Introduction

Several studies revealed that secondary metabolites of microbial origin represent unexplored sources for potential bioactive compounds, where endophytes have the ability to synthesize novel lead molecules with diverse structural and abroad bioactivities (Falade et al. 2021; Abdul-Razek et al. 2020; Gunatilaka 2006; Okoye et al. 2015). Plants that contain endophytes are much healthier than endophyte-free plants, since endophytes provide growth and protection for the host plant by different mechanisms (Busby et al. 2016; Rachel et al. 2022). Fungi are plant-like organisms that lack chlorophyll and are represented by several fungal species. There are 1.5 million species approximately, of which 74,000 are known (Hawksworth 2001). Endophytic fungi are present in all kinds of plants, including trees, grasses, algae, and herbaceous plants (Hyde and Soytong 2008, Bacon and White 2000). Several bioactivities of endophytic fungi can be attributed to synthesizing a number of secondary metabolites, including phenolics, alkaloids, quinones, lignans, peptides, flavonoids, steroids, isocoumarins, and flavonoids (Khalil et al. 2021; Talukdar et al. 2021). Many compounds with antimicrobial, antimalarial, and anticancer potential have been isolated from endophytic fungi (Hridoy et al. 2022; Dramae et al. 2022; Li et al. 2018). Therefore, endophytes are a vast repository for an accumulated wealth of unique chemical structures that can be utilized to treat numerous diseases.

The Euphorbiaceae family is one of the largest plant families, with over 330 genera and 8000 species. Several Euphorbia plants have been used since ancient times as traditional medicinal herbs in India and China for the treatment of different ailments such as asthma, cough, tumors, and antiviral with diverse chemical classes of secondary metabolites (Diop et al. 2018, Ernst et al. 2015, Olounladé et al. 2017, Zengin et al. 2017). In folk medicine, Euphorbia milii has been used to treat hepatitis, warts, and cancer, and it is also reported to have antiviral and cytotoxic properties (Chaman et al. 2019; Delgado et al. 2003) as well as antifungal, antinociceptive, and molluscicidal properties (Opferkuch and Hecker 1982; Rauf et al. 2014). The antiproliferation potential of E. milii using an exquisite combination of phytopharmacological and advanced computational techniques revealed that the chloroform fraction of methanol crude extract had the highest antioxidant and significant cytotoxicity (Talha et al. 2020). Phytochemical studies revealed the presence of sterols, sesquiterpenes, triterpenes, phenolic acids, flavonoids, coumarin, alkaloid, and ellagic acid (Hammad et al. 2019; Hemalatha et al. 2015; Marie and Ronnie 2018). The previous studies of endophytic fungi isolated from Euphorbia species demonstrated that Chaetomium strumarium isolated from E. hirta (Anitha and Mythili 2017), Fusarium sp. from E. pekinensis (Dai et al. 2008), and laccase enzyme producing fungi from E. milii (Rao et al. 2018). Endophytic fungi isolated from medicinal plants have not been investigated yet for the discovery of bioactive metabolites, and limited numbers of endophytes from medicinal plants have been reported (Uzma et al. 2019). Therefore, scientists of different disciplines focus on the biological evaluation of fungal secondary metabolites. Only one report investigated the laccase enzyme production ability of endophytic fungi from E. milli (Rao et al. 2018). However, antimicrobial and identification of corresponding metabolites have not been previously reported. Plant extracts composition including nine euphorbia plants as well as quantification of flavonoids and phenolic acids were previously identified using LC–MS/MS technique (Bouhafsoun et al. 2018; Ceylan et al. 2016; Yener et al. 2018). GC–MS is a powerful tool validation for qualitative and quantitative investigation of some chemical, volatile and thermally stable compounds (Derya et al. 2020; Mehmet et al. 2016).

Therefore, the present study aimed to evaluate the antimicrobial potential of endophytic fungus strains isolated from E.milii and identify the main secondary metabolites using GC–MS and LC–MS/MS techniques.

Materials and methods

Plant material

The plant sample of Euphorbia milii was collected from Orman Garden (30°1ʹ45ʺN, 31°12ʹ47ʺE) Giza, Egypt. Samples were placed in polyethylene bags, labeled, transported to the laboratory, and refrigerated at 4 °C.

