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The α-l-rhamnosidase (rha1) gene was homologously expressed in Aspergillus niger strains CCTCC 206047 and CCTCC 206047ΔpyrG, using hygromycin B and auxotrophic as selection markers. The engineered A. niger strains RHA001-1 and RHA003-1 were screened, yielding α-l-rhamnosidase activities of 20.81 ± 0.56 U/mL and 15.35 ± 0.87 U/mL, respectively. The copy numbers of the rha1 gene in strains RHA001-1 and RHA003-1 were found to be 18 and 14, respectively. Correlation analysis between copy number and enzyme activity in the A. niger strains revealed that α-l-rhamnosidase activity increased with the copy number of the rha1 gene. Recombinant α-l-rhamnosidase was utilized for the enzymatic debittering of Ougan juice, and its process conditions were optimized. Furthermore, the primary bitter substance neohesperidin (2.22 g/L) in Ougan juice was converted into hesperetin 7-O-glucoside (1.47 g/L) and hesperidin (0.143 g/L). This study presents a novel approach for the production of food-grade α-l-rhamnosidase and establishes a technical foundation for its application in the beverage industry. [ABSTRACT FROM AUTHOR]

In order to investigate the effect of mixed-mold fermentation on the bacterial community structure and quality of fish sauce made from mandarin fish viscera, changes in the bacterial community structure of mandarin fish viscera inoculated with a mixture of Aspergillus oryzae and Monascus (fish sauce A) or Aspergillus niger (fish sauce B) at a ratio of 3:1 during the fermentation process were analyzed using high-throughput sequencing. Additionally, changes in various quality parameters including pH, total acid content, amino nitrogen content, total soluble nitrogen content, total volatile basic nitrogen (TVB-N) content, volatile component contents, and free amino acid contents were evaluated. The results showed that mixed-mold fermentation significantly influenced the bacterial community. The diversity of bacterial community decreased during the fermentation process. Staphylococcus was found to be the dominant genus. The pH of fish sauce A and B decreased significantly, and consequently the content of total acids increased significantly throughout the fermentation. At the end of fermentation, the contents of amino nitrogen were 1.23 and 1.02 g/100 mL in fish sauce A and B, respectively, and the contents of total soluble nitrogen were 1.62 and 1.53 g/100 mL, respectively, both of which meet the standard for first-grade fish sauce. The TVB-N contents of fish sauce A and B were 152.81 and 154.12 mg/100 mL, respectively, complying with the national limit requirements. Gas chromatography-mass spectrometry (GC-MS) analysis identified 48 and 54 volatile components in fish sauce A and B, respectively, with the major one being 2,5-dimethylpyrazine at concentrations of 192.79 and 169.04 µg/mL, respectively. The contents of umami taste amino acids and sweet amino acids were significantly higher in fish sauce A and B than in unfermented fish sauce (P < 0.05). The correlation analysis results indicated that Staphylococcus made the greatest contribution to the quality of fish sauce and played a significant role in the formation of key characteristic flavor compounds in the late stage of fermentation. Overall, mixed-mold fermentation could effectively improve the quality of fish sauce. Fish sauce A had higher contents of amino nitrogen and total soluble nitrogen compared with fish sauce B, and consequently better overall quality.

Abstract Epothilones are one of the common prescribed anticancer drugs for solid tumors, for their exceptional binding affinity with β-tubulin microtubule, stabilizing their disassembly, causing an ultimate arrest to the cellular growth. Epothilones were initially isolated from Sornagium cellulosum, however, their extremely slow growth rate and low yield of epothilone is the challenge. So, screening for a novel fungal endophyte dwelling medicinal plants, with higher epothilone productivity and feasibility of growth manipulation was the objective. Aspergillus niger EFBL-SR OR342867, an endophyte of Latania loddegesii, has been recognized as the heady epothilone producer (140.2 μg/L). The chemical structural identity of the TLC-purified putative sample of A. niger was resolved from the HPLC, FTIR and LC–ESI–MS/MS analyses, with an identical molecular structure of the authentic epothilone B. The purified A. niger epothilone B showed a resilient activity against MCF-7 (0.022 μM), HepG-2 (0.037 μM), and HCT-116 (0.12 μM), with selectivity indices 21.8, 12.9 and 4, respectively. The purified epothilone B exhibited a potential anti-wound healing activity to HepG-2 and MCF-7 cells by ~ 54.07 and 60.0%, respectively, after 24 h, compared to the untreated cells. The purified epothilone has a significant antiproliferative effect by arresting the cellular growth of MCF-7 at G2/M phase by ~ 2.1 folds, inducing the total apoptosis by ~ 12.2 folds, normalized to the control cells. The epothilone B productivity by A. niger was optimized by the response surface methodology, with ~ 1.4 fold increments (266.9 μg/L), over the control. The epothilone productivity by A. niger was reduced by ~ 2.4 folds by 6 months storage as a slope culture at 4 °C, however, the epothilone productivity was slightly restored with ethylacetate extracts of L. loddegesii, confirming the plant-derived chemical signals that partially triggers the biosynthetic genes of A. niger epothilones. So, this is the first report emphasizing the metabolic potency of A. niger, an endophyte of L. loddegesii, to produce epothilone B, that could be a new platform for industrial production of this drug.

This study examined the fermentation duration in relation to the effectiveness of tannin levels in mangrove (Sonneratia alba) fruit during the fermentation process using Aspergillus niger. The tested durations were 7, 10, 13, and 16 days in anaerobic conditions. The outcomes measured included crude fat, crude fibre, and nitrogen-free extract digestibility. Microbial biomass, protozoa population, and methane gas production were also recorded as responses to the rumen microbial activity. The results showed that 16 days of fermentation gave the highest average for all responses. The protozoa population reached around 4.07 × 105 cells/ml and methane gas amounted to 33.9 ml/g of dry matter (DM). This is caused by a decrease in the anti-nutrient tannin content in mangrove (S. alba) fruit due to fermentation by A. niger according to treatment. The conclusion of this research is that the 16-day fermentation treatment (T4) of mangrove fruit is the optimal time to be used as a source of concentrate feed for livestock in terms of the increase in nutritional value and gastrointestinal microbes represented by total protozoa population, crude fibre digestibility, crude fat digestibility, and the highest nitrogen-free extract digestibility. However, microbial biomass and methane gas production were not significantly different in this study.

Abstract Among the several threats to humanity by anthropogenic activities, contamination of the environment by heavy metals is of great concern. Upon entry into the food chain, these metals cause serious hazards to plants and other organisms including humans. Use of microbes for bioremediation of the soil and stress mitigation in plants are among the preferred strategies to provide an efficient, cost-effective, eco-friendly solution of the problem. The current investigation is an attempt in this direction where fungal strain PH1 was isolated from the rhizosphere of Parthenium hysterophorus which was identified as Aspergillus niger by sequence homology of the ITS 1 and ITS 4 regions of the rRNA. The strain was tested for its effect on growth and biochemical parameters as reflection of its potential to mitigate Pb stress in Zea mays exposed to 100, 200 and 500 µg of Pb/g of soil. In the initial screening, it was revealed that the strain has the ability to tolerate lead stress, solubilize insoluble phosphate and produce plant growth promoting hormones (IAA and SA) and other metabolites like phenolics, flavonoids, sugar, protein and lipids. Under 500 µg of Pb/g of soil, Z. mays exhibited significant growth retardation with a reduction of 31% in root length, 30.5% in shoot length, 57.5% in fresh weight and 45.2% in dry weight as compared to control plants. Inoculation of A. niger to Pb treated plants not only restored root and shoot length, rather promoted it to a level significantly higher than the control plants. Association of the strain modulated the physio-hormonal attributes of maize plants that resulted in their better growth which indicated a state of low stress. Additionally, the strain boosted the antioxidant defence system of the maize there by causing a significant reduction in the ascorbic acid peroxidase (1.5%), catalase (19%) and 1,1-diphenyl-2 picrylhydrazyl (DPPH) radical scavenging activity (33.3%), indicating a lower stress condition as compared to their non-inoculated stressed plants. Based on current evidence, this strain can potentially be used as a biofertilizer for Pb-contaminated sites where it will improve overall plant health with the hope of achieving better biological and agricultural yields.

Abstract Background Research on protein production holds significant importance in the advancement of food technology, agriculture, pharmaceuticals, and bioenergy. Aspergillus niger stands out as an ideal microbial cell factory for the production of food-grade proteins, owing to its robust protein secretion capacity and excellent safety profile. However, the extensive oxidative folding of proteins within the endoplasmic reticulum (ER) triggers ER stress, consequently leading to protein misfolding reactions. This stressful phenomenon results in the accelerated generation of reactive oxygen species (ROS), thereby inducing oxidative stress. The accumulation of ROS can adversely affect intracellular DNA, proteins, and lipids. Result In this study, we enhanced the detoxification of ROS in A. niger (SH-1) by integrating multiple modules, including the NADPH regeneration engineering module, the glutaredoxin system, the GSH synthesis engineering module, and the transcription factor module. We assessed the intracellular ROS levels, growth under stress conditions, protein production levels, and intracellular GSH content. Our findings revealed that the overexpression of Glr1 in the glutaredoxin system exhibited significant efficacy across various parameters. Specifically, it reduced the intracellular ROS levels in A. niger by 50%, boosted glucoamylase enzyme activity by 243%, and increased total protein secretion by 88%. Conclusion The results indicate that moderate modulation of intracellular redox conditions can enhance overall protein output. In conclusion, we present a strategy for augmenting protein production in A. niger and propose a potential approach for optimizing microbial protein production system.

