The primordial metabolism: an ancestral interconnection between leucine, arginine, and lysine biosynthesis
© Fondi et al; licensee BioMed Central Ltd. 2007
Published: 16 August 2007
It is generally assumed that primordial cells had small genomes with simple genes coding for enzymes able to react with a wide range of chemically related substrates, interconnecting different metabolic routes. New genes coding for enzymes with a narrowed substrate specificity arose by paralogous duplication(s) of ancestral ones and evolutionary divergence. In this way new metabolic pathways were built up by primordial cells. Useful hints to disclose the origin and evolution of ancestral metabolic routes and their interconnections can be obtained by comparing sequences of enzymes involved in the same or different metabolic routes. From this viewpoint, the lysine, arginine, and leucine biosynthetic routes represent very interesting study-models. Some of the lys, arg and leu genes are paralogs; this led to the suggestion that their ancestor genes might interconnect the three pathways. The aim of this work was to trace the evolutionary pathway leading to the appearance of the extant biosynthetic routes and to try to disclose the interrelationships existing between them and other pathways in the early stages of cellular evolution.
The comparative analysis of the genes involved in the biosynthesis of lysine, leucine, and arginine, their phylogenetic distribution and analysis revealed that the extant metabolic "grids" and their interrelationships might be the outcome of a cascade of duplication of ancestral genes that, according to the patchwork hypothesis, coded for unspecific enzymes able to react with a wide range of substrates. These genes belonged to a single common pathway in which the three biosynthetic routes were highly interconnected between them and also to methionine, threonine, and cell wall biosynthesis. A possible evolutionary model leading to the extant metabolic scenarios was also depicted.
The whole body of data obtained in this work suggests that primordial cells synthesized leucine, lysine, and arginine through a single common metabolic pathway, whose genes underwent a set of duplication events, most of which can have predated the appearance of the last common universal ancestor of the three cell domains (Archaea, Bacteria, and Eucaryotes). The model proposes a relative timing for the appearance of the three routes and also suggests a possible evolutionary pathway for the assembly of bacterial cell-wall.
However, in spite of the available data, no evolutionary model explaining the extant scenario has been proposed. The aim of this work was to try to trace the evolutionary history of the three metabolic pathways and to shed some light on the ancestral route(s) and interrelationships existing between them and (eventually) with other metabolic routes. To this purpose, a comparative analysis of the extant leucine, arginine, and lysine metabolic pathways from (micro)organisms whose genome has been completely sequenced was carried out.
Results and discussion
Distribution of leucine, arginine and lysine biosynthetic genes
i) Lysine (AAA) biosynthetic genes are very rarely represented in Bacteria, in that just two organisms harbour the complete set of AAA biosynthetic genes, i.e. T. thermophilus and D. radiodurans. No other bacterium possesses the complete set of enzymes required to synthesize lysine via the AAA route. Six Archaea display a complete set of lysine (AAA) biosynthetic genes, namely Pyrococcus and Sulfolobus strains, and Thermococcus kodakaraensis.
ii) Lysine (DAP) biosynthetic genes are widespread among Bacteria. Among them, 18 (micro)organisms possess a complete set of genes (9) for lysine biosynthesis through the DAP route. The small number of lysine (DAP) biosynthetic genes in some bacterial strains is very likely due to the absence of the corresponding metabolic route, which, in turn, is related to the parasitic lifestyle of these organisms. Such a lifestyle may allow these bacteria to acquire essential compounds directly from the metabolic activities of their host and the adaptation to this environmental condition might have caused the loss of entire metabolic routes or parts thereof.
Although some Archaea are known to synthesize lysine through the DAP pathway [23–28], it is not still completely clear which of the possible variants they use. Nonetheless, no archaeon possesses a number of genes compatible with the number required by the succinylasic variant. When the ddh sequence of Corynebacterium glutamicum, whose product is involved in the dehydrogenasic variant of lysine (DAP) pathway, was used in a BLAST probing, the only ddh archaeal homolog sequence was found in Archaeoglobus fulgidus genome (data not shown).
iii) The complete set of leucine biosynthetic genes is present in most of Bacteria and Archaea that possess either all the five leucine biosynthetic genes or four of them (lacking the last gene of leucine biosynthetic route, ilvE). This different distribution of ilvE, had already been observed by Velasco et al. .
iv) Arginine biosynthetic genes are widespread among Archaea and Bacteria. Even though a complete set is found only in a restricted number of organisms, most of them possess more than half (from five up to eight) of the enzymes required for the biosynthesis of ornithine and arginine, confirming the previous observation that they are synthesized through N-acetylated intermediates both in Bacteria and in Archaea .
Structure of leucine, arginine, and lysine biosynthetic pathways
In most of archaeal, bacterial, and eukaryotic (micro)organisms each of the three amino acid is synthesized through a specific metabolic route and each enzyme catalyzes a single step of the metabolic pathway it belongs to. The only exception is represented by the archaeon Pyrococcus horikoshii (see below); moreover a bifunctional enzyme, coded for by argD, interconnecting arginine and lysine biosyntheses was identified and characterized in Escherichia coli (see below).
