Next Article in Journal
Functional Genomics of Novel Secondary Metabolites from Diverse Cyanobacteria Using Untargeted Metabolomics
Next Article in Special Issue
Microcystin-LR and Cylindrospermopsin Induced Alterations in Chromatin Organization of Plant Cells
Previous Article in Journal
Chitosan Nanoparticles Attenuate Hydrogen Peroxide-Induced Stress Injury in Mouse Macrophage RAW264.7 Cells
Previous Article in Special Issue
Pharmacological Studies of Tentacle Extract from the Jellyfish Cyanea capillata in Isolated Rat Aorta

Mar. Drugs 2013, 11(10), 3601-3616; doi:10.3390/md11103601

Review
Advances in the Study of the Structures and Bioactivities of Metabolites Isolated from Mangrove-Derived Fungi in the South China Sea
Xin Wang 1,2,3, Zhi-Gang Mao 1, Bing-Bing Song 2,3, Chun-Hua Chen 2,3, Wei-Wei Xiao 2,3, Bin Hu 1, Ji-Wen Wang 1, Xiao-Bing Jiang 1, Yong-Hong Zhu 2,3,* and Hai-Jun Wang 1,*
1
Department of Neurosurgery and Pituitary Tumour Center, the First Affiliated Hospital of Sun Yat-sen University, No. 74, Zhongshan Road 2, Guangzhou 510080, China; E-Mails: wangx357@mail2.sysu.edu.cn (X.W.); mmh222111@yahoo.com.cn (Z.-G.M.); warm0809@qq.com (B.H.); 104956978@qq.com (J.-W.W.); 81939338@qq.com (X.-B.J.)
2
Department of Histology and Embryology, Medical school of Sun Yat-sen University, No. 74, Zhongshan Road 2, Guangzhou 510080, China; E-Mails: hd_sbb@163.com (B.-B.S.); 1149755456@qq.com (C.-H.C.); xiaoweiweigz@163.com (W.-W.X.)
3
Key Laboratory of Functional Molecules from Marine Microorganisms, Department of Education of Guangdong Province, Sun Yat-sen University, No. 74, Zhongshan Road 2, Guangzhou 510080, China
*
Authors to whom correspondence should be addressed; E-Mails: zhuyongh@mail.sysu.edu.cn (Y.-H.Z.); wzwxr_1995@aliyun.com (H.-J.W.); Tel.: +86-20-8733-2323 (Y.-H.Z.); +86-20-2882-3388-8215 (H.-J.W.); Fax: +86-20-8733-1451 (Y.-H.Z.); +86-20-8733-1655 (H.-J.W.).
Received: 1 August 2013; in revised form: 21 August 2013 / Accepted: 3 September 2013 /
Published: 30 September 2013

Abstract

: Many metabolites with novel structures and biological activities have been isolated from the mangrove fungi in the South China Sea, such as anthracenediones, xyloketals, sesquiterpenoids, chromones, lactones, coumarins and isocoumarin derivatives, xanthones, and peroxides. Some compounds have anticancer, antibacterial, antifungal and antiviral properties, but the biosynthesis of these compounds is still limited. This review summarizes the advances in the study of secondary metabolites from the mangrove-derived fungi in the South China Sea, and their biological activities reported between 2008 and mid-2013.
Keywords:
marine metabolites; fungus; mangrove; biological activity; south China sea

1. Introduction

The oceans, which cover more than 70% of the earth’s surface, are not only rich in minerals but also have various marine organisms. The international census of marine life (CoML) has claimed that the marine microorganisms amount to 5–10 million, which is far more than the original estimate of 200,000, and far more than the sum of plant and animal species across the world. However, to date, approximately 5000 kinds of marine microorganisms have been officially named and described. The recent advances in natural product chemistry, underwater exploration, bioassays, and genome mining have stimulated interest in the search for new products from this unexplored wealthy habitat [1]. Nowadays, the marine world is a major source for discovery drugs from natural products [2,3]. Such as Cod-liver oil is rich in vitamins A and D, and it probably was the first marine natural products widely commercialized. Arabinofuranosyl-adenine (Ara-A) was isolated from the gorgonian Eunicella cavolini in 1984, it potent used for antitumor and antiviral therapy in the clinic [4,5]. In addition, cephalosporins, digenicacid, active absorbable calcium, bataan, didemnin B, and Ara-C, have gone into clinical use. The biological diversity of the marine ecosystem has provided many promising compounds. In addition, the marine compounds have potent biological activities such as analgesic, antiallergic, antiviral, anticancer, anti-inflammatory, and immunomodulatory activities [6,7].

Marine-derived fungi are a rich source of promising natural products that have biological activities [8]. The secondary metabolites are a diverse group of organic compounds but most of them do not appear to participate directly in the normal growth, development, or reproduction of an organism [9,10]. With an increase in the research on marine microorganisms, an increasing number of new, bioactive, and structurally unique metabolites are being found from marine fungi. In addition, various studies have shown that mangrove-derived fungi yield many novel or bioactive secondary metabolites that are indispensable for drug development [11,12]. In this review, we have summarized the sources and structures of 110 compounds that have been extracted from mangrove-derived fungi from the South China Sea and focused on their bioactivity reported between 2008 and mid-2013.

2. Metabolites Derived from the Mangrove Fungi in the South China Sea

Many bioactive metabolites, including anthracenediones, xyloketals, sesquiterpenoids, chromones, lactones, coumarin and isocoumarin derivatives, xanthones, and peroxides, etc. have been isolated from various mangrove-derived fungi in the South China Sea. The sources, marine products, biological activities, and articles related to these products are listed as shown in Table 1.

Table Table 1. Metabolites from diverse mangrove fungi.

