Next Article in Journal
BP-M345, a New Diarylpentanoid with Promising Antimitotic Activity
Previous Article in Journal
SugarDrawer: A Web-Based Database Search Tool with Editing Glycan Structures
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Molecules
Volume 26
Issue 23
10.3390/molecules26237144
molecules-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Oxandrastins: Antibacterial Meroterpenes from an Australian Mud Dauber Wasp Nest-Associated Fungus, Penicillium sp. CMB-MD14

by
Ahmed H. Elbanna
1,2,
Zeinab G. Khalil
1 and
Robert J. Capon
1,*
1
Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia
2
Current address: Department of Pharmacognosy, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt
*
Author to whom correspondence should be addressed.
Molecules 2021, 26(23), 7144; https://doi.org/10.3390/molecules26237144
Submission received: 9 November 2021 / Revised: 22 November 2021 / Accepted: 24 November 2021 / Published: 25 November 2021
(This article belongs to the Section Natural Products Chemistry)
Browse Figures
Versions Notes

Abstract

:
The ethyl acetate extract of an ISP-2 agar cultivation of the wasp nest-associated fungus Penicillium sp. CMB-MD14 exhibited promising antibacterial activity against vancomycin-resistant enterococci (VRE), with a bioassay guided chemical investigation yielding the new meroterpene, oxandrastin A (1), the first andrastin-like metabolite with an extra oxygenation at C-2. A culture media optimisation strategy informed a scaled-up rice cultivation that yielded 1, together with three new oxandrastins B–D (2–4), two known andrastins C (5) and F (6), and a new meroterpene of the austalide family, isoaustalide F (7). Structures of 1–7 were assigned based on detailed spectroscopic analysis and chemical interconversion. A GNPS molecular networking analysis of the rice cultivation extract detected the known austalides B (8), H (9), and H acid (10), tentatively identified based on molecular formulae and co-clustering with 7. That the anti-VRE properties of the CMB-MD14 extract were exclusively attributed to 1 (IC50 6.0 µM, MIC99 13.9 µM), highlights the importance of the 2-OAc and 3-OAc moieties to the oxandrastin anti-VRE pharmacophore.

1. Introduction

The widespread emergence of antibiotic resistance is seriously undermining the capacity of modern antibiotics to protect against infectious disease. Antibiotic resistance is not just a problem for patients presenting with a primary infection, as secondary infections also drive high levels of morbidity and mortality. For example, patients with genetic, cardiovascular, and/or respiratory diseases, or with compromised immune systems, or even post-operative patients, are at risk from secondary infection. The magnitude of the antibiotic crisis is further exacerbated by the fact that most pharmaceutical companies have exited the antibiotic space, leaving an under resourced and depleted drug development pipeline desperately in need of innovation and renewal. As a result, current infection control is hostage to the residual efficacy of a handful of resistance compromised antibiotics.
For the latter half of the last century, science and industry successfully exploited microbial chemical defences, fuelling a knowledge revolution that inspired new pharmaceuticals and agrochemicals, driving global commerce, and improving quality of life. This led to some of the most widely recognised and successful antibiotic classes, including the penicillins, erythromycins, cephalosporins, tetracyclines, streptomycins, vancomycins, and rifampicins. Notwithstanding this success, when confronted by lower returns on investment and the perception of a near exhausted microbial resource, late last century industry turned elsewhere for inspiration. Two decades on, and confronted by surging antibiotic resistance, and a community demand for better, safer, and more effective antibiotics, the need for inspiration is more urgent than ever.
As part of our ongoing investigations into the chemistry of Australian fungi, we assembled a library of fungi co-isolated from a mud dauber wasp (×15), and a mud dauber wasp nest (×21), both sourced from an urban location in Pullenvale, Queensland, Australia. Collectively, this wasp-derived fungal library proved to be an excellent source of novel natural products with Aspergillus sp. CMB-W031, yielding an unprecedented nitro depsi-peptide diketopiperazine (waspergillamide A) [1]. Talaromyces sp. CMB-W045 yielding new non-cytotoxic siderophores (talarazines A–E) [2], a new a p-terphenyl (talarophenol sulfate), and polyketides (talarophilones) [3]. Penicillium sp. CMB-MD22 yielded an extensive family of stereo-complex and selectively antifungal neobulgarone bianthrones [4]. Turning our attention to the need for new antibiotic classes, and prompted by promising antibacterial activity against vancomycin-resistant enterococci (VRE), this current report describes an investigation into the antibacterial natural products of the mud dauber wasp nest-derived Penicillium sp. CMB-MD14. Bioassay guided fractionation of a scaled-up ISP-2 agar cultivation yielded the new anti-VRE meroterpene 1, closely related to the known antibacterial inactive fungal meroterpene andrastins [5,6] as well as the atlantinones [7,8], citreohybridones, isocitreohybridones and citreohybriddiones [9,10]. The first andrastin-like metabolite to be reported with C-2 oxygenation, 1 was assigned the trivial name oxandrastin A. To better explore the anti-VRE oxandrastin pharmacophore a media optimisation strategy was employed, with a scaled-up rice cultivation of CMB-MD14 yielding oxandrastin A (1), as well as three new oxandrastins B–D (2–4), two known andrastins C (5), F (6) [5,6] and a new meroterpene of the austalide family, isoaustalide F (7) (Figure 1).
A GNPS molecular networking analysis of the unfractionated CMB-MD14 rice cultivation extract confirmed separate clusters for oxandrastins/andrastins and isoaustalides/austalides (Figure 2), with the latter including nodes tentatively attributed to the known austalides B (8) [11,12], H (9) [13] and H acid (10) [14]. Subsequent UPLC-MS analysis with single ion extraction (SIE) detected 1–10 in the fresh extract, which together with GNPS analyses confirmed their natural product status. Structures were assigned 1–7 based on detailed spectroscopic analysis and chemical interconversion, and tentatively to 8–10 on the basis of molecular formulae and GNPS co-clustering with 7. An account of these structure determinations together with commentary on anti-VRE structure activity and biosynthetic relationships is outlined below.

