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Review

Sulfur-Containing Compounds from Endophytic Fungi: Sources, Structures and Bioactivities

by
Yaqin Fan
1,†,
Zhiheng Ma
1,†,
Yan Zhang
1,
Yufei Wang
2,
Yousong Ding
3,
Cong Wang
2,* and
Shugeng Cao
4,*
1
Shandong Provincial Key Laboratory of Applied Mycology, School of Life Sciences, Qingdao Agricultural University, Qingdao 266109, China
2
Key Laboratory of Chemistry and Engineering of Forest Products, State Ethnic Affairs Commission, Guangxi Collaborative Innovation Center for Chemistry and Engineering of Forest Products, School of Chemistry and Chemical Engineering, Guangxi Minzu University, Nanning 530006, China
3
Department of Medicinal Chemistry, Center for Natural Products, Drug Discovery and Development, College of Pharmacy, University of Florida, Gainesville, FL 32610, USA
4
Department of Pharmaceutical Sciences, Daniel K. Inouye College of Pharmacy, University of Hawai’i at Hilo, 200 W. Kawili St., Hilo, HI 96720, USA
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
J. Fungi 2022, 8(6), 628; https://doi.org/10.3390/jof8060628
Submission received: 29 May 2022 / Revised: 10 June 2022 / Accepted: 10 June 2022 / Published: 13 June 2022
(This article belongs to the Special Issue Secondary Metabolites from Fungi—in Honour of Prof. Dr. Ji-Kai Liu's 60th Birthday)
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Abstract

:
Endophytic fungi have attracted increasing attention as an under-explored source for the discovery and development of structurally and functionally diverse secondary metabolites. These microorganisms colonize their hosts, primarily plants, and demonstrate diverse ecological distribution. Among endophytic fungal natural products, sulfur-containing compounds feature one or more sulfur atoms and possess a range of bioactivities, e.g., cytotoxicity and antimicrobial activities. These natural products mainly belong to the classes of polyketides, nonribosomal peptides, terpenoids, and hybrids. Here, we reviewed the fungal producers, plant sources, chemical structures, and bioactivities of 143 new sulfur-containing compounds that were reported from 1985 to March 2022.

1. Introduction

Sulfur is one of the prime elements on Earth and the eighth most abundant element in the human body. It is a group 6A (or VIA) member of the periodic table, with a larger atomic size and a weaker electronegativity than oxygen. Sulfur has unique characteristics, such as five different oxidation states, and sulfur-containing molecules often participate in biological redox reactions and electron transfer processes. Notably, two essential amino acids, l-methionine and l-cysteine, both contain a sulfur atom, further highlighting the importance and indispensability of sulfur in biology [1]. Indeed, one fifth (20%) of the FDA-approved drugs contain at least one sulfur atom. These sulfur-containing drugs have different structure skeletons such as sulfonamides, β-lactams, thioethers, thiazoles, thiophenes, phenothiazines, sulfoxides, S=C and S=P structures, thionucleotides, sulfones, sulfates and macrocyclic disulfides. Of note, many sulfur-containing drugs are natural products or their derivatives (i.e., rosuvastatin, ecteinascidin 743 and ixabepilone) [2].
Fungi are a major group of microorganisms that produce a broad array of compounds with novel structures and unique bioactivities. One type of fungi colonizes the intercellular and/or intracellular regions of healthy plant tissues at a particular time and has no interference with and causes no pathogenic symptoms to the host [3]. These endophytic microorganisms are an important but less-explored source for the discovery of structurally novel natural products in drug research. This paper reviews new sulfur-containing compounds isolated from endophytic fungi since 1985 (Table 1). Based on their major chemical features, these compounds will be categorized into peptides, disulfides, polyketides, hybrids and terpenoids. The fungal strains that producing sulfur-containing compounds, host plants, structure uniqueness and biological activities of these compounds will be discussed (Table 1).

