Metabolic peculiarities of Aspergillus niger disclosed by comparative metabolic genomics
© Sun et al.; licensee BioMed Central Ltd. 2007
Received: 27 February 2007
Accepted: 4 September 2007
Published: 04 September 2007
Aspergillus niger is an important industrial microorganism for the production of both metabolites, such as citric acid, and proteins, such as fungal enzymes or heterologous proteins. Despite its extensive industrial applications, the genetic inventory of this fungus is only partially understood. The recently released genome sequence opens a new horizon for both scientific studies and biotechnological applications.
Here, we present the first genome-scale metabolic network for A. niger and an in-depth genomic comparison of this species to seven other fungi to disclose its metabolic peculiarities. The raw genomic sequences of A. niger ATCC 9029 were first annotated. The reconstructed metabolic network is based on the annotation of two A. niger genomes, CBS 513.88 and ATCC 9029, including enzymes with 988 unique EC numbers, 2,443 reactions and 2,349 metabolites. More than 1,100 enzyme-coding genes are unique to A. niger in comparison to the other seven fungi. For example, we identified additional copies of genes such as those encoding alternative mitochondrial oxidoreductase and citrate synthase in A. niger, which might contribute to the high citric acid production efficiency of this species. Moreover, nine genes were identified as encoding enzymes with EC numbers exclusively found in A. niger, mostly involved in the biosynthesis of complex secondary metabolites and degradation of aromatic compounds.
The genome-level reconstruction of the metabolic network and genome-based metabolic comparison disclose peculiarities of A. niger highly relevant to its biotechnological applications and should contribute to future rational metabolic design and systems biology studies of this black mold and related species.
Metabolic network reconstruction based on the knowledge of annotated genomic sequences is a prerequisite to fully understand and exploit the metabolic potential of industrially relevant organisms. Modern fast DNA-sequencing methods as well as state-of-the-art bioinformatic tools are nowadays available for the reconstruction and cross-comparison of these networks among related species as well as among specific strains in order to elucidate their metabolic peculiarities.
Among the filamentous genus Aspergillus, A. niger, A. awamori (a subspecies of A. niger) and A. oryzae are the industrially important producers of both metabolites and enzymes . For example, citric acid is nowadays almost exclusively produced using A. niger, although this "well-working black box" is not yet fully understood . In addition, A. niger has also revealed some potential in bioremediation [3–6] and, moreover, it is a well-known producer of extracellular fungal enzymes. For example, glucoamylase in 20 grams per liter quantities have been reported . Based on these secretion capacities, many efforts have also been undertaken to develop A. niger as a producer of heterologous proteins such as biopharmaceuticals [8, 9], most often with limited success. Thus, there is a great need for a better knowledge of the genomic potential of A. niger, which could be used for rational strain improvement.
By now, the full genomes of A. nidulans , A. oryzae , and the human pathogen A. fumigatus  have been determined. Compared to A. nidulans, which has been widely used as the model organism for studies on fungal physiology and genetics, very little is known about the genetic background of A. niger. Only recently, the annotated genomic sequence of A. niger became publicly available , now allowing a more in-depth analysis of the metabolic potential of this important black fungus as well as the application of modern 'omics' technologies to further improve its performance.
A small-scale metabolic network can be reconstructed based on experimental evidence derived from the literature. However, reconstruction of a more complete, or so-called genome-scale, metabolic network relies on having the genome sequence and high-quality genome annotation [14, 15]. Briefly, a list of enzymes, especially Enzyme Commission (EC) numbers, is extracted from the genome annotation and searched in an established biochemical reaction database to acquire their corresponding reactions. The biochemical reactions are then connected to each other according to certain rules . Such information can be further interpreted as a network and analyzed by many computer programs, such as Cytoscape .
The model of A. niger central metabolism was reported previously [13, 17]. In this study, we reconstructed a genome-scale metabolic network from the annotated genome of A. niger CBS 513.88 . Moreover, from raw genomic data (three-fold coverage) of A. niger ATCC 9029 (Integrated Genomics, Chicago, IL, USA), protein coding sequences (CDSs) were identified, annotated and used for a more complete metabolic network reconstruction. The high-resolution A. niger metabolic network was cross-compared between the two A. niger strains as well as to other Aspergillus species (A. nidulans, A. oryzae, A. fumigatus, A. flavus) and other filamentous fungi, such as Fusarium graminearum and Neurospora crassa, and to the yeast Saccharomyces cerevisiae for identification of unique genes and metabolic peculiarities. Finally, selected genes from the citric acid production pathway of A. niger CBS 513.88 and A. niger ATCC 9029 were cross-compared to the respective genes of A. niger ATCC 1015, whose genome was recently released by the Joint Genomics Institute ahead of annotation .
