysporum,Alternaria alternata, andBotrytis cinerea. It also reduced the sporulation and spore germination ofFusarium solaniand disrupted its redox balance. Transcriptome analysis showed changes in gene expression related to basic metabolic pathways. Molecular docking suggested that CEP binds to the FsCFEM1 protein, and molecular dynamics simulations confirmed stable binding, with key roles for residues THR748 and LEU950. These results suggest that CEP is a potential bio-based antifungal agent and provide novel insights into its mechanism againstFusarium solani.

CAS / MDL: 100-10-7
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PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY · 2025 · IF 4

Thyme essential oil-based nano-fungicide for managing Fusarium wilt in Anoectochilus roxburghii

Xia Liu,Wanxin Huang,Zifeng Zhu,Liyuan Yu,Yiru Chen,Yihui Bai,Xuexiang Weng,Yongming Ruan

This study develops a thyme essential oil (TEO)-based bio-fungicide, encapsulated in amino-functionalized mesoporous silica nanoparticles (AMSNs), and evaluates its antifungal efficacy. In vitro , the TEO@AMSNs formulation demonstrated 93.23 % mycelial growth inhibition at 3.84 mg/mL, outperformed free TEO (67.77 % inhibition), with a 13.44 % loading rate. Mechanistic studies indicated that this efficacy results from continuous and strong membrane disruption and high reactive oxygen species (ROS) overaccumulation in fungal cells. Density functional theory (DFT) calculations confirmed that the stable release profiles was driven by hydrogen bonding interactions between the AMSNs carrier and the essential oil. In vivo trials on Anoectochilus roxburghii (A. roxburghii) , a medicinal crop susceptible to F. oxysporum , showed that TEO@AMSNs significantly reduced disease symptoms and promoted root development. Inoculated plants treated with TEO@AMSNs at 2 MIC exhibited nearly normal lateral root counts (∼42) compared to 23 in untreated controls. Microscopic analyses revealed intact chloroplasts and preserved polysaccharide levels in treated plants, suggesting reduced oxidative stress and metabolic disruption. Flavonoid accumulation was also enhanced, further supporting the formulation's role in mitigating pathogen-induced stress. These findings highlight TEO@AMSNs as a promising, sustainable bio-fungicide for managing Fusarium infections and enhancing crop resilience.

CAS / MDL: 1336-21-6 141-78-6
研究领域: 植物病理学 · 纳米技术 · 农学 · 精油研究 · 可持续农业
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REACTIVE & FUNCTIONAL POLYMERS · 2022 · IF 4.966

Fluorine-containing amphiphilic quaternary ammonium salts for the suppression of Banana fusarium wilt

Yaling Lin,Deqiang Zhang,Shijie Shan,Wei Zhang,Rui Li,Anqiang Zhang

As the pathogen of banana Fusarium wilt, Fusarium oxysporum f . sp. cubense race 4 (Foc4) has the strongest toxicity and pathogenicity due to its long-term viability in soil, but there is still no effective way to control it at present. Based on the activity parameters of polymeric quaternary ammonium salt in our previous work, this paper hopes to enhance the amphiphilicity of polymeric quaternary ammonium salt by introducing a fluoroalkyl group to improve the antifungal property of polymeric quaternary ammonium salt and achieve stable adsorption and long-term inhibition of saprophytic Foc4 conidia in soil. Here, we prepared a series of fluorine-containing ammonium salts with random and block structures by atom transfer radical polymerization (ATRP), and we systematically studied the effects of the introduction of fluoroalkyl groups, the proportion of hydrophobic segments and polymer structure on micelle properties, antifungal properties, adsorption, migration and long-term antifungal properties against Foc4 in soil. Finally, the preferred polymeric quaternary ammonium salts were selected for pot experiments in the prevention and control of banana Fusarium wilt caused by Foc4, and positive experimental results were achieved. In conclusion, we made an exploratory attempt at the practical application of polymeric amphiphilic quaternary ammonium salt in plant disease control.

研究领域: 植物病理学 · 农业化学
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APPLIED AND ENVIRONMENTAL MICROBIOLOGY · 2023 ·Vol. 89 ·期 3 · IF 4.4

A Fungal P450 Enzyme from Fusarium graminearum with Unique 12β-Steroid Hydroxylation Activity

Ling Wang,Xiaowei Wu,Chenghua Gao,Lingrui Wei,Qian Li,Aitao Li

In this study, a new cytochrome P450 enzyme, namely, CYP68J5_Fusarium graminearum (CYP68J5_fg), was identified from Fusarium graminearum via a combination of transcriptome sequencing and heterologous expression in Saccharomyces cerevisiae. The biotransformation of progesterone by whole-cells of S. cerevisiae expressing CYP68J5_fg revealed that the CYP68J5_fg possessed steroidal 12β- and 15α-hydroxylase activities. To the best of our knowledge, this is the first time that a fungal P450 enzyme with 12β-hydroxylase activity has been identified. This advance offers opportunities to boost the efficiency and selectivity of the CYP68J5_fg hydroxylating system and thus shows great potential for further applications of this enzyme for the synthesis of steroid drugs.IMPORTANCE Regioselective and stereoselective hydroxylation is of vital importance in the functionalization of steroids, which remains challenging in organic synthesis. In particular, the C12-hydroxy steroids play a significant role in the synthesis of many important steroidal drugs. In this study, a novel fungal P450 enzyme with 12β-hydroxylation activity was identified, and it shows different substrate specificity and regioselectivity, compared to the bacterial and fungal steroidal hydroxylases that are known to date. This lays the foundation for the creation of effective biocatalysts for the process of 12β-hydroxylation, although further understanding of the molecular structural basis of this fungal P450 is needed to facilitate the engineering of this enzyme for industrial applications.

CAS / MDL: 57-83-0
研究领域: 生物化学 · 酶学 · 药学 · 微生物学
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Microorganisms · 2023 ·Vol. 11 ·期 12 ·2954 · IF 4.5

Effects of 2-Phenylethanol on Controlling the Development of Fusarium graminearum in Wheat

Shufang Sun,Nawen Tang,Kun Han,Qunqing Wang,Qian Xu

Applying plant-derived fungicides is a safe and sustainable way to control wheat scab. In this study, volatile organic compounds (VOCs) of wheat cultivars with and without the resistance geneFhb1were analyzed by GC-MS, and 2-phenylethanol was screened out. The biocontrol function of 2-phenylethanol onFusarium graminearumwas evaluated in vitro and in vivo. Metabolomics analysis indicated that 2-phenylethanol altered the amino acid pathways ofF. graminearum, affecting its normal life activities. Under SEM and TEM observation, the mycelial morphology changed, and the integrity of the cell membrane was destroyed. Furthermore, 2-phenylethanol could inhibit the production of mycotoxins (DON, 3-ADON, 15-ADON) byF. graminearumand reduce grain contamination. This research provides new ideas for green prevention and control of wheat FHB in the field.Keywords:2-phenylethanol;Fusarium graminearum;volatile organic compounds (VOCs);antifungal mechanism;metabolomics

研究领域: 植物病理学 · 农学 · 真菌学
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