2. Peptides

2.1. Sulfide (R-S-R′)

A rare diketopiperazine bionectin D (1) (Figure 1) was obtained from a fungal strain Bionectria sp. Y1085 that was isolated from the plant Huperzia serrata. Bionectin D (1) consists of a tryptophan and a threonine moiety, and the α-carbon of its tryptophan moiety carries a single methylthio substitution. Compound 1 exhibited antibacterial activity against Staphylococcus aureus, Escherichia coli, and Salmonella typhimurium ATCC 6539 with the same minimal inhibitory concentration (MIC) of 25 μg/mL [4]. Lasiodiplines A-C (2–4) and E-F (5–6) are new sulfureous diketopiperazines that were produced by Lasiodiplodia pseudotheobromae F2 isolated from the apparently normal flower of Illigera rhodantha. The structure elucidation of these compounds was accomplished using a combination of spectroscopic and computational approaches, and the structure of 2 was further confirmed in conjunction with low-temperature (100 K) single-crystal X-ray diffraction. Lasiodiplines E (5) displayed antibacterial activity against Veillonella parvula, Actinmyces israelili, Streptococcus sp., Bacteroides vulgates and Peptostreptococcus sp. with the MIC values of 0.25, 32.0, 0.12, 0.12 and 0.12 μg/mL, respectively [5].
Botryosulfuranols A and B (7–8), two spirocyclic thiodiketopiperazines, were purified from Botryosphaeria mamani. The fungal strain was isolated from the fresh leaves of Bixa orellana L. (Bixaceae) collected in Peru. These two unique compounds, each of which contains two spiro centers, were derived from two l-phenylalanines with two methylthio substitutions at the α-carbon and β-carbon of the two building blocks, respectively. Botryosulfuranols A (7) was active against four cancer cell lines (HT-29, HepG2, Caco-2, HeLa) with IC50 values of 8.0, 11.4, 18.2, 23.5 and 9.3 μM, respectively. Botryosulfuranols B (8) was active against three cancer cell lines (HT-29, HepG2, HeLa) with the IC50 values of 63.2, 56.1, 61.2, 49.9 and 64.7 μM, respectively [6]. Outovirin A (9) was a thiodiketopiperazine derived from two molecules of l-phenylalanine. It was produced by Penicillium raciborskii, an endophytic fungus isolated from Rhododendron tomentosum [7]. Compound 9 contains a nitrogen-oxygen bond in the oxazinane ring between diketopiperazine and conduritol-like rings, and it has a sulfide bridge between the α- and β-carbons rather than the typical α−α bridging. Nine new thiodiketopiperazines, epicoccin I (10), ent-epicoccin G (11), and epicoccins J-P (12–18), have been isolated from the endophytic fungus Epicoccum nigrum. Compounds 10, 17, and 18 all have a sulfide bridge between the α-carbon and the 2′/3′-position of the reduced benzene ring. Ent-epicoccin G (11) and epicoccins M (15) showed potent in vitro activities against the release of β-glucuronidase in rat polymorphonuclear leukocytes induced by the platelet-activating factor, with IC50 values of 3.07 and 4.16 µM, respectively [8].
Tilachlidium sp. (CANU-T988) isolated from a decaying wood sample was reported to produce T988 B (19). Compound 19 has an unusual dimerized indole moiety with a 3-3 linkage, and it displayed potent cytotoxicity against P388 leukemia cells with an IC50 of 2.18 µM [9]. Bisdethiobis(methylsulfanyl)apoaranotin (20) was produced by Aspergillus terreus BCC 4651, which was isolated from a tree hole in Nam Nao National Park, Thailand. Compound 20 was derived from two molecules of l-phenylalanine with one benzene ring being oxidized to a 4,5-dihydrooxepine ring. Compound 20 exhibited weak antimycobacterial activity [10]. Chaetocochin G (21), oidioperazine E (22), and chetoseminudin E (23) were obtained from Chaetomium sp 88194, which was isolated from Cymbidium goeringii, a plant native to China, Japan and Korea. Chaetocochin G (21) is a dimer of serine-tryptophan diketopiperazines. Its structure including the absolute configuration was established by spectroscopic data interpretation and single-crystal X-ray diffraction analysis. Chaetocochin G (21) showed cytotoxicity against MCF-7 [11]. Fusaperazine E (24) and colletopiperazine (25) were obtained from Penicillium crustosum and Colletotrichum gloeosporioides, respectively. Both strains were isolated from Viguiera robusta Gardn. (Asteraceae). [12].
Chetoseminudin F and G (26–27) were purified from Chaetomium sp. SYP-F7950, which was isolated from the root of Panax notoginseng collected from Wenshan, Yunnan, P. R. China. Chetoseminudin F (26) displayed cytotoxicity against MDA-MB-231 with an IC50 of 26.49 μM [13]. Four thiodiketopiperazines penicibrocazines F–I (28–31) were purified from Penicillium brocae MA-231, which was isolated from the fresh tissue of the marine mangrove plant Avicennia marina collected at Hainan Island, P. R. China. Penicibrocazines H (30) displayed activity against V. harveyi, E. coli, A. hydrophilia and V. parahaemolyticus with MICs of 16.0, 16.0, 32.0, and 16.0 μg/mL, respectively. Penicibrocazines I (31) displayed activity against V. harveyi with an MIC of 32.0 μg/mL [14].
Two new compounds 6-octenoic acid, 3-hydroxy-2,4,6-trimethyl-5-oxo-, (5S,5aS,7aR,8R,14aR)-5,5a,7a,8,14a,15-hexahydro-8,12-dihydroxy-7a,14a-bis(methylthio)-7,14-dioxo-7H,14H-oxepino[3″,4″:4′,5′]pyrrolo[1′,2′:4,5]pyrazino[1,2-a]indol-5-yl ester (6E) (32) and bisdethiobis(methylthio)deacetylapoaranotin (33) were purified from the seed fungus Menisporopsis theobromae BCC3975. Compound 32 is a hybrid of diketopiperazine and polyketide. Both compounds showed antimycobacterial activity with MICs of 1.24 and 7.14 µM, respectively. Compound 32 displayed cytotoxicity against NCI-H187 cell line and antimalarial activity with IC50 of 20.3 and 2.95 μM, respectively [15].
Two new compounds, Sch 54794 (34) and Sch 54796 (35) (Figure 2), were separated from the fermentation culture of ToJypocJadium sp. The microorganism ToJypocJadium sp. was isolated from dead twigs from a Quercus virginiana Miller, an old live oak tree in the state of Tamalupas, Mexico. The structures of Sch 54794 (34) and Sch 54796 (35) were determined as cis and trans isomers in the spectroscopic analysis. The trans isomer, which was similar to other diketopiperazines reported as platelet-activating factor (PAF) inhibitors in the literature, displayed weak inhibitory activity in PAF assay with an IC50 of 50 μM. However, the cis isomer appeared inactive (IC50 > 100 μM) [16].
Four new dioxopiperazine alkaloids, penispirozines A−D (36–39), were produced by Penicillium janthinellum HDN13-309, which was isolated from the root of the mangrove plant Sonneratia caseolaris. Penispirozine A (36) contains an unusual pyrazino[1,2]oxazadecaline coupled with a thiophane ring system, and compound 37 possesses a 6/5/6/5/6 pentacyclic ring system with two rare spirocyclic centers. Penispirozines C (38) and penispirozines D (39) increased the expression of superoxide dismutase 2 (SOD2) and heme oxygenase-1 (HO-1) at 10 μM [17]. A fermentation broth of Phoma lingam isolate Leroy obtained from rapeseeds generated a new compound sirodesmin H (40) [18]. The octahydrocyclopenta[b]pyrrole moiety in 40 might be derived from l-phenylalanine, which reacted with an isoprenyl group (C5) to form a spiro-furanone system. Two new thiodiketopiperazines phomazines A (41) and B (42) were purified from Phoma sp. OUCMDZ-1847, which was isolated from the mangrove plant Kandelia candel at Wenchang, Hainan, P. R. China. Compound 42 displayed inhibitory activity against MGC-803 cells with an IC50 of 8.5 μM [19].
Two new pentacyclic diketopiperazines spirobrocazines A (43) and B (44) were obtained from Penicillium brocae MA-231, which was derived from the marine mangrove plant Avicennia marina [20]. Compound 43 exhibited moderate antibacterial activities against Escherichia coli, S. aureus and Vibrio harveyi with MIC values of 32.0, 16.0 and 64.0 μg/mL, respectively. Three new epipolythiodioxopiperazines, penicisulfuranols D–F (45–47), were isolated from a marine mangrove plant, Sonneratia caseolaris-derived Penicillium janthinellum HDN13-309 [21]. The piperazine-2,5-dione core in each of these compounds (45–47) was flanked by a 1,2-oxazadecaline moiety and a spiro-benzofuran ring. Compounds 45–47 were tested inactive against HeLa and HL-60 cell lines. Five pentacyclic diketopiperazines, penicibrocazines A–E (48–52), were obtained from Penicillium brocae MA-231, a fungus obtained from the fresh tissue of the marine mangrove plant Avicennia marina. In the antimicrobial screening, penicibrocazine B (49), penicibrocazine C (50) and penicibrocazine D (51) showed activity against Staphylococcus aureus, with MIC values of 32.0, 0.25, 8.0 μg/mL, respectively, which are comparable with that of the positive control, chloromycetin (MIC = 4.0 μg/mL). Penicibrocazines C (50) also showed activity against Micrococcus luteus with an MIC of 0.25 μg/mL, which is stronger than that of the positive control, chloromycetin (MIC = 2.0 μg/mL). Moreover, penicibrocazines B (49) and D (51) exhibited activity against the plant pathogen Gaeumannomyces graminis with MIC values of 0.25 and 8.0 μg/mL, respectively, while the positive control amphotericin B has an MIC of 16.0 μg/mL [22].
The chemical investigation of a culture of Exserohilum holmii, a pathogenic fungus of the weedy plant Dactyloctenium aegyptium, yielded two linearly fused pentacyclic diketopiperazines exserohilone (53) and 9,10-Dihydroexserohilon (54) [23]. The fermentation of Nigrospora sphaerica, which was isolated from a germinating fescue seed, on shredded wheat medium generated a novel pentacyclic diketopiperazine, epoxyexserohilone (55), a congener of the known phytotoxin, exserohilone [24]. The investigation of Setosphaeria rostrata led to the discovery of three pentacyclic diketopiperazines, rostratazines A-C (56–58). The fungal strain was isolated from the fresh leaf tissues of the medicinal plant C. speciosus collected from Colombo, Sri Lanka. Rostratazine B (57) inhibited porcine pancreatic alpha-amylase activity with an IC50 of 578 μM [25]. A pentacyclic diketopiperazine with a 4,5-dihydrooxepine moiety versicolor A (59) was isolated from Aspergillus versicolor 0312. The fungal strain was isolated from the stems of Paris polyphylla var. yunnanensis collected in Kunming, Yunnan Province, P. R. China. Compound 59 displayed cytotoxicity against the contraction of the MOLT-4 cell line with an IC50 of 29.6 μM [26].