Results and discussion
Genomic annotation of the low-coverage genome of A. nigerATCC 9029
Unique protein coding sequences (CDSs) in selected fungi revealed by comparative genomic analysis
Unique CDSs in comparison to
A. niger CBS 513.88*
A. niger ATCC 9029
The strain-specific genes in the two A. niger strains are listed in Additional data file 3. Among the genes unique to A. niger CBS 513.88, some encode enzymes for primary metabolism (such as alcohol dehydrogenase (NADP+) (An10g00010), fructose-1,6-bisphosphate aldolase (An16g00110), NADH dehydrogenase (An06g00130)), some for secondary metabolism (such as cephalosporin acylase, An16g00140), and some for transcription factors/regulators. A large gene cluster spans over 90 genes (from An08g11200 to An08g12140), of which 52 are unique to A. niger CBS 513.88 and most have unknown functions. Seven transposable elements are located in or next to this cluster, giving hints to its potential evolutionary origin by horizontal gene transfer. Interestingly, 25 of the CDSs unique to A. niger ATCC 9029, including glucokinase (Anig00906), UDP-N-acetylmuramoylalanine-D-glutamate ligase (Anig04708), UDP-N-acetylglucosamine-N-acetylmuramyl-(Pentapeptide) pyrophosphoryl-undecaprenol N-acetylglucosamine transferase (Anig04709) and five proteins involved in transport, have strong similarity (70-95% identical) to bacterial or bacteriophage proteins, indicating a possible bacterial origin of these proteins. The majority of the remaining genes unique to ATCC 9029 do not show any significant homology to the NCBI protein database.
In some cases the unique CDSs are just duplicates: their homologs can be found in both CBS 513.88 and ATCC 9029 (refer to Additional data file 3). For example, in addition to the unique gene An16g00110, CBS 513.88 has three further copies of genes coding for fructose-1,6-bisphosphate aldolase, An14g04410, An05g02040 and An02g07470, which are orthologous to the three copies of fructose-1,6-bisphosphate aldolase in ATCC 9029, Anig06338, Anig11911 and Anig08668, respectively.
In summary, the results from comparative genomics show that the A. niger strains are closely related to each other but exhibit large differences from the other fungal species compared. In the following paragraphs we address the impact of these differences on the metabolic peculiarities of A. niger.
Reconstruction and comparative analysis of the metabolic network
Metabolic network reconstruction
Distribution of reactions and metabolites of the inferred genome-wide metabolic network in different functional categories
Amino acid metabolism
Metabolism of other amino acids
Glycan biosynthesis and metabolism
Biosynthesis of polyketides and nonribosomal peptides
Metabolism of cofactors and vitamins
Biosynthesis of secondary metabolites
Xenobiotics biodegradation and metabolism
A comparative assessment of the central metabolic network
The metabolic network reconstructed from the genomic data was compared to the network of central carbon metabolism of A. niger reconstructed by David et al. . The network of David et al. was mainly based on literature data of A. niger and the genomic information of A. nidulans and other fungi. It contains 335 reactions, 284 metabolites and 129 EC numbers. In general, there is a good agreement between these two metabolic networks regarding central metabolism. Only 14 ECs in the metabolic network of David et al. could not be found in the genome-wide network reconstructed by us in this work, most of which belong to enzymes poorly characterized in the literature in terms of protein sequences. The reason for such minor discrepancies is discussed in detail in Additional data file 8.
Unique enzyme-coding genes and unique EC numbers
Unique enzymes of A. niger in comparison to selected filamentous fungi
Closest homolog in A. niger CBS 513.88
Closest homolog in other Aspergilli
ABC transport system ATP-binding protein
S-adenosylmethionine tRNA ribosyltransferase
Biosynthesis of melanin
Protocatechuate 3,4-dioxygenase, beta subunit
Benzoate and 2,4-dichlorobenzoate degradation
It should be noted that in most cases, the unique enzyme-coding genes mentioned above do have paralogs in other fungi or even in A. niger itself (refer to Materials and methods for the definition of uniqueness). These paralogs were carefully verified not to be orthologs since they are orthologous to other CDSs of A. niger. Gene redundancy or duplication has also been reported in A. niger previously [13, 28], and is commonly found in eukaryotes [26, 29, 30]. Due to slackened selective constraints, the duplicated genes have greater potential for mutation to undergo slight changes in function, such as different substrate or ligand specificity, to achieve different temporal or spatial distribution, to be differently regulated, or even to gain completely new functions . It is interesting to ask what are the biological functions of these unique but paralogous enzymes in A. niger. As can be seen in Table 3, only two enzymes of A. niger have no homolog in the other fungi, namely 4,5-dihydroxyphthalate decarboxylase (EC 220.127.116.11), involved in 2,4-dichlorobenzoate degradation, and S-adenosylmethionine tRNA ribosyltransferase (EC 5.4.99.-), involved in tRNA modification. The finding concerning S-adenosylmethionine tRNA ribosyltransferase is somewhat surprising, because this enzyme is exclusively present in eubacteria for de novo biosynthesis of queuosine, which is an essential nutrient for many eucaryotes [31, 32] (see Additional data file 11 for a detailed analysis).
