Fungal Strains Research Articles

Morphological and phylogenetic analyses reveal two new species of the Fusarium fujikuroi (Hypocreales, Nectriaceae) species complex in China

The Fusarium fujikuroi species complex (FFSC) encompasses a diverse array of more than 80 phylogenetic species with both phytopathological and clinical importance. A stable taxonomy is crucial for species in the FFSC due to their economical relevance. Fungal strains used in this study were obtained from Castanea mollissima and Rubus lambertianus, collected from Beijing and Shaanxi Province. We employ morphological and phylogenetic analyses based on partial gene fragments of the translation elongation factor 1-alpha (tef1), beta-tubulin (tub2), calmodulin (CaM), RNA polymerase largest subunit (rpb1), and RNA polymerase II second largest subunit (rpb2), as well as the pairwise homoplasy index tests. Studies have shown that these phylospecies are clustered in the Asian clade of the FFSC. The present study delineates two novel Fusarium species within the FFSC, named F. castaneophilum and F. rubicola, complemented by illustrations and descriptions.

Design and development of pyrazol-5-ylbenzamide derivatives containing chiral oxazoline moiety as fungicides based on molecular docking.

Development of novel chiral antifungal agents for effective control of plant pathogens is urgently needed. In this study, a series of pyrazol-5-yl-benzamide derivatives containing chiral oxazoline moiety were rationally designed and developed based on molecular docking. The in vitro antifungal assay results indicated that compounds (rac)-4h (R1 = Et), (S)-4 h (R1 = S-Et) and (R)-4 h (R1 = R-Et) exhibited remarkable antifungal activities against Valsa mali with median effective concentration (EC50) values of 0.24, 0.06 and 1.08 mg/L, respectively. Preliminary structure-activity relationships (SARs) revealed that the modification of the chiral substituent group at the oxazoline moiety significantly affected the antifungal activities of the target compounds. Furthermore, compounds (S)-4h (87.5%) and (R)-4h (84.3%) exhibited in vivo protective activities comparable to tebuconazole (87.5%) against V. mali. Subsequent molecular docking analysis, succinate dehydrogenase (SDH) enzyme inhibition assays and molecular dynamic (MD) simulations verified that the potential target enzyme of this class of derivatives could be SDH and helped to explain the large difference in antifungal activities of compounds (S)-4h and (R)-4h. Confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM) observations confirmed that these two compounds severely disrupted the mycelial morphology of V. mali. Theoretical calculation studies provided some insight into the subsequent modification of such pyrazol-5-yl-benzamide derivatives. Resistance frequency studies showed that (S)-4h and (R)-4h treatments were less likely to produce resistant fungal strains than tebuconazole. Meanwhile, compounds (S)-4h and (R)-4h exhibited no apparent toxicity to the Apis mellifera L. Therefore, these derivatives are potential candidates for the development of novel chiral fungicides for crop protection. © 2025 Society of Chemical Industry.

New Evidence for Cotinus coggygria Scop. Extracts Application in Gastrointestinal Ailments

Background/Objectives: Cotinus coggygria Scop. is traditionally used for treatment of various gastrointestinal ailments. In this study, we investigated the phytochemical profile and biological activities of leaves, bark and flowers extracts of C. coggygria. Methods: Phytochemical analysis was performed using HPLC. The antimicrobial activity of water and methanolic extracts of C. coggygria leaves, bark and flowers towards various oral fungal and bacterial strains of clinical origin was tested by use of a microdilution assay. Additionally, their cytotoxic activity was determined against different gastrointestinal carcinoma cell lines (CAL27, FaDu, SW480, HCT116 and MRC-5) in concentrations ranging from 3.125 to 400 µg/mL for 48 and 72 h. Results: The presence of numerous flavonoid and phenolic compounds such as sulfuretin, gallic acid, rutin, hyperoside, and isoquercitrine was detected. Micrococcus luteus, Streptococcus parasanguinis, and Candida tropicalis were the most sensitive microbiological species, with MICs of 0.12 mg/mL for the most effective extracts. Additionally, the cytotoxic activity of the samples against different gastrointestinal carcinoma cell lines (CAL27, FaDu, SW480, HCT116, and MRC-5) was determined in concentrations ranging from 3.125 to 400 µg/mL. Among the tested samples, the methanolic leaf extract exhibited the highest cytotoxic capacity, and the possible mechanism could be related to its inhibitory effect on the release of proinflammatory cytokine in CD4+ cells. Conclusions: The traditional use of C. coggygria for gastrointestinal diseases may be substantiated by its ability to inhibit the growth of harmful microorganisms and its promising cytotoxic properties. The methanolic leaf and flower extracts show significant potential for future clinical applications, and further studies are warranted to explore their mechanisms and applications in medical treatments.