Abstract Palm leaf manuscripts (PLMs), venerable historical artefacts containing Buddhist scriptures, history, mathematics and literature, which are carried by palm leaves (Corypha umbraculifera) and are highly susceptible to microbial degradation during prolonged storage. This degradation results in significant alterations to both the appearance and material properties of PLMs, but the precise mechanism underlying this deterioration remains a mystery. To this end, the present study focused on ancient PLMs from Xishuangbanna Dai Autonomous Prefecture in Yunnan Province, China. The objective of present study was to isolate, culture and identify the microorganisms typically found in these manuscripts and to use them to biodegrade the carriers of PLMs. Detailed observations of the biodegradation behavior of these microorganisms on the carriers of PLMs were carried out, together with characterizations of the hierarchical structure and mechanical properties of the leaf fiber cell walls. This comprehensive analysis provided insights into the deterioration mechanisms of the carriers of PLMs. The study revealed the presence of the common fungus Aspergillus niger on ancient PLMs. Aspergillus niger can secrete cellulase, lipase, and acidic substances after colonizing on the carriers of PLMs. These substances sequentially damage the carrier's epidermal cells, mesophyll cells, and leaf fibers, leading to the separation of different tissue structures. At the molecular level, the lipids on the surface of the leaves were degraded initially, and sequential depolymerization of hemicellulose, amorphous cellulose, and crystalline cellulose occurred. Additionally, this study firstly applied nanoindentation technology in the research of PLMs. The mechanical properties of the cell walls underwent notable alterations due to the modifications in chemical and crystalline structure of the carriers of PLMs upon the biodegradation of Aspergillus niger. Specifically, the hardness and elastic modulus of leaf fiber cell walls showed an initial increasing and then decreasing trend, consistent with the trend of cellulose crystallinity, which also provided a new reference for assessing the degree of deterioration of PLMs.

In the present study, copper oxide (CuO) nanoparticles were biosynthesized from an Aspergillus niger cell-free extract (CFE), and several optimal operating parameters that affected the formation and dimensions of the CuO nanoparticles were determined, as follows: 15 mmol/L metal salt and 90 mL of CFE at room temperature for 24 h, to achieve an average size of 77 nm. Spectroscopic studies revealed an association between alcohol, alkene, and amine functional groups and the grain-shaped CuO nanoparticles. The elemental composition of the nanoparticles was confirmed by energy dispersive X-ray spectroscopy (EDX) data. Mycogenic CuO nanoparticles exhibited excellent antibacterial activity against Gram-positive bacterial species compared with Gram-negative bacterial species, i.e., Streptococcus pneumoniae MTCC 2672, Staphylococcus aureus MTCC 737, Micrococcus luteus MTCC 11948, Pseudomonas aeruginosa MTCC 424, and Escherichia coli MTCC 443, at 200 mg/mL, with inhibition zones of 9.2, 8.3 7.7, 7.2, and 6.1 mm, respectively. Finally, myogenic CuO nanoparticles exhibited good antifungal activity against Aspergillus fumigatus and Aspergillus versicolor.

Aspergillus niger is an efficient cell factory for organic acids production, particularly l-malic acid, through genetic manipulation. However, the traditional method of collecting A. niger spores for inoculation is labor-intensive and resource-consuming. In our study, we used the CRISPR-Cas9 system to replace the promoter of brlA, a key gene in Aspergillus conidiation, with a xylose-inducible promoter xylP in l-malic acid-producing A. niger strain RG0095, generating strain brlAxylP. When induced with xylose in submerged liquid culture, brlAxylP exhibited significant upregulation of conidiation-related genes. This induction allowed us to easily collect an abundance of brlAxylP spores (>7.1 × 106/mL) in liquid xylose medium. Significantly, the submerged conidiation approach preserves the substantial potential of A. niger as a foundational cellular platform for the biosynthesis of organic acids, including but not limited to l-malic acid. In summary, our study offers a simplified submerged conidiation strategy to streamline the preparation stage and reduce labor and material costs for industrial organic acid production using Aspergillus species.

Aspergillus niger is a highly versatile fungal strain utilized in industrial production. The expression levels of recombinant genes in A. niger can be enhanced by increasing the copy number. Nevertheless, given the prolonged gene editing cycle of A. niger, a “one-step” strategy facilitating the simultaneous integration of recombinant genes into multiple genomic loci would provide a definitive advantage. In our previous study, a visual multigene editing system (VMS) was designed to knock out five genes, employing a tRNA-sgRNA array that includes the pigment gene albA and the target genes. Building upon this system, hybrid donor DNAs (dDNAs) were introduced to establish a clustered regularly interspaced short palindromic repeats (CRISPR)-based multiplex integration toolkit. Firstly, a CRISPR-Cas9 homology-directed repair (CRISPR-HDR) system was constructed in A. niger by co-transforming the CRISPR-Cas9 plasmid (with a highly efficient sgRNA) and the dDNA, resulting in precise integration of recombinant xylanase gene xynA into the target loci (the β-glucosidase gene bgl, the amylase gene amyA, and the acid amylase gene ammA). Subsequently, the length of homology arms in the dDNA was optimized to achieve 100% editing efficiency at each of the three gene loci. To achieve efficient multiplex integration in A. niger, the CRISPR plasmid pLM2 carrying a sgRNA-tRNA array was employed for concurrent double-strand breaks at multiple loci (bgl, amyA, ammA, and albA). Hybrid dDNAs were then employed for repair, including dDNA1-3 (containing xynA expression cassettes without selection markers) and dDNAalbA (for albA knockout). Among the obtained white colonies (RLM2′), 23.5% exhibited concurrent replacement of the bgl, amyA, and ammA genes with xynA (three copies). Notably, the xynA activity obtained by simultaneous insertion into three loci was 48.6% higher compared to that obtained by insertion into only the bgl locus. Furthermore, this multiple integration toolkit successfully enhanced the expression of endogenous pectinase pelA and Candida antarctica lipase CALB. Hence, the combined application of VMS and the CRISPR-HDR system enabled the simultaneous application of multiple selection markers, facilitating the rapid generation in the A. niger cell factories.

Biopolymers embedded with nanoparticles of metal oxides (MOs) demonstrate a wide range of bio-functions. Chitosan-incorporated MOs are an interesting class of support matrices for enhancing the biological function, compared to other support matrices. Therefore, the importance of this study lies in exploiting chitosan as a carrier not of one metal as in previous studies, but of two metals in the form of a nanocomposite to carry out several biological functions. The coprecipitation approach was employed to synthesize chitosan/Fe2O3/ZnO-nanocomposite in the present research. The characterization of chitosan/Fe2O3/ZnO-nanocomposite was performed to find out the morphology and dispersion properties of chitosan/Fe2O3/ZnO-nanocomposite. The X-ray diffraction (XRD) investigation revealed that these were crystalline. Fourier transforms infrared (FTIR) spectrum bands were viewed at 400/cm and 900/cm, due to the stretching vibration of Fe and Zn oxygen bond. TEM showed that chitosan/Fe2O3/ZnO-nanocomposite was of 20–95 nm in size. chitosan/Fe2O3/ZnO-nanocomposite exhibited inhibitory potential against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Candida albicans with inhibition zones of 25 ± 0.1, 28 ± 0.2, 27 ± 0.1, and 27 ± 0.2 mm, respectively while didn't inhibited Aspergillus niger. MIC value of nanocomposite was 15.62 ± 0.33 µg/mL for C. albicans, B. subtilis and E. coli, while it was 62.50 ± 0.66 µg/mL for Pseudomonas aeruginosa. Ranged values of nanocomposite MBC (15.62 ± 0.33 to 125 ± 1 µg/mL) were attributed to all tested bacteria. Different concentrations of chitosan/Fe2O3/ZnO-nanocomposite MBC (25, 50, and 75%) reflected anti-biofilm activity against E. coli (85.0, 93.2, and 96.0%), B. subtilis (84.88, 92.21, and 96.99%), S. aureus 81.64, 90.52, and 94.64%) and P. aurogenosa (90.11, 94.43, and 98.24%), respectively. The differences in the levels of antimicrobial activities may depend on the type of examined microbes. Antioxidant activity of chitosan/Fe2O3/ZnO-nanocomposite was recorded with excellent IC50 values of 16.06 and 32.6 µg/mL using DPPH and ABTS scavenging, respectively. Wound heal by chitosan/Fe2O3/ZnO-nanocomposite was achieved with 100% compared to the untreated cells (76.75% of wound closer). The cytotoxicity outcomes showed that the IC50 of the chitosan/Fe2O3/ZnO-nanocomposite was 564.32 ± 1.46 µg/mL normal WI-38 cells. Based on the achieved findings, the chitosan/Fe2O3/ZnO-nanocomposite is a very promising agent for perform pharmacological activities. [ABSTRACT FROM AUTHOR]

