Journal of the Chilean Chemical Society
version ISSN 0717-9707
J. Chil. Chem. Soc. vol.56 no.1 Concepción 2011
J. Chil. Chem. Soc., 56, No 1 (2011), págs.: 625-627
NEW BUTYROLACTONE FROM A MARINE-DERIVED FUNGUS ASPERGILLUS SP
AURELIO SAN-MARTÍN1*, JUANA ROVIROSA1, INMACULADA VACA1, KAREN VERGARA1, LAURA ACEVEDO2, DOLORES VIÑA2, FRANCISCO ORALLO†2 AND MARÍA CRISTINA CHAMY3
1 Departamento de Química, Facultad de Ciencias, Universidad de Chile, Las Palmeras 3425, Ñuñoa, Santiago, Chile.
2 Departamento de Farmacología, Facultad de Farmacia e Instituto de Farmacia Industrial, Universidad de Santiago de Compostela, Campus Universitario Sur, 15782, Santiago de Compostela, España.
3Departamento de Química, Facultad de Ecología y Recursos Naturales, Sede Viña del Mar, Universidad Andrés Bello, Avda Los Fresnos 52, Viña del Mar, Chile
Four compounds that belong to two structure types, namely dibenzylbutyrolactone and sesterterpenoids, were obtained from the extract of the strain Aspergillus sp. (2P-22), isolated from a marine sponge, Cliona chilensis. Among them, compound 1 was identified as new, namely butylrolactone-VI. The structures of these compounds were characterized on the basis of spectroscopic data. Biological activities of these fungal metabolites, are described.
Keywords: marine-derived fungus, Aspergillus sp. (2P-22); dibenzylbutyrolactone; sesterterpenoids.
In the search for novel and bioactive molecules, terrestrial fungi have yielded many biologically active compounds. More recently, marine microorganisms have gained attention as important sources of chemically interesting and biologically active secondary metabolites, due to the diversity in chemical structures and biological activities1,2. However, compared with other marine organisms, relatively few investigations of the secondary metabolites from marine fungi have been reported3. Fungi isolated from various organisms in the marine environment, e.g., from mangroves4, algae5, mollusks6 and particularly sponges7, have been examined for their secondary metabolite content.
As part of our research on marine fungi, we report here the results regarding the secondary metabolite chemistry of 2P-22 strain, Aspergillus sp., isolated from the marine sponge Cliona chilensis collected in Los Molles, IV Region, Chile. This study led to the isolation of a new compound 1, together with three known compounds previously isolated from other fungal sources 8-11 (Figure 1). The new compound is structurally related to the known butyrolactone I isolated from Aspergillus terreus.12 We described the isolation, structure elucidation, and biological activities of these fungal metabolites.
General experimental procedures.
1H and 13C-NMR spectra were recorded on a Bruker AMX2-400 spectrometer, operating at 400.13 for 1H and 100.6 MHz for 13C. Chemical shifts are reported in ppm (S) and coupling constant (J) are given in Hz. The spectra were obtained in CDCl3 solutions and are referred to the residual peaks of CHCl3 at S 7.26 ppm and 77.0 ppm for 1H and 13C respectively. Mass spectra were taken at 70 eV (probe) in a Micromass Autospec spectrometer. Semipreparative HPLC was carried out with a Beckman System Gold 125P. Dry column chromatography was performed on Merck (0.02-0.063 mm) silica gel.
The fungi isolate was recovered from the surface of the sponge Cliona chilensis collected in the Pacific Sea, Los Molles (IV Región, Chile), during September 2007. A sample of this strain was deposited in the Laboratory of Marine Natural Products of the Universidad de Chile coded as 2P-22 and kept in agar slants with potato dextrose agar (PDA) as culture medium. The strain was seeded in Petri dishes with PDA culture medium in seawater and incubated for 7 days at 280C. Then, a solution of Tween 80 (0.05%) in sterile distilled water was used to obtain a spore suspension. This suspension was poured into an Erlenmeyer flask containing 150 mL of Czapeck medium (5g of yeast extract, 30g of sucrose, 2g of KNO3, 0.5g of KCl, 0.01g of FeSO4 x7H2O, 0.5g of MgSO4 x7H2O, 1g of KH2PO4, 1L of seawater) and cultured at 270C with 230 rpm for 48 h to prepared a stock inoculum. The large-scale fermentation was performed in Erlenmayer flask (10 x 1L each) containing 200 mL of Czapeck medium and 20 mL of inoculum. The cultures were incubated on an orbital shaker (230 rpm) at 270C for 25 days.