Citric acid production as a case study
A versatile metabolic conversion center
In view of the importance of citric acid production by A. niger, the metabolic reactions contributing to citric acid production are selected as an example to explore the capability of the constructed metabolic network. Although citric acid production has been studied extensively in the past, there are still many questions that need to be answered to fully understand the citric acid formation process . The pathways related to citric acid production from glucose were extracted from the genome-wide metabolic network together with the metabolites directly connected to these pathways (Figure 3; refer to Additional data file 12 for details). The extensive connections of the 25 intermediates of glycolysis/tricarboxylic acid (TCA) cycle from/to the 146 metabolites of other pathways demonstrate the complexity and large interactions of the central metabolism. Eighteen substrates, such as starch, sucrose, dextrin, maltose, lactose, cellulose, α,α-trehalose, sorbitol, D-glucoside, N-glycan, and so on, require only a one-step reaction to enter this pathway via glucose. In comparison to other filamentous fungi, A. niger has redundant unique genes for the conversion of seven of these substrates (reactions marked as red in Figure 3). Degradation products from many pathways, including xenobiotic and amino acid metabolism, enter this citrate biosynthesis sub-network via pyruvate or acetyl-CoA for further processing. Acetyl-CoA and pyruvate belong to the metabolites having the highest connectivity (involved in 65 and 57 reactions, respectively) in the metabolic network of A. niger. They are directly used for biosynthesis of amino acids, lipids, vitamins, and so on. 2-Oxoglutarate and dihydroxyacetone phosphate from this sub-network are two other metabolites involved in many pathways for biosynthesis (lipids and amino acids, respectively). Anaplerotic pathways of the TCA cycle were identified from the metabolic map, including reactions from the glyoxylate cycle, from phosphoenolpyruvate to oxaloacetate, or from pyruvate to oxaloacetate or malate. The versatile conversion center TCA cycle can potentially offer a sufficient amount of oxaloacetate for the formation of oxalic acid, often an unwanted acidic by-product in A. niger cultivations.
Additional copies of genes encoding alternative mitochondrial oxidoreductase and citrate synthase in the citric acid production strain
Distribution of alternative mitochondrial oxidoreductase and citrate synthase genes in Aspergillus and selected fungi
The second example is the citrate synthase (Table 4) catalyzing the biosynthesis of citric acid from acetyl-CoA and oxaloacetate. Table 4 shows the relevant orthologs across the selected fungi. The A. niger strains share five isoenzymes of citrate synthase, including methylcitrate synthase, which also shows citrate synthase activity , whereas A. oryzae has only four, and A. fumigatus and A. nidulans have only three copies. The genetic multiplicity of citrate synthase was also reported in A. niger . Here, we identified that the ortholog group 12065 is unique to all three A. niger strains. Interestingly, A. niger ATCC 1015, the strain used in the first patented citric acid process, has an additional unique citrate synthase gene, jgi|Aspni1|46236 (Table 4). Its ortholog was not found in A. niger CBS 513.88 or A. niger ATCC 9029. The sequence of this protein is identical to gb|EAV74068.1, citrate synthase I of Delftia acidovorans SPH-1 (β-proteobacteria). This partial gene is found on a small contig, scaffold_1409, whose nucleotide sequence is also identical to the genomic sequence of Delftia acidovorans SPH-1. The presence of this additional and bacteria-originated citrate synthase in A. niger ATCC 1015 needs to be carefully verified by genome sequencing or PCR to rule out the possibility of sequence contamination. Furthermore, a detailed phylogenetic analysis of 1,134 homolog sequences (homologous to any of the six groups of citrate synthase in A. niger at E-value 1E-20) from the NCBI nr protein database showed that the sequences of the first two ortholog groups (361 and 2397) in Table 4 are clearly clustered with the sequences mainly from eukaryotes while those of the last four ortholog groups are clustered with prokaryotic sequences (Additional data file 13), suggesting different origins of citrate synthase in A. niger. Since the members of the A. niger unique ortholog group 12065 is tightly clustered with the other two ortholog groups, these genes probably originated after speciation by gene duplication events. As revealed by the analysis above, gene duplication or redundancy seems to be a general strategy evolved in this black mould. These newly found extra copies of genes in A. niger strains, most remarkably the second AOX and the additional citrate synthases, may contribute to the high citrate production efficiency of A. niger.
14,000 protein coding sequences were predicted from the raw low-coverage genome sequence of A. niger ATCC 9029 and approximately 60% of them were assigned to at least one functional category (GO, KO, COG, EC and pathways). This enabled a comparative genomic analysis of two different A. niger strains. It is found that the genomic content of A. niger ATCC 9029 is very similar to that of A. niger CBS 513.88; merely around 600 genes are exclusively found in each strain. A further comparative genomic analysis among six Aspergilli and other selected eucaryotes revealed more than 4,000 CDSs unique to A. niger. Based on the functional annotation of the two A. niger strains, we reconstructed the metabolic network of A. niger and systematically compared it with those of seven other fungi. Comparative metabolic genomics revealed the high metabolic peculiarity of A. niger by more than 1,100 unique enzyme-encoding genes. Many of these unique genes are additional copies (paralogs) of those genes that are common (orthologs) in the compared fungi, indicating that genetic multiplicity might be a key strategy of A. niger to keep its versatile metabolic capacities and its robustness to adapt to different environmental conditions. Only nine genes were identified to encode enzymes with EC numbers exclusively found in A. niger, mostly involved in the biosynthesis of complex secondary metabolites and degradation of aromatic compounds. Moreover, we identified additional copies of genes, such as the ones encoding alternative mitochondrial oxidoreductase and citrate synthases, which could have an impact on the overproduction of citric acid by this black mould.