Medicinal chemistry highly values the benzimidazole scaffold as a pharmacophore owing to its versatile range of biological functions. In the present study, 17 derivatives of 2‐aryl‐N1‐arylacetamido benzimidazoles 3(a–q) were synthesized by nucleophilic substitution reactions between different 2‐chloro‐N‐(aryl)‐acetamides 2(a–q) and 2‐(4‐chlorophenyl)‐1H‐benzo[d]imidazole (1) in N, N‐dimethylformamide, and evaluated for in vitro anti‐HIV and antifungal activities. Of these derivatives, compounds 3 a, 3 b, 3 i, and 3 n showed moderate inhibitory efficacy against HIV‐1 RT, whereas the remaining compounds showed negligible activity compared to the standard drug efavirenz. In contrast, most of the test compounds demonstrated significant efficacy against fungal strains such as Candida albicans and Aspergillus niger. Compounds 3 a, 3 f, 3 m, and 3 n were the most effective antifungal agents. We applied computational approaches to rationalize the potency of the newly synthesized inhibitors. [ABSTRACT FROM AUTHOR]

The objective of this work was to optimize the application of an enzymatic blend produced by Aspergillus niger ATCC 1004 on the Pimenta dioica fruits for essential oil extraction. The enzyme blend was obtained from the fermentation of cocoa bean shells, an agro‐industrial residue. The effects of the enzymatic pre‐treatment on the extraction yield, the chemical composition of the oil through gas chromatography, and the fruit structure through scanning electron microscopy (SEM) were assessed. A Doehlert design was used to optimize the process conditions, resulting in an extraction with 117 mL of enzyme during 77 min, which increased the extraction yield by 387.5%. The chemical composition was not altered, which proves that the enzyme blend preserves the quality of the essential oil extracted. The content of eugenol (70%), the major compound in the P. dioica essential oil, had a great increase in its concentration (560%). The enzyme activity analyses showed the presence of endoglucanase (0.4 U/mL), exoglucanase (0.25 U/mL), β‐glucosidase (0.19 U/mL), and invertase (135.08 U/mL). The microscopy analyses revealed changes in the morphology of fruit surface due to the enzymatic action. These results demonstrate the great potential of using enzyme blends produced by filamentous fungi from agro‐industrial residues for the essential oils extraction of interest for the pharmaceutical and food industries. [ABSTRACT FROM AUTHOR]

Epothilones are one of the common prescribed anticancer drugs for solid tumors, for their exceptional binding affinity with β-tubulin microtubule, stabilizing their disassembly, causing an ultimate arrest to the cellular growth. Epothilones were initially isolated from Sornagium cellulosum, however, their extremely slow growth rate and low yield of epothilone is the challenge. So, screening for a novel fungal endophyte dwelling medicinal plants, with higher epothilone productivity and feasibility of growth manipulation was the objective. Aspergillus niger EFBL-SR OR342867, an endophyte of Latania loddegesii, has been recognized as the heady epothilone producer (140.2 μg/L). The chemical structural identity of the TLC-purified putative sample of A. niger was resolved from the HPLC, FTIR and LC–ESI–MS/MS analyses, with an identical molecular structure of the authentic epothilone B. The purified A. niger epothilone B showed a resilient activity against MCF-7 (0.022 μM), HepG-2 (0.037 μM), and HCT-116 (0.12 μM), with selectivity indices 21.8, 12.9 and 4, respectively. The purified epothilone B exhibited a potential anti-wound healing activity to HepG-2 and MCF-7 cells by ~ 54.07 and 60.0%, respectively, after 24 h, compared to the untreated cells. The purified epothilone has a significant antiproliferative effect by arresting the cellular growth of MCF-7 at G2/M phase by ~ 2.1 folds, inducing the total apoptosis by ~ 12.2 folds, normalized to the control cells. The epothilone B productivity by A. niger was optimized by the response surface methodology, with ~ 1.4 fold increments (266.9 μg/L), over the control. The epothilone productivity by A. niger was reduced by ~ 2.4 folds by 6 months storage as a slope culture at 4 °C, however, the epothilone productivity was slightly restored with ethylacetate extracts of L. loddegesii, confirming the plant-derived chemical signals that partially triggers the biosynthetic genes of A. niger epothilones. So, this is the first report emphasizing the metabolic potency of A. niger, an endophyte of L. loddegesii, to produce epothilone B, that could be a new platform for industrial production of this drug. [ABSTRACT FROM AUTHOR]

In this study, green synthesis of Ag doped ZnO (AZNPR) has been carried out using the sol-gel method at pH 8.0, using two types of microbial cells, namely Aspergillus niger and Bacillus subtilis as capping and reducing agents. This work centred on the phytomediated biosynthesis and characterisation of AZNPR and its biological utility. Based on infrared analysis, phytochemicals present in microbial cells are extracellular enzymes namely proteolytic, amylolytic, lipolytic, cellulolytic, and pectinase, which can be extracted from A. niger and B. subtilis and are responsible for controlling the growth of AZNPR. The formation of AZNPR was characterised using different analyses. The FTIR shows absorption band located at ∼864 cm−1 that shows the interaction between Ag and ZnO. The XRD results showed the presence of crystalline AZNPR in the forms of hexagonal wurtzite ZnO and Ag. Microstructural and size examination showed that AZNPR was in the form of nanorods with homogeneous distribution with a size of rods in A. nige r media 137.0 nm, while in B. subtili s media 197.4 nm. The Ag–ZnO nanorods revealed the ability to inhibit Candida albicans species, a fungus causing infectious disease, with an inhibition zone measuring 2.1–3.2 mm at 24 h. [ABSTRACT FROM AUTHOR]

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This study aimed to biosynthesize zinc oxide nanoparticles (ZnO-NPs) using extracts from various seaweeds, including Ulva lactuca, Ulva intestinalis (Chlorophyta), and Sargassum muticum (Phaeophyceae). The biosynthesized ZnO-NPs were characterized using UV spectroscopy, Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, and zeta potential analysis. Their antimicrobial activity was assessed using the disk diffusion method, revealing significant efficacy against two bacterial species (Klebsiella pneumoniae and Escherichia coli) and two fungal species (Candida albicans and Aspergillus niger). Additionally, the antioxidant potential of the ZnO-NPs was evaluated based on the total antioxidant capacity, ferric reducing antioxidant power, and DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging assays. The antioxidant activity of the ZnO-NPs was confirmed using the three antioxidant assays. The ZnO-NPs of U. lactuca recorded the highest antioxidant activity. The cytotoxicity of the ZnO-NPs was tested on different cell lines using the MTT assay. The ZnO-NPs of U. lactuca showed very weak cytotoxic effects on WI 38 (84.98 ± 4.6 µg/mL) and 23, and this result confirmed its safety on normal cells. The ZnO-NPs of U. lactuca showed moderate cytotoxic effects on the HepG-2 (46.66 ± 2.8 µg/mL) and MCF-7 (30.60 ± 2.1 µg/mL) cell lines. In an in vivo study, the ZnO-NPs of U. lactuca showed a decrease in tumor volume, weight, and serum malondialdehyde in experimental mice, while the total antioxidant capacity of the serum was increased. Histopathological changes in ZnO-NPs indicated a reduction in tumor size, a lower number of mitosis divisions, and a rise in apoptosis correlated with the ZnO-NPs of the U. lactuca-treated groups. In conclusion, biosynthesized ZnO-NPs from seaweed showed potent antimicrobial, antioxidant, and antitumor activities, which can be used in the pharmaceutical industry. [ABSTRACT FROM AUTHOR]

In the paper, five quaternary ammonium salts derived from rosin were synthesized, characterized and their antifungal activities against different molds were studied. Choline quaternary ammonium salt and tetramethylammonium hydroxide were synthesized from dehydroabietic acid and the rosin ethanolamine ester quaternary ammonium salts which are new compounds were synthesized from propylene pimaric acid. Their structures were confirmed by FTIR, 1HNMR, 13CNMR, and high resolution mass spectrometry. The antifungal activities of the synthesized quaternary ammonium salts from rosin acid were tested by Oxford cup method, and their minimum inhibitory concentration was determined. The results show that quaternary ammonium salts derived from rosin acid have inhibitory effects on bamboo slices to some extent. Among them, propylene pimaric acid ethanolamine ester quaternary ammonium salts (A1 and A2) showed obvious antifungal activity in the Oxford cup test. The Oxford cup activity test and anti-mildew effect of quaternary ammonium salts (B1 and B2) synthesized from rosin acid are significant, and there are almost no mould growth on bamboo slices. It can be inferred that A1, A2, B1 and B2 are expected to be used as bamboo mildew inhibitors. Five quaternary ammonium salts derived from rosin were synthesized and characterized; and their antifungal activities against different molds were studied. [ABSTRACT FROM AUTHOR]

