- freely available
Metabolites 2012, 2(1), 100-133; doi:10.3390/metabo2010100
Published: 30 January 2012
Abstract: Secondary metabolites are small molecules that show large structural diversity and a broad range of bioactivities. Some metabolites are attractive as drugs or pigments while others act as harmful mycotoxins. Filamentous fungi have the capacity to produce a wide array of secondary metabolites including polyketides. The majority of genes required for production of these metabolites are mostly organized in gene clusters, which often are silent or barely expressed under laboratory conditions, making discovery and analysis difficult. Fortunately, the genome sequences of several filamentous fungi are publicly available, greatly facilitating the establishment of links between genes and metabolites. This review covers the attempts being made to trigger the activation of polyketide metabolism in the fungal model organism Aspergillus nidulans. Moreover, it will provide an overview of the pathways where ten polyketide synthase genes have been coupled to polyketide products. Therefore, the proposed biosynthesis of the following metabolites will be presented; naphthopyrone, sterigmatocystin, aspyridones, emericellamides, asperthecin, asperfuranone, monodictyphenone/emodin, orsellinic acid, and the austinols.
Aspergillus nidulans, teleomorph Emericella nidulans, is one of the most significant biological model systems in the fungal kingdom. This was pioneered by Pontecorvos’  work in the middle of the last century, which demonstrated that A. nidulans, in addition to the asexual state, also proliferate via sexual and parasexual life cycles, hence, offering an ideal platform for genetic studies. Related species in the genus Aspergillus include important industrial cell factories, A. niger and A. oryzae, species that cause allergic diseases, A. clavatus, as well as opportunistic pathogens, such as A. fumigatus.
A common feature of aspergilli and filamentous fungi in general is their capacity to produce secondary metabolites (SMs). As opposed to the primary metabolites, SMs are not essential for cellular growth, but provide fungi, as well as bacteria and plants, with a competitive advantage in nature, e.g., by serving as agents for chemical warfare or as signal molecules. Hence, an impressive range of compounds with broad ranging bioactivities has evolved. SMs can be divided into four main chemical classes: Polyketides (PK), terpenoids, shikimic acid derived compounds, and non-ribosomal peptides (NRP). Moreover, hybrid metabolites composed of moieties from different classes are common, as in the meroterpenoids, which are fusions between PKs and terpenes. Hybrid molecules significantly add to the complexity and variety of the fungal metabolomes.
In addition to their likely important ecological roles in their natural biological niches, SMs also have a considerable impact on human life. For instance aflatoxins, ochratoxins, and fumonisins act as mycotoxins by having a detrimental effect on humans and livestock, whereas others are beneficial and serve as food additives, pigments, cholesterol-lowering drugs, immunosuppressants, antibiotics and anticancer agents. The different aspects of SM action and application have spurred a tremendous interest in fungal secondary metabolites, which is further underlined by the fact that around 63% of all small molecule drugs, which reached the market from 1981–2006 were inspired by natural products or derivatives thereof .
In filamentous fungi, the competitive race in SM development and the cost of producing and secreting complex compounds have resulted in the evolution of a multifaceted regulation of SM biosynthesis to avoid unnecessary use of resources. This hampers their discovery since production of most SMs is not induced under laboratory conditions. Analysis of full genome sequences of eight different aspergilli have demonstrated that for the majority of genes that putatively encode enzymes for SM production, the product is not known or detected. In this review, we will provide highlights of the use of genome mining, sophisticated molecular biological and chemical tools to trigger the production of SMs from cryptic gene clusters and discuss how these techniques have accelerated our understanding of PK production and regulation in A. nidulans.
1.1. Polyketide Biosynthesis in A. nidulans
PKs in fungi are synthesized by the use of acyl-CoA units. They act as the general substrates for large multi-domain enzymes named polyketide synthases (PKSs), which resemble eukaryotic fatty-acid synthases (FASs) in domain architecture. PKSs are divided into three types of PKSs based on their catalytic organization, however, only the iterative type I PKS (iPKS) has been reported in A. nidulans. The iPKS repeat the use of a single module containing several catalytic domains until the growing chain of acyl-CoA units block further elongation. For descriptions of PKSs in general, excellent reviews by Crawford , Hertweck  and Cox  can be consulted. The most commonly encountered catalytic activities in fungal PKSs will be addressed as a general introduction to fungal PKSs in the following three paragraphs.
Three fundamental domains are found in all iPKSs in A. nidulans like in filamentous fungi in general; β-ketosynthase (KS), acyltransferase (AT), and the acyl carrier protein (ACP). The KS catalyzes the C–C bond formation via decarboxylation reactions through Claisen condensations between thioesters. The ACP domain is responsible for transiently holding the growing acyl chain, hereby allowing the loading of malonyl extender units. The acyl groups are transferred from CoA by AT onto KS and ACP. The iterative use of the three domains results in a non-reduced PK, a β-keto thioester. Additional domains can be present in the PKS allowing the introduction of further chemical complexity.
iPKSs in fungi can, based on their catalytic domains, be classified as non-reducing (NR-PKSs), partially reducing (PR-PKSs), or highly reducing (HR-PKSs) . This is based on their ability to reduce the β-keto carbon. In PR- and HR-PKSs, reduction occurs through the β-ketoreductase (KR) domain that converts the β-ketone to a hydroxyl group. The resulting hydroxyl can go all the way to saturation by elimination of water through the dehydratase (DH) domain followed by hydrogenation by enoyl reductase (ER). In addition, reducing PKSs can also possess a methyltransferase domain (MT) responsible for C-methylation of the growing PK chain, using S-adenosylmethionine (SAM) as a carbon-donor. The degree of modifications and their position in the PK product is always the same for the individual PKSs. However, it is presently unknown how deployment of the various modifying domains is programmed into the PKS enzyme.
NR-PKSs differ in domain architecture from reducing PKS by not having any of the reducing domains and by having an N-terminal starter unit-ACP transacylase (SAT) domain and an internal product template (PT) domain. The SAT domain is responsible for selecting the starter unit to be extended by the enzyme , while the PT domain is responsible for folding and cyclization of the non-reduced PK backbone [3,8]. The number of iterations within the PKS and thereby the display of functional groups and the size of the final product is likely determined by the size of the active site cavity in the iPKS . Once the length of the final product has been achieved, the PK chain is released from the PKS, catalyzed by either a thioesterase (TE), a Claisen cyclase (CLC) domain if present, or by accessory enzymes. A more detailed discussion on PKS release mechanisms is reviewed by Du and Lou .
It should be noted that it currently is impossible to reliably predict the product of iPKSs based on their amino acid sequences and domain architecture. This is in part due to the inability to predict the number of iterations performed by the iPKS and in part due the lack of understanding of how deployment of tailoring domains in individual iterations are programmed into the enzyme.
Interestingly, the PKS encoding gene tends to reside in clusters of genes coding for a broad range of enzymatic activities. The compound coming directly from the PKS rarely seem to be the final product in the biosynthesis, but usually undergoes further modifications by tailoring enzymes from small decorations to drastic and large intervention and couplings.
Through inspection of the genome sequence (genome mining), the latest estimate of genes encoding PKSs in A. nidulans is 32 open reading frames (ORFs)  (Figure 1), indicating that the number of PK containing end products in A. nidulans should count at least 32 plus stable intermediates. The compounds detected under a given condition do not necessarily reflect the final outcome of a PK pathway, since the presence of intermediates and shunt products depends on other downstream enzymes and regulation.
At present, a total of nine PKS genes have been coupled to the polyketome (collection of PKs and their synthesis) in A. nidulans, and numerous endeavors are currently attempting to unveil the mechanisms of PK metabolism in this model fungus. The pathways described in this review will follow in chronological order with respect to the discovery from PK to genes. For each of the PK gene clusters that have been linked to products so far we will focus on the PK compounds, their discovery, genetics as well as their biosynthetic pathway: Naphthopyrone, sterigmatocystin, aspyridones, emericellamides, asperthecin, asperfuranone, monodictyphenone (emodin), orsellinic acid, and the austinols.
Spores from A. nidulans are characterized by a dark grey-green macroscopic appearance. This is due to deposition of pigments in the conidial wall as shown by ultrastructure studies using transmission electron microscopy (TEM) . The responsible pigment is based on the PK-naphthopyrone YWA1 and the function of the pigment layer has been shown to include quenching of reactive oxygen species  and increased resistance to UV radiation . The work on naphthopyrone synthesis in A. nidulans has paved the way for understanding iPKS domain structure.
The study of conidial pigmentation in A. nidulans has been extremely valuable for genetic screens. The first pigment mutant recorded in literature was the spontaneous white alba (wa) strain reported by Yuill in 1939 . In addition to the white mutant class, yA− mutants producing yellow conidia were discovered. These available color variants served as easy recognizable markers (green, white, and yellow) that allowed the establishment of fundamental genetic tools in A. nidulans . Interestingly, sexual crossing showed that the wA− mutation masked the effect of the yA− mutation (epistatic) [1,16]. Clutterbuck and co-workers  proposed that WA synthesized the yellow pigment that was observed in yA mutants and that the YA enzyme converted this compound into the green conidial pigment. In 1967, Agnihotri and co-workers  found that the wild type strains if grown under copper limiting conditions could mimic the yellow phenotype of the yA− strain. yA (AN6635) and wA (AN8209) were isolated and mapped to loci, chromosome I and II respectively, by complementation of a cosmid based library in 1989 and 1990, respectively [18,19]. Later, cross-feeding experiments performed by Clutterbuck  revealed that the yA phenotype was caused by the lack of a copper dependent extracellular laccase (p-diphenol oxidase). The wA functionality in pigment formation was confirmed by gene-deletion studies . The lack of clustering of the two A. nidulans conidial pigment genes also became evident by their different expression patterns and the finding that they are controlled by different regulatory systems [20,21]. The yA gene is expressed in phialide cells and primary sterigmata (metulae) , and controlled by BrlA and AbaA , while wA is expressed only in phialides  and controlled by WetA . Interestingly, none of the genes are expressed in the conidia. Characterization of the WA PKS was accomplished by Northern blotting, which revealed that wA encoded a 7.5 kb large transcript , and sequencing of the locus . Re-sequencing of the 3′ region in 1998 led to a revised gene model of the PKS with the following domain structure KS-AT-ACP-CLC. This novel CLC domain  catalyzed release of the product and cyclization of the second aromatic ring of YWA1 via a Claisen condensation reaction .
Heterologous expression of wA in A. oryzae resulted in the production of the yellow compound, as observed in yA− mutants, which was identified to be the heptaketide naphthopyrone named YWA1 . In 2002, wA was used for constructing a collection of chimeric PKSs (cPKS) by mixing its domains with those of Colletotrichum lagenarium pks1, known to produce the tetraketide 1,3,6,8-tetrahydroxynaphthalene (T4HN). One of the resulting cPKSs, SW-B, produced several new compounds including both tetra- and pentaketides . The results prompted a reanalysis of the two PKSs, which revealed the existence of two previously overlooked conserved domains; an N-terminal and a central domain. These domains were later identified as a SAT and PT domain, respectively, thus providing the full domain structure SAT-KS-AT-PT-ACP-CLC [3,7,8]. With the organization within WA in mind, the biosynthetic pathway can be envisioned as condensations of an acetyl-CoA with six malonyl-CoA units in six successive reactions resulting in the formation of YWA1  (Figure 2).
