- Research article
- Open Access
Genome-scale reconstruction of metabolic network for a halophilic extremophile, Chromohalobacter salexigens DSM 3043
© Ates et al; licensee BioMed Central Ltd. 2011
- Received: 4 June 2010
- Accepted: 21 January 2011
- Published: 21 January 2011
Chromohalobacter salexigens (formerly Halomonas elongata DSM 3043) is a halophilic extremophile with a very broad salinity range and is used as a model organism to elucidate prokaryotic osmoadaptation due to its strong euryhaline phenotype.
C. salexigens DSM 3043's metabolism was reconstructed based on genomic, biochemical and physiological information via a non-automated but iterative process. This manually-curated reconstruction accounts for 584 genes, 1386 reactions, and 1411 metabolites. By using flux balance analysis, the model was extensively validated against literature data on the C. salexigens phenotypic features, the transport and use of different substrates for growth as well as against experimental observations on the uptake and accumulation of industrially important organic osmolytes, ectoine, betaine, and its precursor choline, which play important roles in the adaptive response to osmotic stress.
This work presents the first comprehensive genome-scale metabolic model of a halophilic bacterium. Being a useful guide for identification and filling of knowledge gaps, the reconstructed metabolic network i OA584 will accelerate the research on halophilic bacteria towards application of systems biology approaches and design of metabolic engineering strategies.
- Metabolic Network
- Enzyme Commission
- Metabolic Model
- Flux Balance Analysis
Extreme environments, generally characterized by abnormal temperature, pH, pressure, salinity, toxicity and radiation levels, are inhabited by various organisms - extremophiles - that are specifically adapted to these particular conditions. Studies on these microorganisms has led to the development of important molecular biology techniques such as polymerase chain reaction (PCR) [1, 2] and hence further research has been largely stimulated by the industry's interest on the fact that the survival mechanisms of these microorganisms could be transformed into valuable applications ranging from wastewater treatment to the diagnosis of infectious and genetic diseases .
Halophilic microorganisms are extremophiles that are able to survive high osmolarity in hypersaline conditions either by maintenance of high salinity in their cytoplasm or by intracellular accumulation of osmoprotectants such as ectoine and betaine . C. salexigens is a halophilic Gammaproteobacterium of the family Halomonadaceae with a versatile metabolism allowing not only fast growth on a large variety of simple carbon compounds as its sole carbon and energy source but also resistance to saturated and aromatic hydrocarbons and heavy metals [5, 6]. C. salexigens with the ability to grow over a wide range of salinities [0.5-4 M NaCl] has been the most euryhaline of the bacteria  and to understand the osmoregulatory mechanisms in halophilic bacteria, it has been used as a model organism [5, 7–9]. Moreover, C. salexigens has also many promising biotechnological applications as a source of compatible solutes, salt-tolerant and recombinant enzymes, biosurfactants and exopolysaccharides .
Genome sequence of extremophiles, such as sulphate-reducing archaeon Archaeaglobus fulgidus, halophilic archaeon Halobacterium species NRC-1  and acidophilic bacterium Acidithiobacillus ferrooxidans have been reported earlier. Since the publication of the genome of C. salexigens DSM 3043  the biological knowledge about this strain has significantly increased and various methods that allow the genomic analysis and genetic manipulation have been developed [15, 16]. On the other hand, systematic analysis of its metabolic and biotechnological capacities have not been performed yet. This is, at some level, due to the lack of an in silico comprehensive metabolic model that enables the integration of canonical experimental data in a coherent fashion.
Metabolic reconstruction is non-automated and iterative decision-making process through which the genes, enzymes, reactions and metabolites that participate in the metabolic activity of a biological system are identified, categorized and interconnected to form a network . The reconstruction process has been reviewed conceptually in literature [17–22] and, recently, a standard operating protocol giving a detailed overview of the necessary data and steps has been published . To date, genome-scale metabolic reconstructions for more than 50 organisms have been published and this number is expected to increase rapidly. Therefore, the need for developing automated, or at least semi-automated, ways to reconstruct metabolic networks is growing. A limited number of software tools, such as Pathway tools , metaSHARK , Simpheny (Genomatica), which aim at assisting and facilitating the reconstruction process are available. However, recent reviews [18, 26] highlight current problems with genome annotations and databases, which make automated reconstructions challenging and thus they require manual evaluation. Genome-scale metabolic reconstructions have been successfully applied to several organisms across eukaryotic (e.g., Saccharomyces cerevisiae[21, 27–29], human , Arabidopsis thaliana), prokaryotic (e.g., Escherichia coli[32–34], Bacillus subtilis, Helicobacter pylori[36, 37], Lactococcus lactis, Staphylococcus aureus[39, 40], Clostridium acetobutylicum, Pseudomonas putida, Pseudomonas aeruginosa, Geobacter metallireducens, Corynebacterium glutamicum), and archaeal (e.g., Methansoarcina barkeri, Halobacterium salinarum species). Being a useful guide for identification and filling of knowledge gaps, these metabolic networks have been used toward simulation of the cellular behavior under different genetic and physiological conditions, contextualization of high-throughput data, directing hypothesis driven discovery, interrogation of multi-species relationships and topological analysis (See  for an extensive review).