2.2. Disulfide (R-S-S-R′) and Multisulfide (R-Sn-S-R′, n = 3 or More)

Bionectin E (60) (Figure 3) was obtained from Bionectria sp. Y1085, which was isolated from Huperzia serrata. Similar to compound 19 (T988 B) [9], compound 60 has an indole moiety attached to the tryptophan-derived 1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole. Interestingly, the other amino acid in the α−α′-bridged disulfide diketopiperazine is a dehydroxylated threonine. Compound 60 showed antibacterial activity against E. coli, S. saureus and Salmonella typhimurium with the same MIC value of 12.5 μg/mL [1]. Derived from the apparently normal flower of Illigera rhodantha, Lasiodiplodia pseudotheobromae F2 produced Lasiodipline D (61) [5]. The α position of the alanine moiety in compound 61 was connected to the β position of the tryptophan moiety via a disulfide bond. Botryosulfuranol C (62) was obtained from the same fungal strain Botryosphaeria mamani as compounds 7 (botryosulfuranols A) and 8 (botryosulfuranols B), but it has an α−β-bridged disulfide bond instead of the sulfide bond in 7 and 8. Botryosulfuranol C (62) showed cytotoxicity against HepG2, HT29, Hela, IEC6 and Vero with IC50 values ranging from 15.9 to 115.7 µΜ [6].
Two new epithiodiketopiperazine natural products, outovirins B (63) and C (64), resembling the antifungal natural product gliovirin have been identified in an extract of Penicillium raciborskii, an endophytic fungus isolated from Rhododendron tomentosum [7]. Compounds 63 and 64 were almost identical to compound 9 (outovirins A) except for an α−β-bridged disulfide and a trisulfide bond in compounds 63 and 64, respectively. Compound 64 inhibited the growth of all tested fungal isolates (Fusarium oxysporum, Botrytis cinerea, and Verticillium dahliae) at a low concentration of 0.38 mM (207 μg/mL), but a more significant growth inhibition was observed at 0.76 mM (413 μg/mL). Compound 64 was the most active against Botrytis cinerea (57% inhibition) and slightly less effective against Verticillium dahliae (45% inhibition). Four new pentacyclic thiodiketopiperazines, epicoccins Q-T (65–68), were discovered from the same fungal strain, Epicoccum nigrum, as compounds 10–18. Epicoccins S (67) showed activity against the release of β-glucuronidase with an IC50 of 4.95 µM [8].
Secoemestrin D (69), a new epitetrathiodioxopiperizine, was obtained from Emericella sp. AST0036, a fungal endophyte of Astragalus lentiginosus. Compound 69 contains an α−α-bridged tetrasulfide bond. A benzoic acid moiety was attached to the 4,5-dihydrooxepine ring. Secoemestrin D (69) exhibited potent cytotoxic activity against a panel of seven cancer cell lines with IC50 values ranging from 0.06 to 0.24 μM [27]. Tilachlidium sp. (CANU-T988), a fungal strain isolated from a decaying wood sample collected in Christchurch, New Zealand, produced two new thiodiketopiperazine derivatives, T988 A (70) and C (71), which have an indole ring connected to the 1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole, structurally similar to compounds 19 and 60. Compound 71 has an α−α-bridged disulfide bond, while compound 70 has an α−α-bridged trisulfide bond. Compounds 70 and 71 displayed cytotoxicity against P388 with IC50 values of 0.25 and 0.56 µM, respectively [9]. Pretrichodermamide A (72) was obtained from Trichoderma sp. BCC 5926, which was collected on a bamboo leaf from Khao Yai National Park, Nakhon Ratchasima Province, Thailand. Under alkaline conditions, compound 72 with an α−β-bridged disulfide bond underwent a rapid transformation to a stable amide, which is composed of a 1,2-oxazadecaline moiety and a coumarin derivative. Compound 72 exhibited antibacterial activity against Mycobacterium tuberculosis H37Ra with an MIC of 12.5 µg/mL [28]. A new epidithiodiketopiperazine, pretrichodermamide G (73), was afforded by Trichoderma harzianum associated with the medicinal plant Zingiber officinale [29]. Although compound 73 is quite similar to compound 72, no chemical transformation under alkaline conditions was reported.
The investigation of Aspergillus tamarii FR02 led to the isolation of a new cyclic pentapeptide, disulfide cyclo-(Leu-Val-Ile-Cys-Cys), named malformin E (74). A. tamarii FR02 was isolated from the root of Ficus carica. Malformin E (74) exhibited cytotoxic activities against MCF-7, A549 and HepG2 with IC50 values of 0.65, 2.42 and 36.02 μM, respectively. Malformin E (74) also showed antimicrobial and antifungal activities against Bacillus subtilis, Staphylococcus aureus, Pseudomonas aeruginosa, Escherichia coli, Penicillium chrysogenum, Candida albicans and Fusarium solani with MIC values ranging from 0.45 to 7.24 μM [30].
Six pentacyclic diketopiperazines, brocazines A-F (75–80), were discovered from Penicillium brocae MA-231, a fungus obtained from the fresh tissue of the marine mangrove plant Avicennia marina. Brocazines A (75), B (76), E (79) and F (80) were cytotoxic to a panel of nine tumor cell lines with IC50 values ranging from 0.89 to 9.0 μM. [31]. A culture of Phoma sp. OUCMDZ-1847 afforded one new phomazine C (81), which should be biogenetically generated from the same precursor as compounds 41 and 42 [19]. Penicillium janthinellum HDN13-309 produced epipolythiodioxopiperazines, penicisulfuranols A−C (82–84), together with compounds 45–47. Compounds 82–84 exhibited cytotoxicity against HeLa and HL-60 with IC50 of 0.1–3.9 μM [21].
Brocazine G (85), a new diketopiperazine, along with compounds 43 and 44 was obtained from Penicillium brocae MA-231 associated with the fresh tissue of the marine mangrove plant Avicennia marina. It showed cytotoxicity against A2780 with an IC50 of 59 μM. Brocazine G (85) also showed inhibitory activity against E. coli, Aeromonas hydrophilia and V. harveyi with the same MIC of 32.0 μg/mL [20]. Five new epipolysulfanyldioxopiperazines, gliocladines A–E (86–90), were isolated from Gliocladium roseum 1A, a fungal strain isolated from submerged wood collected from fresh water in Yunnan Province, P. R. China. Both compounds 86 and 87 are dimers with each monomer being derived from l-alanine and l-tryptophan, while each of compounds 88–90 is a diketopiperazine with an indole ring connected to the 1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole. These compounds exhibited nematicidal activities toward C. elegans, P. redivivus and B. xylophilus with ED50 values ranging from 25 to 250 μg/mL [32].
An analog of compounds 86 and 87, 6-Formamide-chetomin (91), was obtained from a culture of Chaetomium sp. M336, isolated from the plant H. serrata (Thunb. ex Murray) Trev. Compound 91 was cytotoxic to HeLa, SGC-7901 and A549 cells with IC50 values of 21.6–27.1 μM. It exhibited activity against Escherichia coli, Staphylococcus aureus, Salmonella typhimurium ATCC 6539 and Enterococcus faecalis with the same MIC of 0.78 μg/mL [33].

