CHEMICAL CONSTITUENTS DERIVED FROM THE CANARIES MARINE SPONGE Myxilla sp.

Abstract

Stigmasterols, ceramides, including ceramide-1-phosphates and pyrimidines were identified in an ethanol extract of the marine sponge Myxilla sp. The compounds were identified by MS and 1D- and 2D-NMR techniques. A simple method based on an ultra-high-performance liquid chromatography coupled with tandem mass spectrometry was developed to investigate the production of the aforementioned ceramides. This is the first report on ceramide-1-phosphates from a marine sponge.

Keywords:
Myxilla; stigmasterols; ceramides; pyrimidines

INTRODUCTION

Marine invertebrates are a rich source of natural compounds that possess various biological activities. The phylum Porifera, Demospongiae class, is the most diverse and species-rich type of these organisms. Among these, the Poecilosclerida Order, Myxillidae Family, Genus Myxilla top the list. In fact, rosacelose, a new anti-HIV polysaccharide was recently isolated from the Myxilla rosacea marine sponge.¹ Zhukova et al.² also isolated glycolipids from Myxilla incrustans, whose molecular structures contained sphingosine, phytosphingosine, fatty acids and phosphorus. Venkateswarlu et al.³ described new ceramides originating from several sponges from the gulf of Mannar. On the basis of these precedents, in this paper we present the chromatographic and spectroscopic study of an ethanolic extract from the Myxilla sp., for which specimens were collected from the Canary Islands.⁴ This study yielded the stigmasterols 1, 3, 5 and 7, the ceramides 9-13, the ceramide-1-phosphates 14-22 and the pyrimidines 23-24.

EXPERIMENTAL

General experimental procedures

Normal-phase chromatography was carried out on silica gel (Scharlau) with a 0.06-0.2 mm particle size for the adsorbent and 0.04-0.06 mm for the stationary phase. The chromatography was performed either at medium pressure (Büchi Chromatography System) or at low pressure with Fluid Metering Inc. motors connected in series with an Ace Glass Inc. column. Normal-phase TLC was performed on silica gel plates (0.25 mm diameter, Tracer Analitica) using a combination of hexane, ethyl acetate (EtOAc), chloroform (Cl₃CH) and methanol (MeOH) as an eluent, in proportions specified for each case. Reverse-phase TLC was carried out on RP18-F₂₅₄ plates (0.25 mm, Merck) with the use of CH₃CN/ CH₃OH/ H₂O (80:18:2) as a mobile phase. In all cases, the spots were revealed by spraying with oleum (4% sulphuric acid, 80% acetic acid, 16% water) and heating at 120 ºC for 20 minutes. ¹H-, ¹³C-, and 2D-NMR experiments were recorded on a Bruker spectrometer, AMX-300 or AMX-500 models, with standard pulse sequences operating at 300 or 500 MHz in ¹H-NMR spectroscopy and 75 or 125 MHz in ¹³C-NMR spectroscopy. Tetramethylsilane was used as an internal standard for the calibration of the ¹H-NMR spectra and deuterated chloroform (δ 77.00)/ deuterated dimethyl sulfoxide (δ 39.70)/ deuterated pyridine (δ 149.80) was used for the calibration of the ¹³C-NMR spectra. Electrospray ionization mass spectrometry (ESI-MS) was performed either at low or high resolutions with a common electron impact mass spectrometer (IE) or by fast atom bombardment (FAB). Positive-mode was carried out on a FAB-MS at 70 eV with a FISONS VG Micromass Autospec apparatus with NBA (3-nitrobencylic alcohol) as the matrix. Melting points were stablished using a Gallenkamp apparatus and were left uncorrected.

