Next Article in Journal
Allylation of Functionalized Aldehydes by Potassium Allyltrifluoroborate Catalyzed by 18-Crown-6 in Aqueous Media
Previous Article in Journal
Fluorescent Probes and Fluorescence (Microscopy) Techniques — Illuminating Biological and Biomedical Research
Article Menu

Export Article

Molecules 2012, 17(12), 14091-14098; doi:10.3390/molecules171214091

Isolation, Identification and Antimicrobial Activities of Two Secondary Metabolites of Talaromyces verruculosus
Fang Miao 1, Rui Yang 2, Dong-Dong Chen 2, Ying Wang 1, Bao-Fu Qin 1, Xin-Juan Yang 1,2,* and Le Zhou 2,*
College of Life Science, Northwest A&F University, Yangling, Shaanxi 712100, China
College of Science, Northwest A&F University, Yangling, Shaanxi 712100, China
Authors to whom correspondence should be addressed; Email: Tel./Fax: +86-29-8709-2226.
Received: 16 October 2012; in revised form: 21 November 2012 / Accepted: 23 November 2012 / Published: 28 November 2012


: From the ethyl acetate extract of the culture broth of Talaromyces verruculosus, a rhizosphere fungus of Stellera chamaejasme L., (−)-8-hydroxy-3-(4-hydroxypentyl)-3,4-dihydroisocoumarin (1) and (E)-3-(2,5-dioxo-3-(propan-2-ylidene)pyrrolidin-1-yl)acrylic acid (2) were isolated and evaluated for their antimicrobial activities. Their structures were elucidated by UV, IR, MS, 1H-NMR, 13C-NMR and 2D NMR spectra. Compound 1 exhibited the significant activities in vitro against two strains of bacteria and four strains of fungi. Compound 2 gave slight activities on the fungi at 100 µg mL−1, but no activities on the bacteria. Compound 1 should be considered as a new lead or model compound to develop new isocoumarin antimicrobial agents.
antimicrobial activity; isocoumarin; Talaromyces verruculosus; rhizosphere microorganism; Stellera chamaejasme L.

1. Introduction

The term rhizosphere microorganism refers to a bacterial or a fungal microorganism that colonizes the region of the soil immediately adjacent (within 1 mm) to plant roots [1]. Rhizosphere microorganisms are different from those living in the nonrhizosphere surrounding soil, both in gross numbers of cells and the variety of strains. The rhizosphere microbial communities influence growth, resistance to disease or even death of the plant host depending on the degree of parasitism and pathogenicity [1,2]. The rhizosphere communities of plant species differ from each other [3,4]. The diversity of microbial strains in the rhizosphere is influenced by different plant species [5,6] and environmental factors affecting plant growth [7]. Recently, rhizosphere microorganisms have been recognized as an important source of a variety of structurally novel active secondary metabolites. As a representative example, Gunatilaka et al. have isolated 18 new natural products and 23 known compounds from nine strains of Sonoran desert plant-associated rhizosphere fungi [8,9,10,11,12,13,14,15]. However, compared with those of endophytes, the secondary metabolites of rhizosphere microorganisms had not received much attention.

Stellera chamaejasme L. (Thymelaeceae) is a perennial herb and widely distributed in North China. Its roots have been used in Chinese traditional herb medicine as an external medicament. Our previous study resulted in the isolation of a fungal strain from the rhizosphere soil of Stellera chamaejasme L. identified as Penicillium verruculosum YL-52, which was revised as Talaromyces verruculosus by Samson et al. in 2011 [16]. Meanwhile, the ethyl acetate extract of the culture broth of the fungus exhibited obvious antifungal activities against 11 strains of plant pathogens and antibacterial activities against four bacterial strains [17]. The aim of the present study was to determine the chemical constituents of the ethyl acetate extract and its active compounds. Herein, we reported the isolation and identification of two compounds from the ethyl acetate extract and their antimicrobial activities.

2. Results and Discussion

2.1. Isolation and Structural Identification

Repeated silica gel column chromatography of the ethyl acetate extract of the culture broth of the fungus YL-52, followed by purification of Sephadex LH-20 column chromatography, revealed two compounds 1 and 2 (Figure 1).