YWA1 is then believed to be dimerized or polymerized by the YA laccase into the green conidial pigment(s) via phenolic oxidative coupling. However, to date no one has succeeded in characterizing the chemical structure of the green conidial pigmentation in detail. As the final product remains elusive, it is impossible to predict if other tailoring enzymes further modify the YWA1 backbone or reactions occur with other metabolites or cellular components, e.g., the cell wall.
Sterigmatocystin, a PK, was first partially purified from a Sterigmatocytis sp. in 1948 by Nekam and Polgar . Hatsuda and co-workers [28,29] successfully isolated sterigmatocystin in 1954 from A. versicolor. The correct relative structure was determined in 1962 by Bullock et al. . By performing degradative experiments it was shown that the stereochemistry of sterigmatocystin was the same as that of aflatoxin , which had the absolute stereochemistry determined in 1967 . The absolute stereochemistry of sterigmatocystin was confirmed via crystallography [33,34].
The aflatoxins are among the most carcinogenic mycotoxins and the research in aflatoxin and sterigmatocystin intensified with the Turkey X disease caused by aflatoxins in the middle of the last century . Aflatoxins are reported to be produced only by a few aspergilli. A. nidulans does not produce aflatoxins, as the biosynthesis stops at sterigmatocystin, a late, yet stable precursor of the pathway. Sterigmatocystin is a powerful mycotoxin, though it is estimated to be 150 times less carcinogenic than the most potent aflatoxin, B1 . Fungi that are able to produce aflatoxins and/or sterigmatocystin are common contaminants of food, feed, and indoor environments and may be mammalian and plant pathogens [37,38]. Due to the high toxicity and prevalence of sterigmatocystin and aflatoxins, they are likely the most extensively studied examples of secondary metabolism in fungi both in terms of biosynthesis and biological function, and there are several excellent and comprehensive reviews for further reading on aflatoxin biosynthesis [39,40]. Studies on the biosynthesis of aflatoxin and sterigmatocystin have been carried out in several fungi (A. flavus, A. nidulans and A. parasiticus) and some of the assigned gene functions in A. nidulans are proposed based on gene homology to these two other species.
The biosynthetic cluster of sterigmatocystin in A. nidulans was first characterized by Brown and co-workers in 1996 . They identified a 60 kb region in the A. nidulans genome responsible for the synthesis of sterigmatocystin. The cluster contains 27 genes named stcA-X (Figure 3), reflecting their order of appearance on the chromosome .
The PKS catalyzing the production of the PK backbone of sterigmatocystin was identified by Yu and co-workers in 1995  and originally named pksST, but was later renamed to stcA by Brown et al.  to simplify nomenclature. Besides the PKS, the stc gene cluster is predicted to contain two transcription factors (aflR, aflJ), six monoxygenases (stcB, stcC, stcF, stcL, stcM, stcS, stcW), two dehydrogenases (stcG, stcV), an esterase (stcI), an O-methyltransferase (stcP), two ketoreductases (stcE, stcU), a VERB synthase (stcN), an oxidase (stcO), a monooxydase/oxidase (stcQ), a Baeyer-Villiger oxidase (stcR), a fatty acid synthase composed by the two subunits HexA and HexB (encoded by stcJ and stcK, respectively), and five unassigned genes (stcD, stcH, stcR, stcT, stcX), which may also be part of the cluster [39,40,41,43,44,45,46,47,41,43].
The stc cluster is a relatively large gene cluster, and studying the gene regulation has led to important discoveries. The two TFs were found to be present within the cluster. The AflR is a Zn2Cys6 TF that regulates transcription of the stc locus in A. nidulans [41,48], while AflJ (also named AflS) have been shown to have a role in the regulation of aflatoxin biosynthesis in A. flavus and is likely to have a similar function in A. nidulans . Interestingly, Bok and Keller  discovered a novel regulator (LaeA) of secondary metabolism in A. nidulans in a mutant screen for loss of aflR expression. Deletion of laeA resulted in a significantly decreased production of different classes of SMs like sterigmatocystin and penicillin. LaeA, a putative methyl transferase was moreover acting in a feedback loop with AflR since overexpression of aflR downregulates laeA expression, and overexpression of laeA could not increase production of sterigmatocystin . LaeA was shown to be a part of the conserved Velvet complex, which is important for regulation of fungal development and secondary metabolism . Another hint on chromatin regulated gene expression came from the deletion of a histone deacetylase, hdaAΔ, which led to significant increase in the expression of two stc cluster genes, stcU and aflR compared to the reference .
Applying this strategy of deleting and overexpressing genes encoding global epigenetic regulators has paved the way for novel discoveries in secondary metabolism. Moreover the alternative of utilizing a chemical epigenetic approach through epigenetic modifier molecules has proven successful in activating gene clusters in A. niger .
The first step in the biosynthesis of sterigmatocystin (Figure 4) is the production of hexanoate by the FAS units, StcJ and StcK . Watanabe and Townsend  showed that the hexanoyl-CoA is not an intermediate freed from the complex, indicating that hexanoate is transferred directly to the SAT domain of the PKS. The PK backbone is assembled by StcA by condensation of the starter unit, hexanoyl-CoA and seven malonyl-CoA extender units followed by cyclization and release of norsolorinic acid anthrone . The oxidation of norsolorinic acid anthrone to norsolorinic acid may be catalyzed by stcM, a monooxygenase ortholog to hypC that converts norsolorinic acid anthrone to norsolorinic acid in A. parasiticus . Norsolorinic acid is the first stable intermediate in the biosynthesis of sterigmatocystin and is converted into averantin by StcE, reducing the hexanoate ketone to an alcohol [41,55,56].
Yabe et al.  showed that 5′-hydroxyaverantin is a step towards aflatoxin in A. parasiticus and a later study showed that the oxidation of averantin into 5′-hydroxyaverantin is catalyzed by StcF . The conversion of 5′-hydroxyaverantin to 5′-oxyaverantin is likely catalyzed by StcG [39,44]. In a study in A. parasiticus by Yabe and co-workers it was shown that both (1′S, 5′S)- and (1′S, 5′R)-hydroxyaveratin are formed in the conversion of averatin to 5′-oxyaveratin . Disruption of aflH in A. parasiticus resulted in the accumulation of 5′-hydroxyaverantin, however, small amounts of O-methylsterigmatocystin present suggested that other enzymes may be involved in the reaction [44,59]. The gene(s) responsible for the conversion of 5′-oxyaverantin to averufin have not been identified [39,60].
Individual disruption of StcB and StcW resulted in elimination of sterigmatocystin and accumulation of averufin, indicating that both enzymes catalyze the conversion of averufin to 1-hydroxyversicolorone . It was not possible for the authors to determine why two monooxygenases were required for this reaction step . No gene products have been identified as being responsible for the conversion of 1-hydroxyversicolorone to versiconal hemiacetal acetate. StcI is thought to catalyze the reaction from 1-hydroxyversicolorone to versiconal based on studies of the ortholog AflJ in A. parasiticus, though other genes capable of this reaction may be present in A. nidulans [44,61].
Deletion of stcN did not result in the production of sterigmatocystin or other intermediates . However, StcN show homology to AflK and the versicolorin B synthase, Vbs, in A. parasiticus, indicating that the biosynthetic step from versiconal to versicolorin B may be catalyzed by StcN [39,44,62]. StcL was shown by Kelkar et al.  to catalyze the conversion of versicolorin B to versicolorin A. Inactivation of stcL resulted in accumulation of dihydrosterigmatocystin, leading to a branching of the sterigmatocystin biosynthesis as seen in the aflatoxin biosynthesis. Addition of versicolorin A to the mutant gave production of sterigmatocystin, and that indicated that this enzyme functions before versicolorin A .
Keller and co-workers [64,65] showed that StcU and StcS are involved in the conversion of versicolorin A to demethylsterigmatocystin. Individual disruption of stcU and stcS led to the accumulation of versicolorin A and eliminated production of sterigmatocystin in A. nidulans [64,65]. Henry and Townsend  studied the same step in the aflatoxin biosynthesis in A. parasiticus and proposed an oxidation-reduction-oxidation mechanism, involving at least a ketoreductase AflM and a monooxygenase AflN, orthologs to stcU and stcS, respectively. Ehrlich et al.  and Cary et al.  identified two enzymes, AflY, a Baeyer-Villiger oxidase and AflX, an oxidoreductase, to be involved in the conversion of versicolorin A to demethylsterigmatocystin in A. parasiticus and A. flavus, respectively. aflX and aflY are homologous to stcQ and stcR, which suggests that these genes might be involved in the biosynthetic step from versicolorin A to demethylsterigmatocystin [46,47].
The final step in the biosynthesis of sterigmatocystin is the methylation of demethylsterigmatocystin catalyzed by StcP . The conversion of sterigmatocystin to aflatoxin involves two additional biosynthetic steps; an O-methylation of sterigmatocystin by aflP followed by involvement of aflQ to produce aflatoxin . Slot and Rokas have recently showed that the sterigmatocystin gene cluster in Podospora anserina was horizontally transferred from Aspergillus, which shows that transfer of large metabolite clusters between fungi are possible .
Aspyridone is a PK-NRP hybrid and a fascinating example on how PK-NRP compounds in A. nidulans can be assembled from the activity of a single fusion enzyme. The aspyridones have shown to display moderate cytotoxicity . The responsible gene cluster was discovered by Bergmann and co-workers  using a genome mining approach. Using the Aspergillus genome sequence, they identified a SM gene cluster, which contained a putative TF (AN8414/apdR) that the authors hypothesized could trigger activation of the genes in the cluster. Accordingly, the authors overexpressed the TF under the control of an inducible alcA promoter by integrating it randomly in the genome. In agreement with the hypothesis, it was demonstrated by Northern blot analysis that six of the nearest neighbor genes were up-regulated in this strain on inductive medium, and that the aspyridones and two intermediates or shunt products could also be detected. Prediction of the catalytic potential for the six upregulated genes (apdA, apdB, apdC, apdD, apdE, and apdG) combined with the structure of the accumulating compounds allowed the authors to propose a model for the biosynthesis of aspyridones including an assignment of the involved enzymes (Figure 5).
The structure of aspyridone A and B suggested that their synthesis involved both PKS and NRPS activity. Indeed, analysis of the AN8412 structure revealed domains characteristic for a HR-PKS as well as NRPS in one ORF spanning more than 11 kb. This is a special subclass of reducing PKSs, where the PKS has been directly fused with a single NRPS module at the C′-terminal end. This architecture allows for the incorporation of amino acids or carboxylic acids into the carboxylic end of the growing PK chain. Only one of these fusion enzymes has been found in A. nidulans, but has been reported in other fungi [70,71]. Since AN8412 is the first enzyme to act in the pathway, the gene was named apdA. ApdA catalyzes the assembly of the PK-amino acid backbone of the aspyridones by three Claisen condensations of malonyl-CoA, and KR-DH-ER-MT carries out full reduction of the β-keto and the methylations, which are required. However, as ApdA lacks a functional ER domain, the ER activity is most likely provided by ApdC, a homolog to an enoyl reductase (LovC) from the lovastatin biosynthetic gene cluster . The resulting triketide is transferred to the NRPS module, where it is linked to tyrosine . Bergmann and co-workers listed the domains through protein homology in the NRPS as condensation (C), adenylation (A), peptidyl carrier protein (PCP) and reductase domain (RED).The release of the PKS-NRPS hybrid product was proposed to be a NADPH-dependent reductive release followed by an intramolecular Knoevenagel condensation and enzymatic oxidation . Biochemical studies of the role of ApdA and ApdC in the biosynthetic pathway of the aspyridones have been performed by Liu et al.  and Xu et al. . Liu and co-workers  defined the NRPS module as C-A-T-R with the latter two being thiolation and reductase, which is an alternative to the more frequent C-A-T-TE found in these modules. However, this reductase domain (R*) in the NRPS module of ApdA is not the standard SDR superfamily dehydrogenase since tyrosine in the Ser-Tyr-Lys catalytic triad is mutated suggesting a redox-independent condensation reaction and the release of a tautomer of preaspyridone from ApdA by a Dieckmann cyclization, which was first shown by Halo and co-workers . This result has been confirmed by Xu et al. who expressed the apdA and apdC genes in Saccharomyces cerevisiae and Escherichia coli, respectively . The purified enzymes (ApdA and ApdC) were incubated in the presence of cofactors and building blocks and the predominant product was preaspyridone .
