Identification, Characterization, and Antibacterial Evaluation of Five Endophytic Fungi from Psychotria poeppigiana Müll. Arg., an Amazon Plant

Endophytic fungi, residing within plants without causing disease, are known for their ability to produce bioactive metabolites with diverse properties such as antibacterial, antioxidant, and antifungal activities, while also influencing plant defense mechanisms. In this study, five novel endophytic fungi species were isolated from the leaves of Psychotria poeppigiana Müll. Arg., a plant from the Rubiaceae family, collected in the tropical Amazon region of Bolivia. The endophytic fungi were identified as a Neopestalotiopsis sp., three Penicillium sp., and an Aspergillus sp. through 18S ribosomal RNA sequencing and NCBI-BLAST analysis. Chemical profiling revealed that their extracts obtained by ethyl acetate contained terpenes, flavonoids, and phenolic compounds. In a bioautography study, the terpenes showed high antimicrobial activity against Escherichia coli. Notably, extracts from the three Penicillium species exhibited potent antibacterial activity, with minimum inhibitory concentration (MIC) values ranging from 62.5 to 2000 µg/mL against all three pathogens: Escherichia coli, Staphylococcus aureus, and Enterococcus faecalis (both Gram-positive and Gram-negative bacteria). These findings highlight the potential of these endophytic fungi, especially Penicillium species as valuable sources of secondary metabolites with significant antibacterial activities, suggesting promising applications in medicine, pharmaceuticals, agriculture, and environmental technologies.


Introduction
Fungi have emerged as a rich source of bioactive and structurally unique secondary features [1,2].Due to the extensive chemical and biological diversity of these secondary metabolites, exploring the fungal genus continues to offer opportunities for discovering novel lead compounds with potential for pharmaceutical drug development and biocontrol agent synthesis [3].In recent years, endophytic fungi have garnered increasing attention in research circles, attributed to the identification of numerous novel compounds [4][5][6].Endophytic fungi, microorganisms residing internally within various host plant tissues asymptomatically without inducing apparent disease [7][8][9], possess the ability to engage in complex interactions with their host plants.Through these interactions, plants can modulate endophytic metabolic processes to produce molecules with protective functions, benefiting both the microbe and host [10,11].
The cohabitation of endophytes within host plants may aid in their adaptation to biotic and abiotic stress factors [7,12].Endophytic fungi have demonstrated the potential to produce bioactive metabolites that influence plant defense mechanisms, thereby enhancing the survival of both symbiotic entities.Generally, leaves exhibit a more diverse community of fungal endophytes compared to other plant parts [7,13].Given their potential as an abundant source of new metabolites, crude extracts from these microorganisms hold promise as an alternative approach, with the capacity for industrial-scale production of bioactive compounds, thereby reducing final product costs and contributing to plant species conservation [14].
Consequently, this research explores the capability of endophytic fungi to generate novel secondary metabolites with diverse biological activities, such as antibacterial, antioxidant, and antifungal properties.Despite being recognized as promising sources of novel active compounds, the true potential of endophytic fungi, in terms of biological activity and biotechnological applications, remains largely unexplored [7], particularly in the context of tropical plant endophytes and their pharmacological potential [15].The Amazon forest harbors the highest diversity of plant species on Earth, alongside an extraordinary abundance of fungi [16,17].Research efforts have focused on collecting biological and ecological data on both rare and common fungal species to develop a deeper understanding of their roles in ecosystem functioning, particularly in light of predictions of global warming [17].However, research on the identification and role of endophytic fungi remains underreported.
Meanwhile, Lidilhone Hamerski et al. conducted a comprehensive review exploring the natural product diversity and pharmacological properties of secondary metabolites produced by endophytic fungi associated with various genera of Rubiaceae [9].Rubiaceae stands as the fourth largest angiosperm family, comprising approximately 617 genera and 13,000 species of herbs, shrubs, and trees, distributed worldwide, with a notable concentration in tropical and warm regions [9,18].This botanical family showcases a remarkable diversity of chemical substances, including iridoids, anthraquinones, indole alkaloids, terpenoids, flavonoids, and alkaloids [9,[18][19][20].Several species within the Rubiaceae family have found extensive use in folk medicine, with evidence of anti-inflammatory, analgesic, antibacterial, mutagenic, antiviral, and antioxidant activities.One such species within Rubiaceae, Psychotria poeppigiana Müll.Arg.(now accepted as Palicourea tomentosa (Aubl.)Borhidi), is native to Central and South America, specifically Bolivia, Venezuela, and Brazil [21].Traditionally, it has been employed in medicinal practices for the treatment of inflammation and pain.Additionally, Cephaelis elata, a synonym for Psychotria poeppigiana, has been utilized for addressing dementia [21].Recent research has delved into the antioxidant, anti-inflammatory, and anti-acetylcholinesterase (AChE) activities of the chemical composition of P. poeppigiana essential oil extracted from its leaves (EOPP) [21].However, investigations into the endophytic fungi associated with P. poeppigiana, particularly concerning their extract's antibacterial activity, have not been performed.
With this context, in this study, P. poeppigiana Müll.Arg., a plant belonging to the Rubiaceae family, was collected from the tropical Amazon region of Cochabamba, Bolivia.From the leaves of this plant, five new species of endophytic fungi (Neopestalotiopsis sp.SMB-23, Aspergillus sp.SMB-27, and three species of Penicillium sp.SMB-24, SMB-25, and SMB-26 were isolated and identified using 18S ribosomal RNA sequences, analyzed through the online NCBI-BLAST tool.Phylogenetic trees were also constructed using the same tool.Subsequently, the resulting extracts underwent antibacterial testing to determine the minimal inhibitory concentration (MIC), revealing significant inhibition against pathogenic bacteria in the extracts from three Penicillium species.The chemical profiles of the extracts were investigated to identify the main groups of chemical compounds.