The mycelium was removed from the culture broth by filtration. Both the broth and the mycelium were studied. First, the broth (10 L) was extracted with EtOAc, (3x 1.5 L). The resulting organic extract was dried under reduced pressure to obtain a brown solid (0.5 g), which was fractionated by column chromatography on silica gel using stepwise gradient elution from 70% hexane in ethyl acetate, to 100% ethyl acetate, to 100% methanol. The volume eluted in each step was 0.5 L, and 10 fractions were obtained and evaporated to dryness. Moreover, the dried mycelium (12 g) was first extracted with CH2Cl2 (3 X 1 L) to give 1 g of dichloromethane extract and then with CH3OH (3 x 1 L) to obtain 11 g of methanol extract. Purification of the resulting fractions of the organic culture broth allowed us to obtain the pure compounds 1-4 as follows: the methanol extract was fractionated on a Sephadex LH-20 column using a 6:2:1 n-hexane/CH2Cl2/MeOH solvent system to obtain 20 fractions. Fraction 10 (100 mg) was further separated using silica gel (200-300 mesh) CC with a gradient solvent system from 50% petroleum ether/EtOAc to 100% EtOAc to yield 27 fractions (50 mL for each fraction). The fractions were monitored by TLC. Further purifications were made by chromatography on silica gel isolating compounds 1 and 2. From the purification by chromatography on silica gel using as mobile phase hexane/EtOAc (8:3), fractions 15 and 18 contained compounds 3 and 4 respectively. Compounds 2 - 4 were identified by comparison of their spectroscopic properties with those reported 8-13.
Compound (1): 1H-NMR(δ, 400 MHz,): 7.59 (2H, d, J= 8.8 Hz, H-5' and H-9'), 6.90 (2H, d, J= 8.8 Hz, H-6' and H-8'), 6.58 (1H, brs, H-5), 6.55 (1H, d, J= 8.3Hz, H-8), 6.52 (1H, dd, J= 2.0, 8.3 Hz, H-9), 4.94 (1H, t, J= 4.9 Hz, H-11), 3.78 (3H, s, OCH3), 3.76 (1H, t, J=4.9 Hz, H-11), 3.53 (1H, d, J=14.7 Hz, H-3a), 3.45 (1H, d, J=14.7 Hz, H-3e), 2.88 (1H, dd, J= 4.6, 17.0 Hz, H-10a), 2.62 (1H, dd, J= 5.1, 17.0 Hz, H-10e), 1.31 (3H, s, Me-13), 1.24 (3H, s, Me 14). 13C-NMR: 169.7 (C-1), 85.9 (C-2), 38.7 (C-3), 128.0 (C-4), 132.1 (C-5), 118.2 (C-6), 151.9 (C-7), 116.7 (C-8), 129.6 (C-9), 31.0 (C-10), 69.6 (C-11), 77.2 (C-12), 24.6 ( C-13), 22.4 (C-14), 169.2 (C-1'), 137.4 (C-2'), 124.7 (C-3'), 128.0 (C-4'), 129.5 (C-5' and C-9'), 116.0 (C-6' and C-8'), 156.6 (C-7'). EIMS m/z (rel. int.): 458[M]+ (1), 440 (3), 422 (2), 405 (15), 391 (4), 319 (5), 237 (7), 217 (12), 216 (63), 202 (8), 154 (6), 149 (10), 122 (9), 104 (13), 99 (36), 94 (57), 93 (5);