Click here to display table

Table 1. Metabolites from diverse mangrove fungi.
SourceCompoundActivityRef.
Halorosellinia sp. (No. 1403)SZ-685C (1)Cytotoxic[13]
Bostrycin (16)Cytotoxic[14]
Halorosellinia sp. (No. 1403) and Guignardia sp. (No. 4382)Compounds (215)Cytotoxic (6)[15]
Nigrospora sp.4-Deoxybostrycin (18)Anti-mycobacteria[16]
Nigrosporin (19)Anti-mycobacteria
Alternaria sp. (ZJ9-6B)Alterporriol K (20), L (21) and M (22)Cytotoxic (20,21)[17]
Paecilomyces sp.Secalonic acid A (23)Cytotoxic[18]
Paecilomyces sp. (tree 1–7) and endophytic fungus No. ZSU44Secalonic acid D (24)Cytotoxic[19,20,21]
Xylaria sp. (No. 2508)Xyloketal B (25)Protects Human umbilical vein endothelial cells from oxidized LDL-induced oxidative injury[22]
Xyloketal J (26) [23]
Xyloester A (27)
Xylaria sp. BL321Eremophilane sesquiterpenes (3335) [24]
07H239-A (36)Effect on α-glucosidase
Aspergillus sp.(+)-methyl sydowate (28)Antibacterial[25]
7-deoxy-7,8-didehydrosydonic acid (29)
7-deoxy-7,14-didehydrosydonic acid (30)
(+)-sydonic acid (31)Antibacterial
(+)-sydowic acid (32)Antibacterial
Aspergillus sp. (16-5c)Asperterpenoid A (37)Anti-Mycobacterium tuberculosis[26]
Aspergillus terreus Gwq-48Isoaspulvinone E (58), pulvic acid (59) and aspulvinone E (60) Anti-influenza A H1N1 virus[27]
Diaporthe sp.Diaporols A–I (3846) [28]
Pestalotiopsis sp.Pestalotiopsones A–F (4752)Cytotoxic (52)[29]
Cytosporones J–N (6872) [30]
Dothiorelone B (73)
Pestalasins A–E (7478)
3-hydroxymethyl-6,8-dimethoxycoumarin (56)
7-hydroxy-2-(2-hydroxypropyl)-5-methylchromone (53)
Phomopsis sp. (ZZF08)Phomopsin A (61)Cytotoxic[31]
Cytochalasin H (62) Cytotoxic
Glucosylceramide (63)
Phomopsis sp. (ZSU-H76)Phomopsin A (61), B (64), C (65) [32]
Cytosporone B (66) and C (67)Antifungal
Phomopsis sp. (No. SK7RN3G1)2,6-dihydroxy-3-methyl-9-oxoxanthene-8-carboxylic acid methyl ester (88) [33]
Penicillium sp. (091402)(3 R*, 4S*)-6,8-dihydroxy-3,4,7-trimethylisocoumarin (79)Cytotoxic[34]
(3 R, 4S)-6,8- dihydroxy-3,4,5-trimethylisocoumarin (80)
(3 R, 4S)-6,8- dihydroxy-3,4,5,7-tetramethylisocoumarin (81)
( S)-3-(3′,5′-dhydroxy-2′,4′-methlphenyl)butan-2-one (82)
Phenol A (83) Cytotoxic
Penicillium sp. (ZZF 32#)Dimethyl 8-methoxy-9-oxo-9H-xanthene-1, 6-dicarboxylate (86) [35]
8-(methoxycarbonyl)-1-hydroxy-9-oxo-9 H-xanthene-3-carboxylic acid (87)Antifungal
Talaromyces flavusTalaperoxides A–D (8992)Cytotoxic[36]
Steperoxide B (93, or merulin A)Cytotoxic
Talaromyces sp. (SBE-14)Tenelate A (108) and B (109) [37]
Tenellic acid C (110)
Sporothrix sp. (#4335)Sporothrins A, B, and C (105107)Cytotoxic[38]
Unidentified fungus (No. B77)Anhydrofusarubin (17)Anti-Gram-positive bacteria, Cytotoxic[39]
Unidentified fungus (No. GX4-1B)1,10-dihydroxy-8-methyl-dibenz[b,e]oxepin-6,11-dione (54) [40]
6-hydroxy-4-hydroxymethyl-8-methoxy-3-methylisocoumarin (55)
3-hydroxymethyl-6,8-dimethoxycoumarin (56)
1,10-dihydroxy-dibenz[b ,e]oxepin-6,11-dione (57)
Unidentified fungus (No. ZH19)1-hydroxy-4,7-dimethoxy-6-(3-oxobutyl)-9 H-xanthen-9-one (84)Cytotoxic[41]
1,7-dihydroxy-2-methoxy-3-(3-methylbut-2-enyl)-9 H-xanthen-9-one (85)Cytotoxic

2.1. Anthracenediones

Anthracenedione is one of the important sources of marine secondary metabolites. They have a great potential of biomedical applications because their novel structures and bioactivities (Figure 1).

A novel marine anthraquinone derivative, SZ-685C (1), was isolated from Halorosellinia sp. (No. 1403), a mangrove-derived fungus in the South China Sea. A previous study showed that SZ-685C inhibits the growth of six tumor cell lines, including human glioma, hepatoma, prostate cancer, and breast cancer (half-maximal inhibitory concentration [IC50] = 3.0–9.6 × 103 μM), and in vivo experiments showed that SZ-685C also inhibits the tumor growth in nude mice by inducing apoptosis via the Akt/FOXO pathway [13]. Subsequently, Zhu et al. found that compound 1 causes apoptosis in adriamycin-resistant human breast cancer cells both in vitro and vivo, and it exerts these antitumor effects through multiple mechanisms mainly involving the suppression of Akt signaling [42]. Recently, Chen et al. [43] reported that SZ-685C significantly inhibited the proliferation of MMQ pituitary adenoma cells and induced apoptosis by downregulation of miR-200c. In addition, this compound showed potent anticancer activity in radiosensitive and radioresistant nasopharyngeal carcinoma cells, and the miR-205-PTEN-Akt pathway is the mechanism underlying the anticancer activity [44]. Zhang et al. isolated 14 anthracenedione derivatives (215) from the mangrove fungi Guignardia sp. (No. 4382) and Halorosellinia sp. (No. 1403). Of these compounds, compound 6 was effective against KBv200 cells and KB cells (IC50 = 3.21 and 3.17 μM, respectively) and induced apoptosis through a mitochondrial pathway [15].