Materials
The materials utilized encompassed basic microbiology and chemistry supplies for the preparation and handling of culture media, bacterial strains, and extracts from endophytic fungal strains.Potato dextrose agar (PDA) and potato dextrose broth (PDB) were meticulously prepared in the laboratory following established protocols [22] or purchased from Merck (Darmstadt, Germany).The culture media for the bacterial strains, Nutrient medium and Brain Heart Infusion BHI, were purchased from MBcell, the Republic of Korea.Commercially procured Mueller-Hinton Agar, Trypto-Casein Soy Broth (TSB), and Trypto-Casein Soy Agar (TSA) were sourced from OXOID manufacturing.Additionally, the Quick-DNA Fungal/bacterial Miniprep Kit Zymo Research (Irvine, CA, USA) and the Gene JET PCR Purification Kit Thermo Scientific, (Waltham, MA, USA) were employed for DNA extraction and purification processes following the protocol introduced by the manufacturer.For polymerase chain reaction (PCR) amplification, specific primers (ITS3, ITS5, EF4f, and Fung5r) were utilized Integrated DNA Technologies IDT, (Coralville, IA, USA).Ethyl acetate, n-hexane, ethanol, sodium hypochlorite, p-anisaldehyde, ferric chloride, and aluminum chloride were acquired from Sigma-Aldrich (Saint Louis, MO, USA).TLC Silica gel 60 F254 chromatographic plates (aluminum sheets 20 × 20 cm, silica gel matrix, fluorescent indicator) and Mueller-Hinton (M-H agar) were purchased from Merck (Darmstadt, Germany).

Isolation of Endophytic Fungi from Psychotria poeppigiana Müll. Arg.
The collection of specimens of P. poeppigiana Müll.Arg., a plant species, was conducted in the Amazon region known as Valle del Sacta at an altitude of 240 m above sea level (17 • 05 ′ 12 ′′ S and 64 • 46 ′ 19 ′′ W), located within the Carrasco province of Cochabamba, Bolivia (Figure 1).

Materials
The materials utilized encompassed basic microbiology and chemistry supplies for the preparation and handling of culture media, bacterial strains, and extracts from endophytic fungal strains.Potato dextrose agar (PDA) and potato dextrose broth (PDB) were meticulously prepared in the laboratory following established protocols [22] or purchased from Merck (Darmstadt, Germany).The culture media for the bacterial strains, Nutrient medium and Brain Heart Infusion BHI, were purchased from MBcell, the Republic of Korea.Commercially procured Mueller-Hinton Agar, Trypto-Casein Soy Broth (TSB), and Trypto-Casein Soy Agar (TSA) were sourced from OXOID manufacturing.Additionally, the Quick-DNA Fungal/bacterial Miniprep Kit Zymo Research (Irvine, CA, USA) and the Gene JET PCR Purification Kit Thermo Scientific, (Waltham, MA, USA) were employed for DNA extraction and purification processes following the protocol introduced by the manufacturer.For polymerase chain reaction (PCR) amplification, specific primers (ITS3, ITS5, EF4f, and Fung5r) were utilized Integrated DNA Technologies IDT, (Coralville, IA, USA).Ethyl acetate, n-hexane, ethanol, sodium hypochlorite, p-anisaldehyde, ferric chloride, and aluminum chloride were acquired from Sigma-Aldrich (Saint Louis, MO, USA).TLC Silica gel 60 F254 chromatographic plates (aluminum sheets 20 × 20 cm, silica gel matrix, fluorescent indicator) and Mueller-Hinton (M-H agar) were purchased from Merck (Darmstadt, Germany).

Isolation of Endophytic Fungi from Psychotria poeppigiana Müll. Arg.
The collection of specimens of P. poeppigiana Müll.Arg., a plant species, was conducted in the Amazon region known as Valle del Sacta at an altitude of 240 m above sea level (17°05′12″ S and 64°46′19″ W), located within the Carrasco province of Cochabamba, Bolivia (Figure 1).This plant, belonging to the Rubiaceae family, was identified using taxonomic keys of the Amazonian flora and the regional flora of the Sacta Valley, corroborated by reference to the "M.Cárdenas" National Forest Herbarium (BOLV).The collected plant parts (small branches with leaves) were stored in chilled containers at 4 °C for transportation to the laboratory [23,24].
Endophytic fungi were isolated from the aerial parts of the P. poeppigiana Müll.Arg.plant.Healthy leaves underwent surface disinfection through sequential washes with This plant, belonging to the Rubiaceae family, was identified using taxonomic keys of the Amazonian flora and the regional flora of the Sacta Valley, corroborated by reference to the "M.Cárdenas" National Forest Herbarium (BOLV).The collected plant parts (small branches with leaves) were stored in chilled containers at 4 • C for transportation to the laboratory [23,24].
Endophytic fungi were isolated from the aerial parts of the P. poeppigiana Müll.Arg.plant.Healthy leaves underwent surface disinfection through sequential washes with running tap water, 70% ethanol for 2 min, 1% hypochlorite for 1 min, and sterilized water for 2 min [23,24].For the isolation of endophytic fungi, the plant material was cut into approximately 5 mm 2 pieces and inoculated into Petri dishes (8-10 fragments per plate) containing (PDA) supplemented with 100 µg/mL chloramphenicol.The dishes were then incubated at 22 • C for 15 days.Mycelium was transferred to new plates, isolated, purified into pure strains, and stored in darkness.Depending on the culturable endophytes isolated, these were transferred to cryovial tubes containing 10% glycerol in PDB medium, cultured for 1 week at room temperature, and stored at −20 • C for later use in fermentations and biological tests [25,26].The isolated fungi were deposited in the Microbiology laboratory of the Centro de Tecnología Agroindustrial (CTA), Universidad Mayor de San Simón Cochabamba, Bolivia.

