Predicted Roles of the Uncharacterized Clustered Genes in Aflatoxin Biosynthesis

Biosynthesis of the toxic and carcinogenic aflatoxins (AFs) requires the activity of more than 27 enzymes. The roles in biosynthesis of newly described enzymes are discussed in this review. We suggest that HypC catalyzes the oxidation of norsolorinic acid anthrone; AvfA (AflI), the ring-closure step in formation of hydroxyversicolorone; HypB, the second oxidation step in conversion of O-methylsterigmatocystin to AF; and HypE and NorA (AflE), the final two steps in AFB1 formation. HypD, an integral membrane protein, affects fungal development and lowers AF production while AflJ (AflS), has a partial methyltransferase domain that may be important in its function as a transcriptional co-activator.


Introduction
The aflatoxins (AFs) are the most studied of all of the fungal toxins (for recent reviews, see references [1][2][3][4][5][6][7][8][9][10]). Not only are they powerful toxins to some animals, they are among the most carcinogenic naturally occurring compounds. The species of Aspergillus that produce aflatoxins are found on all continents with a temperate climate [11]. They are commonly found in the soil where they survive on many plant and animal debris and insect waste [12]. Under favorable conditions for the fungi, they can also become pathogens of plant seeds. They reproduce by forming spores and sclerotia. These reproductive structures are extremely hardy and can survive in the soil for years [13]. Because of their toxicity, the amounts of AFs allowed in crops intended for human and animal consumption are OPEN ACCESS carefully regulated [14]. The levels allowed range from 20 to 200 ppb in corn, cottonseed and tree and ground nuts in the United States and most other countries [15].
The biosynthesis of AFs has been extensively studied [3,16]. The genes that encode enzymes and transcription regulatory factors for their biosynthesis are maintained on a 75 kDa subtelomeric gene cluster on chromosome 3 [17,18]. Approximately 29 genes have been identified in the cluster. The characterized genes encode enzymes involved in biosynthetic steps starting from the precursors, malonyl and acetylCoA. Since their discovery in 1960, the main biosynthetic steps have been identified and detailed reviews of the chemistry and biosynthesis of AF formation are available [4,16,[19][20][21][22]. It is the intention of this review to focus only on the proteins whose roles in biosynthesis have not been adequately described in previous reviews. Surprisingly, detailed characterization of many of the enzymes involved in the catalysis of the biosynthetic steps is sorely lacking even when the genes involved in biosynthesis were characterized in detail. In fact, only 11 of the 29 enzymes and regulatory factors involved in the biosynthesis have been isolated and their activity characterized by kinetic studies, and, of these, only some have been assigned to specific catalytic steps in the biosynthesis pathway. Because of this inadequate knowledge of protein function, some of this review's conclusions on the role of the enzymes will be, of necessity, speculative. However, because the literature regarding AF biosynthesis is so extensive, placing the newly discovered hypothetical enzymes and some of the older, as yet, uncharacterized enzymes into the biosynthetic puzzle should help to better understand the complexity of the biosynthesis and the logic behind some of these steps.

Gene Clusters and Aflatoxin Biosynthesis
It is fortunate for understanding the function of the genes and proteins involved in AF biosynthesis in A. flavus and A. parasiticus that all of the genes are maintained in a 75 kbp gene cluster [23,24] ( Figure 1). The cluster contains not only the genes that encode the enzymes necessary for biosynthesis, but also the genes that encode the two key regulatory proteins necessary for transcription. The AF cluster like so many gene clusters in eukaryotes represents a regulatory island, presumably, to allow coordinated production of the catalytic machinery necessary for all of the steps in biosynthesis [25,26]. Related clusters are also shown in Figure 1 [1,[27][28][29][30][31]. Three of these, the A. nidulans ST cluster, the A. ochraceoroseus AF cluster and the Mycosphaerella pini dothistromin biosynthesis clusters encode some of the same biosynthetic proteins as do the genes in the AF cluster. Three separated regions form the dothistromin cluster. Since no transcription regulatory protein was identified in the dothistromin clusters, the regulation of expression of genes in this cluster may be different from that of the AF and ST clusters. The A. ochraceoroseus AF cluster possesses most but not all of the AF biosynthesis genes. Genes for conversion of ST to AF formation are encoded by genes outside of the cluster. Two fungi known to be highly virulent to humans, namely, A. fumigatus and Coccidioides posadasii/immitis, have gene clusters resembling the AF/ST cluster. These small clusters may be capable of producing an anthraquinone precursor, but no metabolites related to these clusters have yet been characterized. Comparison of secondary metabolite gene clusters in six species of fungi that contain some of the genes related to AF production. The genes whose function is considered in this paper are shown above the A. flavus AF cluster schematic. Vertical lines link gene orthologs in the ST and AF clusters. Vertical red arrows are known AflR-binding sites.

