Species Diversity and Secondary Metabolites of Sarcophyton-Associated Marine Fungi

Soft corals are widely distributed across the globe, especially in the Indo-Pacific region, with Sarcophyton being one of the most abundant genera. To date, there have been 50 species of identified Sarcophyton. These soft corals host a diverse range of marine fungi, which produce chemically diverse, bioactive secondary metabolites as part of their symbiotic nature with the soft coral hosts. The most prolific groups of compounds are terpenoids and indole alkaloids. Annually, there are more bio-active compounds being isolated and characterised. Thus, the importance of the metabolite compilation is very much important for future reference. This paper compiles the diversity of Sarcophyton species and metabolites produced by their associated marine fungi, as well as the bioactivity of these identified compounds. A total of 88 metabolites of structural diversity are highlighted, indicating the huge potential these symbiotic relationships hold for future research.


Soft Corals
Soft corals, also known as octocorals, are Anthozoans (Ehrenberg, 1834) classified under the subclass Octocorallia (Haeckel, 1866). They belong to the Phylum Cnidaria, making them closely related to the sea anemones, hard corals and jellyfishes. Unlike hard corals that are the building blocks of the coral reef, soft corals act as shelter for juvenile fishes and food to some marine organisms. As the name octocoral is derived from Latin "octo", which means eight, soft coral species comprise of eight-tentacle polyps and eight mesenteries, with minimal variance within the clade. The polyp in octocorals is an individual zooid, and they together play important roles in the essential functions of a colony, including growth, food capture, transport of nutrients, defence, irrigation of seawater and reproduction [1]. As suspension feeders, soft coral food intake relies on environmental conditions, especially water currents [2]. For small organic particles (<20 mm), octocoral polyps can filter them from the water column, whereas larger particles (such as zooplankton and larvae) could be captured or intercepted by the tentacles. Since octocorals have simple stinging cells (nematocysts), their food is restricted to weaklyswimming, small plankton [3].
Octocorals are widely distributed, with their presence recorded from the intertidal zone to depths up to 6400 m and from tropical to polar regions [4]. Their distribution is heavily influenced by several environmental factors, for example, distance from the coast, suspended organic matter and the presence of strong currents [5]. For instance, the distribution of cold-water species is closely related to salinity, temperature, productivity, oxygen, the broad scale of the highest diversity of soft corals in the world, of which are mostly endemic [6,7]. However, the greatest diversity of octocorals is recorded in

Diversity of Sarcophyton
In 1982, Verseveldt revised the classification scheme of Sarcophyton based on a systematic examination of the morphology and microscopic images of Sarcophyton-like specimens [14]. According to his revision on Sarcophyton taxonomy, the genus Sarcophyton contained 35 valid species, and since then, there have been reports on new species of Sarcophyton. To date, there have been approximately 50 Sarcophyton species as shown in Table 1. Most Sarcophyton species were identified in the Indo-Pacific regions. Table 1. Sarcophyton species diversity.

Sarcophyton-Fungal Associations
Coral-associated microbes consist of endolithic algae, endosymbiotic dinoflagellates, bacteria, fungi, alveolates, archaea, and viruses. The consortium of coral and its associated internal and external microbes is often considered as the holobiont [43,44]. The associated microorganisms provide extra carbon and nitrogen sources for their host, as well as play a part in detoxification, nutrient cycling, genetic exchange, ultra violet (UV) protection, and chemical defence [43,45]. In some populations of gorgonian, fungal diseases are common, but relatively few investigations have been conducted on the causal marine fungi from these octocorals [43]. In particular, the genera Aspergillus and Penicillium have often been found in the Caribbean Gorgonia ventalina [46,47], Leptogorgia species distributed in the Eastern Pacific regions [48], and many octocorals in the South China Sea [49] as well as Singapore [50]. Other frequently identified octocoral-associated fungi include the genera Cladosporium [46][47][48], Fusarium [48,50,51], Nigrospora [48,51], and Tritirachium [46][47][48]50]. As for the soft coral genus Sarcophyton, Aspergillus terreus was obtained from the Sarcophyton subviride, which was collected from the coast of Xisha Island in the South China Sea [52]. The marine fungus Penicillium bialowiezense was also isolated from the same soft coral species [53]. Additionally, Chondrostereum sp. was isolated from Sarcophyton tortuosum of the South China Sea as well [54].
The surrounding environment and host substrate have an impact on the composition of fungal communities [51], with a varied abundance of the most common associated fungal species. Knowledge of the fungal isolates is mainly obtained from culture-based techniques, thus favouring species likely to be cultivated in the laboratory conditions [50,51]. Nonetheless, cultured marine fungi have been a promising reservoir of bioactive secondary metabolites, usually with unique chemical structures, thus making octocoral-derived fungi potential bio-prospecting sources [13]. Despite limited knowledge about the exact ecological functions of these fungal species, some possess potential antifungal, antibacterial properties and might have a role in maintaining holobiont health and regulating the microbiome [13]. Table 2 summarises the soft coral Sarcophyton and its associated fungi.