2. Results and Discussion

HRESI(+)MS analysis of 1 revealed a molecular formula (C30H42O8) requiring 10 double bond equivalents (DBE). The 1D NMR (CDCl3) data for 1 (Table S1, Figures S7 and S8) revealed three ester (δC 170.6, 2-CO; 171.0, 3-CO, and 168.4, 14-CO2) and two ketone (δC 210.7, C-15, and δC 209.5, C-17) carbonyls, and a trisubstituted double bond (δH 5.58, br s, H-11; δC 126.8, C-11; δC 135.1, C-12), accounting for 6 DBE and requiring that 1 be tetracyclic. Diagnostic 2D NMR COSY and HMBC correlations established the planar structure for 1, while ROESY correlations defined the full relative configuration (Figure 3). More specifically, ROESY correlations between H-2, H3α-4, H3-10, and H3-8 confirmed a co-facial (α) orientation, while correlations between Hβ-1, H-5, Hβ-7, H-9, and H-16 confirmed a co-facial (β) orientation. Supportive of these assignments, the magnitude of J1α,2 (4.0 Hz), J1β,2 (12.4 Hz), and J2,3 (3.1 Hz) confirmed the axial and equatorial orientation of H-2 and H-3, respectively, and the structure for oxandrastin A (1) (relative configuration only) as shown. Of note, the NMR (methanol-d4) data for 1 (Table 1, Table 2 and Table S2; Figures S10 and S11) revealed an alternate ring D enol tautomer and, as the 13C NMR (MeOH-d4) resonances for the C-15 and C-17 were not detectable (broadened), it seemed likely that ring D was an equilibrating mixture of tautomers (Figure 4). A search of the literature revealed that many of the above mentioned related fungal meroterpenes (e.g., andrastins and citreohybridonol) exhibited a comparable solvent dependent ring D keto-enol tautomerism [5,7,10,15]. Significantly, this solvent effect was of added importance when acquiring optical measurements. For example, the [α]D for 1 measured in CHCl3 (–64) was larger than that measured in MeOH (–18.3).
HRMS(+)ESI analysis of 2 and 3 revealed isomeric molecular formulae (C28H40O7) suggestive of deacetylated analogues of 1. As 2 exhibited limited solubility in CDCl3, comparison of the 1D NMR (methanol-d4) data for 2 (Table 1, Table 2 and Table S3; Figures S13 and S14) with 1 confirmed the loss of resonances for an acetyl moiety, with a corresponding upfield shift of H-2 in 2 (ΔδH = −1.18) attributed to conversion of the 2-OAc in 1 to a 2-OH in 2. In addition, values for J1α,2 (4.1 Hz), J1β,2 (12.1 Hz), and J2,3 (2.8 Hz) in 2 confirmed an axial H-2 and equatorial H-3 in common with 1. Diagnostic 2D NMR COSY and HMBC correlations (Figure 5) supported the planar structure, while ROESY correlations permitted assignment of the complete relative configuration for oxandrastin B (2) as shown.
Comparison of the NMR (methanol-d4) data for 3 (Table 1, Table 2 and Table S4; Figures S16 and S17) with 1 also confirmed the loss of resonances for an acetyl moiety, with a corresponding upfield shift of H-3 in 3 (ΔδH = −1.52) attributed to conversion of the 3-OAc in 1 to a 3-OH in 3. In addition, values for J1α,2 (4.1 Hz), J1β,2 (12.1 Hz), and J2,3 (2.7 Hz) in 3 confirmed an axial H-2 and equatorial H-3 in common with 1. Diagnostic 2D NMR COSY and HMBC correlations (Figure 5) supported the planar structure, while ROESY correlations permitted assignment of the complete relative configuration for oxandrastin C (3) as shown.
A global natural products social (GNPS) molecular networking analysis of the unfractionated rice cultivation extract detected an array of minor metabolites including 4 (Figure 2 and Figure S34), speculated on the basis of its molecular formula (C26H38O6) to be the deacetylated homologue of the monoacetates 2 and 3. Although only an exceptionally minor metabolite in the extract, alkaline hydrolysis of 2, yielded pure semi-synthetic 4, which co-eluted on UPLC and had an MS/MS fragmentation in common with the natural product 4 (Figures S4 and S5), which was identified by detailed spectroscopic analysis. Comparison of the NMR (methanol-d4) data for 4 (Table 1, Table 2 and Table S5; Figures S19–S21) with 1 confirmed the loss of two acetyl moieties, with corresponding upfield shifts of H-2 and H-3 in 4 (ΔδH = −1.31 and −1.64, respectively) attributed to conversion of the 2-OAc and 3-OAc in 1 to 2-OH and 3-OH moieties in 4. Diagnostic 2D NMR COSY and HMBC correlations (Figure 5), together with chemical interconversion with 2, permitted assignment of the structure for oxandrastin D (4) as shown (relative configuration).
Spectroscopic analysis of the co-metabolites 5 (C28H40O6) and 6 (C26H38O5) (Tables S6 and S7; Figures S23, S24, S26 and S27) readily identified them as the known fungal metabolites andrastin C and andrastin F [5,6] respectively. Significantly, as the absolute configuration of 5 had been established in 1996 by X-ray analysis of its co-metabolite andrastin A [5] and the optical properties of our re-isolation ([α]D = −16.5 in MeOH; −134.4 in CHCl3) corresponded well with those reported in the scientific literature ([α]D = −30.3 in MeOH; −143.4 in CHCl3), on biosynthetic grounds we inferred the absolute configuration of oxandrastins A–D (1–4), as shown. A plausible biosynthesis of the meroterpene andrastins and oxandrastins was summarised in Figure 6.
The GNPS analysis of CMB-MD14 (Figure 2 and Figure S35) disclosed a second family of meroterpenes, which following fractionation, yielded 7 (C26H34O9) isomeric and sharing a common UV-vis chromophore with the known fungal metabolite austalide F (11) (Figure 7). Comparison of the 1D NMR (methanol-d4) data for 7 (Table 3 and Table S8; Figures S29 and S30) with 11 suggested the presence of a C-15 2°-OH in 7 (H-15 δH 3.71, dd, 10.5, and 5.9; C-15 δC 68.8) as opposed to the C-16 2°-OH in 11. This hypothesis was confirmed by 2D NMR correlations, which together with diagnostic ROESY correlations established the structure and relative configuration (Figure 7), with the absolute configuration for isoaustalide F (7) assigned on the basis of comparable experimental ECD spectra and specific rotations ([α]D = −43), with those reported for the known austalides F ([α]D = −57.7) [11]. A ([α]D = −84.4) [11] and T ([α]D = −88) [16] (Figure S32). The absolute configurations of known austalides have been confirmed by either ECD calculations, an X-ray structure analysis for a derivatized austalide D, or total synthesis of some analogues, such as austalide B [14,16,17,18].
Minor GNPS nodes within the CMB-MD14 austalide family (Figure 2 and Figures S35) were tentatively identified based on correlations within the GNPS databases as the known austalides B (8) (m/z 475), H (9) (m/z 477) and H acid (10) (m/z 463). Both 8 and 9 were firstly reported from the toxigenic Aspergillus ustus (Bainier) Thom. and Church (strain MRC 1163) [11,12,13], while 10 was later isolated from the alga-derived fungi Penicillium thomii (Maire) and Penicillium lividum (Westling) [14]. The natural product status of 8–10 in the CMB-MD14 extract was confirmed by UPLC-QTOF analysis with single ion extraction (SIE) monitoring (Figure S36). A plausible biosynthesis linking austalide F (11) and isoaustalide F (7) is summarised in Figure 8.
The CMB-MD14 metabolites 1–7 did not exhibit growth inhibitory activity (IC50 > 30 μM) against the Gram −ve bacteria Escherichia coli ATCC11775, the Gram +ve bacteria Staphylococcus aureus ATCC25923, the fungus Candida albicans ATCC10231, or human colorectal (SW620) and lung (NCI-H460) carcinoma cells (Figures S37 and S38). Significantly, the anti-VRE properties of the CMB-MD14 extract were exclusively attributed to 1, which exhibited growth inhibitory activity against a clinical isolate of vancomycin resistant Enterococcus (VRE) (IC50 6.0 µM, MIC99 13.9 µM), with slightly improved activity against a vancomycin susceptible Enterococcus faecalis ACM 5184 (IC50 1.9 µM, MIC99 6.1 µM) (Figure S37), suggesting that 2-OAc and 3-OAc moieties were pivotal to the anti-VRE properties of the oxandrastin pharmacophore.