Figure 1. The structures of compounds 1 and 2.
Figure 1. The structures of compounds 1 and 2.
Molecules 17 14091 g001 1024

Compound 1, isolated as white needle crystals, showed a quasi-molecular ion peak at m/z 251.1279 [M+H]+ in HRMS corresponding to the molecular formula C14H18O4. The molecular formula indicated six degrees of unsaturation within the molecule. IR spectrum revealed the presence of OH groups (3419, 1239, 1120 cm−1), C=O group (1657 cm−1) and benzene ring (3080, 1617, 1584 cm−1). UV absorption maxima at λmax 246 nm (logε 3.75) and 314 nm (logε 3.56) disclosed the presence of a conjugated system. The 1H-NMR displayed the presence of three aromatic hydrogen atoms (δH 7.44, 6.92, 6.72). Based on the multiplicity and coupling constant of each peak, the three hydrogen atoms above were considered as a system of three vicinal aromatic protons. In addition, the 1H-NMR spectrum showed the presence of one methyl group (δH 1.25, d), two oxygenated methenyl groups (δH4.59–4.65, 3.88) and one phenolic hydroxyl group (δH 11.04). In the 13C-NMR spectrum, fourteen carbon atom signals were observed. The DEPT spectrum showed one signal for one carbonyl carbon atom, six signals for sp2-hybridized carbon atoms (3 × C and 3 × CH), and seven signals for sp3-hybridized carbon atoms (1 × CH3, 2 × OCH and 4 × CH2). The signals at δC 162.0 suggested the presence of one oxygenated aromatic carbon atom.

The UV and IR data were good agreement with those published for 3-(2-hydroxypropyl)-8-hydroxy-3,4-dihydroisocoumarin isolated from the Chinese mangrove associate Catunaregam spinosa [18], suggesting that compound 1 contained an 8-hydroxy-3,4-dihydroisocoumarin moiety. The 13C-NMR spectrum was very similar to that of 3-(2-hydroxypropyl)-8-hydroxy-3,4-dihydroisocoumarin, except for the presence of two additional methylenes. Moreover, the location of the hydroxyl group at C-14 was determined by the HMBC correlations between H-15 (δH 1.25) and C-14 (δC 67.8) and between the proton of 14-OH and C-14, as well as the coupling relationship between H-15 (δH 1.25) and H-14 (δC 3.88) in 1H-NMR spectrum. The assignment of all proton signals in 1H-NMR spectrum was carried out by HSQC and HMBC correlations. Based on the facts above, 1 was established as 3-(4-hydroxypentyl)-8-hydroxy-3,4-dihydroisocoumarin. The optical rotation ([α]D25 −40.4 (c 0.19, acetone)) showed that 1 was an optically pure chiral compound, but the configurations at C-3 and C-14 remained unsolved because the crystal of 1 was too fragile for an X-ray crystallographic determination. A similar case was observed for 3-(2-hydroxypropyl)-8-hydroxy-3,4-dihydro-isocoumarin [17].

Compound 2 was obtained as a white powder, and established as (E)-3-(2,5-dioxo-3-(propan-2-ylidene)pyrrolidin-1-yl) acrylic acid by X-ray crystallographic analysis in our previous study [18]. Herein, we further reported its other previously unpublished spectroscopic data. Compound 2 possessed a molecular formula of C10H11NO4, as deduced from its quasi-molecular ion peak at m/z 210.0762 [M+H]+ in HR-ESI-MS. The molecular formula indicated six degrees of unsaturation. The IR spectrum revealed the presence of an OH group (3431, 1234 cm−1), C=O groups (1714, 1628 cm−1) and CH3 groups (2924, 1359 cm−1); The UV disclosed absorption maxima at λmax 262 nm (logε 4.01), due to the presence of a conjugated system; The 1H-NMR spectrum exhibited the presence of two methyl groups at δH 2.35 (3H, s) and 1.93 (3H, s), two olefinic protons at δ 7.78 (1H, d) and 6.91 (1H, d), and one methylene group at δH 3.35 (2H, s). The above findings were further supported by the DEPT spectrum. The 13C-NMR spectrum displayed 10 signals, of which five were assigned to quaternary carbon atoms by DEPT. Based on the large coupling constant of the signals at δH7.78 (1H, d, J = 14.8) and 6.91 (1H, d, J = 14.8), a trans configuration was established for the ∆6-double bond. In the HMBC spectrum, the correlations between H-6 and C-2, C-5, C-8 suggested that the CH=CHCO2H group was attached to a nitrogen atom, and the correlations between H-10 and C-3, C-9, C-11 and between H-11 and C-3, C-9, C-10 suggested the occurrence of one propan-2-ylidene moiety at the C-3 position. From the foregoing, it was concluded that compound 2 was (E)-3-(2,5-dioxo-3-(propan-2-ylidene)pyrrolidin-1-yl) acrylic acid, in agreement with its X-ray crystallographic analysis result [19].