Identification of Endophytic Fungi
Five fungi were isolated from the leaves of the P. poeppigiana Müll.Arg.plant and underwent identification using both classical taxonomies, based on morphological characteristics and molecular techniques.The macromorphological characteristics were analyzed after seven days of culturing at 30 • C in Petri dishes (10 mm × 100 mm) containing PDA. Macroscopic vegetative traits, including color, texture, topography, diffuse pigmentation, and colony border, were examined.Additionally, the back topography of the colony was assessed [27].Microscopic morphology, encompassing hyphae and reproductive structures, was evaluated using the microculture technique in PDA for 5-7 days and YES for 7-10 days [28].Stained macroscopic glass slides using Lactophenol blue solution (Merck, Stockholm, Sweden) were observed under an optical microscope (LRI-OLYMPUS-100×/0.65, Tokyo, Japan) [10,29], and the obtained results were compared with taxonomic keys [28,30,31].
Furthermore, molecular taxonomy was employed for identification using specific PCR primers to amplify the endophyte ITS1-5.8S-ITS2region and 530 bp conserved region of the 18S rDNA gene.Fungal samples (50-100 mg wet weight) were obtained from fresh cultures grown in Petri dishes containing PDA for 7 to 15 days at a temperature between 28 and 30 • C [29,32,33].Genomic DNA extraction from the fungi was performed using the Quick-DNA extraction kit Zymo Research (Irvine, CA, USA), following the manufacturer's instructions, and stored at −20 • C in 100 µL DNA elution buffer.
The amplification of the ITS1-5.8S-ITS2region and 530 bp conserved region of the 18S rDNA gene was conducted via polymerase chain reaction (PCR) using the primers listed in Table 1.The EF4f/Fung5r primers were used for SMB-24, 26 and 27, while the forward ITS5F/ITS3R primer was used for SMB-25.The PCR reactions were carried out in a T100 Thermal Cycler BIO-RAD Laboratories Inc., (Hercules, CA, USA) under specified conditions (Table 1).The PCR products were visualized via agarose gel electrophoresis by running 2 µL of the PCR product in 1.0% (w/v) agarose gel with 19 tris/borate electrophoresis buffer (TBE).The gel was stained with GelGreen Nucleic Acid Gel Strain, 10,000× in water Fisher Scientific, (El Paso, TX, USA), and compared with a reference marker, GeneRuler 1 Kb DNA Ladder, Thermo Fisher Scientific (Waltham, MA, USA).The PCR products were purified using a PCR purification kit following the manufacturer protocol and were then subjected to direct sequencing using the same PCR primers, which were performed by Eurofins Scientific (Augsburg, Germany) [10,29].
Following sequencing, sequence analysis and alignment were performed using the online BLASTtool (blastn) in NCBI GenBank databases (website: www.ncbi.nlm.nih.gov/blast.accessed on 13 May 2024) to assess DNA similarities.The sequence of the endophytic fungal isolate was aligned with representative sequences of reference taxa, including members from other orders, obtained from GenBank.This alignment was crucial for resolving phylogenetic relationships.
To construct the phylogenetic trees, multiple sequence alignment and molecular phylogeny were conducted using Molecular Evolutionary Genetics Analysis (MEGA) 10.2.4 [29].The phylogenetic trees were constructed from models generated by MEGA software (www.megasoftware.net,freeware, Accessed on 15 April 2024), with bootstrap analysis performed using 1000 replications to assess the reliability of the node tree [34].Finally, the obtained sequences were deposited in GenBank for future reference and analyses.

Preparation and Chemical Profile of Extract from Endophytic Fungi
Five fragments of fungal mycelium (each measuring 5 × 5 mm 2 ), from every strain of endophytic fungus under investigation, were excised from the PDA plates and inoculated into 500 mL Erlenmeyer flasks containing 200 mL of PDB liquid medium composed of potato broth (200 g/L) and dextrose (20 g/L) [22].The cultures were incubated under shaking conditions at 200 rpm and 30 • C for 15 days, following the methodology outlined by Bose et al. [35], with certain modifications.To monitor biomass production under these culture conditions, the amount of biomass produced by each strain over the 15-day fermentation period was quantified.At the end of the cultivation, the mycelium was separated from the liquid medium through filtration using filters in a Büchner funnel.For the liquid-medium fraction, a liquid-liquid extraction technique was employed using ethyl acetate with a volume ratio of 1:1, and three extractions were performed.
The remaining mycelium portion underwent maceration with twice its volume of ethyl acetate for 24 h.Subsequently, the extracted fractions from both mycelium and broth were combined, and the solvent was evaporated.Thereafter, the extract was preserved at −10 • C for later use in biological tests.Following extraction, the total dry extract obtained from 200 mL of culture media and mycelium was weighed for control purposes.
For chemical profiling, the extracts were subjected to a TLC experiment to identify the main groups of chemical compounds present in the samples.Forty milligrams of the extract were dissolved in 1 mL of ethyl acetate, and 1 µL of the sample, corresponding to 40 µg of extract, was placed on the TLC plate.A mixture of n-hexane and ethyl acetate (1:1) was used as the mobile phase.To detect the chemical classes, ultraviolet light at 254 nm and 365 nm and the following chemical developers were used.To prepare the p-anisaldehyde developer, 0.5 mL of p-anisaldehyde was mixed with 10 mL of acetic acid, 85 mL of methanol, and 5 mL of concentrated H 2 SO 4 in that order.The ferric chloride solution was obtained by diluting 3 g of FeCl 3 in 100 mL of ethyl alcohol.The aluminum chloride solution was prepared by dissolving 1 g of AlCl 3 in 100 mL of ethyl alcohol.The partition factors (Rf) were calculated as the ratio of the distance migrated by the compound to the distance migrated by the eluent [10,36].
An ultra performance liquid chromatography (UPLC) system (ACQUITY H-Class, Waters, MA, USA) equipped with a quaternary pump, auto-sampler, photodiode array detector, QDa Mass detector, and BEH C18 column (2.1 × 100 mm, 1.7 µm) was utilized for the analysis of major compounds.The gradient elution was performed using solvent A (0.1% formic acid in water) and solvent B (acetonitrile) at a flow rate of 0.4 mL/min as follows: 0-2 min, 2% B; 2-15 min, 2-20% B; 15-20 min, 20-100% B; 20-23 min, 100% B; 23-26 min, 100-2% B; and 26-28 min, 2% B. Detection was set at a wavelength of 230 nm.The column temperature was maintained at 40 • C, the injection volume was 2 µL, and the flow rate was 0.4 mL/min.A QDa mass detector was used together with an electrospray ionization (ESI) source in positive mode under the following conditions: capillary voltage, 1.5 kV; cone voltage, 15 V; sampling frequency, 5 Hz; and probe temperature, 600 • C. The MS full scan was acquired in the range of m/z 120-1200.
Gas chromatography-mass spectrometry (GC-MS) was performed using a 431-GC and 210-MS system (Varian, Palo Alto, CA, USA) with a FactorFour Capillary column, VF-1 ms (15 m × 0.25 mm).The initial column oven temperature was ramped from 50 • C to 250 • C at a rate of 20 • C/min.Samples diluted with acetonitrile to a concentration of 0.1-0.5 mg/mL were injected in split injection mode at 275 • C, with a split ratio of 10:1.