3. Materials and Methods

3.1. General Experimental Procedures

Chiroptical measurements ([α]D) were obtained on a JASCO P-1010 polarimeter (JASCO International Co. Ltd., Tokyo, Japan) in a 100 × 2 mm cell at specified temperatures. Electronic Circular Dichroism (ECD) measurement were obtained on a JASCO J-810 spectropolarimeter (JASCO International Co. Ltd., Tokyo, Japan) in a 0.1 cm path-length cell. Nuclear magnetic resonance (NMR) spectra were acquired on a Bruker Avance 600 MHz spectrometer (Bruker Pty. Ltd., Alexandria, NSW, Australia) with either a 5 mm PASEL 1H/D-13C Z-Gradient probe or 5 mm CPTCI 1H/19F-13C/15N/DZ-Gradient cryoprobe. In all cases, spectra were acquired at 25 °C deuterated solvents as indicated, with referencing to residual 1H or 13C signals. High-resolution ESIMS spectra were obtained on a Bruker micrOTOF mass spectrometer (Bruker Daltonik Pty. Ltd., Preston, VIC, Australia) by direct injection in MeOH at 3 μL/min using sodium formate clusters as an internal calibrant. Liquid chromatography-diode array-mass spectrometry (HPLC-DAD-MS) data were acquired either on an Agilent 1260 series separation module equipped with an Agilent G6125B series LC/MSD mass detector (Agilent Technologies Inc., Mulgrave, VIC, Australia) and diode array detector or on Shimadzu LCMS-2020 LCMS. Semi-preparative HPLCs were performed using Agilent 1100 series HPLC instruments (Agilent Technologies Inc., Mulgrave, VIC, Australia) with corresponding detectors, fraction collectors, and software inclusively. UPLC chromatograms were obtained on Agilent 1290 infinity UPLC system equipped with diode array multiple wavelength detector (Zorbax C8 RRHD 1.8 μm, 50 × 2.1 mm column, 0.417 mL/min with a 2.50 min gradient from 90% H2O/MeCN to MeCN with a constant 0.01% TFA modifier). UPLC-QTOF analysis was performed on UPLC-QTOF instrument comprising an Agilent 1290 Infinity II UPLC (Zorbax C8 RRHD 1.8 μm, 50 × 2.1 mm column, eluting at 0.417 mL/min with a 2.50 min gradient elution from 90% H2O/MeCN to 100% MeCN with a constant 0.1% formic acid modifier) coupled to an Agilent 6545 Q-TOF. MS/MS analysis was performed on the same instrument for ions detected in the full scan, at an intensity above 1000 counts at 10 scans/s, with an isolation width of 4 ~m/z using a fixed collision energy and a maximum of 3 selected precursors per cycle. Chemicals were purchased from Sigma-Aldrich or Merck unless otherwise specified. Analytical-grade solvents were used for solvent extractions. Chromatography solvents were of HPLC grade supplied by Labscan or Sigma-Aldrich and filtered/degassed through 0.45 μm polytetrafluoroethylene (PTFE) membrane prior to use. Deuterated solvents were purchased from Cambridge Isotopes. Microorganisms were manipulated under sterile conditions using a Laftech class II biological safety cabinet and incubated in either MMM Friocell incubators (Lomb Scientific, NSW, Australia) or an Innova 42R incubator shaker (John Morris, NSW, Australia).

3.2. Fungal Isolation

The fungus Penicillium sp. CMB-MD14 was isolated from a specimen of mud dauber wasp nests collected from an urban location in Pullenvale, Queensland, Australia, by cultivation on ISP-2 agar plate at 26.5 °C for 8 days.