Metabolites of Marine Fungi Derived from Sarcophytons
Marine organisms are an important source of natural products with potential for drug discovery. To date, more than 40,000 marine natural products (MNPs) have been identified from the marine environment. Coral reefs are among the most productive ecosystems and exhibit a large group of structurally unique biosynthetic products [60]. The coral reef is a prolific source of metabolites synthesised by a wide range of organisms such as sponges, cnidarians, tunicates, molluscs, echinoderms, bryozoans, macroalgae and microorganisms. Interestingly, recent records have shown an upward trend in MNPs from marine microorganisms, with approximately 57% of the total metabolites reported in 2017 [60]. These MNPs can be classified into terpenoids, alkaloids, steroids, lactones, polyketides, peptides, phenols, and lipids based on their biosynthesis pathways. Most of these metabolites are of pharmaceutical interest due to the varying bioactivity exhibited, such as cytotoxic, antimicrobial, anti-inflammatory, antimalarial, and antidiabetic activities [61].
Due to the lack of calcium carbonate skeletons for physical protection, soft corals depend heavily on chemical defence mechanisms in order to resist predators and prevent overgrowth and fouling by accumulating a variety of secondary metabolites in their bodies and releasing them to the environment [62]. The soft coral genus Sarcophyton hosts a wide diversity of marine fungi that interacts with the soft corals in multiple ways. The microorganisms are expected to synthesise various secondary metabolites to adapt and survive in their cohabitating environment either as a symbiont or as a parasite [62]. The fungal genus Aspergillus, for instance, was once thought to be pathogenic; however, it was not only found in diseased gorgonians but also healthy ones [46]. Therefore, it is now considered as an opportunist rather than a pathogen. Soft coral-associated fungi have an influence on the maintenance of holobiont health and regulation of the microbiome. Previous studies have demonstrated that coral-associated bacteria communities regulate the settlement of bacteria on the coral surface, thus controlling the resistance against coral disease [63]. The protective mechanisms include competition for food and space, as well as the production of antibiotics from the mucus or coral tissues [45]. Although corals naturally produce a mucus microbiome as a defence system against pathogens [64], changes in the microbiome could lead to the emergence of coral diseases. However, associated bacterial communities produce antibiotic metabolites to inhibit the settlement and growth of many pathogenic species, like Vibrio coralliilyticus, V. shiloi and Serratia marcescens [45]. Even though there is no such study carried out on associated fungi, they could play a similar role to coral-associated bacteria.
The conventional view of microbial symbionts has been that their biosynthesis of natural products contributes greatly to the wide range of metabolites from sessile marine invertebrates. In the case of sponges, there have been debates on the source of metabolites from this organism. Eventually, it was determined that the microorganisms within are the main contributors of secondary metabolites [65]. In the case of hard corals, the production of mycosporin amino acids (MAA) provides protection for the corals against solar radiation [66]. Similarly to the relationship between fungi and soft corals, the metabolites produced by the fungi are of interest. The bioactivity exhibited can be associated with the protective role of the soft corals. Additionally, this work also confirms that the metabolites produced by the fungi are totally different from those reported from the soft corals, ascertaining that the soft coral metabolites are synthesised by the coral itself. Even though most octocoral-derived marine fungi are obtained through cultivation-dependent methods, these fungi produce a variety of bioactive natural products, usually exhibiting an unusual chemical structure [13]. Thus, octocoral-derived fungi provide a great candidate for bioprospecting. The following sections compile the soft coral-fungal associated metabolites that have been reported over the years 2010-2020. Most of the secondary metabolites belong to the chemical sgroup sesquiterpene and indole alkaloid. A list of compounds with bio-activity is shown in Table 3.  (70) significant anti-inflammatory activity against NO production [52] territrem A (72) lovastatin (75) Penicillium bialowiezense 8-O-methyl mycophenolic acid (78) 3-hydroxy mycophenolic acid (79) 6-(5-carboxy-3-methylpent-2-enyl)-7-hydroxy-3,5dimethoxy-4-methylphthalan-1-one (80) inhibitory activity against inosine-50-monophosphate dehydrogenase (IMPDH2) 6-(5-methoxycarbonyl-3-methylpent-2-enyl)-3,7dihydroxy-5-methoxy-4-methylphthalan-1-one (81) 6-(3-carboxybutyl)-7-hydroxy-5-methoxy-4methylphthalan-1-one (82) and [53] 6-[5-(2,3-dihydroxy-L-carboxyglyceride)-3methylpent-2-enyl]-7-hydroxy-5-methoxy-4methylphthalan-1-one (83) in vitro immunosuppressive activity against the proliferation of T-lymphocytes