Antibacterial Test: Determination of Minimum Inhibitory Concentration (MIC), Disk Diffusion, and TLC-Bioautography
For the evaluation of the antimicrobial activity, the minimum inhibitory concentration (MIC) was determined through microdilution tests in extracts according to the Clinical and Laboratory Standard Institute [37][38][39][40], with modifications.All compounds were subjected to MIC tests against three pathogenic species of bacteria.The bacterial strains Staphylococcus aureus (KCTC 3881, Gram-positive), Enterococcus faecalis (KCTC 2011, Gram-positive), and Escherichia coli (KCTC 1039, Gram-negative) were used.Bacterial strains were cultured in each medium.E. coli and E. faecalis were cultured at 37 • C in aerobic conditions in nutrient medium (MBcell, Seoul, Republic of Korea), and E. faecalis was cultured at 37 • C in a fecaltative anaerobic condition in BHI medium (MBcell, Republic of Korea).
The cultured bacterial medium was then diluted until the absorbance at 660 nm reached 0.03 (equivalent to 1-2 × 10 7 CFU/mL).The microplate wells were inoculated with the bacterial culture medium 20 min before the test.
Fungal extracts were solubilized in each medium at a concentration of 2000 µg/mL, followed by twofold serial dilutions to concentrations of 1000, 500, 250, 125, and 62.5 µg/mL.In a sterilized 96-well plate (Falcon, Dublin, OH, USA), 1 mL of sample was added, and 10 µL of the bacterial culture medium was inoculated.The plate was then incubated for 12 h in a shaking incubator at 150 rpm.Inhibition rates were determined using photometry (BIO-RAD Laboratories Inc., USA) at OD620 nm.Ampicillin was used as the positive control, with a MIC90 of 1.25 µg/mL for E. coli and E. faecalis, and a range of 20~0.625 µg/mL for S. aureus (MIC90 not determined).
The disk diffusion method was used according to the methodology established by the Clinical and Laboratory Standards Institute (CLSI 2015) and the European Committee on Antimicrobial Susceptibility Testing [38].An E. coli culture was spread on Petri dishes containing Mueller-Hinton agar, and filter paper discs treated with extracts (100 µg/disc) were placed on the agar.Antibacterial activity was assessed after 24 to 48 h of incubation at 37 • C. The presence of a clear zone around the discs indicated the antibacterial nature of the endophytic fungal extracts.
For the TLC-bioautography assay, the extracts were applied to TLC plates using the same method as in the chemical profiling experiments.The plates were then overlaid with a layer of E. coli on Mueller-Hinton agar, with an initial concentration corresponding to 0.5 on the McFarland scale (1.5 × 10 8 cells) [41,42].The inhibition zones on the TLC plates were compared to identify the main groups of chemical compounds, correlating these results with those from the chemical profiling.

Isolation and Molecular Identification of Endophytic Fungi from Psychotria poeppigiana Müll. Arg. (Rubiaceae)
Five endophytic fungi were successfully isolated from leaves of P. poeppigiana collected in the tropical Amazon area, a plant known for its traditional medicinal uses as an analgesic and anti-inflammatory agent.The fungal isolates underwent both morphological and molecular identification processes.All five strains were effectively amplified using primers ITS5/ITS3 for strain 25 and EF4f/Fung5r for strains SMB-23, 24, 26, and 27.BLAST searches revealed their identities as members of three different genera: one Neopestalotiopsis sp.(SMB-23), one Aspergillus sp.(SMB-27), and three Penicillium sp.(SMB-24, SMB-25, and SMB-26), all classified as endophytic fungi (Figures 2-6).
cal and molecular identification processes.All five strains were effectively amplified using primers ITS5/ITS3 for strain 25 and EF4f/Fung5r for strains SMB-23, 24, 26, and 27.BLAST searches revealed their identities as members of three different genera: one Neopestalotiopsis sp.(SMB-23), one Aspergillus sp.(SMB-27), and three Penicillium sp.(SMB-24, SMB-25, and SMB-26), all classified as endophytic fungi (Figures 2-6).Phylogenetic trees constructed using the partial sequence ITS of 18S rRNA gene sequences depicted a close phylogenetic relationship with partial sequences of fungal strains and some fungal species.The challenges in species-level determination and the scarcity of molecular data for comparison underscore the difficulties encountered in identifying many species of endophytic fungi [43].Figures 2-6 present the results of the phylogenetic trees depicting the endophytic fungal strains isolated from P. poeppigiana Müll.Arg.Phylogenetic trees constructed using the partial sequence ITS of 18S rRNA gene sequences depicted a close phylogenetic relationship with partial sequences of fungal strains and some fungal species.The challenges in species-level determination and the scarcity of molecular data for comparison underscore the difficulties encountered in identifying many species of endophytic fungi [43].Figures 2-6 present the results of the phylogenetic trees depicting the endophytic fungal strains isolated from P. poeppigiana Müll.Arg.
The sequences were analyzed using the neighbor-joining method, and the best-fit model was selected based on the closest sequences for constructing the phylogenetic trees.The sequences obtained in this study were deposited in GenBank (Table 2).Given the low probability and the limited approach to the genus level, it is evident that an alternative locus is required for proper molecular identification and to expand the sequence data (Figures 2-6).
The sequences were analyzed using the neighbor-joining method, and the best-fit model was selected based on the closest sequences for constructing the phylogenetic trees.The sequences obtained in this study were deposited in GenBank (Table 2).Given the low probability and the limited approach to the genus level, it is evident that an alternative locus is required for proper molecular identification and to expand the sequence data (