Marinedrugs 11 03601 g001 1024
Figure 1. Chemical structures of metabolites anthracenediones.

Click here to enlarge figure

Figure 1. Chemical structures of metabolites anthracenediones.
Marinedrugs 11 03601 g001 1024

Xu et al. [14] showed that an anthracenedione with phytotoxic properties, bostrycin (16), was collected from the same strain Halorosellinia sp. (No. 1403). They showed that this compound was cytotoxic against yeast cells, and it might induce apoptosis through a mitochondria-mediated apoptotic pathway. Another novel anthraquinone, anhydrofusarubin (17) isolated from the endophytic fungus No. B77, showed an inhibitory effect on the gram-positive bacterium Staphylococcus aureus (ATCC27154; minimum inhibitory concentration [MIC] = 43.4 μM) [45] and showed a significant inhibition of the growth of HEp2 and HepG2 cells (IC50 = 8.67 and 3.47 μM, respectively) [39].

A natural anthraquinone, 4-deoxybostrycin (18), and its deoxy derivative, nigrosporin (19), were obtained from Nigrospora sp. A primary bioassay showed that both compounds showed inhibitory effects against mycobacteria, and compound 18 showed significant inhibition of some clinical multidrug-resistant (MDR) Mycobacterium Tuberculosis strains (MIC < 15.7 μM) [16]. Huang et al. isolated alterporriol K (20), L (21), and M (22), three new bianthraquinone derivatives, from the endophytic mangrove fungus Alternaria sp. ZJ9-6B. Of these three derivatives, compounds 20 and 21 were moderately active against MDA-MB-435 and MCF-7 human breast cancer cell lines (IC50 = 13.1–29.1 μM) [17].

2.2. Secalonic Acid Family

Secalonic acid A (SAA) (23) was isolated from the marine fungi Paecilomyces sp. and has been reported to have strong antitumor activities (Figure 2). Zhai et al. [18] found that pretreatment with SAA has neuroprotective effects in cultured rat cortical neurons, which was associated with the suppression of c-Jun N-terminal kinase (JNK), calcium influx, p38 mitogen-activated protein kinase (MAPK), and the activation of caspase-3. Moreover, compound 23 may rescue dopaminergic neurons from 1-methyl-4-phenylpyridinium (MPP+)-induced cell death through the mitochondrial apoptotic pathway, and this protective effect of 23 was observed in mice with Parkinson’s disease [46].

Marinedrugs 11 03601 g002 1024
Figure 2. Chemical structures of metabolites secalonic acid family and xyloketals.

Click here to enlarge figure

Figure 2. Chemical structures of metabolites secalonic acid family and xyloketals.
Marinedrugs 11 03601 g002 1024

Another promising metabolite, secalonic acid D (SAD) (24), was initially isolated from Penicillium oxalicum by Steyn PS in 1969 and was investigated as a teratogenic fungal metabolite with strong toxicity [47]. In the following decades, studies on SAD mainly focused on its toxicity in mice. Several studies showed that SAD could cause cleft palate through the inhibition of G1/S-phase-specific CDK2 activity [48]. SAD inhibited the proliferation of human embryonic palatal mesenchymal cells by suppressing cell cycle progression and altering the expression of cell cycle regulatory proteins, p21 and cyclin E [49].

Recent studies have shown that SAD has strong anticancer activities. Hong [50] showed that SAD might act as a novel DNA topoisomerase I inhibitor (MIC = 0.4 µM) and be a potential anticancer drug; SAD was separated from the fermentation broth of marine sediments-derived fungi Gliocladium sp. T31 obtained from the South Pole.

Some studies have shown that SAD was extracted from the secondary metabolites of the mangrove-derived fungi No. ZSU44. Zhang et al. [19] found that SAD showed significant cytotoxic activities and induced apoptosis in K562 and HL60 myeloid leukemia cell lines (IC50 = 0.43 and 0.38 μM, respectively), and it exerted this effect by blocking the G1 phase of the cell cycle through the GSK-3β/β-catenin/c-Myc pathway. Recently, Hu et al. [20] suggested that SAD was active against MDR cells and reduced the percentage of side population cells in lung cancer through downregulation of the expression levels of ABCG2. Liao et al. [21] reported that SAD was isolated from Paecilomyces sp. (tree 1–7); SAD inhibited the proliferation of murine pituitary adenoma GH3 cells and induced apoptosis in a dose-dependent manner. SAD exerted its cytotoxic effect mainly through cell cycle arrest by activating caspase. In addition, SAD inhibited the expression of growth hormone in GH3 cells.

2.3. Xyloketals

A novel bioactive marine compound, xyloketal B (25), has been isolated from the mangrove fungus Xylaria sp. (no. 2508). Chen et al. showed for the first time that xyloketal B protected human umbilical vein endothelial cells from oxidized low-density lipoprotein-induced oxidative injury by suppressing NADPH oxidase-derived generation of reactive oxygen species, recovering the expression levels of Bcl-2, and increasing nitric oxide (NO) production [22]. Subsequently, Zhao et al. [51] found that compound 25 could protect rat pheochromocytoma PC12 cells against oxygen glucose deprivation (OGD)-induced cell damage.

In the same mangrove fungus, Xu et al. [23] found two metabolites, xyloketal J (26) and xyloester A (27). Compound 26 showed results similar to those observed in compound 25; however, in their primary bioactivity test, the two metabolites were inactive against bacteria.