The formation of preaspyridone into aspyridone A and B was proposed by Bergmann et al. , (and outlined in Figure 5a) using the predicted functions of the remaining genes of the apd gene cluster. The proposed biosynthesis involved ApdB and ApdE which shows similarity to cytochrome P450 oxygenases and cytochrome P450 alkane hydroxylases, respectively, and were believed to catalyze the formation of hydroxypreaspyridone . Based on the study of pyridone rearrangement in metabolites related to aspyridone it was suggested that ApdE or ApdB were involved in the pyridone rearrangement [68,75,76,77]. Moreover, aspyridone A was hypothesized to be converted into aspyridone B by ApdD, a putative FAD-dependent monooxygenase, which is related to other ring hydroxylases . Aspyridone has a similar structure to other pyridines isolated from fungi, e.g., tenellin whose biosynthetic gene cluster also has been identified [75,76]. The proposed biosynthesis of aspyridone was, as described above, based on predicted gene functions and not isolated intermediates. However, a study on the biosynthesis of the related metabolite tenellin by Halo and co-workers  showed that the suggested biosynthesis may be incorrect and an alternative biosynthesis was suggested (as shown in Figure 5b). In this biosynthesis preaspyridone is not converted into hydroxyaspyridone but ring expanded by ApdE to aspyridone A similar to the biosynthesis of tenellin . Halo et al. also showed that the hydroxylated metabolite of pretenellin is a shunt metabolite as it could not be converted into tenellin.
The emericellamides are other examples of hybrid compounds that are formed between PKs and NRPs. In this case the biosynthesis requires a PKS and a NRPS rather than a fusion PKS-NRPS as used in the production of the aspyridones. Emericellamides are cyclic depsipeptides and a total of five variants, A, C–F, of these metabolites have been found in A. nidulans. Initially, emericellamide A and B were isolated and described from an unidentified marine-derived Emericella strain in a screen due to their antibacterial activity against methicillin-resistant Staphylococcus aureus .
In order to discover novel natural products, Chiang and co-workers  searched the genome sequence of A. nidulans for NRPS gene candidates. Subsequently, six of these genes were randomly chosen and deleted by gene targeting. One of the resulting mutants, AN2545Δ, showed a metabolite profile where emericellamide A was missing. Furthermore, HPLC profiles and dereplication using mass spectrometry and database searches revealed four additional compounds, which disappeared in the mutant metabolite profile. Since these compounds had not previously been described in A. nidulans, they were purified and their structures solved by NMR analysis revealing that they were novel analogues of emericellamide A and B, thus named emericellamide C–F .
To investigate whether AN2545, now called easA, defines a gene cluster encoding all necessary enzymatic activities in the emericellamide biosynthetic pathway, the genes from AN2542 to AN10325, a total of ten, were deleted . Most of these gene deletions did not affect emericellamide production as judged by LC-MS analysis, demonstrating that they do not participate in the biosynthesis. However, the emericellamides were absent in four of the deletion strains, now named easA-easD, indicating that these genes are involved in the pathway.
Bioinformatic analysis of the three additional genes suggested that they all encode activities that are relevant for emericellamide biosynthesis. Specifically, easB (AN2547), a PKS, easC (AN2548), an acyl transferase, and easD (AN2549), an acyl-CoA ligase. Based on these putative activities, the authors proposed a biosynthetic pathway for emericellamide production (Figure 6). In this model, the biosynthesis is initiated by EasB, a HR-PKS composed of the domains KS-AT-MT-DH-ER-KR-ACP. Since the PK component of the different emericellamide variants differ with respect to chain length and methylation pattern, it indicates that iterativity of this PKS is flexible .
Next, the PK carboxylic acid is converted to a CoA thioester by the acyl-CoA ligase, EasD, loaded onto the acyltransferase EasC, and then transferred to the thiolation (T) domain of EasA. This NRPS is a multi-modular enzymatic assembly containing 18 domains grouped into five modules. Among those, the authors propose that the first T domain is responsible for accepting the incoming PK from EasC (Figure 6). Moreover, the remaining domains fit well with the fact that five amino acids are incorporated into emericellamides. The authors note that this NRPS does not contain a TE domain at the end of module 5, indicating that this enzymatic activity is not necessary for cyclization of the emericellamides .
Asperthecin is a PK compound that was first isolated from A. quadrilineatus by Howard and Raistrick in 1955 , however, the structure was not fully determined until six years later . Initially, various chemical derivatizations and spectroscopic data determined a partial structure of asperthecin . Neelakantan and co-workers  reduced the number of possible structures to two, and further derivatizations of asperthecin by Birkinshaw and Gourlay resulted in the final structure . A. quadrilineatus is a member of the A. nidulans group, therefore Howard and Raistrick  extended the search of asperthecin to additional members of the A. nidulans group. No other was as rich in asperthecin production as A. quadrilineatus, yet small amounts of crystallized asperthecin could be obtained from cultures of A. nidulans and A. rugulosus indicating that production of asperthecin was possible in other aspergilli .
About 50 years later, Szewczyk and co-workers  used a molecular genetics approach to find the gene cluster responsible for the production of asperthecin in A.nidulans. Since many aspects of the regulation in the polyketome were unknown, the authors speculated whether sumoylation had an effect. SUMO is a small ubiquitin-like protein which is post-translationally added to proteins in the cell, as it plays a role in regulating transcription. A. nidulans contains one SUMO encoding gene, sumO , deletion of which led to a decrease in the production of SMs such as austinol, dehydroaustinol, and sterigmatocystin, and an increase in the production of a metabolite identified to be asperthecin, whereas the production of emericellamides were not affected . Due to the aromatic structure of asperthecin, Szewczyk et al.  studied the domain prediction in 27 putative PKS-protein sequences using the A. nidulans genome sequence and available tools, in order to identify potential producers of non-reduced PKs. Ten NR-PKSs were identified and a deletion series of all NR-PKS genes was performed in the sumO∆ background . While nine of the PKS-deletion strains still produced asperthecin, the AN6000 (aptA) PKS-deletion strain failed to synthesize asperthecin . With the notion that most end compounds in PK biosynthesis are made by a clustered gene collective, six candidate genes surrounding aptA were picked in an attempt to identify the apt biosynthetic cluster. Two of these genes, aptB (AN6001) and aptC (AN6002), were found to be required for asperthecin production . One strain (AN5999Δ) had a significantly lower production of asperthecin compared to the reference strain, but asperthecin was still present in the metabolite extracts, and as the strain showed poor growth, it was not included in the apt gene cluster.
Interestingly, AptA was shown to have SAT-KS-AT-PT-ACP domains, but lack a TE/CLC domain [83,85,86,87,88]. Independent groups have used this case as a model system to study the mode of PK release, and two alternating mechanisms for the biosynthesis of asperthecin are shown in Figure 7 [86,87]. The first model suggests the formation of the PK backbone by condensations of one acetyl-CoA and seven malonyl-CoA units , with the β-lactamase AptB releasing the octaketide from AptA . This assumption was based on a study by Awakawa and co-workers  in A. terreus, where there was a release of atrochrysone carboxylic acid from the atrochrysone carboxylic acid synthase (ACAS) lacking a TE/CLC domain, in the presence of the atrochrysone carboxylic ACP thioesterase (ACTE), a member of the β-lactamase superfamily . The unstable atrochrysone carboxylic acid then undergoes a series of reactions; decarboxylation, dehydration, and various oxidations where the monooxygenase AptC is believed to be involved, and in the end yielding asperthecin .
In another approach, Li et al.  introduced aptA, aptB, and aptC into S. cerevisiae, which resulted in the production of a nonaketide (here called preasperthecin), and not the octaketide as proposed by Chiang et al. . Expressing aptA and aptB without aptC resulted in a product identical to preasperthecin except for the lack of C2-OH, confirming that AptC is responsible for this step . Expression of aptA and aptC alone did not lead to the production of preasperthecin or any other traceable compounds, confirming that AptB is needed for release of the PK from AptA . These results were confirmed by an in vitro assay after expressing aptA, aptB and aptC in E. coli . Further insight into AptA functionality came from expressing the AptA-PT domain in E. coli, and combining it with the Gibberellafujikuroi PKS4, which can produce nonaketide products in vitro . The experiment revealed that AptA-PT can catalyze C6-C11 cyclization, and most likely also the C4-C13 cyclization. Further, a spontaneous C2-C15 cyclization was followed by a C1-C17 esterification . The apt gene cluster appears likely to consist of additional genes, which are responsible for the conversion of preasperthecin into asperthecin.
Asperfuranone is an example of a novel PK metabolite discovered through genetic mining in A. nidulans, as this compound had not previously been reported in the literature before Chiang and co-workers  in 2009. Asperfuranone was later shown to possess bioactive properties as it inhibited proliferation of human non-small A549 cancer cells . Investigating the loci containing putative PKS gene clusters, Chiang and co-workers  noticed that a NR-PKS gene (AN1034, afoE) and a HR-PKS gene (AN1036, afoG) were located close to each other on chromosome VIII. Since no products had ever been detected from activity of this locus, and due to the rare constellation of two neighbor PKSs, the authors speculated whether a novel metabolite could be revealed. A putative transcriptional activator (AN1029, afoA) was found near the PKS and the authors replaced the upstream sequence of afoA, estimated to be the native promoter, with the inducible alcA promoter . This indeed turned on the expression of the cluster, since asperfuranone and a precursor metabolite were detected. The structure of asperfuranone was determined based on one- and two-dimensional NMR experiments and the absolute configuration by a modified Mosher’s method, whereas the precursor preasperfuranone had already been determined in the literature [89,91]. With these two compounds being identified, a gene-deletion strategy was performed to map the other genes assigned to the afo gene cluster, which involved twelve surrounding genes including the two PKSs . Four deletion strains afoD∆, afoE∆, afoF∆, and afoG∆ fully eliminated asperfuranone production whereas afoB∆ and afoC∆ strongly reduced production of asperfuranone . The deletions confirmed that both afoE and afoG were responsible for the production of asperfuranone, and that the deletion of afoD, encoding a putative hydroxylase, resulted in the production of preasperfuranone . Deletion of afoB reduced the production of asperfuranone and due to a high homology to efflux pumps, Chiang and co-workers  suggested that it was responsible for the transport of asperfuranone out of the cell.