Toward an Efficient Differentiation of Two Diaporthe Strains Through Mass Spectrometry for Fungal Biotyping

Considering that fungi display a great morphological, ecological, metabolic, and phylogenetic diversity, their taxonomic identification is extremely important because it helps us establish important information about each species and its possible biochemical and ecological roles. Traditionally, the identification of fungi at the species level has been carried out with molecular tools such as DNA sequencing, but it still represents a huge challenge today due to the heterogeneity of the fungal kingdom, making the task of identification a complex and difficult process. Biotyping, a type of chemotaxonomy, has been developed in the field of the identification/differentiation and classification of micro-fungi through tools such as mass spectrometry (MS). Here, two endophytic strains isolated from two different hosts were cultivated and studied regarding their morphology and molecular biology. Morphology analysis determined the strains as Diaporthe, and the molecular analysis results grouped them as D. melongenae. We sought a faster and less complex way of differentiating these fungal strains of interest through an MS chemical profile and MS/MS data using a low-resolution mass spectrometer. Additionally, we linked this information with the structure of compounds previously isolated in the genus Diaporthe. Studies conducted using this technique allowed us to propose the structure of distinctive molecules that are unique to each strain and share compounds common to this genus (13 compounds in total). In addition, this is the first report of secondary metabolites in D. melongenae. The dataset demonstrates that the two strains under investigation can be distinguished via mass spectrometry, suggesting host affinity; both exhibits pronounced differences in their chemical profiles across all culture media and incubation periods with the parameters described herein.

Anti-Neuroinflammatory Effects of Prenylated Indole Alkaloids from the Antarctic Fungus Aspergillus sp. Strain SF-7367

Inflammation has always been considered a trigger or consequence of neurodegenerative diseases, and the inhibition of inflammation in the central nervous system can effectively protect nerve cells. Several studies have indicated that various natural products inhibit neuroinflammation. Among these, Antarctic fungal metabolites have pharmacological activities and a developmental value. Therefore, this study aimed to evaluate the anti-neuroinflammatory activity of an Antarctic fungus belonging to Aspergillus (strain SF-7367). Secondary metabolites of SF-7367 were isolated using high-performance liquid chromatography followed by validation of their anti-inflammatory effects in lipopolysaccharide-stimulated BV2 microglia and RAW264.7 macrophages. Chemical analysis of metabolites from the fungal strain revealed five known compounds: epideoxybrevianamide E (1), brevianamide V/W (2), brevianamide K (3), brevianamide Q (4), and brevianamide R (5). Among these compounds, brevianamide K showed significant anti-inflammatory activity against both cell types. Results of Western blotting and molecular docking showed that brevianamide K could regulate the activation of nuclear factor kappa-light-chain-enhancer of activated B cell (NF-κB) signaling. This indicates that brevianamide K present in Aspergillus sp. (strain SF-7367) can inhibit inflammatory responses by reducing lipopolysaccharide-induced nuclear translocation of NF-κB (p65). These findings suggest that Aspergillus sp. (strain SF-7367) and brevianamide K are candidate agents for treating neurodegenerative diseases.

Pharmacognistic, proximate and phytochemical analysis of stem of Cistanche tubulosa (Schenck) Hook. F.

A medicinal plant is any plant that in one or more of its organs contains substances that can be used by it or their constituent for therapeutic purposes. The present work was done to evaluate pharmacognostic, fluorescence, proximate and phytochemical analysis of ethanolic extracts of Cistanche tubulosa (Orobanchaceae) along with antimicrobial activity. Antimicrobial activity against four bacterial strains S. aureus, E. coli, P. aeruginosa, S. typhi along with five fungal strains such as F. oxyfurum, P. notatum, Candida albicans, A. fumigatus, and A. niger evaluate using agar well diffusion method. The powder drug study of various tissues of plants revealed higher concentrations (20.29 mg/l) of essential macro and micronutrients. Fluorescence analysis of the stem powdered with various chemical reagents showed different colors. Proximate analysis showed the presence of crude substances such as proteins (8.5 %), fat (1.5 %), fibres (6.6 %), carbohydrates (73.87 %), moisture contents (3.23 %) and ash contents (6.3 %) respectively. Phytochemical screening revealed the presence of carbohydrates, proteins and dozen other important secondary metabolites. The presence of these bioactive constituents associated with the antimicrobial activity of S. aureus showed the maximum zone of inhibition (15.1 ± 3.7 mm), while in antifungal activity C. albicans showed the highest zone of inhibition (11.0 ± 3.15 mm). The pharmacognostic study, fluorescence analysis and antimicrobial activity are helpful in the standardization of the drug establishing a good support for the use of C. tubulosa in traditional medicine.