2.2. Bioactivity

The antimicrobial activities of 1 and 2 were determined against pathogenic bacteria and fungi as listed in Table 1. The results showed that 1 had obvious antibacterial activities against Staphylococcus aureus and Escherichia coli, with minimum inhibitory concentration (MIC) values of 2.5 µg mL−1 and 5.0 µg mL−1, respectively, but 1 was less active than the standard drug ceftriaxone sodium (a broad-spectrum antibiotic) with an MIC value of 0.625 µg mL−1. For plant pathogenic fungi, 1 disclosed significant growth inhibitions of 92.6 ± 2.1%, 97.3 ± 3.3%, 87.2 ± 2.8% and 94.9 ± 1.9% at 50 µg mL−1 against Alternaria solani, Valsa mali, Curvularia lunata and Botryosphaeria berengeriana, respectively. Under the same conditions, the growth inhibitions of thiabendazole, a broad-spectrum antifungal drug, were 54.7 ± 2.6%, 100 ± 0.0%, 51.5 ± 4.1, compound 2 was inactive for both the tested bacteria and fungi, although it showed slight antifung% and 92.8 ± 3.7%. Obviously, 1 had higher activities than thiabendazole against phytopathogenic fungi. Under the same conditions al activities at a concentration of 100 µg mL−1.

Table 1. In vitro antimicrobial activities of 1 and 2 (50 µg mL−1).
Table 1. In vitro antimicrobial activities of 1 and 2 (50 µg mL−1).
CompoundGrowth inhibition (%, mean ± SD)MIC (µg mL−1)
A. solaniV. maliC. lunataB. berengerianaS. aureusE. coli
192.6 ± 2.197.3 ± 3.387.2 ± 2.894.9 ±
2N a (16.3 ± 5.4) bN (21.3 ± 4.6)N (25.6 ± 5.4)N (19.7 ± 3.8)>100>100
Thiabendazole54.7 ± 2.6100 ± 0.051.5 ± 4.192.8 ± 3.7
Ceftriaxone sodium0.6250.625

a: N: No inhibition of growth was observed at 50 µg mL−1; b: The numbers in parentheses were growth inhibition rates at 100 µg mL−1.

3. Experimental

3.1. General

Optical rotations: Horiba SEPA-300 digital polarimeter. IR spectra: Nexus FT-IR 400 spectrometer; with KBr pellets; in cm−1. UV spectra: SP-2100 UV/VIS spectrometer; λmax (logε) in nm. NMR spectra were recorded on Bruker AV-400 spectrometers with TMS as an internal standard. MS spectra were recorded with a VG Autospec-3000 spectrometer. HR-ESI-MS were recorded with an API QSTAR Pulsar 1 spectrometer; in m/z. Column chromatography was carried out on silica gel (200–300 mesh, Qingdao Marine Chemical Inc., Qingdao, China) and Sephadex LH-20 (Pharmacia, New Jersey, NJ, USA). Fractions were monitored by TLC and spots were visualized by heating silica gel plates sprayed with 10% H2SO4 in ethanol.

3.2. Plant and Fungal Strain Materials

The fungal strain was isolated in the rhizosphere soil of Stellera chamaejasme L. collected in the Qinling Mountains of Taibai town in Shaanxi Province, China, in August 2007 and deposited in the Laboratory of Natural Product Research, Northwest A&F University, Shaanxi Province, China (culture collection number YL-52). The fungus was identified as Penicillium verruculosum YL-52 (the revised name: Talaromyces verruculosus) by the streak plate method, morphological characteristics, sequence analysis of ITS and comparison analysis with GenBankB data [16].

3.3. Fermentation

Cultures of YL-52 maintained on potato-dextrose-agar (PDA) medium slants were subcultured in Petri dishes prior to testing. Two fungal cakes (d = 13 mm) were added to a 250 mL conical flask containing 100 mL potato-dextrose broth (PDB), and cultured for 9 d at 25 °C with a 150 r/min frequency in a rocking bed. A 60 L culture broth was obtained from 600 fermentation flasks.