In all of the organisms analyzed, leucine is synthesized through the typical biosynthetic pathway, consisting of the enzymatic steps catalyzed by 3-isopropylmalate synthase, 2-isopropylmalate isomerase, 3-isopropylmalate dehydrogenase, and α-ketoisocaproate transaminase, respectively. The four enzymes are coded for by the procaryotic leuA, leuCD, leuB, and ilvE genes, or by the eucaryotic LEU9\4, LEU1, LEU2, and BAT1\2 (Figures 3, 4, 5).
The lysine biosynthesis is much more intriguing; the amino acid can be synthesized through either the AAA or the DAP pathway (see Background). The AAA pathway was found in T. thermophilus and D. radiodurans, and a modified version of it was found in S. cerevisiae (Figure 4a and Figure 5a). The first four metabolic steps are shared by the two organisms and are evolutionarily related to the corresponding ones of leucine biosynthesis [8, 19]. The second moiety of these two AAA versions is different. In T. thermophilus lysine biosynthesis is achieved by the products of lysZ, Y, J, and K, whose sequences are homologous to argB, C, D, and E, respectively, whereas in S. cerevisiae lysine biosynthesis is completed by LYS2, LYS9, LYS1, that have no homolog among the genes of the biosynthetic pathways we took into account.
In the other Bacteria and in some Archaea, lysine is synthesized through the DAP pathway. Even in this case, several alternatives are possible. In the γ-proteobacterium E. coli (Figure 4c) the product of DapB is converted in LL-meso-diaminopimelate through four sequential enzymatic steps, known as the succinylate variant, and performed by DapD, ArgD, DapE, and DapF. Moreover, the enzyme coded for by argD exhibits both N-acetyl-ornithine and N-succinyl-L,L-diaminopimelate aminotransferase activities, with a very similar catalytic efficiency and identical kinetic mechanism, suggesting that this enzyme can play a role in both lysine and arginine biosynthesis . In C. glutamicum (Figure 4b) another version of the pathway has been disclosed: tetrahydrodipicolinate can be converted into meso-diaminopimelate by the activity of diaminopimelate dehydrogenase (ddh) in a single metabolic step. It is highly likely that this catalytic step is present also in the DAP pathway of the archaeon Haloarcula hispanica (Figure 3a) . Interestingly, in C. glutamicum two distinct enzymes (ArgD and DapC) can perform the reaction that in E. coli is carried out by a single one. Thus, the enzymes encoded by argD and dapC in C. glutamicum can be considered specific for the biosynthetic routes of arginine and lysine, respectively.
Arabidopsis thaliana is known to synthesize lysine through the DAP pathway [15, 31]. A DAP variant has been recently identified in this plant that utilizes a novel transaminase (LL-aminoadipate aminotransferase, the product of ORF At4g33680) that specifically catalyzes the conversion of tetrahydrodipicolinate to LL-diaminopimelate, a reaction requiring three enzymes in the DAP-pathway variant found in E. coli .
The archaeon P. horikoshii represents the main exception. In fact, in this organism just one pathway for the biosynthesis of all these three amino acids has been identified so far (Figure 3b). On the basis of sequence comparison and phylogenetic analyses, it has been suggested  that ORF PH1722, PH1724, PH1726, and PH1727 (see Figure 3b) from P. horikoshii might be involved in leucine biosynthesis as well as in the AAA variant of lysine biosynthesis, and that ORF PH1720, PH1718, PH1716, and PH1715 (Figure 3b) might be involved in the biosynthesis of both lysine (through the AAA one) and arginine. Even though it cannot be ruled a priori out the possibility that other uncharacterized routes for the biosynthesis of these amino acids may exist , it has been suggested that P. horikoshii possesses a unique amino acid biosynthetic system by which several amino acids are synthesized by a limited number of enzymes with broad substrate specificity .
A hypothetical ancestral pathway for lysine, leucine, and arginine
Data shown in Figures 3, 4 and 5 reveal that some steps of lysine, leucine, and arginine biosynthetic pathways are strongly conserved among the organisms we have taken into account. These steps are the first three of leucine route (performed by LeuA, LeuCD, and LeuB), the central ones of the arginine route (performed by ArgB, ArgC, ArgD, and ArgE), and the first two of lysine (DAP) route (performed by Ask and Asd). Moreover, these enzymes, share a significant degree of sequence similarity with some of those involved in the AAA lysine biosynthesis . As shown in Figure 1, leuA, leuCD, and leuB appeared to be paralogous to lysS, lysTU, and homoisocitrate dehydrogenase coding gene, respectively. A similar paralogy exists between argB, ask, and lysZ, as well as among argC, asd, and lysY. Velasco et al.  suggested that all of them are the outcome of one or more duplication events of an ancestral set of genes. According to the patchwork hypothesis , these ancestral genes might have encoded enzymes possessing broad substrate specificity and have been involved in different metabolic pathways.