Study of the Antagonism of Biocontrol Strains Against the Blue-Stain Fungus of Rubberwood

Wood blue staining is one of the most common wood defects, which commonly occurs in rubberwood and Masson pine. It not only affects the appearance of the wood, but also its properties. In this study, rubberwood from Xishuangbanna was examined. During the process, blue-stain fungi and endophytic fungi were isolated and identified. The antagonism of biocontrol strains against blue-stain fungi was studied, and their inhibitory effects were evaluated by inoculating the biocontrol strains on non-blue-stained rubberwood. The morphology and distribution of the strains on the wood were observed using polarized light and fluorescence microscopy, infrared spectroscopy, scanning electron microscopy (SEM–EDS), and X-ray diffraction (XRD). The effects of biocontrol strains on the blue stain of the wood were then evaluated. The results showed that at room temperature, the fungus causing the blue stain in rubberwood was identified as Lasiodiplodia theobromae, and the biocontrol strains of endophytic fungi isolated were Trichoderma koningii and Trichoderma reesei. It was found that T. reesei was more effective than T. koningii in inhibiting the development of L. theobromae. Based on these findings, T. reesei was suggested as a biocontrol strain for preventing and controlling blue stain in rubberwood.

Bioprocess development for microbial production and purification of cellobiose lipids by the smut fungus Ustilago maydis DSM 4500.

Cellobiose lipids (CBLs) are a class of glycolipid biosurfactants produced by various fungal strains. These compounds have gained significant interest due to their surface-active and antifungal properties, which are comparable to traditional synthetic surfactants and antimicrobials. Despite their potential applicability in various cosmetic, pharmaceutical, and agricultural formulations, significantly less research has been focused on their production and purification in comparison to other glycolipid biosurfactants, such as mannosylerythritol lipids (MELs) and sophorolipids. Hence, this work proposes the development of a bioprocess that involves the microbial production and high-level chromatographic purification of CBLs from a submerged culture of Ustilago maydis DSM 4500. After a highly purified CBL product was obtained, the factors affecting the production of this glycolipid were investigated. It was demonstrated that U. maydis DSM 4500 produces a specific structural variant of CBLs at a concentration of 1.36g/L on an optimized the growth medium. Also, it was established that when the C/N ratio was decreased, the CBL titer increased by 2.3-fold. Furthermore, supplementing the culture with ZnSO4 at a concentration of 0.04mg/L further increased CBL concentration to 4.95g/L, representing the highest CBL titer achieved in a single-stage bioprocess to date. This study developed a methodology for utilizing U. maydis as a high-level CBL producer, which could challenge other familiar CBL producers, such as Sporisorium scitamineum and Cryptococcus humicola.

Impact of Fungal Symbionts of Co-occurring Orchids on the Seed Germination of Serapias orientalis and Spiranthes spiralis.

Interactions with mycorrhizal fungi are increasingly recognized as crucial ecological factors influencing orchids' distribution and local abundance. While some orchid species interact with multiple fungal partners, others show selectivity in their mycorrhizal associations. Additionally, orchids that share the same habitat often form relationships with different fungal partners, possibly to reduce competition and ensure stable coexistence. However, the direct impact of variations in mycorrhizal partners on seed germination remains largely unknown.We examined how fungal associates' specific identity and originaffect seed germination in Spiranthes spiralis and Serapias orientalis through in situ symbiotic germination experiments. A total of four fungal isolates, Tulasnellaceae and Ceratobasidiaceae were successfully isolated and cultured from S. spiralis and S. orientalis and two additional orchid species found in the same habitat: Neotinea tridentata and Orchis provincialis. While all fungal strains facilitated the swelling of seed embryos, only the fungal associate, a member of the Ceratobasidiaceae family isolated from N. tridentata, (NT2)was capable of inducing protocorm formation and subsequent seedling growth of S. spiralis seeds. Another fungal associate belonging to the Tulasnellaceae family and isolated from O. provincialis (OP3)supported seed germination up to the seedling stage of S. orientalis seeds. However, the remaining two fungal strains did not support seed germination. We conclude that fungal associates of co-occurring orchids can promote seed germination and seedling growth in S. spiralis and S. orientalis.