Materials and methods
Genome sequence of A. niger
The genome (approximately 32 Mb, haploid 8 chromosomes) sequence of A. niger ATCC 9029 was obtained from Integrated Genomics Inc (Chicago, IL, USA), which has a genome coverage of about three-fold and was generated by using a whole-genome shotgun strategy without finishing. The assembled genomic sequence contains 9,510 contigs corresponding to 33.7 Mb. The average length of the contigs is 3.5 kb. The largest contig is 34.9 kb. The genome of A. niger CBS 513.88 and its annotation were kindly provided by the company DSM ahead of publication . The genome of A. niger ATCC 1015 and its gene prediction were downloaded from the Joint Genome Institute under its data release agreement . Genome sequences of other fungal strains were downloaded from KEGG and NCBI.
Prediction and annotation of protein-coding sequences
To predict the CDSs and to reconstruct the metabolic network of organisms with unannotated, low coverage genome sequences, we recently developed a new algorithm called 'IdentiCS' . This homology-based algorithm was demonstrated to be able to cope with sequences of low genome coverage and, thus, potentially high error rates. It was successfully used to predict CDSs and to infer the metabolic networks of several bacteria, including Klebsiella pneumoniae and Salmonella typhimurium , Escherichia coli 1917  and Bacillus megaterium . In this study, this algorithm was extended for the prediction and annotation of eukaryotic CDSs by considering the intron and extron structure of genes (see Additional data file 1).
Complementation of 'IdentiCS' by GenScan and GeneWise for the prediction of protein-encoding genes
GeneWise, another useful software applying a homology-based approach to predict gene structure , was used to refine and confirm the prediction of 'IdentiCS' as described above. Like all other homology-based methods, 'IdentiCS' is unable to predict new genes for which no homologue is present in the available protein database. Thus, a homology-independent program called GenScan was used. GenScan is a general-purpose gene identification program that determines the most likely 'parse' (gene structure) by using a probabilistic model of the gene structural and compositional properties of the genomic DNA for the given organism .
Refinement of the annotation
We combined several strategies to refine the annotation. First, all CDSs predicted were submitted to the KEGG Automatic Annotation Server  which applies a best-best algorithm to associate the submitted sequence to known KO number, COG, EC number, GO number and biochemical reactions. Second, we used HT-GO-FAT (High Throughput Gene Ontology Functional Annotation Toolkit) , another useful software toolkit that utilizes a custom-curated BLAST database to annotate sequences to GO, EC number, KEGG pathways and so on. EC numbers can be deduced from the associated GO numbers by this program. Third, text mining was used to assign EC number when an obvious enzyme could not be associated to an EC number or a complete EC number through the above-mentioned methods. For this purpose, the name of the enzyme was queried in the KEGG Ligand database [42, 43] for synonyms or searched via a general search engine such as Google . The hits were manually evaluated.
Proteins predicted from the unfinished genomic sequences of A. niger ATCC 9029 and the proteins from A. niger CBS 513.88 were cross-compared with the proteins of seven selected fungal species and another 26 representative eukaryotic organisms to identify their orthologous relationships. The seven selected fungi included A. oryzae (used in Asian food fermentation), A. fumigatus (a human pathogen), A. nidulans (a model organism for genetic studies), F. graminearum (a plant pathogen but also used in food production), Magnaporthe grisea (a plant pathogen), N. crassa (a model organism) and S. cerevisiae (used in baking and brewing but also a model organism). The protein ortholog relationship among A. niger and the selected fungi was detected by the program OrthoMCL  with relatively strict parameters, such as p value cutoff 1E-20, identity cutoff 40%, percentage-of-match cutoff 50% and inflation factor 5. OrthoMCL detects the many-to-many ortholog groups including recent paralogs based on all-against-all sequence alignment. This algorithm is suitable to work with more genomes. Blast  and PatternHunter  were used for sequence alignment.
