Cytotoxic and Antimicrobial Compounds from the Marine-Derived Fungus, Penicillium Species.

The organic extract of liquid cultures of the marine-derived Penicillium sp. was investigated. Fractionation of the extracts of the fungus led to the purification and identification of two new compounds, penicillatides A (1) and B (2), together with the previously reported cyclo(R-Pro-S-Phe) (3) and cyclo(R-Pro-R-Phe) (4). The structures of compounds 1-4 were assigned by extensive interpretation of their NMR and high-resolution mass spectrometry (HRMS). The antiproliferative and cytotoxic activities of the compounds against three human cancer cell lines as well as their antimicrobial activity against several pathogens were evaluated. Compounds 2-4 displayed variable cytotoxic and antimicrobial activities.

1. Introduction

Members of the genus Penicillium are among the most investigated fungi by natural products chemists and are considered a major source for drug discovery. Prominent fungal-derived drugs include the antibiotic n class="Chemical">penicillin, which was obtained from Penicillium chrysogenum, and the antifungal griseofulvin from Penicillium griseofulvum. Nowadays, the genus Penicillium still represents a major producer of secondary metabolites with diverse bioactivities, as reported in many recent reviews [1,2,3,4,5].

In the last decade, a significantly increased interest in secondary metabolites from marine microbes has been reported [2]. 2,5-Diketopiperazines (n class="Chemical">2,5-DKPs) are obtained from different organisms, including marine microbes. They represent an important group of cyclic dipeptides with diverse structures and significant biological activities [2]. Since the number of reported compounds with significant biological properties is increasing, several reviews covering the structural determinations, biological activities, and proposed biosynthetic pathways of this class of compounds have been reported [6,7,8]. Consequently, marine fungi appear to be a promising source of these interesting dipeptides. Several members of the 2,5-DKP class displayed cytotoxic, anti-inflammatory, and antimicrobial activities [9,10,11,12].

Our growing interest in identifying secondary metabolites from marine microbes resulted in the identification of several compounds with different bioactivities [13,14,15,16,17]. The organic extract of the fungus Penicillium sp. gave two new compounds, named n class="Chemical">penicillatides A and B (1 and 2), together with cyclo(d-Pro–l-Phe) {cyclo(R-Pro–S-Phe)} (3) [18] and cyclo(R-Pro–R-Phe) (4) [19] (Figure 1). Structural determinations of the compounds were supported by interpretation of their spectroscopic data as well as comparison of available NMR data in the literature. In this paper, the structural determinations and the cytotoxic and antimicrobial activities of the compounds are reported.

Figure 1

Chemical structures of compounds 1–4.

2. Results and Discussion

2.1. Structure Elucidation of Compounds

The high-resolution electrospray ionization mass spectrometry (HRESIMS) and NMR spectra (Figures S1–S4) of compound 1 (Figure 1) support the molecular formula of C11H18N2O3. The n class="Chemical">13C-NMR (Figure S2) spectrum of 1 (Figure S2) displayed signals for 11 carbons, including two methyls, four methylenes, two aliphatic methines, one aldehydic methine, and two quaternary amidic carbonyls (Table 1). Tracing of the 1H–1H couplings in the COSY spectrum (Figure S3) allowed the assignment of two structural subunits in 1: N-formylleucine (subunit A) and 2-oxopyrrolidine (subunit B) moieties (Figure 1 and Table 1). The first 1H–1H COSY coupling system led to the assignment of the N-formyl-leucine moiety as established from the multiplicity-edited HSQC spectral data (Figure S4) at δH/C 6.10 (NH), 173.7 (qC, C-1), 5.81/49.9 (CH, H-2/C-2), 1.62, 1.42/41.5 (CH2, H2–3/C-3), 1.74/25.0 (CH, H-4/C-4), 1.05/21.0 (CH3, H3–5/C-5), 0.92/23.5 (CH3, H3-6/C-6), and 8.21/160.6 (CH, H-11/C-11) (Table 1). The 1H/13C chemical shift at δH/C 8.21/160.6 is typical for an N-formyl moiety and in agreement with reported values [20]. The placement of the N-formyl moiety was supported by HMBC of H-2/C-11, H-11/C-2 as well as NOESY correlations of NH/H-2 and NH/H-11 (Figure 2). Further HMBC correlations (Figure S5) within the leucine moiety are shown in Table 1 and Figure 2. The second coupling system allowed the assignment of the 2-oxopyrrolidine subunit based on the continuous 1H–1H COSY coupling system of H2-8/H2-9/H2-10 and the 1H/13C NMR signals at δH/C 174.8 (qC, C-7), 2.64, 2.61/33.4 (CH2, H2-8/C-8), 2.09/17.3 (CH2, H2-9/C-9), and 3.88, 3.77/45.6 (CH2, H2-10/C-10). The HMBC correlations of H2-8/C-7, H2-9/C-7, and H2-10/C-7 supported the assignment of subunit B (Figure 2). Finally, the connection between the two subunits of 1 at C-1 and the amidic nitrogen of the 2-oxopyrrolidine moiety was secured from the HMBC correlation from H2-10 to C-1 (Figure 2), supporting the assignment of 1 as N-(N-formylleucyl)-2-oxopyrrolidine.