2.3. Sulfoxide (R-SO-R′) and Sulfone (R-SO2-R′)

An indole alkaloid with a rare methylsulfonyl unit, 21-Epi-taichunamide D (92), was obtained from Aspergillus versicolor F210 (Lycoris radiata). The strain was isolated from the bulbs of Lycoris radiata collected from Yichang City in Hubei Province, P. R. China. Compound 92 inhibited anticancer activity toward HL-60 and A549 cells with IC50 values of 26.8 and 32.5 μM, respectively [34].

3. Polyketides

3.1. Sulfide

A new cytotoxic compound, isocochlioquinones D (93) (Figure 4), was purified from Bipolaris sorokiniana A606. The endophytic fungus was isolated from the medicinal plant Pogostemon cablin, also known as patchouli or “Guanghuoxiang” in traditional Chinese medicine (TCM) [35]. Isocochlioquinones D (93) is a hybrid of a polyketide and a sesquiterpenoid with a rare benzothiazin-3-one moiety. Compound 93 demonstrated antiproliferative activity toward SF-268, MCF-7, NCI-H460 and HepG-2 with IC50 values of 32.8, 28.3, 42.6 and 38.6 µM, respectively.
Paraphaeosphaeria neglecta FT462 yielded paraphaeosphaerides E (94), F (95), H (96) and methyl ester of paraphaeosphaeride F (97) [36]. P. neglecta FT462 was isolated from the Hawaiian plant Lycopodiella cernua, synonym Palhinhaea cernua (Lycopodiaceae). Paraphaeosphaeride E (94) was active against E. coli JW2496 at 20 μg/mL. Paraphaeosphaeride E (94) inhibited nuclear factor kappa B (NF-κB) with an IC50 of 7.1 μM. Paraphaeosphaerides E (94) and F (95) also showed inducible nitric oxide synthase (iNOS) with IC50 values of 47.9 and 43.2 μM, respectively. Paraphaeosphaeride A (98) with the unique 4-pyranone-γ-lactam-1,4-thiazine moiety was obtained from P. neglecta FT462 [37].
The first natural sulfur-containing benzophenone dimer, named guignasulfide (99), was isolated from the culture of Guignardia sp. IFB-E028, an endophytic fungus residing in the healthy leaves of Hopea hainanensis. Guignasulfide (99) exhibited cytotoxicity against HepG2 with an IC50 of 5.27 μM. It also showed antimicrobial activity against Helicobacter pylori with an MIC of 42.9 μM [38].
Cladosporium cladosporioides MA-299 yielded four 12-membered macrolides, thiocladospolides A-D (100–103). C. cladosporioides MA-299 is an endophytic fungus obtained from the leaves of the mangrove plant Bruguiera gymnorrhiza. Thiocladospolide A (100) was active against E. tarda, E. ictarda and C. glecosporioides with MIC values of 1, 8 and 2 μg/mL, respectively. Thiocladospolide B (101) was active against C. glecosporioides, P. piricola Nose and F. oxysporum f. sp.cucumerinum with MIC values of 2, 32 and 1 μg/mL, respectively. Thiocladospolide C (102) was active against the same three strains as 101 with MIC values of 1, 32 and 32 μg/mL, respectively. Thiocladospolide D (103) was active against E. ictarda, C. glecosporioides, P. piricola Nose and F. oxysporum f. sp.cucumerinum with MIC values of 1, 1, 32, and 1 μg/mL, respectively [39]. The investigation of the mangrove-derived fungus Cladosporium sp. SCNU-F0001 afforded a new 12-membered macrolide, thiocladospolide E (104) [40]. A mangrove-derived fungus, Cladosporium oxysporum, yielded five 12-membered macrolides, thiocladospolides F–J (105–109), and they showed a broad spectrum of antimicrobial activity with MIC values ranging from 4 to 32 μg/mL [41].
Two cytochalasan analogs, cyschalasins A (110) and B (111), were obtained from Aspergillus micronesiensis, which was isolated from the root of the traditional Chinese medicinal plant Phyllanthus glaucus collected from LuShan Mountain, Jiangxi Province, P. R. China. Cyschalasins A (110) and B (111) exhibited cytotoxicity against HL60, A549, Hep3B, MCF-7 and SW480 with IC50 values in the range of 3.0 to 19.9 μM except for 110, which was inactive toward A549 at 20 μM. Cyschalasins A (110) and B (111) also demonstrated antimicrobial activity with MIC50 values ranging from 10.6 to 94.7 μg/mL [42].
An amide of a coumarin moiety and l-phenylalanine-derived 1,2-oxazadecaline moiety, trichodermamide G (112), was isolated from Trichoderma harzianum D13. The fungal strain was isolated from the internal tissues of the root of Excoecaria agallocha, distributed in the mangrove regions of various parts of India [43].
Two sulfur-containing xanthones, sydoxanthone A (113) and sydoxanthone B (114), were purified from A. sydowii, occurring in the liverwort Scapania ciliata S. Lac. Sydoxanthone B (114) was active on the concanavalin A-induced and lipopolysaccharide (LPS)-induced proliferation of mouse splenic lymphocytes with IC50 of 22.53 and 15.30 μg/mL, respectively [44]. Sydoxanthones D (115) and E (116) were discovered from Pseudopestalotiopsis theae, which was isolated from the leaves of Caloncoba welwitschii [45].

3.2. Disulfide

A new natural compound, a symmetrical disulfide dimer dodecyl 3,3″-dithiodipropionate (117) (Figure 5), was isolated from the ethyl acetate extract of fermentation broth of an endophytic fungus, Sphaceloma sp. LN-15. The fungal strain was isolated from the leaves of Melia azedarach L., commonly known as the chinaberry tree, pride of India, Persian lilac, and some other names [46]. The structure of 117 was determined by NMR and MS and was further confirmed by chemical synthesis.