3.3. Fungal Taxonomy

Genomic DNA for CMB-MD14 was extracted from its mycelia using the DNeasy Plant Mini Kit (Qiagen), as per the manufacturers protocol. The 18s rRNA gene was amplified by PCR using the universal primers ITS-1 (5ʹ-TCCGTAGGTGAACCTGCGG-3ʹ) and ITS-4 (5ʹ-TCCTCCGCTTATTGATATGC-3ʹ) purchased from Sigma-Aldrich. The PCR mixture (50 μL) contained genomic DNA (2 μL, 20–40 ng), EmeraldAmpn GT PCR Master Mix (2X Premix) (25 μL), primer (0.2 μM, each), and H2O (up to 50 μL). PCR was performed using the following conditions: initial denaturation at 95 °C for 2 min, 30 cycles in series of 95 °C for 20 s (denaturation), 56 °C for 20 s (annealing), and 72 °C for 30 s (extension), followed by one cycle at 72 °C for 5 min. PCR products were purified with PCR purification kit (Qiagen, Victoria, Australia). Amplification products were examined by agarose gel electrophoresis. The DNA sequencing was performed by the Australian Genome Research Facility (AGRF) at The University of Queensland. A BLAST analysis (NCBI database) on the resulting ITS gene sequence (GenBank accession no. MW185842) for CMB-MD14 revealed 99% identity with the fungal strain Penicillium panissanguineum 580833 (Figures S1 and S2) [19,20,21].

3.4. Global Natural Product Social (GNPS) Molecular Networking

Aliquots (1 μL) of dried fraction (100 μg/mL in MeOH) were analysed on an Agilent 6545 Q-TOF LC/MS equipped with an Agilent 1290 Infinity II UPLC system, utilising an Agilent SB-C8 1.8 μm, 2.1 × 50 mm column, eluting with 90% H2O/MeCN to MeCN at a 0.417 mL/min over 2.5 min with an isocratic 0.1% formic acid modifier. UPLC-QTOF-(+)MS/MS data acquired for all samples at collision energy of 10, 20, and 40 eV were converted from Agilent MassHunter data files (.d) to mzXML file format using MSConvert software and transferred to the GNPS server (gnps.ucsd.edu). Molecular networking was performed using the GNPS data analysis workflow [22] using the spectral clustering algorithm with a cosine score of 0.6 and a minimum of 5 matched peaks. The resulting spectral network was imported into Cytoscape software (version 3.7.1) [23] and visualized using a ball-stick layout where nodes represent parent masses and the cosine score was reflected by edge thickness. Furthermore, group abundances were set as pie charts, which reflected the intensity of MS signals.

3.5. Extraction and Fractionation of an ISP-2 Agar Cultivation of CMB-MD14

The fungus Penicillium sp. CMB-MD14 was incubated on ISP-2 agar plates (×20) at 26.6 °C for 8 days, after which the diced agar was extracted with EtOAc (400 mL), filtered, and the organic phase concentrated in vacuo at 40 °C to yield an EtOAc extract (70 mg). The EtOAc extract was subjected to sequential solvent trituration (2 × 20 mL) to afford after concentration in vacuo n-hexane (21 mg) and MeOH (47 mg) solubles. The MeOH solubles were subjected to preparative reversed phase HPLC fractionation (PrepHT SB-C8 5 μm, 21.2 × 150 mm column, 20 mL/min gradient elution over 20 min from 90% H2O/MeCN to MeCN inclusive of an isocratic 0.1% TFA modifier) to yield the anti-VRE active oxandrastin A (1) (2 mg, 2.8%). (see Scheme S1).

3.6. Extraction and Fractionation of a Rice Cultivation of CMB-MD14

A culture flask (2 L) containing medium grain rice (200 g) inoculated with the fungus CMB-MD14 was incubated at room temperature for 6 weeks, after which it was extracted with EtOAc (2 × 400 mL), and the combined organic phase filtered and concentrated in vacuo at 40 °C to yield the EtOAc extract (1.6 g). The EtOAc extract was subjected to solvent trituration (2 × 50 mL) to afford after concentration in vacuo n-hexane (850 mg) and MeOH (750 mg) solubles. A portion of the MeOH solubles (600 mg) was fractionated by preparative reversed phase HPLC (Phenomenex Luna-C8 10 μm, 21.2 × 250 mm column, 20 mL/min gradient elution over 20 min from 90% H2O/MeCN to MeCN inclusive of an isocratic 0.1% TFA modifier) to yield fractions A–E (prioritized based on UPLC-DAD and UPLC-QTOF analyses). Fraction A (12.5 mg) was subjected to a semi-preparative reversed phase HPLC (ZORBAX SB-C8 5 μm, 9.4 × 250 mm column, 3 mL/min gradient elution over 5 min from 90% H2O/MeCN to 60% H2O/MeCN, followed by isocratic elution over 30 min with 60% H2O/MeCN, inclusive of an isocratic 0.1% TFA/MeCN modifier) to yield isoaustalide F (7) (6.5 mg, 0.4%). A portion of fraction B (40 of 120 mg) was subjected to semi-preparative reversed phase HPLC (ZORBAX SB-Phenyl 5 μm, 9.4 × 250 mm column, 3 mL/min gradient elution over 20 min from 80% H2O/MeCN to 20% H2O/MeCN inclusive of an isocratic 0.1% TFA/MeCN modifier) to yield oxandrastin B (2) (26 mg, 4.87%). Fraction C (27 mg) was subjected to a semi-preparative reversed phase HPLC (ZORBAX SB-C18 5 μm, 9.4 × 250 mm column, 3 mL/min isocratic elution over 21 min with 45% H2O/MeCN inclusive of an isocratic 0.1% TFA/MeCN modifier) to yield oxandrastin C (3) (13 mg, 0.81%). Fraction D (27 mg) was subjected to a semi-preparative reversed phase HPLC (ZORBAX SB-C3 5 μm, 9.4 × 250 mm column, 3 mL/min isocratic elution over 35 min with 53% H2O/MeCN inclusive of an isocratic 0.1% TFA/MeCN modifier) to yield oxandrastin A (1) (19.3 mg, 1.2%) and andrastin F (6) (1.3 mg, 0.08%). Fraction E (14 mg) was subjected to a semi-preparative reversed phase HPLC (ZORBAX SB-Phenyl 5 μm, 9.4 × 250 mm column, 3 mL/min isocratic elution over 35 min with 47% H2O/MeCN inclusive of an isocratic 0.1% TFA/MeCN modifier) to yield andrastin C (5) (6 mg, 0.37%) (see Scheme S2). (Note: % yields estimated on a mass-to-mass basis against the weight of the EtOAc extract).