Terpenoids Sesquiterpene
Soft-coral associated fungi are reported to be an important source of sesquiterpenes. The earliest reports on sesquiterpenes from soft-coral associated fungi are the isolation and characterisation of the hirsutane sesquiterpenes hirsutanol A (1), E (2) and F (3) in 2011 from the marine fungus Chondrostereum sp., which was isolated from the soft coral Sarcophyton tortuosum [67]. The laboratory-cultured fungal isolate was extracted in over ethyl acetate prior to fractionation using petroleum ether (Petr Eth), ethyl acetate (EtOAc) and methanol (MeOH) as a mobile phase. A 60% gradient reverse phased high-performance liquid chromatography (RP-HPLC) profiling led to the isolation of the hirsutanols A (1), E (2) and F (3). Initial reports on hirsutanol A (1) were from the marine sponge Jaspis cf. johnstoni fungal isolate in 1986, which was also isolated from an unidentified fungal strain from the Haliclona sponge along with hirsutanol F (3) [73]. Hirsutanol E (2) (C l5 H 24 O 3 ) comprises of three methyls, five methylenes, two methines, five quaternary carbons, and three hydroxy groups. According to nuclear magnetic resonance (NMR) and single-crystal X-ray diffraction data, the structure of hirsutanol F (3) was regarded the same as gloeosteretriol, despite the opposite optical rotations [67]. Hirsutanol A was characterised as C l5 H 18 O 3 with potential cytotoxicity against many types of human cancer cell lines and induction of autophagical cell death through increased Reactive Oxygen Species (ROS) levels. An investigation into the anticancer mechanism of hirsutanol A (1) towards MCF-7 breast cancer cells exhibited the inhibition of cell proliferation, enhanced ROS production, apoptosis and autophagy. Hirsutanol A (1) could lead to apoptosis and autophagy through accumulated ROS production, and MCF-7 cells could be sensitised if co-treated with an autophagy inhibitor [74]. The bioactivity of hirsutanol A (1) was attributed to the presence of an α-methylidene oxo group, which was absent in hirsutanols E (2) and F (3) [67].
In 2012, an additional hirsutane type sesquiterpene, hirsutanol C (4) was isolated along with five triquinane-type sesquiterpenoids, chondrosterins A-E (5-9) from the fungus Chondrostereum sp. isolated from tissues of Sarcophyton tortuosum [54]. The isolated fungi were laboratory-cultured in potato dextrose broth (PDB) medium that was eventually extracted over EtOAc. A two-stage column chromatography fractionation with Petr Eth/EtOAc followed by EtOAc/MeOH and an RP-HPLC purification with a 60-100% acetonitrile (MeCN) gradient system through a Shim-Pack Octadecylsilyl (ODS) column (250 × 20 mm) yielded hirsutanol C (4). Subsequent Sephadex LH-20 gel column chromatography and RP-HPLC purification of the fungal fractions yielded chondrosterins A-E (5-9) [54]. Hirsutanol C (4), C 15 H 20 O 3 , isolated as powder, was previously characterised by Wang et al. (1998) [73] from an unidentified fungus of the marine sponge Haliclona sp. that yielded the hirsutanols A (1) and F (3) [54]. The relative configuration of hirsutanol C (4) was determined via single-crystal X-ray diffraction. It was inactive against the human lung cancer cell line (A549), human nasopharyngeal carcinoma cell line (CNE2), and human colon cancer cell line (LoVo) at IC 50 (half maximal inhibition concentration) concentrations >200 μM [54]. Chondrosterins A (5) and B (6) were both isolated as yellowish oil. With the presence of a α-methylene ketone group in its tricyclic system, chondrosterin A (5) showed significant cytotoxic activities against various cancer lines A549 (IC 50 = 2.45 μM), CNE2 (IC 50 = 4.95 μM), and LoVo (IC 50 = 5.47 μM) [54]. The metabolites from Chondrostereum sp. cultured in PDB medium showed a difference from those in the glucose peptone yeast (GPY) medium. This investigation also evaluated the difference in metabolite presence through alteration of the fermentation conditions, such as the ratios of the carbon and nitrogen source and inorganic salts, leading to the detection of the previously reported hirsutanol E (2) in the GPY culture strain. This confirms that the Chondrostereum sp. is able to produce diverse hirsutane derivatives under different conditions [54] Chondrosterin C (7) is a compound with a hydroxyl, ketone carbonyl, α,β-unsaturated carbonyl functionality, and its planar skeleton is determined entirely by 1 H-1 H correlated spectroscopy (COSY) and Heteronuclear Multiple Bond Correlation (HMBC) analysis [54]. Chondrosterin D (8) was isolated as a colourless crystal. Similar to chondrosterin C (7), this compound also possesses three ketone carbonyl groups. Infrared absorptions at 1737, 1687 and 1610 cm −1 confirmed the presence of ketones and α,β-unsaturated carbonyls. X-ray crystallography was used to confirm its relative configuration [54]. The fifth compound from the cultured Chondrostereum sp. is chondrosterin E (9), which was reported as a white solid. Compared to the other metabolites isolated from this study, chondrosterin E (9) is the only compound where the carbonyl was positioned at C-5 instead of C-4 [54].