Conversion of Lignocellulosic Biomass Into Valuable Feed for Ruminants Using White Rot Fungi.

White rot fungi can degrade lignin and improve the nutritional value of highly lignified biomass for ruminants. We screened for excellent fungi-biomass combinations by investigating the improvement of digestibility of wheat straw, barley straw, oat straw, rapeseed straw, miscanthus, new reed, spent reed from thatched roofs, and cocoa shells after colonisation by Ceriporiopsis subvermispora (CS), Lentinula edodes (LE), and Pleurotus eryngii (PE) (indicated by increased in vitro gas production [IVGP]). First, growth was evaluated for three fungi on all types of biomass, over a period of 17 days in race tubes. CS grew faster than LE and PE on all types of biomass. LE did not grow on cocoa shells, while growth rate of CS and PE on cocoa shells was lower compared to other types of biomass. After this first screening, all types of biomass, excluding the cocoa shells, were colonised by the three fungal strains for 8 weeks. Treatment with CS and LE improved IVGP more than treatment with PE. Methane production was reduced in six combinations of biomass with CS, four with LE, and three with PE. Six types of biomass were selected for treatment with CS and four were selected for treatment with CS and LE, to determine the net improvement of nutritional value (increased IVGP corrected for dry matter loss) after 2, 4, 6, 7 and 8 weeks of treatment. The highest net improvement was found for CS and LE treated rapeseed straw (86% and 20%, respectively) and spent reed (80% and 43%, respectively). All treatments decreased dry matter, lignin and hemicellulose, the latter two both in absolute amount and content. In conclusion, net improvement of highly lignified biomasses by CS was greater than LE, with the nutritional value of rapeseed straw and spent reed being significantly improved by both fungi.

Synthesis and anti-microbial evaluation with in silico studies of novel 2-aminothiazole benzohydrazide derivatives

BackgroundThe development of novel anti-microbial drugs for multidrug-resistant (MDR) is a significant challenge. This study aimed to synthesize various derivatives of (Z)-4-(2-aminothiazol-5-yl)-N-benzohydrazide (DT01-DT10) that are effective against a wide variety of anti-bacterial and antifungal pathogens.ResultsThe binding energy of the compounds ranged from − 9.0 to − 10.0 kcal/mol. Molecular simulations produced a major result in improving the representation of the real biological conditions with an average RMSD of 0.110 nm. The derivatives DT03, DT04, and DT06 showed overall good anti-microbial activity at lower concentrations of 1.8 µg/ml. Compound DT03 showed significant activity against Gram-positive, Gram-negative bacteria and fungal strains, with inhibition zone diameters of 17, 19 and 16 mm, respectively. Compound DT04 showed promising anti-bacterial effects against S.mutans and C.albicans, with inhibition zone diameters of 18 and 17 mm, and moderate activity against B. cereus. Compound DT06 showed enhanced activity against P.aeruginosa.ConclusionThe derivative 4-(2-amino-1,3-thiazol-5-yl)-N′-(Z)-(2-nitrophenyl) methylidene benzohydrazide (DT06), which contained a nitro group displayed potent activity at 1.8 µg/ml with an IC50 of 50.31 and a selectivity index of 61.33.Graphical abstract

Pseudocercospora fengxinensis, a new species causing sooty spot of kiwifruit in China.