2.4. Sesquiterpenoids

Wei et al. obtained three new phenolic bisabolane-type sesquiterpenoids along with two known fungi-derived metabolites from the marine-derived fungus Aspergillus sp. (Figure 3). They were (+)-methyl sydowate (28), 7-deoxy-7,8-didehydrosydonic acid (29), 7-deoxy-7,14-didehydrosydonic acid (30), (+)-sydonic acid (31), and (+)-sydowic acid (32). Out of which, compound 28, 30, and 31 were weakly active against S. aureus, however, they displayed inactive effects against methicillin-resistant S. aureus [25]. Song et al. reported three new eremophilane sesquiterpenes (3335) along with a known analogue 07H239-A (36) obtained from the marine-derived fungus Xylaria sp. BL321. Out of these, compound 36 activated α-glucosidase at a concentration of 0.15 μM, and compound 36 exhibited an inhibitory effect against α-glucosidase at increased concentrations (IC50 = 6.54 μM) [24].

A novel sesterterpenoid, asperterpenoid A (37), isolated from a mangrove endophytic fungus Aspergillus sp. 16-5c, efficiently inhibited M. tuberculosis protein tyrosine phosphatase B (IC50 = 2.2 μM) [26]. Another new sesquiterpenoid, diaporol A (38), and eight other novel drimane sesquiterpenoids, diaporols B–I (3946), were obtained from a culture of the marine-derived endophytic fungus Diaporthe sp., but a primary bioassay indicated that they were not cytotoxic [28].

2.5. Chromones

Pestalotiopsones A–F (4752), the new chromones have been reported by Xu et al., together with the known derivative 7-hydroxy-2-(2-hydroxypropyl)-5-methylchromone (53) obtained from the mangrove-derived endophyte Pestalotiopsis sp. isolated from Rhizophora mucronata leaves (Figure 4). A preliminary biological activity test showed that compound 52 was moderately cytotoxic against the mouse L5178Y lymphoma cell line, while the other six metabolites were inactive [29].

Marinedrugs 11 03601 g003 1024
Figure 3. Chemical structures of metabolites sesquiterpenoids.

Click here to enlarge figure

Figure 3. Chemical structures of metabolites sesquiterpenoids.
Marinedrugs 11 03601 g003 1024
Marinedrugs 11 03601 g004 1024
Figure 4. Chemical structures of metabolites chromones.

Click here to enlarge figure

Figure 4. Chemical structures of metabolites chromones.
Marinedrugs 11 03601 g004 1024

2.6. Lactones

Lactones continue to be a great source for new bioactive natural products (Figure 5). Two new aromatic lactones, 1,10-dihydroxy-8-methyl-dibenz[b,e]oxepin-6,11-dione (54) and 6-hydroxy-4-hydroxymethyl-8-methoxy-3-methylisocoumarin (55), along with two known compounds, 3-hydroxymethyl-6,8-dimethoxycoumarin (56) and 1,10-dihydroxy-dibenz[b,e]oxepin-6,11-dione (57), were collected from an unidentified endophytic fungus No. GX4-1B, which was obtained from Bruguiera gymnoihiza (L.), but their bioactivities have not been examined in this research [40].

Marinedrugs 11 03601 g005 1024
Figure 5. Chemical structures of metabolites lactones, coumarins, and isocoumarin derivatives.

Click here to enlarge figure

Figure 5. Chemical structures of metabolites lactones, coumarins, and isocoumarin derivatives.
Marinedrugs 11 03601 g005 1024

Recently, Gao et al. [27] isolated a new butenolide isoaspulvinone E (58) and two known butenolides pulvic acid (59) and aspulvinone E (60) from Aspergillus terreus Gwq-48. All the three compounds were moderately against influenza A H1N1 virus (IC50 = 101.3, 94.5, and 192.2 μM, respectively).

Tao et al. [31] isolated a novel marine product named phomopsin A (61) along with two known compounds cytochalasin H (62) and glucosylceramide (63) from the mangrove endophytic fungus Phomopsis sp. (ZZF08). Bioactivity assay of these compounds showed that compound 61 was moderately active against KBv200 cells and KB cells (IC50 = 66.4 μM and 110.7 μM, respectively) and compound 62 showed significant cytotoxic activity against KBv200 cells and KB cells (IC50 < 2.5 μM). Huang et al. [32] found phomopsin B (64) and C (65) from the endophytic fungus, Phomopsis sp. ZSU-H76, along with two known compounds cytosporone B (66) and C (67) from the stem of a Chinese mangrove plant Excoecaria agallocha. Compounds 66 and 67 inhibited two fungi Fusarium oxysporum and Candida albicans (MIC = 115.1–198.8 μM). Cytosporones J–N (6872) and two known compounds, dothiorelone B (73) and cytosporone C (67) were obtained from the mangrove fungi Pestalotiopsis sp. [30]. Compound 6872 were inactive against cancer cells.

2.7. Coumarins and Isocoumarin Derivatives

Mangrove fungi isolated from the South China Sea also yielded a variety of coumarins and isocoumarin derivatives with novel structures.

Five novel coumarins, pestalasins A–E (7478), and a known compound 3-hydroxymethyl-6,8-dimethoxycoumarin (56) were isolated from the Chinese mangrove Rhizophora mucronata-derived Pestalotiopsis sp. [30]. These compounds were isolated from a mangrove fungus for the first time by Xu et al. A new compound (3R*, 4S*)-6,8-dihydroxy-3,4,7-trimethylisocoumarin (79) was obtained from the mangrove endophytic Penicillium sp. 091402 from the plant Bruguiera sexangula together with four known derivatives (3R, 4S)-6,8-dihydroxy-3,4,5-trimethylisocoumarin (80) and (3R, 4S)-6,8-dihydroxy-3,4,5,7-tetramethylisocoumarin (81), (S)-3-(3′,5′-dihydroxy-2′,4′-methlphenyl) butan-2-one (82), and phenol A (83), the structures of which were consistent with that of the decomposition product of citrinin. Of these compounds, compound 80 was cytotoxic against cancer cell line K562 (IC50 = 84.7 μM), and compound 83 showed weak cytotoxicity against the cancer cell line SGC-7901(IC50 = 195.7 μM) [34].