Even though these ancestral enzymes may have been the backbone of the hypothetical common route, some others might have been necessary to complete the biosynthesis of all the corresponding products. An ancestor of the extant IlvE might have catalyzed the conversion of 2-oxoisocaproate into leucine, the final step of leucine biosynthesis, whereas an unspecific aminotransferase may have accomplished the transamination of α-aminoadipate, the extant role of LysN.
Moreover, an ancestral copy of LysX, which is evolutionarily related to E. coli RimK , was probably involved in the modification of α-aminoadipate to N-acetyl-α-aminoadipate, releasing the substrate of LysZ/ArgB/Ask ancestor. As shown in Figure 5, the model proposed does not contemplate the biosynthesis of LL-diaminopimelate in primordial cells, implying that the AAA pathway predated the appearance of the DAP pathway.
In conclusion, ancestral organisms may have been able to synthesize lysine, leucine and ornithine using just one pathway, consisting of a small number of enzymes endowed with a broad substrate specificity, permitting a clear interconnection of different metabolic routes.
A model for the evolution of lysine, leucine, and arginine metabolic routes
On the basis of the structure and the relationships existing in the extant biosynthetic routes leading to lysine, leucine, or arginine we depict a possible evolutionary model that might explain the (complex) extant scenario.
If the idea of an ancestral common pathway for the biosynthesis of lysine, leucine and arginine is correct, this raises the question of how did the extant routes originate. Besides, which was the timing of their appearance? Here we propose a model that is in agreement with the Nishida's idea and predicts that the extant biosynthetic routes might have emerged after a set of duplication events involving the genes of the ancestral common pathway (Figure 7). According to the model, the first step (or one of the first steps) might have been the duplication of the genes encoding the enzymes catalysing the sixth and seventh steps of the route common to lysine and ornithine. These events gave raise to the ancestors of ask and asd genes and to the overall metabolic "grid" that has been found in P. horikoshii (Figures 3b and 7b). This idea is also supported by the phylogenetic analysis (see next section).
Later on, the duplication of the genes encoding the first three steps of the ancestral pathway and the further evolutionary divergence of the new copies might have originated the ancestor of leuA, leuCD, and leuB, which coded for enzymes with a more narrow substrate specificity, rendering the leucine biosynthesis independent from the ancestral common pathway (Figure 7c). The central steps of arginine biosynthesis, catalyzed by ArgB, ArgC, ArgD and ArgE, might have arisen from the duplication and further evolutionary divergence of the corresponding ancestral aspecific genes (Figure 7d). In this way the four metabolic routes leading to leucine, lysine, arginine, and methionine\threonine, respectively, became one independent from each other. This metabolic scheme corresponds to that found in T. thermophilus and D. radiodurans.
A further duplication of the bottom genes of the ancestral pathway led to the appearance of DapC and DapE; during this step the branch of the "DAP pathway" leading to lysine was completely assembled (Figure 7e) with the recruitment of dapC and dapE (that are homolog to the extant lysJ/argD and lysZ/argB, respectively), dapF, and lysA. On the basis of the available data, it is not still possible to discern between the possibility that the product of the reaction catalyzed by Asd directly interacts with DapC, or if other enzymes (possibly the ancestor of the extant dapA, dapB, and dapD) were required to complete the DAP route. However, it is possible that once the assembly of the lysine-branch of the DAP pathway was completed the primordial cells possessed two alternative ways to synthesize lysine. If the model we propose here is correct, it is possible that, in this context, the entire AAA pathway became superfluous. Hence, the fourth step (Figure 7e) of the model predicts that, after the completion of the DAP pathway to lysine, genes belonging to the AAA pathway were progressively lost; therefore those organisms lacking the DAP pathway, maintained the ability to synthesize lysine through the AAA route. The final step of the model (Figure 7f) predicts that lysine (DAP) may have been completely assembled, with the appearance of all the extant variants (deacetylasic, desuccynilasic, and dehydrogenasic), leading to the metabolic patterns found in E. coli and in many other microorganisms. The development of the DAP pathway might allow bacterial cells to acquire the possibility to insert LL-diaminopimelate and meso-diaminopimelate, that are both intermediaries of the DAP route, into their cell wall.
In our opinion, the duplication events from Figure 7a to Figure 7e would have predated the appearance of the Last Universal Common Ancestor (LUCA), which, according to Woese , would have been a complex community of progenotes, highly dynamic from a genomic viewpoint, a mix of heterogeneous primordial cells with different metabolic abilities that could be easily exchanged between the different entities of the community. According to this idea, cells with different metabolic grids such as those represented in Figure 7b and 7d might have co-existed in the "LUCA community". The model also predicts, according to Cavalier-Smith , that if the primordial cells were surrounded by a cell wall containing peptidoglycan, ornithine should have been one of the first, if not the very first, component of peptidoglycan (see Conclusions).