Pseudocercospora is a large cosmopolitan genus of plant pathogenic fungi that are commonly associated with leaf and fruit spots as well as blights on a wide range of plant hosts. P. actinidiae is a member of this genus, causing sooty spot on kiwifruit worldwide. With the expansion of kiwifruit cultivation, the incidence of sooty spot has become severe in Fengxin County, Jiangxi Province, China. Based on a survey conducted in 2022 across nine kiwifruit cultivars in six local orchards, the results showed that the disease incidence was higher in 'Donghong', 'Jinyan', 'Jinkui', 'Fenghuang No. 1' and 'Jinguo'. In contrast, it was lower in 'Gold3' and 'Hongshi No. 2'. No lesions were observed on 'Kuilv' and 'Miliang No. 1'. 31 fungal strains were isolated from infected leaves using single-spore isolation. Phylogenetic analysis of combined sequence data from the internal transcribed spacer region of ribosomal DNA (ITS), partial actin (actA), translation elongation factor 1-alpha (tef1), and the second largest subunit of RNA polymerase II (rpb2) sequence data, using maximum-likelihood (ML) and Bayesian inference (BI), revealed their taxonomic placement within Pseudocercospora. Both morphological and molecular phylogenetic analysis supported Pseudocercospora fengxinensis as a new taxon within Pseudocercospora. Pathogenicity tests confirmed P. fengxinensis as the causal agent of sooty spot on kiwifruit. This study is the first report of P. fengxinensis causing sooty spot of kiwifruit worldwide, enriching our understanding of Pseudocercospora diversity in China and providing a foundation for improved disease management strategies.

Recent Developments in Azetidinone-Azole Conjugates: Emerging Antimicrobial Potentials.

The emergence of multidrug-resistant microbial strains poses a significant challenge to global public health. In response, researchers have been exploring innovative antimicrobial agents with enhanced efficacy and novel mechanisms of action. One promising approach involves the synthesis of hybrid molecules combining azetidinone and azole moieties, capitalizing on the respective antimicrobial properties of both structural elements. Natural and synthetic azetidinone derivatives hold a prominent position among medicinally significant compounds due to their varied and potent antibiotic activities. Interest persists in discovering new synthetic methods and refining existing ones, as well as applying these methods to create novel, biologically active azetidinone derivatives. Additionally, azoles are highly regarded in pharmaceuticals for their broad efficacy, tolerability, and oral availability. By merging these two pharmacophores, researchers aim to create compounds with synergistic or additive antimicrobial effects, potentially overcoming existing resistance mechanisms. Various synthetic strategies, including click chemistry and multicomponent reactions, have been employed to prepare these hybrid molecules efficiently. The antimicrobial potential of azetidinone-azole conjugates has been extensively evaluated against a spectrum of pathogens, including bacteria, fungi, and protozoa. These studies have demonstrated promising results, with several compounds exhibiting potent activity against both Gram-positive and Gramnegative bacteria, as well as clinically relevant fungal strains. Furthermore, SAR studies have provided valuable insights into the key structural features governing the antimicrobial properties of these conjugates, facilitating further optimization and rational design. In conclusion, the development of azetidinone-azole hybrids represents a promising avenue in the quest for novel antimicrobial agents. This study presents a comprehensive overview of recent advancements in synthesis and antimicrobial evaluation of azetidinone-azole conjugates.

In vitro Investigation of Antimicrobial and Antioxidant Properties of Green Silver Nanoparticles Synthesized Using Ephedra gerardiana Plant Extract.

The increasing prevalence of antibiotic-resistant bacteria necessitates exploring nanotechnology as a potential solution for microbial elimination. This study aimed to investigate the antimicrobial and antioxidant effects of silver nanoparticles synthesized using aqueous extract from the Ephedra gerardiana (E. gerardiana) plant (EG@AgNPs). Optimal synthesis conditions, including silver nitrate concentration, time, and temperature, were determined. Characterization of EG@AgNPs was conducted, which was followed by antimicrobial assessment against eight bacterial strains and one fungal strain. Additionally, the antioxidant properties of EG@AgNPs were evaluated using the DPPH method. XRD analysis confirmed EG@AgNPs synthesis. DLS analysis revealed a hydrodynamic diameter of 22 nm. FT-IR analysis confirmed the presence of functional groups from the E. gerardiana plant extract in EG@AgNPs. FESEM and TEM images depicted spherical nanoparticles ranging in size from 10 to 20 nm. Antimicrobial investigations using the broth microdilution method demonstrated that E. gerardiana plant extract at 7.5 mg/ml inhibited only Streptococcus mutans and Candida albicans growth, with no antimicrobial effects observed at lower concentrations. However, EG@AgNPs significantly enhanced the antimicrobial properties of the E. gerardiana plant extract. Notably, these nanoparticles exhibited the most significant effect on E. coli and the least on S. salivaris, with MIC value of 125 and 2000 μg/ml, respectively. Furthermore, they inhibited C. albicans growth at a concentration of 62.5 μg/ml. An assessment of the antioxidant properties of EG@AgNPs indicated a significant increase in antioxidant activity. The E. gerardiana plant extract has emerged as a promising option for silver nanoparticle synthesis. These nanoparticles have been found to exhibit potent antimicrobial properties against Gram-positive and Gram-negative bacterial species, as well as C. albicans. Additionally, they have demonstrated antioxidant properties.