In a separate study, following the successful characterisation of chondrosterins A-E (5-9), additional hirsutane sesquiterpenoids chondrosterin F (10), incarnal (11) and anthrosporone (12) were reported from the soft coral species Sarcophyton tortuosum-associated marine fungus Chondrostereum sp. collected from South China Sea in 2013 [68]. Using the similar culture and isolation protocol involving two stages of column chromatography followed by RP-HPLC purification as the previously mentioned metabolites, chondrosterin F (10) was isolated in the form of a colourless oil. This compound was determined to have a rearranged hirsutane skeleton believed to be caused by the migration of a methyl functionality from C-2 to C-3 as well as the formation of a lactone through the conversion of a cyclic ketone [68].
The hirsutane incarnal (11), a compound previously first reported from fungus Gloeostereum incarnatum, was isolated as red solids from the soft-coral-associated Chondrostereum sp. [68]. Compared to the reference data, the J value coupling constant of the protons H-11α and H-11β reported in this study was calculated as 14.0 Hz instead of an oddly lower value of 5.1 Hz that was previously reported. Incarnal (11) [68]. Based on these data, it is evident that the α-methylene ketone functional group plays an important role in the cytotoxic activities of hirsutane sesquiterpenoids. Arthrosporone (12) is another hirsutane sesquiterpenoid originally reported from an unidentified arthroconidial fungus and Macrocystidia cucumis [75]. In comparison with chemical data from the literature, it was confirmed that arthrosporone (12) was also produced by the investigated soft-coral-associated fungi. Arthrosporone (12) was not reactive in oxidation reactions, which is a common characteristic of the tertiary hydroxyl groups present in the compound [68].
In 2014, two more hirsutane sesquiterpenoids, chondrosterins I and J (13 and 14), were obtained from yet again the marine fungus Chondrostereum sp., which originated from Sarcophyton tortuosum and cultured in a liquid medium with glycerol as the carbon source [69]. The compounds were isolated through repeated Petr Eth/EtOAc and EtOAc/MeOH column chromatography on the EtOAc extract followed by RP-HPLC purification. Though cultured in a different medium, the fungal extract contained the previously reported hirsutanol A (1), chondrosterins A (5) and incarnal (11). Compared to the previously mentioned hirsutane sesquiterpenoids, chondrosterins I (13) and J and (14) exhibited a switch in methyl position from C-2 to C-6 and a presence of carboxylated methyl at C-3 [69]. Chondrosterin I (13) was isolated as a colourless solid. The absolute configuration of chondrosterin I (13) was determined as 1R, 6S, 8S and confirmed by X-ray single-crystal diffraction. Chondrosterin J (14) was isolated as a white solid. The absolute configuration for this compound was established as 1R, 6S, 7S, 8S. These compounds were screened for cytotoxicity against the human nasopharyngeal cancer cell line CNE-1 and CNE-2, where chondrosterin J (14) was cytotoxic against CNE-1 and CNE-2 cell lines with the IC 50 values of 1.32 and 0.56 μM [69].
The mycelia of Chondrostereum sp. of Sarcophyton tortuosum cultured in GPY liquid medium was reported to contain four sesquiterpenoids, which included three triquinanetype sesquiterpenoids, chondrosterins K-M (15-17) and a previously identified metabolite, anhydroarthrosporone (18) [70]. A similar fractionation and purification technique was applied in order to isolate and characterise the compounds 15-18. The use of GPY medium often results in an altered metabolite profile compared to those cultured in PDB medium. Chondrosterin K (15), C 15 [70].
Further investigation into the Sarcophyton tortuosum-derived fungi Chondrostereum sp. cultivated in GPY medium continued to yield two more additional hirsutane-type sesquiterpenoids, chondrosterins N (19) and O (20) [55]. These were isolated from its EtOAc extract after repeated column chromatography followed by RP-HPLC over a 70% MeCN mobile phase [55]. Both chondrosterins N (19) and O (20) were isolated as colourless oil. Chondrosterin N (19) is comprised of an α, β-unsaturated carbonyl chromophore as indicated by UV absorption at 239 nm. On the other hand, chondrosterin O (20) was identified as a stereoisomer to chondrosterin N (19). Both compounds were initially determined as identical based on 1 H-1 H COSY and HMBC spectra; however, the differences in the chemical shifts of H-4 and its coupling constants were able to distinguish these compounds from each other [55]. They were screened against seven cancer cell lines: CNE1, CNE2, HONE1, SUNE1, A549, GLC82 and HL7702, and were categorised as inactive with IC 50 values exceeding 100 μM. Chemical structures of all the highlighted I-associated fungi hirsutane sesquiterpenes are exhibited in Figure 1.