Problems in Gene Characterization
Conversion of precursors to AFs involves several major steps: 1) formation of the anthraquinone polyketide; 2) a series of oxidations of the C-6 hydrocarbon side chain on the anthraquinone to convert the first stable metabolite, norsolorinic acid (NA) to averufin (AVF) and versicolorin A (VERA); 3) oxidation of the anthraquinone moiety and rearrangement of VERA to the xanthone, sterigmatocystin (ST); 4) oxidation and rearrangement of the xanthone to the AF coumarin nucleus. There is substantial evidence that the key enzymes involved in the various conversion steps are coordinately regulated and that, therefore, most of the polyketide "decorating" enzymes are simultaneously available for carrying out the steps in the biosynthesis [20]. This observation implies that the sequence of reductions, oxidations, hydrolyses, and rearrangements is mainly dictated by the differential chemical susceptibilities of the different portions of the initially formed anthraquinone, rather than by its position on a chemical assembly line, where the sequential steps are dictated by relationships of the catalytic proteins to one another, as may be the case for the formation of some of the secondary metabolites in bacteria [32]. That being said, it is possible that the gene arrangement has some role to play in the sequential attack on the precursors as they are formed and that the precursors, while susceptible to other oxidative enzymes in the cell, are shielded from others. The "leakiness" (retention of the ability to form AFs) of some of the mutations could result from the presence of functional homologs in the cell or, in some cases, homologs in the AF cluster as will be discussed below. The genes that give a "leaky" phenotype upon disruption are listed in Table 1. Table 1. Comparison of genes in the A. flavus aflatoxin gene clusters. The leaky mutation phenotype is defined as a knockout transformant that still produces some aflatoxin. Derailment products are by-product metabolites that in some cases cannot be converted directly to aflatoxins by feeding experiments [16,24,33]. Although the structures of most of the AF precursors have been known for many years [34], and have helped define the biosynthetic steps, where the presumed precursor is sufficiently unstable to be isolated, identification of which enzyme catalyzes which step may be unclear. Furthermore, possible precursors might not survive the isolation process or the acidic growth medium, with pH values between 3 and 6, in which AF production occurs in most of the known producing organisms. Besides "leakiness" some of the mutations give derailment products that can be mistaken for precursors. Both known stable metabolites and characterized derailment products are also listed in Table 1. In AF biosynthesis 18 true precursor metabolites have been identified. In several of the AF biosynthesis steps, knockout of different genes led to accumulation of the same precursor metabolite, thereby obscuring the relationships among the enzymes implicated in the conversion process for that step.

Non-leaky mutations
As mentioned above, some of the conversion steps require multiple precursors and, based on structure, some of these are unlikely to be sufficiently stable to be isolable. By knowing, or guessing at, probable enzyme functionalities based on sequence comparisons, we have attempted to assign roles for predicted enzymes encoded by genes in the aflatoxin cluster whose functions have not yet been assigned. Wherever possible, experimental data is given to provide added evidence for the assignments.