Cellulose nanocrystals are an important class of bio‐based crystalline nanostructures, finding application in several technological fields, including paper and textile coating, biocomposite engineering, biocatalysts immobilization, etc. This study explores enzymatic hydrolysis of Avicel, using endoglucanase from Aspergillus niger, to find an environmentally friendly method to extract cellulose nanocrystals from cellulose sources. Enzymatic hydrolysis has the advantage of reduced energy consumption and higher environmental friendliness compared to acid hydrolysis. In this work, we report for the first time very high nanocrystals yield by combining mechanical pretreatment of the cellulose starting material with a ball miller and endoglucanase hydrolysis, as a result of an extensive optimization of reaction conditions. In particular, a ball milling pretreatment carried out for 50 minutes at 3 Hz, allowed to isolate enzymatic CNCs with 76 % yield and with crystallinity as high as 75 %. The materials were characterized by X‐Ray diffractometry, attenuated total reflectance Fourier transform infrared (ATR‐FTIR) spectroscopy, dynamic light scattering, zeta potential and field emission scanning electron microscopy (FE‐SEM). Their characteristics were compared with the properties of sulfated CNCs, prepared from Avicel by sulfuric acid hydrolysis. Our results are technologically relevant, as they contribute to the accessibility and sustainability of CNCs for a wide range of applications in various industries. [ABSTRACT FROM AUTHOR]

A series of new 7‐{3‐[3‐(Benzylidene‐amino)‐[1,2,4]triazole‐1‐yl]‐propoxy}‐4‐methyl‐chromen‐2‐one molecular hybrids 7(a–k) were synthesized using molecular hybridization approach. The synthesized new benzylidene‐triazole tethered coumarin molecular hybrids were characterized by spectroscopic studies and elemental analysis. The coumarin molecular hybrids have been explored for their antifungal efficacy in terms of tubulin inhibitors using molecular modelling studies against tubulin alphabeta hetero dimer protein. The results clearly demonstrated strong binding affinity of coumarin molecular hybrids with indole substituted and 2,4‐dihydroxy substituted as antagonists with respective binding scores of −10.5 and −10.7 kcal/mol towards tubulin alphabeta hetero dimer protein which was higher in comparison to standards griseofulvin (−8.2 kcal/mol) and fluconazole (−8.1 kcal/mol). In addition, broth dilution method was used to conduct in‐vitro antifungal studies against three fungal strains namely Candida albicans, Aspergillus niger and Aspergillus fumigatus. The results obtained clearly illustrate the antifungal activity of indole and 2,4‐dihydroxy substituted compounds which are consistent with docking simulations. Out of all the synthesized molecular hybrids, indole and 2,4‐dihydroxy substituted compounds depict outstanding antifungal activity with Minimum Inhibitory Concentration (MIC) value of 31.25 μg/ml and 62.5 μg/ml towards C.albicans and with MIC value of 31.25 for both these molecules towards A.niger in each case which is quite higher than griseofulvin and fluconazole respectively. Present work clearly demonstrates the potential efficacy of synthesized indole and 2,4‐dihydroxy substituted coumarin molecular hybrids to be considered as lead compounds for the development of new agents against resistant strains for the treatment of fungal infection. [ABSTRACT FROM AUTHOR]

[Objective] To explore the optimal potassium dissolving conditions of Aspergillus niger J6 on potassium mineral powder. [Method] Based on Cha’s culture medium, the potassium dissolving capacity of A. niger J6 on potassium mineral powder was determined. The singlefactor test and orthogonal design test were used to optimize the potassium dissolving fermentation conditions of A. niger J6. [Result] The optimum potassium-dissolving medium for A. niger J6 was 2% soluble starch, 0. 5% soybean meal, 0. 003% FeSO4 and 0. 008% ZnSO4 . The optimal culture conditions for its potassium dissolution were an initial pH of 8. 5, a culture temperature 32 ℃, a culture time of 28 days, and an inoculation amount of 2. 5%. [Conclusion] This study provides a reference for the effective utilization of microbial transformation technology for low-grade mineral potassium and the production of biological potassium fertilizer. [ABSTRACT FROM AUTHOR]

This study evaluates the biocontrol efficacy of three bacterial strains (Pseudomonas fluorescens DTPF-3, Bacillus amyloliquefaciens DTBA-11, and Bacillus subtilis DTBS-5) and two fungal strains (Trichoderma harzianum Pusa-5SD and Aspergillus niger An-27) antagonists, along with their combinations at varying doses (5.0, 7.5, and 10.0 g/kg of seeds), against wheat powdery mildew. The most effective dose (10 g/kg seeds) was further analyzed for its impact on induced resistance and plant growth promotion under greenhouse conditions. The study measured defense enzyme activities, biochemical changes, and post-infection plant growth metrics. All tested microbial antagonists at 10 g/kg significantly reduced PM severity, with B. subtilis strain DTBS-5 outperforming others in reducing PM severity and achieving the highest biocontrol efficacy. It was followed by B. amyloliquefaciens strain DTBA-11 and P. fluorescens strain DTPF-3, with the fungal antagonists showing no significant effect. Wheat crops treated with B. subtilis strain DTBS-5 exhibited substantial increases in defense-related enzyme activities and biochemicals, suggesting an induced resistance mechanism. The study found a 45% increase in peroxidase (POD) activity, a 50% increase in catalase (CAT) activity, a 30% increase in phenolic content, and a 25% increase in soluble protein content in the wheat plants treated with microbial antagonists. The study highlights the effectiveness of microbial antagonists, particularly B. subtilis strain DTBS-5, in managing wheat PM through biocontrol, induced resistance, and enhanced plant growth, offering a sustainable alternative to chemical treatments. [ABSTRACT FROM AUTHOR]

A Schiff base (imine) ligand, (E)-4-((2-hydroxy-3,5-diiodobenzylidene)amino)-N-(4,6-dimethylpyrimidin-2-yl)benzenesulfonamide (HL), was synthesized by condensation of 3,5-diiodosalicylaldehyde with sulfamethazine. The ligand was then complexed with Zn(II), Cu(II), Ni(II), Co(II) and Fe(II) employing a metal to ligand ratio of 1:2 to form chelates (1-5), [M(L)2(H2O)2]. Characterization was done by UV-visible, FTIR, 1H and 13C NMR spectroscopy, elemental analysis, magnetic moments, thermogravimetric analyses (TGA) and conductance studies. The Schiff base behaved as a bidentate ligand and metal chelates assumed octahedral geometry. MOE-docking was employed to assess binding of the Schiff base (HL) and its chelates (1-5) with 1T2P, 1VVQ, 2W61, 3U2D, 4H8E and 5K18 proteins. Results indicated that Zn(II) chelate (1) and Fe(II) chelate (5) are the most potent compounds. Antibacterial and antibiofilm activities were executed against Enterococcus faecalis, Staphylococcus aureus, Proteus mirabilis and Klebsiella pneumoniae. Antifungal activities were performed against Candida albicans and Aspergillus niger. The Schiff base exhibited moderate antibacterial/antifungal activities that were enhanced on chelation with metal ions. Zinc(II) chelate (1) and Fe(II) chelate (5) show excellent antibacterial/antifungal activities. Complex 2 exhibited good antibiofilm activity. [ABSTRACT FROM AUTHOR]

Red seaweed Gelidium is used for agar extraction, generating large quantities of by-products (red seaweed by-product - GBP). Its carbohydrate and protein-rich composition makes it a suitable substrate to produce value-added compounds through solid-state fermentation (SSF). For the first time, GBP was used in SSF with Aspergillus ibericus and Aspergillus niger for carbohydrases production and protein enrichment. SSF was performed with unsupplemented GBP, supplemented with Mandel salt solution, and mixed at equal dry mass proportion with plant feedstuffs and with the seaweed Ulva rigida. A. niger CECT 2915 was the best strain under SSF obtaining the maximum xylanase activity (498 ± 49Ug-1), in GBP mixed with sunflower cake and the maximum of cellulase activity (382 ± 37Ug-1) in GBP mixed with rapeseed cake. In these mixtures, protein content increased 1.2-fold by SSF, as well as in GBP mixed with rice bran (1.3-fold). Scale-up of SSF using GBP mixed with sunflower cake from flasks to tray-type bioreactors demonstrated SSF reproducibility, achieving similar xylanase and cellulase activities. In the stirred-drum bioreactor, aeration and low agitation favored both enzymes production. Bioprocessing of GBP with plant feedstuffs using SSF was a cost-effective strategy to produce high-value enzymes, valorizing this seaweed by-product. [ABSTRACT FROM AUTHOR]

Bread is one of the fast food products because it is very easy to get and as one of the staple food ingredients consumed globally. However, bread is easily damaged which can be caused by bacteria and fungi that affect health. This study aims to identify contamination or contaminants of bacteria and fungi in bakery products. Bread samples were obtained from several school canteens, stalls, and markets in Yogyakarta City. In identifying bacteria, Nutrient Agar, Mannitol Salt Agar, and Baird Parker agar mediums are needed, while mushrooms are grown on Malts Extract agar medium in petri dishes. The selection of bacterial colonies into single colonies is carried out by biochemical tests. Bacterial confirmation tests were performed with API Staph and molcululent tests with nuc and sea marker genes using PCR. Fungal isolates were identified macromorphologically through observation of colony shape and micromorphology through cell observation with slide culture technique. The type of bacteria found in the sample was Staphylococcus aureus (identified API 52.8%, 97.7%, and 97.7%). The suspected isolate of S. aureus with an ID percentage of 52.8% was detected to have the sea gene but did not have the nuc gene. Suspected isolate. The type of fungus found in the sample is Aspergillus niger. [ABSTRACT FROM AUTHOR]