3.4. Extraction and Isolation

The culture broth (60 L) was extracted with ethyl acetate (50 L × 3). The combined ethyl acetate solution was concentrated under vacuum to yield 12.8 g of crude extract. Ten grams of the extract were subjected to column chromatography over silica gel using CHCl3-CH3OH (stepwise gradient: 100:1, 50:1, 25:1, 10:1, 5:1, 1:1, 0:1, v/v) to furnish the corresponding fractions A-1 (0.8 g), A-2 (3.80 g), A-3 (1.44 g), A-4 (1.21 g), A-5 (0.32 g), A-6 (0.30 g) and A-7 (1.95 g). Fractions A-2 and A-3 were combined and subjected to column chromatography over silica gel using petroleum ether-EtOAc (stepwise gradient: 20:1, 15:1, 10:1, 5:1, 1:1, 0:1; petroleum ether: b.p. 60–90 °C) to obtain corresponding subfractions B-1 (0.57 g), B-2 (0.76 g), B-3 (0.97 g), B-4 (0.86 g), B-5 (0.94 g) and B-6 (0.90 g). Subfractions B-3 and B-4 were combined, and subjected to column chromatography on SiO2 with petroleum ether-acetone (stepwise gradient: 10:1, 8:1, 5:1, 2:1, 1:1, 0:1). The petroleum ether–acetone (5:1) eluate was sequentially subjected to preparative silica gel TLC using petroleum ether–acetone (2:1) and Sephadex LH-20 column chromatography with methanol. Compound 1 (16 mg) was obtained as colorless needle-like crystals (petroleum ether–EtOAc, 1:1). Fractions A-5 and A-6 were combined and repeatedly subjected to column chromatography over silica gel using petroleum ether–acetone mixture (stepwise gradient: 5:1, 2:1, 1:1, 0.5:1). The petroleum ether-acetone (0.5:1) eluate was purified by preparative silica gel TLC (CHCl3–CH3OH, 1:1)and Sephadex LH-20 column chromatography using methanol to provide 2 (14 mg) as a white powder.

3-(4-Hydroxypentyl)-8-hydroxy-3,4-dihydroisocoumarin (1). White needle-like crystals (petroleum ether–ethyl acetate), Rf = 0.35 (petroleum ether–acetone, 2:1), 0.56 (CHCl3–CH3OH, 8:1), m.p. 80–81 °C, [α]D25 −40.4 (c 0.19, acetone); UV (95% EtOH): λmax (logε) = 212 (4.30), 246 (3.75), 314 (3.56) nm; IR (KBr): νmax = 3419, 3080, 2946, 1657, 1617, 1584, 1462, 1239, 1120 cm−1; 13C-NMR (100 MHz, CDCl3) δ ppm: 169.8 (C-1), 162.0 (C-8), 139.3 (C-10), 136.1 (C-6), 117.9 (C-5), 116.1 (C-7), 108.3 (C-9), 79.6 (C-3), 67.8 (C-14), 38.7 (C-13), 34.7 (C-11), 32.8 (C-4), 23.6 (C-15), 21.1 (C-12); 1H-NMR (400 MHz, CDCl3) δ ppm: 11.04 (1H, s, 8-OH), 7.44 (1H, t-like, J = 8.0 Hz, H-6), 6.92 (1H, d, J = 8.4 Hz, H-7), 6.72 (1H, d, J = 7.6 Hz, H-5), 4.59-4.65 (1H, m, H-3), 2.96-2.99 (2H, m, H-4), 1.89–2.00 (1H, m, H-11a), 1.77-1.85 (1H, m, H-11b), 1.60–1.77 (2H, m, H-12), 1.50–1.56 (2H, m, H-13), 3.88 (1H, hepta, J = 6.4, 11.6, 17.6 Hz, H-14), 1.25 (3H, d, J = 6.4 Hz, H-15), 1.69 (1H, s, 14-OH); Main HMBC correlations: δH 2.96–2.99 (H-4) / δC 79.6 (C-3), 117.9 (C-5), 108.3 (C-9), 139.3 (C-10); δH 6.72 (H-5) / δC 32.8 (C-4), 108.3 (C-9); δH7.44 (H-6) / δC 116.1 (C-7), 139.3 (C-10); δH 6.92 (H-7) / δC 117.9 (C-5), 108.3 (C-9); δH1.89-2.00 (H-11a), 1.77-1.85 (H-11b) / δC 79.6 (C-3); δH 1.50–1.56 (H-13) / δC 23.6 (C-15); δH 1.25 (H-15) / 67.8 (C-14), 38.7 (C-13); δH1.69 (14-OH) / 67.8 (C-14), 23.6 (C-15); (+)-ESI MS m/z = 251.0 [M+H]+; (+)-ESI HR MS m/z = 251.1279 [M+H]+ (calcd. for C14H19O4, 251.1283).