According to the model proposed, the metabolic pathway leading to methionine and threonine diverged from the ancestral pathway before lysine, leucine, and arginine biosynthetic ones. However, (at least) another plausible scenario can be depicted, involving the previous appearance of the leucine pathway and the further assembly of the others biosynthetic routes. In other words, is it possible to establish the relative timing of the separation of the extant three pairs of genes involved in lysine, arginine, threonine, and methionine biosynthesis, that is lysZ and lysY, argB and argC, and ask and asd?
Ask sequences form a unique cluster, which is clearly separated from the other one containing all the ArgB and LysZ sequences involved in arginine and lysine (AAA) biosynthesis, respectively (Figure 8a).
Asd sequences form a unique cluster separated from ArgC and LysY sequences, involved in arginine and lysine biosynthesis, respectively (Figure 8b).
Hence, the topology of the tree in Figure 8a suggests that ArgB and LysZ sequences share a degree of sequence similarity higher than that exhibited with Ask, respectively. Similarly, the tree shown in Figure 8b, revealed that ArgC and LysY sequences share a degree of similarity higher than that exhibited with Asd. The overall body of phylogenetic data suggests that the first duplication event(s) involving the ancestral common genes might have originated the ancestor of the extant ask and asd genes; hence, argB and argC might be the outcome of a later duplication event of their corresponding ancestral sequences.
In this work a likely model for the evolution of genes involved in the biosynthesis of lysine, leucine, and arginine is depicted. The model proposed is based on the analysis of the structure of these biosynthetic routes and the phylogenetic distribution of their genes. The phylogenetic analysis performed allowed us also to determine a possible relative timing of the appearance of genes that are involved in the extant lysine (DAP) and arginine biosynthetic routes. This analysis gave a strong support to the hypothesis that extensive gene duplication events played a key role in shaping the extant biosynthetic routes of lysine, leucine and arginine. According to the model proposed in this work a common metabolic pathway for the biosynthesis of these three amino acids predated the appearance of the last universal common ancestor. This ancestral metabolic route was probably composed of a set of unspecific enzymes able to react with chemically related substrates interconnecting different biosynthetic routes (Figure 6). The occurrence of multiple gene duplication events (Figure 7) would have led to the appearance of specific metabolic pathways responsible for the biosynthesis of each amino acid. The evolutionary history of lysine, leucine, and arginine biosynthetic routes strongly supports the hypothesis on the origin and evolution of metabolic pathways proposed by Jensen , strengthening the idea that the gene duplication and the recruitment of genes encoding enzymes with a broad substrate specificity played a key role in the assembly of primitive metabolic routes.
Hence, starting from a metabolic network whose (highly interconnected) nodes represent unspecific enzymes (Figure 6), novel metabolic networks have emerged, consisting of highly specialized (and less interconnected) enzymes (Figure 1). In this way, ancestral enzymes belonging to a given metabolic route, have been "recruited" to serve a single or other (novel) pathways.
One of the main consequences of this evolutionary pathway, i.e. gene duplication followed by evolutionary divergence, is the separation of metabolic routes that were originally fused in a single, common one. The biological significance of this cascade of duplication events might rely on both (i) the appearance and refinement of regulatory mechanisms specific to each novel metabolic pathway and on (ii) the increased robustness acquired by the whole metabolic network, i.e. its ability to respond to environmental changes or to "knock-out" mutations falling within biosynthetic genes (while maintaining unchanged biosynthetic activity). In fact, the removal of one of the multifunctional enzymes belonging to the ancestral common pathway of lysine, leucine and arginine (Figure 6) would lead to auxotrophy to all of the three amino acids. On the contrary, mutations silencing one of the extant, specific biosynthetic genes may generate auxotrophy only for the amino acid whose biosynthetic route has been interrupted, whereas all the others may still be synthesized. In this latter case, the presence of a paralogous copy may still account for the reaction catalyzed by the product of the silenced gene, permitting the biosynthesis of the corresponding amino acid and avoiding the occurrence of any other auxotrophy. In this context the dapC and argD genes (Figure 14b, 4c) represent a paradigmatic example. In E. coli (Figure 4c) the argD product exhibits both N-acetyl-ornithine and N-succinyl-L,L-diaminopimelate aminotransferase activities  whereas in C. glutamicum two distinct enzymes, DapC and ArgDrespectively, perform these reactions . Although the genetic inactivation of E. coli argD and the consequences of this disruption are still under investigation, it is likely that it may generate auxotrophy to both diaminopimelate (and lysine) and L-arginine . On the contrary, the simultaneous deletion of the dapC gene and ddh in C. glutamicum does not generate auxotrophy to lysine, suggesting that the product of argD may substitute the DapC function . Since the simultaneous deletion of dapC, ddh and argD genes from C. glutamicum does not affect its growth, the existence of another aminotransferase able to substitute ArgD and DapC, has been invoked . This, in turn, is in agreement with the well-established low substrate specificity of aminotransferases , that may allow the enzymes carrying this activity to serve several different metabolic pathways.