Alkaloids Indole Type Alkaloid
Indoles are bicyclic molecules built by a six-membered benzene ring fused to a fivemembered pyrrole ring. These compounds are commonly produced by a wide variety of microorganisms. As for the Sarcophyton associated fungi, in 2013, two cytochalasin compounds, aspochalasin A1 (21) and cytochalasin Z24 (22), were reported from a Sarcophyton sp.-derived marine fungi Aspergillus elegans, originating from the South China Sea [58]. The alkaloids reported in this study were isolated from the EtOAc extract that was subjected to a petroleum ether/EtOAc followed by a chloroform (CHCl 3 ) fractionation over Sephadec LH-20 [58]. The reported compounds were purified over HPLC using an ODS Kromasil C18 column with the mobile phase between 60 to 85% MeOH. Aspochalasins are a subgroup of cytochalasans, consisting of a macrocyclic ring, isoindolone moiety and a 2-methyl-propyl side chain. According to high-resolution electrospray ionisation mass spectrometry (HRESIMS), aspochalasin A1 (21), isolated as a white powder, was characterised as C 24 H 35 NO 5 . The presence of a (2-methylpropyl) isoindolone moiety is an indication of aspochalasin A1 (21) from a typical cytochalasin skeleton [58]. Cytochalasin Z24 (22) was also isolated as a white powder and possesses a 10-phenyl-substituted 6,7epoxyperhydroisoindol-1-one type skeleton. Both compounds, aspochalasin A1 (21) and cytochalasin Z24 (22), were determined to share identical macrocyclic properties similar to other known cytochalasins reported. The absolute configuration of cytochalasin Z24 (22) was determined as 3S,4S,5S,6R,7S,8S,9S,13E,16S,18S,19E [58]. Eight additional cytochalasin-derivatives (23-30) were also reported from the Aspergillus elegans [58]. All these cytochalsins were previously reported from various sources of fungi from the genus Aspergillus. Aspochalasins B (23), a yellowish powder and D (24), were previously reported from the Aspergillus niveus that was associated with a marine crustacean [77], while aspochalasin H (25) was first identified from the aspochalasin Dproducing strain, Aspergillus sp. The common detection of a broad infra-red band at 1685 cm −1 shows the presence of lactone and ketone carbonyl in aspochalasins B (23) and D (24). The carbon position C-18 of aspochalasin D (24) was attached to a hydroxyl moeity instead of a carbonyl as in aspochalasin B (23). Aspochalasin H (25), C 24 H 35 NO 5 was isolated as a colourless powder [78] and was reported to have an identical stereochemistry to aspochalasin D (24). Additionally, the double bond between carbons C-19 and 20 was replaced by an epoxy in aspochalasin H (25), which differed both these compounds structurally. Aspochalasins I (26) and J (27) were obtained from Aspergillus flavipes associated with the rhizosphere of Ericameria laricifolia, a turpentine bush [79]. Aspochalasin I (26) was isolated as a white powder [79], while aspochalasin J (27) was isolated as a white solid. The difference between aspochalasins (26) and J (27) was the presence of only one oxygenated methine bearing a hydroxyl with α-orientation in compound 27 [79]. The acetylation of aspochalasin J (27) yields the monoacetyl derivative acetyl aspochalasin J confirming the presence of hydroxyl (-OH) in the compound.
Aspergillin PZ (28) is a compound that was previously reported from the soil fungi Aspergillus awamori as a colourless crystal [80]. Aspergillin PZ (28) shares an identical skeleton to the compound aspochalasin C, which is also produced by fungi from the genus Aspergillus. The addition of a hydroxyl followed by cyclisation of aspochalasin C produced aspergillin PZ (28). Zygosporin D (29) was previously isolated from the fungus Metarrhizium anisopliae [81], while rosellichalasin (30), a solid colourless needle, has been reported from an Aspergillus strain from China [82]. Zygosporin D (29) is reported as a deacetyl derivative of the compound cytochalasin D. These compounds are classified as cytochalasins, a group of fungal alkaloids with diverse biological activities targeting cytoskeletal processes. They can bind to actin filaments and block polymerisation and the elongation of actin. The isolated compounds were screened for their bio-activity against six terrestrial pathogenic bacteria (Staphylococcus epidermidis, S. aureus, Escherichia coli, Bacillus subtilis, B. cereus and Micrococcus luteus) and two marine pathogenic bacteria (Vibrio parahaemolyticus and Listonella anguillarum) [58].
Aspochalasin D (24) demonstrated a wide spectrum of antibacterial properties, especially towards four pathogenic bacteria, S. epidermidis, S. aureus, E. coli and B. cereus [58]. In contrast, aspochalasin I (26) displayed moderate minimum inhibition activity (MIC) against the bacteria S. epidermidis (MIC = 20 μM) and S. aureus (MIC = 10 μM). In addition, compounds aspochalasin D, H-J (24-27) also showed strong antifouling activity against the larval settlement of the barnacle, Balanus amphitrite, with EC 50 values of 6.2, 37, 34 and 14, respectively [58]. Despite the small differences in their structures, aspochalasin D (24), which possessed an α,β-unsaturated lactone moiety, demonstrated that the electrophilic α,β-unsaturated carbonyl moiety plays an important role in the antifouling activity of these cytochalasins [58]. Since aspochalasin D (24) had higher antifouling activity than aspochalasin H (25), the presence of a double-bond at C-19 and C-20 was deduced to be the possible active site for cytochalasin antifouling activities [58]. The chemical structures of these compounds are shown in Figure 2.