(E)-3-(2,5-Dioxo-3-(propan-2-ylidene)pyrrolidin-1-yl)acrylic acid (2). White powders, Rf = 0.54 (chloroform–methanol–EtOAc, 2:3:3), 0.76 (chloroform–methanol, 1:1), m.p. 194–195 °C; UV (95%EtOH): λmax (logε) = 262 (4.01) nm; IR (KBr): νmax = 3431, 2924, 1714, 1628, 1359, 1234 cm−1; 13C-NMR (100 MHz, CDCl3) δ ppm: 173.9 (C-8), 170.9 (C-5), 168.3 (C-2), 154.1 (C-9), 133.2 (C-6), 119.3 (C-3), 110.9 (C-7), 48.6 (C-4), 24.4 (C-11), 21.0 (C-10); 1H-NMR (400 MHz, CDCl3) δ ppm: 7.78 (1H, d, J =14.8 Hz, H-6), 6.91 (1H, d, J = 14.8 Hz, H-7), 3.35 (2H, s, H-4), 2.35 (3H, s, H-10), 1.93 (3H, s, H-11); Main HMBC correlations: δH 7.78 (H-6) / δC 173.9 (C-8), 170.9 (C-5), 168.3 (C-2); δH 6.91 (H-7) / δC 133.2 (C-6); δH 2.35 (H-10) / δC 154.1 (C-9), 119.3 (C-3), 24.4 (C-11); δH 1.93 (H-11) / δC 154.1 (C-9), 119.3 (C-3), 21.0 (C-10); (+)-ESI MS m/z = 209.9 [M+H]+; (+)-ESI HR MS m/z = 210.0762 [M+H]+ (calcd. for C10H12NO4, 210.0766).

3.5. Antibacterial Assay

The antibacterial activity was determined by method reported in the literature [20]. A LB (Luria-Bertani) broth (50 mL) was used for culturing E. coli and S. aureus. Half milliliter of the 24 h cultured fresh broth at 37 °C was diluted by 50 mL of the same broth to indicate a 0.5 McFarland (McF) turbidity (ca. 1.5 × 108colony forming unit). A tested compound was dissolved in dimethylsulfoxide (DMSO) to provide a sample solution of 0.8 mg mL−1, and then double-fold serial dilutions (0.625–160 μg mL−1) were made by adding Mueller-Hinton broth. Each sample solution (100 μL) was completely mixed with the bacterial suspension (100 μL) in a well of 96-well polystyrene plate. After incubation of the plates for 24 h at 37 °C, the absorbance of each well was measured at 630 nm with a microtiter plate reader (BioRad). According to the same, were prepared and used as positive control. Five percent DMSO in the same broth served method as the tested compounds, the double-fold serial solutions of ceftriaxone sodium (0.156–2.50 μg mL−1), a broad spectrum antibiotics as negative control. All experiments were performed in triplicate. The minimal inhibitory concentration (MIC, μg mL−1) was defined as the concentration of a compound required to reduce the absorbance to less than 50% of that of the negative control.

3.6. Antifungal Assay

The antifungal activity in vitro was assayed by the growth rate method [21] with slight modifications. The tested pathogenic fungi were Alternaria solani, Valsa mali, Curvularia lunata and Botryosphaeria berengeriana, provided by the Institute of Pesticides, Northwest A&F University. Cultures of the test fungi maintained on potato-dextrose-agar (PDA) medium slants were subcultured in Petri dishes prior to testing. Sample solution (1 mg mL−1) in acetone was completely mixed with the autoclaved PDA medium to provide the medium containing 50 µg mL−1 of sample, and poured into Petri dishes. Five percent acetone in PDA medium served as negative control. PDA medium containing 50 (or 100) µg mL−1 of thiabendazole, a broad-spectrum antifungal drug, was used as positive control. When the medium in the plates was partially solidified, a 5-mm thick and 4 mm diameter disc of fungus cut from earlier subcultured Petri dishes was placed at the centre of the semi-solid medium. The treated and control dishes were kept in an incubator at 26 (±2) °C for 72 h. The diameters (in mm) of inhibition zones were measured in three different directions. Growth inhibition rates were calculated according to the following formula and expressed as means ± SD:

%Growth inhibition rate = (dcds) / (dcd0) × 100
where d0: Diameter of the fungus cut, dc: Diameter of the untreated control fungus, ds: Diameter of the sample-treated fungus.