Animal material

In the summer of 2006, we started a marine sponge bioprospecting campaign near the effluent pipe of a fish farm, in Castillo del Romeral, Santa Lucía, Gran Canaria island (27º47´53´´N; 15º26´51´´W), at 5 m depth. As a result of it, specimens of a marine sponge classified as Myxilla sp. were collected. A voucher sample (Por.11) was deposited at the "Colección de Zoología ZCM, Universidad de Las Palmas de Gran Canaria (www.gbif.es)", Canary Islands, as communicated in a conference.⁴

Extraction and isolation

Fresh sponge (3399 g) was extracted exhaustively with acetone (3 L, x3) and ethanol (3 L, x3). The combined extract (67,11 g) was chromatographed at medium pressure (Büchi Chromatography System) on silica gel (Scharlau, 0.04-0.06 mm) as the stationary phase. A gradient elution from hexane to EtOAc, then from EtOAc to Cl₃CH, and later still from Cl₃CH to MeOH was used (the amount and proportion of each solvent is specified in Table 1S). The 100 mL fractions collected were monitored by normal-phase TLC on silica gel plates (0.25 mm diameter) using a combination of hexane (x%) and EtOAc [(100-x)%] as eluents and pooled together to obtain three TLC homogeneous fractions, namely: 1) the sterol mixture, 2) the ceramide mixture and 3) the pyrimidinic nucleobase mixture.

The sterol mixture (1+3+5+7)

White amorphous solid; m.p. 277-278 ºC; [α]_D ^25ºC = -15.2º (c 0.2; CHCl₃). Both values are in agreement with those reported in literature for the β-sitosterol (m.p. = 277-278 ºC,⁵ [α]_D^25ºC = -15.2º (c 0.2; CHCl₃).⁶ For ¹H- and ¹³C-NMR spectra, see Table 2S. ESI-MS m/z 414.39, 412.39, 386.36, 368.30, 273.28, 255.23; HR-ESI-MS m/z 414.3854 (calcd for C₂₉H₅₀O 414.3862); 386.3903 (calcd for C₂₈H₅₀ 386.3913).

The acetate of the sterol mixture (2+4+6+8)

The sterol mixture (50 mg) was dissolved in pyridine (1 mL) and acetic anhydride was added (2 mL). After 24 hours stirring at room temperature, 5 g of crushed ice was added and stirred for 30 minutes. By extraction with diethyl ether, washing with 2N HCl and 10% NaHCO₃, drying on anhydrous Na₂SO₄, filtrating and evaporating with a rotary evaporator, a white amorphous solid was obtained. Crystals of this mixture of compounds were obtained from MeOH; for ¹H- and ¹³C-NMR spectra, see Table 2S and discussion for the lateral chain; ESI-MS m/z 456.38, 442.38; HR-ESI-MS m/z 456.3976 (calcd for C₃₁H₅₂O₂ 456.3967).

The ceramide mixture (9-13)

White amorphous solid; m.p. 87-88 ºC; [α]_D^20ºC = -2.6º (c 0.945; Cl₃CH); TLC, R_f = 0.60 in Cl₃CH (50 mL)/MeOH (30 mL)/AcOH (8 mL)/H₂O (7 mL) as eluent. ¹H-NMR, (Cl₃CD, 300 MHz) δ 6.26 (1H, d, J=7.26 Hz), 5.77 (1H, dt, J_4,5=15.3, J_5,6=6.6 Hz), 5.53 (1H, dd, J_3,4=6.4 Hz, J_4,5=15.3 Hz), 3.60-4.31 (4H, m, 1a-H, 1b-H, 2-H, 3-H), 2.80 (1H, br s, OH), 2.23 (2H, t, J=7.6 Hz, 2´-H), 2.04 (2H, m, 6-H), 1.66 (1H, br s, OH), 1.63 (2H, m, 3´-H), 1.25 (34H, CH₂), 1.22 (22H, CH₂), 0.88 (3H, t, J=6.6 Hz, CH₃), 0.87 (3H, t, J=6.6 Hz, CH₃). ¹³C-NMR (Cl₃CD, 75 MHz) δ 173.95, 134.31, 128.76, 74.66, 62.49, 54.46, 36.84, 32.28, 31.92, 29.69, 29.36, 25.75, 22.68, 14.11. ¹³C-NMR (Py-D₅, 125 MHz) δ 175.44, 134.36, 134.24, 75.29, 64.14, 58.85, 38.87, 34.12, 34.10, 32.00, 31.98, 31.90, 31.87, 31.84, 31.76, 31.71, 31.61, 31.59, 31.55, 28.42, 24.92, 16.26. ESI-MS m/z 362.31 (3.0%), 350.31 (3.2%), 336.29 (5.4%), 323.28 (3.46%). HR-ESI-MS m/z 672.6302 ([M+Na]⁺, C₂₄-ceramide) (calcd for C₄₂H₈₃NO₃Na 672.6302); 658.6120 ([M+Na]⁺, C₂₃-ceramide) (calcd for C₄₁H₈₁NO₃Na 658.6114); 644.6007 ([M+Na]⁺, C₂₂-ceramide) (calcd for C₄₀H₇₉NO₃Na 644.5958); 630.5812 ([M+Na]⁺, C₂₁-ceramide) (calcd for C₃₉H₇₇NO₃Na 630.5812); 616.5662 ([M+Na]⁺, C₂₀-ceramide) (calcd for C₃₈H₇₅NO₃Na 616.5645).