In the present study, six mononuclear Zinc(II) complexes, [Zn(L1)(6-Methyl-2,2′-bpy)] (1), [Zn(L1)(1,10-Phen)] (2), [Zn(L1)(5-Amino-1,10-Phen)] (3), [Zn(L2)(6-Methyl-2,2′-bpy)] (4), [Zn(L2)(4,4′-Di-tert-butyl-2,2′-bpy)] (5), and [Zn(L2)(1,10-Phen)] (6) formed from Schiff bases, 2-methyl-1-phenyl-1-(pyridin-2-ylmethylimino)propan-2-ol (L1) and 4-chloro-5-methyl-2-(1-(pyridin-2-ylmethylimino)ethyl)phenol (L2) were synthesized. The synthesized Schiff base ligands and metal complexes were characterized by different spectroscopic techniques such as FTIR, UV–Visible, 1H & 13C NMR spectroscopy, in addition to Powder X-ray diffraction and cyclic voltammetry. Further, the synthesized metal complexes (1–6) and their parental Schiff bases (L1, L2) were evaluated for antibacterial, antifungal, and antioxidant activities. Of those, Complex 1 was shown to have significant antibacterial activity against all of the evaluated microorganisms. Schiff base ligands, L1 and L2, complexes 1, 4, and 5 were shown to have superior antifungal activity against Aspergillus niger than the standard drug, fluconazole. In addition, the synthesized compounds achieved good antioxidant activities when compared to the standard Ascorbic acid. [ABSTRACT FROM AUTHOR]

Rose (Rosa chinensis) is subjected to various biotic and abiotic stresses. In this study, rose leaves with blight symptoms were collected and based on microscopic, morphological, and genetic analyses, the disease-causing pathogen was identified as Aspergillus niger. To our knowledge, this is the first report of leaf blight of R. chinensis in Pakistan. To control this disease, iron oxide nanoparticles (Fe 2 O 3 NPs) were synthesized in the seed extract of Trachyspermum ammi. Suitable formation of synthesized Fe 2 O 3 NPs was tested using reliable techniques. Fourier transformed infrared (FTIR) spectrum of Fe 2 O 3 NPs determined the presence of reducing agent like alcohol, alkyl halide and amine on the surface of NPs. X-Ray diffraction (XRD) analysis depicted crystal-like nature and size (41 nm) of NPs, while scanning electron microscopy (SEM) depicted their spherical shape. Sharp Fe and O peaks were observed by energy dispersive X-ray (EDX) analysis. All concentrations of Fe 2 O 3 NPs (0.25, 0.5, 0.75, 1 and 1.5 mg/ mL) inhibited mycelial growth, in vitro and the greatest inhibition (88.9 %) was observed at 1.0 mg/ mL concentration. SEM micrographs showed severe shrinking and structural decomposition of mycelia at this concentration. In pot experiment, Fe 2 O 3 NPs adeptly controlled blight disease of rose leaves by improving various physiological and biochemical attributes and superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT) activities. Findings of Real-Time Quantitative Reverse Transcription PCR (qRT-PCR) showed the higher expression of RcWRKY29 by the application of Fe 2 O 3 NPs, depicting its probable role in plant defense mechanism. These results proved that the application of Fe 2 O 3 NPs can efficiently prevent the spread of blight disease. [Display omitted] • Fe 2 O 3 nanoparticles were used to control leaf blight of Rosa chinensis. • Application of NPs increased the activity of antioxidant enzymes. • Interaction of NPs also up-regulated the expression of RcWRKY29. • qRT-PCR and KEGG pathway demonstrated plant-defense mechanism. • These NPs can efficiently prevent the spread of blight disease.s. [ABSTRACT FROM AUTHOR]

In this study, submerged and solid-state fermentation studies were performed for xylanase production simultaneously to determine ideal carbon and nitrogen sources together with necessary production parameters from the laboratory scale to the pilot scale. The results showed that barley malt sprout is effective as a nitrogen and a good carbon source. Under optimum conditions, xylanase activities 71.74 ± 2.70 U/mL, 56.95 ± 3.6 U/mL, 65.8 ± 8 U/mL and 46.05 ± 0.1 U/mL were achieved in shake flasks, 2, 10 and 30 L bioreactors, respectively. In solid-state fermentation studies, maximum activity in flasks was 759.15 ± 36.16 U/g production media, and maximum activity in pilot-scale tray bioreactor productions was 1312 ± 137.85 U/g dry substrate. Bread-making trials showed that using xylanase at 100 U/100g flour resulted in a significant increase in the loaf volume of wheat flour bread and whole wheat flour bread. [ABSTRACT FROM AUTHOR]

To investigate the effect and mechanism of plasma-activated water (PAW) on Aspergillus niger, PAW was prepared using a needle array–plate dielectric barrier discharge plasma system. The concentrations of long-lived reactive oxygen and nitrogen species (RONS), namely, H2O2, NO2−, and NO3−, in the PAW were 48.76 mg/L, 0.046 mg/L, and 172.36 mg/L, respectively. Chemically activated water (CAW) with the same concentration of long-lived RONS was also prepared for comparison. A. niger A32 was treated with PAW and CAW. After treatment, the treated strains were observed and analyzed with scanning electron microscopy (SEM) and transmission electron microscopy (TEM) to screen probable mutants. The results indicated that the pH, conductivity, and ORP values of PAW were 2.42, 1935 μS/cm, and 517.07 mV, respectively. In contrast, the pH and ORP values of CAW were 6.15 and 301.73 mV, respectively, which differed significantly from those of PAW. In addition, the conductivity of CAW showed no change. SEM and TEM analyses revealed that A. niger A32 treated with CAW exhibited less damage compared with the control. In contrast, A. niger A32 treated with PAW showed significant shrinkage, deformation, and exudate attachment over time. Following PAW treatment, after four passages, a high cellulase-producing stable mutant strain A-WW5 was screened, exhibiting a filter paper enzyme activity of 29.66 U/mL, a cellulose endonuclease activity of 13.79 U/mL, and a β-glucosidase activity of 27.13 U/mL. These values were found to be 33%, 38%, and 2.1% higher than those of the original fungus sample, respectively. In total, 116 SNPs and 61 InDels were present in the genome of the mutant strain A-WW5. The above findings indicate that the impact of PAW on A. niger is not only attributed to long-lasting H2O2, NO2−, and NO3− particles but also to other short-lived active particles; PAW is expected to become a new microbial breeding mutagen. [ABSTRACT FROM AUTHOR]

The study aimed to screen fungal diversity and ochratoxin A levels on culinary spice and herb samples sold in open-air markets and supermarkets in Nairobi County, Kenya. All herbs were grown in Kenya, while locally-produced and imported spices were purchased from both types of retail outlet. The results showed a high frequency of Aspergillus and Penicillium species contaminating the samples. The isolated species included Aspergillus ochraceous, Aspergillus nomiae, Aspergillus niger, Aspergillus flavus, Aspergillus ustus, Aspergillus terrus, Aspergillus nidulans, Aspergillus clavutus, Penicillium crustosum, Penicillium expansum, Penicillium brevicompactum, Penicillium glabrum, Penicillium thomii, Penicillium citrinum, Penicillium polonicum, and Cladosporium cladosporioides. Total fungal count on spice and herb samples collected from various sources varied between 6 and 7 CFU/mL. Of imported spices, garlic had the highest fungal diversity, while cardamom had the least. For spices from both open market and supermarket outlets, cloves had the highest fungal diversity, while white pepper had the least. For the herbs sampled from the open markets, basil was the most contaminated, while sage was the least. In supermarket samples, parsley, sage, and mint had the highest fungal diversity, and bay had the least. The results indicate the contamination of spices and herbs with OTA at high concentrations. The calibration curve was saturated at 40 µg/kg; with samples of garlic, cinnamon, red chili, basil, thyme, mint, sage, and parsley having levels above this. Of the spices, imported ginger had the highest OTA levels (28.7 µg/kg), while turmeric from the open market had the least, 2.14 µg/kg. For herb samples, parsley from the open market had the highest OTA levels at 29.4 µg/kg, while marjoram from the open market had the lowest at 6.35 µg/kg. The results demonstrate the presence of mycotoxigenic fungi and OTA contamination of marketed culinary herbs and spices beyond acceptable limits. Hence, there is a need for informed and sustainable mitigation strategies aimed at reducing human exposure in Kenya to OTA mycotoxicosis through dietary intake of spices and herbs. [ABSTRACT FROM AUTHOR]