On the basis of gene distribution analysis, Velasco et al.  proposed that the DAP pathway appeared earlier than the AAA one. The model we have proposed is in disagreement with this view, in that it suggests that the AAA pathway is the oldest one and that both pathways might have been simultaneously (and transiently) present in the "LUCA community". Since most bacteria, with the only exception of T. thermophilus and D. radiodurans (TD group), lack the AAA pathway, we suggest that, during the separation of Archaea from Bacteria, the latter may have lost the AAA pathway, maintaining the DAP pathway for the biosynthesis of lysine, LL-diaminopimelate, and meso-diaminopimelate (Figure 7e). The presence of the AAA pathway in the TD group might be the result of an event of horizontal gene transfer between an ancestor of P. horikoshii and the ancestor of the (micro)organisms belonging to the TD group as suggested by Nishida . Alternatively, T. thermophilus and D. radiodurans have maintained the AAA pathway. The model proposed fits with the metabolic schemes shown in Figures 2, 3, 4 and the timing of some duplication events is supported by the phylogenetic analysis of triads of paralogous genes.
The distribution of the AAA and the DAP pathway in Archaea defies a simple explanation since all currently known pathways for lysine biosynthesis in Bacteria and Eucarya exist also in the domain of Archaea . Hence, in the case of Archaea, a lineage specific maintenance of the DAP or the AAA pathway for lysine biosynthesis seems to be the most reliable hypothesis.
Lastly, on the basis of the scenario depicted in this work, the evolutionary history of lysine, leucine, and arginine biosynthetic routes might supply useful hints to disclose the origin and the assembly of bacterial cell wall. In the extant bacteria, the rigidity of the cell wall is due to a huge macromolecule containing acylated amino sugars and three to six different amino acids. This heteropolymer, the peptidoglycan, is built out of glycan strands cross linked through short peptides. In contrast to the uniform structure of the glycan, the peptide moiety reveals considerable variations. The greatest variation occurs at position 3 of the peptide moiety, where usually a diamino acid is found. The most widely distributed diamino acid is meso-diaminopimelate. It is present in gram-negative bacteria and in many other (micro)organisms, such as some species of bacilli, clostridia, lactobacilli, corynebacteria, propionibacteria, actinomycetales, myxobacteriales, rickettsiae, and cyanobacteria. Some studies have shown that the L-asymmetric carbon of meso-diaminopimelate is bound to the peptide subunit (see  and references therein). Studies on the amino acid composition and sequence of the peptidoglycans of different gram-negative bacteria have also shown that there is no great variation within this group. The peptidoglycan of these bacteria contains mainly meso-diaminopimelate, although D-glutamate and L-alanine can replace it.
The gram-positive bacteria reveal, contrary to the gram-negative organisms, a great variability in the composition and structural arrangement of their peptidoglycan since it can alternatively contain, at position 3, L-lysine, L-ornithine, D-glutamate, and LL-diaminopimelate.
Lastly, archaeal cells possess a fundamentally different type of peptidoglycan. Its glycan moiety contains L-talosaminuronic acid instead of muramic acid, and its peptide moiety lacks D-amino acids, but it is present L-lysine (see  and references therein).
As expected by the lack of DAP pathway, all those bacterial (micro)organisms biosynthesizing lysine through the AAA pathway (T. thermophilus, D. radiodurans) do not have diaminopimelic acid within their cell wall [41, 42]. In these microorganisms diaminopimelic acid is replaced by ornithine. In addition to this, LL-diaminopimelate and meso-diaminopimelate, intermediaries of the DAP pathway (Figure 1), are compounds that can be found in the cell wall of extant Bacteria , whereas they are absent in the archaeal cell wall of Archaea . Hence we suggest that the maintenance of the DAP pathway for the biosynthesis of lysine, at least in Bacteria, might be correlated with the appearance of the extant structure of their cell wall. The ability of inserting these molecules in the cell wall, might be an "invention" of Bacteria. In our opinion, the primordial cells had ornithine as a component of peptidoglycan. This is in agreement with the recent suggestion that the presence of ornithine within the cell wall might be an ancestral feature  whose biosynthesis, in the primordial organisms, might have occurred through the previously proposed common route (Figure 6).
This evolutionary step corresponds to the last one that is depicted in the evolutionary model that we have previously proposed (Figure 7f). This view might support the idea that the insertion of the meso-diaminopimelate and, probably, the appearance of the fully assembled DAP pathway might be a metabolic invention of Bacteria.
Amino acid sequences were retrieved from GenBank and KEGG databases and were used to build a local database for BLASTp  probing that was performed using default parameters. Orthologs identification was achieved according to the bidirectional best-hit (BBH) criterion [45, 46]. The relationship between gene x in genome A and gene y in genome B is called best-best hit when x is the best hit of query y against all genes in A and vice versa, and it is often used as an operational definition of ortholog [45, 47].
Phylogenetic trees were obtained with Mega 3 software  using the Neighbor-Joining (NJ) and the Minimum Evolution (ME) methods.