3.3. Sulfoxide

LC-UV/MS-based metabolomics analysis of the Hawaiian endophytic fungus Paraphaeosphaeria neglecta FT462 led to the identification of unique mercaptolactated γ-pyranol–γ-lactams, paraphaeosphaerides G (118). The fungal strain was isolated on potato dextrose agar (PDA) medium from a healthy leaf of the Hawaiian indigenous plant Lycopodiella cernua (L.) Pic. Serm, which was collected in the Mokuleia Forest Reserve in 2014 [36].

3.4. Sulfones

Two new polyketides modified with a rare methyl sulfonyl group, neosartoryone A (119) and 3-methoxy-6-methyl-5-(methylsulfonyl)benzene-1,2,4-triol (120), were isolated from Neosartorya udagawae HDN13-313 cultivated with the DNA methyltransferase inhibitor 5-azacytidine. N. udagawae HDN13-313 was isolated from the root of the mangrove plant Aricennia marina [47]. Compound 119 decreased the lipid accumulation elicited by oleic acid at 10 μM.

3.5. Sulfates and Sulfonates

Two new alkyl sulfate-containing aromatic compounds, penixylarins B (121) and D (122), were isolated from a mixed culture of the Antarctic deep-sea-derived fungus Penicillium crustosum PRB-2 and the fungus Xylaria sp. HDN13-249 [48]. Xylaria sp. HDN13-249 was isolated from the root of Sonneratia caseolaris collected from the mangrove conservation area of Hainan, P. R. China. Penixylarins B (121) showed weak antibacterial activity against Bacillus subtilis with an MIC50 of 100 μM.
Alternariol 5-O-sulfate (123) and alternariol 5-O-methyl ether-4′-O-sulfate (124) were produced by Alternaria sp., which was isolated from fresh healthy leaves of the wild Egyptian medicinal plant Polygonum senegalense Meisn. (Polygonaceae) [49]. Alternariol 5-O-sulfate (123) was cytotoxic against L5178Y with an EC50 of 4.5 μg/mL. Compound 123 also showed inhibition toward a panel of protein kinases at the micromolar level.
The extracts of cultures grown in liquid or on solid rice media of the fungal endophyte Ampelomyces sp. isolated from the medicinal plant Urospermum picroides exhibited considerable cytotoxic activity against L5178Y cells. The extract obtained from liquid cultures afforded two sulfated anthraquinones, macrosporin-7-O-sulfate (125) and 3-O-methylalaternin-7-O-sulfate (126) [50]. However, neither compound showed any cytotoxic or antimicrobial activities.
A 2-hydroxyl 6-alkylated benzaldehyde derivative, pestalols E (127), was isolated from the endophytic fungus Pestalotiopsis sp. AcBC2, which was derived from the Chinese mangrove plant Aegiceras corniculatum, commonly known as black mangrove or river mangrove [51].
Oreganic acid (128) and its trimethyl esters (129) were obtained from the extract of an endophytic fungus MF6046 isolated from living leaves of Berberis oregano [49]. Oreganic acid (128) is a highly potent and specific farnesyl protein transferase (FPTase) inhibitor (IC50 = 14 nM) [49].
A novel metabolite containing a sulfonate group, fusaodavinvin (130), was isolated from an endophytic fungus Fusarium sp. (CTGU-ZL-34). The fungal strain was isolated from a healthy plant Davidia involucrata. Compound 130 displayed inhibitory activity against A549, HepG2, Caski and MCF-7 cell lines with IC50 values of 11.5, 15.3, 15.2 and 60.5 μg/mL, respectively [53].

4. Hybrids

4.1. Sulfides

A fungal strain Pestalotiopsis sp. HS30 was isolated from the fresh stems of Isodon xerophilus collected at Kunming Botanical Garden, Yunnan Province, P. R. China [54]. Pestaloamides A (131) and B (132), two novel alkaloids featuring an unprecedented spiro[imidazothiazoledione-alkylidenecyclopentenone] scaffold, were obtained from the cultures of Pestalotiopsis sp. HS30. Compounds 131 and 132 were derived from a polyketide and a Phe-Cys dipeptide together with C2 and C5 moieties. Both compounds could enhance the cell surface engagement of NKG2D ligands in HCT116 cells at 40 μM [54].

4.2. Disulfides

PM181110 (133) was a new depsipeptide obtained from Phomopsis glabrae, which was isolated from the leaves of Pongamia pinnata (Fabaceae) [55]. Compound 133 was derived from two molecules of l-cysteine and one C12 polyketide. It exhibited potent cytotoxic activity toward 40 human cancer cell lines at the nanomolar level (mean IC50 = 89 nM) and 24 human tumor xenografts with the mean IC50 of 245 nM [55].
FE399 (134), a dehydroxylated 133, was isolated from Ascochyta sp. AJ 117309, an endophytic strain separated from a raw leaf of Taxus cuspidata var. nana Rehd. [56]. Compound 134 also demonstrated potent cytotoxic activity against SWS948, K562T, Colon26, CHO-K1 and P388 cells with IC50 values ranging from 75 to 400 ng/mL [56].

4.3. Thiols

Fusarium chlamydosporium, an endophytic fungus isolated from the leaves of Anvillea garcinii (Burm.f.) DC. (Asteraceae), produced a new benzamide derivative, fusarithioamide A (135), which is composed of a 2-aminobenzamide moiety, an l-alanine and a 3-mercaptopropan-1-ol moiety derived from l-cysteine. Compound 135 displayed cytotoxicity against SK-MEL, KB, BT-549 and SKOV-3 cells with IC50 values of 9.3, 7.7, 0.4 and 0.8 μM, respectively. It was also active against S. aureus, B. cereus, E. coli, P. aeruginosa and C. albicans with MIC values of 4.4, 3.1, 6.9, 100 and 2.6 μg/mL, respectively [57].
Fusarithioamide B (136), a new aminobenzamide derivative with an unprecedented carbon skeleton, was separated from an EtOAc extract of Fusarium chlamydosporium isolated from Anvillea garcinii (Burm.f.) DC. leaves (Asteraceae) [58]. Fusarithioamide B (136) displayed antifungal activity toward C. albicans with an MIC of 1.9 μg/mL. It also showed high antibacterial activity against E. coli, S. aureus and B. cereus with MIC values of 3.4, 2.9 and 3.9 μg/mL, respectively. Compound 136 exhibited cytotoxic activity toward BT-549, MCF-7, HCT-116, SKOV-36, KB and SK-MEL with IC50 values of 0.09, 0.21, 0.59, 1.23, 6.9 and 11.2 µM, respectively [58].

5. Terpenoids

5.1. Sulfide/Thiophene

Leptosphin A (137), a new sesquiterpenoid with a benzo[b]thiophene moiety, was obtained from a culture of Leptosphaeria sp. XL026 isolated from the leaves of Panax notoginseng [59]. Leptosphin A (137) displayed antifungal and antibacterial activity with MIC values ranging from 25 to 100 μg/mL [59].