3.7. Metabolite Characterization

Oxandrastin A (1) White powder; [α]D = −18.3 (c 0.44, MeOH) and [α]D = −64 (c 0.51, CHCl3); NMR (CDCl3) see Table S1, Figures S7 and S8; NMR (methanol-d4) see Table 1, Table 2 and Table S2, Figures S10 and S11; ESI(+)MS m/z 531 [M+H]+; HRESI(+)MS m/z 553.2772 [M + Na]+ (calcd for C30H42O8Na, 553.2772).
Oxandrastin B (2) White powder; [α]D = −39.8 (c 0.68, MeOH); NMR (methanol-d4) see Table 1, Table 2 and Table S3, Figures S13 and S14; ESI(+)MS m/z 489 [M+H]+; HRESI(+)MS m/z 511.2666 [M + Na]+ (calcd for C28H40O7Na, 511.2666).
Oxandrastin C (3) White powder; [α]D = −24.7 (c 0.45, MeOH); NMR (methanol-d4) see Table 1, Table 2 and Table S4, Figures S16 and S17; ESI(+)MS m/z 489 [M+H]+; HRESI(+)MS m/z 511.2665 [M + Na]+ (calcd for C28H40O7Na, 511.2666).
Oxandrastin D (4) White powder; [α]D = −15.1 (c 0.07, MeOH); NMR (methanol-d4) see Table 1, Table 2 and Table S5, Figures S19–S21; ESI(+)MS m/z 447 [M+H]+; HRESI(+)MS m/z 469.2561 [M + Na]+ (calcd for C26H38O6Na, 469.2561).
Andrastin C (5) White powder; [α]D = −16.5 (c 0.45, MeOH) and [α]D = −134.4 (c 0.38, CHCl3); NMR (methanol-d4) see Table S6, Figures S23 and S24; ESI(+)MS m/z 473 [M+H]+; HRESI(+)MS m/z 495.2722 [M + Na]+ (calcd for C28H40O6Na, 495.2717).
Andrastin F (6) White powder; [α]D = −28.0 (c 0.10, MeOH) and [α]D = −81.5 (c 0.09, CHCl3); NMR (methanol-d4) see Table S7, Figures S26 and S27; ESI(+)MS m/z 431 [M+H]+; HRESI(+)MS m/z 453.2613 [M + Na]+ (calcd for C26H38O5Na, 453.2611).
Isoaustalide F (7) White powder; [α]D = −68.3 (c 0.30, MeOH) and [α]D = −43 (c 0.38, CHCl3); NMR (methanol-d4) see Table 3 and Table S8, Figures S29 and S30; ESI(+)MS m/z 491 [M+H]+; HRESI(+)MS m/z 513.2095 [M + Na]+ (calcd for C26H34O9Na, 513.2095).

3.8. Hydrolysis of Oxandrastin B (2) to Oxandrastin D (4)

A mixture of 2 (2 mg) and K2CO3 (0.1 mg) in MeOH (1 mL) was stirred at room temperature for 12 h, with aliquots (2 μL) taken at 1, 4, and 12 h. Each aliquot was diluted with acetonitrile (200 μL) and analysed by UPLC-QTOF, to reveal complete conversion of 2 to 4 after 12 h. The 12 h hydrolysis reaction mixture was dried under N2, extracted with MeCN + 0.01% TFA modifier (2 mL) and purified by semi-preparative HPLC (ZORBAX SB-C8 5 μm, 9.4 × 250 mm column, and 3 mL/min gradient elution over 20 min from 90% H2O/MeCN to MeCN, inclusive of an isocratic 0.1% TFA/MeCN modifier) to yield oxandrastin D (4) (0.8 mg) (Figures S4 and S5).

3.9. Antibiotic Assays

Antibacterial and antifungal assays were performed using prior published methods [24,25,26] as documented in the Supporting Information (Figure S37).

3.10. Cytotoxicity Assays

Cytotoxicity assays were performed using prior published methods [24,25,26] as documented in the Supporting Information (Figure S38).

Supplementary Materials

The following are available online, Fungal taxonomy, NMR spectra and tabulated data for 1–7, bioassay methods and results, and GNPS analyses.

Author Contributions

Conceptualization: R.J.C.; isolation and characterization of metabolites and GNPS analyses: A.H.E.; Assignments of molecular structures of metabolites: A.H.E. and Z.G.K.; biological assays: Z.G.K.; construction of the Supplementary Materials document: A.H.E. and Z.G.K.; whole data revision and writing—original draft preparation: R.J.C. with support from A.H.E. and Z.G.K.; writing—review and editing: all authors. All authors have read and agreed to the published version of the manuscript.

Funding

This work was funded in part by the Institute for Molecular Bioscience and The University of Queensland.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable

Data Availability Statement

Data is contained within the article or Supplementary Materials.

Acknowledgments

The authors thank A. D. Patterson and H. Zowawi (UQ Centre for Clinical Research) for providing the multidrug-resistant bacterial isolate, S. Bates and R. Robey (NCI) for providing the SW620 cell line, and P. Dewapriya for isolating the mud dauber wasp nest-associated Penicillium sp. CMB-MD14. A. H. Elbanna thanks The University of Queensland for an International Postgraduate Scholarship.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Not available.