Morphological Characteristics of Endophytic Fungi
The description of cultural and morphological characteristics of fungal endophytes, along with microphotographs of their morphological structures, is presented in Table 3 and Figure 7.

Morphological Characteristics of Endophytic Fungi
The description of cultural and morphological characteristics of fungal endophytes, along with microphotographs of their morphological structures, is presented in Table 3 and Figure 7.
Colonies of endophytic fungi typically exhibit rapid growth on PDA medium at 30 • C, ranging between 3 and 7 days.However, growth is comparatively slower on yeast extract sucrose agar (YES) culture medium [28], taking between 7 and 10 days.

Aspergillus niger
The growth is initially white but changes to black after a few days, producing conidial spores.The edges of the colonies appear pale yellow, producing radial fissures.
Cottony appearance, initially white to yellow and then turning black.The reverse rough yellow on PDA.In YES, the color is and more orange on the reverse.
Filamentous fungus that forms filamentous hyphae that make them look like small plants.
The conidial heads appear radial, they are smooth and hyaline.The conidiophore becomes dark at the apex and terminating in a globose vesicle which is 30-75 µm in diameter.Produce conidia of brown coloration, and have a diameter of 4-5 µm.
[  Colonies of endophytic fungi typically exhibit rapid growth on PDA medium at 30 °C, ranging between 3 and 7 days.However, growth is comparatively slower on yeast extract sucrose agar (YES) culture medium [28], taking between 7 and 10 days.
The endophytic fungus SMB-23 belongs to the genus Neopestalotiopsis, sharing morphological characteristics akin to the genus Discosia.When isolated, SMB-23 exhibited a The endophytic fungus SMB-23 belongs to the genus Neopestalotiopsis, sharing morphological characteristics akin to the genus Discosia.When isolated, SMB-23 exhibited a colony with rapid vegetative growth, appearing cottony, irregular, and flat, ranging in color from whitish to gray toward the center, with a lightly colored reverse side and dense mycelial culture (Figure 7, Table 3).However, sporulation was notably slow, which is a result identical with that in the literature [46].Microscopically, SMB-23 displays septate, hyaline, thin, and dense hyphae, along with cylindrical, fusiform conidia featuring obtuse ends, which are smooth-walled, hyaline, aseptate, and relatively scarce.The presence of appressoria is abundant, with some being globose, others clavate, and some displaying complex structures with irregular lobes; all were aseptate and white in color (Figure 7, Table 3).Generally, the color of the median conidial cells facilitates the differentiation of three genera: Neopestalotiopsis, Pestalotiopsis, and Pseudopestalotiopsis [46].Conidia with versicolored median cells are characteristic of the genus Neopestalotiopsis, which is believed to have evolved from the lineage of Pseudopestalotiopsis, characterized by dark concolorous conidial median cells, while Pestalotiopsis typically presents three light concolorous conidial median cells [46].The morphology of Pestalotiopsis-like taxa exhibits variability depending on the environment and host from which they were isolated, rendering species separation based on phenotypic characteristics challenging.Neopestalotiopsis can be easily distinguished from Pestalotiopsis by its fusiform conidia with five cells and versicolored median cells [47].
The three strains belonging to the Penicillium genus exhibit rapid colony growth, initially appearing white and later developing a yellowish-green hue with a creamy yellow reverse side.Their texture is flat, filamentous, and either velvety or cottony.SMB-24 and SMB-26 display drops of exudate after 10 days of growth on PDA.The colonies of Penicillium strains SMB-24, 25, and 26 possess a cotton-like texture, albeit with varying shades; SMB-24 and 26 tend towards a more yellow-green hue, while SMB-25 appears greenish (Figure 7, Table 3).In contrast, strain SMB-23 exhibits a rough surface texture, with aerial mycelium resembling cotton in white layers.
Strain Aspergillus SMB-27 displays abundant black conidia on the surface and lacks a cottony appearance (Figure 7).For the genus Aspergillus, ascospore sizes and morphologyespecially diagnostic ornamentation such as roughening, rims, wings, and furrows-play a crucial role in species identification [30].Strain SMB-27 of Aspergillus forms filamentous hyphae, resembling miniature plants.The initial mycelium color is white and contains growth which turned black within two days on PDA, accompanied by the production of conidial spores.The colony's reverse side appears yellow.