This article has been published as part of BMC Evolutionary Biology Volume 7 Supplement 2, 2007: Second Congress of Italian Evolutionary Biologists (First Congress of the Italian Society for Evolutionary Biology). The full contents of the supplement are available online at http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2148/7?issue=S2
- Fani R: Gene duplication and gene loading. Microbial evolution: gene establishment, survival and exchange. Edited by: Miller RV, Day MJ. 2004, Washington DC: ASM Press, 67-81.Google Scholar
- Jensen RA: Enzyme Recruitment in Evolution of New Function. Annual Review of Microbiology. 1976, 30: 409-425. 10.1146/annurev.mi.30.100176.002205.View ArticlePubMedGoogle Scholar
- Ohno S: Evolution by Gene Duplication. 1970, New York: Springer-VerlagView ArticleGoogle Scholar
- Vogel HJ: Lysine biosynthesis and evolution. Evolving genes and proteins. Edited by: Bryson V, Vogel HJ. 1965, New York Academic Press, 25-40.Google Scholar
- Umbarger HE: Amino acid biosynthesis and its regulation. Annu Rev Biochem. 1978, 47: 532-606. 10.1146/annurev.bi.47.070178.002533.View ArticlePubMedGoogle Scholar
- Bhattacharjee JK: Evolution of α-aminoadipate pathway for the synthesis of lysine in fungi. The Evolution of Metabolic Function. Edited by: Mortlock RP. 1992, Boca Raton, Florida CRC Press, 47-80.Google Scholar
- Kosuge T, Hoshino T: Lysine is synthesized through the α-aminoadipate pathway in Thermus thermophilus. FEMS Microbiol Lett. 1998, 169: 361-367.PubMedGoogle Scholar
- Nishida H, Nishiyama M, Kobashi N, Kosuge T, Hoshino T, Yamane H: A Prokaryotic Gene Cluster Involved in Synthesis of Lysine through the Amino Adipate Pathway: A Key to the Evolution of Amino Acid Biosynthesis. Genome Res. 1999, 9: 1175-1183. 10.1101/gr.9.12.1175.View ArticlePubMedGoogle Scholar
- Nishida H: Distribution of genes for lysine biosynthesis through the aminoadipate pathway among prokaryotic genomes. Bioinformatics. 2001, 17: 189-191. 10.1093/bioinformatics/17.2.189.View ArticlePubMedGoogle Scholar
- Schafer S, Paalme T, Vilu R, Fuchs G: 13C-NMR study of acetate assimilation in Thermoproteus neutrophilus. Eur J Biochem. 1989, 186: 695-700. 10.1111/j.1432-1033.1989.tb15262.x.View ArticlePubMedGoogle Scholar
- Ragan MA: Biochemical pathways and the phylogeny of the eukariotes. The hierarchy of life. Edited by: Fernhulm B, Bremer K, Jornvall H. 1989, New York: Elsevier, 145-160.Google Scholar
- Matsuda M, Ogur M: Separation and specificity of the yeast glutamate-α-ketoadipate transaminase. J Biol Chem. 1969, 244: 3352-3358.PubMedGoogle Scholar
- Rowley B, Tucci AF: Homoisocitric dehydrogenase from yeast. Arch Biochem Biophys. 1970, 141: 499-510. 10.1016/0003-9861(70)90167-0.View ArticlePubMedGoogle Scholar
- Weidner G, Steffan B, Brakhage AA: The Aspergillus nidulans lysF gene encodes homoaconitase, an enzyme involved in the fungus-specific lysine biosynthesis pathway. Mol Gen Genet. 1997, 255: 237-147. 10.1007/s004380050494.View ArticlePubMedGoogle Scholar
- Vogel HJ: On biochemical evolution: lysine formation in higher plants. Proc Natl Acad Sci USA. 1959, 45: 1717-1721. 10.1073/pnas.45.12.1717.PubMed CentralView ArticlePubMedGoogle Scholar
- Lèjohn HB: Enzyme Regulation, Lysine Pathways and Cell Wall Structures as Indicators of Major Lines of Evolution in Fungi. Nature. 1971, 231: 164-168. 10.1038/231164a0.View ArticlePubMedGoogle Scholar
- Cirillo JD, Weisbrod TR, Banerjee A, Bloom BR, Jacobs WR: Genetic determination of the meso-diaminopimelate biosynthetic pathway of mycobacteria. J Bacteriol. 1994, 176: 4424-4429.PubMed CentralPubMedGoogle Scholar
- Wehrmann A, Phillipp B, Sahm H, Eggeling L: Different Modes of Diaminopimelate Synthesis and Their Role in Cell Wall Integrity: a Study with Corynebacterium glutamicum. J Bacteriol. 1998, 180: 3159-3165.PubMed CentralPubMedGoogle Scholar