2.8. Xanthones and Peroxides

Xanthones and peroxides play an important role in the source of promising drugs (Figure 6). They produce several structurally diverse, bioactive metabolites.

Huang et al. [41] isolated two novel xanthone derivatives, 1-hydroxy-4,7-dimethoxy-6-(3-oxobutyl)-9H-xanthen-9-one (84) and 1,7-dihydroxy-2-methoxy-3-(3-methylbut-2-enyl)-9H-xanthen-9-one (85), from a mangrove endophytic fungus (No. ZH19). Compounds (84) and (85) inhibited KB cells (IC50 = 3.5 × 104 and 2.0 × 104 μM, respectively) and KB(V)200 cells (IC50 = 4.1 × 104 and 3.0 × 104 μM, respectively). Dimethyl 8-methoxy-9-oxo-9H-xanthene-1, 6-dicarboxylate (86), and 8-(methoxycarbonyl)-1-hydroxy-9-oxo-9H-xanthene-3-carboxylic acid (87) were other novel xanthones isolated from the culture broth of the mangrove fungus Penicillium sp. (ZZF 32#) from the South China Sea. Among these, compound 87 was active against Fusarium oxysporum f. sp. cubense with moderate antifungal activity (MIC = 39.8 μM) [35].

Marinedrugs 11 03601 g006 1024
Figure 6. Chemical structures of metabolites xanthones and peroxides.

Click here to enlarge figure

Figure 6. Chemical structures of metabolites xanthones and peroxides.
Marinedrugs 11 03601 g006 1024

Recently, a novel xanthone, 2,6-dihydroxy-3-methyl-9-oxoxanthene-8-carboxylic acid methyl ester (88), was isolated from the marine fungus Phomopsis sp. (No. SK7RN3G1) by Yang et al. Primary bioassays showed that compound 88 was cytotoxic against HepG2 and HEp-2 cells (IC50 = 30 and 26.7 μM, respectively) [33].

Talaperoxides A–D (8992), four new norsesquiterpene peroxides, and steperoxide B (93), a known analogue, were isolated from the mangrove-derived fungus Talaromyces flavus. All the four compounds, in particular compounds 90 and 92, were cytotoxic against several human tumor cell lines HeLa, HepG2, MCF-7, PC-3, and MDA-MB-435 (IC50 = 2.8–9.4 μM) [36].

2.9. Other

There are several other metabolites with biological activities (Figure 7). Tao et al. examined 87 natural products isolated from the mangrove fungus in the South China Sea [52]. From these products, 11 (94104) showed potent cytotoxicity in KBv200, A549, KB, MCF-7/adr, and MCF-7 cells (IC50 < 50 μM). Compared to normal liver cells, the compounds 94, 102, 103, and 104 were more sensitive against cancer cells in this research (IC50 were at least 1.35 fold more potent against cancer cells). In addition, while compound 95 and 99 showed complete inhibition of the growth of LO2 cells, the other compounds were inactive.

Sporothrins A, B, and C (105107), three bioactive metabolites, were collected from the mangrove fungus Sporothrix sp. (#4335). Compound 105 and 106 showed moderate cytotoxic activity against HepG2 cell lines (IC50 = 108.2 and 41.8 μM, respectively). Moreover, compound 105 significantly inhibited the activity of acetylcholine esterase (AChE) in vitro (IC50 = 1.05 μM) [38]. Liu et al. [37] identified two novel metabolites and known compounds named tenelate A (108), B (109), and tenellic acid C (110); these compounds were separated from the marine-derived fungus Talaromyces sp. (SBE-14). The bioactivities of these compounds have not been examined in this study.

Marinedrugs 11 03601 g007 1024
Figure 7. Chemical structures of other metabolites.

Click here to enlarge figure

Figure 7. Chemical structures of other metabolites.
Marinedrugs 11 03601 g007 1024

3. Conclusions

The oceans are the largest underexploited wealthy resource of potential drugs. Mangrove fungi are increasingly being explored in the studies on novel and bioactive molecules from marine sources. Several new bioactive compounds of potential therapeutic have been isolated and identified from mangrove fungi during the last 5 years. Some of them have a high toxicity toward cancer cells; however, they are also cytotoxic to normal cells. These compounds require structural modifications to decrease the toxicity and increase the anticancer activity. In addition, the bioactivity of the compounds was mainly examined in vitro; thus, further in vivo and preclinical studies are required to determine the bioactive compounds with potential therapeutic applications. The side effects of these metabolites should be examined in future studies.

Further, for the industrial large-scale production of these metabolites, there is an important hurdle that mass culture of the fungi and compound purification. Because the biosynthesis of these compounds is limited, large amounts of active materials cannot be obtained from mangrove fungi. In recent research, this may mean increased production through changing the function of the genes and enzymes, seed culture methods, and larger field of the metabolic engineering of culturable microorganisms. With the technical advancements in isolation and cultivation of marine microorganisms, we infer that marine natural products will lead to a new surge of drugs, and fungi and other marine microorganisms will be promising sources for novel therapeutic agents.

Acknowledgments

This research was supported in part by two grant from the National Natural Science Foundation of China (No. 41076092, 30971538) and two grant from the Guangdong Provincial National Natural Science Foundation of China (No.1051008901000176, S2012010009194).