Formation of Norsolorinic Acid (NA), the First Stable Metabolite in AF Biosynthesis
The predicted product from polyketide biosynthesis is norsolorinic acid anthrone (NAA) (Scheme 1). It had been widely assumed that NAA is converted to NA spontaneously, by non-enzymatic O 2 oxidation [22,[35][36][37][38][39]. Oxidation of bacterial anthrones is known to be catalyzed by an unusual low molecular weight (less that 20 kDa) monooxygenase that does not require a co-factor [40,41]. The catalytic active site of this protein consists of amino acids, NXXQWESQAY, near the middle of the protein about 60-70 amino acids from the amino terminus. The single Trp residue in this catalytic motif is assumed to activate the anthrone and the oxidation by molecular oxygen is then mediated by a neighboring Arg residue about 14 aa closer to the carboxyl end of the enzyme. The Trp residue involved in the catalysis may form a charge transfer complex with the anthrone enabling a more favorable energetic state for oxygen addition. A presumed anthrone oxidase involved in conversion of emodin anthrone to emodin was partially purified from a microsomal fraction from Aspergillus terreus [42,43]. Its reported size of 50 kDa is much larger than that of the bacterial proteins (14 kDa). Its amino acid and the gene coding sequence have not yet been reported.  In AF clusters from section Flavi fungi (A. parasiticus, A. flavus, A. nomius and others) two hypothetical genes, hypC and hypB, are predicted to encode closely related 17 kDa proteins. In A. nidulans and A. ochraceoroseus only one copy of these hypothetical genes was found in the cluster. Based on EST data, the genes hypC and hypB (originally named hypB1 and hypB2), are expressed under conditions conducive to AF production, but not under non-conducive conditions. The putative promoter regions for both genes have TCGN 5 CGA motifs, the canonical binding sequence for the AF pathway transcriptional regulatory factor, AflR. Disruption of hypC gave mutant fungi that accumulated excess amounts of NA, a small amount of NAA, and lower amounts of AFs than did selection marker-transformed recipient fungi ( Figure 2A) whereas no precursor metabolite accumulated after disruption of hypB ( Figure 2B). Expression of hypC (codon-optimized for E. coli expression) in bacteria gave a protein fraction that catalyzed conversion of synthetic NAA to NA ( Figure 2C). Incubation of NAA with HypB, also expressed in E. coli, did not catalyze this conversion. These results demonstrate that HypC, but not HypB, is the anthrone oxidase involved in the catalytic conversion of NAA to NA. The ability of the disruption mutant to still produce AFs suggests that either a hypC homolog is able to complement the defect or non-enzymatic oxidation is a significant alternative pathway allowing the enzymatic loss to be bypassed. A tBlastN search of the Broad Institute Aspergillus comparative database (http://www.broad.mit.edu/annotation/genome/aspergillus_terreus/MultiHome.html) or the Multi-fungi database (http://www.broadinstitute.org/cgi-bin/annotation/fgi/blast_page.cgi), containing sequenced genomes of many fungal species, revealed numerous HypC orthologs. Only some of potential orthologs are listed in the alignment in Figure 3. Included in the list is StcM, the candidate anthrone oxidase from A. nidulans, a species that produces the AF precursor, ST. In fact, all of the known producers of AF precursor-like metabolites were found to have genes predicted to encode proteins similar to the small HypC-like anthrone oxidase. Comparison of the predicted amino acid sequence of suspected HypC orthologs revealed potential catalytic sites similar to those characterized in known bacterial anthrone oxidases. In the comparison of fungal anthrone oxidases, of the several possible Trp residues, the one that fits best with the bacterial active site has the motif QLXXQWSRIFY. Since Gln (Q) and Asp (N) have interchangeable properties, the assignment of this motif as the catalytic site is plausible. HypB, while also possessing several key Trp residues is missing this one, thus providing an explanation for why HypB is unable to catalyze NAA oxidation in our in vitro studies. The anthrone oxidase from A. terreus was characterized previously as a much larger molecule [42]. We suggest that the HypC and HypC-like proteins are the actual fungal anthrone oxidases and have a size similar to those of bacteria. During the studies of the oxidation of synthetic NAA and emodin anthrone (also produced synthetically, results not shown) we found that the substrate was quite sensitive to buffer conditions and to air oxidation when the pH of the environment was sufficiently basic (pH 7.5 or higher). Under these conditions the substrate was converted, partially to a red pigment that remained at the origin under the conditions used for TLC. Previously, the anthrone oxidase assays were done by spectophotometric determination of the red shift that occurs when emodin anthrone is converted to emodin [42]. Formation of the red pigment at the origin observed by TLC would also give a red shift that could have been easily mistaken for catalytic conversion. Furthermore, a smear of protein on the SDS-PAGE gel shown in their study suggests that their sample was quite impure and, therefore, molecular weight was probably not accurately determined in their electrophoretic analysis.