Chloroquine (CQ) has been a good treatment for antimalarial mainstay for several decades; additionally discovered, it has a significant therapeutic impact on some instances of fungal inhibition. This study focused on the effect of novel CQ compounds on the activity of two different species of fungi, Aspergillus niger and Aspergillus falves. The activity of each CQ derivative was monitored using Nuclear magnetic resonance spectroscopy (NMR), minimal inhibitory concentration and physical parameters such as optical microscopy, UV/visible absorbance and optical band gap. NMR indicated the conjugation between the substrate and amino acid. The optical microscopic images indicated homogeneously distributed and uniform density distribution of CQ-derivative particles on the glass substrates. The samples' presented absorption peaks at 203, 207 and 220 nm wavelengths, suggesting the important electronic transition with reducing the indirect bandgap from 4.1 eV to 3.95 eV. These compounds have the best antifungal growth inhibitory properties and excellent features, indicating cosmetics use. [ABSTRACT FROM AUTHOR]

Due to the significant pharmacophoric role of 1,4‐naphthoquinone moiety, which is found in numerous biologically active natural products and well‐known chemotherapeutic drugs, including doxorubicin, shikonin, and alkannin, a newly prepared ligand ((E)‐1‐((2‐mercaptophenyl)imino)naphthalen‐2(1H)‐one) can be obtained from the condensation of 2‐aminothiophenol with diketone (1,2‐naphthoquinone) to form Schiff base (HL), which has been characterized using elemental analyses, FT‐IR, 1H‐NMR, and mass spectra. The inner ((La(III), Er(III), and Yb(III)) and outer ((Fe(III), Co(II), and Zn(II)) transitionmetal complexes have been prepared in 1:2 ratio and identified by several spectroscopic instruments. Different characterization tools have been used as elemental analyses, 1H‐NMR, molar conductivity, 13C‐NMR, FT‐IR, thermal decomposition (TG and DTG), UV‐vis, X‐ray diffraction, mass spectrometry, solid reflectance, and magnetic moment. All of them are conjugated to confirm the proposed structures of the metal complexes and are complementary. Also, molecular docking studies for the ligand and its Zn(II) and Yb(III) complexes (using MOE program) have been performed to support the experimental biological activity. Molecular docking studies recommended that (Yb(HL)2)Cl3·6H2O complex is more potent against Aspergillus niger fungus when docked with 1Y43 (aspergilloglutamic peptidase enzyme from A. niger) receptor, while Zn(II) complex recorded the strongest binding energy among the docked compounds against 2W3Z(the crystal structure of a Streptococcus mutans CE4 esterase) and 7AB4 (the crystal structure of the Escherichia coli toxin‐antitoxin system HipBST [HipT S59A]) proteins receptors, respectively. Experimental applications of the free ligand and its metal chelates as antimicrobial and antioxidant activities have been carried out. The former occurred against two fungal species (Aspergillus niger [ATCC:16404] and Candida albicans [ATCC:10231]), two G‐positive bacterial species (S. mutans [ATCC:25175] and Staphylococcus aureus [ATCC:13565]) and two G‐negative bacterial species (Klebsiella pneumonia [ATCC:10031] and E. coli [ATCC:10536]). The DPPH scavenging method has been used to measure the antioxidant activity of the tested compounds. [ABSTRACT FROM AUTHOR]

Objective: Due to wide range of biological activities exhibited by pyran derivatives such as antibacterial, antioxidant, anticancer and other activities, we have synthesized and investigated the biological activity of some pyran derivatives. Methods: A series of 4-hydroxy-6-methyl-5,6-dihydro-2H-pyran-2-one based azo dyes (IIIa–IIIf) have been synthesized by a conventional diazo coupling reaction. The antioxidant activity was determined via DPPH assay and Antimicrobial activity through disc diffusion test. Results and Discussion: Compound (IIIb) has shown excellent radical scavenging activity with an IC50 value of 20.22 ± 7.36 µg/mL compared to the standard. Furthermore, compounds (IIIc) and (IIId) showed a good antibacterial and antifungal activity against Escherichia coli and Aspergillus niger compared to other prepared azo compounds. Conclusions: We propose that in future, synthesized compounds may act as a promising antimicrobial drugs. [ABSTRACT FROM AUTHOR]

Background and Objectives: The ocular surface is perpetually exposed to the external environment, rendering it susceptible to microbial contamination. The ocular surface microbiota consists of non-pathogenic microorganisms that inhabit the conjunctiva and cornea. This study's objective was to extensively review the prevalence of bacterial and fungal organisms in the conjunctiva of healthy and diseased cats. (Herpes-and Calici-infected groups). Materials and Methods: The current study was performed on 240 cats that had visited veterinary health centers (Tehran, Iran) for examination. Sterile swabs from each cat's eyes were investigated for microbiological assessment. After sample collection, viral pathogens (Herpes and Calici viruses) were isolated and identified using the PCR method. The ages of the investigated group were 3.76, 3.93, and 4.15 months. Results: The highest frequency of bacteria in the normal, Herpes-infected/Calici-infected, and Herpes/Calici-infected groups were associated with Staphylococcus intermedius and Streptococcus agalactiae, Staphylococcus epidermidis, and Staphylococcus intermedius, respectively. In addition, it was found that the high prevalence of fungal microorganisms in the isolated samples was related to yeasts, Aspergillus (Aspergillus fumigatus, Aspergillus niger), and Penicillium species. Conclusion: Bacterial prevalence was significantly higher in all groups than the prevalence of fungi in the eyes of cats. The statistical comparison between the study groups regarding microbial and fungal frequency showed that significant differences were found between them, such that the frequency was higher in all disease groups, against the control group. In addition, a significant relation was observed between the Herpes-infected and Calici-infected groups regarding microbial and fungal prevalence. [ABSTRACT FROM AUTHOR]

Fungi can adapt their metabolism to different cultivation conditions, which may accompany changes in secondary metabolites, but few cost-effective approaches were presented. Therefore, Aspergillus niger CBMAI 2766 was studied aiming at the obtention of antibacterial compounds using KBr, an innocuous and inexpensive salt. The addition of this salt to culture medium was an interesting strategy for obtention of natural products at higher concentrations, as observed by the increased extract mass that favored the isolation of biologically active compounds. Furthermore, an experimental design with temperature, pH, and KBr concentration was performed to maximize the obtained products. Seven compounds were isolated: the phenylalanine derivatives Aspernigrin A 1 and Pestalamide B 2, the polyketides RF-3192C 3 , Foncesinone A 6 and Aurasperone A 7 , and the bicoumarins Orlandin 4 and Kotanin 5. The bactericidal activity of 5 against Gram-positive bacteria was observed for the first time in this study. Furthermore, antimicrobial activities of the isolated metabolites 3–7 were described in the literature. In summary, the employed experimental design showed that 34 °C and 10 g.L−1 KBr were optimal conditions for producing the bioactive compounds 5 - 7 , employing this inexpensive salt as medium modifier. Thus, indicating that this proposal presents potential for enhancing antimicrobials production. [Display omitted] • The safe and inexpensive salt KBr increased antimicrobials production by A. niger. • Concentrations of phenylalanines, polyketides, and bicoumarins were differentiated. • Foncesinone A, Aurasperone A, and Kotanin production were optimized. • The antimicrobial activity of 4 from 7 isolated compounds already was reported. • Kotanin activity against Gram-positive bacteria was reported for the first time. [ABSTRACT FROM AUTHOR]

Prolyl Endopeptidase (PEP) has the unique ability to hydrolyze the carboxyl terminal peptide bonds of Proline. This enzyme holds great value in various fields including medical research, disease treatment, human diet, and food production. Aspergillus niger is a significant food-grade protein expression system renowned for its high safety. It is considered an ideal system for producing Aspergillus -derived PEP due to its ability to secrete a large amount of endogenous proteins. Our research group successfully constructed the Aspergillus niger PEP engineering strain in the early stages by eliminating the background protein AsaA, thereby increasing secretion protein production. In this article, we explore new solutions to further enhance production. Experimental investigations were conducted to regulate secretory protein production at different levels by modifying the 5′UTR and reconstructing the secretion pathways. The results demonstrate that the strain modified by the 5′UTR and Kozak sequence (glaA5'UTR-GCCACC, glaA::protA) exhibited a 1.88-fold increase in gene transcription and a 105% increase in extracellular PEP activity compared to the non-modified strain. Co-expression of the ERdjs gene AnScj1 further increased extracellular PEP activity by 168%. However, deletion of derA or vps10 , key genes in the Aspergillus niger secretory protein degradation pathway, resulted in reduced levels of gene transcription and secretory expression. This article holds practical significance in enhancing the secretion and expression of PEP, obtaining higher-yield strains, and exploring optimization strategies for highly expressed proteins. [Display omitted] • 5'UTR modification enhances the expression of prolyl endopeptidase. • The ER-located DnaJ family member AnScj1 improves the expression of secretory protein. • Deletion of derA or vps10 does not always favor secretory protein expression. [ABSTRACT FROM AUTHOR]