Compound(1a): 1H-NMR (δ, 400 MHz): 7.72 (2H, d, J= 8.8 Hz, H-5' and H-9'), 7.20 (2H, d, J= 8.8 Hz, H-6' and H-8'), 6.62 (1H, dd, J= 1.5, 8.5 Hz, H-9), 6.58 (1H, d, J= 8.5 Hz, H-8), 6.48 (1H, brs, H-5), 4.94 (1H, t, J= 5.2 Hz, H-11), 3.78 (3H, OCH3), 3.56 (1H, d, J=14.8 Hz, H-3a), 3.45 (1H, d, J=14.8 Hz, H-3e), 2.90 (1H, dd, J= 5.1, 17.3 Hz, H-10a), 2.60 (1H, dd, J= 5.3, 17.3 Hz, H-10e), 2.33 (3H, s, Me-18), 2.02 (3H, s, Me-16), 1.25 (6H, s, Me-13 and Me 14). 13C-NMR: 170.6 (C-1), 86.0 (C-2), 38.5 (C-3), 126.6 (C-4), 131.7 (C-5), 117.9 (C-6), 151.9 (C-7), 116.8 (C-8), 129.6 (C-9), 28.1 (C-10), 70.9 (C-11), 75.1 (C-12), 24.8 (C-13), 22.6 (C-14), 169.6 (C-15), 21.1 (C-16), 168.7 (C-17), 21.0 (C-18), 169.1 (C-1'), 138.8 (C-2'), 124.4 (C-3'), 127.2 (C-4'), 128.9 (C-5' and C-9'), 122.2 (C-6' and C-8'), 151.0 (C-7'); EIMS m/z (rel. int.): 542[M]+ (1), 525 (9), 524 (5), 465 (28), 405 (18), 412 (11), 352 (12), 313 (21), 261 (10), 231 (28), 256 (30), 216 (10), 173 (35), 99 (12), 88(2);
The antibacterial activity was determined in solid media by the paper disc diffusion method14. The MIQ was measured as the minimal quantity that showed a transparent halo of growth inhibition. Five phytopathogen bacterial strains were used in the bioassay: Pseudomonas syringae pv syringae, Xanthomonas arboricola pv juglandis 833, Erwinia carotovora, Agrobacterium tumefaciens A348 (Gram-negative bacterias) and Clavibacter michiganensis 807 (Gram-positive bacteria). Benzylpenicillin potassium salt (Sigma-Aldrich) and streptomycin sulfate (Calbiochem) were used as positive antibiotics.
Antitumor activity of compounds was assessed with the potato disc method described by McLaughlin and Rogers in 199815. In brief, potato tubers were surface sterilized in 1% NaClO for 20 min. Potato discs (5 mm thick) were made with cork borer and placed on 2% agar plates (5 discs per plate). To each potato disc was applied 0.05 mL of a solution containing 2 mL of a broth culture of A. tumefaciens (48 h culture in Lauria-Bertani broth medium), 1.5 mL of sterile water and 0.5 mL of the solution of the compound tested (8 mg of compound in 2 mL of dimethyl sulfoxide, DMSO). Control discs were prepared with DMSO. A minimum of three Petri dishes (% discs/dish) (n= 1525) were used for each test compound and the control. After preparation, the Petri dishes were placed in an incubator at 270 C for 12-21 days. The crown galls on the potato tuber discs were observed by the naked eye. Numbers of tumors per disc were counted, and percent inhibition for each concentration was determined as % inhibition= 100- (average number of tumors of sample/ ditto for the control) x100.
Functional (contraction/relaxation) studies in rat isolated thoracic aorta rings: _
Endothelium-denuded vascular rings were prepared from aortae of male Wistar rats weighing 210-270 g, essentially as described elsewhere16. Contraction studies were performed following the general procedure previously reported17. In the present study, however, isometric contractions were recorded by means of force-displacement transducers (Dynamometer UF1, Pioden Controls Ltd.,) connected to a MacLab® system (ADInstruments Pty Ltd,), controlled by a Power Macintosh 5500-225 computer.