Since no other characterization was reported, we strongly suggest that HypC is the actual fungal anthrone oxidase and closely resembles its bacterial counterparts in size and in activity.

Assignment of a Role for AvfA in Averufin Oxidation
The chemical steps in the conversion of averufin to hydroxyversicolorone have been partially worked out [44][45][46][47] and recently, the cytochrome P450 oxidoreductase CypX (AflV), has been unequivocally assigned to this conversion [46]. Based on complementation studies, two groups found that the gene avfA (aflI) is also involved in this conversion [23,48]. AvfA encodes a presumed flavin dependent oxidoreductase of uncertain catalytic functionality. Both knockout of cypX or avfA led to accumulation of averufin (AVF), with loss of accumulation of metabolites beyond AVF in the biosynthesis. A precise role for AvfA in the oxidation of AVF has never been determined.
There are stereochemical constraints on the rearrangement. As discussed by Townsend, et al. [49], the rearrangement involves a 1,2-aryl shift. The reaction is probably initiated by hydride abstraction from the 2'-carbon by the cytochrome P450, CypX, which may be facilitated by interaction with the aryl hydroxyl at carbon-1 (Scheme 2). Oxidation at one of the secondary carbons of AVF is consistent with the expected functionality of CypX, which has closest similarity to a cytochrome P450 monooxygenase involved in oxidation of a secondary carbon of a trichothecene precursor. This allows rearrangement to proceed across one face of the closed form of the ketal side chain of AVF to be consistent with the stereochemistry of the resulting product, hydroxyversicolorone (HVN), even though there is a required ring-opening reaction, in which the stereochemistry of the rearrangement could be lost. Townsend, et al. convincingly showed that a Favorskii-type rearrangement via formation of a cyclopropanone ring is highly unlikely [45]. Furthermore they proved that nidurufin, a known hydroxylation product of AVF, is not a precursor but rather a shunt metabolite [50]. Nidurufin does not accumulate in cultures from gene knockouts of cypX or avfA, confirming their results [46]. The bridged intermediate in Scheme 2 would be expected to open to give the stereochemically correct configuration of the aldehyde. Since the aldehyde has not been identified as an intermediate in the conversion, it is possible that oxidation of the hydrated CypX intermediate may be catalyzed by AvfA as shown in Scheme 2. To explain why only AVF accumulates in transformants lacking AvfA, we hypothesize that AvfA may form a complex with CypX that aids the electron transfer to flavin necessary for formation of the carbonium ion. precursor by retaining the dehydration functionality of OrdB. It is highly unlikely that CypX alone carries out the oxidation, hydration, and alcohol dehydrogenase closure steps.

The Last Steps in AF Formation
Formation of AFB 1 is initiated by the cytochrome P450 monooxygenase, OrdA (AflQ), mediated oxidation of O-methylsterigmatocystin (OMST) (Scheme 4) [53,54]. Knockout of the gene for this enzyme led to accumulation of OMST. Feeding of OMST to yeast cells containing ordA allowed formation of AFB 1 [53,55], a result suggesting that OrdA is the only enzyme required for this complicated multistep chemical conversion. Townsend has shown that 11-hydroxyOMST (HOMST) is also an AFB 1 precursor and is the likely initial product of OMST oxidation by OrdA. Further oxidative rearrangement to the coumarin ring system in AFB 1 must be consistent with the following observations: 1) NADPH is utilized in the conversion; 2) an "NIH hydride shift" must occur to allow the C-11 hydrogen to be retained; 3) an oxygen atom and C-11 in the A-ring of OMST are lost as carbon dioxide; and 4) an oxygen atom incorporated into the pyrone ring (Scheme 4) is retained [55]. The "reuse" of OrdA for the second required oxidation step is implausible. Not only would the enzyme have very different substrate specificity from that of the first oxidation, but the ring opening that follows would not be a catalyzed step. In the conversion originally postulated [55], after oxidation of HOMST a 370 Da seven-member ring lactone is formed (Scheme 4). The 370 Da intermediate accumulates in detectable amounts in cultures of A. parasiticus with disrupted norA, nadA, or norB [33]. HOMST another postulated intermediate in the conversion was also detected in extracts of these knockout cultures [33].