With the gene cluster and predicted functionalities of the gene products defined, a biosynthetic pathway of asperfuranone was proposed (Figure 8) . The assembly of the primary reduced tetraketide is synthesized by AfoG from one acetyl-CoA, three malonyl-CoA, and two SAM. The tetraketide is transferred to the SAT domain of AfoE and extended with four malonyl-CoA and one SAM . The octaketide is released from AfoE after aldol condensation and reductive release from a C-terminal reductase (R) domain, which resembles a reductive release mechanism to generate the aldehydes described by Bailey et al. , forming the aldehyde preasperfuranone . The biosynthetic steps from preasperfuranone to asperfuranone are uncharacterized and the suggestions are not based on identified metabolites . Accumulation of preasperfuranone in the afoDΔ suggested AfoD to be the next enzyme in the biosynthesis of asperfuranone. The deletions of afoF, encoding a putative FAD/FMN-dependent oxygenase and afoC, initially believed to code for a homologue to citrinin biosynthesis oxidoreductase, did not reveal any intermediates, the order of reactions and the exact enzymatic functions for AfoF and AfoC have not been determined. In afoC∆, the production of asperfuranone was not fully eliminated, which Chiang and co-workers  suggested could be due to other enzymes catalyzing the reaction, however less efficiently.
Other puzzling discoveries have been made in connection to the asperfuranone production. When trying to activate a cryptic NRPS gene cluster containing two NRPSs, inpA (AN3495) and inpB (AN3496), by overexpression of a regulatory gene, scpR (AN3492), Bergmann et al.  also activated asperfuranone. This is an interesting example of a regulatory gene located on chromosome II that activates the afo cluster located on chromosome VIII . Lui et al.  have attempted to engineer the production of a new metabolite by swapping the SAT domain of AfoE with the StcA-SAT. This led to the production of a new metabolite though having the same length as the native AfoE product, asperfuranone .
The PK monodictyphenone was first reported in A. nidulans in 2005  and the genes behind the production of monodictyphenone were mapped four years later . This discovery not only enabled the establishment of a biosynthesis model for monodictyphenone in A. nidulans, it has subsequently revealed that more than ten different stable products among different classes of related polyketides can be linked to monodictyphenone biosynthesis [11,96,97,98]. These metabolites count monodictyphenone, emodin and the emodin derivates 2-hydroxyemodin, 2-aminoemodin, ω-hydroxy emodin, and emodic acid. Moreover, the arugosins and prenyl-xanthones are also coupled to the pathway [11,98]. The compound emodin has been studied for more than a century , and is an anthraquinone found in a wide array of both plants and fungi [100,101]. Emodin and several derivatives (e.g. emodic acid) have been shown to possess anti-bacterial and cancer preventive properties [102,103,104,105,106].
The presence of the SM clusters in silent areas of chromosomes, e.g. near telomeres and centromeres, suggests that chromatin remodeling factors can influence the expression of genes responsible for SMs. As rationalized by Bok and co-workers , removal of histone-tail methylation could open heterochromatic regions for transcription. The authors deleted an ortholog, cclA, to the yeast BRE2 gene, encoding an enzyme partner of the COMPASS transcriptional regulator complex conserved in eukaryotes, which rendered A. nidulans defective in di- and trimethylation of lysine 4 of the histone 3 tails (H3K4). The cclA deletion was established in a mutant strain, stcJΔ, to avoid interference of high amounts of sterigmatocystin in purification of other metabolites. The effect was striking as the loss of CclA in HPLC analysis showed an altered chemical landscape compared to the stcJΔ reference .
As the compounds appearing were UV-active suggesting high conjugation likely due to aromaticity, the ten NR-PKSs investigated in the asperthecin and asperfuranone studies were individually deleted in the cclAΔ stcJΔ double deletion background. This screen revealed six products that all were linked to one PKS, AN0150 (mdpG) . Delineation of the cluster was achieved by inspecting the genome sequence for possible cluster candidates followed by Northern blotting for gene-expression analysis in the cclAΔ stcJΔ, where the products were detected. The cluster was found to span 12 putative ORFs (AN10021-AN10023 (mdpA-L))  of which two genes AN0147 (mdpD) and AN10035 (mdpI), did not show altered expression from the reference [96,97]. The mdp-cluster candidates were also deleted in the cclAΔ stcJΔ mutant strain to confirm the expression analysis data and to draw the borders of the cluster . The authors suggest that two transcriptional activators are present within the cluster; MdpE as a main activator (homologue to AflR) and that MdpA is a co-activator. The mdp locus is located near the telomere of chromosome VIII, and activation of the genes in the cclAΔ strain supports the hypothesis of epigenetic regulation in these areas through chromatin remodeling .
Two groups cultivated A. nidulans on complex growth media, which revealed six additional metabolites. First Sanchez et al.  discovered that emericillin, variecoxanthone A, shamixanthone, and epi-shamixanthone were also products of the mdp cluster, and subsequently Nielsen and co-workers  added arugosin A and H to the pathway. Since these PKs are prenylated, a BLAST search of the A. nidulans genome sequence was performed and pathway-candidate genes were deleted. Two prenyl transferases encoded by xptA and xptB, and one neighbor GMC oxidoreductase encoded by xptC, were found to be involved in the pathway, though they were located on other chromosomes than the mdp cluster (for cluster overview see Sanchez et al. ). This is an intriguing example of SM-cluster members located on more than one chromosome, however, prenyl transferases are known to have broad substrate specificity, and it is currently not known whether they are involved in other processes than prenyl-xanthone formation .
MdpG synthesizes the main PK backbone. Since MdpG lacks a CLC/TE domain, MdpF, a putative zinc dependent hydrolase, is believed to catalyze the release of the PK from MdpG . The mechanism is believed to follow the case of ACAS and ACTE as introduced previously in the asperthecin section. Awakawa and co-workers  demonstrated that the direct product of the ACAS/ACTE is not emodin anthrone as proposed earlier [107,108], but more likely atrochrysone carboxylic acid (Figure 9). Atrochrysone carboxylic acid was not observed in vitro, instead the decarboxylated product atrochrysone was the major product in the assays and therefore proposed to be an intermediate to emodin, as suggested by Couch and Gautier . Conversion of atrochrysone to emodin requires dehydration (forming emodin anthrone) and a final oxidation (Figure 9), however, Awakawa and co-workers  observed small amounts of both emodin anthrone and emodin in vitro showing that these reactions may occur non-enzymatically. Based on these observations, Chiang and co-workers  proposed that mdpH encodes a decarboxylase, catalyzing the conversion of atrochrysone carboxylic acid to atrochrysone. The deletion of mpdH resulted in accumulation of a shunt product endocrocin produced via endocrocin anthrone. Enzymes responsible for dehydration of atrochrysone or modification of emodin into the observed derivatives have not yet been identified.
The first stable intermediate following emodin towards the prenyl-xanthones is monodictyphenone [97,98], and gene-deletion studies points to at least the five following enzymes are involved; a dehydratase (MdpB), a ketoreductase (MdpC), a glutathione S transferase (MdpJ), an oxidoreductase (MdpK), and a Baeyer-Villiger oxidase (MdpL) . The mechanism has been proposed to be analogous to the conversion of versicolorin A to demethylsterigmatocystin which is known to proceed through oxidation-reduction-oxidation catalyzed by a cytochrome P450 monooxygenase (VerA) and a ketoreductase (StcU) [45,65,110]. However, none of the above mentioned Mdp enzymes appear to be homologous to VerA, and the role of the individual enzymes has not been investigated further .
The biosynthesis of the six monodictophenone derived metabolites is based on hydroxylation (MdpD), C-prenylation (XptA), O-prenylation (XptB), and carboxylic acid reduction (unidentified enzyme) [11,98]. Central in the pathway is the hydroxylation of C2 in monodictyphenone accompanied by reduction of the carboxylic acid. The carboxylic acid is suggested by Sanchez and co-workers  to be reduced to a hydroxy group, the B-ring is closed by dehydration and the intermediate is O-prenylated at C2 to yield variecoxanthone A, which in turn is C-prenylated to emericillin (Figure 10). The final known step in prenyl-xanthone biosynthesis gives rise to the stereoisomers shamixanthone and epishamixanthone and is catalyzed by XptC . Alternatively, Nielsen and co-workers include synthesis of arugosins by partially reducing the carboxylic acid to an aldehyde, followed by C-prenylation, yielding arugosin H and O-prenylation to give arugosin A. Subsequent reduction of the aldehyde to a hydroxyl group, and ring closure by dehydration then gives emericillin and shamixanthones .
9. Orsellinic Acid
In addition to the mdp cluster, the loss of CclA also led to the discovery of another gene cluster driven by an NR-PKS . Two PK products, the cathepcin K inhibitors F-9775A and F-9775B, first isolated from Paecilomyces carneus , were detected and mapped to AN7909. Following this discovery, Schroeckh and co-workers  found the primary metabolite from AN7909 (orsA) to be orsellinic acid, an archetypal metabolite . Moreover, the metabolite lecanoric acid typically found in lichens and produced by mycobiots such as Umbilicaria antarctica  was linked to OrsA . Following the initial observations, the number of detected metabolites from the orsA gene cluster has expanded to gerfelin, a C10-deoxy-gerfelin, diorcinol, orcinol, cordyol C, and violaceol I and II [115,116]. The biosynthetic activities of the orsA cluster are as yet not elucitated, and this illustrates the need for applying different eloquent strategies to trigger production of these metabolites.
The deficiency in methylation of H3K4 in the cclAΔ strain resulted in activation of both mdp and ors gene clusters. Expression analysis revealed that the annotated ORFs from AN7909-AN7915 were possible cluster members, hereby indicating candidates for a gene cluster . The ors gene cluster, orsB-orsE, was identified by Schroeckh and co-workers  as four additional ORFs spanning AN7911-AN7914, which was confirmed by Sanchez et al. , who deleted all genes from AN7901 to AN7915. Interestingly, the neighbor PKS to the ors locus, AN7903, was deleted by Nielsen et al.  and the resulting strain failed to produce F-9775A and B like AN7909Δ under the conditions tested. Schroeckh and co-workers  defined orsA-E using gene-expression analysis through both an Aspergillus secondary metabolism array (ASMA) and relative expression analysis in quantitative reverse-transcriptase PCR (qRT-PCR). The induction of orsA was achieved by co-cultivating with a soil bacterium, Streptomyces rapamycinicus (initially named S. hygroscopicus) and extracting mRNA from the fungus . This response on SM level was further investigated by Nützmann and co-workers . Since the loss of H3K4 methylation induced gene expression in ors locus , the rationale was that the transcriptional activation of silent secondary-metabolism genes by acetylation of lysines on histone tails, especially H3K9, is equally important and the search for histone acetyl transferases (HATs) in the genome sequence was commenced . Forty HATs were found and deleted, and only four proved to be essential. Of the 36 deletions of nonessential HATs in A. nidulans, the deletions of gcnE and adaA, both essential core parts of the multi-subunit Saga/Ada complex, an important complex for HAT activity in A. nidulans, significantly lowered the ors transcripts investigated . Thus, Saga/Ada plays a role in the response to S. rapamycinicus and loss of this complex downregulated orsellinic acid metabolites, as well as sterigmatocystin, terrequinone, and penicillin .
Four additional orsellinic acid derived compounds were found in a defect COP9 signalosome (CSN) mutant strain . The multiunit CSN complex is found in higher eukaryotes, albeit with different functional roles depending on the tissues. In A. nidulans the CSN is required for fruiting body formation and is not essential for asexual growth. By deleting csnE; orcinol, cordyol C, and violaceol I+II were produced, and the genes orsA-orsE were shown to be differentially expressed . The link of the violaceol metabolites to ors was confirmed by Nielsen and co-workers  who applied an OSMAC strategy on their reference strain and compared this to their deletion library.