Pseudoindole A (31) was isolated as an amorphous brown powder, consisting of one methylene group, six methine groups, three quaternary carbon atoms and is built of two identical structural moieties comprising an ortho-disubstituted aromatic ring and 3-substituted indole connected at the electronegative carbon C-9 [59]. Chemically, pseudoindole A (31) was deduced as 1,3-di(1H-indol-3-yl)propan-2-ol. Pseudoindole B (32) is also made up of a similarly identical skeleton connected at the methine carbon C-8, which bears a chain with a sulfoxide moiety. Compounds 33 to 37 share a common basic structure comprising two identical groups of ortho-disubstituted aromatic ring and 3-substituted indole joined at carbon C-8, making them a member of the bisindole alkaloid class. Similar to compound 31 and 32, 3,3 -cyclohexylidenebis(1H-indole) (33) was also isolated as a brown amorphous powder [59]. It can be synthesised by reacting an indole with cyclohexanone. This compound exhibited a 140% enhancing potential towards the Am80-induced HL-60 (myeloid leukemic cell lines) cell. When treated with eight human cancer cell lines (A549, GLC82, CNE1, CNE2, HONE1, SUNE1, BEL7402 and the human hepatocarcinoma cell line (SMMC7721)), compound 33 showed cytotoxicity with IC 50 values of 22.84, 22.04, 18.69, 20.84, 26.62, 20.54, 27.52 and 22.50 μM, respectively [59]. 3,3-bis(3-indolyl)butane-2-one (34) was previously reported as a synthesised product but was later isolated as a natural metabolite from the bacterium Vibrio parahaemolyticus of the North Sea, as a pale yellowish solid [83]. Another indole reported from the soft-coral-derived fungi is 2-[2,2-di(1H-indol-3-yl) ethyl] aniline (35), which was previously isolated from the bacterium Aeromonas sp. derived from seawater collected from the South China Sea [84]. It is also a common product produced by various other bacterial sources and exhibits weak toxicity against the A549 cell line with an IC 50   The compounds 3,3 -diindolyl(phenyl)-methane (36) and 1,1-(3,3 -diindolyl)-2phenylethane (37) were reported from the bacteria Edwardsiella tarda [85]. 3,3 -diindolyl (phenyl)-methane (36) was obtained as a red solid, while 1,1-(3,3 -diindolyl)-2-phenylethane (37) was reported as a yellowish solid. The compound 3,3 -diindolyl(phenyl)methane (36) was found to exhibit weak antibacterial properties against the pathogen Clostridium perfringens [86]. Perlolyrin (38), a type of β-carboline derivative isolated as a yellow powder, was originally reported as a fluorescent compound from soy sauce. It is also often associated with plants, such as Ginseng and several Asiatic plants. These derivatives are strongly associated with its antitumour and anti-oxidative properties [67]. Pityriacitrin (39), on the other hand, was previously reported from the marine bacterium Paracoccus sp. and the yeast Malassezia furfur [87]. It appeared as a bright yellow band in thin layer chromatography and was isolated as a yellow solid. Pityriacitrin (39) was characterised as a natural UV filter in cultures of the yeast Malassezia furfur [88].
Along with the bisindole alkaloids, several β-carboline type indoles were also reported from the soft-coral associated Pseudallescheria boydii. 1-acetyl-β-carboline (40) is a fluorescent compound first reported from the marine sponge Tedania ignis [59]. Prior records of this metabolite were from a terrestrial plant Ailanthus malabarica [67]. Similarly, the other derivative is 3-Hydroxy-β-carboline (41), which was first obtained in its natural form as a yellowish amorphous solid from the stems of a medicinal plant Picrasma quassioides collected in China. This carboline derivative was previously described as a synthesised product [89]. The final two indoles reported from the investigation of Yuan and team (2019) [59] were 1-(9H-pyrido [3,4-b]indol-1-yl)ethan-1-ol (42), initially reported from the heartwood of Dicorynia guianensis as a yellowish powder [90] and N b -acetyltryptamine (43), which was isolated from an unidentified marine fungus derived from the red alga Gracilaria verrucose as a yellowish oil. Previous records on N b -acetyltryptamine had been as a bio-transformed product of tryptamine from the fungus Streptomyces staurosporeus [91]. All the chemical structures of these compounds are shown in Figure 3.