Table 1

NMR data of compound 1 (CDCl3, 850 and 213 MHz).

No.	δC (mult.)	δH (mult., J (Hz))	HMBC	NOESY
1	173.7, qC		H-2, H2-10
2	49.9, CH	5.81 (dt, 11.5, 3.0)	H-11	NH
3	41.5, CH2	1.62 (m), 1.42 (m)	H-2, H3-5, H3-6
4	25.0, CH	1.74 (m)	H3-5, H3-6
5	21.0, CH3	1.05 (d, 6.5)	H3-6
6	23.5, CH3	0.92 (d, 6.5)	H3-5
7	174.8, qC		H2-8, H2-9, H2-10
8	33.4, CH2	2.64 (dd, 9.5, 1.5)2.61 (dd, 9.5, 7.0)	H2-9, H2-10
9	17.3, CH2	2.09 (m)	H2-7, H2-8
10	45.6, CH2	3.83 (m), 3.77 (m)	H2-8, H2-9
11	160.6, CH	8.21 (s)	H-2	NH
NH		6.10 (brs)		H-2, H-11

Figure 2

Key COSY and HMBC correlations of 1 and 2.

The absolute configuration of C-2 of the leucine residue was determined by Marfey’s method (Scheme 1) [21]. HPLC analysis of the derivative of n class="Chemical">1-fluoro-2,4-dinitrophenyl-5-l-alanine amide (FDAA, Marfey’s reagent) with the hydrolytic product of 1 gave the same retention time as the derivative prepared from an authentic l-leucine, and therefore the l-configuration was assigned to the leucine residue. Thus, compound 1 was assigned as (S)-N-(4-methyl-1-oxo-1-(2-oxopyrrolidin-1-yl)pentan-2-yl)formamide. The name penicillatide A was given to 1, and it is reported here as a new natural compound.

Scheme 1

Reaction of 1-fluoro-2,4-dinitrophenyl-5-l-alanine amide (FDAA) with the hydrolytic product of compound 1 (l-leucine).