5.2. Sulfates

An endophytic fungus S49 was isolated from the bark of Cephalotaxus hainanensis, known as Hainan plum-yew. S49 afforded two new sesquiterpenoids 1,10,11,12-guaianetetrol (138) and 1,10,11,12-guaianetetrol (139) [60]. Two new isopimarane diterpenoids, 16-O-sulfo-18-norisopimar-7-en-4α,16-diol (140) and 9-deoxy-hymatoxin A (141), were isolated from the culture broth of an endophytic fungus, Xylaria sp. YM 311647, obtained from Azadirachta indica. Compounds (140) and (141) were active against C. albicans YM 2005, A. niger YM 3029, P. oryzae YM 3051, F. avenaceum YM 3065 and H. compactum YM 3077 with MIC values in the range of 32–128 μg/mL, while compound 141 had the same MIC of 16 μg/mL toward C. albicans and P. oryzae [61].

6. Others

A new thiazole derivative, colletotricole A (142), was obtained from Colletotrichum gloeosporioides A12, an endophytic fungus derived from Aquilaria sinensis [62]. A sulfur-containing anticandidal compound, N-[(2S,3aR,6S,7aS)-6-acetamido-octahydro-l,3-benzothiazoi-2-yl]2-(adamantan-l-yl) acetamide (143), was isolated from Emericella sp. from Azadirachta indica [63].

7. Discussion and Conclusions

From 1985 to March 2022, 143 new sulfur-containing compounds were obtained from endophytic fungi. This review summarized the fungal producers, host plants, chemical structures and biological activities of these fungal metabolites (Table 1). The majority of these compounds (109 out of 143) were reported in 2010, 2014, 2015, 2017, 2019 and 2020 (Figure 6). There was a trend that more sulfur-containing compounds were reported in recent years except 2021. Only one sulfur-containing compound was reported in 2021, most likely due to the outbreak of COVID-19 in 2020. A total of 24 journals reported these compounds (Figure 7). The J. Nat. Prod. has published the highest number of papers (16) that reported sulfur-containing compounds, followed by Phytochemistry (8) (Figure 7). This is not unexpected because both J. Nat. Prod. and Phytochemistry are prominent natural product journals.
These sulfur-containing compounds demonstrate functional and structural diversity and exhibited many bioactivities. Among the reported biological activities, 42% of these compounds were antimicrobial, while 37% were cytotoxic (Figure 8), which is not surprising because the majority of the FDA-approved antimicrobial and anticancer drugs are either natural products or derived from natural products. For example, Secoemestrin D (69), a diketopiperazine, was very active against a panel of seven cancer cell lines with IC50 values ranging from 0.06 to 0.24 μM [27], while PM181110 (133) [55] and FE399 (134) [56], hybrids of polyketides and peptides, exhibited potent anticancer activity with IC50 values at the nM level. These compounds also possess other bioactivities. For instance, oreganic acid (128), a fatty acid derivative, inhibited FPTase with an IC50 of 14 nM [49]. The majority of sulfur-containing compounds (92) were peptides, followed by polyketides (38), hybrids (6), terpenoids (5) and others (2) (Figure 9). All 92 of these peptides are diketopiperazines, and the sulfur atoms in these molecules are mainly derived from l-cysteine that contains a reactive sulph-hydryl group.

8. Prospects

Some plants are rich in sulfur, for example, allium vegetables, legumes and cruciferous plants. These plants should be great sources of endophytic fungi that produce sulfur-containing compounds. Large amounts of sulfur are released during volcanic eruptions. Hence, plants in volcanic areas and hot springs might also be excellent sources for endophytic fungi producing sulfur-containing compounds.
Most of the compounds reviewed in this article were tested for their antimicrobial and antiproliferative or anticancer activities. We believe that other biological properties could be identified if fungal metabolites were evaluated in a broader range of biological settings. For example, sinuxylamides A and B were obtained from Xylaria sp. FM1005, an endophytic fungus isolated from Sinularia densa (leather coral) collected in the offshore region of the Big Island, Hawaii [64]. Sinuxylamides A and B showed no antibacterial activity or cytotoxicity at 40 μM, but they strongly inhibited the binding of fibrinogen to purified integrin IIIb/IIa in a dose-dependent manner with IC50 values of 0.89 and 0.61 μM, respectively.
Diketopiperazines are expected to be biosynthetically assembled from two amino acid building blocks by nonribosomal peptide synthetases [65]. On the other hand, the biogenesis of many sulfur-containing compounds remains incompletely understood. For example, the structures of compounds 20 [10], 40 [18], 98 [37], 136 [58], 142 [62] and 143 [63] are unique. It would be interesting to investigate how these molecules are biogenetically synthesized. Presumably, the 4,5-dihydrooxepine ring in 20 is derived from the benzene ring of l-phenylalanine through ring expansion. On the other hand, the spiro[cyclopenta[b]pyrrole-5,2′-furan] moiety in 40 might be formed through the constriction of the benzene ring of l-phenylalanine followed by the merge of the octahydrocyclopenta[b]pyrrole ring with an isoprenyl (C5) group. We previously isolated compound 98 [37]. The precursor of the side chain at the 14-position in compound 98 could be l-cysteine, which is converted to mercaptolactate. The nucleophilic addition of the mercaptolactate thiol to C-14 of paraphaeosphaeride C generates an intermediate that is oxidized to another intermediate. It is also plausible that the second intermediate is generated from mercaptopyruvate and paraphaeosphaeride C. The nitrogen atom in the second intermediate undergoes intramolecular nucleophilic addition to the ketone of the mercaptopyruvate moiety, leading to the formation of the third intermediate. The dehydration of the third intermediate yields the final product 98 [37]. However, the experimental details of the biosynthesis of compound 98 are still not available. Compound 136 is composed of five fragments, including a 2-amino benzoic acid moiety, an l-alanine, a 2-amino-2-methylsuccinic acid fragment that might be derived from an isoprenyl group (C5), and l-glycine and l-cysteine-derived 3-mercaptopropanoic acid moieties. Compound 142 carries a 2-hydroxyl propanoic acid ester. The thiazole ring in 142 is probably derived from acetate and l-cysteine, while the linker (-CH2-CH2-) might be derived from another acetate. It would be interesting to investigate how 142 is synthesized biogenetically. Investigating the biosynthesis of diamond-like compound 143 should be very challenging and interesting. Recent advances in genome mining and synthetic biology offer new opportunities to discover new natural products [66]. It becomes routine to sequence the (meta)genomes of fungal isolates, and capable bioinformatics tools (e.g., antiSMASH fungal version) [67] are increasingly available for identifying potential biosynthetic gene clusters (BGCs) of fungal natural products [68]. These predicted BGCs can suggest new chemotypes, enzymology and bioactivities. Subsequently, native and engineered BGCs can be expressed in multiple synthetic biology chasses, such as Aspergillus nidulans [69] and Saccharomyces cerevisiae [70]. In this regard, biosynthetic research is critical for laying the basis for the genome mining of BGCs of new fungal sulfur-containing compounds with bioactivities, particularly those whose biogenesis remains unclear.