Isolation and purification of endophytic fungi

After surface sterilization of the host plant sample; fresh, healthy parts of leaves and stem of Euphorbia milii have been cut into pieces and placed in Potato dextrosw agar (PDA) (Greenfield et al. 2015). After a week of incubation at 28 °C temperature, when fungal mycelium tips were observable, each hyphal tip was transferred onto a fresh PDA slant. For purification of the fungal strains, this step was repeated several times until the colony was deemed uniform. All pure isolates were numbered and stored on the surface of PDA slants at 4 °C (Hanlin 2000). Fungal characterizations were made according to their macroscopic and microscopic characteristics. The cultural and morphological characteristics of the isolate were compared with species descriptions reported in the standard taxonomic manuals to identify the fungal genera and species. Light micrographs were captured using an Olympus CX40 RF100 light microscope coupled to a Canon A620 digital camera (Hanlin 2000). Based on the antagonistic screening; the most active fungal isolate was selected for biological activity studies.

Genotypic identification of the most active fungal isolates

Sequencing and molecular phylogenetics

Based on the preliminary screening; the most potent fungal isolate representing the highest antimicrobial activity was inoculated on PDA and colony morphology was recorded after 48 h of incubation at 25 °C. Microscopic observations were made on the fungus stained with lactophenol cotton blue under the microscope. The molecular characterization was performed through isolation of 18S rDNA. The ITS1–5.8S–ITS2 genomic region was amplified from genomic DNA, using the forward primer ITS1 (5-TCCGTAGGTGAACCTGCGG-3) and the reverse primer ITS4 (5-TCCTCCGCTTATTGATATGC-3) (Hemalatha et al. 2015; White et al. 1990). In short, the reaction conditions for polymerase chain reaction are performed with 2 μl of 10 X Taq PCR buffer, 1.6 μl from 2.5 mM dNTP mixture, 1 μl of both forward and reverse primers (10 pmol/μl), 2 μl template genomic DNA (20 ng/μl), 0.2 μl from KOMATaq. (2.5 U/μl), and distilled water (HPLC grade) up to 20 μl. The reaction mixture was as follows: initial denaturation at 95 °C for 1 min, 30 cycles dent. 95 °C for 30 s, annealing 55 °C for 2 min, extension 68 °C for 1.5 min, final extension 68 °C for 10 min for 1 cycle. After completion, the PCR products were electrophoresed on 1% agarose gels, containing ethidium bromide (10 mg ml), to ensure that a fragment of the correct size had been amplified. The amplification products were purified by Montage PCR clean up kit (Millipore). The purified PCR products were sequenced, using the 2 primers that were used before in the PCR reaction. Sequencing was performed by big Dye Terminator Cycle Sequencing kit V.3.1 (Applied Biosystems, USA). PCR products were resolved on an Applied Biosystems model 3730XL automated DNA sequencing system (Applied Biosystems, USA) at the Macrogen, INC, Seoul Korea.

Phylogenetic data were obtained by aligning the nucleotides of different 18S rRNA retrieved from BLAST algorithm (www.ncbi.nlm.nih.gov/BLAST), MEGA6 BLAST and fast minimum evolution method were used for tree formation. The further parameters in the tree were inserted through MEGA-X software, and the sequence obtained was submitted to NCBI database.

Fermentation and crude extract preparation

The most active fungal endophyte was cultivated on PDA medium and incubated at 28 °C, statically. After 21 days of incubation, secondary metabolites were extracted by soaking in methanol 70% overnight. The cultures were filtered under vacuum through filter paper (Whatman No. 4; Brentford, UK). After drying, the extraction process by ethyl acetate was carried out three times for complete extraction. The organic phase was concentrated to dryness under reduced pressure using a rotary evaporator to obtain the crude fungal extract. A part of crude ethyl acetate extract was partitioned using n-hexane and the other part was fractionated on column chromatography using silica gel to afforded six sub-fractions (F1–F6). The 6 fractions were obtained by applying ethyl acetate extract on silica gel column using n-hexane/ethyl acetate in the order of increasing polarity; 5, 10, 20, 30, 40, and 50%, respectively. TLC was used to collect the similar fractions and detection was performed under UV lamp (254 and 356 nm) as well as spraying reagents. TLC showed a major compound for F2 which further purified on Sephadex LH-20 using chloroform/methanol followed by two successive column on silica gel using dichloromethane/methanol (8:2) to afford a crude compound 1 (1.5 mg).