References

  1. Quezada, M.; Shang, Z.; Kalansuriya, P.; Salim, A.A.; Lacey, E.; Capon, R.J. Waspergillamide A, a Nitro depsi-Tetrapeptide Diketopiperazine from an Australian Mud Dauber Wasp-Associated Aspergillus sp. (CMB-W031). J. Nat. Prod. 2017, 80, 1192–1195. [Google Scholar] [CrossRef]
  2. Kalansuriya, P.; Quezada, M.; Espósito, B.P.; Capon, R.J. Talarazines A-E: Noncytotoxic Iron(III) Chelators from an Australian Mud Dauber Wasp-Associated Fungus, Talaromyces sp. (CMB-W045). J. Nat. Prod. 2017, 80, 609–615. [Google Scholar] [CrossRef] [PubMed]
  3. Kalansuriya, P.; Khalil, Z.G.; Salim, A.A.; Capon, R.J. Talarophenol sulfate and talarophilones from the Australian mud dauber wasp-associated fungus, Talaromyces sp. CMB-W045. Tet. Lett. 2019, 60, 151157. [Google Scholar] [CrossRef]
  4. Elbanna, A.H.; Khalil, Z.G.; Bernhardt, P.V.; Capon, R.J. Neobulgarones Revisited: Anti and Syn Bianthrones from an Australian Mud Dauber Wasp Nest-Associated Fungus, Penicillium sp. CMB-MD22. J. Nat. Prod. 2021, 84, 762–770. [Google Scholar] [CrossRef] [PubMed]
  5. Uchida, R.; Shiomi, K.; Inokoshi, J.; Sunazuka, T.; Tanaka, H.; Iwai, Y.; Takayanagi, H.; Omura, S. Andrastins A-C, new protein farnesyltransferase inhibitors produced by Penicillium sp. FO-3929. II. Structure elucidation and biosynthesis. J. Antibiot. 1996, 49, 418–424. [Google Scholar] [CrossRef] [PubMed]
  6. Matsuda, Y.; Awakawa, T.; Abe, I. Reconstituted biosynthesis of fungal meroterpenoid andrastin A. Tetrahedron 2013, 69, 8199–8204. [Google Scholar] [CrossRef]
  7. Wang, X.; Filho, J.G.S.; Hoover, A.R.; King, J.B.; Ellis, T.K.; Powell, D.R.; Cichewicz, R.H. Chemical epigenetics alters the secondary metabolite composition of guttate excreted by an atlantic-forest-soil-derived Penicillium citreonigrum. J. Nat. Prod. 2010, 73, 942–948. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Dalsgaard, P.W.; Petersen, B.O.; Duus, J.Ø.; Zidorn, C.; Frisvad, J.C.; Christophersen, C.; Larsen, T.O. Atlantinone A, a Meroterpenoid Produced by Penicillium ribeum and Several Cheese Associated Penicillium Species. Metabolites 2012, 2, 214–220. [Google Scholar] [CrossRef] [Green Version]
  9. Kosemura, S. Meroterpenoids from Penicillium citreo-viride B. IFO 4692 and 6200 hybrid. Tetrahedron 2003, 59, 5055–5072. [Google Scholar] [CrossRef]
  10. Özkaya, F.C.; Ebrahim, W.; Klopotowski, M.; Liu, Z.; Janiak, C.; Proksch, P. Isolation and X-ray structure analysis of citreohybridonol from marine-derived Penicillium atrovenetum. Nat. Prod. Res. 2017, 32, 840–843. [Google Scholar] [CrossRef]
  11. Horak, R.M.; Steyn, P.S.; Vleggaar, R.; Rabie, C.J. Metabolites of Aspergillus ustus. Part 1. Application of the heteronuclear selective population inversion (SPI) n.m.r. technique to the structure elucidation of the austalides A–F, novel ortho ester meroterpenoids. J. Chem. Soc. Perkin Trans. 1 1985, 345–356. [Google Scholar] [CrossRef]
  12. Horak, R.M.; Steyn, P.S.; Rooyen, P.H.V.; Vleggaar, R.; Rabie, C.J. Structures of the austalides A–E, five noval toxic metabolites from Aspergillus ustus. J. Chem. Soc. Chem. Commun. 1981, 1265–1267. [Google Scholar] [CrossRef]
  13. Horak, R.M.; Steyn, P.S.; Vleggaar, R.; Rabie, C.J. Metabolites of Aspergillus ustus. Part 3. Structure elucidation of austalides G–L. J. Chem. Soc. Perkin Trans. 1 1985, 363–367. [Google Scholar] [CrossRef]
  14. Zhuravleva, O.I.; Sobolevskaya, M.P.; Leshchenko, E.V.; Kirichuk, N.N.; Denisenko, V.A.; Dmitrenok, P.S.; Dyshlovoy, S.A.; Zakharenko, A.M.; Kim, N.Y.; Afiyatullov, S.S. Meroterpenoids from the Alga-Derived Fungi Penicillium thomii Maire and Penicillium lividum Westling. J. Nat. Prod. 2014, 77, 1390–1395. [Google Scholar] [CrossRef] [PubMed]
  15. Nielsen, K.F.; Dalsgaard, P.W.; Smedsgaard, J.; Larsen, T.O. Andrastins A-D, Penicillium roqueforti Metabolites consistently produced in blue-mold-ripened cheese. J. Agric. Food. Chem. 2005, 53, 2908–2913. [Google Scholar] [CrossRef] [PubMed]
  16. Peng, J.; Zhang, X.; Wang, W.; Zhu, T.; Gu, Q.; Li, D. Austalides S-U, New Meroterpenoids from the Sponge-Derived Fungus Aspergillus aureolatus HDN14-107. Mar. Drugs 2016, 14, 131. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Dillen, J.L.M.; Horak, R.M.; Maharaj, V.J.; Marais, S.F.; Vleggaar, R. Absolute configuration and biosynthesis of the austalides, meroterpenoid metabolites of Aspergillus ustus: Mode of cyclisation of the farnesyl moiety. J. Chem. Soc. Chem. Commun. 1989, 7, 393–394. [Google Scholar] [CrossRef]