- Velasco AM, Leguina JI, Lazcano A: Molecular Evolution of the Lysine Biosynthetic Pathways. Journal of Molecular Evolution. 2002, 55: 445-449. 10.1007/s00239-002-2340-2.View ArticlePubMedGoogle Scholar
- Fondi M, Brilli M, Fani R: On the origin and evolution of biosynthetic pathways: integrating microarray data with structure and organization of the Common Pathway genes. BMC Bionformatics. 2007, 8 (Suppl 1): S12-10.1186/1471-2105-8-S1-S12.View ArticleGoogle Scholar
- Irvin SD, Bhattacharjee JK: A Unique Fungal Lysine Biosynthesis Enzyme Shares a Common Ancestor with Tricarboxylic Acid Cycle and Leucine Biosynthetic Enzymes Found in Diverse Organisms. Journal of Molecular Evolution. 1998, 46: 401-408. 10.1007/PL00006319.View ArticlePubMedGoogle Scholar
- Miyazaki J, Kobashi N, Fujii T, Nishiyama M, Yamane H: Characterization of a lysK gene as an argE homolog in Thermus thermophilus HB27. FEBS Lett. 2002, 512: 269-274. 10.1016/S0014-5793(02)02290-1.View ArticlePubMedGoogle Scholar
- Hochuli M, Patzelt H, Oesterhelt D, Wüthrich K, Szyperski T: Amino Acid Biosynthesis in the Halophilic Archaeon Haloarcula hispanica. Journal of Bacteriology. 1999, 181: 3226-3237.PubMed CentralPubMedGoogle Scholar
- Bakhiet N, Forney FW, Stahly DP, Daniels L: Lysine biosynthesis in Methanobacterium thermoautotrophicum is by the diaminopimelic acid pathway. Current Microbiology. 1984, 10: 195-198. 10.1007/BF01627254.View ArticleGoogle Scholar
- Bult CJ, White O, Olsen GJ, Zhou L, Fleischmann RD, Sutton GG, Blake JA, FitzGerald LM, Clayton RA, Gocayne JD, Kerlavage AR, Dougherty BA, Tomb J-F, Adams KD, Reich CI, Overbeek R, Kirkness EF, Weinstock KG, Merrick JM, Glodek A, Scott JL, Geoghagen NS, Weidman JF, Fuhrmann JL, Nguyen D, Utterback TR, Kelley JM, Peterson JD, Sadow PW, Hanna MC, Cotton MD, Roberts KM, Hurst MA, Kaine BP, Borodovsky M, Klenk H-P, Fraser CM, Smith HO, Woese CR, Venter J: Complete Genome Sequence of the Methanogenic Archaeon, Methanococcus jannaschii. Science. 1996, 273: 1058-1073. 10.1126/science.273.5278.1058.View ArticlePubMedGoogle Scholar
- Klenk H-P, Clayton RA, Tomb J-F, White O, Nelson KE, Ketchum KA, Dodson RJ, Gwinn M, Hickey EK, Peterson JD, Richardson DL, Kerlavage AR, Graham DE, Kyrpides NC, Fleischmann RD, Quackenbush J, Lee NH, Sutton GG, Gill S, Kirkness EF, Dougherty BA, McKenney K, Adams MD, Loftus B, Peterson S, Reich CI, McNeil LK, Badger JH, Glodek A, Zhou L, Overbeek R, Gocayne JD, Weidman JF, McDonald L, Utterback T, Cotton MD, Spriggs T, Artiach P, Kaine BP, Sykes SM, Sadow PW, D'Andrea KP, Bowman C, Fujii C, Garland SA, Mason TM, Olsen GJ, Fraser CM, Smith HO, Woese CR, Venter JC: The complete genome sequence of the hyperthermophilic, sulphate-reducing archaeon Archaeoglobus fulgidus. Nature. 1997, 390: 364-370. 10.1038/37052.View ArticlePubMedGoogle Scholar
- Selkov E, Maltsev N, Olsen GJ, Overbeek R, Whitman WB: A reconstruction of the metabolism of Methanococcus jannaschii from sequence data. Gene. 1997, 197: GC11-26. 10.1016/S0378-1119(97)00307-7.View ArticlePubMedGoogle Scholar
- Smith DR, Doucette-Stamm LA, Deloughery C, Lee H, Dubois J, Aldredge T, Bashirzadeh R, Blakely D, Cook R, Gilbert K: Complete genome sequence of Methanobacterium thermoautotrophicum deltaH: Functional analysis and comparative genomics. J Bacteriol. 1997, 179: 7135-7155.PubMed CentralPubMedGoogle Scholar
- Caldovic L, Tuchman M: N-acetylglutamate and its changing role through evolution. Biochem J. 2003, 372 (2): 279-290. 10.1042/BJ20030002.PubMed CentralView ArticlePubMedGoogle Scholar
- Ledwidge R, Blanchard JS: The dual biosynthetic capability of N-acetylornithine aminotransferase in arginine and lysine biosynthesis. Biochemistry. 1999, 38: 3019-3024. 10.1021/bi982574a.View ArticlePubMedGoogle Scholar
- Bryan JK: Synthesis of the aspartate family and branched chain amino acids. The biochemistry of plants. Edited by: Miflin BJ. 1980, New York: Academic Press, 5: 402-452.Google Scholar