In vitro antibacterial and antifungal assay

Antimicrobial activity was measured by an agar diffusion method against Gram-positive bacteria (Bacillus subtilis ATCC 6633), Gram-negative bacteria (Escherichia coli ATCC 25,922), unicellular yeast fungi (Candida albicans ATCC 10,321), and filamentous fungi (F. solani NRC15 and F. oxysporum). Bacteria and yeast strains were obtained from the American Type Culture Collection, while fungi were obtained from the culture collection of the Chemistry of Natural and Microbial Products Department, National Research Centre, Egypt. Thiophenicol (Thiamphenicol, Sanofiaventis, France) and Treflucan (Fluconazole, Egyptian Pharmaceutical Industries Company EIPICO) were used as antibacterial and antifungal positive controls, respectively, in a concentration of 100 μg/disk and DMSO was used as a negative control. The disks (1 mg/5 μl) were applied on inoculated nutrient agar and PDA media plates and incubated for 24 h at 37 °C for bacteria and 72 h at 28 °C for fungal strains, respectively. The zone of inhibition was recorded and compared with the positive control treatments.

MIC of endophytic strains and their fractions

Endophytic strain C. ovatoascomatis NRC, n-hexane fraction, and sub-fractions F1-F6 were screened in vitro against Gram-positive bacteria (Bacillus subtilis ATCC 6633, Staphylococcus aureus ATCC29213 and Lactobacillus cereus ATCC14579), Gram-negative bacteria (Escherichia coli ATCC 25922 and Salmonella enteric ATCC 25566), unicellular yeast fungi (Candida albicans ATCC 10321), and filamentous fungi (Aspergillus niger NRC53, F. solani NRC15 and F. oxysporum). The minimum inhibitory concentration of each sample against tested microorganisms was determined by microtiter broth dilution method: MIC was performed on the extracts, fractions and isolated compounds by serial dilution as previously described (Eloff 1998; Teh et al. 2017) according to the Clinical and Laboratory Standards Institute (CLSI) guidelines. The serial dilutions from the stock solution were made ranges 500, 250, 125 and 62.5 using Nutrient broth and Potato dextrose broth for Bacteria and fungi, respectively, in 96-well microplates. The bacterial suspension containing approximately 5 × 105 colony-forming units/mL was prepared from a 24 h culture plate. From this suspension, 100 μl was inoculated into each well. A sterility control well and a growth control well were also studied for each strain. Thiophenicol and Treflucan were used as positive controls for antibacterial and antifungal activity in a concentration of 500, 250, 125 and 62.5 μg. The microtiter plates were incubated at 37 °C, 24 h for bacteria and 28 °C, 48 h for fungi. After incubation; the MIC values visually determined. The lowest concentration of each extract displaying no visible growth was recorded as the minimum inhibitory concentration.

GC–MS analysis

GC–MS analysis was performed using a Thermo Scientific, Trace GC Ultra/ISQ Single Quadrupole MS, TG-5MS fused silica capillary column (30 m, 0.251 mm, 0.1 mm film thickness). For GC–MS detection, an electron ionization system with ionization energy of 70 eV was used, Helium gas was used as the carrier gas at a constant flow rate of 1 mL/min. The injector and MS transfer line temperature was set at 280 °C. The oven temperature was programmed at an initial temperature 50 °C (hold 2 min) to150 °C at an increasing rate of 7 °C/min then to 270 at an increasing rate 5 °C/min (hold 2 min) then to 310 as a final temperature at an increasing rate of 3.5 °C/min (hold 10 min). The quantification of all the identified components was investigated using a percent relative peak area. A tentative identification of the compounds was performed based on the comparison of their relative retention time and mass spectra with those of the NIST (National Institute of Standards and Technology, Gaithersburg, MD, USA), WILEY library data of the GC–MS system.

LC-ESI-TOF–MS analysis

Sample preparation

A stock solution of the extract was prepared from 50 mg of the lyophilized ethyl acetate extract dissolved in 1000 µL of the solvent mixture composed of water: methanol: acetonitrile (H2O:MeOH: ACN) in a ratio of 2:1:1. Complete solubility of stock solution was obtained by sample vortexed and ultra-sonication at 30 kHz for 10 min. An aliquot, 20 µL of the stock solution was again diluted with 1000 µL of the H2O: MeOH: ACN (2:1:1) and centrifuged at 10,000 rpm for 5 min, and 10 µL (1 µg/mL) was used for injection. The LCMS analysis was also performed for blank and quality control samples/internal standard (IS) for confidence in the experiment. The sample was injected in negative mode.