Identification of the ceramide-1-phosphates (14-22) in the ceramide mixture

These minor metabolites were detected by high-resolution mass spectrometry (HRMS) and an ultra high-pressure liquid chromatography tandem mass spectrometry technique (UHPLC-MS/MS).

Reagents used in the UHPLC-MS method

Stock solutions containing 1000 mg L^-1 of ceramide-1-phosphates mixture were prepared by dissolving the mixture in tetrahydrofuran (Fischer Chemical, Madrid, Spain). The solutions were stored in glass-stoppered bottles at -20 ºC before use. Working solutions were prepared daily using acetonitrile as solvent (Panreac Química, Barcelona, Spain). LC-MS grade methanol, LC-MS water as well as formic acid, used to adjust the pH of the mobile phases, were obtained from Panreac Química (Barcelona, Spain).

Instrumentation used in the UHPLC-MS method

The mass spectrum was performed in a UHPLC-MS/MS system from Waters (Madrid, Spain), with a Quaternary Solvent Manager (QSM) used to load samples and wash and recondition the analytical column, a 2777C sample manager equipped with a 25 µL syringe, a tray to hold 2 mL vials, and an ACQUITY triple quadrupole (TQD) mass spectrometer with an electrospray ionization (ESI) interface. All Waters components (Madrid, Spain) were controlled using the MassLynx Mass Spectrometry Software. Electrospray ionization parameters were fixed as follows: the capillary voltage was 4 kV in positive mode, the cone voltage was 80V, the source temperature was 120 ºC, the desolvation temperature was 450 ºC, and the desolvation gas flow rate was 1000 L hour^-1. Nitrogen was used as the desolvation gas and argon was employed as the collision gas.

Chromatographic conditions in the UHPLC-MS method

For the chromatographic separation, the analytical column was a 50 mm × 2.1 mm ACQUITY UHPLC BEH Waters C₁₈ with a particle size of 1.7 µm (Waters Chromatography, Barcelona, Spain) operating at a temperature of 30 ºC. Analytes separation was carried out in isocratic mode, 95:5, using water with 5 mM formic acid (A) and methanol (B). The sample volume injected was 10 µL.

The pyridinic nucleobase mixture (23+24)

Two heterocyclic compounds appear mixed as a white amorphous solid. After integration of the ¹H-NMR spectrum of the mixture, the composition was deduced to be C_uracil/C_thymine = 1.1.

Thymine (23). Amorphous white solid. ¹H-NMR (DMSO-D₆, 300 MHz) δ 11.02 (1H, br s), 10.63 (1H, br s), 7.26 (1H, br s), 1.73 (3H, d, 𝐽 = 0.6 Hz). ¹³C-NMR (DMSO-D₆, 75 MHz) δ 165.2, 151.7, 138.0, 107.9, 12.0.

Uracil (24). Amorphous white solid. ¹H-NMR (DMSO-D₆, 300 MHz) δ 11.00 (1H, br s), 11.00 (1H, br s), 7.40 (1H, d, 𝐽 = 7.5 Hz), 5.46 (1H, d, 𝐽 = 7.5 Hz). ¹³C-NMR (DMSO-D₆, 75 MHz) δ 164.7, 151.7, 142.5, 100.4.