Compound 2 (Figure 1) exhibited a molecular formula of C14H16N2O3 as established by HRESIMS. The n class="Chemical">1H/13C NMR signals (Figures S6 and S7, Table 2) at δH/C 6.13 (1H, brs, NH-1), 166.9 (qC, C-2), 2.85/59.6 (CH, H-3/C-3), and 166.1 (qC, C-5) suggested a diketopiperazine moiety as part of a cyclic dipeptide skeleton. The NMR data of compound 2 (Table 2) are very close to those of 3. However, compound 2 displayed a signal for an oxygenated quaternary carbon at δC 83.4 and 1H singlet at δH 4.36 (1H, OH) instead of the methine of H-6/C-6 at δH/C 4.20/59.1 in 3, suggesting the presence of a hydroxyl moiety at C-6 in 2. The placement of the OH at C-6 was supported by HMBC correlations of H2-10/C-6, H2-10/C-5, and OH/C-5 (Figure 2 and Table 2). Furthermore, the COSY (Figure S8), HSQC (Figure S9) and HMBC experiments (Figure S10) supported the assignment of the structure of 2 as cyclo(Pro–2-OH–Phe) (Table 2 and Figure 2). The absolute configuration of C-3 of the proline residue was determined by Marfey’s method [21]. HPLC analysis of the FDAA derivative of the hydrolytic product of 2 gave the same retention time as the derivative prepared from an authentic (l)-proline, and therefore the l-configuration was assigned to the proline residue (Scheme 2). The absolute configuration at C-6 of the phenylalanine residue was not determined by Marfey’s method, because the hydroxyphenylalanine residue decomposed under acidic conditions. The relative configuration at C-6 was established by comparing the chemical shift values of C-6 and H2-10/C-10 with a similar compound containing the α-hydroxylated phenylalanine moiety, namely (3R,6S)-3-benzyl-3-hydroxy-1,4-dimethyl-6-((4-nitro-1H-indol-3-yl)methyl)piperazine-2,5-dione [22]. The δH/C of 3.14, 3.05/47.8 (H2-10/C-10), and 83.4 (C-6) in 2 were very close to the values in the literature [22], supporting the configuration of OH at C-6, as shown in Figure 1. Furthermore, the configuration of the OH at C-6 in 2 was also confirmed by the NOESY experiment, in which a strong correlation between H-3 (δH 2.85) and 6-OH (δH 4.36) was observed (Figure 3). Further studies are needed to determine the absolute configuration at C-6 in 2. Thus, the relative configuration at C-6 was assigned as R*. Accordingly, compound 2 was assigned as (3R*,8aS)-3-benzyl-3-hydroxyhexahydropyrrolo[1,2-a]pyrazine-1,4-dione. The name penicillatide B was given to compound 2, and it is reported here as a new natural product.

Table 2

NMR data of compound 2 (CDCl3, 600 and 150 MHz).

No.	δC (mult.)	δH (mult., J (Hz))	HMBC
1 (NH)		6.13 (brs)
2	166.9, qC		H-1, H-3, H2-9
3	59.6, CH	2.85 (dd, 10.2, 6.8)	H-1, H2-8, H2-9
5	166.1, qC		H-1, H2-7, H2-10
6	83.4, qC		H2-10
7	45.5, CH2	3.63 (m)3.41 (ddd, 12.8, 8.5, 2.5)	H-3, H2-9
8	22.1, CH2	1.98 (m), 1.71 (m)	H2-7
9	28.7, CH2	2.17 (m), 1.83 (m)	H-3, H2-8
10	47.8, CH2	3.14 (d, 13.6)3.05 (d, 13.6)	H-12/H-16
11	133.1, qC		H2-10, H-12/H-16, H-13/H-15
12	130.6, CH	7.29 (m)	H-14
13	129.4, CH	7.40 (m)	H-14
14	128.1, CH	7.30 (m)	H-12/H-16, H-13/H-15
15	129.4, CH	7.40 (m)	H-14
16	130.6, CH	7.29 (m)	H-14
OH		4.36 (brs)

Scheme 2

Reaction of FDAA with the hydrolytic product of compound 2 (l-proline).

Figure 3

MM2 energy-minimized drawing of 2 showing an important NOE correlation.

Compounds 3 and 4 were assigned as cyclo(d-Pro–l-Phe) {n class="Chemical">cyclo(R-Pro–S-Phe)} (3) [18] and cyclo(R-Pro–R-Phe) (4) by interpretation of their NMR (Figures S11–S20) and HRMS data.

2.2. Biological Activities of Compounds

Compounds 2–4 were evaluated for their cytotoxic and antiproliferative activities against n class="Disease">colorectal carcinoma (HCT 116), hepatocellular carcinoma (HepG2), and breast cancer (MCF-7) using a sulforhodamine assay, as previously described [23]. Compounds 2 and 3 showed significant activity against HCT-116, with IC50 of 23.0 and 38.9 µM, while compound 4 was weakly active against this cell line. Compounds 3 and 4 were weakly active against MCF-7, with IC50 of 102 and 104 µM, respectively. Finally, none of the compounds showed activity against HepG2 (≥50 µM).

In addition, 2–4 were evaluated for their antimicrobial activity against several microbes: S. aureus, n class="Species">Vibrio anguillarum, and C. albicans. Compounds 2–4 showed significant activity against V. anguillarum, with inhibition zones of 20, 24, and 25 mm, respectively. Similarly, compounds 2–4 showed moderate activity against both S. aureus and C. albicans, with inhibition zones between 10 and 19 mm (Table 3).