References

  1. Vinothkumar, S.; Parameswaran, P.S. Recent advances in marine drug research. Biotechnol. Adv. 2013. in press. [Google Scholar]
  2. Montaser, R.; Luesch, H. Marine natural products: a new wave of drugs? Future Med. Chem. 2011, 3, 1475–1489. [Google Scholar] [CrossRef]
  3. Xiong, Z.Q.; Wang, J.F.; Hao, Y.Y.; Wang, Y. Recent advances in the discovery and development of marine microbial natural products. Mar. Drugs 2013, 11, 700–717. [Google Scholar] [CrossRef]
  4. De Rosa, S. Marine natural products—Analysis, structure elucidation, bioactivity and potential use as drugs. In Mediterranean Marine Organisms as Source of New Potential Drugs, Proceedings of the Phytochemical Society of Europe, Fund calouste gulbenkian, Lisbon, Portugal, April 2000; Rauter, A.P., Palma, F.B., Justino, J., Araujo, M.E., PinaDosSantos, S., Eds.; Springer: Dordrecht, The Netherlands, 2002; pp. 441–461. [Google Scholar]
  5. Newman, D.J.; Cragg, G.M. The Discovery of Anticancer Drugs from Natural Sources; Humana Press Inc: Totowa, NJ, USA, 2005; pp. 129–168. [Google Scholar]
  6. Singh, R.; Sharma, M.; Joshi, P.; Rawat, D.S. Clinical status of anti-cancer agents derived from marine sources. Anticancer Agents Med. Chem. 2008, 8, 603–617. [Google Scholar]
  7. Yasuhara-Bell, J.; Lu, Y. Marine compounds and their antiviral activities. Antiviral Res. 2010, 86, 231–240. [Google Scholar] [CrossRef]
  8. Saleem, M.; Ali, M.S.; Hussain, S.; Jabbar, A.; Ashraf, M.; Lee, Y.S. Marine natural products of fungal origin. Nat. Prod. Rep. 2007, 24, 1142–1152. [Google Scholar] [CrossRef]
  9. Fraenkel, G.S. The raison d′etre of secondary plant substances; these odd chemicals arose as a means of protecting plants from insects and now guide insects to food. Science 1959, 129, 1466–1470. [Google Scholar]
  10. Secondary metabolite. Available online: http://en.wikipedia.org/wiki/Secondary_metabolites (accessed on 15 August 2013).
  11. Xu, J. Biomolecules produced by mangrove-associated microbes. Curr. Med. Chem. 2011, 18, 5224–5266. [Google Scholar] [CrossRef]
  12. Blunt, J.W.; Copp, B.R.; Keyzers, R.A.; Munro, M.H.; Prinsep, M.R. Marine natural products. Nat. Prod. Rep. 2013, 30, 237–323. [Google Scholar] [CrossRef]
  13. Xie, G.; Zhu, X.; Li, Q.; Gu, M.; He, Z.; Wu, J.; Li, J.; Lin, Y.; Li, M.; She, Z.; et al. SZ-685C, a marine anthraquinone, is a potent inducer of apoptosis with anticancer activity by suppression of the Akt/FOXO pathway. Br. J. Pharmacol. 2010, 159, 689–697. [Google Scholar] [CrossRef]
  14. Xu, C.; Wang, J.; Gao, Y.; Lin, H.; Du, L; Yang, S.; Long, S.; She, Z.; Cai, X.; Zhou, S.; et al. The anthracenedione compound bostrycin induces mitochondria-mediated apoptosis in the yeast Saccharomyces cerevisiae. FEMS Yeast Res. 2010, 10, 297–308. [Google Scholar] [CrossRef]
  15. Zhang, J.Y.; Tao, L.Y.; Liang, Y.J.; Chen, L.M.; Mi, Y.J.; Zheng, L.S.; Wang, F.; She, Z.G.; Lin, Y.C.; To, K.K.; et al. Anthracenedione derivatives as anticancer agents isolated from secondary metabolites of the mangrove endophytic fungi. Mar. Drugs 2010, 8, 1469–1481. [Google Scholar] [CrossRef]
  16. Wang, C.; Wang, J.; Huang, Y.; Chen, H.; Li, Y.; Zhong, L.; Chen, Y.; Chen, S.; Wang, J.; Kang, J.; et al. Anti-mycobacterial activity of marine fungus-derived 4-deoxybostrycin and nigrosporin. Molecules 2013, 18, 1728–1740. [Google Scholar] [CrossRef]
  17. Huang, C.H.; Pan, J.H.; Chen, B.; Yu, M.; Huang, H.B.; Zhu, X.; Lu, Y.J.; She, Z.G.; Lin, Y.C. Three bianthraquinone derivatives from the mangrove endophytic fungus Alternaria sp. ZJ9-6B from the South China Sea. Mar. Drugs 2011, 9, 832–843. [Google Scholar] [CrossRef]
  18. Zhai, A.; Zhang, Y.; Zhu, X.; Liang, J.; Wang, X.; Lin, Y.; Chen, R. Secalonic acid A reduced colchicine cytotoxicity through suppression of JNK, p38 MAPKs and calcium influx. Neurochem. Int. 2011, 58, 85–91. [Google Scholar] [CrossRef]
  19. Zhang, J.Y.; Tao, L.Y.; Liang, Y.J.; Yan, Y.Y.; Dai, C.L.; Xia, X.K.; She, Z.G.; Lin, Y.C.; Fu, L.W. Secalonic acid D induced leukemia cell apoptosis and cell cycle arrest of G(1) with involvement of GSK-3beta/beta-catenin/c-Myc pathway. Cell Cycle 2009, 8, 2444–2450. [Google Scholar] [CrossRef]