RESULTS AND DISCUSSION

The sterols

The fractions that contained sterols were eluted with a mixture of hexane/EtOAc 80:20, and were repeatedly chromatographied, thereby allowing the identification of the following compounds: stigmast-5-en-3β-ol (β-sitosterol) (1, 75%), stigmast-5,25-dien-3β-ol (3, 7%), stigmast-5,24(25)-dien-3β-ol (5, 2%) and stigmast-5,23-dien-3β-ol (7, 16%). The high resolution mass spectrum (HRMS) showed a peak at m/z 414.3854 corresponding to the molecular ion which in turn corresponds to the molecular formula C₂₉H₅₀O. The presence of secondary products with one unsaturation on the side chain is demonstrated by the observation of a molecular ion at m/z 412 (C₂₉H₄₈O). On the basis of the intensity of the molecular peaks -414 vs 412- we can deduce that the unsaturated side chain compounds are present at a final concentration of 25%. The ¹H-NMR spectrum showed a signal at δ 5.35 (1H, overlapped double doublets) characteristic of a double bond between the carbons 5 and 6 of the four sterols with the same skeleton as β-sitosterol. A signal at δ 5.16 in the form of a deformed triplet revealed the minor presence (16%) of the regioisomer stigmast-5,23-dien-3β-ol (7). Two broad singlets at δ 4.71 and δ 4.67 (both in a ratio 1:1) revealed the olefinic methylene of stigmast-5,25-dien-3β-ol (3). The ¹³C-NMR spectrum of the aforementioned mixture showed the presence of peaks that can be assigned to all carbons of the steroidal nucleus present in the four steroids (Table 2S). The signals that give evidence of the four side chains of the mixture were observed, giving the following results: signals assignable to C25 and C26 were emitted by stigmast-5,25-dien-3β-ol 3 (δ 145.6 and 116.4 respectively), to C23 and C24 from stigmast-5,23-dien-3β-ol 7 (δ 135.9 and 131.7 respectively) and to C24 and C25 from stigmast-5,24(25)-dien-3β-ol 5 (δ 124.0 and 126.1 respectively).

On the other hand, the mixture of sterols was acetylated as usual to give the corresponding mixture of acetates, stigmast-5-en-3β-ol acetate (2, 75%), stigmast-5,25-dien-3β-ol acetate (4, 7%), stigmast-5,24(25)-dien-3β-ol acetate (6, 2%) and stigmast-5,23-dien-3β-ol acetate (8, 16%). The ¹H-NMR spectrum of this mixture of acetates revealed a sole steroid skeleton and also shows up the different side chains of the mixture. Therefore, a triplet centered at δ 5.16 corresponds to stigmast-5,23-dien-3β-ol acetate (8) and two signals at δ 4.71 and δ 4.65 revealed the methylene of the stigmast-5,25-dien-3β-ol acetate (4).

Again, the integral curves of these signals are consistent with the proportion assigned in Figure 1. In the ¹³C-NMR spectrum (Table 2S) the expected signals were also found, including the minority signals in the olefinic zone of the spectrum (δ 116-146) produced by the unsaturated stigmasterol acetates (4, 6 and 8).

Figure 1
Sterols identified in Myxilla sp. (1,3,5,7) and their acetates (2,4,6,8)

The ceramides

The ceramides mixture (Figure 2) is a white solid, and homogeneous by TLC. The physical constants of the mixture are: m.p. 87-88 ºC, [α]_D^20ºC= -2.6 (Cl₃CH, c 0.945). Both chromatographic (R_f) and spectroscopic data (¹H and ¹³C NMR spectra) revealed the typical characteristics of ceramides, consistent with literature.⁷ That is, erythro configuration (2S, 3R) and a 4,5-trans double bond in the base component, the latter linked to long-chain fatty acids (more than 16 carbons) via an amide bond. Carbons 2S and 3R cause shifts in the ¹³C NMR spectrum at δ 54.46 and 74.66 respectively, and the trans double bond yields a coupling constant of 15.3 Hz in the ¹H-NMR spectrum for the two vinylic protons.

Figure 2
Ceramides identified in Myxilla sp.