  18. Paquette, L.A.; Wang, T.-Z.; Sivik, M.R. Total Synthesis of (-)-Austalide B. A Generic Solution to Elaboration of the Pyran/p-Cresol/Butenolide Triad. J. Am. Chem. Soc. 1994, 116, 11323–11334. [Google Scholar] [CrossRef]
  19. Yang, Z.; Goldman, N.; Friday, A. Comparison of models for nucleotide substitution used in maximum-likelihood phylogenetic estimation. Mol. Biol. Evol. 1994, 11, 316–324. [Google Scholar] [PubMed] [Green Version]
  20. Edgar, R.C. MUSCLE: A multiple sequence alignment method with reduced time and space complexity. BMC Bioinform. 2004, 5, 113. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Okonechnikov, K.; Golosova, O.; Fursov, M.; UGENE team. Unipro UGENE: A unified bioinformatics toolkit. Bioinformatics 2012, 28, 1166–1167. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Wang, M.; Carver, J.J.; Phelan, V.V.; Sanchez, L.M.; Garg, N.; Peng, Y.; Nguyen, D.D.; Watrous, J.; Kapono, C.A.; Luzzatto-Knaan, T.; et al. Sharing and community curation of mass spectrometry data with Global Natural Products Social Molecular Networking. Nat. Biotechnol. 2016, 34, 828–837. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Shannon, P.; Markiel, A.; Ozier, O.; Baliga, N.S.; Wang, J.T.; Ramage, D.; Amin, N.; Schwikowski, B.; Ideker, T. Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks. Genome Res. 2003, 13, 2498–2504. [Google Scholar] [CrossRef] [PubMed]
  24. Shang, Z.; Salim, A.A.; Khalil, Z.; Quezada, M.; Bernhardt, P.V.; Capon, R.J. Viridicatumtoxins: Expanding on a Rare Tetracycline Antibiotic Scaffold. J. Org. Chem. 2015, 80, 12501–12508. [Google Scholar] [CrossRef] [PubMed]
  25. Elbanna, A.H.; Khalil, Z.G.; Bernhardt, P.V.; Capon, R.J. Chrysosporazines A-E: P-Glycoprotein Inhibitory Piperazines from an Australian Marine Fish Gastrointestinal Tract-Derived Fungus, Chrysosporium sp. CMB-F214. Org. Lett. 2019, 21, 8097–8100. [Google Scholar] [CrossRef] [PubMed]
  26. Mohamed, O.G.; Salim, A.A.; Khalil, Z.G.; Elbanna, A.H.; Bernhardt, P.V.; Capon, R.J. Chrysosporazines F-M: P-Glycoprotein Inhibitory Phenylpropanoid Piperazines from an Australian Marine Fish Derived Fungus, Chrysosporium sp. CMB-F294. J. Nat. Prod. 2020, 83, 497–504. [Google Scholar] [CrossRef] [PubMed]
Molecules 26 07144 g001 550
Figure 1. Metabolites 1–10 from Penicillium sp. CMB-MD14.
Figure 1. Metabolites 1–10 from Penicillium sp. CMB-MD14.
Molecules 26 07144 g001
Molecules 26 07144 g002 550
Figure 2. GNPS molecular networking revealing cluster for (left) oxandrastins/adrastins and (right) austalides; (pink) CMB-MD14 rice extract; (green) 1 and 5–7; (blue) 2; (red) 3; (red dashed) sodiated adducts of 1–3 and 5–6.
Figure 2. GNPS molecular networking revealing cluster for (left) oxandrastins/adrastins and (right) austalides; (pink) CMB-MD14 rice extract; (green) 1 and 5–7; (blue) 2; (red) 3; (red dashed) sodiated adducts of 1–3 and 5–6.
Molecules 26 07144 g002
Molecules 26 07144 g003 550
Figure 3. Diagnostic 2D NMR (CDCl3) correlations for oxandrastin A (1).
Figure 3. Diagnostic 2D NMR (CDCl3) correlations for oxandrastin A (1).
Molecules 26 07144 g003
Molecules 26 07144 g004 550
Figure 4. Tautomeric keto-enol forms of 1 present in aprotic versus protic solvents.
Figure 4. Tautomeric keto-enol forms of 1 present in aprotic versus protic solvents.
Molecules 26 07144 g004
Molecules 26 07144 g005 550
Figure 5. Diagnostic 2D NMR (methanol-d4) correlations for oxandrastins B–D (2–4).
Figure 5. Diagnostic 2D NMR (methanol-d4) correlations for oxandrastins B–D (2–4).
Molecules 26 07144 g005
Molecules 26 07144 g006 550
Figure 6. Proposed biosynthesis of the meroterpene andrastins and oxandrastins.
Figure 6. Proposed biosynthesis of the meroterpene andrastins and oxandrastins.
Molecules 26 07144 g006
Molecules 26 07144 g007 550
Figure 7. Diagnostic 2D NMR (methanol-d4) correlations for isoaustalide F (7), and the structure for austalide F (11).
Figure 7. Diagnostic 2D NMR (methanol-d4) correlations for isoaustalide F (7), and the structure for austalide F (11).
Molecules 26 07144 g007
Molecules 26 07144 g008 550
Figure 8. Proposed biosynthesis of the meroterpene austalide F and isoaustalide F (7).