Very little is known about the biosynthesis of the metabolites of the ors locus. One acetyl-CoA and three malonyl-CoA units can yield a C8 aldol intermediate, and as proposed by Nielsen et al. , this can lead to the tetraketide orsellinic acid through loss of water and enolization and to the C7 compound orcinol by decarboxylation and enolization. Oxidation of orcinol in the para position then leads to 5-methyl-benzene-1,2,3-triol which is believed to either dimerize with the loss of water to give violaceol I and II, Figure 11, or to give F-9775A+B, Figure 12, in an unknown series of synthesis steps. Another outcome is the formation of lecanoric acid by dimerization of orsellinic acid. Though the steps in the pathway have been hypothesized, most steps are not accounted for. It has been reported that OrsA having the domains SAT-KS-AT-PT-ACP-TE is responsible solely to form orsellinic acid. OrsA, OrsB, and OrsC seem to be sole responsible for F-9775A+B formation. Moreover, it has been shown that gerfelin and a C10-deoxy derivative of gerfelin accumulate in orsBΔ, whereas diorcinol was found in high amounts in the orsCΔ strain . Gerfelin, C10-deoxy gerfelin and cordyol C are all dimers built up of two of the three suggested monomer units, orsellinic acid, orcinol and 5-methylbenzene-1,2,3-triol.
Recently Scherlach and co-workers  continuously cultivated A. nidulans under nitrogen-limitation and carbon-limitation. At nitrogen limiting conditions in continuous cultivations two novel products, denoted as spiroanthrones, were found. They could not be detected at batch cultivation. The metabolites were based on anthraquinone and orsellinic acid derived phenols. The induced expression of both mdpG and orsA confirmed increased activity under the N-limiting continuous cultivation conditions.
10. Austinol and Dehydroaustinol
The meroterpenoids austinol and the related compound dehydroaustin were first isolated from A. ustus by Simpson and co-workers in 1982 , where the structure of austinol was elucidated by 1H and 13C NMR. Austinol and dehydroaustinol are just two examples out of many meroterpenoids that are derived from 3,5-dimethyl orsellinic acid as presented in the excellent review by Geris and Simpson .
The two austinols were detected for the first time in A. nidulans four years ago , where it was further substantiated that austinol was indeed of partly PK origin. Deletion of the phosphopantheteinyl transferase (PPTase) cfwA/npgA in A. nidulans resulted in a strain that among many other compounds did not produce austinol and dehydroaustinol . The PPTase is responsible for attaching the phosphopantetheine moiety to the acyl carrier domain of the PKSs and NRPSs, thus it is an activator of the enzyme complexes. Hence, the abolition of austinol and dehydroaustinol production in the PPTase deficient strain strongly suggests a PK origin of these compounds.
In 2011, Nielsen and co-workers  discovered the PKS responsible for synthesis of the PK part of austinol and dehydroaustinol in A. nidulans. A deletion library of all 32 putative PKS genes in A. nidulans was created and screened using an OSMAC approach  to enable activation of different clusters on different media. One single strain deleted in AN8383 (ausA) failed to produce austinol and dehydroaustinol . This discovery was supported by the introduction of a point mutation at the phosphopantetheine attachment site, thus abolishing activation of the enzyme by the PPTase to ensure the loss of austinols was not an indirect effect e.g., at chromatin level. The ausAΔ strain was complemented by re-introducing the ausA gene into the deletion strain. Introducing the gene under control of the inducible alcA promoter revealed that 3,5-dimethyl orsellinic acid (3,5-MOA) was indeed the precursor for austinol and dehydroaustinol in A. nidulans, as shown experimentally via labeling studies by Simpson and co-workers 20 years earlier [11,123,124].
A more detailed understanding of the biosynthesis of the austinols has not been established yet. However, it is well established that 3,5-dimethyl orsellinic acid is synthesized from condensation of an acetyl-CoA unit with 3 malonyl-CoA units to form the PK backbone, which is methylated twice, catalyzed by AusA. The PK part is then alkylated with farnesyl pyrophosphate to form a transient intermediate (Figure 13), which can then act as a precursor for several similar meroterpenoids, such as andibenins, austin, berkeleyones and andrastins . Recently we tentatively identified neoaustin and austinolide in A. nidulans extracts by LC-MS analysis (unpublished data), which makes us hypothesize that the biosynthesis towards the austinols involves (i) oxidation and acyl shift in the D ring (ii) lactonization from the substituent groups of the D ring, a Baeyer-Villiger type oxidation and 1,2 alkyl shift in the A ring to give neoaustin. Neoaustin is subsequently oxidized in the D ring by another Baeyer-Villiger type oxidation to give austinolide that upon further oxidation and ring condensation leads to austinol and dehydroaustinol, Figure 13.
11. Concluding Remarks
Secondary metabolism represents chemical diversity and span in biological functionality to the extreme. As shown above, individual compound classes can even form hybrid molecules to other compound classes. There is a high commercial interest in discovery and utilization of SMs in general as drugs or additives, or to avoid mycotoxins in food and feeds. Mapping PK biosynthesis to genes in A. nidulans as presented in this review involves great complexity. One challenge is to find and activate the genes required to produce the compounds. As shown, it takes in-depth understanding of fungal biology, nutrient sensing, chromatin remodeling, as well as analysis on all levels from DNA to metabolites to unveil cryptic gene clusters and their products. Moreover, the majority of the pathways described in this review have been elucidated in a relatively short time span. This has been possible due to bioinformatics. The availability of the genome sequence, as well as resources and tools in, e.g., Aspergillus Comparative Database (ACD), Aspergillus Genome Database (AspGD), and the Central Aspergillus REsource (CADRE) have been key aids to perform the extensive genome mining.
The ability to predict enzymatic function based on gene sequences has proven fruitful in characterization of secondary metabolism, since this has revealed the location of e.g., PKS genes. Additionally, the presence of gene cluster specific TFs was utilized in activation of silent SM clusters both in the case of aspyridones and asperfuranone. The asperfuranone biosynthesis is moreover an example of a previously unknown compound, with a potential to be a novel drug, has been found in a well-known filamentous fungus. Another case of a metabolite with attractive properties is emodin, which has been known for more than a century, but just recently had the biosynthetic machinery uncovered in A. nidulans. Both asperthecin and the emericellamides were firstly discovered and isolated from less well described aspergilli, however, after the compounds were observed in A. nidulans, the candidates for responsible genes in biosynthesis were found in a few months. The study of conidial pigment biosynthesis in A. nidulans has contributed to our basic understanding of fungal development and PKS organization, and provided researchers with an easy assayable marker system for genetic studies. Interestingly, the structure of the final pigment(s) still remains unknown after more than 70 years of research, underlining the difficulties in elucidating structures of highly polymerized PKs.
Epigenetic regulation through chromatin remodeling has shown to be involved in activation of several SM gene clusters. Conserved chromatin remodeling factors have influenced both local activation of some SM clusters and more global responses within the genome. Gene clusters producing sterigmatocystin, orsellinic acid, emodins, and austinols have shown to respond to specific factors. The presence of SM producing genes outside gene clusters, e.g., in prenyl-xanthone production, is probably more common than observed so far. Moreover, cross-talk between pathways is frequently observed, as more pathways become known. This can open a discussion whether common pools of intermediates or enzymes can exist. In addition, the compartmentalization of SM production is an area to be explored. Furthermore, controlling compartmentalization of production as well as secretion will influence yields and downstream applications which are important factors for exploiting SM production commercially. Existing compounds can be modified genetically to add/remove chemical groups on existing drugs, mix moieties from different SM classes or species by for example domain swapping, and to considerably increase/abolish a specific production.
Altogether the recent uncovering of secondary metabolism in A. nidulans is an illustrative example of strong interdisciplinary efforts requiring strong expertise within chemistry, biology, microbiology, molecular genetics, protein chemistry, computer science, and engineering. Ultimately, the efforts described in this review can form the basis for uncovering of the specific biological roles of the chemical arsenal in the fungus.
This work was supported by the Danish Research Agency for Technology and Production grant # 09-064967, FOBI, DTU, and Novozymes. Additionally, we thank Maria Månsson for critical proof reading of the manuscript and for suggestions.
Conflict of Interest
The authors declare no conflict of interest.
References and Notes
- Pontecorvo, G.; Roper, J.A.; Hemmons, L.M.; MacDonald, K.D.; Bufton, A.W.J. The genetics of Aspergillus nidulans. Adv. Genet. Incorp. Mol. Genet. Med. 1953, 5, 141–238.
- Newman, D.J.; Cragg, G.M. Natural products as sources of new drugs over the last 25 years. J. Nat. Prod. 2007, 70, 461–477, doi:10.1021/np068054v.
- Crawford, J.M.; Townsend, C.A. New insights into the formation of fungal aromatic polyketides. Nat. Rev. Microbiol. 2010, 8, 879–889, doi:10.1038/nrmicro2465.
- Hertweck, C. The biosynthetic logic of polyketide diversity. Angew. Chem. Int. Ed. 2009, 48, 4688–4716, doi:10.1002/anie.200806121.
- Cox, R.J. Polyketides, proteins and genes in fungi: Programmed nano-machines begin to reveal their secrets. Org. Biomol. Chem. 2007, 5, 2010–2026, doi:10.1039/b704420h.
- Bingle, L.E.H.; Simpson, T.J.; Lazarus, C.M. Ketosynthase domain probes identify two subclasses of fungal polyketide synthase genes. Fun. Gen. Biol. 1999, 26, 209–223, doi:10.1006/fgbi.1999.1115.
- Crawford, J.M.; Vagstad, A.L.; Ehrlich, K.C.; Townsend, C.A. Starter unit specificity directs genome mining of polyketide synthase pathways in fungi. Bioorg. Chem. 2008, 36, 16–22, doi:10.1016/j.bioorg.2007.11.002.
- Crawford, J.M.; Thomas, P.M.; Scheerer, J.R.; Vagstad, A.L.; Kelleher, N.L.; Townsend, C.A. Deconstruction of iterative multidomain polyketide synthase function. Science 2008, 320, 243–246, doi:10.1126/science.1154711. 18403714
- Yadav, G.; Gokhale, R.S.; Mohanty, D. Towards prediction of metabolic products of polyketide synthases: An in silico analysis. PLoS Comp. Biol. 2009, 5, e1000351–1, doi:10.1371/journal.pcbi.1000351.
- Du, L.; Lou, L. PKS and NRPS release mechanisms. Nat. Prod. Rep. 2010, 27, 255–278, doi:10.1039/b912037h.
- Nielsen, M.L.; Nielsen, J.B.; Rank, C.; Klejnstrup, M.L.; Holm, D.K.; Brogaard, K.H.; Hansen, B.G.; Frisvad, J.C.; Larsen, T.O.; Mortensen, U.H. A genome-wide polyketide synthase deletion library uncovers novel genetic links to polyketides and meroterpenoids in Aspergillus nidulans. FEMS Microbiol. Lett. 2011, 321, 157–166, doi:10.1111/j.1574-6968.2011.02327.x.
- Chung, Y.S.; Kim, J.M.; Han, D.M.; Chae, K.S.; Jahng, K.Y. Ultrastructure of the cell wall of a null pigmentation mutant, npgA1, in Aspergillus nidulan. J. Microbiol. 2003, 41, 224–231.