Author Contributions

Y.D., C.W. and S.C.: Conceptualization. Y.F., Z.M., Y.Z. and Y.W.: discussion of the contents. C.W. and S.C.: writing—original draft preparation. Y.F., Z.M., Y.Z., Y.W., Y.D., C.W. and S.C.: writing—review and editing. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the National Natural Science Foundation of China (42006096), the Natural Science Foundation of Shandong Province (ZR2020QD098), the China Postdoctoral Science Foundation (2020M682266) and the Talents of High-Level Scientific Research Foundation of Qingdao Agricultural University (Grants 6651120031). Y.D. is partially supported by NIH R35 GM128742.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Jof 08 00628 g001 550
Figure 1. Structures of compounds 1–33.
Figure 1. Structures of compounds 1–33.
Jof 08 00628 g001
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Figure 2. Structures of compounds 34–59.
Figure 2. Structures of compounds 34–59.
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Figure 3. Structures of compounds 60–92.
Figure 3. Structures of compounds 60–92.
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Figure 4. Structures of compounds 93–116.
Figure 4. Structures of compounds 93–116.
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Figure 5. Structures of compounds 117–143.
Figure 5. Structures of compounds 117–143.
Jof 08 00628 g005
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Figure 6. Annual numbers of sulfur-containing compounds identified from 1985 to 2022. (Keywords: sulfur-containing compound, plant endophytic fungi; Databases: SciFinder, PubMed).
Figure 6. Annual numbers of sulfur-containing compounds identified from 1985 to 2022. (Keywords: sulfur-containing compound, plant endophytic fungi; Databases: SciFinder, PubMed).
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Figure 7. The journal names and numbers for the papers that reported sulfur-containing compounds.
Figure 7. The journal names and numbers for the papers that reported sulfur-containing compounds.
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Figure 8. The percentages of the biological activity among sulfur-containing compounds from endophytic fungi.
Figure 8. The percentages of the biological activity among sulfur-containing compounds from endophytic fungi.
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Figure 9. The structural classes of sulfur-containing compounds isolated from endophytic fungi.
Figure 9. The structural classes of sulfur-containing compounds isolated from endophytic fungi.
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Table
Table 1. Sulfur-containing compounds isolated from plant endophyte fungi.
Table 1. Sulfur-containing compounds isolated from plant endophyte fungi.
Compound StructuresProducing StrainHost Plant etc.BioactivityReference(s)
Jof 08 00628 i001Bionectria sp. Y1085Huperzia serrataAntibacterial[4]
Jof 08 00628 i002
Jof 08 00628 i003
Jof 08 00628 i004		Lasiodiplodia pseudotheobromaeFlower of Illigera rhodantha (Hernandiaceae)Antibacterial (5)[5]
Jof 08 00628 i005
Jof 08 00628 i006		Botryosphaeria mamaniFresh leaves of Bixa orellana L. (Bixaceae)Anticancer[6]
Jof 08 00628 i007Penicillium raciborskii (TRT59)Rhododendron tomentosum [7]
Jof 08 00628 i008
Jof 08 00628 i009
Jof 08 00628 i010
Jof 08 00628 i011
Jof 08 00628 i012		Epicoccum nigrumLeaves of Lysidice rhodostegiaInhibition of β-
Glucuronidase release (11 and 15)		[8]
Jof 08 00628 i013Tilachlidium sp. (CANU-T988)Decaying wood sample collected in ChristchurchCytotoxicity[9]
Jof 08 00628 i014Aspergillus terreus BCC 4651Tree holeWeak antimycobacterial activity[10]
Jof 08 00628 i015
Jof 08 00628 i016
Jof 08 00628 i017		Chaetomium sp. 88194Cymbidium goeringiiCytotoxicity (21)[11]
Jof 08 00628 i018
Jof 08 00628 i019		Penicillium crustosum and Colletotrichum gloeosporioides, respectivelyViguiera robusta [12]
Jof 08 00628 i020Chaetomium sp. SYP-F7950Panax notoginsengCytotoxic (26)[13]
Jof 08 00628 i021
Jof 08 00628 i022
Jof 08 00628 i023
Jof 08 00628 i024		Penicillium brocae MA-231Fresh tissue of the marine mangrove plant Avicennia marinaAntibacterial (30 and 31)[14]
Jof 08 00628 i025
Jof 08 00628 i026		Menisporopsis theobromae BCC 3975SeedAntimycobacterial
Cytotoxic (32)		[15]
Jof 08 00628 i027TolypocJadium sp.Quercus virginiana MillerPAF inhibition (35)[16]
Jof 08 00628 i028
Jof 08 00628 i029
Jof 08 00628 i030		Penicillium janthinellum HDN13-309Root of Sonneratia caseolarisCytoprotective (38 and 39)[17]
Jof 08 00628 i031Phoma lingam isolate LeroyRapeseed [18]
Jof 08 00628 i032
Jof 08 00628 i033		Phoma sp. OUCMDZ-1847Mangrove plant Kandelia candelCytotoxic (42)[19]
Jof 08 00628 i034
Jof 08 00628 i035		Penicillium brocae MA-231Avicennia marinaAntimicrobial (43)[20]
Jof 08 00628 i036Penicillium janthinellum HDN13-309Root of Sonneratia caseolaris [21]
Jof 08 00628 i037
Jof 08 00628 i038
Jof 08 00628 i039
Jof 08 00628 i040
Jof 08 00628 i041		Penicillium brocae MA-231Fresh tissue of the marine mangrove plant Avicennia marinaAntimicrobial[22]
Jof 08 00628 i042
Jof 08 00628 i043		Exserohilum holmiiDactyloctenium aegyptium [23]
Jof 08 00628 i044Nigrospora sphaericaGerminating fescue seed [24]
Jof 08 00628 i045
Jof 08 00628 i046
Jof 08 00628 i047		Setosphaeria rostrataFresh asymptomatic leaf tissues of the medicinal plant Costus speciosusInhibiting porcine pancreatic alpha-amylase (57)[25]
Jof 08 00628 i048Aspergillus versicolor 0312Stems of Paris polyphylla var. yunnanensisCytotoxic[26]
Jof 08 00628 i049Bionectria sp. Y1085Huperzia serrataAntibacterial[9]