We have reinterpreted a scheme offered by Udwary, et al. (Scheme 9 of reference [55]) to include involvement of oxidative enzymes encoded by three of the uncharacterized genes in the AF biosynthesis gene cluster. In Scheme 4, rather than the ring-opening of HOMST involving a second OrdA-catalyzed oxidation, oxidation by HypB, the HypC homolog, could introduce an oxygen into the keto-tautomer of HOMST, followed by rearrangement to the 370 Da intermediate. Such an oxidation would be similar to the anthrone oxidation by HypC, namely, oxidation by molecular oxygen at an activated phenolic ring. As Udwary, et al. suggested [55], the oxidation route shown in their Scheme 9, involving nucleophilic attack by molecular oxygen on the keto tautomer of HOMST would require little motion of the substrate relative to the catalytic center and would lead directly to Baeyer-Villigerlike rearrangement to the seven-membered ring 370 Da lactone. Since ST is not a substrate for OrdA it may be that the presence of the methoxy group in OMST enforces the hydroquinone oxidation state in the A-ring and maintains the syn-geometry after ring-opening to favor five-member ring formation in the proposed decarboxylative aldol reaction. The 370 Da intermediate must be sufficiently stable to be identifiable by mass spectrometry and to be the probable substrate for CypA-catalyzed oxidation required for formation of AFG 1 [56]. Scheme 4. Involvement of HypB in the second oxidation step leading from OMST to the 370 Da 7-membered ring lactone precursor for AFB1 and AFG1 formation.
Further rearrangements that allow formation of AFB 1 are shown in Scheme 5. Hydrolysis and ring-opening of the 370 Da lactone could occur spontaneously or involve the action of hydrolytic enzymes encoded by genes that are not part of the AF cluster. In the absence of isolable intermediates from gene disruption studies, assignments of catalytic steps in Scheme 5 is based mainly on fitting plausible reaction steps in the conversion to the enzymes' putative functions. Just as we recently reported that NadA and NorB (AflF) are involved in AFG 1 formation from a CypA (AflU)-created intermediate [56], we now suggest that HypE and the homolog to NorB, NorA (AflE), are involved in the last steps in AFB 1 formation. OrdB, described above, may catalyze an oxidative decarboxylation/dehydration to give the 326 Da metabolite shown in Scheme 5.
Demethylation of the 326 Da metabolite to AFB 1 is also likely to be enzymatically catalyzed. To produce either AFB 1 or AFG 1 the A-ring methyl residue derived from OMST must be removed. Whether or not demethylation occurs concomitantly with decarboxylation and ring-closure is not known. However, the enzyme, HypE, which is part of the AF cluster, has a catalytic domain that would be suitable for ether hydrolysis. Blast search of the translated nucleotide database revealed the presence of orthologs of HypE in many fungi ( Figure 4). These proteins possess an ethD domain, a domain that previously was only reported in a protein from bacteria [57] that is required for ethyl-t-butyl ether degradation [58]. The specific role of the 103 amino acid bacterial protein in ethyl-t-butyl ether degradation has not been determined, but it is known that it works in conjunction with a bacterial cytochrome P450 oxidase. Holmes found that disruption of hypE in A. flavus gave isolates that accumulated a compound with the intense blue fluorescence characteristic of aflatoxins, but which migrated much faster than AFB 1 or AFG 1 on TLC (Robert Holmes' PhD Thesis: http://www.lib.ncsu.edu/theses/available/etd-08182008-112539/unrestricted/etd.pdf [57]). A preliminary analysis of the metabolite mixture from a hypE knockout culture by mass spectrometry identified a compound with mass 328. A plausible candidate for this compound is the 328 Da methyl ether that could be a reduction product of the 326 Da enol ether expected to result from ring closure following decarboxylation as shown in Scheme 5. Upon oxidation of the methyl residue with an unknown cytochrome P450 enzyme and the ethD domain protein (HypE) the resulting oxidized product from the 326 Da intermediate would lose the methyl as formaldehyde to directly give AFB 1 . The 328 Da compound, after demethylation, would require an additional oxidation step to give AFB 1 . A similar series of steps can be envisioned for formation of AFG 1 upon reduction, ether hydrolysis, and re-oxidation. An AF cluster-encoded aryl