- Jahn, B.; Boukhallouk, F.; Lotz, J.; Langfelder, K.; Wanner, G.; Brakhage, A.A. Interaction of human phagocytes with pigmentless Aspergillus conidia. Infect. Immun. 2000, 68, 3736–3739, doi:10.1128/IAI.68.6.3736-3739.2000.
- Wright, P.J.; Pateman, J.A. Ultraviolet-light sensitive mutants of Aspergillus nidulans. Mutation Res. 1970, 9, 579–587, doi:10.1016/0027-5107(70)90103-X.
- Yuill, E. Two new Aspergillus mutants. J. Bot. 1939, 77, 174–175.
- Clutterbuck, A.J. Absence of laccase from yellow-spored mutants of Aspergillus nidulans. J. Gen. Microbial. 1972, 70, 423–435, doi:10.1099/00221287-70-3-423.
- Agnihotri, V.P. Role of trace elements in the growth and morphology of five ascosporic Aspergillus species. Can. J. Bot. 1967, 45, 73–79, doi:10.1139/b67-005.
- O’Hara, E.B.; Timberlake, W.E. Molecular characterization of the Aspergillus nidulans yA locus. Genetics 1989, 121, 249–254. 2659435
- Mayorga, M.E.; Timberlake, W.E. Isolation and molecular characterization of the Aspergillus nidulans wA gene. Genetics 1990, 126, 73–79. 2227390
- Marshall, M.A.; Timberlake, W.E. Aspergillus nidulans wetA activates spore-specific gene expression. Mol. Cell. Biol. 1991, 11, 55–62. 1986246
- Adams, T.H.; Wieser, J.K.; Yu, J.H. Asexual sporulation in Aspergillus nidulans. Microbiol. Mol. Biol. Rev. 1998, 62, 35–54. 9529886
- Mayorga, M.E.; Timberlake, W.E. The developmentally regulated Aspergillus nidulans wA gene encodes a polypeptide homologous to polyketide and fatty acid synthases. Mol. Gen. Genet. 1992, 235, 205–212, doi:10.1007/BF00279362.
- Watanabe, A.; Ono, Y.; Fujii, I.; Sankawa, U.; Mayorga, M.E.; Timberlake, W.E.; Ebizuka, Y. Product identification of polyketide synthase coded by Aspergillus nidulans wA gene. Tetrahedron Lett. 1998, 39, 7733–7736, doi:10.1016/S0040-4039(98)01685-2.
- Fujii, I.; Watanabe, A.; Sankawa, U.; Ebizuka, Y. Identification of Claisen cyclase domain in fungal polyketide synthase WA, a naphthopyrone synthase of Aspergillus nidulans. Chem. Biol. 2001, 8, 189–197, doi:10.1016/S1074-5521(00)90068-1.
- Watanabe, A.; Fujii, I.; Sankawa, U.; Mayorga, M.E.; Timberlake, W.E.; Ebizuka, Y. Re-identification of Aspergillus nidulans wA gene to code for a polyketide synthase of naphthopyrone. Tetrahedron Lett. 1999, 40, 91–94, doi:10.1016/S0040-4039(98)80027-0.
- Watanabe, A.; Ebizuka, Y. A novel hexaketide naphthalene synthesized by a chimeric polyketide synthase composed of fungal pentaketide and heptaketide synthase. Tetrahedron Lett. 2002, 43, 843–846, doi:10.1016/S0040-4039(01)02251-1.
- Nekam, L.; Polgar, P. The inhibitory effect of a mold upon Staphylococcus. Urol. Cutan. Rev. 1948, 52, 372–373. 18871089
- Hatsuda, Y.; Kuyama, S. Studies on the metabolic products of Aspergillus versicolor. Part 1. Cultivation of Aspergillus versicolor, isolation and purification of metabolic products. J. Agric. Chem. Soc. Jpn. 1954, 28, 989–991.
- Hatsuda, Y.; Kuyama, S.; Terashima, N. Studies on the metabolic products of Aspergillus versicolor. Part 2. Physical and chemical properties and the chemical structure of sterigmatocystin. J. Agric. Chem. Soc. Jpn. 1954, 28, 992–998.
- Bullock, E.; Underwood, J.G.V.; Roberts, J.C. Studies in mycological chemistry. 11. Structure of isosterigmatocystin and an amended structure for sterigmatocystin. J. Chem. Soc. 1962, 10, 4179–4183.
- Holker, J.S.E.; Mulheirn, L.J. Biosynthesis of sterigmatocystin. Chem. Comm. 1968, 24, 1574–1579.
- Brechbühler, S.; Buchi, G.; Milne, G. Absolute configuration of aflatoxins. J. Org. Chem. 1967, 2641–2642.
- Fukuyama, K.; Hamada, K.; Tsukihara, T.; Katsube, Y.; Hamasaki, T.; Hatsuda, Y. Crystalstructures of sterigmatocystin and O-methylsterigmatocystin, metabolites of genus Aspergillus. Bull. Chem. Soc. Jpn. 1976, 49I, 1153–1154.
- Fukuyama, K.; Tsukihara, T.; Katsube, Y.; Tanaka, N.; Hamasaki, T.; Hatsuda, Y. Crystal and molecular structure of p-bromobenzoate of sterigmatocystin. Bull. Chem. Soc. Jpn. 1975, 48, 1980–1983, doi:10.1246/bcsj.48.1980.
- Blount, W.P. Turkey “X” disease. Turkey 1961, 61, 55–58.
- Terao, K. Sterigmatocystin—A masked potent carcinogenic mycotoxin. J. Toxicol. Toxin Rev. 1983, 2, 77–110, doi:10.3109/15569548309006494.
- Bennett, J.W.; Klinch, M. Mycotoxins. Clin. Microbiol. Rev. 2003, 16, 497–516, doi:10.1128/CMR.16.3.497-516.2003.
- Bhatnager, D.; Yu, J.; Ehrlich, K.C. Toxins of filamentous fungi. Chem. Immunol. 2002, 81, 167–206, doi:10.1159/000058867.
- Yu, J.; Chang, P.K.; Ehrlich, K.C.; Cary, J.W.; Bhatnagar, D.; Cleveland, T.E.; Payne, G.A.; Linz, J.E.; Woloshuk, C.P.; Bennett, J.W. Clustered pathway genes in aflatoxin biosynthesis. Appl. Environ. Microbiol. 2004, 70, 1253–1262, doi:10.1128/AEM.70.3.1253-1262.2004. 15006741
- Yabe, K.; Nakajima, H. Enzyme reactions and genes in aflatoxin biosynthesis. Appl. Microbiol. Biotechnol. 2004, 64, 745–755, doi:10.1007/s00253-004-1566-x.
- Brown, D.W.; Yu, J.H.; Kelkar, H.S.; Fernandes, M.; Nesbitt, T.C.; Keller, N.P.; Adams, T.H.; Leonard, T.J. Twenty-five coregulated transcripts define a sterigmatocystin gene cluster in Aspergillus nidulans. Proc. Natl. Acad. Sci. USA 1996, 93, 1418–1422, doi:10.1073/pnas.93.4.1418. 8643646
- Yu, J.H.; Leonard, T.J. Sterigmatocystin biosynthesis in Aspergillus nidulans requires a novel type I polyketide synthase. J. Bacteriol. 1995, 177, 4792–4800. 7642507
- McDonald, T.; Hammond, T.; Noordermeer, D.; Zhang, Y.Q.; Keller, N. The sterigmatocystin cluster revisited: lessons from a genetic model. In Food Science and Technology/Aflatoxin and Food Safety; Abbas, H.K., Ed.; CRC Press: Boca Raton, FL, USA, 2005; pp. 117–136.
- Ehrlich, K.C.; Li, P.; Scharfenstein, L.; Chang, P.K. HypC, the anthrone oxidase involved in aflatoxin biosynthesis. Appl. Environ. Microbiol. 2010, 76, 3374–3377, doi:10.1128/AEM.02495-09. 20348292
- Henry, K.M.; Townsend, C.A. Ordering the reductive and cytochrome P450 oxidative steps in demethylsterigmatocystin formation yields general insights into the biosynthesis of aflatoxin and related fungal metabolites. J. Am. Chem. Soc. 2005, 127, 3724–3733, doi:10.1021/ja0455188.
- Ehrlich, K.C.; Montalbano, B.; Boué, S.M.; Bhatnagar, D. An aflatoxin biosynthesis cluster gene encodes a novel oxidase required for conversion of versicolorin A to sterigmatocystin. Appl. Environ. Microbiol. 2005, 71, 8963–8965, doi:10.1128/AEM.71.12.8963-8965.2005. 16332900
- Cary, J.W.; Ehrlich, K.C.; Bland, J.M.; Montalbano, B.G. The aflatoxin biosynthesis cluster gene, aflX, encodes an oxidoreductase involved in conversion of versicolorin A to demethylsterigmatocystin. Appl. Environ. Microbiol. 2006, 72, 1096–1101, doi:10.1128/AEM.72.2.1096-1101.2006.
- Yu, J.H.; Butchko, R.A.E.; Fernandes, M.; Keller, N.P.; Leonard, T.J.; Adams, T.H. Conservation of structure and function of the aflatoxin regulatory gene aflR from Aspergillus nidulans and A. flavus. Curr. Genet. 1996, 29, 549–555, doi:10.1007/BF02426959.
- Meyers, D.M.; Obrian, G.; Du, W.L.; Bhatnagar, D.; Payne, G.A. Characterization of aflJ, a gene required for conversion of pathway intermediates to aflatoxin. Appl. Environ. Microbiol. 1998, 64, 3713–3717. 9758789
- Bok, J.W.; Keller, N.P. LeaA, a regulator of secondary metabolism in Aspergillus spp. Eukaryot. Cell 2004, 3, 527–535, doi:10.1128/EC.3.2.527-535.2004.
- Krappmann, S.; Ni, M.; Bok, J.W.; Helmstaedt, K.; Valerius, O.; Braus-Stromeyer, S.; Kwon, N.J.; Keller, N.P. VelB/VeA/LaeA complex coordinates light sighal with fungal development and secondart metabolism. Science 2008, 320, 1504–1506, doi:10.1126/science.1155888. 18556559
- Shwab, E.K; Bok, J.W.; Tribus, M.; Galehr, J.; Graessle, S.; Keller, N.P. Histone deacetylase activity regulates chemical diversity in Aspergillus.. Eukaryot. Cell 2007, 6, 1656–1664, doi:10.1128/EC.00186-07.
- Fisch, K.M.; Gillaspy, A.F.; Gipson, M.; Henrikson, J.C.; Hoover, A.R.; Jackson, L.; Najar, F.Z.; Wägele, H.; Cichewicz, R.H. Chemical induction of silent biosynthetic pathway transcription in Aspergillus niger. J. Ind. Microbiol. Biotechnol. 2009, 36, 1199–1213, doi:10.1007/s10295-009-0601-4.
- Watanabe, C.M.H.; Townsend, C.A. Initial characterization of a type I fatty acid synthase and polyketide synthase multienzyme complex NorS in the biosynthesis of aflatoxin B1. Chem. Biol. 2002, 9, 981–988, doi:10.1016/S1074-5521(02)00213-2.