Chemical Profile of Endophytic Fungi Extracts
The secondary metabolites were extracted from five endophytic fungi using ethyl acetate.Cultures of Neopestalotiopsis sp.SMB-23, Penicillium sp.SMB-24, sp.SMB-25, and sp.SMB-26 and Aspergillus sp.SMB-27 were grown for 15 days in 200 mL of medium, resulting in extract yields of 31.8 mg, 138.6 mg, 201.9 mg, 161.9 mg, and 12.2 mg, respectively.In cultures of 9, 12, 15, 18, and 30 days for the endophytic fungi, similar metabolite profiles in TLC were obtained after 12 days.The chemical profiles of the extracts were investigated using thin-layer chromatography (TLC) and staining methods to identify the main groups of chemical compounds (Figure 8).
The TLC analysis did not reveal any chemical compounds with chromophores or high unsaturation visible under normal light (Figure 8A).However, the presence of conjugated double bonds was observed under UV light at 254 nm in samples from SMB-24, SMB-25, and SMB-26, with an Rf value of 0.35 (Figure 8B).Flavonoid compounds, stained with aluminum chloride, were observed in all extracts under UV light at 365 nm (Figure 8C).After developing the TLC plate with p-anisaldehyde, purple spots were observed in all extracts at Rf values of 0.96 and 0.88, indicating the presence of terpenes (Figure 8D).Additionally, red spots at Rf 0.60 in SMB-25 and SMB-26, and at Rf 0.35 in all three Penicillium extracts (SMB-24, SMB-25, and SMB-26), indicated the presence of flavonoids.These flavonoids were also observed under UV light at 254 nm (Figure 8B), showing conjugated double bonds and corroborating the identified compounds.The presence of phenolic compounds was indicated by brown spots developed with ferric chloride in extracts SMB-23, SMB-24, SMB-25, and SMB-26, all at an Rf value of 0.58 (Figure 8E).The TLC analysis did not reveal any chemical compounds with chromophores or high unsaturation visible under normal light (Figure 8A).However, the presence of conjugated double bonds was observed under UV light at 254 nm in samples from SMB-24, SMB-25, and SMB-26, with an Rf value of 0.35 (Figure 8B).Flavonoid compounds, stained with aluminum chloride, were observed in all extracts under UV light at 365 nm (Figure 8C).After developing the TLC plate with p-anisaldehyde, purple spots were observed in all extracts at Rf values of 0.96 and 0.88, indicating the presence of terpenes (Figure 8D).Additionally, red spots at Rf 0.60 in SMB-25 and SMB-26, and at Rf 0.35 in all three Penicillium extracts (SMB-24, SMB-25, and SMB-26), indicated the presence of flavonoids.These flavonoids were also observed under UV light at 254 nm (Figure 8B), showing conjugated double bonds and corroborating the identified compounds.The presence of phenolic compounds was indicated by brown spots developed with ferric chloride in extracts SMB-23, SMB-24, SMB-25, and SMB-26, all at an Rf value of 0.58 (Figure 8E).

Antimicrobial Activity of Extracts from Endophytic Fungi
The extracts were assessed for antimicrobial activity against pathogenic bacteria, including Staphylococcus aureus (Gram-positive), Escherichia coli (Gram-negative), and Enterococcus faecalis (Gram-positive), by determining their minimum inhibitory concentrations (MICs, mg/mL).

Relationship between Antibacterial Activity and Chemical Profile
Since Penicillium SMB-24, SMB-25, and SMB-26 possess antibacterial properties against both Gram-positive and Gram-negative pathogenic bacteria (Tables 4 and 5), the extract from these strains were subjected to identify the relationship between antibacterial activity and chemical profile classified (Figure 11).As a control, the antimicrobial activity was confirmed using Gram-positive E. coli, and showed clear zones in all three strains and positive control (Figure 11A).In the TLC-bioautography assay, the area of terpene (around Rf 0.35) showed high activity against E. coli for the extracts of endophytic fungi, Penicillium species (SMB-24, 25 and 26) (Figure 11B,C).Therefore, this observation and relationship can propose that the responsible active compound is classified as a terpene compound.Furthermore, Penicillium species can be a rich source of the terpene compound, which was present in high amounts in TLC (Figure 8D).
Since Penicillium SMB-24, SMB-25, and SMB-26 exhibited antibacterial properties against both Gram-positive and Gram-negative pathogenic bacteria (Tables 4 and 5); their extracts were analyzed to identify the relationship between antibacterial activity and chemical profile (Figure 11).and (Figure 11B,C).This observation suggests that the active compound responsible for the antibacterial activity is likely a terpene.Furthermore, the Penicillium species appear to be rich sources of terpene compounds, as indicated by the high content observed in the TLC analysis (Figure 8D).Meanwhile, the extracts from both the mycelium and the medium showed similar chemical profiles in TLC analysis, especially in the extracts of Penicillium species; the mycelium contained 1-2 times more the amount of the extracts.

Discussion
A species of Rubiaceae, P. poeppigiana Müll.Arg.(accepted as Palicourea tomentosa (Aubl.)Borhidi), was collected in the Amazon region of Bolivia.Bolivia is renowned for its rich biological diversity, boasting a vast array of plant species estimated to range between 17,000 and 20,000 vascular plants, thus contributing significantly to global biodiversity.
The indigenous communities of Bolivia possess profound knowledge of the medicinal properties of the surrounding flora, passed down through generations via oral traditions and direct observation.P. poeppigiana Müll.Arg. has long been utilized in traditional medicine for treating inflammation and pain, with Cephaelis elata serving as a synonym for dementia treatment [21].As a control, the antimicrobial activity was confirmed using Gram-negative E. coli, which showed clear inhibition zones for all three strains and the positive control (Figure 11A).In the TLC-bioautography assay, the terpene region (around Rf 3.5) demonstrated high activity against E. coli for the extracts from the Penicillium species SMB-24, SMB-25, and SMB-26 (Figure 11B,C).This observation suggests that the active compound responsible for the antibacterial activity is likely a terpene.Furthermore, the Penicillium species appear to be rich sources of terpene compounds, as indicated by the high content observed in the TLC analysis (Figure 8D).Meanwhile, the extracts from both the mycelium and the medium showed similar chemical profiles in TLC analysis, especially in the extracts of Penicillium species; the mycelium contained 1-2 times more the amount of the extracts.