After an equilibration period of at least 1 h, isometric contractions induced by L-phenylephrine (1 µM) were obtained. When contraction of the tissue in response to this vasoconstrictor agent had stabilized (after about 20 min), cumulatively increasing concentrations of the tested compounds (1-200 µM) were added to the bath at 5-10 min intervals (the time needed to obtain steady-state relaxation). Control tissues were subjected to the same procedures simultaneously, but omitting the compounds and adding the vehicle (appropriate dilutions of DMSO).
Contractile responses to phenylephrine are expressed as a percentage of the maximal contraction produced by this vasoconstrictor agent before the addition of the tested compounds. Sigmoidal concentration-response curves for the vasorelaxant effects of compounds were fitted using the program Origin 7.0 (Microcal Software, Inc., Northampton, USA), with estimation of IC50 values (i.e. concentrations inducing 50% relaxation) for phenylephrine-induced contractions.
Significant differences between two means (p < 0.05 or p < 0.01) were determined by one-way analysis of variance (ANOVA) followed by the Dunnett's post-hoc test.
Appropriate dilutions of the above drugs were prepared every day immediately before use in deionized water from the following concentrated stock solutions kept at -20oC: the tested compounds (100 mM) in DMSO; L-phenylephrine (100 mM) in deionized water. In our experiments, neither deionized water nor appropriate dilutions of the vehicle used had significant pharmacological effects.
RESULTS AND DISCUSSION
Chromatographic separation of compounds extracted from the culture of 2P-22 strain, Aspergillus sp. led to the isolation of 4 compounds 14: one new, 1, and three known compounds, named butyrolactone I, 211, and the two sesterterpenoids terretonin A, 3 and terretonin B, 48,9. The structures of the known compounds were confirmed by comparing their spectroscopic properties with those reported8-13.
Compound 1 was obtained as colourless crystals. Its molecular formula was established as C24H26O9 (m/z 458.0). The 13C NMR and DEPT spectra of 1 showed 24 carbon signals for two methyl, one methoxy, two methylene, eight methines and 11 quaternary carbon atoms including two carbonyl carbons and a sp3 carbon bearing a hydroxyl group. The 1H NMR spectra of 1 displayed signals for a 1,4-disubstituted phenolic moiety at δ 7.59 (2H, d, J= 8.8 Hz) and 6.90 (2H, d, J= 8.8 Hz), three aromatic proton signals of a 1,2,4-trisubstituted phenol (δ 6.58, 6.55 and 6.52 ppm ), a signal at 8 3.78 (3H, s, OMe), a triplet at δ 3.76 (J= 4.9 Hz) corresponding to a hydrogen geminal to a hydroxyl group, a pair of doublets at 8 3.53 and 3.45 (1H each, d, J=14.7 Hz) corresponding to the methylene connecting the butyrolactone with the trisubstituted aromatic ring, two double doublets at δ 2.88 (1H, dd, J = 4.7, 17.0 Hz) and 2.62 (1H, dd, J=5.03, 17.0 Hz), and two methyl groups at 1.31 and 1.24 ppm ( See Experimental). The 1H-NMR data of compound 1 closely resembled those of butyrolactone I, 2 (Figure 1), with the only difference being the chemical shift of the prenyl residue, ie. the absence of a double bond in 2 and the appearance of a triplet at 8 3.76 in 1 corresponding to a hydrogen geminal to a hydroxyl group.
In order to verify this structure, compound 1 was treated with acetic anhydride in pyridine affording compound 1a. The comparison of the 1H-NMR spectra of compounds 1 and 1a showed only minor differences. The signal at 8 3.76 was shifted to 4.94 ppm in 1a, which suggested that the hydroxyl group at C-11 was acetylated, and the protons of 1,4-disubstituted phenol where shifted from 8 7.59 and 6.90 ppm in 1 to 7.72 and 7.20 ppm, indicating the acetylation of the 1,4 disubstituted phenol.