- Yabe, K.; Nakamura, Y.; Nakajima, H.; Ando, Y.; Hamasaki, T. Enzymatic conversion of norsolorinic acid to averufin in aflatoxin biosynthesis. Appl. Environ. Microbiol. 1991, 57, 1340–1345. 1854196
- Trail, F.; Chang, P.K.; Cary, J.; Linz, J.E. Structural and functional analysis of the nor-1 gene involved in the biosynthesis of aflatoxins by Aspergillus parasiticus.. Appl. Environ. Microbiol. 1994, 60, 4078–4085. 7993094
- Keller, N.P.; Watanabe, C.M.H.; Kelkar, H.S.; Adams, T.H.; Townsend, C.A. Requirement of monooxygenase-mediated steps for sterigmatocystin biosynthesis by Aspergillus nidulans.. Appl. Environ. Microbiol. 2000, 66, 359–362, doi:10.1128/AEM.66.1.359-362.2000.
- Yabe, L.; Matsuyama, Y.; Ando, Y.; Nakajima, H.; Hamasaki, T. Stereochemistry during aflatoxin biosynthesis: Conversion of norsolorinic acid to averufin. Appl. Environ. Microbiol. 1993, 59, 2486–2492. 8368836
- Chang, P.K.; Yu, J.; Ehrlich, K.C.; Boue, S.M.; Montalbano, B.G.; Bhatnagar, D.; Cleveland, T.E. adhA in Aspergillus parasiticus is involved in conversion of 5′-hydroxyaverantin to averufin. Appl. Environ. Microbiol. 2000, 66, 4715–4719, doi:10.1128/AEM.66.11.4715-4719.2000. 11055914
- Sakuno, E.; Yabe, K.; Nakajima, H. Involvement of two cytosolic enzymes and a novel intermediate 5’-oxoaverantin in the pathway from 5′-hydroxyaverantin to averufin in aflatoxin biosynthesis. Appl. Environ. Microbiol. 2003, 69, 6418–6426, doi:10.1128/AEM.69.11.6418-6426.2003.
- Chang, P.K.; Yabe, K.; Yu, J. The Aspergillus parasiticus estA-encoded esterase converts versiconal hemiacetal acetate to versiconal and versiconol acetate to versiconol in aflatoxin biosynthesis. Appl. Environ. Microbiol. 2004, 70, 3593–3599, doi:10.1128/AEM.70.6.3593-3599.2004. 15184162
- Silva, J.C.; Minto, R.E.; Barry, C.E., III; Holland, K.A.; Townsend, C.A. Isolation and characterization of the versicolorin B synthase gene from Aspergillus parasiticus. J. Biol. Chem. 1996, 271, 13600–13608, doi:10.1074/jbc.271.23.13600. 8662689
- Kelkar, H.S.; Skloss, T.W.; Haw, J.F.; Keller, N.P.; Adams, T.H. Aspergillus nidulans stcL encodes a putative cytochrome P-450 monooxygenase required for bisfuran desaturation during aflatoxin/sterigmatocystin biosynthesis. J. Biol. Chem. 1997, 272, 1589–1594, doi:10.1074/jbc.272.3.1589. 8999832
- Keller, N.P.; Kantz, N.J.; Adams, T.H. Aspergillus nidulans verA is required for production of the mycotoxin sterigmatocystin. Appl. Environ Microbiol. 1994, 60, 1444–1450. 8017929
- Keller, N.P.; Segner, S.; Bhatnagar, D.; Adams, T.H. stcS, a putative P-450 monooxygenase, is required for the conversion of versicolorin A to sterigmatocystin in Aspergillus nidulan. Appl. Environ. Microbiol. 1995, 61, 3628–3632. 7486998
- Kelkar, H.S.; Keller, N.P.; Adams, T.H. Aspergillus nidulans stcP encodes an O-methyltransferase that is required for sterigmatocystin biosynthesis. Appl. Environ. Microbiol. 1996, 62, 4296–4298. 8900026
- Slot, J.C.; Rokas, A. Horizontal transfer of a large and highly toxic secondary metabolic gene cluster between fungi. Curr. Biol. 2011, 21, 134–139, doi:10.1016/j.cub.2010.12.020.
- Bergmann, S.; Schümann, J.; Scherlach, K.; Lange, C.; Brakhage, A.A.; Hertweck, C. Genomics-driven discovery of PKS-NRPS hybrid metabolites from Aspergillus nidulans. Nat. Chem. Biol. 2007, 3, 213–217, doi:10.1038/nchembio869. 17369821
- Chiang, Y.M.; Szewczyk, E.; Nayak, T.; Davidson, A.D.; Sanchez, J.F; Lo, H.C.; Ho, W.Y.; Simityan, H.; Kuo, E.; Praseuth, A.; et al. Molecular genetic mining of the Aspergillus secondary metabolome: Discovery of the emericellamide biosynthetic pathway. Chem. Biol. 2008, 15, 527–532, doi:10.1016/j.chembiol.2008.05.010.
- Sims, J.W.; Fillmore, J.P.; Warner, D.D.; Schmidt, E.W. Equisetin biosynthesis in Fusarium heterosporum. Chem. Commun. 2005, 186–188.
- Song, Z.; Cox, R.J.; Lazarus, C.M.; Simpson, T.J. Fusarin C biosynthesis in Fusarium moniliforme and Fusarium venenatum. ChemBioChem 2004, 5, 1196–1203, doi:10.1002/cbic.200400138.
- Liu, X.; Walsh, C.T. Cyclopiazonic acid biosynthesis in Aspergillus sp.: Characterization of a reductase-like R* domain in cyclopiazonate synthetase that forms and releases cyclo-acetoacetyl-L-tryptophan. Biochemistry 2009, 48, 8746–8757, doi:10.1021/bi901123r.
- Xu, W.; Cai, X.; Jung, M.E.; Tang, Y. Analysis of intact and dissected fungal polyketide synthase-nonribosomal peptide synthetase in vitro and in Saccharomyces cerevisiae. J. Am. Chem. Soc. 2010, 132, 13604–13607, doi:10.1021/ja107084d. 20828130
- Halo, L.M.; Marshall, J.W.; Yakasai, A.A., Song; Butts, C.P.; Crump, M.P.; Heneghan, M.; Bailey, A.M.; Simpson, T.J.; Lazarus, C.M.; Cox, R.J. Authentic heterologous expression of the tenellin iterative polyketide synthase nonribosomal peptide synthetase requires coexpression with an enoyl reductase. ChemBioChem 2008, 9, 585–594, doi:10.1002/cbic.200700390. 18266306
- Eley, K.L.; Halo, L.M.; Song, Z.; Powles, H.; Cox, R.J.; Bailey, A.M.; Lazarus, C.M.; Simpson, T.J. Biosynthesis of the 2-pyridone tenellin in the insect pathogenic fungus Beauveria bassiana. ChemBioChem 2007, 8, 289–297, doi:10.1002/cbic.200600398.
- Fujita, Y.; Oguri, H.; Oikawa, H. Biosynthetic studies on the antibiotics PF1140: a novel pathway for a 2-pyridone framework. Tetrahedron Lett. 2005, 46, 5885–5888, doi:10.1016/j.tetlet.2005.06.115.
- McInnes, A.G.; Smith, D.G.; Wat, C.K. Tenellin and Bassianin, Metabolites of Beauveria Species. Structure elucidation with 15N- and doubly 13C-enriched compounds using 13C nuclear magnetic resonance spectroscopy. J. Chem. Soc. Chem. Commun. 1974, 8, 281–282.
- Halo, L.M.; Heneghan, M.N.; Yakasai, A.A.; Song, Z.; Williams, K.; Bailey, A.M.; Cox, R.J.; Lazarus, C.M.; Simpson, T.J. Late stage oxidations during the biosynthesis of the 2-pyridone tenellin in the entomopathogenic fungus Beauveria bassiana. J. Am. Chem. Soc. 2008, 130, 17988–17996, doi:10.1021/ja807052c. 19067514
- Oh, D.C.; Kauffman, C.A; Jensen, P.R.; Fenical, W. Induced production of emericellamides A and B from the marine-derived fungus Emericella sp. in competing co-culture. J. Nat. Prod. 2007, 70, 515–520, doi:10.1021/np060381f.
- Howard, B.H.; Raistrick, H. Studies in the biochemistry of micro-organism. 94. The colouring matters of species in the Aspergillus nidulans group. Part I. Asperthecin, a crystailline colouring matter of Aspergillus quadrilineatus Thom & Raper. Biochem. J. 1955, 59, 475–484. 14363122
- Birkinshaw, J.H.; Gourlay, R. Studies in the biochemistry of micro-organisms. 109. The structure of asperthecin. Biochem. J. 1961, 81, 618–622. 13869399
- Neelakantan, S.; Pocker, A.; Raistrick, H. Studies in the biochemistry of micro-organisms. 101. The colouring matters of species in the Aspergillus nidulans group. Part 2. Further observations on the structure of asperthecin. Biochem. J. 1957, 66, 234–237. 13445677
- Szewczyk, E.; Chiang, Y.M.; Oakley, C.E.; Davidson, A.D.; Wang, C.C.C; Oakley, B.R. Identification and characterization of the asperthecin gene cluster of Aspergillus nidulans.. Appl. Environ. Microbiol. 2008, 74, 7607–7612, doi:10.1128/AEM.01743-08. 18978088
- Wong, K.H.; Todd, R.B.; Oakley, B.R.; Oakley, C.E.; Hynes, M.J.; Davis, M.A. Sumoylation in Aspergillus nidulans: sumO inactivation, overexpression and live-cell imaging. Fungal Genet. Biol. 2008, 45, 728–737, doi:10.1016/j.fgb.2007.12.009.
- Awakawa, T.; Yokota, K.; Funa, N.; Doi, F.; Mori, N.; Watanabe, H.; Horinouchi, S. Physically discrete β-lactamase-type thioesterase catalyzes product release in atrochrysone synthesis by iterative type I polyketide synthase. Chem. Biol. 2009, 16, 613–623, doi:10.1016/j.chembiol.2009.04.004.
- Chiang, Y.M.; Oakley, B.R.; Keller, N.P.; Wang, C.C.C. Unraveling polyketide synthesis in members of the genus Aspergillus. Appl. Microbiol. Biotechnol. 2010, 86, 1719–1736, doi:10.1007/s00253-010-2525-3.
- Li, Y.; Chooi, Y.H.; Sheng, Y.; Valentine, J.S.; Tang, Y. Comparative characterization of fungal anthracenone and naphthacenedione biosynthetic pathways reveals an α-hydroxylation-dependent claisen-like cyclization catalyzed by a dimanganese thioesterase. J. Am. Chem. Soc. 2011, 133, 15773–15785, doi:10.1021/ja206906d. 21866960
- Li, Y.; Xu, W.; Tang, Y. Classification, prediction, and verification of the regioselectivity of fungal polyketide synthase product template domains. J. Biol. Chem. 2010, 285, 22764–22773, doi:10.1074/jbc.M110.128504.
- Chiang, Y.M.; Szewczyk, E.; Davidson, A.D.; Keller, N.; Oakley, B.R.; Wang, C.C.C. A gene cluster containing two fungal polyketide synthases encodes the biosynthetic pathway for a polyketide, asperfuranone, in Aspergillus nidulan. J. Am. Chem. Soc. 2009, 131, 2965–2970, doi:10.1021/ja8088185. 19199437
- Wang, C.C.C; Chiang, Y.M.; Praseuth, M.B.; Kuo, P.L.; Liang, H.L.; Hsu, Y.L. Asperfuranone from Aspergillus nidulans inhibits proliferation of human non-small cell lung cancer A549 cells via blocking cell cycle progression and inducing apoptosis. Basic Clin. Pharmacol. Toxicol. 2010, 107, 583–589, doi:10.1111/j.1742-7843.2010.00545.x.