4. Conclusions

In conclusion, the present study described the isolation, characterization and antimicrobial activities of two secondary metabolites 1 and 2 of Talaromyces verruculosus isolated in the rhizosphere soil of Stellera chamaejasme L. and reported their UV, IR, MS, 1D and 2D NMR spectroscopic data for the first time. Compound 1 showed significant antimicrobial activities against four strains of fungi (A. solani, V. mali, C. lunata, B. berengeriana) at 50 µg mL−1 and two strains of bacteria (S. aureus and E. coli) with MIC values of 2.5 µg mL−1 and 5.0 µg mL−1, respectively. Compound 2 was slightly active against the fungi at 100 µg mL−1and its MIC values on the bacteria were more than 100 µg mL−1. Compound 1 should be considered as a new lead or model compound to develop new isocoumarin antimicrobial agents.


This project was supported by the National Natural Science Foundation of China (NNSF; No. 31172365, 31000865, 31101469).

  • Sample Availability: Samples of the compounds 1 and 2 are available from the authors.


  1. Whipps, J.M. Microbial interactions and biocontrol in the rhizosphere. J. Exp. Bot. 2001, 52, 487–511. [Google Scholar] [CrossRef]
  2. Trejo-Estrada, S.R.; Paszczynski, A.; Crawford, D.L. Antibiotics and enzymes produced by the biocontrol agent Streptomyces violaceusniger YCED-9. J. Ind. Microbiol. Biotech. 1998, 21, 81–90. [Google Scholar] [CrossRef]
  3. Smalla, K.; Wachtendorf, U.; Heuer, H.; Liu, W.-T.; Forney, L. Analysis of BIOLOGGN substrate utilization patterns by microbial communities. Appl. Environ. Microbiol. 1998, 64, 1220–1225. [Google Scholar]
  4. Grayston, S.J.; Wang, S.Q.; Campbell, C.D.; Edwards, A.C. Selective influence of plant species on microbial diversity in the rhizosphere. Soil Biol. Biochem. 1998, 30, 369–378. [Google Scholar] [CrossRef]
  5. Rovira, A.D. Plant root excretions in relation to the rhizosphere effect I. Plant Soil 1956, 7, 178–194. [Google Scholar] [CrossRef]
  6. Berg, G.; Zachow, C.; Lottmann, J.; Gotz, M.; Costa, R.; Smalla, K. Impact of plant species and site on rhizosphere-associated fungi antagonistic to Verticillium dahliae Kleb. Appl. Environ. Microbiol. 2005, 71, 4203–4213. [Google Scholar] [CrossRef]
  7. Rovira, A.D. Root excretions in relation to the rhizosphere effect. IV. Influence of plant species, age of plant, light, temperature, and calcium nutrition on exudation. Plant Soil 1959, 11, 53–64. [Google Scholar] [CrossRef]
  8. Gunatilaka, A.A.L. Natural products from plant-associated microorganisms: distribution, structural diversity, bioactivity, and implications of their occurrence. J. Nat. Prod. 2006, 69, 509–526. [Google Scholar] [CrossRef]
  9. He, J.; Wijeratne, E.M.; Bashyal, B.P.; Zhan, J.; Seliga, C.J.; Liu, M.X.; Pierson, E.E.; Pierson, L.S., III; VanEtten, H.D.; Gunatilaka, A.A. Cytotoxic and other metabolites of Aspergillus inhabiting the rhizosphere of Sonoran desert plants. J. Nat. Prod. 2004, 67, 1985–1991. [Google Scholar] [CrossRef]
  10. Kobayashi, A.; Hino, T.; Yata, S.; Itoh, T.J.; Sato, H.; Kawazu, K. Unique spindle poisons, curvularin and its derivatives, isolated from Penicillium specie. Agric. Biol. Chem. 1988, 52, 3119–3123. [Google Scholar] [CrossRef]