alcohol dehydrogenase, NorA, may catalyze the re-oxidation as described below. HypE may act in conjunction with one of the five AF biosynthesis cluster cytochrome P450 monooxygenases (possibly CypX or OrdA) to hydroxylate the methyl ether to give, first, an acetal intermediate and then, AFB 1 , after loss of formaldehyde. Previously, the role of NorA in AF biosynthesis was not defined [59]. Orthologs of genes encoding NorA and NorB are found in non-aflatoxigenic fungi, including yeast, so it is possible that such aryl alcohol dehydrogenases have several functions in biosynthesis of secondary or primary metabolites. Mutants of norA in A. parasiticus produced the same mixture of metabolites as the wild-type fungi while disruptants of norA in A. flavus accumulated a bright blue fluorescent metabolite in addition to smaller quantities of AFB 1 compared to the untransformed control. The bright blue fluorescent metabolite was identified as deoxyAFB 1 by its mass spectrum (m/z = 297) and its co-migration on TLC and HPLC with deoxyAF prepared by dehydration of aflatoxicol (AFOH) [60]. To account for the formation of deoxyAF, in the absence of NorA, AFOH is formed in norA disruptant cultures, either prior to or after formation of AFB 1 , and is dehydrated in the acidic growth medium (Scheme 5). In these studies no evidence was found for accumulation of the 326 Da metabolite, but such a metabolite was obtained by knockout of norB in A. parasiticus [33]. Both the predicted 328 and 326 Da ethers would be expected to be rapidly demethylated to yield AFB 1 or AFOH, respectively, by HypE-mediated cytochrome P450 monooxygenase oxidation. NorA may catalyze the oxidization of AFOH back to AFB 1 and, thereby serve as a maintenance oxidase. .

Possible Involvement of HypD in AF Accumulation and Fungal Development
Based on expressed sequence tag data, another small gene, hypD, predicted to encode a 129 Da integral membrane binding protein with a DUF6 domain, was discovered in the AF cluster. The high degree of sequence conservation of HypD orthologs in many fungi ( Figure 5) suggests these proteins have an important functional role in fungi. Disruption of hypD in AF-producing A. parasiticus gave isolates that had markedly increased ability to sporulate compared to the wild-type control ( Figure 6) but diminished yield of both AFB 1 and AFG 1 . These results suggest that HypD affects processes that involve both development and secondary metabolism. Integral membrane proteins can act as permeases or metabolite transporters or function as subunits of proteins such as oxidoreductases or glucan synthases [61][62][63]. At this point we cannot say if HypD plays a role in AF efflux or cytochrome P450 enzyme activity or both. Consistent with the function of integral membrane proteins HypD might assist OrdA in oxidation of OMST [64][65][66] and enable AF efflux from the cell. It is known that AF is mostly excreted from fungal cells, but the only other AF cluster gene with homology to a transporter, namely aflT, is not involved in AF efflux [67]. It is possible that HypD functions as a permease and that in knockout cultures, in the absence of HypD function, causes feedback inhibition of AF biosynthesis with a concomitant increase in formation of conidia. There is known inverse relationship between the developmental and secondary metabolite production pathways that would explain the reduction in AF formation and the increase in conidia in hypD knockout cultures [68,69].   T  L  T  T  T  T  F  i   T  I  I  I  I  I  I  i   F  A  F  I  I  I  P  i   I  I  I D  D  D  D  i   I  I  I  I  I  I  I 1 3 1 1 2 9 1 2 9 1 2 9 1 2 9 1 2 9 1 3 5 w

New Insights into the Involvement of AflJ in AF Biosynthesis Regulation
Previous research sought a role for AflJ (AflS) in regulation of transcription of AF biosynthesis genes [70][71][72][73]. It was established in 1998 that disruption of aflJ caused loss of AF production as well as the production of all AF biosynthesis proteins. There was some confusion as to whether or not transcripts were still made from AF genes in aflJ disruptants, but attempts to complement aflJ mutants by feeding AF precursors were unsuccessful. aflJ and aflR share a common intergenic region and aflJ transcription is regulated by AreA, the global transcription factor for nitrate utilization [74], as well as by the pathway-specific transcription regulatory protein, AflR. These results suggested that AflJ plays knockout wild-type WT KO A B .