  20. Hu, Y.P.; Tao, L.Y.; Wang, F.; Zhang, J.Y.; Liang, Y.J.; Fu, L.W. Secalonic acid D reduced the percentage of side populations by down-regulating the expression of ABCG2. Biochem. Pharmacol. 2013, 85, 1619–1625. [Google Scholar] [CrossRef]
  21. Liao, G.; Zhou, J.; Wang, H.; Mao, Z.; Xiao, W.; Wang, H.; She, Z.; Zhu, Y. The cell toxicity effect of secalonic acid D on GH3 cells and the related mechanisms. Oncol. Rep. 2010, 23, 387–395. [Google Scholar]
  22. Chen, W.L.; Qian, Y.; Meng, W.F.; Pang, J.Y.; Lin, Y.C.; Guan, Y.Y.; Chen, S.P.; Liu, J.; Pei, Z.; Wang, G.L. A novel marine compound xyloketal B protects against oxidized LDL-induced cell injury in vitro. Biochem. Pharmacol. 2009, 78, 941–950. [Google Scholar] [CrossRef]
  23. Xu, F.; Zhang, Y.; Wang, J.; Pang, J.; Huang, C.; Wu, X.; She, Z.; Vrijmoed, L.L.; Jones, E.B.; Lin, Y. Benzofuran derivatives from the mangrove endophytic Fungus Xylaria sp. (#2508). J. Nat. Prod. 2008, 71, 1251–1253. [Google Scholar] [CrossRef]
  24. Song, Y.; Wang, J.; Huang, H.; Ma, L.; Wang, J.; Gu, Y.; Liu, L.; Lin, Y. Four eremophilane sesquiterpenes from the mangrove endophytic fungus Xylaria sp. BL321. Mar. Drugs 2012, 10, 340–348. [Google Scholar] [CrossRef]
  25. Wei, M.Y.; Wang, C.Y.; Liu, Q.A.; Shao, C.L.; She, Z.G.; Lin, Y.C. Five sesquiterpenoids from a marine-derived fungus Aspergillus sp. isolated from a gorgonian Dichotella gemmacea. Mar. Drugs 2010, 8, 941–949. [Google Scholar] [CrossRef]
  26. Huang, X.; Huang, H.; Li, H.; Sun, X.; Huang, H.; Lu, Y.; Lin, Y.; Long, Y.; She, Z. Asperterpenoid A, a new sesterterpenoid as an inhibitor of Mycobacterium tuberculosis protein tyrosine phosphatase B from the culture of Aspergillus sp. 16-5c. Org. Lett. 2013, 15, 721–723. [Google Scholar] [CrossRef]
  27. Gao, H.; Guo, W.; Wang, Q.; Zhang, L.; Zhu, M.; Zhu, T.; Gu, Q.; Wang, W.; Li, D. Aspulvinones from a mangrove rhizosphere soil-derived fungus Aspergillus terreus Gwq-48 with anti-influenza A viral (H1N1) activity. Bioorg. Med. Chem. Lett. 2013, 23, 1776–1778. [Google Scholar] [CrossRef]
  28. Zang, L.Y.; Wei, W.; Guo, Y.; Wang, T.; Jiao, R.H.; Ng, S.W.; Tan, R.X.; Ge, H.M. Sesquiterpenoids from the mangrove-derived endophytic fungus Diaporthe sp. J. Nat. Prod. 2012, 75, 1744–1749. [Google Scholar] [CrossRef]
  29. Xu, J.; Kjer, J.; Sendker, J.; Wray, V.; Guan, H.; Edrada, R.; Lin, W.; Wu, J.; Proksch, P. Chromones from the endophytic fungus Pestalotiopsis sp. isolated from the chinese mangrove plant Rhizophora mucronata. J. Nat. Prod. 2009, 72, 662–665. [Google Scholar] [CrossRef]
  30. Xu, J.; Kjer, J.; Sendker, J.; Wray, V.; Guan, H.; Edrada, R.; Muller, W.E.; Bayer, M.; Lin, W.; Wu, J.; et al. Cytosporones, coumarins, and an alkaloid from the endophytic fungus Pestalotiopsis sp. isolated from the Chinese mangrove plant Rhizophora mucronata. Bioorg. Med. Chem. 2009, 17, 7362–7367. [Google Scholar] [CrossRef]
  31. Tao, Y.; Zeng, X.; Mou, C.; Li, J.; Cai, X.; She, Z.; Zhou, S.; Lin, Y. 1H and 13C NMR assignments of three nitrogen containing compounds from the mangrove endophytic fungus (ZZF08). Magn. Reson. Chem. 2008, 46, 501–505. [Google Scholar] [CrossRef]
  32. Huang, Z.; Cai, X.; Shao, C.; She, Z.; Xia, X.; Chen, Y.; Yang, J.; Zhou, S.; Lin, Y. Chemistry and weak antimicrobial activities of phomopsins produced by mangrove endophytic fungus Phomopsis sp. ZSU-H76. Phytochemistry 2008, 69, 1604–1608. [Google Scholar] [CrossRef]
  33. Yang, J.X.; Qiu, S.X.; She, Z.G.; Lin, Y.C. A new xanthone derivative from the marine fungus Phomopsis sp. (No. SK7RN3G1). Chem. Nat. Compd. 2013, 49, 31–33. [Google Scholar] [CrossRef]
  34. Han, Z.; Mei, W.L.; Zhao, Y.X.; Deng, Y.Y.; Dai, H.F. A new cytotoxic isocoumarin from endophytic fungus Penicillium sp. 091402 of the mangrove plant Bruguiera sexangula. Chem. Nat. Compd. 2009, 45, 805–807. [Google Scholar] [CrossRef]
  35. Shao, C.; Wang, C.; Wei, M.; Gu, Y.; Xia, X.; She, Z.; Lin, Y. Structure elucidation of two new xanthone derivatives from the marine fungus Penicillium sp. (ZZF 32#) from the South China Sea. Magn. Reson. Chem. 2008, 46, 1066–1069. [Google Scholar]