The chemical structures were confirmed by HRMS, DEPT-135, DEPT-90 and two-dimensional nuclear magnetic resonance spectroscopy (COSY, NOESY, HSQC and HMBC).

Several nitrogenous fragments were detected in the mass spectrum at m/z 362.31 (C₂₃H₄₀NO₂, 3.0%), 350.31 (C₂₂H₄₀NO₂, 3.2%), 336.29 (C₂₁H₃₈NO₂, 5.4%), 323.28 (C₂₀H₃₇NO₂, 3.46%) and the molecular ions as sodium adducts at m/z 672.6302 ([M+Na]⁺, C₂₄-ceramide, 31.79%), 658.6120 ([M+Na]⁺, C₂₃-ceramide, 11.52%), 644.6007 ([M+Na]⁺, C₂₂-ceramide, 40.25%), 630.5812 ([M+Na]⁺, C₂₁-ceramide, 7.97%) and 616.5662 ([M+Na]⁺, C₂₀-ceramide, 8.47%).

In the DEPT-135 experiment, the four methines and two methyls (positive signals) were separated from rest of methylenes (negative signals). C1 is included in the latter. In the DEPT-90 experiment only the four methines were separated (positive signals). The COSY spectrum showed the following correlations: (2,NH); (3,4); (5,6); (1a,1b); (6,7); (2´,3´) and (3´,4´), among others. In the NOESY spectrum the correlation between hydroxyl group protons in C-1 and C-3 is to be highlighted. The HSQC spectrum provides the correlation between proton and their attached carbon (H_1a and H_1b to C₁, H₂ to C₂, etc.), whereas in the HMBC spectrum each proton is correlated to carbons that are separated by two or three bonds (H₃ to C₁, C₂, C₄ and C₅, etc).

The ceramide-1-phosphates

The ceramide-1-phosphates mixture was detected as an impurity of the previous ceramides mixture. The high-resolution mass spectrum obtained showed different phosphorated fragments [m/z 490.3287 (C₂₅H₄₉NO₆P, 4.5%, Figure 4), 476.3143 (C₂₄H₄₇NO₆P, 2.5%), 472.3176 (C₂₅H₄₇NO₅P, 15.7%) and 462.2969 (C₂₃H₄₅NO₆P, 8.1%, Figure 4)]. On the other hand, the molecular ions of the compounds indicated in Figure 3, from n=11 (ceramide-1-phosphate-C₁₆ or Cer1PC₁₆, 14) to n=19 (ceramide-1-phosphate-C₂₄ or Cer1PC₂₄, 22) were detected by direct injection in the ultra-high performance liquid chromatography mass spectrometer (UHPLC-MS). The percentage composition of the mixture was calculated using the relative intensities of the molecular ions, and gave the highest percentage for ceramide-1-phosphate-C18 or Cer1PC₁₈ which is made up of stearic acid.

Figure 3
Ceramide-1-phosphates identified in Myxilla sp.

Figure 4
Fragmentation schema of the mixture of ceramide-1-phosphates isolated from Myxilla sp. observed in high-resolution mass spectrum

The ceramide-1-phosphates spectrum was obtained by the direct injection of a 1 mg L^-1ceramides mixture solution into the detector at a flow rate of 10 µL minute^-1. The spectra showed nine molecular ions belonging to the positive ionized ceramide-1-phosphates. Each ion increased its mass by 14 units with the addition of each new methylene group. The ion with the largest intensity was m/z = 644.60 corresponding to (Cer1PC₁₈-H)⁺.

After the mass spectrum was obtained, a solution of ceramide-1-phosphates was injected in the UHPLC-MS system to obtain the chromatographic separation of the ceramide-1-phosphates. However, the compounds could not be chromatographically separated because of the similarity of their structures, as it can be observed in Figure 5. The detection was performed using the first quadrupole because no stable "daughter ion" was obtained in the fragmentation of the "parent ions".