Table 3

Cytotoxic and antimicrobial activities of compounds 2–4.

Compound	IC50 (µM)			Inhibition Zone (mm)@100 µg/disc
	HCT-116	HepG2	MCF-7	S. aureus	V. anguillarum	C. albicans
2	23.0	≥50	≥50	19	20	10
3	38.9	≥50	102.0	14	24	11
4	94.0	≥50	114.0	16	25	15
Doxorubicin a	0.789	0.621	0.415
Ciprofloxacin b				22	26
Ketoconazole c						30

a Positive cytotoxic control; b positive antibacterial control (5 μg/disc); c positive antifungal control (50 μg/disc).

The results in Table 3 clearly show that compounds 2–4 were selective against HCT-116 without any activity against HepG2. In comparison to 3 and 4, the n class="Chemical">hydroxylation of C-6 (in 2) potentiated the cytotoxic activity against HCT-116. In the antimicrobial screen, 2–4 were almost identically active against S. aureus and C. albicans, suggesting no effect for the OH at C-6. In addition, 2 and 3 were more active than 2 against V. anguillarum and showed similar activity to the positive control ciprofloxacin.

3. Materials and Methods

3.1. General Experimental Procedures

One- and two-dimensional NMR spectra (chemical shifts in ppm, coupling constants in Hz) were recorded on Bruker Avance DRX 600 MHz (Bruker, Rheinstetten, Germany) and Bruker Ascend™ 850 (850 MHz) (Bruker BioSpin, Billerica, MA, USA) spectrometers using n class="Chemical">CDCl3 as solvent. NMR spectra were referenced to the residual protonated solvent signals (CHCl3: 7.26 ppm for 1H and 77.0 ppm). Positive ion HRESIMS data were obtained with a Micromass Q-ToF equipped with leucine enkephalin lockspray, using m/z 556.2771 (M + H)+ as a reference mass. For column chromatography, silica gel (Merck, 70–230 mesh ASTM, Sigma-Aldrich, Darmstadt, Germany) and Sephadex LH-20 (0.25–0.1 mm, Pharmacia, Piscataway, NJ, USA) were used. Precoated silica gel 60 F-254 plates (Merck) were used for TLC. HPLC purifications were performed on a semipreparative HPLC column (RP18, 5 μm, ARII Cosmosil, 250 × 10 mm, Waters, Nacalai, Inc., San Diego, CA, USA).

3.2. Biological Materials

The marine-derived fungus Penicillium sp. was isolated from the Red Sea tunicate n class="Species">Didemnum sp., and the fungus was identified as previously described [13].

3.3. Culture Condition and Extraction

Large-scale culture of the fungus Penicillium sp. was carried out in 20 flasks (each 2 L). Each flask contained 500 mL of n class="Chemical">Sabouraud Dextrose (HiMedia Laboratories, Vadhani Ind. Est., LBS Marg, Mumbai, India) Broth (SDB) liquid medium. The prepared liquid cultures were shaken on an orbital shaker at 28 °C continuously for 14 days. After 2 weeks of shaking and incubation, the cultures were filtered using clean gauze to separate the formed fungal mycelia from the broth. The culture broth from each flask was extracted with EtOAc (3 × 300 mL). The mycelia formed during the shaking were lyophilized and extracted with MeOH. The ethyl acetate and methanolic extracts were combined and evaporated under vacuum, and the resulting extracts were used for fractionation and purification of the compounds.

3.4. Isolation and Purification of Compounds

The combined extracts of the broth and mycelia (0.76 g) were flash chromatographed on reverse-phase SiO2 using n class="Chemical">H2O-MeOH gradients, giving 6 subfractions (A–F). Fraction B (120 mg), eluted with 25% MeOH in H2O, was fractionated on Sephadex LH-20 column using MeOH as eluent, giving 6 main subfractions (B1–B6). Fraction B3 (56 mg) was purified on C18 HPLC column using 50% CH3CN to give compounds 3 (5.5 mg) and 4 (3.5 mg). Similarly, subfraction B4 (30 mg) was purified on C18 HPLC column using 45% CH3CN to give compounds 1 (2.7 mg) and 2 (2.3 mg).