Discussion
A species of Rubiaceae, P. poeppigiana Müll.Arg.(accepted as Palicourea tomentosa (Aubl.)Borhidi), was collected in the Amazon region of Bolivia.Bolivia is renowned for its rich biological diversity, boasting a vast array of plant species estimated to range between 17,000 and 20,000 vascular plants, thus contributing significantly to global biodiversity.
The indigenous communities of Bolivia possess profound knowledge of the medicinal properties of the surrounding flora, passed down through generations via oral traditions and direct observation.P. poeppigiana Müll.Arg. has long been utilized in traditional medicine for treating inflammation and pain, with Cephaelis elata serving as a synonym for dementia treatment [21].
Recent studies have unveiled the antioxidant, anti-inflammatory, and antiacetylcholinesterase (AChE) activities of essential oil derived from P. poeppigiana leaves (EOPP) [21].However, the endophytic fungi associated with P. poeppigiana have not been thoroughly explored, particularly concerning their antibacterial properties.The traditional use of the plant and its ecological habitat are crucial factors to consider when isolating endophytes, as regions with high biodiversity harbor endophytes with potentially diverse properties [23,24].
In this study, five novel species of endophytic fungi were isolated from the leaves of P. poeppigiana Müll.Arg. and identified as Neopestalotiopsis sp.SMB-23, Aspergillus sp.SMB-27, and Penicillium sp.SMB-24, SMB-25, and SMB-26.Furthermore, the extracts obtained from these fungi cultured in potato dextrose broth (PDB) were evaluated for antibacterial activity, specifically the minimum inhibitory concentration (MIC), against Escherichia coli, Staphylococcus aureus, and Enterococcus faecalis.Among them, the extracts from the three Penicillium species exhibited potent antibacterial activity against all three pathogens (both Gram-positive and Gram-negative bacteria), MIC values ranging from 62.5 to 2000 µg/mL.Additionally, the study on the relationship between antibacterial activity and TLC-bioautography suggested that the active compound responsible for the observed antibacterial activity is a terpene.There is also a possibility of a synergistic effect of the metabolites, as non-selective solvent extracts often exhibit such interactions.
The Penicillium species SMB-24, SMB-25, and SMB-26 demonstrated high terpene content in the TLC analysis (Figure 8D).These species produced significant yields of the active compound, with extract yields of 138.6 mg, 201.9 mg, and 161.9 mg, respectively, indicating their potential as rich sources of terpenes on a large scale.Furthermore, the secretion of an active compound, a terpen, in the medium suggests the potential for developing a continuous process in a bioreactor, where metabolites can be harvested directly from the medium.
Over the past three decades, the rise in antimicrobial resistance among pathogenic microbes has posed significant challenges, compelling scientists, professionals, and clinical specialists to seek new solutions [7,15].Certain bioactive metabolites with unique structures have been identified within endophytic fungi, holding promise for combating increasing antimicrobial resistance [6].For instance, ethyl acetate extracts of F. lateritium and Xylaria sp., isolated from Rhizophora mucronata, demonstrated inhibition against the tested bacterial pathogens at varying concentrations [7].For these two fungi, crude extracts at 500 µg/mL were sufficient for inhibiting E. coli and P. aeruginosa, while 1000 µg/mL was needed to inhibit S. aureus, and the highest concentration, at 2000 µg/mL, was required for B. subtilis.
Previous reports have also demonstrated similar results with Penicillium species.For instance, ethyl acetate extracts of endophytic Penicillium lanosum (PL) and Penicillium radiatolobatum (PR) showed minimum inhibitory concentrations (MICs) ranging from 31.25 to 500 µg/mL against Gram-positive and Gram-negative pathogens such as B. cereus, S. aureus, L. monocytogenes, E. coli, and S. enterica [55].Additionally, Mosquera (2020) reported the antibacterial activity of an endophytic fungus of the genus Penicillium spp.isolated from M. americana and M. oleifera against E. coli and S. aureus, with MICs of 1000 and 2000 µg/mL, respectively [56].Another strain of endophytic fungi, Penicillium sp.isolated from the mangrove plant (Rhyzopora mucronata), exhibited antibacterial activity against S. aureus ATCC 9144 and E. coli ATCC 8739 [57].
However, extracts from Neopestalotiopsis SMB-23 and Aspergillus SMB-27 showed no activity up to the concentration of 2000 µg/mL in this study.Neopestalotiopsis was initially grouped with Pestalotiopsis but was re-classified as a separate genus based on morphological and DNA data in 2014 [46,58].A secondary metabolite, Neopestalotin B, purified from the endophytic fungus Neopestalotiopsis sp., exhibited inhibitory effects against Grampositive bacteria, including B. subtilis, S. aureus, and S. pneumoniae, with MIC values of 10, 20, and 20 µg/mL, respectively [58].Additionally, chloroform-methanol (1:1) crude extracts of Neopestalotiopsis and Pestalotiopsis species isolated from the Manilkara zapota plant were found to be inactive against E. coli (ATCC 25922 and ATCC 35218), S. aureus, and E. faecalis [59].
Meanwhile, an endophytic fungus, Aspergillus sp.EJC08, isolated from the medicinal plant Bauhinia guianensis, exhibited higher activity against B. subtilis with its hexane extract, while the methanol extract showed greater efficacy against S. aureus.The isolated pure-alkaloid substances, including fumigaclavine C and pseurotin A, were approximately 10 times more potent than the ethyl acetate extract from which they were derived, with MIC values 7810 µg/mL [59].Consequently, the antimicrobial activity of crude extracts from Neopestalotiopsis and Aspergillus species may generally be lower compared to Penicillium species.
Filamentous fungi of the Aspergillus genus are characterized by their filament-like cell chains, known as hyphae.Given their ability to release multiple enzymes and their role in fermentations, the peptides they produce are of considerable interest and warrant exploration and study.The biotechnological potential of the Aspergillus genus is therefore underscored, as these microorganisms play a crucial role in producing molecules and enzymes of scientific and pharmaceutical significance, as well as in various industries, particularly in food production [30].
These findings highlight the potential of these endophytic fungi, particularly Penicillium species, as valuable sources of secondary metabolites with significant biological activities.This suggests promising applications in medicine, pharmaceuticals, agriculture, and environmental technologies.