Figure 8. Proposed biosynthesis of the meroterpene austalide F and isoaustalide F (7).
Molecules 26 07144 g008
Table
Table 1. Diagnostic 1H NMR (methanol-d4) data for oxandrastins A–D (1–4).
Table 1. Diagnostic 1H NMR (methanol-d4) data for oxandrastins A–D (1–4).
PositionδH, Mult (J in Hz)
(1)(2)(3)(4)
1α. 1.82, dd (12.3, 4.2)α. 1.81, dd (12.3, 4.1)α. 1.72, dd (12.0, 4.1)α. 1.71, dd (12.0, 4.1)
β. 1.27, dd (12.3, 12.3)β. 1.14, dd (12.3, 12.1)β. 1.36, dd (12.1, 12.0)β. 1.17, dd (12.1, 12.0)
25.25, ddd (12.3, 4.2, 2.4)4.07, ddd (12.1, 4.1, 2.8)5.17, ddd (12.1, 4.1, 2.7)3.94, ddd (11.9, 4.3, 3.0)
34.96, d (2.4)4.91, d (2.8)3.44, d (2.7)3.32, d (3.0) A
51.40, dd (12.1, 2.2)1.33, dd (12.1, 2.9)1.45, dd (12.1, 2.0)1.39, dd (11.7, 2.7)
6α. 1.56, ddd
(13.3, 12.9, 3.0)		α. 1.53, ddd
(12.8, 12.4, 3.1)		α. 1.52, ddd
(13.1, 12.8, 3.1)		α. 1.51, ddd
(12.8, 12.4, 3.2)
β. 1.52, mβ. 1.49, mβ. 1.46, mβ. 1.48, m
7α. 2.13, br d (13.4)α. 2.11, ddd
(12.8, 3.2, 3.1)		α. 2.09, ddd
(13.1, 3.1, 2.4)		α. 2.07, ddd
(13.2, 3.0, 2.8)
β. 2.77, m β. 2.75, ddd
(12.8, 12.4, 5.0)		β. 2.76, ddd
(13.1, 12.8, 4.4)		β. 2.74, m
91.88, br s1.85, br s1.86, br s1.82, br s
115.40, br s5.44, br s5.39, br s5.44, br s
2-COCH31.92, s-2.03, s-
3-COCH32.07, s2.07, s--
4-CH3 (α)1.00, s0.959, s0.91, s0.86, s
4-CH3 (β)0.90, s0.88, s0.99, s0.99, s
8-CH31.31, s1.30, s1.29, s1.28, s
10-CH31.03, s0.99, s1.00, s0.95, s
12-CH31.80, s1.80, br s1.78, br s1.79, br s
13-CH31.18, s1.18, s1.17, s1.17, s
14-CO2CH33.57, s3.56, s3.56, s3.56, s
16-CH31.60, s1.59, s1.57, s1.57, s
A obscured by solvent signal.
Table
Table 2. Diagnostic 13C NMR (methanol-d4) data for oxandrastins A–D (1–4).
Table 2. Diagnostic 13C NMR (methanol-d4) data for oxandrastins A–D (1–4).
PositionδC, Type
(1)(2)(3)(4)
139.6CH242.8CH238.8CH242.2CH2
269.4CH65.6CH71.9CH67.0CH
378.5CH81.6CH77.2CH79.7CH
439.3C39.4C40.0C39.6C
550.0CH49.9CH48.4CH48.3CH
618.6CH218.6CH218.7CH218.8CH2
734.1CH234.1CH234.2CH234.3CH2
843.5C43.5C43.5C43.6C
954.5CH54.6CH54.6CH54.6CH
1039.5C39.4C39.4C39.2C
11125.6CH125.9CH126.0CH126.4CH
12137.2C136.9C136.7C136.3 aC
1358.6 aC58.4 aC58.4C58.8 aC
1468.9 aC68.9 aC68.8C68.8 aC
15NDCNDCNDCNDC
16114.8C114.6C114.8C114.9 aC
17NDC201.8 aC202.3 aCNDC
2-COCH3172.3C--172.7C--
2-COCH321.1CH3--21.3CH3--
3-COCH3172.6C173.1C----
3-COCH320.9CH321.2CH3----
4-CH3 (α)21.7CH321.9CH322.0CH322.1CH3
4-CH3 (β)28.2CH328.3CH329.1CH329.2CH3
8-CH318.3CH318.4CH318.3CH318.4CH3
10-CH318.4CH318.5CH318.5CH318.7CH3
12-CH319.9CH319.9CH319.9CH319.9CH3
13-CH316.2CH316.2CH316.2CH316.2CH3
14-CO2CH3172.0C172.0C172.1C172.1C
14-CO2CH352.2CH352.2CH352.1CH352.1CH3
16-CH36.4CH36.4CH36.4CH36.4CH3
ND not detected; a resonances detected from HMBC data.
Table
Table 3. Diagnostic 1H and 13C NMR (methanol-d4) data for isoaustalide F (7).
Table 3. Diagnostic 1H and 13C NMR (methanol-d4) data for isoaustalide F (7).
PositionδH, Mult (J in Hz)δCType
15.21, br s69.9CH2
2-171.9C
3-108.4C
4-156.7C
5-117.5C
6-160.0C
7-116.2C
8-147.6C
9-77.6C
10a. 2.33, dd (15.7, 2.0)43.4CH2
b. 2.16, dd (15.7, 4.3)
114.16, dd (3.9, 2.0)69.7CH
12-87.5C
13-87.0C
14-120.1C
153.71, dd (10.5, 5.9)68.8CH
16a. 2.18, dd (13.9, 5.9)40.5CH2
b. 1.68, dd (13.9, 10.5)
17-44.6C
182.40, d (8.1)39.4CH
19a. 3.01, d (18.6)19.2CH2
b. 2.94, dd (18.6, 8.1)
7-CH32.07, s10.8CH3
9-CH31.23, s28.3CH3
13-CH3(a)1.52, s29.3CH3
13-CH3(b)1.63, s26.7CH3
17-CH31.03, s18.8CH3
4-OCH34.06, s62.4CH3
14-OCH33.41, s49.3 ACH3
A resonance obscured by residue solvent.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Elbanna, A.H.; Khalil, Z.G.; Capon, R.J. Oxandrastins: Antibacterial Meroterpenes from an Australian Mud Dauber Wasp Nest-Associated Fungus, Penicillium sp. CMB-MD14. Molecules 2021, 26, 7144. https://doi.org/10.3390/molecules26237144

AMA Style

Elbanna AH, Khalil ZG, Capon RJ. Oxandrastins: Antibacterial Meroterpenes from an Australian Mud Dauber Wasp Nest-Associated Fungus, Penicillium sp. CMB-MD14. Molecules. 2021; 26(23):7144. https://doi.org/10.3390/molecules26237144

Chicago/Turabian Style

Elbanna, Ahmed H., Zeinab G. Khalil, and Robert J. Capon. 2021. "Oxandrastins: Antibacterial Meroterpenes from an Australian Mud Dauber Wasp Nest-Associated Fungus, Penicillium sp. CMB-MD14" Molecules 26, no. 23: 7144. https://doi.org/10.3390/molecules26237144

Article Metrics

Back to TopTop