A range of fungal species showed variable abilities to colonize and penetrate a mortar substrate. Calcium biomineralization was a common feature with calcium-containing crystals deposited in the microenvironment or encrusting hyphae, regardless of the specific mortar composition. Several species caused significant damage to the mortar surface, exhibiting burrowing and penetration, surface etching, and biomineralization. In some cases, extensive biomineralization of hyphae, probably by carbonatization, resulted in the formation of crystalline tubes after hyphal degradation on mortar blocks, including those amended with Co or Sr carbonate. Ca was the only metal detected in the biomineralized formations with Co or Sr undetectable. Aspergillus niger , Stemphylium sp. and Paecilomyces sp. could penetrate mortar with differential responses depending on the porosity. Fluorescent staining of thin sections recorded penetration depths of ∼530 um for A. niger and ∼620 um for Stemphylium sp. Penetration depth varied inversely with porosity and greater penetration depths were achieved in mortar with a lower porosity (lower water/cement ratio). These results have provided further understanding of biodeteriorative fungal interactions with cementitious substrates that can clearly affect structural integrity. The potential significance of fungal colonization and such biodeteriorative phenomena should not be overlooked in built environment contexts, including radionuclide storage and surface decontamination. [ABSTRACT FROM AUTHOR]

Phellinus caribaeo‐quercicola is a basidiomycetous fungus, isolated as an endophyte in this study from the healthy and symptomless leaves of Inula racemosa Hook. f., an important medicinal herb growing in Kashmir Himalaya. This study combines morphological, molecular and phylogenetic techniques to identify the fungal endophyte, using the ITS sequence of nrDNA. A detached leaf assay was conducted to assess the pathogenicity of the fungal endophyte suggesting its mutually symbiotic relationship with the host. The authors also investigated the antifungal potential of the isolated endophytic strain to ascertain its use as a biocontrol agent. The study shows that P. caribaeo‐quercicola INL3‐2 strain exhibits biocontrol activity against four key fungal phytopathogens that cause significant agronomic and economic losses: Aspergillus flavus, Aspergillus niger, Fusarium solani, and Fusarium oxysporum. Notably, P. caribaeo‐quercicola INL3‐2 strain is highly effective against A. flavus, with an inhibition percentage of 57.63%. In addition, this study investigates the antioxidant activity of P. caribaeo‐quercicola INL3‐2 strain crude extracts using ethyl acetate and methanol as solvents. The results showed that the methanolic fraction of P. caribaeo‐quercicola exhibits potential as an antioxidant agent, with an IC50 value of 171.90 ± 1.15 µg/mL. This investigation is first of its kind and marks the initial report of this fungal basidiomycete, P. caribaeo‐quercicola, as an endophyte associated with a medicinal plant. The findings of this study highlight the potential of P. caribaeo‐quercicola INL3‐2 strain as a dual‐action agent with both biocontrol and antioxidant properties consistent with the medicinal properties of Inula racemosa. This endophytic fungus could be a promising source of natural compounds for use in agriculture, medicine, and beyond. [ABSTRACT FROM AUTHOR]

A study was conducted using twenty-one (21) West African Dwarf (WAD) goats with an average weight of 10.50 ± 0.36 kg to evaluate the nutrient intake, weight gain, and nitrogen balance of WAD goats fed microbial-treated Bambara nutshell diets. The chemical and mineral compositions of the diets were also determined. The goats were allotted to seven dietary treatments, replicated three times in a completely randomized design. The Bambara nutshells were sterilized for 15 minutes, inoculated with 25, 50, and 75 ml of each Pleurotus pulmonaris and Aspergillus niger, incubated for 7 days and air dried. The treated Bambara nutshell was incorporated into the diets at the rate of 0ml (Diet A), 25 ml P. pulmonaris (Diet B), 50 ml P. pulmonaris (Diet C), (Diet D), 75 ml P. pulmonaris (Diet E), 25 ml A. niger (Diet F) 50 ml A. niger and (Diet G) 75 ml A. niger respectively. The experimental period lasted for 56 days excluding 2 weeks of adaptation. Results showed that the proximate compositions were significantly influenced (p<0.05) by the treatment except for crude protein (CP). Diet F had the highest dry matter (DM) values (94.77%) and CP (20.33%) while Diet C had the least (92.33%) DM and Diet G (19.16%) had the least CP. Goats fed Diet D had the highest daily weight gain (107.14 g/day), and best feed/gain ratio of 6.20. Conclusively, microbial treatment of Bambara nutshell will help in the conversion of these wastes to better quality ruminant feed for better performance. [ABSTRACT FROM AUTHOR]

Lytic polysaccharide monooxygenase (LPMO) of Auxiliary Activity 9 family has great potential for lignocellulose biomass degradation, and obtaining AA9 LPMOs with high catalytic activity and thermalstability is necessary for its industrial application. In this study, rational design and molecular modification was conducted on AnLPMO15g from Aspergillus niger to boost its performance on lignocellulose hydrolysis. The catalytic performance of mutant AnLPMO15g-293 (C293F) and AnLPMO15g-351 (S351F) with increased α-helix content in the secondary structure were improved. The catalytic efficiency (Kcat/Km) of C293F and S351F on 2,6-dimethoxyphenol was 1.27 and 1.17 times higher than that of AnLPMO15g respectively, and their activities on Avicel® increased by 81.17% and 40.78%, respectively. The half-life of C293F and S351F at 55 ℃ was 1.5 and 2.5 times longer than that of AnLPMO15g. Surface plasmon resonance analysis showed that the association velocity constant (Ka) of S351F increased tenfold compared with that of AnLPMO15g, indicating the substrate affinity of S351F was significantly improved. When C293F and S351F acted together with cellulase on straw powder, the reducing sugar yields increased by 1.81 and 1.53 times and the synergistic degree increased 30.7% and 11.8%, respectively. This study provides a good alternative for preparing efficient enzyme cocktails to hydrolyze lignocellulosic biomass. [ABSTRACT FROM AUTHOR]

The present study explores the influence of Cobalt oxide nanoparticles(Co3O4 NPs) on the physicochemical characteristics of Poly(vinylalcohol)/ Chitosan (PVA/Cs) blend. Using a variety of techniques, the pure blend and the nanocomposites' composition, structure, optical, thermal, and mechanical properties, and antibacterial activity were characterized. The Co3O4 NPs were produced by precipitation method utilizing cobalt salt as the raw material. The crystalline nature of the nanoparticles and semi-crystalline behavior of the PVA/Cs are demonstrated by the XRD data. Adding nanoparticles to the pure blend reduced the intensity of the semi-crystalline. The rise in absorption intensity observed in UV-visible spectra upon the incorporation of Co3O4 NPs into the PVA/Cs blend indicates an improved dispersion of the nanoparticles within the blend. When Co3O4 NPs are added, the energy band-gap Egdir and Egind of PVA/Cs–Co3O4 samples greatly decrease. According to TGA data, the thermal stability of nanocomposites was significantly higher than that of the PVA/Cs blend, and it rose as the concentration of nanoparticles increased. When compared to neat PVA/Cs film, mechanical property investigation of PVA/Cs–Co3O4 nanocomposites films revealed enhanced features. The effectiveness of the PVA/Cs–Co3O4 nanocomposite films in inhibiting the growth of microorganisms was assessed by evaluating their antimicrobial activity (ANMAC) against a range of bacteria and fungi. The inclusion of Co3O4 NPs led to an increase in activity against Gram-positive Staphylococcus aureus (S. aureus) and Gram-negative Escherichia coli (E. coli) bacteria as well as fungi Candida albicans and Aspergillus niger (C. albicans and A. niger). The addition of Co3O4 NPs to the PVA/Cs blend effectively improved the material's optical, thermal, mechanical, and antibacterial properties. This remarkable improvement stems from the Co3O4 NPs, which were introduced into the PVA/Cs blend in different amounts, leading to the development of novel nanocomposites. The outstanding properties of Co3O4/PVA/Cs nanocomposite films suggest their potential for applications in optoelectronics and food packaging. [ABSTRACT FROM AUTHOR]

In the current investigation, the enhanced cytotoxic impact of gold nanoparticle–loaded camptothecin—a bioactive metabolite produced by a soil isolate of Aspergillus niger against breast cancer cell line (MCF 7)—was studied. Camptothecin (CPT) was isolated from Aspergillus niger biomass followed by loading with chemogenic gold nanoparticles, and the synthesized nano-drug conjugate was characterized by suitable techniques. Anticancer activity against MCF 7 cell line was studied by determination of cell viability and morphometric changes including apoptosis, biochemical, and molecular marker expression pattern. Active principles of CPT were readily extracted with chloroform + methanol extract of A. niger biomass. The maximum yield of CPT was 0.132 g/L. Extracted CPT was loaded onto chemically synthesized gold nanoparticles (CPT-AuNp) that brought about a highly stable core shell-like structure with particle sizes ranging from 60 to 70 nm. Prepared nanoformulation recorded noteworthy anticancer activity against breast cancer cells. Cell viability of the cancer cells was highly reduced in CPT-AuNp treatment. The lethal concentration (IC50) was recorded at 50.5 µg, whereas free gold nanoparticles and free camptothecin were at 301 and 295 µg, respectively, which showed the enhanced cytotoxicity of AuNp-CPT against the tested cancer cell line. Most significantly, CPT-AuNp treatment induced apoptosis and characteristic changes in enzymatic antioxidants which includes catalase (CAT), superoxide dismutase (SOD), and glutathione s-transferase (GST). Expression pattern changes of gene-like PARP and Bax genes revealed a marked impact on the molecular markers. From these findings, it is clear that the nanoformulated camptothecin can be used as an effective and safe anticancer agent against life-threatening diverse cancer types. [ABSTRACT FROM AUTHOR]