Figure 5
Chromatograms of the ceramide-1-phosphates mixture obtained by UHPLC-MS

Figure 6
Structures of thymine (23) and uracil (24)

Sponges of genus Myxilla are emerging as a source of natural products with the carbon skeleton of sphingosine. Sphingosine-1-phosphate has been described in Myxilla incrustans.⁸ Apparently, ceramides and ceramide-1-phosphates have antagonistic functions, and a correct balance between the concentrations of both metabolites is needed for cell and tissue homeostasis. The mixture of ceramide-1-phosphates is made up of metabolites involved in the sphingomyelin cycle, as these are sphingolipids that are analogous to phosphatidic acid. These metabolites are formed from the ceramides thanks to the action of a specific ceramide kinase, which is related to but distinct from the sphingosine kinase that synthesizes sphingosine-1-phosphate.

The pyrimidinic bases

The more polar fractions of the extract yielded two nucleobases, thymine (23) and uracil (24). Both bases appear mixed as a white amorphous solid, which spontaneously precipitates from hexane/EtOAc. With the integration of the ¹H-NMR spectrum of the mixture, the composition was deduced to be C_uracil / C_thymine = 1.1. After repeated chromatographies on the silica gel at low pressure, a sample of pure thymine was obtained. This product provided spectroscopic data in agreement with literature reports.⁹With its substraction, from the spectrum of the mixture, we can deduce the presence of spectrum of uracil, also in agreement with the literature.⁹

In past studies these bases were isolated from marine sponges from Indonesia.¹⁰ Nevertheless, this is the first time that they have been described for the genus Myxilla.

CONCLUSIONS

The chemical study of an ethanolic extract of the Myxilla sp. sponge by chromatographic and spectroscopic techniques, afforded natural products of the type of stigmasterol, ceramides, ceramide-1-phosphates and pyrimidines. This study reports for the first time the isolation of ceramide-1-phosphates from a marine sponge. A facile method based on ultra-high performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS) has been established in order to investigate the production of aforementioned ceramides in the future.

Table 1
Parent ions of the mixture of ceramide-1-phosphates isolated from Myxilla sp. detected by direct injection into the UPLC-MS system. The relative intensities give the relative amounts (percentage) of each compound in the mixture.

Observed ion and formula	Concentration (% w/w)	Ceramide (n value in Figure 3)
616.57 (M-1+) C34H67NO6P	12.96	Cer1PC16 (14, n=11)
617.58 (M+) C34H68NO6P
630.58 (M-1+) C35H69NO6P	6.21	Cer1PC17 (15, n=12)
631.59 (M+) C35H70NO6P
644.60 (M-1+) C36H71NO6P	28.34	Cer1PC18 (16, n=13)
645.60 (M+) C36H72NO6P
658.61 (M-1+) C37H73NO6P	13.90	Cer1PC19 (17, n=14)
659.62 (M+) C37H74NO6P
672.63 (M-1+) C38H75NO6P	21.05	Cer1PC20 (18, n=15)
673.63 (M+) C38H76NO6P
686.64 (M-1+) C39H77NO6P	9.18	Cer1PC21 (19, n=16)
687.65 (M+) C39H78NO6P
700.56 (M-1+) C40H79NO6P	3.51	Cer1PC22 (20, n=17)
701.57 (M+) C40H80NO6P
714.58 (M-1+) C41H81NO6P	0.81	Cer1PC23 (21, n=18)
715.59 (M+) C41H82NO6P
728.60 (M-1+) C42H83NO6P	4.05	Cer1PC24 (22, n=19)
729.60 (M+) C42H84NO6P

ACKNOWLEDGEMENTS

The authors would like to thank the Canary government (Agencia Canaria de Investigación, Innovación y Sociedad de la Información, ACIISI) for the PhD fellowship granted to Pere Ferriol, and the financial support given to the project SI-697 (ULPAPD-08/01-5).

SUPPLEMENTARY MATERIAL

A photograph of the sponge Myxilla sp. and select ¹H-NMR, ¹³C-NMR, DEPT, COSY, NOESY, HSQC, HMBC and MS spectra of the compounds identified (1-24) can be seen at http://quimicanova.sbq.org.br, in a free-access PDF file. Further spectroscopy dates are available upon request from the authors.

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Publication Dates

• Publication in this collection
  Mar 2018

History

• Received
  10 Sept 2017
• Accepted
  21 Nov 2017