  36. Li, H.; Huang, H.; Shao, C.; Huang, H.; Jiang, J.; Zhu, X.; Liu, Y.; Liu, L.; Lu, Y.; Li, M.; et al. Cytotoxic norsesquiterpene peroxides from the endophytic fungus Talaromyces flavus isolated from the mangrove plant Sonneratia apetala. J. Nat. Prod. 2011, 74, 1230–1235. [Google Scholar] [CrossRef]
  37. Liu, F.; Li, Q.; Yang, H.; Cai, X.L.; Xia, X.K.; Chen, S.P.; Li, M.F.; She, Z.G.; Lin, Y.C. Structure elucidation of three diphenyl ether derivatives from the mangrove endophytic fungus SBE-14 from the South China Sea. Magn. Reson. Chem. 2009, 47, 453–455. [Google Scholar] [CrossRef]
  38. Wen, L.; Cai, X.; Xu, F.; She, Z.; Chan, W.L.; Vrijmoed, L.L.; Jones, E.B.; Lin, Y. Three metabolites from the mangrove endophytic fungus Sporothrix sp. (#4335) from the South China Sea. J. Org. Chem. 2009, 74, 1093–1098. [Google Scholar] [CrossRef]
  39. Shao, C.; Wang, C.; Zheng, C.; She, Z.; Gu, Y.; Lin, Y. A new anthraquinone derivative from the marine endophytic fungus Fusarium sp. (No. b77). Nat. Prod. Res. 2010, 24, 81–85. [Google Scholar] [CrossRef]
  40. Huang, H.; Li, Q.; Feng, X.; Chen, B.; Wang, J.; Liu, L.; She, Z.; Lin, Y. Structural elucidation and NMR assignments of four aromatic lactones from a mangrove endophytic fungus (No. GX4-1B). Magn. Reson. Chem. 2010, 48, 496–499. [Google Scholar]
  41. Huang, Z.; Yang, R.; Yin, X.; She, Z.; Lin, Y. Structure elucidation and NMR assignments for two xanthone derivatives from a mangrove endophytic fungus (No. ZH19). Magn. Reson. Chem. 2010, 48, 80–82. [Google Scholar]
  42. Zhu, X.; He, Z.; Wu, J.; Yuan, J.; Wen, W.; Hu, Y.; Jiang, Y.; Lin, C.; Zhang, Q.; Lin, M.; et al. A marine anthraquinone SZ-685C overrides adriamycin-resistance in breast cancer cells through suppressing Akt signaling. Mar. Drugs 2012, 10, 694–711. [Google Scholar] [CrossRef]
  43. Chen, C.H.; Xiao, W.W.; Jiang, X.B.; Wang, J.W.; Mao, Z.G.; Lei, N.; Fan, X.; Song, B.B.; Liao, C.X.; Wang, H.J.; et al. A novel marine drug, SZ-685C, induces apoptosis of MMQ pituitary tumor cells by downregulating miR-200c. Curr. Med. Chem. 2013, 20, 2145–2154. [Google Scholar] [CrossRef]
  44. Wang, D.; Wang, S.; Liu, Q.; Wang, M.; Wang, C.; Yang, H. SZ-685C exhibits potent anticancer activity in both radiosensitive and radioresistant NPC cells through the miR-205-PTEN-Akt pathway. Oncol. Rep. 2013, 29, 2341–2347. [Google Scholar]
  45. Shao, C.L.; Wang, C.Y.; Deng, D.S.; She, Z.G.; Gu, Y.C.; Lin, Y.S. Crystal Structure of a Marine Natural Compound, Anhydrofusarubin. Chinese J. Struct. Chem. 2008, 27, 824–828. [Google Scholar]
  46. Zhai, A.; Zhu, X.; Wang, X.; Chen, R.; Wang, H. Secalonic acid A protects dopaminergic neurons from 1-methyl-4-phenylpyridinium (MPP)-induced cell death via the mitochondrial apoptotic pathway. Eur. J. Pharmacol. 2013, 713, 58–67. [Google Scholar] [CrossRef]
  47. Steyn, P.S. The isolation, structure and absolute configuration of secalonic acid D, the toxic metabolite of Penicillium oxalicum. Tetrahedron 1970, 26, 51–57. [Google Scholar] [CrossRef]
  48. Dhulipala, V.C.; Welshons, W.V.; Reddy, C.S. Cell cycle proteins in normal and chemically induced abnormal secondary palate development: A review. Hum. Exp. Toxicol. 2006, 25, 675–682. [Google Scholar] [CrossRef]
  49. Dhulipala, V.C.; Maddali, K.K.; Ray, B.K.; Welshons, W.V.; Reddy, C.S. Role of p21 and cyclin E in normal and secalonic acid D-inhibited proliferation of human embryonic palatal mesenchymal cells. Hum. Exp. Toxicol. 2011, 30, 1222–1232. [Google Scholar] [CrossRef]
  50. Hong, R. Secalonic acid D as a novel DNA topoisomerase I inhibitor from marine lichen-derived fungus Gliocladium sp. T31. Pharm. Biol. 2011, 49, 796–769. [Google Scholar] [CrossRef]
  51. Zhao, J.; Li, L.; Ling, C.; Li, J.; Pang, J.Y.; Lin, Y.C.; Liu, J.; Huang, R.; Wang, G.L.; Pei, Z.; et al. Marine compound Xyloketal B protects PC12 cells against OGD-induced cell damage. Brain Res. 2009, 1302, 240–247. [Google Scholar] [CrossRef]
  52. Tao, L.Y.; Zhang, J.Y.; Liang, Y.J.; Chen, L.M.; Zhen, L.S.; Wang, F.; Mi, Y.J.; She, Z.G.; To, K.K.; Lin, Y.C.; et al. Anticancer effect and structure-activity analysis of marine products isolated from metabolites of mangrove fungi in the South China Sea. Mar. Drugs 2010, 8, 1094–1105. [Google Scholar] [CrossRef]
Mar. Drugs EISSN 1660-3397 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert