Kunlong Li
Jian Cai1,2
Yonghong Liu
Xuefeng Zhou
Huaming Tao- 1CAS Key Laboratory of Tropical Marine Bio-Resources and Ecology/Guangdong Key Laboratory of Marine Materia Medica, South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China
- 2College of Earth and Planetary Sciences, University of Chinese Academy of Sciences, Beijing, China
- 3School of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China
- 4State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China
A growing body of evidence indicates that glycosylated natural products have become vital platforms for the development of many existing first-line drugs. This review covers 205 new glycosides over the last 22 years (1997–2018), from marine microbes, including bacteria, cyanobacteria, and fungi. Herein, we discuss the structures and biological activities of these compounds, as well as the details of their source organisms.
Introduction
Sugars are ubiquitous in nature and have a multitude of functions, ranging from serving as a simple source of energy to contributing to molecular-recognition scaffolds that are critical to the interactions/communication among a wide array of biomolecules, cells, tissues, and organisms (Gantt et al., 2011). Not only do sugars work alone in the processes of life, but also they play an important role by combing with secondary metabolites. For instance, glycolipids are carbohydrate-attached lipids, which are widely distributed throughout organisms and involved in the biosynthesis of glycoproteins and serve as ligands for toxins, lectins, bacteria, and viruses. In addition, sugars are also attached to the anomeric carbon of a non-sugar moiety via a glycosidic linkage, such as quinones, lactones, peptides, terpenoids, and alkaloids etc., performed by more than 80 families of glycosyl transferases and those secondary metabolites derive multiple drugs, such as gentamycin, vancomycin, bleomycin, and erythromycin etc. (Grynkiewicz et al., 2008; Yu et al., 2012). Although some glycosides are simply attached to saccharides and saccharide parts in which glycosides are mostly inactive in terms of activity, sometimes they are crucial for overall effects, such as the improvement of a drug's pharmacokinetics and/or dose-limiting toxicities and the improvement for a drug's solubility and selective/non-selective uptake into cells/organs of interest (Gantt et al., 2011; Yu et al., 2012).
Oceans cover more than 70% of the Earth's surface and host considerable diversity of species. Approximately 30,000 marine natural products had already been identified by the end of 2017 (Jimenez, 2018). The roles of marine natural products in biomedical research and drug development are significant and promising. Many marine natural products have been in clinical stages and the interest in marine natural products is increasing every year (Wang L. et al., 2018). Among these compounds, seven structural types of approved therapeutic agents are considered derivatives of marine natural products, including two nucleosides—the anticancer cytarabine (ara-C, FDA-approved in 1969) and the antiviral vidarabine (ara-A, FDA-approved in 1976)—derived from two natural arabinonucleosides (Figure 1) (Dyshlovoy and Honecker, 2018). Hence, glycosides have served as a validated platform for the development of many existing front-line drugs (Blanchard and Thorson, 2006).
Figure 1. Two FDA-approved nucleosides.
Given the vital role of glycosides in drug discovery, this review provides a comprehensive overview of the structures and biological activities of 205 glycosides (discovered 1997–2018) from marine-sourced bacteria, cyanobacteria, and fungi, along with the details of their source organisms.
Discussion
Marine-Sourced Bacteria Derived Natural Products
Quinones
Four quinone-containing metabolites, halawanones A–D (1–4, Figure 2), have been isolated from Streptomycete sp. BD-18T(41) collected from shallow water sediment. The fraction containing halawanones A–B (1–2) exhibited inhibitory activity against Bacillus subtilis and Staphylococcus aureus at 100 μg/disk, but did not inhibit Escherichia coli at 100 μg/disk in a disk diffusion assay (Ford et al., 1998).
Figure 2. Chemical structures of compounds 1–17 derived from marine-sourced bacteria.
An anthracycline, komodoquinone A (5, Figure 2), with an amino sugar was isolated from the marine Streptomyces sp. KS3, derived from marine sediment. Komodoquinone A (5) was the first example of all anthracyclines and displayed neurogenic activity against a neuroblastoma cell line (Neuro 2A) at 1 μg/ml (Itoh et al., 2003). Four new anthracycline derivatives—(7S*9R*10R*)-pyrromycin (6), (7R*9R*10R*)-pyrromycin (7), 1-hydroxyauramycin T (8), and 1-hydroxysulfurmycin T (9, Figure 2)—were given by a strain Streptomycete sp. (CANU Fox 21-2-6) isolated from the mouth of the Fox River. The bioactivity evaluation showed that all four compounds displayed considerable cytotoxicity against P388 cultured cells, with 50% infectious dose (ID50) values ranging from 0.4 to 0.06 μg/ml (Phipps et al., 2004). Two anthracyclines, 5-iminoaranciamycin (10) and tetracenoquinocin (11), were isolated from a culture broth of Streptomyces sp. Sp080513GE-26, originally derived from the marine sponge, Haliclona sp. Tetracenoquinocin (11) exhibited modest cytotoxicity in HeLa and HL-60 cells (IC50 120 and 210 μM, respectively) (Motohashi et al., 2010).
Further chemical investigation of the actinomycete Saccharothrix espanaensis An 113, associated with the marine mollusk Anadara broughtoni, led to the isolation of two angucyclines saccharothrixmicine A (12) and B (13, Figure 2). Bioassay results indicated that the saccharothrixmicine-containing fraction exhibited activity toward Candida albicans and Xanthomonas sp. pv. Badrii (Kalinovskaya et al., 2008, 2010). Based on bioassay-guided analyses and the detection of genes encoding for the biosynthesis of secondary metabolites, the marine Streptomyces sp. strain HB202, which was isolated from the sponge Halichondria panacea, showed profound antibiotic activity and yielded a benz[α]anthracene derivative called mayamycin (14, Figure 2). This compound exhibited potent activity against several human cancer cell lines (IC50 0.15–0.33 μM) and inhibited growth of a number of bacteria including antibiotic-resistant strains (IC50 0.31–31.2 μM) (Schneemann et al., 2010).
Arenimycin (15, Figure 2) from a strain Salinispora arenicola CNR-647 associated with ascidian Ecteinascidia turbinate showed significant activity against HCT-116 cells (IC50 1.16 μg/ml). In addition, antibacterial testing with a panel of human Gram-positive pathogens—including various MRSA strains, such as Enterococcus feacalis and Enterococcus faecium—showed that arenimycin (15) exhibited MIC values at or <1 μg/ml (Asolkar et al., 2010). Isolated from the culture broth of Actinomadura sp., a polycyclic xanthone, IB-00208 (16, Figure 2), showed potent cytotoxic activity against several lines of human and murine tumor cell. Moreover, IB-00208 (16) exhibited considerable antibiotic activity against Gram-positive organisms (MIC 0.09–1.4 nM) (Malet-Cascon et al., 2003; Rodriguez et al., 2003). Pseudonocardians C (17, Figure 2), a diazaanthraquinone derivative, was produced by the strain SCSIO 01299, which is a marine actinomycete member of the genus Pseudonocardia and showed certain in vitro cytotoxic activities against the tumor cell lines, SF-268 (human glioma cell line), and MCF-7 (human breast adenocarcinoma cell line) with IC50 values of 6.70 and 8.02 μM, respectively (Li S. et al., 2011).
Gutingimycin (18, Figure 3) is a natural product with a trioxacarcin skeleton from Streptomyces B8652 isolated from a sediment (Maskey et al., 2002, 2004b). The same Streptomyces species also yielded trioxacarcins D–F (19–21, Figure 3) along with three known trioxacarcins, A–C. Bioactivity tests showed that trioxacarcins A–E exhibited strong antibacterial activity against a range of test organisms—including B. subtilis, Streptomyces viridoch-romogenes Tu 57, S. aureus, and E. coli—with MIC values of 0.15–2.5 μg/ml, compared with the MIC values >20 μg/ml for gutingimycin. In addition, an experiment against the large-cell lung cancer xenograft LXFL 529 in vitro indicated that the activity of trioxacarcin D (19) was similar to that previously reported for trioxacarcins A–C, with an IC50 value of 0.26 ng/ml (Maskey et al., 2004a). An unattainable bis-nitroglycosylated anthracycline, keyicin (22, Figure 3), was produced from coculturing of the producer Micromonospora strain with Rhodococcus. Biological activity indicated that it inhibited B. subtilis and methicillin-sensitive S. aureus (MSSA) with MIC values of 8 μg/ml (9.9 μM) and 2 μg/ml (2.5 μM), respectively (Adnani et al., 2017). Six natural products with antibiotic activity—dechromose-A chromomycin A2 (23), dechromose-A chromomycin A3 (24), chromomycin A2(25), chromomycin A3(26), 4B-O-demethylchromomycin (27), and chromomycin A4 (28, Figure 3)—were found from the marine sediment-associated strain Streptomyces sp. KMM 9048. Among them, compounds 23 and 24 were established as chromomycin analogs. Antimicrobial activity showed that compounds 25, 26, and 27 were mostly active against B. subtilis at concentrations of 4.1, 4.2, and 4.3 μM, respectively. In addition, at a concentration of 5 nM, compound 25 exhibited strong inhibition of colony formation of human melanoma RPMI-7951 and SK-Mel-28 cells by 82 and 72%, respectively (Kalinovskaya et al., 2017).
Figure 3. Chemical structures of compounds 18–36 derived from marine-sourced bacteria.
Three angucycline glycosides, designated grincamycins I–K (29–31, Figure 3), were isolated from the marine-derived actinomycete, Streptomyces lusitanus SCSIO LR32. In antitumor tests in five human cancer cells—namely MDA-MB-435, MDA-MB-231, NCI-H460, HCT-116, and HepG2—and human normal breast epithelial cell MCF10A cells, grincamycin J (30) showed cytotoxicity with IC50 values ranging from 2.6 to 5.4 μM; grincamycin I (29) showed strong cytotoxicity against MCF10A with an IC50 value of 2.9 μM; however, grincamycin K (31) did not exhibit cytotoxic activity. Structure–activity relationships suggested that classical angucyclines and the absence of the disaccharide at 3-O-position helped to enhance cytotoxic activity (Lai et al., 2018). With the application of the “Metal Stress” strategy for activating silent gene clusters, the Streptomyces pratensis strain NA-ZhouS1, isolated from marine sediment, produced two angucycline antibiotics stremycin A–B (32–33, Figure 3). The structures of 32 and 33 showed moderate antibiotic activities with equal MIC values of 16 μg/ml against Pseudomonas aeruginosa, MRSA, Klebsiella pneumonia, and Escherchia coli. In addition, both compounds showed inhibition against B. subtilis at an MIC value of around 8–16 μg/ml, respectively (Akhter et al., 2018).
Guided by a biochemical induction assay, two dimeric diazobenzofluorene glycosides, lomaiviticins A–B (34–35, Figure 3), were isolated from the halophilic actinomycete LL-37I366, which was found to be a new species, Micromonospora lomaivitiensis. Both showed potent DNA-damaging activity at a minimum induction concentration ≤0.1 ng/spot and lomaiviticin A (34) exhibited cleaved double-stranded DNA under reducing conditions. In an assay against a number of cancer cell lines, lomaiviticin A (34) also possessed a unique cytotoxicity profile with IC50 values ranging from 0.01 to 98 ng/ml as compared to those of known DNA-damaging drugs, such as adriamycin and mitomycin C. Both lomaiviticins A–B (34–35) also exhibited potent antibiotic activity against S. aureus and E. faecium (He et al., 2001). Continuous searching for benzo[b]fluorene led to the discovery of nenestatin A (36, Figure 3) produced from the deep sea-derived Micromonospora echinospora SCSIO 04089. Comparative bioinformatic analysis has indicated a high similarity of nenestatin A (36) and lomaiviticin gene clusters and has led to elucidation of similar biosynthetic pathways, including a conserved set of enzymes for the formation of a diazo group (Jiang X. et al., 2017).
Macrocyclic Lactones
With the application of bioassay-guided analyses, the macrolide antibiotic, chalcomycin B (37, Figure 4), was produced by the marine Streptomycete sp. B7064 derived from the mangrove sediment. Chalcomycin B (37) displayed activity against some microorganisms and microalgae (Asolkar et al., 2002). During the course of searching for bioactive secondary metabolites, the marine microbe Streptomycetes sp. strain HK-2006-1 from a marine sediment, produced six 16-membered macrolides, aldgamycins J–O (38–43, Figure 4), some of which exhibited strong antibacterial activity against S. aureus 209P, such as aldgamycins M–O (41–43), which possessed MIC values of 16–32 μg/ml. Structure–activity relationships showed that OH-8 and the double bonds from C-10 to C-13 were beneficial for antibacterial activities (Wang et al., 2016). Further investigation for the Streptomycetes sp. strain HK-2006-1 led to a macrolide, chalcomycin E (44, Figure 4; Jiang S. et al., 2017). 7-O-α-D-glucopyranoside (45, Figure 4), a macrolide with a rare α-D-glucopyranose substituent, was isolated from marine actinomycete Pseudonocardia sp. HS7, originated from the cloacal aperture of sea cucumber Holothuria moebii. A bioassay test indicated that compound 45 displayed modest activity against cancer cell lines with IC50 values of 20.84–81.01 μM (Ye et al., 2016). Further investigation for a strain of Streptomyces hygroscopicus OUPS-N92 obtained from the marine fish Halichoeres bleekeri led to a macrolide, halichoblelide (46, Figure 4), with potent cytotoxic activity against the murine P388 cell line and against 39 human cancer cell lines (Yamada et al., 2002). A glycosylated macrolide, macrolactin W (47, Figure 4), together with two known macrolides, macrolactins A and Q from the marine Bacillus sp. 09ID194 exhibited potent activity against B. subtilis (KCTC 1021), S. aureus (KCTC 1916), E. coli (KCTC 1923), and P. aeruginosa (KCTC 2592) with an MIC value of 64 μg/ml (Mondol et al., 2011).
Figure 4. Chemical structures of compounds 37–58 derived from marine-sourced bacteria.
Two derivatives of kijanimicin, lobophorins A–B (48–49, Figure 4), were produced from the fermentation broth of the marine actinomycete strain # CNC-837 obtained from the surface of the Caribbean brown alga, Lobophora variegate, and both of them exhibited potent antiinflammatory activities in a Phorbol-Myristate-Acetate (PMA)-induced mouse ear edema model (Jiang et al., 1999). Another two analogs, lobophorins C–D (50–51, Figure 4), produced by the actinomycete Streptomyces carnosus AZS17 obtained from marine sponges Hymeniacidon sp. Lobophorin C (50), displayed strong cytotoxic activity against the cellular proliferation of 7,402 hepatoma cells with an IC50 value of 0.6 μg/ml. In addition, lobophorin D (51) had a potent inhibitory effect on the growth of the human breast cancer cell line, MDA-MB 435, with an IC50 value of 7.5 μM (Wei et al., 2011). On the basis of bioassays, seven kijanimicin derivatives, microsporanates A–F (52–57) and tetrocarcin P (58, Figure 4), were isolated from the marine-derived Micromonospora harpali SCSIO GJ089. Among them, compounds 52–54 displayed vital growth-inhibiting activities against B. subtilis BS01 and Bacillus thuringiensis BT01, with MIC values of 0.016–0.5 μg/ml, and compounds 55–58 exhibited moderate activities against B. subtilis BS01 and B. thuringiensis BT01 with MIC values of 1.0–8.0 μg/ml (Gui et al., 2017).
Lipids
Two unique glycolipopeptides, ieodoglucomides A–B (59–60, Figure 5), were produced by the marine-derived bacterium Bacillus licheniformi and acted as broad spectrum, moderately active antimicrobial agents. In addition, ieodoglucomide B (60) displayed cancer growth inhibition against lung cancer (NCI-H23) and stomach cancer (NUGC-3) cell lines, with GI50 values of 25.18 and 17.78 μg/ml, respectively (Tareq et al., 2012). Based on bioassay-guided purification, strain Pseudomonas BNT1, isolated from Antarctic sub-sea sediments, produced two rhamnolipids (61–62, Figure 5), and in an antibacterial experiment, compound 61 had the lowest MBC values against Burkholderia cenocepacia (3.12 μg/ml) and S. aureus (3.12 μg/ml) (Tedesco et al., 2016).
Figure 5. Chemical structures of compounds 59–67 derived from marine-sourced bacteria.
Terpenoids
A acyl glyco-carotenoic acid, diapolycopenedioic acid xylosyl ester (63, Figure 5), was produced from the marine bacterium Rubritalea squalenifaciens, belonging to the first subdivision of Verrucomicrobia and possessed potent antioxidative activity with an IC50 value of 4.6 μM (10.9 μM for β-carotene) (Shindo et al., 2007). Another three analogs, diapolycopenedioic acid xylosyl esters A–C (64–66, Figure 5), were obtained from the marine bacterium R. squalenifaciens, which was isolated from the marine sponge Halichondria okadai. Of the three compounds, compound 64 exhibited 1O2 suppression activity with an IC50 of 5.1 μM (Shindo et al., 2008a). With the same 1O2 suppression activity as compound 64, methyl glucosyl-3, 4-dehydro-apo-8′-lycopenoate (67, Figure 5) was produced by the marine bacterium Planococcus maritimus strain iso-3 (Shindo et al., 2008b).
Alkaloids
Twelve indolocarbazoles 68–70, 71–76, and 77–79 (Figure 6) were isolated from the marine-derived Streptomyces sp. A68, Streptomyces sp. DT-A61, and Streptomyces sp. A65, respectively. Bioactivity testing showed that these indolocarbazoles had cytotoxic activities toward PC-3 cell lines with IC50 values of 0.8–41.3 μM. In addition, most of these indolocarbazoles also showed potent kinase inhibitory activities against protein kinase C alpha (PKCα), Roh associated protein kinase 2 (ROCK2), Bruton's tyrosine kinase (BTK), and apoptosis signal-regulating kinase 1 (AKS1). For instance, compound 7 displayed a notable inhibitory effect against ROCK2 with an IC50 value of 5.7 nM, which was similar to that of the positive control, staurosporine (IC50 = 7.8 nM). Structure–activity relationships for this set of indolocarbazoles suggested that when the sugar, connected with the K252c unit, was similar to that of staurosporine, the compound would be more effective than those without sugar moiety or those with only a single attachment of the sugar to the aromatic aglycone (Qin et al., 2018; Wang J. N. et al., 2018; Zhou et al., 2018).
Figure 6. Chemical structures of compounds 68–89 derived from marine-sourced bacteria.
Two rare N-glycosyl indoles, kahakamides A–B (80–81, Figure 6), were given by the actinomycete Nocardiopsis dassonvillei, isolated from a shallow water sediment sample. Bioassay testing indicated that kahakamide A (80) showed slight inhibition of B. subtilis in a disc-diffusion assay (Schumacher et al., 2001). From an actinomycete belonging to the family Nocardiopsaceae, Marinactinospora thermotolerans SCSIO 00652, methylpendolmycin-14-O-α-glucoside (82, Figure 6) was identified and found to exhibit antiplasmodial activities against the Plasmodium falciparum lines Dd2 and 3D7 with IC50 values of 5.03 and 10.43 μM, respectively (Huang et al., 2011). One deoxyuridine (83, Figure 6), obtained from the Streptomyces microflavus strain, No. HVG29, represents the first example of acetyl deoxyuridine from marine-derived actinomycetes which was isolated from the marine sponge, Hymeniacidon perlevis (Li K. et al., 2011). Tunicamycin E (84, Figure 6), a new natural nucleoside antibiotic, was isolated from marine-derived Streptomyces xinghaiensis SCSIO S15077 and exhibited moderate antifungal activity against B. thuringiensis, B. thuringiensis, and C. albicans with MIC values of 2.0, 0.5, and 8.0 μg/ml, respectively (Zhang et al., 2018).
A diketopiperazine glycoside, maculosin-O-α-L-rhamnopyranoside (85, Figure 6), was obtained from a culture of the marine-derived actinomycete Streptomyces sp. ZZ446. Bioassay testing showed that compound 85 displayed antimicrobial activity against methicillin-resistant S. aureus, E. coli, and C. albicans with MIC values of 27.0–37.0 μg/ml (Chen et al., 2018). Cyanogrisides A–D (86–89, Figure 6) were four bipyridine cyclic glycosides from the actinomycete Actinoalloteichus cyanogriseus WH1-2216-6. Cyanogrisides A (86) and C (88) were moderately cytotoxic to three multidrug resistant (MDR) and drug-sensitive parental cell lines, and cyanogrisides B (87) reversed the multidrug resistance of K562/A02,MCF-7/Adr, and KB/VCR cells at a concentration of 10 μM, with reversal-fold values of 1.7, 1.2, and 3.6, respectively (Fu et al., 2011).
Peptides
Based on a multi-drug resistant E. faecium (MREF) assay, two thiazolyl peptide glycosides, nocathiacins I–II (90–91, Figure 7), were isolated from the cultured broth of Nocardia sp. WW-12651 (ATCC 202099). The nocathiacins exhibited strong in vitro activity against a broad spectrum of Gram-positive bacteria, with MIC values of 0.1–60 ng/ml. In addition, they also showed good in vivo efficacy in a systemic S. aureus infection mouse model (Leet et al., 2003; Li et al., 2003). One peptide-polyketide glycoside totopotensamide A (92, Figure 7) produced by a Streptomyces sp. 1053U.I.1a.1b, cultivated from the gastropod mollusk Lienardia totopotens, contains a previously undescribed 2,3-diaminobutyric acid-containing macrolactam and an amino acid, 4-chloro-5,7-di- hydroxy-6-methylphenylglycin (Lin et al., 2012).
Figure 7. Chemical structures of compounds 90–103 derived from marine-sourced bacteria.
Other Classes
A flavonoid-like glycoside, actinoflavoside (93, Figure 7), was detected in the culture broth of the marine Streptomyces sp. CNB-689 and showed only weak antibacterial activity against Gram-positive bacteria (Jiang et al., 1997). Further biological and chemical investigation of Salinispora strains led to the discovery of a third species with this genus, Salinispora pacifica, which produced two chlorinated cyclopenta[α]indene glycosides, cyanosporasides A–B (94–95, Figure 7; Oh et al., 2006). Isolated from the marine actinomycetes Micromonospora matsumotoense M-412, the first compound of the paulomycin family lacking the paulomycose structure, paulomycin G (96, Figure 7), displayed excellent cytotoxic activities against several human tumor cell lines—such as MiaPaca_2, MCF-7, and HepG2—with IC50 values of 2.70, 1.58, and 4.30 μM, respectively (Sarmiento-Vizcaino et al., 2017).
Two antitumor pyranone glycosides, PM050511 (97) and PM0060431 (98, Figure 7), along with their aglycones PM050463 and PM060054, were obtained from the marine-derived Streptomyces albus, POR-04-15-053. Bioassay testing suggested that compounds 97–98 showed excellent cytotoxicity against three human tumor cell lines with GI50 values in the range of 0.24–2.69 μM (Schleissner et al., 2011). A cytotoxic piericidin derivative, glucopiericidin C (99, Figure 7), was isolated from the marine-derived Streptomyces species B8112 and showed a concentration-dependent cytotoxicity toward a panel of 36 human tumor cell lines with an IC50 value of 2.0 μM (mean IC70 = 4.2 μM), in addition to the same antibacterial activity as glucopiericidin A (Shaaban et al., 2011). One flavonoid derivative, flavoside A (100, Figure 7), was produced from the EtOAc extract of the culture broth of the sea urchin (Anthocidaris crassispina)-derived actinobacterium, Streptomyces sp. HD01 (Guo et al., 2019). According to the HPLC-UV profile, the Streptomyces sp. CMN-62 isolated from an unidentified sponge sample was selected for its chemical investigation and produced two anthranilate-containing alkaloids, anthranosides A–B (101–102, Figure 7; Che et al., 2018). Chemical analysis of these actinomycete strains using LC/MS identified a Streptomyces sp. SNM31 and led to a metabolite, mohangic acid E (103, Figure 7), which was the first glycosylated compound discovered in the p-aminoacetophenonic acid family and exhibited good quinone-reductase induction activity at a concentration of 20 μM (Bae et al., 2016).
Marine-Sourced Cyanobacteria Derived Natural Products
Macrocyclic Lactones
Lyngbya bouillonii Hoffmann and Demoulin is a “superproducer,” which is a filamentous, non-heterocystous, blue-green alga up to 50 μm wide (Klein et al., 1997). Guided by cancer viability assays and the aid of LC-MS, six macrolide glycosides—lyngbyaloside (104), lyngbyaloside B (105), lyngbouilloside (106), 2-epi-lyngbyaloside (107), and the regioisomeric 18E- and 18Z-lyngbyalosides C (108-109, Figure 8)—were isolated from L. bouillonii. Bioassay testing suggested that lyngbyaloside B (105) exhibited weak cytotoxicity against KB cells, with an IC50 value of 4.3 μM and showed a smaller effect on LoVo cells (IC50 ≈ 15 μM); additionally, lyngbouilloside (106) was only moderately cytotoxic to neuro-2a neuroblastoma cells (IC50 = 17 μM) (Klein et al., 1997; Luesch et al., 2002; Tan et al., 2002; Matthew et al., 2010).
Figure 8. Chemical structures of compounds 104–116 derived from marine-sourced cyanobacteria.
Bioassay-guided investigation of the marine cyanobacterium Lyngbya sp., collected in Okinawa Prefecture, led to an 18-membered macrolide glycoside, biselyngbyaside (110, Figure 8). Biselyngbyaside (110) exhibited broad-spectrum cytotoxicity in a panel of human tumor cell lines and likely inhibited cancer cell proliferation through a mechanism indicated by COMPARE analyses (Teruya et al., 2009). Chemical investigation of the marine cyanobacterium Lyngbya sp., collected from the Tokunoshima Island, Japan, led to three new analogs of biselyngbyaside (110), biselyngbyasides B–D (111–113, Figure 8). Biselyngbyaside B (111) was shown to induce apoptosis in HeLa S3 cells and HL60 cells. Further investigation of this activity in HeLa S3 cells indicated that apoptosis is likely mediated through increasing cytosolic Ca2+ concentrations (Morita et al., 2012).
The dimeric macrolide xylopyranoside, cocosolide (114, Figure 8), was obtained from the marine cyanobacterium preliminarily identified as Symploca sp. and reduced IL-2 production without significantly affecting cell viability. Comparison of the activities of analogs indicated the importance of sugars and dimeric structures to the target recognition and engagement process (Gunasekera et al., 2016). Bioassay-guided fractionation of the extract of Leptolyngbya sp., collected from the coast of Itoman City in the Okinawa Prefecture (Japan), led to the separation of two macrolactones, leptolyngbyolides A–B (115–116, Figure 8), both of which showed strong growth inhibition against HeLa S3 cells with IC50 values of 0.1 and 0.16 μM, respectively. In addition, structure–activity relationships suggested that the sugar moiety did not affect growth-inhibitory activity (Cui et al., 2017).
The polycavernoside analog, polycavernoside D (117, Figure 9), was isolated from a red-colored Okeania sp. and had moderate activity against the human lung carcinoma cell line H-460 (EC50 = 2.5 μM). Importantly, polycavernoside D (117) was obtained from the Atlantic, whereas polycavernosides previously isolated were derived from the Western Pacific, suggesting that these toxins occur over a much wider geographical range than originally thought (Navarro et al., 2015). Two glycosylated swinholides, ankaraholides A–B (118–119, Figure 9), were produced by the cyanobacterium, Geitlerinema sp., from a Madagascar field collection. Bioassay testing indicated that ankaraholide A (118) inhibited proliferation (IC50 values) in NCI-H460 (119 nM), Neuro-2a (262 nM), and MDA-MB-435 (8.9 nM) cell lines (Andrianasolo et al., 2005). Under bioassay-guided separation in combination with the MS2-based molecular-networking dereplication tool, nine glycosylated swinholide-type compounds, samholides A–I (120–128, Figure 9), were separated from the American Samoan marine cyanobacterium cf. Phormidium sp. All of these samholides showed potential activities against the human lung cancer cell line H-460 with IC50 values ranging from 170 to 910 nM. Comparison of the activities of these samholides suggested that the sugar and glyceric-acid units played important roles in enhancing the cytotoxic activity (Tao et al., 2018).
Figure 9. Chemical structures of compounds 117–128 derived from marine-sourced cyanobacteria.
Lipids
Further investigation of the marine cyanobacterium Lyngbya majuscula from Curafao yielded one glycoside metabolite, malynsamide J (129, Figure 10). Bioassay testing suggested that malynsamide J (129) was toxic to both brine shrimp and fish (Wu et al., 1997). Bartolosides A–D (130–133, Figure 10), which are unique glycolipids featuring aliphatic chains with chlorine substituents and C-glycosyl parts, were isolated from the filamentous cyanobacterium Nodosilinea sp. LEGE 06102 and Synecho-cystis salina LEGE 06155, respectively. The determination of the planar structure of bartolosides through key pathway intermediates illustrates the importance of genomics for structure elucidation. In addition, the biosynthesis of the diglycosylated dialkylresorcinol skeleton of bartolosides B–D (131–133) involves first the head-to-head condensation of an α, β-unsaturated fatty acyl-ACP thioester with a β-keto-fatty acyl-ACP thioester, catalyzed by the ketosynthase, BrtD (Leao et al., 2015). Another seven analogs, bartolosides E–K (134–140, Figure 10), produced from Synechocystis salina LEGE 06099, a strain closely related to the Synecho-cystis salina LEGE 06155 and bartoloside E (134), showed antitumor activities against the MG-63, RKO, and T-47D cell lines with IC50 values of 39, 40, and 22 μM, respectively (Afonso et al., 2016). One cerebroside, mooreaside A (141, Figure 10), was produced by the marine cyanobacterium Moorea producens, collected from the Red Sea and displayed moderate activity toward the MCF-7 cancer cell line with an IC50 value of 20.5 μM (Youssef et al., 2016).
Figure 10. Chemical structures of compounds 129–144 derived from marine-sourced cyanobacteria.
Alkaloids
Chemical investigation of the crude organic extract of L. majuscula from Puerto Rico resulted in the quinoline alkaloid 142 (Figure 10), the geometry of which was established as (E) by 1H-13C coupling constant measurements from HSQMBC NMR experiments (Nogle and Gerwick, 2003). Except for the mooreaside A (141), the marine cyanobacterium M. producens also yielded two nucleoside derivatives, 3-acetyl-2′-deoxyuridine (143) and 3-phenylethyl-2′-deoxyuridine (144, Figure 10), both of which showed moderate activity toward the MCF-7 cancer cell line with IC50 values of 18.2 and 22.8 μM, respectively (Youssef et al., 2016).
Marine-Sourced Fungi Derived Natural Products
Quinones
A anthracene glycoside, asperflavin ribofuranoside (145, Figure 11), was isolated from the marine-derived fungus Microsporum sp. Compound 145 showed radical scavenging activity against DPPH with an IC50 value of 14.2 μM and also exhibited moderate antibacterial activity against the methicillin-resistant and multidrug-resistant S. aureus with an MIC value of 50.0 μg/ml (Li et al., 2006). The xanthone O-glycoside, 3-O-(6-O-α-L-arabinopyranosyl)-β-D-gluco- pyranosyl-1,4-dimethoxyxanthone (146, Figure 11), was obtained from the mangrove endophytic fungus Phomopsis sp. ZH76 and was found to display cytotoxicity against HEp-2 and HepG2 cells with IC50 values of 9 and 16 μmol/ml, respectively (Huang et al., 2013). In the assessment of a library of marine-derived fungi (240 strains) for growth inhibitory activity against Mycobacterium phlei (M. phlei), the extract of the sponge-derived fungus Metarhizium anisopliae mxh-99 displayed promising levels of anti-M. phlei activity and produced two naphtho-γ-pyrones glycosides, indigotides G–H (147–148, Figure 11; Kong et al., 2013).
Figure 11. Chemical structures of compounds 145–156 derived from marine-sourced fungi.
Esters
The 3,4-dihydroisocoumarin derivative, R-(–)-mellein-8-O-β-D-glucopyranoside (149, Figure 11), was yielded from the marine-derived fungus Paraconiothyrium sporulosum YK-03 (Zhang et al., 2017). Another two isocoumarin glucosides, halorosellins A–B (150–151, Figure 11), were produced from a culture broth of the marine fungus, Halorosellinia oceanica 187q BCC 5149 (Chinworrungsee et al., 2002). Based on bioassay test, another two isocoumarin derivatives, acremonones H (152), and penicimarins D (153, Figure 11), were produced from the mangrove-derived fungus Acremonium sp. PSU-MA70 and the sponge-derived fungus, Penicillium sp. MWZ14-4, respectively (Rukachaisirikul et al., 2012; Qi et al., 2013). One mycophenolic acid derivative, penicacid B (154, Figure 11), was given by a fungus, Penicillium sp. SOF07 derived from a marine sediment in the South China Sea and was found to inhibit inosine-monophosphate dehydrogenase (IMPDH) (Chen et al., 2012). The marine-derived fungus Cosmospora sp. SF-5060, isolated from inter-tidal sediment, produced the depside derivative, aquastatin A (155, Figure 11). Aquastatin A was found to display potent selective inhibitory activity against protein tyrosine phosphatase 1B (PTP1B) with an IC50 value of 0.19 μM in a competitive manner (Seo et al., 2009). Another C-glycosidic depside, stromemycin (156, Figure 11), was identified from the crude extract of the fungus Emericella variecolor derived from the marine sponge Haliclona valliculata (Bringmann et al., 2003).
Lipids
Two cerebroside analogs, flavicerebrosides A and B (157–158, Figure 12), were obtained from the cultivated mycelium of the marine-derived fungus Aspergillus flavipes, isolated from the sea anemone Anthopleura xanthogrammica and exhibited cytotoxic activity against the KB cell line with IC50 values of 20.1 and 14.3 μg/ml, respectively (Jiang et al., 2004). The Quanzhou marine fungus Aspergillus niger (MF-16) produced another two cerebrosides, asperiamides B and C (159–160, Figure 12; Wu et al., 2008). With the constant effort to isolate microbes from hypersaline environments, the marine-derived halotolerant fungal strain (THW-18), Alternaria raphani, was isolated and afforded three cerebrosides, alternarosides A–C (161–163, Figure 12). Bioassay testing indicated that compounds 161–163 showed small antibacterial activity against E. coli, B. subtilis, and C. albicans (Wang et al., 2009). Flavusides A–B (164–165, Figure 12), two new antibacterial cerebroside derivatives, were identified from the fermentation broth of the marine-derived fungus Aspergillus flavus and showed weak inhibitory activities against S. aureus and methicillin-resistant S. aureus (Yang et al., 2011).
Figure 12. Chemical structures of compounds 157–173 derived from marine-sourced fungi.
In order to explore bromodomains (BRD) inhibitors, the secondary metabolites of Alternaria sp. NH-F6, a fungus obtained from deep-sea sediment samples, were analyzed and led to a cerebroside (166, Figure 12) along with two perylenequinones (Ding et al., 2017). Under continuous searching for bioactive natural products from Red-Sea marine-derived fungi, the fungus Penicillium was isolated from the tunicate Didemnum and led to two cerebrosides, penicillosides A–B (167–168, Figure 12). In an agar diffusion assay, penicilloside A (167) exhibited antifungal activity against C. albicans, while penicilloside B (168) showed antibacterial activities against S. aureus and E. coli (Murshid et al., 2016). Four highly methylated glycolipids—roselipins 1A (169), 1B (170), 2A (171), and 2B (172, Figure 12)—were obtained from the marine fungus Gliocladium roseum KF-1040. In an enzyme assay system using rat liver microsomes, roselipins inhibited the enzyme, diacylglycerol acyl transferase (DGAT) with IC50 values of 17–22 μM (Omura et al., 1999; Tabata et al., 1999). One fatty acid, glucoside (173, Figure 12), was isolated from the endophytic fungus A1 of mangrove plant, Scyphiphora hydrophyllacea Gaertn. F. Through using a filter-paper disc-agar-diffusion method, compound 173 possessed modest inhibitory activity on Staphylococcus aureus and methicillin-resistant S. aureus (Zeng et al., 2012).
Terpenoids
The fungus Acremonium striatisporum was originally obtained from the holothurian Eupentacta fraudatrix, and multiple investigations for metabolites of this strain led to the isolation of 21 glycosides, namely virescenosides M–X (174–185), Z (186), R1-R3 (187–189), and Z4-Z8 (190–194, Figure 13). Bioassay testing showed that virescenosides M–U (174–182) displayed cytotoxic action against tumor cells Ehrlich carcinoma (IC50 = 10–100 μM) in vitro. In addition, virescenosides M–N (174–175) and P (177) displayed cytotoxic effects on developing eggs of the sea urchin, Strongylocentrotus intermedius (IC50 = 2.7–20 μM) (Afiyatullov et al., 2000, 2002, 2004, 2006, 2011, 2016). Two phenylspirodrimane-type glucosidic meroterpenoids, stachybosides A–B (195–196, Figure 13), were seperated from the sponge-derived fungus, Stachybotrys chartarum MXH-X73 (Ma et al., 2013). The polyketide glycoside, cladionol A (197, Figure 13), was produced from the culture broth of the fungus Gliocladium sp. L049 collected from the sea grass Syringodium isoetifolium and was found to exhibit modest cytotoxicity against murine leukemia L1210 cells and human epidermoid carcinoma KB cells with IC50 values of 5 and 7 μg/ml, respectively (Kasai et al., 2005). The carotenoid glycosyl ester, neurosporaxanthin β-D-glucopyranoside (198, Figure 13), was isolated from cultured cells of the marine microorganism, Fusarium sp., collected from the seawater surface and was the first naturally occurring neurosporaxanthin glycoside that was discovered (Sakaki et al., 2002).
Figure 13. Chemical structures of compounds 174–198 derived from marine-sourced fungi.
Other Classes
Three polyketide glucosides containing a pyrone ring—neofusapyrone (199), fusapyrone (200), and deoxyfusapyrone (201, Figure 14)—were obtained from the marine-derived fungus Fusarium sp. FH-146. All three compounds exhibited moderate active against Aspergillus clavatu with MIC values of 6.25, 25, and 3.12 μg/ml, respectively (Hiramatsu et al., 2006). The fungus Aspergillus sydowii derived from the marine sponge, Stelletta sp., produced the β-D-glucopyranosyl, aspergillusene A (202, Figure 14), which was the first glycoside of phenolic bisabolane sesquiterpenes that was discovered and exhibited mild antitumor activities against KB, HepG2 and HCT-116 cell lines (Liu et al., 2017). Three hydroquinone glycosides—acremonin A1-O-β-D-glucopyranoside (203), gliomastin E1-O-β-D-glucopyranoside (204), and 6′-O-acetyl-isohomoarbutin (205, Figure 14)—were isolated from the marine-derived fungus, Gliomastix sp., originally derived from the hard coral, Stylophora sp. (Elnaggar et al., 2017).
Figure 14. Chemical structures of compounds 199–205 derived from marine-sourced fungi.
Conclusions
According to an estimation, ~70% of global drug leads derive directly from natural products, many of which are glycosylated metabolites (Thorson et al., 2001). Chemical investigation for 205 glycosides of the last 22 years (1997–2018) suggests that these compounds are classified as quinones, macrocyclic lactones, esters, lipids, terpenoids, alkaloids, peptides, and other classes. Macrocyclic lactones and quinone glycosides comprise roughly 42% of all these compounds (Figure 15A), and bacteria were the main source of new glycosides at 50% (104/205) (Figure 15B). Given the importance of glycoprotein to many biological processes, although peptide glycosides only account for 1% of these compounds, the peptide glycosides have a considerable potential for the discovery of drug leads.
Figure 15. The percent of each class glycosides out of all glycosides (A); the distribution of each class glycosides in marine microbes (B); the percent of each class bioactive glycosides out of all glycosides (C).
In this review, the bioactivities of 129 glycosides were summarized in Tables S1–S3. In measured activities for these compounds, more than 50% (Figure 15C) display antitumor and antimicrobial activities, some of which also possess strong cytotoxicity. For example, IB-00208 (16) had a strong antibiotic activity against Gram-positive organisms with MIC values ranging from 0.09 to 1.4 nM, and lomaiviticin A (34) had a unique cytotoxicity profile against cancer cell lines with IC50 values ranging from 0.01 to 98 ng/ml. At present, two FDA-approved marine drugs, ara-C and ara-A, are antitumor and antiviral nucleosides, which are consistent with the main activity summarized in this review. This suggests that antitumor and antimicrobial drugs may be the main research direction for marine natural products. In addition, some glycosides also exhibited enzyme-inhibitory, antioxidative, DNA-damaging, anti-inflammatory, and anti-plasmodial activities. The recent in-depth study of glycosides has revealed their dynamic potential as therapeutic agents in the treatment of different disorders. Based on these findings, it may be possible to discover and develop glycosides with higher selectivities and efficacies.
Author Contributions
KL and XZ designed and elaborated the manuscript. JC, ZS, BY, XZ, and YL added valuable comments. XZ, JH, and HT critically revised and improved the manuscript. All authors read and approved the final version of the manuscript.
Funding
This research was supported by grants from the Guangdong MEPP Funds (GDME-2018C010, GDOE[2019]A28, 2019-017), National Natural Science Foundation of China (81973235 and 21977102), Drug Innovation Major Project of China (2018ZX09735001-002-003), Guangzhou Science and Technology Project (201804010462), Guangdong Basic and Applied Basic Research Foundation (2018A0303130219 and 2019B151502042), and Project from Institution of South China Sea Ecology and Environmental Engineering, CAS (No. ISEE2018PY04).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2019.00879/full#supplementary-material
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Keywords: marine microbes, bacteria, cyanobacteria, fungi, glycosides
Citation: Li K, Cai J, Su Z, Yang B, Liu Y, Zhou X, Huang J and Tao H (2020) Glycosylated Natural Products From Marine Microbes. Front. Chem. 7:879. doi: 10.3389/fchem.2019.00879
Received: 15 October 2019; Accepted: 05 December 2019;
Published: 10 January 2020.
Edited by:
Huiming Ge, Nanjing University, ChinaReviewed by:
Michele Mari, Department of Biomolecular Sciences, School of Pharmacy, University of Urbino Carlo Bo, ItalyCheng Fang, Biogen Idec, United States
Copyright © 2020 Li, Cai, Su, Yang, Liu, Zhou, Huang and Tao. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xuefeng Zhou, xfzhou@scsio.ac.cn; Jingxia Huang, 13694217880@163.com; Huaming Tao, taohm@smu.edu.cn