.         T  T  T  M   A  A  A  L  T  T  T  T   V  V  A  L  T  T  T  S   I  I  I  a regulatory role in biosynthesis. By yeast two-hybrid studies, Chang found that AflJ bound to AflR [70]. We expanded these studies and found that AflJ also interacts with another protein that acts globally as a regulator of secondary metabolite biosynthesis, namely the methyltransferase, LaeA [25,[75][76][77][78][79]. Transformant A. parasiticus isolates possessing additional copies of AflJ produced higher levels of AF and precursor metabolites [70]. AflJ has three membrane spanning domains and a microbodies signaling sequence at its C-terminal end. By tBlastN analysis, AflJ and AflJ-like proteins were found only in fungi. No conserved domains were detected. However, some of the AflJ-orthologs identified by the tBlastN search contain a conserved methyltransferase-2 (O-methyltransferase) domain. When these and the AflJ orthologs from AF-producing fungi were aligned, several regions in AflJ that are conserved in methyltransferase-2 domain proteins were missing (Figure 7). This explains why Blast search was unable to pick up the methyltransferase-2 domain in AflJ. Nonetheless, a partial domain could still retain biological function, namely, it could bind to another methyltransferase, e.g., LaeA, and become a key nuclear protein for activating specific secondary metabolism gene clusters [25,[75][76][77][78][79]. While unproven, LaeA may modulate chromatin activity at the site of secondary metabolism gene clusters. We suggest that LaeA requires a specific interacting partner, namely AflJ or an AflJ-like protein to allow it to target specific secondary metabolite gene clusters. AflJ is a good candidate for such a partner. It is expected to be nuclear membrane bound, interacts with AflR, and aids formation of the transcription complex. All that is still needed is to ensure a region of open chromatin to allow robust transcriptional activity. Loss of high level transcriptional activity of AF cluster genes has been observed when the genes are cloned into a different locus. When non-AF biosynthesis genes are cloned into the AF cluster they have high levels of transcription [80,81]. Another role for AflJ could be related to its ability to bind to components of the de-ubiquitination pathway, for example CsnF and Nedd8, components of the COP9 signalosome [82,83], a multiprotein complex that prevents protein degradation due to ubiquitination [84][85][86]. Both activation of transcription and stabilization of the protein products formed from the mRNA are necessary to assure the production of high levels of secondary metabolites.

Conclusions
The biosynthetic steps leading to formation of AFB 1 and G 1 from OMST most likely involve multiple enzymes rather than just OrdA for catalysis as was previously suggested. Until the catalytic properties of the individual enzymes are characterized in detail, their role in the conversion schemes reported in this review must remain speculative. To date few such detailed characterizations have been done. Our data allow functional classification of certain previously hypothetical enzymes. HypC and HypC-like proteins are probable oxygenases that are able to catalyze the introduction of oxygen into activated aryl moieties. AflJ and AflJ-like proteins are associated with many secondary metabolite biosynthesis gene clusters in fungi and may form complexes with proteins that affect chromatin activity, such as LaeA. NADH:flavin reductases similar to OrdB and AvfA are often associated with secondary metabolite clusters and our data suggests they are involved in ring closure steps with or without decarboxylation or loss of water. These assignments of function should help to better understand the roles of genes commonly associated with secondary metabolite gene clusters that are not now well understood.