Comparative genomics revealed a huge number of species-specific genes, even when two closely related sub-species were compared to each other. We found 3,976 CDSs unique to A. niger ATCC 9029 compared to A. niger CBS 513.88, and 4,306 unique to A. niger CBS 513.88 compared vice versa. We argue that this number is too high to be true because the sequence alignment of the two subspecies usually showed very high identity (close to 100%), indicating that the speciation is really a recent evolutionary event and a huge difference in genomic content is thus impossible. Failure of gene prediction in the genome annotation process can cause failure in ortholog detection. To avoid this problem, the protein sequence of each A. niger strain was compared against the genomic sequences of the other A. niger strain by applying strict criteria (aligned region >80% and identity >80% or log10(e2) < 0.8*log10(e1), where e2 is the E-value of the query protein against the genome while e1 is the E-value of the query protein against itself) in addition to the criteria mentioned above. This procedure ensures the detection of near-identical genes (ortholog or inparalog ) even in cases where they were not predicted as genes in one of the compared strains by the initial genome annotation process. The results were surprising: many nearly identical genomic regions were predicted as genes in A. niger ATCC 9029 but not in A. niger CBS 513.88, or vice versa, strongly demonstrating the necessity for improvement of current gene finding strategies, for instance, by integrating results from comparative genomics study. By this procedure, the number of genes truly specific to one of the A. niger strains is greatly reduced (see Table 1 for the results). This procedure was not applied for the cross-comparison of A. niger with the other fungi due to lack of an operational criterion.
Uniqueness of genes or CDSs
In this work, if not specified, the uniqueness of a gene or CDS from organism A is defined according to the orthologous relationship table established above. If the ortholog of a gene from organism A is absent in organism B, we define that this gene is unique or specific to organism A in comparison to organism B. This does not imply there is no homolog (namely paralog) of the gene from organism A in organism B. In some cases, this gene is just an additional copy of another gene whose orthologs are found in both organisms. This also does not imply that this gene is found only in organism A. For example, the ortholog of this gene may be found in organism C from the relationship table or another strain or species that is not compared in this work.
Metabolic network reconstruction
Two methods were used to reconstruct and visualize the metabolic network based on the annotation of CDSs. One method was based on mapping the annotation information to knowledge bases such as the KEGG pathways through 'IdentiCS' . The metabolic pathways and network reconstructed this way are intuitive with respect to our knowledge on biochemical pathways. They can be used for a straightforward comparison with the network of other sequenced organisms . The metabolic network was also constructed based on the connection matrix of reactions according to Ma and Zeng . Thirty-one non-enzymatic reactions were also considered in the latter approach. The connection matrix of reactions published by Ma and Zeng  was substantially improved in this work by: updating the enzyme reaction database to the newer version of KEGG Ligand (Status Nov. 2005) ; integrating the information of reversibility from KEGG pathway maps (Status Nov. 2005)  and confirming it with the BRENDA enzymatic database ; and considering the complete set of reactions available in the Ligand database. In the end, the new version contains 6,442 reactions instead of the 3,805 in the former version. In addition, half of the reactions from the former version were updated in term of reversibility and connection pairs (Additional data file 14; also, check the authors' website  for an updated version). The software Cytoscape [16, 50] and yEd (a Java Graph Editor from the company yWorks)  were used as layout tools for the genome-wide network. The phylogenetic tree was built by using the software ClustalW (version 1.83 for Windows) .
Additional data files
The following additional data are available with the online version of this paper. Additional data file 1 describes the methods for prediction and annotation of protein-coding sequences. Additional data file 2 is a table listing the orthologous groups of genes from selected fungi and their functions. Additional data file 3 is a table listing the strain-specific CDSs identified by cross-comparing the two A. niger strains. Additional data file 4 shows the genome-wide metabolic network of A. niger as a reaction graph where nodes are reactions and links are common reactants (substrate or product) of two successive reactions. The color of the nodes represents different functional categories. Additional data file 5 is a clickable version of Figure 2 where nodes (metabolites) are linked to the KEGG Ligand database for detailed information. Additional data file 6 is a clickable version of Additional data file 4 where nodes (reactions) are linked to the KEGG Ligand database for detailed information. Additional data file 7 is a table listing all the reactions used for reconstruction of the A. niger metabolic network. The corresponding EC numbers and genes are also shown. Additional data file 8 shows the results of a comparative assessment of the central metabolic network. Additional data file 9 is a table listing the enzyme-encoding genes unique to one of the two A. niger strains in comparison with the other selected fungi. Additional data file 10 is a table listing the enzyme-encoding genes common in both A. niger strains and unique to them in comparison with the other selected fungi. Additional data file 11 is a phylogenetic analysis of the S-adenosylmethionine tRNA ribosyltransferase. Additional data file 12 is a detailed version of Figure 3, showing a network view from glucose to citrate, including the names of all metabolites. Additional data file 13 is a phylogenetic analysis of citric acid synthases (CS), where 1,123 sequences from the NCBI nr protein database homologous to any of the six CSs of A. niger (cutoff E-value 1E-20, partial sequence ignored) were aligned together with the CSs from A. niger ATCC 9029 and ATCC 1015 to build the phylogenetic tree with 1,000 time bootstraps, using the software ClustalW. Part A is an overview while part B is the full phylogenetic tree with GI number, strain name, taxonomy, and bootstrap values. Additional data file 14 is the reaction database used for reconstruction of the metabolic network. Additional data file 15 is the protein database of A. niger ATCC 9029.
Clusters of Orthologous Groups
- EC number:
Enzyme Commission number
- TCA cycle:
tricarboxylic acid cycle.
This study was carried out as a collaborative effort in the Sonderforschungsbereich 578 (Projects B4 and B6), supported by the German Research Foundation (DFG). The team for the KEGG Automatic Annotation Server receives our thanks for assigning the CDSs to functional categories (GO, KO and EC). We greatly acknowledge DSM for the access to A. niger CBS 513.88 database ahead of publication. The sequence data of A. niger ATCC 9029 were obtained from Integrated Genomics, Inc. The sequence data of A. niger ATCC 1015 were generated by the US Department of Energy Joint Genome Institute.
- Bodie EA, Bower B, Berka RM, Dunn-Coleman NS: Economically important organic acid and enzyme products. Aspergillus: 50 Years On. Edited by: Martinelli SD, Kinghorn JR. 1994, Amsterdam, Lausanne, NewYork, Oxford, Shannon, Tokyo: Elsevier, 561-602.Google Scholar
- Karaffa L, Kubicek CP: Aspergillus niger citric acid accumulation: do we understand this well working black box?. Appl Microbiol Biotechnol. 2003, 61: 189-196.PubMedView ArticleGoogle Scholar
- Bejaoui H, Mathieu F, Taillandier P, Lebrihi A: Biodegradation of ochratoxin A by Aspergillus section Nigri species isolated from French grapes: a potential means of ochratoxin A decontamination in grape juices and musts. FEMS Microbiol Lett. 2006, 255: 203-208. 10.1111/j.1574-6968.2005.00073.x.PubMedView ArticleGoogle Scholar
- Kanaly RA, Kim IS, Hur HG: Biotransformation of 3-methyl-4-nitrophenol, a main product of the insecticide fenitrothion, by Aspergillus niger. J Agric Food Chem. 2005, 53: 6426-6431. 10.1021/jf050679w.PubMedView ArticleGoogle Scholar
- Mathialagan T, Viraraghavan T: Biosorption of pentachlorophenol by fungal biomass from aqueous solutions: a factorial design analysis. Environ Technol. 2005, 26: 571-579.PubMedView ArticleGoogle Scholar
- Volke-Sepulveda T, Gutierrez-Rojas M, Favela-Torres E: Biodegradation of high concentrations of hexadecane by Aspergillus niger in a solid-state system: kinetic analysis. Bioresour Technol. 2006, 97: 1583-1591. 10.1016/j.biortech.2005.07.026.PubMedView ArticleGoogle Scholar
- Finkelstein DB: Improvement of enzyme production in Aspergillus. Antonie van Leeuwenhoek. 1987, 53: 349-352. 10.1007/BF00400559.PubMedView ArticleGoogle Scholar
- Wiebe MG, Karandikar A, Robson GD, Trinci APJ, Flores Candia JL, Trappe S, Wallis G, Rinas U, Derkx PMF, Madrid SM, et al: Production of tissue plasminogen activator (t-PA) in Aspergillus niger. Biotechnol Bioeng. 2001, 76: 164-174. 10.1002/bit.1156.PubMedView ArticleGoogle Scholar
- Joosten V, Lokman C, van den Hondel CAMJ, Punt PJ: The production of antibody fragments and antibody fusion proteins by yeasts and filamentous fungi. Microb Cell Fact. 2003, 2: 1-10.1186/1475-2859-2-1.PubMedPubMed CentralView ArticleGoogle Scholar
- Galagan JE, Calvo SE, Cuomo C, Ma LJ, Wortman JR, Batzoglou S, Lee SI, Basturkmen M, Spevak CC, Clutterbuck J, et al: Sequencing of Aspergillus nidulans and comparative analysis with A. fumigatus and A. oryzae. Nature. 2005, 438: 1105-1115. 10.1038/nature04341.PubMedView ArticleGoogle Scholar
- Machida M, Asai K, Sano M, Tanaka T, Kumagai T, Terai G, Kusumoto K, Arima T, Akita O, Kashiwagi Y, et al: Genome sequencing and analysis of Aspergillus oryzae. Nature. 2005, 438: 1157-1161. 10.1038/nature04300.PubMedView ArticleGoogle Scholar
- Nierman WC, Pain A, Anderson MJ, Wortman JR, Kim HS, Arroyo J, Berriman M, Abe K, Archer DB, Bermejo C, et al: Genomic sequence of the pathogenic and allergenic filamentous fungus Aspergillus fumigatus. Nature. 2005, 438: 1151-1156. 10.1038/nature04332.PubMedView ArticleGoogle Scholar
- Pel HJ, de Winde JH, Archer DB, Dyer PS, Hofmann G, Schaap PJ, Turner G, de Vries RP, Albang R, Albermann K, et al: Genome sequencing and analysis of the versatile cell factory Aspergillus niger CBS 513.88. Nat Biotechnol. 2007, 25: 221-231. 10.1038/nbt1282.PubMedView ArticleGoogle Scholar
- Francke C, Siezen RJ, Teusink B: Reconstructing the metabolic network of a bacterium from its genome. Trends Microbiol. 2005, 13: 550-558. 10.1016/j.tim.2005.09.001.PubMedView ArticleGoogle Scholar
- Ma H, Zeng AP: Reconstruction of metabolic networks from genome data and analysis of their global structure for various organisms. Bioinformatics. 2003, 19: 270-277. 10.1093/bioinformatics/19.2.270.PubMedView ArticleGoogle Scholar
- Shannon P, Markiel A, Ozier O, Baliga NS, Wang JT, Ramage D, Amin N, Schwikowski B, Ideker T: Cytoscape: a software environment for integrated models of biomolecular interaction networks. Genome Res. 2003, 13: 2498-2504. 10.1101/gr.1239303.PubMedPubMed CentralView ArticleGoogle Scholar
- David H, Akesson M, Nielsen J: Reconstruction of the central carbon metabolism of Aspergillus niger. Eur J Biochem. 2003, 270: 4243-4253. 10.1046/j.1432-1033.2003.03798.x.PubMedView ArticleGoogle Scholar
- Joint Genomics Institute (JGI). [http://genome.jgi-psf.org]
- Birney E, Clamp M, Durbin R: GeneWise and Genomewise. Genome Res. 2004, 14: 988-995. 10.1101/gr.1865504.PubMedPubMed CentralView ArticleGoogle Scholar
- Burge C, Karlin S: Prediction of complete gene structures in human genomic DNA. J Mol Biol. 1997, 268: 78-94. 10.1006/jmbi.1997.0951.PubMedView ArticleGoogle Scholar
- Sun J, Wang W, Hundertmark C, Zeng AP, Jahn D, Deckwer W-D: A protein database constructed from low-coverage genomic sequence of Bacillus megaterium and its use for accelerated proteomic analysis. J Biotechnol. 2006, 124: 486-495. 10.1016/j.jbiotec.2006.01.033.PubMedView ArticleGoogle Scholar
- Li L, Stoeckert CJ, Roos DS: OrthoMCL: identification of ortholog groups for eukaryotic genomes. Genome Res. 2003, 13: 2178-2189. 10.1101/gr.1224503.PubMedPubMed CentralView ArticleGoogle Scholar
- Sun J, Zeng AP: IdentiCS - identification of coding sequence and in silico reconstruction of the metabolic network directly from unannotated low-coverage bacterial genome sequence. BMC Bioinformatics. 2004, 5: 112-10.1186/1471-2105-5-112.PubMedPubMed CentralView ArticleGoogle Scholar
- Blumenthal CZ: Production of toxic metabolites in Aspergillus niger, Aspergillus oryzae, and Trichoderma reesei: justification of mycotoxin testing in food grade enzyme preparations derived from the three fungi. Regul Toxicol Pharmacol. 2004, 39: 214-228. 10.1016/j.yrtph.2003.09.002.PubMedView ArticleGoogle Scholar
- Kondrashov FA, Kondrashov AS: Role of selection in fixation of gene duplications. J Theor Biol. 2006, 239: 141-151. 10.1016/j.jtbi.2005.08.033.PubMedView ArticleGoogle Scholar
- Hurles M: Gene duplication: The genomic trade in spare parts. Plos Biology. 2004, 2: 900-904. 10.1371/journal.pbio.0020206.View ArticleGoogle Scholar
- Cerniglia CE: Fungal metabolism of polycyclic aromatic hydrocarbons: past, present and future applications in bioremediation. J Ind Microbiol Biotechnol. 1997, 19: 324-333. 10.1038/sj.jim.2900459.PubMedView ArticleGoogle Scholar
- Cullen D: The genome of an industrial workhorse. Nat Biotechnol. 2007, 25: 189-190. 10.1038/nbt0207-189.PubMedView ArticleGoogle Scholar
- Freilich S, Spriggs RV, George RA, Al Lazikani B, Swindells M, Thornton JM: The complement of enzymatic sets in different species. J Mol Biol. 2005, 349: 745-763. 10.1016/j.jmb.2005.04.027.PubMedView ArticleGoogle Scholar
- Langkjaer RB, Cliften PF, Johnston M, Piskur J: Yeast genome duplication was followed by asynchronous differentiation of duplicated genes. Nature. 2003, 421: 848-852. 10.1038/nature01419.PubMedView ArticleGoogle Scholar
- Morris RC, Elliott MS: Queuosine modification of tRNA: a case for convergent evolution. Mol Genet Metab. 2001, 74: 147-159. 10.1006/mgme.2001.3216.PubMedView ArticleGoogle Scholar
- Slany RK, Bosl M, Crain PF, Kersten H: A new function of S-adenosylmethionine: the ribosyl moiety of AdoMet is the precursor of the cyclopentenediol moiety of the tRNA wobble base queuine. Biochemistry. 1993, 32: 7811-7817. 10.1021/bi00081a028.PubMedView ArticleGoogle Scholar
- Kirimura K, Yoda M, Usami S: Cloning and expression of the cDNA encoding an alternative oxidase gene from Aspergillus niger WU-2223L. Curr Genet. 1999, 34: 472-477. 10.1007/s002940050422.PubMedView ArticleGoogle Scholar
- Kirimura K, Yoda M, Shimizu H, Sugano S, Mizuno M, Kino K, Usami S: Contribution of cyanide-insensitive respiratory pathway, catalyzed by the alternative oxidase, to citric acid production in Aspergillus niger. Biosci Biotechnol Biochem. 2000, 64: 2034-2039. 10.1271/bbb.64.2034.PubMedView ArticleGoogle Scholar
- Kubicek CP, Zehentgruber O, El Kalak H, Röhr M: Regulation of citric acid production by oxygen: Effect of dissolved oxygen tension on adenylate levels and respiration in Aspergillus niger. App Microbiol Biotechnol. 1980, 9: 101-115. 10.1007/BF00503505.View ArticleGoogle Scholar
- Juszczuk IM, Rychter AM: Alternative oxidase in higher plants. Acta Biochim Pol. 2003, 50: 1257-1271.PubMedGoogle Scholar
- Kirimura K, Ogawa S, Hattori T, Kino K: Expression analysis of alternative oxidase gene (aox1) with enhanced green fluorescent protein as marker in citric acid-producing Aspergillus niger. J Biosci Bioeng. 2006, 102: 210-214. 10.1263/jbb.102.210.PubMedView ArticleGoogle Scholar
- Maerker C, Rohde M, Brakhage AA, Brock M: Methylcitrate synthase from Aspergillus fumigatus. Propionyl-CoA affects polyketide synthesis, growth and morphology of conidia. FEBS J. 2005, 272: 3615-3630. 10.1111/j.1742-4658.2005.04784.x.PubMedView ArticleGoogle Scholar
- Sun J, Gunzer F, Westendorf AM, Buer J, Scharfe M, Jarek M, Gossling F, Blocker H, Zeng AP: Genomic peculiarity of coding sequences and metabolic potential of probiotic Escherichia coli strain Nissle 1917 inferred from raw genome data. J Biotechnol. 2005, 117: 147-161. 10.1016/j.jbiotec.2005.01.008.PubMedView ArticleGoogle Scholar
- The KEGG Automatic Annotation Server. [http://www.genome.jp/kegg/kaas]
- The High Throughput Gene Ontology Functional Annotation Toolkit (HT-GO-FAT). [http://liru.ars.usda.gov]
- KEGG Ligand Database. [http://www.genome.jp/ligand]
- Kanehisa M, Goto S, Hattori M, Aoki-Kinoshita KF, Itoh M, Kawashima S, Katayama T, Araki M, Hirakawa M: From genomics to chemical genomics: new developments in KEGG. Nucleic Acids Res. 2006, 34: D354-D357. 10.1093/nar/gkj102.PubMedPubMed CentralView ArticleGoogle Scholar
- Google. [http://www.google.com]
- Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997, 25: 3389-3402. 10.1093/nar/25.17.3389.PubMedPubMed CentralView ArticleGoogle Scholar
- Ma B, Tromp J, Li M: PatternHunter: faster and more sensitive homology search. Bioinformatics. 2002, 18: 440-445. 10.1093/bioinformatics/18.3.440.PubMedView ArticleGoogle Scholar
- KEGG Pathway Maps. [http://www.genome.jp/kegg/xml]
- The BRENDA Enzymatic Database. [http://www.brenda-enzymes.info/]
- The Institute of Bioprocess and Biosystems Engineering at the Hamburg University of Technology. [http://www.tu-harburg.de/ibb]
- The Software Cytoscape. [http://www.cytoscape.org]
- The Software yEd from the Company yWorks. [http://www.yworks.com]
- The Software ClustalW from EBI. [http://www.ebi.ac.uk/clustalw]
- Yokoyama S, Nishimura S: Modified nucleosides and codon recognition. tRNA: Structure, Biosynthesis and Function. Edited by: Söll D, RajBhandary UL. 1995, Washington, DC: ASM Press, 207-223.View ArticleGoogle Scholar
- Gaur R, Varshney U: Genetic analysis identifies a function for the queC (ybaX) gene product at an initial step in the queuosine biosynthetic pathway in Escherichia coli. J Bacteriol. 2005, 187: 6893-6901. 10.1128/JB.187.20.6893-6901.2005.PubMedPubMed CentralView ArticleGoogle Scholar
- Siedenberg D, Mestric S, Ganzlin M, Schmidt M, Punt PJ, van den Hondel CAMJ, Rinas U: GlaA promoter controlled production of a mutant green fluorescent protein (S65T) by recombinant Aspergillus niger during growth on defined medium in batch and fed-batch cultures. Biotechnol Prog. 1999, 15: 43-50. 10.1021/bp980105u.PubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.