Instruments and acquisition method

Small molecules were separated on an ExionLC system (AB Sciex, Framingham, MA, USA) connected with an autosampler system, an in-line filter disks pre-column (0.5 µm × 3.0 mm, Phenomenex, Torrance, CA, USA), and an Xbridge C18 (3.5 µm, 2.1 × 50 mm) column (Waters Corporation, Milford, MA, USA) was maintained at 40 °C, and at a flow rate of 300 µL/min was utilized. The mobile phase consisted of solution (A): 5 mM ammonium formate in 1% methanol, pH adjusted to 8.0 by using sodium hydroxide, and solution (B): consisting of acetonitrile (100%). The gradient elution was performed with the following program: 0–20 min, 10% B; 21–25 min, 90% B; 25.01–28 min, 10% B; and then 90% B for equilibration of the column. The mass spectrometry (MS) was performed on a Triple TOF 5600 + system equipped with a Duo-Spray source operating in the ESI mode (AB SCIEX, Concord, ON, Canada). The sprayer capillary and declustering potential voltages were − 4500 and − 80 V. The source temperature was set at 600 °C, the curtain gas was 25 psi, and gas 1 and gas 2 were 40 psi. The collision energy − 35 V (negative mode) with CE spreading 20 V and the ion tolerance for 10 ppm were used. The TripleTOF5600 + was operated using an information dependent acquisition (IDA) protocol. Batches for MS and MS/MS data collection were created using Analyst-TF 1.7.1. The IDA method was used to collect full-scan MS and MS/MS information simultaneously. The method consisted of high-resolution survey spectra from 50 to 1100 m/z and the mass spectrometer was operated in a pattern where a 50-ms survey scan was detected. Subsequently, the top 15 intense ions were selected for acquiring MS/MS fragmentation spectra after each scan (Fayek et al. 2019).

LC–MS data processing

MS-DIAL 3.70 open-source software (Tsugawa et al. 2015) was used for non-targeting, small molecule comprehensive analysis of the sample. According to the acquisition mode, ReSpect negative (1573 records) databases were used as reference databases. The search parameters were set as MS1 and MS2 mass tolerance: 0.01 Da and 0.05 Da for data collection, for peak detection; minimum peak height: 100 amplitude, mass slice width: 0.05 Da, smoothing level: 2 scans, minimum peak width: 6 scans, for identification MS1 and MS2 tolerance: 0.2 Da/each, for alignment; retention time tolerance: 0.05 min and MS1 tolerance: 0.25 Da. The MS-DIAL output was used to run again on PeakView 2.2 with the MasterView 1.1 package (AB SCIEX) for feature (peaks) confirmation from Total Ion Chromatogram (TIC) based on the criteria; aligned features having signal-to-noise ratio greater than 5 and intensities of the sample: blank greater than 5.

Results and discussion

Microorganisms isolation and antimicrobial screening

Euphorbia milii yielded a total of 5 fungal isolates belonging to the following genera: Alternaria, Aspergillus, Fusarium, and Chaetomium. Antimicrobial assays of microorganism’s fungal isolates are shown in Table 1. The ethyl acetate extract of fungal isolate coded (MP2) Chaetomium ovatoascomatis revealed a promising activity against Gram-negative E. coli ATCC25922, and Gram-positive B. subtilis with inhibition zones 15 and 22 mm, respectively, and showed moderate activity against tested yeast C. tropicalis with inhibition zone 7 mm as well as a considerable effect against tested fungal strains F. solani and F. oxsporium with inhibition zone 7 and 13 mm, respectively. The strain Chaetomium ovatoascomatis was selected for phytochemical investigation using LC–MS/MS and GC–MS analysis based on the screening process results.

Table 1 Antimicrobial assays of microorganism's fungal isolates
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Identification of the most active isolates based on molecular phylogenetic analysis

Morphological identification revealed the formation of colonies on PDA fast-growing, reaching around 7 cm diam. After seven days after incubation at 25 °C, the colony was sparse, rough, raised with an entire edge, thinly hairy, and well defined at the margin; colony from above; rough, sparse, whitish; from below, pale brown. Sporulate on PDA, these morphological characteristics agreed with (Raza et al. 2019). The phylogenetic analysis of the isolated fungal strain MP2 Chaetomium ovatoascomatis revealed 98% identity with ITS sequences of rRNA genes of related species using BLAST programs (Fig. 1). (Selim et al. 2014).

Fig. 1
figure 1

Phylogenetic analysis of fungal strains

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Phytochemical analysis

Endophytic fungi are an abundant source of secondary metabolites such as coumarins, terpenoids, glycosides, and flavonoids, which contain a multitude of antifungal, anticancer, and antibacterial compounds. Terpenoids demonstrated several pharmacological effects, including antibacterial, antitumor, antiviral, anti-inflammatory as well as cardiovascular disease treatment (Yang et al. 2020). Flavonoids possess antifungal activity via diverse mechanisms such as mitochondria and plasma membrane destruction (Al Aboody and Mickymaray 2020). Flavonoids exert their antibacterial effect by damaging the cytoplasmic membrane, thereby impeding the synthesis of nucleic acids (Zhenyou et al. 2022). Phytochemical analysis of ethyl acetate extract of Chaetomium ovatoascomatis NRC and its nonpolar hexane fraction was performed by LC–MS/MS and GC–MS, respectively.

Identification of the crude compound 1 of Chaetomium ovatoascomatis NRC

The major crude compound 1 was identified by a combination of LC–MS, LC–MS/MS, and NMR tools. Negative and positive mode LC–MS analysis of crude 1 showed molecular ion peak at m/z 328 and 330, respectively, suggesting molecular weight of 329 Daltons (Fig. 2, 3). LC–MS/MS analysis (negative mode) of Chaetomium ovatoascomatis total extract was used to predict the molecular formula corresponding to m/z 329 by using PeakView software program which suggested molecular formula of C17H13O7, [M–H]−. The precursor ion peak m/z 329.066 exhibited to daughter ions at m/z 314, 311, 301, 283 corresponding to [M–H–CH3]–, [M–H–H2O]–, [M–H–CO]–, [M-H–CO–H2O]–, respectively. Analysis and comparison to the references public database HMBD and FOODB for precursor and daughter ions peaks were consistent with aflatoxin G2. 13C–NMR and HSQC of crude compound 1 exhibited the unresolved mixture with expected signals of aflatoxin G2 (Fig. 4).

Fig. 2
figure 2

LC–MS of a crude compound 1 in positive (above) and negative mode

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Fig.3
figure 3

UV absorbance (above) and mass spectrum for crude compound 1 in positive mode

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Fig. 4
figure 4

13C–NMR (above) and HSQC spectrum of crude compound 1

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LC–MS/MS of ethyl acetate extract of Chaetomium ovatoascomatis NRC

LC–MS/MS analysis of ethyl acetate extract (Fig. 5) revealed the presence of an additional compound with precursor ion m/z 339.0499 with a predicted molecular formula of C18H11O7 [M–H]–. The daughter ions were shown at m/z 321 (C18H9O6), 307 (C17H7O6), 295 (C17H11O5), 265 (C16H9O4). Comparison to the references public database (HMBD, FOODB) for the precursor ion and fragment daughter ions suggested the presence of grevilline B which belongs to catechols.

Fig. 5
figure 5

Chromatogram of LC–MS/MS of ethyl acetate extract of Chaetomium ovaoascomatis

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The same procedures were followed, and a number of metabolites were tentatively identified (Table 2) by comparison with the public reference database and reported data, including austdiol, apigenin, citreaoisocoumarin, macrosporin, quinalizatrine, alternariol, and questinol. The mass spectrum of the major identified compounds is shown in Fig. 6.

Table 2 LC–MS/MS of Chaetomium ovatoascomatis NRC, Adduct ion as [M–H]–
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Fig.6
figure 6

Mass spectrum of grevilline B, apigenin and aflatoxin G2

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GC–MS analysis

GC–MS analysis of the nonpolar hexane fraction tentatively identified 30 compounds (Table 3), where 9,12-octadecadienoic acid methyl ester was the major compound (35.6%), followed by 9-octadecenoic acid methyl ester (16.1%) then hexadecanoicacid methyl ester (13.9%). In the range of 4.94 to 3.10 percent, additional compounds were tentatively identified as 2-ethyl4-methyl-2, 5-dihydrooxazole, l-Limonene, 2-Methyl-2(1,4-dimethylcyclohexyl) cyclopentanone, and octadecanoic acid, methyl ester.

Table 3 GC–MS of n-hexane fraction
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Antibacterial activity

Endophyte fungi are promising sources of novel bioactive compounds that can be utilized for pharmaceutical, medicinal and agricultural applications (Manganyi and Ateba 2020). Several studies on fungal endophytes have reported significant antimicrobial activity due to the presence of different classes of bioactive molecules (Rao et al. 2015; Rodriguez et al. 2009). In the present study, ethyl acetate extract of Chaetomium ovatoascomatis NRC, n-hexane fraction, and sub-fractions (1F-6F) was evaluated against Gram-positive bacteria (Bacillus subtilis ATCC 6633, Staphylococcus aureus ATCC29213 and Lactobacillus cereus ATCC14579), Gram-negative bacteria (Escherichia coli ATCC 25922 and Salmonella enteric ATCC 25566), unicellular yeast fungi (Candida albicans ATCC 10321), and filamentous fungi (Aspergillus niger NRC53, F. solani NRC15 and F. oxysporum). Antibacterial results (Table 4) revealed a promising activity of ethyl acetate extract of Chaetomium ovatoascomatis against Gram-negative (E. coli ATCC25922, Salmonella enteric ATCC 25,566) and Aspergillus niger NRC53 with MIC of 62.5ug and considerable effect against Gram-positive (Staphylococcus aureus ATCC29213, Lactobacillus cereus ATCC14579) and Candida albicans ATCC 10321 with MIC value of 125.0ug. The most significant activity was recorded for n-hexane and F2 fractions against Gram-positive, Gram-negative, yeast, and filamentous fungi with MIC of 62.5 ug for both fractions. Whereas, n-hexane has higher activity against F. solani NRC15 while F2 is more effective against Aspergillus niger NRC53. F4 fraction demonstrated its activity against 2 Gram-positive (Bacillus subtilis ATCC 6633, Lactobacillus cereus ATCC14579.) and two Gram-negatives (Escherichia coli ATCC 25922, Salmonella enteric ATCC 25566) and Aspergillus niger NRC53. F1 exhibited antibacterial activity against Gram-positive (Staphylococcus aureus ATCC29213, Bacillus subtilis ATCC 6633) and Gram-negative (Escherichia coli ATCC 25922, Salmonella enteric ATCC 25566). The antimicrobial activity of fractions F3, F5, and F6 was significantly lower than that of the previous fractions. The antimicrobial activity of ethyl acetate extract of Chaetomium ovatoascomatis is due to the presence of major metabolites belonging to aflatoxin, catechol, and flavonoid classes. Aflatoxin G2 is a highly toxic secondary metabolite previously produced by Chaetomium species (Koyama et al. 1991). Grevilline B belongs to catechols compounds demonstrating significant antimicrobial activity (Jeong et al. 2009). Apigenin has several medicinal properties, including antiviral, antibacterial, and antioxidant (Thirukumaran et al. 2019), as well as significant antimicrobial activities of flavonoids (Zhenyou et al. 2022; Al Aboody and Mickymaray 2020). The antimicrobial results of n-hexane can be attributed to the presence of 9,12-octadecadienoic acid methyl ester and 9-octadecenoic acid methyl as major constituents consistent with the previously reported activity of fatty acid methyl esters (Chandrasekaran et al. 2008; Agoramoorthy et al. 2007). Currently, chromatographic identification of the obtained fractions is being conducted to determine the chemical constituents and rationalize their antimicrobial activities.

Table 4 MIC of fungal endophyte strain and their fractions
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Conclusion

Chaetomium ovatoascomatis NRC strain was isolated herein for the first time from E.milli and demonstrated promising antimicrobial activity against tested pathogens. In addition, n-hexane and sub-fractions of the strain exhibited broader activity against Gram-positive and Gram-negative bacteria, yeast, and filamentous fungi with a higher MIC value than the positive control. LC–MS/MS of ethyl acetate extract of Chaetomium ovatoascomatis revealed the presence of aflatoxin G2, grevilline B, and apigenin with potential antimicrobial activity. The GC–MS analysis of n-hexane revealed 9,12-octadecadienoic acid methyl ester as the major antimicrobial component. The combination of LC–MS/MS and NMR would be helpful in identifying impure metabolites with few milligrams.