- Matsuzaki, K.; Tahara, H.; Inokoshi, J.; Tanaka, H.; Masuma, R.; Omura, S. New brominated and halogen-less derivatives and structure-activity relationship of azaphilones inhibiting gp120-CD4 binding. J. Antibiot. 1998, 51, 1004–1011, doi:10.7164/antibiotics.51.1004.
- Bailey, A.M.; Cox, R.J.; Harley, K.; Lazarus, C.M.; Simpson, T.J.; Skellam, E. Characterisation of 3-methylorcinaldehyde synthase (MOS) in Acremonium strictum: First observation of a reductive release mechanism during polyketide biosynthesis. Chem. Commun. 2007, 39, 4053–4055.
- Bergmann, S.; Funk, A.N.; Scherlach, K.; Schroeckh, V.; Shelest, E.; Horn, U.; Hertweck, C.; Brakhage, A.A. Activation of a silent fungal polyketide biosynthesis pathway through regulatory cross talk with a cryptic nonribosomal peptide synthetase gene cluster. Appl. Environ. Microbiol. 2010, 76, 8143–8149, doi:10.1128/AEM.00683-10. 20952652
- Liu, T.; Chiang, Y.M.; Somoza, A.D.; Oakley, B.R.; Wang, C.C.C. Engineering of an “unnatural” natural product by swapping polyketide synthase domains in Aspergillus nidulans. J. Am. Chem. Soc. 2011, 133, 13314–13316, doi:10.1021/ja205780g. 21815681
- Lu, P.; Zhang, A.; Dennis, L.M.; Dhal-Roshak, A.M.; Xia, Y.Q.; Arison, B.; An, Z.; Tkacz, J.S. A gene (pks2) encoding a putative 6-methylsalicylic acid synthase from Glarea lozoyensis. Mol. Gen. Genomics 2005, 273, 207–216, doi:10.1007/s00438-005-1132-y.
- Bok, J.W.; Chiang, Y.M.; Szewczyk, E.; Reyes-Dominguez, Y.; Davidson, A.D.; Sanchez, J.F.; Lo, H.C.; Watanabe, K.; Strauss, J.; Oakley, B.R.; et al. Chromatin-level regulation of biosynthetic gene clusters. Nat. Chem. Biol. 2009, 5, 462–464, doi:10.1038/nchembio.177.
- Chiang, Y.M.; Szewczyk, E.; Davidson, A.D.; Entwistle, R.; Keller, N.P.; Wang, C.C.C.; Oakley, B.R. Characterization of the Aspergillus nidulans monodictyphenone gene cluster. Appl. Environ. Microbiol. 2010, 76, 2067–2074, doi:10.1128/AEM.02187-09.
- Sanchez, J.F.; Entwistle, R.; Hung, J.H.; Yaegashi, J.; Jain, S.; Chiang, Y.M.; Wang, C.C.C.; Oakley, B.R. Genome-based deletion analysis reveals the prenyl xanthone biosynthesis pathway in Aspergillus nidulans. J. Am. Chem. Soc. 2011, 133, 4010–4017, doi:10.1021/ja1096682. 21351751
- Jowett, H.A.D.; Potter, C.E. CXXVII—The constitution of chrysophante acid and of emodin. J. Chem. Soc. Trans. 1903, 83, 1327–1334, doi:10.1039/ct9038301327.
- Beal, G.D.; Okey, R. The qualitative identification of the drugs containing emodin. J. Am. Chem. Soc. 1917, 39, 716–725, doi:10.1021/ja02249a023.
- Gatenbeck, S. Incorporation of labelled acetate in emodin in Penicillum islandicum. Acta Chem. Scand. 1958, 12, 1211–1214, doi:10.3891/acta.chem.scand.12-1211.
- Basu, S.; Ghosh, A.; Hazra, B. Evaluation of the antibacterial activity of Ventilago madraspatana Gaertn., Rubia cordifolia Linn. and Lantana camara Linn.: Isolation of emodin and physcion as active antibacterial agents. Phytother. Res. 2005, 19, 888–894, doi:10.1002/ptr.1752.
- Chen, J.; Zhang, L.; Zhang, Y.; Zhang, H.; Du, J.; Ding, J; Guo, Y.; Jiang, H.; Shen, X. Emodin targets the β-hydroxyacyl carrier protein dehydratase from Helicobactor pylori: Enzymatic inhibition assay with crystal structural and thermodymamic characterization. BMC Microbiol. 2009, 9, 91–1, doi:10.1186/1471-2180-9-91. 19433000
- Huang, Q.; Lu, G.; Shen, H.M.; Chung, M.C.M.; Ong, C.N. Anti-cancer properties of anthraquinones from rhubarb. Med. Res. Rev. 2007, 27, 609–630, doi:10.1002/med.20094.
- Srinivas, G.; Babykutty, S.; Sathiadevan, P.P.; Srinivas, P. Molecular mechanism of emodin action: Transition from laxative ingredient to an antitumor agent. Med. Res. Rev. 2007, 27, 591–608, doi:10.1002/med.20095.
- Zargar, B.A.; Masoodi, M.H.; Ahmed, B.; Ganie, S.A. Phytoconstituents and therapeutic uses of Rheum emodi wall. Ex Meissn. Food Chem. 2011, 128, 585–589, doi:10.1016/j.foodchem.2011.03.083.
- Chen, Z.G., Fujii; Ebizuka, Y.; Sankawa, U. Purification and characterization of emodinanthrone oxygenase from Aspergillus terreus.. Phytochemistry 1995, 38, 299–305, doi:10.1016/0031-9422(94)00543-3.
- Huang, K.X.; Fujii, I.; Ebizuka, Y.; Gomi, K.; Sankawa, U. Molecular cloning and heterologous expression of the gene encoding dihydroheodin oxidase, a multicopper blue enzyme from Aspergillus terreus. J. Biol. Chem. 1995, 270, 21495–21502, doi:10.1074/jbc.270.37.21495.
- Couch, R.D.; Gaucher, G.M. Rational elimination of Aspergillus terreus sulochrin production. J. Biotech. 2004, 108, 171–178, doi:10.1016/j.jbiotec.2003.10.021.
- Henry, K.M.; Townsend, C.A. Synthesis and fate of o-carboxybenzophenones in the biosynthesis of aflatoxin. J. Am. Chem. Soc. 2005, 127, 3300–3309, doi:10.1021/ja045520z. 15755146
- Sato, S.; Morishita, T.; Hosoya, T.; Ishikawa, Y. Novel pentacyclec compounds, F-9775A and F-9775B, their manufacture with Paecilomyces carneus, and their use for treatment of osteoporos. Japan Pat. JP11001480A 19990106, 1999.
- Schroeckh, V.; Scherlach, K.; Nützmann, H.W.; Shelest, E.; Schmidt-Heck, W.; Schuemann, J.; Martin, K.; Hertweck, C.; Brakhage, A.A. Intimate bacterial-fungal interaction triggers biosynthesis of archetypal polyketides in Aspergillus nidulans. Proc. Natl. Acad. Soc. USA 2009, 106, 14558–14563, doi:10.1073/pnas.0901870106.
- Gaucher, G.M.; Sherpherd, M.G. Isolation of orsellinic acid synthase. Biochem. Biophys. Res. Commun. 1968, 32, 664–671, doi:10.1016/0006-291X(68)90290-8.
- Leo, H.; Yamamoto, Y.; Kim, J.A.; Jung, J.S.; Koh, Y.J.; Hur, J.S. Lecanoric acid, a secondary lichen substance with antioxidant properties from Umbilicaria antarctica in maritime Antarctica (King George Island). Polar Biol. 2009, 32, 1033–1040, doi:10.1007/s00300-009-0602-9.
- Sanchez, J.F.; Chiang, Y.M.; Szewczyk, E.; Davidson, A.D.; Ahuja, M.; Oakley, C.E.; Bok, J.W.; Keller, N.P.; Oakley, B.R.; Wang, C.C.C. Molecular genetic analysis of the orsellinic acid/F9775 gene cluster of Aspergillus nidulans. Mol. BioSyst. 2010, 6, 587–593, doi:10.1039/b904541d.
- Nahlik, K.; Dumkow, M.; Bayram, Ö.; Helmstaedt, K.; Busch, S.; Valerius, O.; Gerke, J.; Hoppert, M.; Schwier, E.; Opitz, L.; et al. The COP9 signalosome mediates transcriptional and metabolic response to hormones, oxidative stress production and cell wall rearrangement during fungal development. Mol. Microbiol. 2010, 78, 964–979, doi:10.1111/j.1365-2958.2010.07384.x.
- Nützmann, H.W.; Reyes-Doninguez, Y.; Scherlach, K.; Schroeckh, V.; Horn, F.; Gacek, A.; Schümann, J.; Hertweck, C.; Strauss, J.; Brakhage, A.A. Bacteria-induced natural product formation in the fungus Aspergillus nidulans requires Saga/Ada-mediated histone acetylation. Proc. Natl. Acad. Soc. USA 2011, 108, 14282–14287, doi:10.1073/pnas.1103523108.
- Scherlach, K.; Sarkar, A.; Schroeckh, V.; Dahse, H.M.; Roth, M.; Brakhage, A.A.; Horn, W.; Hertweck, C. Two induced fungal polyketide pathways converge into antoproliferative spiroanthrones. ChemBioChem 2011, 12, 1836–1839, doi:10.1002/cbic.201100132.
- Simpson, T.J.; Stenzel, D.J.; Bartlett, A.J.; O’Brien, E.; Holker, J.S.E. Studies on fungal metabolites. Part 3. 13C-NMR spectral and structural studies on Austin and new related meroterpenoids from Aspergillus ustus, Aspergillus variecolor, Penicillum diversum. J. Chem. Soc. Perkin Trans. I 1982, 11, 2687–2692.
- Geris, R.; Simpson, T.J. Meroterpenoids produced by fungi. Nat. Prod. Rep. 2009, 26, 1063–1094, doi:10.1039/b820413f.
- Márquez-Fernández, O.; Trigos, Á.; Ramos-Balderas, J.L.; Viniegra-González, G.; Deising, H.B.; Aguirre, J. Phosphopantetheinyl transferase CfwA/NpgA is required for Aspergillus nidulans secondary metabolism and asexual development. Eukaryot. Cell 2007, 6, 710–720, doi:10.1128/EC.00362-06.
- Bode, H.B.; Bethe, B.; Höfs, R.; Zeeck, A. Big effects from small changes: possible ways to explore nature’s chemical diversity. ChemBioChem 2002, 3, 619–627, doi:10.1002/1439-7633(20020703)3:7<619::AID-CBIC619>3.0.CO;2-9.
- Simpson, T.J.; Stenzel, D.J. Biosynthesis of austin, a polyketide-terpenoid metabolite of Aspergillus ustus. JCS Chem. Commun. 1981, 20, 1042–1043.
- Scott, F.E.; Simpson, T.J.; Trimble, L.A.; Vederas, J.C. Biosynthesis of the meroterpenoid austin by Aspergillus ustus: Synthesis and incorporation of 13C, 18O-labelled ethyl 3,5-dimethylorsellinate. J.C.S. Chem. Comm. 1986, 3, 214–215.
© 2012 by the authors; licensee MDPI, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).