Anthraquinones Derivates
Anthraquinones are aromatic compounds with the 9,10-anthracenedione core and are often referred to as 9,10-dioxoanthracene with a keto functionality in its central ring. There have been nearly 100 naturally occurring anthraquinones, and about 20 have been identified to be the products of marine fungi derived from the soft-coral genus Sarcophyton. In 2012, Zheng et al. isolated tetrahydroaltersolanol B (44), five hydroanthraquinone derivatives named tetrahydroaltersolanols C-F (45)(46)(47)(48) and dihydroaltersolanol A (49), from the liquid culture of Alternaria sp. derived from a Sarcophyton sp. collected from the Weizhou coral reef in the South China Sea [49]. The crude extract of the cultured fungi was fractioned using column chromatography with the mobile phase combination between Petr Eth: EtOAc (1:2). The immunosuppressive potential of the fractions exhibited activity at concentrations 1.48 ± 0.15 and 11.83 ± 0.83 μg/mL [49]. Repeated Sephadex column chromatography followed by HPLC over methanol through a Zorbax SB-C18 (9.4 mm × 25 cm) yielded the above-mentioned metabolites.
Tetrahydroaltersolanol B (44), isolated as a colourless crystal, is a hexahydroanthronol type anthraquinone isolated only from the fungi Alternaria solani [49]. So far there have been two records of this metabolite from the fungi. Likewise, tetrahydroaltersolanol C (45) was also isolated as a colourless crystal. According to the spectroscopic features, compound 45 bears a great deal of structural similarity to the compound tetrahydroaltersolanol B (44) with differences in the α, β positioning of the proton and hydroxyl at carbon C-3 and C-9, respectively [49]. Tetrahydroaltersolanol C (45) was isolated as a new metabolite at the point of report, along with tetrahydroaltersolanols D-F (46-48) from the soft-coral associated Alternaria sp. It exhibited antiviral activity when screened against the porcine reproductive and respiratory syndrome virus (PRRSV) [49].
Tetrahydroaltersolanol D (46) was also obtained in the form of colourless crystal. Though tetrahydroaltersolanol D (46) is structurally identical to tetrahydroaltersolanol B (44), it varied stereochemically at carbon positions C-1a and C-4a [49]. The relative configurations of all asymmetric carbons in tetrahydroaltersolanol D (46) were confirmed as 1aβ, 3β, 4aα, 9β, and 11β, identical to those of tetrahydroaltersolanol B (44). Likewise, tetrahydroaltersolanol E (47) was isolated as a colourless crystal of similar nature to compounds (45) and (46). Since its chemical shifts resembled tetrahydroaltersolanol B (44), it was eventually determined as 3-epi-tetrahydroaltersolanol B [49]. Tetrahydroaltersolanol F (48) was isolated as amorphous pink powder. It shows close structural resemblance to tetrahydroaltersolanol B (44), despite obvious differences in the presence of a singlet methyl at 2.14 ppm and the downfield shift of H-3 in 1 H-NMR. The final compound in the set of hydroanthraquinones reported from the Alternaria sp. was dihydroaltersolanol A (49), isolated as colourless crystals as well [49]. The relative configurations of all asymmetric carbons in dihydroaltersolanol A (49) were determined as 1α, 1aα, 3β, 9β, and 11β. None of these compounds exhibited antimicrobial potential as screened [49].
Further investigation of the marine fungi Alternaria sp. from the Sarcophyton soft coral yielded six alterporriol-type anthranoid dimers, altersolanols B-C (50-51), altersolanol L (52), ampelanol (53), macrosporin (54) and alterporriol C (55), together with five more analogues, alterporriols N-R (56-60) were isolated and characterised [49]. The Alternaria sp. isolated from the soft coral was cultured in potato glucose liquid medium before being extracted in EtOAc. Column fractions of extract were subjected to repeated column chromatography over Sephadex LH-20 and purification via HPLC using a Kromasil C18 preparative HPLC column to yield the reported compounds [49].