Antifungal activity of different extractions of drone larvae (apilarnil)

Drone larvae (DL) has many biological activities thanks to the bioactive components it contains, but there are very few studies on its antimicrobial activity. The aim of this research was to determine the antifungal activity of DL (raw and lyophilised) water and ethanol extracts against fluconazole (FLU) sensitive and resistant yeast strains. The 87 fungal strains obtained from clinical samples were identified by phenotypic and molecular methods, and broth microdilution test was used for antifungal activity. All DL extracts had antifungal activity. The ethanolic extract of lyophilised DL showed higher antifungal activity. Total phenolic substance content and antioxidant activity of lyophilised DL ethanolic extract were found to be higher than other extracts. According to these results, the observed antifungal activity of DL extracts can be attributed not only to phenolic components, but also to synergistic effect of phenolic components with other bioactive components it contains.

Polysaccharide biocomposites with tunable adsorption and antipathogen activity via surface immobilization of chitosan onto modified flax fibers

Flax fiber modified composite (FFMC) duplex systems with unique sorbent and antipathogen properties were developed by physisorption of chitosan onto modified flax fibers by a facile method. Complementary characterization of the FFMCs (Raman, NMR, and IR, SEM, XRD, TGA and BET analysis) revealed variable composite morphology with incremental chitosan doping and supramolecular interactions between the fiber substrate and immobilized chitosan. Dye adsorption profiles of FFMCs with Rose Bengal corroborated the role of physisorption with an adsorption capacity that rises to 17.9 mg/g, whereas the water sorption capacity reaches an impressive value ca. 11 g/g, which indicated the role of synergism upon chitosan immobilization. Anti-microbial and fungal properties were supported by antimicrobial tests. The FFMCs have high antimicrobial potency toward gram negative (E. coli), gram positive (Streptococcus aureus) and a fungal strain (Candida albicans) based on the low FFMC dosages required to achieve 100 % microbial elimination. This versatile class of unique biocomposites displayed unique structure-function relationships related to synergistic water sorption and antipathogenic effects, as compared to available literature reports. FFMCs are a diversiform class of biocomposites with unique physicochemical and biological properties that extend the field of adsorption science and technology from environmental remediation to biomedical devices.

Cosmopolitan but still untapped: Antimicrobial, antibiofilm and in silico molecular docking study on Caulerpa racemosa, Dictyopteris polypodioides and Padina pavonica

Egyptian seaweeds contain diverse bioactive compounds, but our understanding of their antimicrobial potential, particularly against multidrug-resistant (MDR) human pathogens, is still limited and underestimated. This study screened the antimicrobial potential of ethanolic extracts of Caulerpa racemosa, Dictyopteris polypodioides, and Padina pavonica against various MDR bacterial and fungal strains using broth microdilution technique. Antibiofilm assay of the seaweed extracts against Pseudomonas aeruginosa clinical isolates was also investigated. Our findings showed that the minimum inhibitory concentrations (MICs) of the tested seaweed extracts ranged between 62 and 500 μg mL−1. P. pavonica displayed the most biofilm inhibition percentages against P. aeruginosa clinical isolate by 31.2 % and 62.5 % for BIC50 and BIC90, respectively, as comparing to D. polypodioides and C. racemosa. Liquid chromatography-high resolution electrospray ionization mass spectrometry (LC-HR-ESI-MS) metabolic profiling of P. pavonica ethanolic extract was characterized. Twenty-seven metabolites were identified and checked for their inhibitory biofilm formation based on molecular docking simulation on LasR protein-specific quorum sensing. Interestingly, squalene (4), hydroperoxy-24 vinyl-24 cholesterol (18), fucoxanthol (21), flavoxanthin (22), and fucoxanthin (23) exhibited adequate interaction energies and formed significant interactions inside the LasR active site, supporting them to possess potent antibiofilm properties. Overall, P. pavonica can be recommended as powerful agent of antibiofilm preparation.