3.5. Determination of Configuration of the Amino Acids in and

About 0.5 mg each of compounds 1 and 2 was heated separately in 1 mL of 6 N HCl at 100 °C for 16 h, followed by removal of the excess n class="Chemical">HCl under vacuum. To each dry hydrolysate, 200 µL of 1% solution of FDAA [21] in acetone and 40 µL of 1.0 M NaHCO3 were added. The reaction mixture was heated at 45 °C for 1.5 h, cooled, and acidified with 20 µL of 2.0 M HCl. Similarly, standard amino acids (d and l) of leucine and proline were derivatized separately. The derivatized standard amino acids and hydrolysates of 1 and 2 were subjected to HPLC on Nova-Pak C18 reverse-phase column (150 × 3.9 mm i.d., 4 mm particle size; Waters, Milford, MA, USA) using the following gradient program. Solvent A was a 50 mM triethylamine–phosphate buffer (pH 3.5) containing 25% (v/v) MeOH, and solvent B was the same buffer containing 70% MeOH. The mobile phase was a linear gradient from 0 to 100% B (100 to 0% A) in 40 min, at a flow rate of 0.65 mL/min at 25 °C. The eluted peaks were monitored at 340 nm. The retention times for FDAA derivatives of standards and compounds 1 and 2 were as follows: (l)-leucine (tR 27.2 min), (d)-leucine (tR 36.0 min), (l)-proline (tR 15.4 min), (d)-proline (tR 19.1 min), compound 1 (tR 27.2 min), and compound 2 (tR 15.4 min).

Penicillatide A (1): White amorphous powder; (α)D = −22° (c 0.05, n class="Chemical">MeOH); NMR data (Table 1); HRESIMS m/z 227.1395 (calcd for C11H19N2O3, (M + H)+, 227.1396).

Penicillatide B (2): White amorphous powder; (α)D = 85° (c 0.08, n class="Chemical">MeOH); NMR data (Table 2); HRESIMS m/z 261.1240 (calcd for C14H17N2O3, (M + H)+, 261.1239).

3.6. Biological Activities of the Compounds

3.6.1. Evaluation of the Cytotoxic Activities of the Compounds

The cytotoxicity of compounds 2–4 against 3 n class="Disease">tumorous cell lines—colorectal carcinoma, breast cancer, and hepatocellular carcinoma—were evaluated using sulforhodamine assay [23]. Briefly, before adding the compounds, the cells were grown in 96-well plates for 24 h. After adding the compounds, incubation of the cells was carried out for another 48 h. The IC50 values of the compounds were obtained from the log dose–response curve. The reported IC50 values were obtained from the means of 3 experiments.

3.6.2. Antibacterial Evaluation of the Compounds

A disc diffusion assay was used to determine the antimicrobial activity of the compounds [24] with replication (n = 3). Staphylococcus aureus, n class="Species">Vibrio anguillarum, and Candida albicans served as target models for bacteria and fungi. A total of 100 μg of each compound was loaded onto 6-mm sterile circular filter-paper discs. The paper discs were left to air-dry. The dried paper discs were placed onto nutrient agar plates that had already been inoculated with a lawn of target microorganisms. After 24 h of incubation, the antimicrobial activity of the compounds was calculated.

4. Conclusions

Investigation of the marine-derived fungus Penicillium sp. gave two new compounds, n class="Chemical">penicillatides A and B (1 and 2), together with the known compounds cyclo(R-Pro–S-Phe) (3) and cyclo(R-Pro–R-Phe) (4). The structures of 1–4 were assigned by interpretation of their spectroscopic data by NMR and high-resolution mass spectroscopy (HRMS). Compounds 2 and 3 displayed significant and selective activity against HCT-116, with IC50 of 6.0 and 9.57 µg/mL, respectively, while they were inactive against HepG2 and MCF-7. These results suggest a selective effect of 2 and 3 against HCT-116. Also, 2–4 showed potent antimicrobial activity against V. anguillarum, with inhibition zones of 20, 24, and 25 mm, respectively. On the other hand, 2–4 were moderately active against S. aureus and C. albicans.