Altersolanol B (50), a red needle and altersolanol C (51) were previously reported from the extract of Alternaria solani, which caused the black spot disease. Both compounds were potent in inhibiting all the Gram-positive bacteria [71]. Altersolanol L (52), isolated as a brown powder, and the white crystal macrosporin (54) reported from the soft coral Alternaria sp. were initially isolated from the endophytic fungus Stemphylium globuliferum derived from a medicinal plant species [92]. Apart from Alternaria, macrosporin (54) is known to be produced by several economically important crop-disease-causing fungal pathogens, such as Cladosporium, Dichotomophthora, Phomopsis, Stemphylium and Dactylaria. Altersolanol L (52) was reported to share a similar skeletal structure to the previously described dihydroaltersolanol A (49). Ampelanol (53), on the other hand, is another metabolite associated with medicinal plant-derived fungus Ampelomyces sp. It was isolated as white crystals and determined to exhibit mild cytotoxicity towards mouse lymphoma cells (L5178Y) [72]. The chemical structures of the anthraquinones compounds 44-54 are shown in Figure 4. Subsequently, several bianthraquinones were isolated from the soft-coral-derived marine fungi as well. Alterporriol C (55) belongs to a modified bianthraquinone and was first isolated from the fungus Alternaria porri as red needles [93]. Alterporriol C (55), which was antibacterial against Escherichia coli and Vibrio parahemolyticus with both MIC values 2.5 μM, is suggested to be made up of the compounds altersolanol A and macrosporin (54) [49]. Alterporriol N (56) was an amorphous powder in red. 13 C NMR spectrum analysis suggested that alterporriol N (56) was a symmetrical dimer of altersolanol C (51) with a C-8 and C-8 linkage [49]. Another symmetrical dimer to altersolanol C (51) isolated from Alternaria sp. was alterporriol O (57), which appeared as a red amorphous powder. Unlike alterporriol N (56), alterporriol O (57) was an anthranoid dimer with a C-4 and C4' linkage [49]. Likewise, alterporriol P (58) was also a red, amorphous powder, with the molecular formula of C 32 H 26 O 12 . Alterporriol P (58), also isolated as a red amorphous powder, was characterised as a sub-unit of the altersolanol C (51) and macrosporin (54) linkage via carbon C-4 and C-6'. This compound was cytotoxic against the human prostate cancer (PC-3) and human colorectal carcinoma (HCT-116) cell lines with the IC 50 values 6.4 and 8.6 μM [49]. In contrast, alterporriol Q (59) was obtained as a yellowish amorphous powder, and the final anthraquinone characterised from Alternaria sp. was alterporriol R (60), which was determined to be an isomer of alterporriol Q 59 [49]. These compounds were comprised of two macrosporin (54) sub-units. The two sub-units of alterporriol Q (59) were linked through carbons C-4 and C-6', while alterporriol R (60) was connected via carbons C-4 and C-8 . Alterporriol Q (59) exhibited antiviral activity against the porcine reproductive and respiratory syndrome virus (PRRSV), with an IC 50 value of 39 μM [49].
All the above-mentioned compounds were isolated via a similar protocol in the choice of culture conditions, mobile phase in column chromatography and HPLC purification. The chemical structures of the reported bianthraquinones are shown in Figure 5.

Amino Acid Derivates
In 2013, a phenylalanine derivative 4 -OMe-asperphenamate (61) was isolated from Aspergillus elegans derived from Sarcophyton sp. [58]. Asperphenamate (62) is another phenylalanine derivative reported from the same study and has an identical basic skeletal structure to the white powdered 4 -OMe-asperphenamate [58]. The only difference observed in the 1 H-NMR spectrum was the presence of a highly electronegative primary methyl signal at δH 3.74 in 4 -OMe-asperphenamate (61) instead of an aromatic proton at δH 7.30 in asperphenamate (62), making it the only detected difference between the two at the carbon position 4 [58]. The compounds were isolated in the same manner as the previously mentioned compounds; column chromatography with Petr Ether and EtOAc mobile phase followed by a Sephadex LH-20 column with chloroform and methanol at a ratio 1:1 and HPLC purification using methanol over a Kromasil C18 preparative column [58]. The chemical structures of compounds (61) and (62) are shown in Figure 6.

Concluding Remarks
The chemical diversity of soft-coral associated symbionts is often limited to bacterial and fungal isolates cultured under laboratory conditions. Nevertheless, there are still many unexplored symbionts in terms of their secondary metabolism and natural-product biosynthesis potential. However, the development of new techniques such as metabolomics for the determination of metabolites produced by specific genes and next generation sequencing creates new dimensions of in-depth investigation of the microbiome. Independent culture methods, such as the next-generation sequencing on sponges, would reveal novel microorganisms, and their guild patterns could be analysed in order to know their association with corals. The role of fungi and their respective host can either be symbiotic or parasitic. As sponges, there have been speculations as to the origin of metabolites isolated from the soft corals. This review study reveals that no common metabolites were shared by the host and its fungi. This confirms that the metabolites isolated from the host are synthesised by the host itself. Due to the diverse bioactivity of the fungal metabolites, we hypothesise that fungal metabolites perform various functions for additional protection to their host, presumably similar to the role of constituents, such as the MAAs. The presence of microorganisms triggers the development of a wide array of secondary metabolites, which function as mutual defences or for adaptive purposes as well as microbial regulation of the octocoral holobionts. Recent studies have shown an increasing trend in bioactive secondary metabolites from Sarcophyton-associated marine fungi. However, many compounds have not been thoroughly evaluated for their bioactivities. In the future, more bioassays could be conducted on the soft coral and its associated fungal chemical compounds.
Funding: Not applicable for the preparation of this review.

Informed Consent Statement: Not applicable.
Acknowledgments: This review is an output as part of the University Malaya BKP grant (BK08-2018) and the Higher Institution Centre of Excellence (HiCoE) grant (IOES-2014G).

Conflicts of Interest:
The authors declare no conflict of interest.