Jof 08 00628 i050Lasiodiplodia pseudotheobromaeApparently normal flower of Illigera rhodantha (Hernandiaceae) [5]
Jof 08 00628 i051Botryosphaeria mamaniFresh leaves of Bixa orellana L. (Bixaceae)Cytotoxic[6]
Jof 08 00628 i052
Jof 08 00628 i053		Penicillium raciborskii (TRT59)Rhododendron tomentosumCytotoxic (64)
Antifungal (64)		[7]
Jof 08 00628 i054
Jof 08 00628 i055		Epicoccum nigrumLeaves of Lysidice rhodostegiaInhibiting the release of β-glucuronidase (67)[8]
Jof 08 00628 i056Emericella sp. AST0036Healthy leaf tissue of Astragalus lentiginosusCytotoxic[27]
Jof 08 00628 i057
Jof 08 00628 i058		Tilachlidium sp. (CANU-T988)Decaying wood sample collected in ChristchurchCytotoxicity[9]
Jof 08 00628 i059Trichoderma sp. BCC 5926Bamboo leafAntibacterial[28]
Jof 08 00628 i060Trichoderma harzianumZingiber officinale [29]
Jof 08 00628 i061Aspergillus tamariiFicus caricaCytotoxic
Antimicrobial		[30]
Jof 08 00628 i062
Jof 08 00628 i063
Jof 08 00628 i064
Jof 08 00628 i065		Penicillium brocae MA-231Fresh tissue of the marine mangrove plant Avicennia marinaCytotoxic (75, 76, 79 and 80)[31]
Jof 08 00628 i066Phoma sp. OUCMDZ-1847Mangrove plant Kandelia candel [19]
Jof 08 00628 i067Penicillium janthinellum HDN13-309Root of Sonneratia caseolarisCytotoxic[21]
Jof 08 00628 i068Penicillium brocae MA-231Fresh tissue of the marine mangrove plant Avicennia marinaCytotoxic
Antimicrobial		[20]
Jof 08 00628 i069
Jof 08 00628 i070		Gliocladium roseum 1ASubmerged woodNematicidal[32]
Jof 08 00628 i071Chaetomium sp. M336Huperzia serrata TrevCytotoxic
Antibacterial		[33]
Jof 08 00628 i072Aspergillus versicolor F210Bulbs of Lycoris radiataAnticancer[34]
Jof 08 00628 i073Bipolaris sorokiniana A606Pogostemon cablinAntiproliferative[35]
Jof 08 00628 i074
Jof 08 00628 i075		Paraphaeosphaeria neglecta FT462Lycopodiella cernuaAntibacterial (94)
Inhibiting NF-kB (94), iNOS (94 and 95)		[36]
Jof 08 00628 i076Paraphaeosphaeria neglecta FT462Lycopodiella cernua (L.) Pic [37]
Jof 08 00628 i077Guignardia sp. IFB-E028Hopea hainanensisCytotoxic
Antimicrobial		[38]
Jof 08 00628 i078
Jof 08 00628 i079
Jof 08 00628 i080		Cladosporium cladosporioides MA-299Bruguiera gymnorrhizaAntimicrobial[39]
Jof 08 00628 i081Cladosporium sp. SCNU-F0001Mangrove plant [40]
Jof 08 00628 i082
Jof 08 00628 i083		Cladosporium oxysporumRoot of Avicennia marina (Forssk.) Vierh. (Acanthaceae)Antimicrobial[41]
Jof 08 00628 i084
Jof 08 00628 i085		Aspergillus micronesiensisPhyllanthus glaucusCytotoxic
Antibacteria		[42]
Jof 08 00628 i086Trichoderma harzianum D13Root of mangrove plant Excoecaria agallocha Linn [43]
Jof 08 00628 i087
Jof 08 00628 i088		Aspergillus sydowiiLivewort Scapania ciliata S. Lac [44]
Jof 08 00628 i089
Jof 08 00628 i090		Pseudopestalotiopsis theaeLeaves of Caloncoba welwitschii [45]
Jof 08 00628 i091Sphaceloma sp. LN-15Leaves of Melia azedarach L. [46]
Jof 08 00628 i092Paraphaeosphaeria neglecta FT462Lycopodiella cernua [36]
Jof 08 00628 i093Neosartorya udagawae HDN13-313Root of the mangrove plant Aricennia marinaDecreasing the lipid accumulation elicited by oleic acid[47]
Jof 08 00628 i094Neosartorya udagawae HDN13-313Root of the mangrove plant Avicennia marina [47]
Jof 08 00628 i095
Jof 08 00628 i096		Penicillium crustosum PRB-2 and Xylaria sp. HDN13-249.Root of Sonneratia caseolarisAntibacterial[48]
Jof 08 00628 i097Alternaria sp.Polygonum senegalense Meisn. (Polygonaceae)Cytotoxic (123)
Inhibiting protein kinases (123)		[49]
Jof 08 00628 i098Ampelomyces sp.Urospermum picroides [50]
Jof 08 00628 i099Pestalotiopsis sp. AcBC2Aegiceras corniculatum [51]
Jof 08 00628 i100MF6046Surface-sterilized leaves of Berberis oregana (Berberidaceae)Inhibiting FPTase (128)[52]
Jof 08 00628 i101Fusarium sp. (CTGU-ZL-34).Davidia involucrataCytotoxic[53]
Jof 08 00628 i102Pestalotiopsis sp. HS30Isodon xerophilusAntitumor[54]
Jof 08 00628 i103Phomopsis glabraeLeaves of Pongamia pinnata (family Fabaceae)Anticancer[55]
Jof 08 00628 i104Ascochyta sp. AJ 117309Raw leaf of Taxus cuspidata var. nana RehdCytotoxic[56]
Jof 08 00628 i105Fusarium chlamydosporiumLeaves of Anvillea garcinia (Burm.f.) DC. (Asteraceae)Cytotoxic
Antimicrobial		[57]
Jof 08 00628 i106Fusarium chlamydosporiumAnvillea garcinii (Burm.f.) DC. leavesAntibacterial Antifungal
Cytotoxic		[58]
Jof 08 00628 i107Leptosphaeria sp. XL026Panax notoginsengAntifungal Antibacterial[59]
Jof 08 00628 i108
Jof 08 00628 i109		S49Bark of Cephalotaxus hainanensis tree [60]
Jof 08 00628 i110
Jof 08 00628 i111		Xylaria sp. YM 311647Azadirachta indicaAntifungal[61]
Jof 08 00628 i112Colletotrichum gloeosporioides A12Aquilaria sinensis [62]
Jof 08 00628 i113Emericella SpAzadirachta indicaAnticandidal[63]
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Fan, Y.; Ma, Z.; Zhang, Y.; Wang, Y.; Ding, Y.; Wang, C.; Cao, S. Sulfur-Containing Compounds from Endophytic Fungi: Sources, Structures and Bioactivities. J. Fungi 2022, 8, 628. https://doi.org/10.3390/jof8060628

AMA Style

Fan Y, Ma Z, Zhang Y, Wang Y, Ding Y, Wang C, Cao S. Sulfur-Containing Compounds from Endophytic Fungi: Sources, Structures and Bioactivities. Journal of Fungi. 2022; 8(6):628. https://doi.org/10.3390/jof8060628

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Fan, Yaqin, Zhiheng Ma, Yan Zhang, Yufei Wang, Yousong Ding, Cong Wang, and Shugeng Cao. 2022. "Sulfur-Containing Compounds from Endophytic Fungi: Sources, Structures and Bioactivities" Journal of Fungi 8, no. 6: 628. https://doi.org/10.3390/jof8060628

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