- Hudson AO, Singh BK, Leustek T, Gilvarg C: An LL-Diaminopimelate Aminotransferase Defines a Novel Variant of the Lysine Biosynthesis Pathway in Plants. Plant Physiology. 2006, 140: 292-301. 10.1104/pp.105.072629.PubMed CentralView ArticlePubMedGoogle Scholar
- Miyazaki K: Bifunctional isocitrate-homoisocitrate dehydrogenase: a missing link in the evolution of beta-decarboxylating dehydrogenase. Biochem Biophys Res Commun. 2005, 331: 341-346. 10.1016/j.bbrc.2005.03.169.View ArticlePubMedGoogle Scholar
- Sakai H, Vassylyeva MN, Matsuura T, Sekine S, Gotoh K, Nishiyama M, Terada T, Shirouzu M, Kuramitsu S, Vassylyev DG: Crystal Structure of a Lysine Biosynthesis Enzyme, LysX, from Thermus thermophilus HB8. J Mol Biol. 2003, 332: 729-740. 10.1016/S0022-2836(03)00946-X.View ArticlePubMedGoogle Scholar
- Woese C: The universal ancestor. PNAS. 1998, 95: 6854-6859. 10.1073/pnas.95.12.6854.PubMed CentralView ArticlePubMedGoogle Scholar
- Cavalier-Smith T: Rooting the tree of life by transition analyses. Biology Direct. 2006, 1: 19-10.1186/1745-6150-1-19.PubMed CentralView ArticlePubMedGoogle Scholar
- Thompson JD, Higgins DG, Gibson TJ: CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res. 1994, 22: 4673-4680. 10.1093/nar/22.22.4673.PubMed CentralView ArticlePubMedGoogle Scholar
- Hartmann M, Tauch A, Eggeling L, Bathe B, Mockel B, Puhler A, Kalinowski J: Identification and characterization of the last two unknown genes, dapC and dapF, in the succinylase branch of the L-lysine biosynthesis of Corynebacterium glutamicum. J Biotechnol. 2003, 104: 199-211. 10.1016/S0168-1656(03)00156-1.View ArticlePubMedGoogle Scholar
- Jensen RA, Gu W: Evolutionary Recruitment of Biochemically Specialized Subdivisions of Family I within the Protein Superfamily of Aminotransferases. Journal of Bacteriology. 1996, 178 (8): 2161-2171.PubMed CentralPubMedGoogle Scholar
- Schleifer KH, Kandler O: Peptidoglycan Types of Bacterial Cell Walls and their Taxonomic Implications. Bacteriological Reviews. 1972, 36: 407-477.PubMed CentralPubMedGoogle Scholar
- Quintela JC, Pittenauer E, Allmaier G, Aran V, Pedro MA: Structure of peptidoglycan from Thermus thermophilus HB8. Journal of Bacteriology. 1995, 177 (17): 4947-4962.PubMed CentralPubMedGoogle Scholar
- Mkarova KS, Aravind L, Wolf YI, Tatusov RL, Minton KW, Koonin EV, Daly MJ: Genome of the extremely radiation-resistant bacterium Deinococcus radiodurans viewed from the perspective of comparative genomics. Microbiol Mol Biol Rev. 2001, 65: 44-79. 10.1128/MMBR.65.1.44-79.2001.View ArticleGoogle Scholar
- Kandlera O, Konig H: Cell wall polymers in Archaea (Archaebacteria). Cell Mol Life Sci. 1998, 54: 305-308. 10.1007/s000180050156.View ArticleGoogle Scholar
- Altschul SF, Madden TL, Schäffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ: Gapped BLAST and PSI-BLAST: A new generation of protein database search programs. Nucleic Acid Res. 1997, 25: 3389-3402. 10.1093/nar/25.17.3389.PubMed CentralView ArticlePubMedGoogle Scholar
- Bono H, Ogata H, Goto S, Kanehisa M: Reconstruction of Amino Acid Biosynthesis Pathways from the Complete Genome Sequence. Genome Res. 1998, 8: 203-210.View ArticlePubMedGoogle Scholar
- Uchiyama I: Hierarchical clustering algorithm for comprehensive orthologous-domain classification in multiple genomes. Nucleic Acids Research. 2006, 34: 647-658. 10.1093/nar/gkj448.PubMed CentralView ArticlePubMedGoogle Scholar
- Kanehisa M, Goto S, Kawashima S, Nakaya A: The KEGG databases at GenomeNet. Nucleic Acids Res. 2002, 30: 42-46. 10.1093/nar/30.1.42.PubMed CentralView ArticlePubMedGoogle Scholar
- Hall TA: BioEdit: a user-friendly biological sequence alignment editor and analysis program for Windows 95/98/NT. Nucl Acids Symp Ser. 1999, 41: 95-98.Google Scholar
- Kumar S, Tamura K, Nei M: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment. Briefings in Bioinformatics. 2004, 5: 150-163. 10.1093/bib/5.2.150.View ArticlePubMedGoogle Scholar
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