  11. Zhou, G.X.; Wijeratne, E.M.; Bigelow, D.; Pierson, L.S., III; VanEtten, H.D.; Gunatilaka, A.A. Aspochalasins I, J, and K: Three new cytotoxic cytochalasans of Aspergillus flavipes from the rhizosphere of Ericameria laricifolia of the Sonoran Desert. J. Nat. Prod. 2004, 67, 328–332. [Google Scholar] [CrossRef]
  12. Wijeratne, E.M.; Turbyville, T.J.; Zhang, Z.; Bigelow, D.; Pierson, L.S., III; VanEtten, H.D.; Whitesell, L.; Canfield, L.M.; Gunatilaka, A.A. Cytotoxic constituents of Aspergillus terreus from the rhizosphere of Opuntia versicolor of the sonoran desert. J. Nat. Prod. 2003, 66, 1567–1573. [Google Scholar] [CrossRef]
  13. Turbyville, T.J.; Wijeratne, E.M.; Whitesell, L.; Gunatilaka, A.A. The anticancer activity of the fungal metabolite terrecyclic acid A is associated with modulation of multiple cellular stress response pathways. Mol. Cancer Ther. 2005, 4, 1569–1576. [Google Scholar] [CrossRef]
  14. Wijeratne, E.M.; Carbonezi, C.A.; Takahashi, J.A.; Seliga, C.J.; Turbyville, T.J.; Pierson, E.E.; Pierson, L.S., III; VanEtten, H.D.; Whitesell, L.; Bolzani, Vda S.; et al. Isolation, optimization of production and structure-activity relationship studies of monocillin I, the cytotoxic constituent of Paraphaeosphaeria quadriseptata. J. Antibiot. 2004, 57, 541–546. [Google Scholar] [CrossRef]
  15. Zhan, J.; Wijeratne, E.M.; Seliga, C.J.; Zhang, J.; Pierson, E.E.; Pierson, L.S., III; VanEtten, H.D.; Gunatilaka, A.A. A new anthraquinone and cytotoxic curvularins of a Penicillium sp. from the rhizosphere of Fallugia paradoxa of the Sonoran desert. J. Antibiot. 2004, 57, 341–344. [Google Scholar] [CrossRef]
  16. Samson, R.A.; Yilmaz, N.; Houbraken, J.; Spierenburg, H.; Seifert, K.A.; Peterson, S.W.; Varga, J.; Frisvad, J.C. Phylogeny and nomenclature of the genus Talaromyces and taxa accommodated in Penicillium subgenus Biverticillium. Stud. Mycol. 2011, 70, 159–183. [Google Scholar] [CrossRef]
  17. Yang, L.Z.; Zhou, L.; Xu, H.; Qin, B.F. Isolation and identification and antifungal activity of a Penicillium. Acta Agric. Boreali-Occid. Sin. 2009, 18, 98–102. [Google Scholar]
  18. Gao, G.C.; Qi, S.H.; Zhang, S.; Yin, H.; Xiao, Z.H.; Li, M.Y.; Li, Q.X. Phenolic compounds and iridoids from the stem bark of Chinese mangrove associate Catunaregam spinosa. Pharmazie 2008, 63, 542–544. [Google Scholar]
  19. Miao, F.; Qin, B.F.; Yang, L.Z.; Yang, X.J.; Zhou, L. (E)-3-[2,5-Dioxo-3-(propan-2-ylidene) pyrrolidin-1-yl]acrylic acid. Acta Cryst. 2010, E66, o634. [Google Scholar]
  20. Guz, N.R.; Stermitz, F.R.; Johnson, J.B.; Beeson, T.D.; Willen, S.; Hsiang, J.-F; Lewis, K. Flavonolignan and flavone inhibitors of a Staphylococcus aureus multidrug resistance pump: structure-activity relationships. J. Med. Chem. 2001, 44, 261–268. [Google Scholar] [CrossRef]
  21. Zhang, J.W.; Li, S.K.; Wu, W.J. The main chemical composition and in vitro antifungal activity of the essential oils of ocimum basilicum Linn. var. pilosum (Willd.) Benth. Molecules 2009, 14, 273–278. [Google Scholar] [CrossRef]
Molecules EISSN 1420-3049 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert
Back to Top