The structure of 1a (Figure 1) was determined based on the 1H-13C long-range correlations of the phenyl proton at δ 7.72 (H-5' and H-9'; δC 128.9) with the carbons at δ 122.2 (C-6' and C-8') and 151.0 ppm (C-7'), and the phenyl protons at δ 7.20 (H-6' and H-8') with the carbons at δ 128.9 (C-5' and C-9') and 151.0 (C-7'); the correlations between the multiplet at δ 6.62 (corresponding to the phenyl protons H-8, δC 116.8 and H-9, δC 129.6) with carbons at δ 38.5 (C-3), 151.9 (C-7) and 131.7 (C-5); the 1H-13C long-range correlations of the methyl protons at δ 1.25 (H-13 and H-14) with the carbons at δ 70.9 (C-11) and 75.1 (C-12). The protons at δ 3.56 and 3.44 (H-3) showed long-range correlations with the carbons at δ 170.6 (C-1), 86.0 (C-2), 126.6 (C-4), 131.7 (C-5) and 129.6 (C-9) indicating that this carbon is the linkage between the butyrolactone and the trisubstituted aromatic ring. The pair of double doublets at δ 2.90 and 2.60 showed 1H-13C long-range correlations with δ 70.9 (C-11), 75.0 (C-12), 117.9 (C-6), 131.7 (C-5) and 151.9 (C-7) indicating that the chain was linked to C-6.
The assignments of the quaternary carbons were determined based on the comparison with butyrolactone I 2.11 Thus, the structure of compound 1 was elucidated as butyrolactone-VI. (Figure 1)
The result of the antibacterial activity assay shows that 1 and 2 were only active against Clavibacter michiganensis. The MIQ value of butyrolactone VI (U was 50 ug. The crown gall tumor bioassay used to test the compounds for antitumor activity was performed essentially according to McLaughlin & Rogers15. It has been demonstrated that the compounds which inhibit these plant tumors have a high predictability of showing activity against the P288 (3PS) leukaemia in mice18 and, in general, of disrupting the cell cycle (mitosis, S phase, etc.) regardless of their mode of action19. Compounds 1 and 2 showed a similar and significant inhibition of the growth of crown gall tumors on potato discs. The values were: butyrolactone I 2 (84, 46%) and butyrolactone VI 1 (71, 64%), which suggests in vivo antitumor activity for both compounds.
Butyrolactone I 2 was acetylated as usual (Py/acetic anhydride) yielding compound 2a. The potential vasorelaxant effects of compounds 2 and 2a were evaluated on endothelium-denuded rat aortic rings precontracted with L-phenylephrine.16,17L-phenylephrine caused slow and sustained contraction of the rat isolated aortic rings without endothelium. The maximal tension (mg) reached was 2053.9 ± 89 (n=5). These contractile effects were maintained without significant tension changes in control rings for at least 90 min. DMSO had no significant effects on phenylephrine-induced contractions in endothelium-denudes rat aortic rings (n=5, p>0.05). The cumulative addition of the tested compounds (20-200 uM) concentration-dependently relaxed the contractions induced by L-phenylephrine (Figure 2). The butyrolactone I acetate was slightly less efficient than butyrolactone I in relaxing these contractions. However, the corresponding IC50 values of both compounds did not present significant differences (Table 1).
Each value represents the mean ± s.e.m from experiments shown in brackets.
In summary, a new cytotoxic compound, butyrolactone VI, 1, has been isolated from a strain of Aspergillus sp, isolated from a Chilean sponge Cliona chilensis. Its structure resembles that of other butyrolactones, previously characterized from marine strain of Aspergillus terreus and Aspergillus sp.10-13. These compounds were tested for antibacterial and antitumor assays and for potential vasorelaxant effects obtaining good responses suggesting that further studies to assess the potential of this type of structure are merited.
Financial support by a Grant Proyecto PBCT, PDA - 13 (Chile), Proyecto Anillo ACT-38, (CHILE) and CSIC-UCHILE Proyecto (02/2007-2008).
This article is dedicated to the memory of Prof. Francisco Orallo, who died in December 2009.
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(Received: October 6, 2010 - Accepted: March 28, 2011)