Synthesis and Evaluation of Antibacterial and Antifungal Activities In vitro and In silico of Novel Morpholinoalkoxychalcones

Introduction: Chalcone compounds exhibit diverse bioactivities, attracting significant interest. Morpholine is a heterocycle commonly used in medicinal chemistry. It could enhance the potency, pharmacokinetics, and bioactivities of its compounds. Methods: Adding morpholine into the chalcone scaffold could help create new compounds with favorable bioactivities. In this study, a new parallel synthesis procedure has been developed. Using this procedure, 18 novel morpholinoalkoxychalcones have been successfully synthesized. They had chains with morpholine appended on ring A or ring B. All the synthesized compounds were evaluated for the antibacterial and antifungal activities by agar diffusion method on 5 bacteria and 2 fungi strains. Results: The compounds with good inhibition were determined with respect to the MIC values by the agar dilution method. Among the tested compounds, B.21 was found to be the best against E. faecalis, with an MIC value of 0.6 mM. B.43 with an MIC value of 2.04 mM has displayed its potential in inhibiting A. niger and C. albicans the best among other compounds. Conclusion: The in silico study has revealed two targets to align with the in vitro results. Longer alkyl chains have enhanced the activity, along with the presence of OH, NH2, and halogen groups on both rings A and B.

New insights into autochthonous fungal bioaugmentation mechanisms for recalcitrant petroleum hydrocarbon components using stable isotope probing.

Autochthonous fungal bioaugmentation (AFB) is a promising strategy for the microbial remediation of petroleum hydrocarbon (PH)-contaminated soils. However, the mechanisms underlying AFB, particularly for degrading recalcitrant PH components, are not fully understood. This study employed stable isotope probing (SIP) and high-throughput sequencing to investigate the AFB mechanisms of two hydrocarbon-degrading fungi, Fusarium solani LJD-11 and Aspergillus fumigatus LJD-29, focusing on three challenging PH components: n-Hexadecane (n-Hex), Benzo[a]pyrene (BaP), and Dibenzothiophene (DBT). Our findings indicate that both fungal strains significantly enhanced pollutant removal rates, with combined application yielding optimal results. AFB treatment reduced the microbial diversity index and altered the soil microbial community, especially affecting fungal populations. A significant correlation between the microbial diversity index and degradation efficiency suggests that greater diversity enhances pollutant removal. SIP analysis showed that LJD-11 and LJD-29 could directly assimilate n-Hex and DBT, but not BaP. Correlation analyses between functional microorganisms and other biological indicators suggest that the removal of pollutants is also attributable to indigenous functional bacteria. Additionally, non-inoculated functional fungi present in the soil play a crucial role in BaP degradation. These findings reveal distinct degradation pathways for the three pollutants. The addition of carrier substrate reduced the complexity of the network, while AFB treatment restored it. In addition, the combined fungal treatment resulted in higher network parameters, leading to a more complex and stable network structure. These results provide insights into the mechanisms of AFB for degrading recalcitrant PH components, underscoring its potential for in situ bioremediation of petroleum-contaminated soils.

Improved production of palitantin by design of experiments and semi-synthesis of palitantin derivatives for bioactivity assessment

A new method for the production and isolation of (+)-palitantin (1) is herein reported, from cultures of the fungal strain Penicillium sp. AMF1a. (+)-Palitantin was isolated in 160 mg/L yield, as an alternative procedure to obtain 1 at a larger scale. The complete spectroscopic characterization, including conformational analysis, is presented for (+)-palitantin (1) and for its derivatives 3-α-palitantol (2), 3-β-palitantol (3), (Z)-palinitrorin (4), (Z)-paliphenin (5), (Z)-palifluorin (6) and (E)-palifluorin (7). The absolute configuration of the palitantin portion was confirmed by X-ray analysis of compound 4. The (4-(trifluoromethyl)benzyl)-hydrazone derivatives (6 and 7) displayed moderate biological activities. (Z)-Palifluorin (6) exhibited moderate antiplasmodial activity, while (E)-palifluorin (7) displayed weak antibacterial activity against E. faecalis and S. aureus, while palitantin itself was inactive in the same bioassays, indicating that the semi-synthesis of nitrogenated derivatives of 1 may be of potential interest to generate bioactive palitantin derivatives.