Introduction: This study aimed to investigate the fungal growth and diversity in the Sabkha marsh. The anti-bacterial properties of the isolated fungi were assessed using an agar disk diffusion assay, and the crude extracts were tested for their anticancer activities. Liquid chromatography-mass spectrometry was employed to identify the active compounds of the fungal secondary metabolites. In-silico studies were conducted to predict the toxicity, pharmacokinetic properties, and safety profiles of the identified compounds. Results: The analysis revealed that the isolated fungi belonged to the Aspergillus species, specifically Aspergillus flavus and Aspergillus niger. The crude extract of A. flavus exhibited significant anticancer activity against various cancer cell lines, while the antifungal activities against pathogenic bacteria varied between the two fungi. Liquid chromatography-mass spectrometry analysis identified several compounds in the fungal isolates. In Aspergillus flavus, the compounds included Aflavinine, Dihydro-24-hydroxyaflavinine, Phomaligin A, Hydroxysydonic acid, Gregatin B, Pulvinulin A, Chrysogine, Aspergillic acid, Aflatoxin B1, and Aflatoxin G1. In Aspergillus niger, the compounds identified were atromentin, fonsecin B, firalenone, rubrofusarin, aurasperone E, aurasperone D, aurasperone C, nigerone, and αβ-dehydrocurvularin. Conclusion: This study demonstrated promising fungal growth and diversity in the Sabkha marsh, with Aspergillus species being the most prevalent. The fungal crude extract showed anticancer activities against various cancer cell lines, while the antifungal activities against pathogenic bacteria varied between the two fungi. Future research should focus on investigating the antimicrobial activities of these fungi against multidrug-resistant bacteria and exploring the genetic changes in bacteria and cancer cells treated with these fungal extracts. Additionally, it is important to test the anticancer activity of the active compounds separately to determine which one is the active agent against cancer cells. This information can be used in drug development trials. [ABSTRACT FROM AUTHOR]

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This study presents a novel approach to producing activated carbon from agro-industrial residues, specifically cocoa fruit peel, using solid-state fermentation (SSF) with Aspergillus niger. The process effectively degrades lignin, a major impediment in traditional activated carbon production, resulting in a high-quality carbon material. This carbon was successfully utilized for enzyme immobilization and aroma synthesis, showcasing its potential as a versatile biocatalyst. The study meticulously evaluated the physical and chemical attributes of activated carbon derived from fermented cocoa peel, alongside the immobilized enzymes. Employing a suite of analytical techniques—electrophoresis, FTIR, XRD, and TG/DTG the research revealed that fermentation yields a porous material with an expansive surface area of 1107.87 m2/g. This material proves to be an excellent medium for lipase immobilization. The biocatalyst fashioned from the fermented biomass exhibited a notable increase in protein content (13% w/w), hydrolytic activity (15% w/w), and specific activity (29% w/w), underscoring the efficacy of the fermentation process. The significant outcome of this research is the development of a sustainable method for activated carbon production that not only overcomes the limitations posed by lignin but also enhances enzyme immobilization for industrial applications. The study's findings have important implications for the agro-industrial sector, promoting a circular economy and advancing sustainable biotechnological processes. [ABSTRACT FROM AUTHOR]

In this study, nutritious and abundant waste generated by sardine canneries was used as the main substrate to assess the effect of fundamental parameters in anaerobic digestion. The temperature range studied, between 37°C and 45°C, allowed for a comparison between the performance of the thermophilic and mesophilic processes. The free water content in the substrate also enabled us to compare fermentation in solid-state fermentation (SSF) with its counterpart, liquid-state fermentation (LSF). The study parameters also included the integration of Aspergillus niger (AN) and molasses. The results revealed significant effects of the AN inoculum and thermophilic conditions in improving biogas production. Optimal biotransformation generated a safe digestate that complies with French standards for use as a biofertilizer. Germination tests demonstrated that it has no inhibitory effect on tomato seeds and has the potential to enhance crop yields better than chemical fertilisers. [ABSTRACT FROM AUTHOR]

Invasive fungal infections (IFI) pose a significant health burden, leading to high morbidity, mortality, and treatment costs. This study aims to develop and characterize nanomicelles for the codelivery of posaconazole and hemp seed oil for IFI via the oral route. The nanomicelles were prepared using a nanoprecipitation method and optimized through the Box Behnken design. The optimized nanomicelles resulted in satisfactory results for zeta potential, size, PDI, entrapment efficiency, TEM, and stability studies. FTIR and DSC results confirm the compatibility and amorphous state of the prepared nanomicelles. Confocal laser scanning microscopy showed that the optimized nanomicelles penetrated the tissue more deeply (44.9µm) than the suspension (25µm). The drug-loaded nanomicelles exhibited sustained cumulative drug release of 95.48 ± 3.27% for 24 h. The nanomicelles showed significant inhibition against Aspergillus niger and Candida albicans (22.4 ± 0.21 and 32.2 ± 0.46 mm, respectively). The pharmacokinetic study on Wistar rats exhibited a 1.8-fold increase in relative bioavailability for the nanomicelles compared to the suspension. These results confirm their therapeutic efficacy and lay the groundwork for future research and clinical applications, providing a promising synergistic antifungal nanomicelles approach for treating IFIs. [ABSTRACT FROM AUTHOR]

Cancer is a threatening disease that needs strong therapy with fewer side effects. A lot of different types of chemotherapy or chemo-drugs are used in cancer treatments but have many side effects. The increasing number of antibiotic-resistant microorganisms requires more study of new antimicrobial compounds and delivery and targeting strategies. This work aims to isolate and identify Azotobacter sp., and extract alginate from Azotobacter sp. As well as fabricating selenium nanoparticles using ascorbic acid as reducing agent (As/Se-NPs), and loading extracted alginate with selenium nanoparticles (Alg-Se-NCMs). The As/Se-NPs and Alg-Se-NCMs were categorized by TEM, EDX, UV–Vis spectrophotometry, FT-IR, and zeta potential. The antifungal activities of both As/Se-NPs and Alg-Se-NCMs were investigated against some human pathogen fungi that cause skin infection such as Aspergillus niger (RCMB 002005), Aspergillus fumigatus (RCMB 002008), Cryptococcus neoformans (RCMB 0049001), Candida albicans (RCMB 005003), and Penicillium marneffei (RCMB 001002). The anticancer activities were determined against HCT-116 colorectal cancer and Hep G2 human liver cancer cells. UV spectra of As/Se-NPs and Alg-Se-NCMs confirmed a surface plasmon resonance at 269 and 296 nm, and zeta potential has negative charges −37.2 and −38.7 mV,. Both As/Se-NPs and Alg-Se-NCMs were hexagonal, size ranging from 16.52 to 97.06 and 17.29 to 44.2. Alg-Se-NCMs had anticancer activities against HCT-116 and HepG2. The Alg-Se-NCMs possessed the highest antifungal activities against Cryptococcus neoformans, followed by Aspergillus niger, but did not possess any activities against Penicillium marneffei. Alginate-capped selenium nanoparticles can be used as antifungal and anticancer treatments. [ABSTRACT FROM AUTHOR]

Among the several threats to humanity by anthropogenic activities, contamination of the environment by heavy metals is of great concern. Upon entry into the food chain, these metals cause serious hazards to plants and other organisms including humans. Use of microbes for bioremediation of the soil and stress mitigation in plants are among the preferred strategies to provide an efficient, cost-effective, eco-friendly solution of the problem. The current investigation is an attempt in this direction where fungal strain PH1 was isolated from the rhizosphere of Parthenium hysterophorus which was identified as Aspergillus niger by sequence homology of the ITS 1 and ITS 4 regions of the rRNA. The strain was tested for its effect on growth and biochemical parameters as reflection of its potential to mitigate Pb stress in Zea mays exposed to 100, 200 and 500 µg of Pb/g of soil. In the initial screening, it was revealed that the strain has the ability to tolerate lead stress, solubilize insoluble phosphate and produce plant growth promoting hormones (IAA and SA) and other metabolites like phenolics, flavonoids, sugar, protein and lipids. Under 500 µg of Pb/g of soil, Z. mays exhibited significant growth retardation with a reduction of 31% in root length, 30.5% in shoot length, 57.5% in fresh weight and 45.2% in dry weight as compared to control plants. Inoculation of A. niger to Pb treated plants not only restored root and shoot length, rather promoted it to a level significantly higher than the control plants. Association of the strain modulated the physio-hormonal attributes of maize plants that resulted in their better growth which indicated a state of low stress. Additionally, the strain boosted the antioxidant defence system of the maize there by causing a significant reduction in the ascorbic acid peroxidase (1.5%), catalase (19%) and 1,1-diphenyl-2 picrylhydrazyl (DPPH) radical scavenging activity (33.3%), indicating a lower stress condition as compared to their non-inoculated stressed plants. Based on current evidence, this strain can potentially be used as a biofertilizer for Pb-contaminated sites where it will improve overall plant health with the hope of achieving better biological and agricultural yields. [ABSTRACT FROM AUTHOR]