New Spiral γ-Lactone Enantiomers from the Plant Endophytic Fungus Pestalotiopsis foedan

(−)-(4S, 8S)-Foedanolide (1a) and (+)-(4R, 8R)-foedanolide (1b), a pair of new spiro-γ-lactone enantiomers, were isolated from the fermentation broth of the plant endophytic fungus Pestalotiopsis foedan by HPLC using a chiral column, achieving over 7% ee. Their structures and absolute configurations were determined on the basis of extensive analysis of NMR spectra combined with computational methods via calculation of the electronic circular dichroism (ECD) and optical rotation (OR). Compounds 1a and 1b showed moderate activities against HeLa, A-549, U-251, HepG2 and MCF-7 tumor cell lines.


Introduction
Endophytic fungi, as one of the most promising resource for natural product discovery, live inside the normal tissues of host plants without causing apparent disease symptoms [1].The study of natural products from plants and their endophytes has shown that endophytes have been found to produce a significant number of interesting novel and bioactive metabolites [2].For example, Taxomyces andreanae, the first report endophytic fungus colonizing the inner bark of Pacific yew Taxus brevifolia, is capable of producing taxol and its analogue baccatin III when grown in semi-synthetic medium [3].One of the most commonly found endophytes is Pestalotiopsis genus [4].Since discovery of the anticancer agent taxol from an endophytic fungal strain Pestalotiopsis microspora [5], interest in searching for bioactive compounds from this fungal genus has increased considerably.Previous chemical studies of some species of this genus have afforded a variety of bioactive metabolites [2,[6][7][8][9].

OPEN ACCESS
During our continuing research for naturally occurring bioactive secondary metabolites from this genus, the present study was undertaken to investigate the chemical constituents of Pestalotiopsis foedan isolated from the branch of Bruguiera sexangula, and have led to the isolation of a pair of new spiro-γ-lactone enantiomers 1a and 1b (Figure 1).Details of the isolation, structure elucidation and cytotoxic evaluation of 1a and 1b are reported herein.

Results and Discussion
Compound 1 was obtained as a white powder.Its molecular formula was determined to be C 14 H 20 O 3 by high-resolution atmospheric pressure chemical ionization mass spectrometry (HR-APCI-MS) ([M+H] + , found 237.1501, calc.237.1485), corresponding to five degrees of unsaturation.The IR spectral data of 1 showed the presence of one α,β-unsaturated ketone group (1780 cm −1 ) and one ester carbonyl group (1712 cm −1 ).Analysis of the 1 H-and 13 C-NMR spectral data (Table 1) revealed that 1 contained one α,β-unsaturated ketone carbonyl group, one ester carbonyl group, two olefinic quaternary carbons, three methyl groups, five methylene groups, one methine group, and one oxygenated sp 3 quaternary carbon.The connectivity of the protons and carbons was established by the HSQC data.Two olefinic quaternary carbons could be assigned to one olefin, together with the two carbonyls accounted for three of the five required degrees of unsaturation.The remaining two degrees of unsaturation had to be accounted for two rings.Further interpretation of NOESYspectrum revealed that no NOE interactions were observed between H-3 and H-8, H-9.Thus, compound 1 may be either a cis or trans structure.
The recorded optical rotation (OR) for 1 was −8 (c = 0.25, MeOH), and the observed CD spectrum has a negative Cotton effect at 221 nm with a  value of 2.0.This is unexpected for a spiro compound due to its quite small optical rotation value, and we predicted that 1 might be isolated as a partially racemic mixture with low ee.Thus, compound 1 was finally separated by preparative HPLC on a Chiralcel OB-H phase to yield (−)-(4S,8S)-foedanolide (1a) and (+)-(4R,8R)-foedanolide (1b), revealing an ee of 7% for the unresolved mixture based on the integration value of HPLC peak areas.The major enantiomer 1a has a OR value of −101.0 (c = 0.11, MeOH), and its CD spectrum has a  value of 21.5 at 221 nm.
Combing with the experimental OR value, the absolute configuration of the major enantiomer 1a was finally determined to be 4S,8S.Compounds 1a and 1b were tested for their cytotoxicity against a small panel of human tumor cell lines including HeLa, A-549, U-251, HepG2 and MCF-7 (Table 2).Both exhibited inhibitory activities against HeLa, HepG2 and MCF-7, and the cytotoxic activities of compound 1b were all higher than compound 1a.Importantly, compound 1b showed significant activity against HeLa tumor cell line with IC 50 value of 5.4 µg mL −1 .Compound 1b also exhibited inhibitory activities against A-549 and U-251 tumor cell lines with IC 50 value of 67.9 and 53.0 µg mL −1 , whereas compound 1a was inactive against A-549 and U-251 cell lines at the same concentrations (IC 50 < 100 µg/mL).It suggested that the stereochemistry of enantiomers could affect their cytotoxicity.Actually, this phenomenon was already reported for other enantiomers.For example, a popular herbicide, metolachlor, its (S)-metolachlor exhibited highly effective toward grasses, while (R)-enantiomer is inactive [16].