Conclusions
In conclusion, this study successfully isolated and identified five novel endophytic fungi from the leaves of P. poeppigiana Müll.Arg, a plant belonging to the Rubiaceae family.These fungi were identified as Neopestalotiopsis sp.SMB-23, three Penicillium sp.SMB-24, 25, and 26, and Aspergillus sp.SMB-27.The extracts obtained from these fungi, cultured in PDB, were evaluated for their antibacterial activity (MIC) against E. coli, S. aureus, and E. faecalis.Remarkably, extracts from the three Penicillium species exhibited potent antibacterial activity against all three pathogens, including both Gram-positive and Gramnegative bacteria, with MIC values ranging from 62.5 to 2000 µg/mL.Conversely, extracts from Neopestalotiopsis and Aspergillus species showed no activity up to a concentration of 2000 µg/mL.
This study has laid the groundwork for further exploration by enabling the isolation of bioactive endophytic fungi from the P. poeppigiana Müll.Arg.plant.It opens avenues for future research to delve into the chemical isolation and elucidation of the secondary metabolites responsible for their activity.Further studies are needed to determine optimal production conditions for active compounds, as factors such as time, temperature, light-dark exposure, and medium composition can significantly influence metabolite production.This can be applied to both batch and continuous processes in a bioreactor, where metabolites can be harvested directly from media.Additionally, deeper identification at the species level could shed light on the importance of fungus-plant associations in the quest for new active compounds.Further tests will be conducted to check for mycotoxins and other bioactivities such as antioxidants, cytotoxicity, and anti-diabetic effects.
Therefore, these findings underscore the potential of these endophytic fungi, particularly the Penicillium species, as valuable sources of secondary metabolites with significant biological activities.This suggests promising applications in various fields, including medicine, pharmaceuticals, agriculture, and environmental technologies.

Figure 2 .
Figure 2. Phylogenetic tree based on the partial sequence of a small-subunit ribosomal RNA gene of the endophytic fungus Neopestalotiopsis sp.SMB-23 (accession no.PP800334) obtained with EF4f/Fung5r, showing its relationship via neighbor-joining with other closely related taxa from NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Kimura 2 (K2).The tree was rooted in Neopestalotiopsis clavispora18S ribosomal RNA gene.SMB-23 was identified as Neopestalotiopsis sp.based on its morphological traits.

Figure 2 .
Figure 2. Phylogenetic tree based on the partial sequence of a small-subunit ribosomal RNA gene of the endophytic fungus Neopestalotiopsis sp.SMB-23 (accession no.PP800334) obtained with EF4f/Fung5r, showing its relationship via neighbor-joining with other closely related taxa from NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Kimura 2 (K2).The tree was rooted in Neopestalotiopsis clavispora18S ribosomal RNA gene.SMB-23 was identified as Neopestalotiopsis sp.based on its morphological traits.

Figure 3 .
Figure 3. Phylogenetic tree based on the partial sequence of a small-subunit ribosomal RNA gene of the endophytic fungus Penicillium sp.SMB-24 (Accession no.PP800436) obtained with EF4f/Fung5r primers, showing a relationship via neighbor-joining with other closely related taxa from the NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Jukes-Cantor (JC).

Figure 3 .
Figure 3. Phylogenetic tree based on the partial sequence of a small-subunit ribosomal RNA gene of the endophytic fungus Penicillium sp.SMB-24 (Accession no.PP800436) obtained with EF4f/Fung5r primers, showing a relationship via neighbor-joining with other closely related taxa from the NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Jukes-Cantor (JC).

Figure 4 .
Figure 4. Phylogenetic tree based on the sequence of mitochondrial substrate/solute carrier gene of the endophytic fungus Penicillium sp.SMB-25 obtained with ITS5f/ITS3r primers, showing a relationship by neighbor-joining with other closely related taxa from NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Tajima-Nei (TN).

Figure 4 .
Figure 4. Phylogenetic tree based on the sequence of mitochondrial substrate/solute carrier gene of the endophytic fungus Penicillium sp.SMB-25 obtained with ITS5f/ITS3r primers, showing a relationship by neighbor-joining with other closely related taxa from NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Tajima-Nei (TN).

Figure 5 .
Figure 5. Phylogenetic tree based on the partial sequence of small-subunit ribosomal RNA gene of the endophytic fungus Penicillium sp.SMB-26 (accession no.PP800338) obtained with EF4f/Fung5r primers, showing a relationship via neighbor-joining with other closely related taxa from NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Jukes-Cantor (JC).

Figure 5 . 23 Figure 6 .
Figure 5. Phylogenetic tree based on the partial sequence of small-subunit ribosomal RNA gene of the endophytic fungus Penicillium sp.SMB-26 (accession no.PP800338) obtained with EF4f/Fung5r primers, showing a relationship via neighbor-joining with other closely related taxa from NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Jukes-Cantor (JC).

Figure 6 .
Figure 6.Phylogenetic tree based on the partial sequence of small-subunit ribosomal RNA gene of the endophytic fungus Aspergillus sp.SMB-27 (accession no.PP800435) obtained with EF4f/Fung5r primers, showing a relationship via neighbor-joining with other closely related taxa from NCBI GenBank.The scale bar indicates nucleotide substitutions per site, using the neighbor-joining method.The numbers of the nodes indicate the bootstrap values of 1000 replicates.The model used was Jukes-Cantor (JC).

Table 2 .
GenBank accession numbers for the endophytic fungi isolates from P. poeppigiana Müll.Arg.

Table 2 .
GenBank accession numbers for the endophytic fungi isolates from P. poeppigiana Müll.Arg.

Table 4 .
Minimum inhibitory concentration (MIC) inhibition activity at various concentrations of crude extract prepared from endophytic fungi against 3 pathogen bacteria.: indicates the sample completely inhibited bacterial growth.++: indicates the sample completely inhibited bacterial growth by more than 90%.+: indicates the sample completely inhibited bacterial growth by more than 70%.-: indicates no or less than 70% inhibition. +++

Table 5 .
Summary of minimum inhibitory concentration (MIC) and inhibition activity at 250 µg/mL of extract prepared from endophytic fungi.