Fungal Material and Cultivation Conditions
Pestalotiopsis foedan was isolated from the branches of Bruguiera sexangula in Hainan, China, in April, 2008, identified by Prof. Jing-Ze Zhang, and assigned the accession number L444.The fungal strain was cultured on slants of potato dextrose agar (PDA) at 28 °C for 7 days, and then inoculated into 500 mL Erlenmeyer flask containing 100 mL of PDB (20.0 g of glucose, 200.0 g of potato (peeled), 3.0 g of KH 2 PO 4 , 1.5 g of MgSO 4 , 0.1 g of citric acid, and 10.0 mg of thiamin hydrochloride, in 1 liter of deionized H 2 O).The final pH of the media was adjusted to 6.5 before sterilization.After 7 days of incubation at 28 °C on rotary shakers at 150 rpm, 25 mL of culture liquid were transferred as seed into each 1,000 mL Erlenmeyer flask containing 250 mL of PDB and fermentation was carried out on a shaker for 30 days.

Extraction and Isolation
The culture broth (40 L) was extracted three times with ethyl acetate (40 L/each time, 12 h).Evaporation of the solvent in vacuo gave a brown oily residue (40.0 g), which was subjected to column chromatography (silica gel) with gradient elution systems of petroleum ether/acetone (from 100:0 to 0:100).The fraction (6.9 g) eluted with 80% petroleum ether was further purified by repeated CC (petroleum ether/acetone, 40:1) and Sephadex LH-20 chromatography (acetone) to afford compound 1 (4.0 mg).Compound 1 was dectected as one spot on TLC by heating silica gel plates sprayed with 10% H 2 SO 4 in ethanol, and which also exhibited one peak monitored by HPLC.The recorded optical rotation (OR) for 1 was −8 (c 0.25 MeOH), the observed CD had a negative Cotton effect at 221 nm with only a  values of 2.0.This is unexpected for a spiral compound.It is doubt that another enantiomer mixed inside.Thus, compound 1 was further isolated by HPLC on a chiralrel OB-H phase (80% n-hexane in 20% isopropanol over 30 min, 1 mL/min, 225 nm, 25 °C), which led to the isolation of (−)-(4S,8S)-foedanolide (1a) (1.7 mg, t R = 13.5 min) and (+)-(4R,8R)-foedanolide (1b) (1.5

Cytotoxicity Assay
Cytotoxicity activity was evaluated against HeLa, A-549, U-251, HepG2 and MCF-7 cells by the MTT method [17].All cell lines were grown in RPMI-1640 medium (GIBCO) supplemented with 10% heat-inactivated bovine serum, 2 nM L-glutamine, 10 5 IU/L penicillin, 100 mg/L streptomycin and 10 mM HEPES, pH 7.4.Cells were kept at 37 °C in a humidified 5% CO 2 incubator.An aliquot (180 μL) of these cell suspensions at a density of 1,500 cell mL −1 was pipetted into 96-well microtiter plates.Subsequently, 180 μL of sample (in DMSO) at different concentrations was added to each well and incubated for 72 h at the above conditions in a CO 2 -incubator.MTT solution (20 µL of 5 mg/L in RPMI-1640 medium) was added to each well and further incubated for 4 h at 37 °C.After addition of 100 µL DMSO and incubation for 1h, the cells were lysed to liberate the formed formazan crystals.The optical density (OD) was read on a Multiscan plate reader at a wavelength of 570 nm.DMSO control well, in which sample was absent, was included in the experiment in order to eliminate the influence of DMSO.The inhibitory rate of cell proliferation was calculated by the following formula: Growth inhibition (%) = [OD control − OD treated /OD control ] × 100% (1) The cytotoxicity of samples on tumor cells was expressed as IC 50 values and calculated by LOGIT method.

Conclusions
A pair of new spiro-γ-lactone enantiomers was isolated from the fermentation broth of the plant endophytic fungus Pestalotiopsis foedan by HPLC using a chiral column.Their absolute configurations were mainly determined by computational methods via calculation of the electronic circular dichroism (ECD) and optical rotation (OR).Preliminary biological assay of 1a and 1b showed that both compounds exhibited moderate activities against HeLa, A-549, U-251, HepG2 and MCF-7 tumor cell lines.

1 H-
COSY spectrum (Figure2).It allowed establishment of two H-atom systems, one is C-2 through C-3, and the other is C-8 through C-9, C-10, C-11 to C-12.HMBC correlations (Figure2) of H-8 with C-4, C-7 and C-9, H-9 with C-4, C-7 and C-8, H-12 with C-10 and C-11, H 3 -13 with C-4, C-5 and C-6, and of H 3 -14 with C-5, C-6 and C-7, indicated that 1 contains the cyclopentenolone moiety with the n-butyl chain attached to C-8 position.Finally, fragment a was established (Figure1).The γ-lactone moiety (fragment b) was established by analysis of the remaining HMBC (Figure2) correlations of H-2 with C-1, C-3 and C-4, and of H-3 with C-1, C-2 and C-4, combined with the only remaining one degree of unsaturation which had to be accounted for one ring.In light of the evidences mentioned above, the planar structure of 1 was established (Figure1).