Here, a genome-scale reconstruction of C. salexigens DSM 3043's metabolism was established based on genomic, biochemical and physiological information. Being the first comprehensive metabolic model of a halophilic bacterium, it was labeled as i OA584 following the naming convention proposed by . The predictive potential of the model was validated not only against literature data on the in vivo C. salexigens phenotypic features, the transport and use of different substrates but also against experimental observations on the choline - betaine and ectoine synthesis pathways which are important parts of the osmoadaptation mechanism.
The complete genome sequence of C. salexigens DSM 3043 has been assembled in 2005 by the Joint Genome Institute  and gene annotations are available online at the web-sites of Computational Biology at ORNL  and Joint Genome Institute , which represent computational platforms enabling the corresponding enzymes in addition to gene catalog. C. salexigens DSM 3043 genome size is 3.696 Mb with 3352 candidate protein-encoding gene models.
For the reconstruction of a genome-scale metabolic network of the halophilic bacterium C. salexigens DSM 3043, a non-automated but iterative decision-making process is designed based on the conceptual reviews [18, 19, 22] and published protocol . In the first stage, a draft reconstruction was built from gene-annotation data [48, 49] coupled with information from online databases, which link genes to functional categories and help bridge the genotype-phenotype gap. For the association of the enzymes to the biochemical reactions, biochemical information databases KEGG , BiGG , ExPASy , BioCyc  and BRENDA , which provide comprehensive information on enzymes and biochemical reactions, were employed to extract metabolic reactions, their stoichiometry and thermodynamic constraints (i.e. reversibility). As a result of the first stage, an initial catalog of gene-enzyme-reaction associations was prepared. In the second stage, the draft reconstruction was refined semi-automatically through gap analysis. Using the draft catalog, the stoichiometric matrix, the reaction and metabolite adjacency matrices  were constructed, metabolic maps were drawn and topological analysis [56, 57] was performed. Analysis of the preliminary version of the network indicated the occurrence of metabolites not connected with the overall metabolic network, i.e. the presence of dead-end metabolites. The resulting shortage was overcome mostly by manually searching biochemical information databases [50–54] and carrying out a comprehensive literature survey on metabolisms of C. salexigens[5–9, 16, 58, 59]. In the last stage, the biomass formation and transport reactions, which describe the intra- and extracellular exchange of metabolites, were added to the metabolic network predominantly based on the experimental evidence on phenotypic characterization of the strain [5–9, 16, 58, 59]. The reconstructed metabolic network was automatically converted into a mathematical model that could be analyzed through constraint-based approaches, and was validated through comparison of model predictions with phenotypic data.
The interconnectivity of metabolites in a biochemical reaction network can be represented by a set of equations defining the stoichiometric conversion of substrates into products . The reconstructed metabolic network was represented by a stoichiometric matrix, S (m × n) where m is the number of metabolites and n is the number of reactions. The corresponding entry in the stoichiometric matrix, S ij , represents the stoichiometric coefficient for the participation of the ith metabolite in the jth reaction. A constraint-based optimization framework, Flux Balance Analysis (FBA) [61, 62], was then recruited to solve the linear programming problem under steady-state criteria represented by the equation () where v is a vector of reaction fluxes. Since the optimization problem belongs to an under-determined system, there exist multiple solutions. To find a particular solution for reaction fluxes, the cellular objective of producing the maximum amount of biomass constituents was optimized . The employment of optimal growth assumption has allowed successful calculation of phenotypic behaviour in FBA of reconstructed metabolic models of several microorganisms [34–36, 38, 40–42, 46, 47], suggesting that their metabolic networks have evolved for the optimization of the specific growth rate under several carbon source limiting conditions. Constraints need to be imposed on the system in the form of inequality () where α and β are the lower and upper limits placed on each reaction flux, respectively. The constraint-based optimization problem was solved using MATLAB 7.4 (The Mathworks, Inc.).
No thorough biomass composition has been published for C. salexigens. The use of a generic biomass formation reaction in FBA simulations was previously tried and led to successful predictions [34, 39, 64]. Hence, based on the experimental evidences on genome similarity , phylogenetic classification and results from the comparative analysis of the C. salexigens metabolic network with other published reconstructed networks [27, 34, 35, 39, 42, 43, 46, 47], the relative production of metabolites required for growth was taken from the published composition of E. coli i AF1260 .
Flux Variability Analysis
The flux variabily analysis was performed  to observe the alternate optimal flux distributions. Briefly, the optimal value of the objective function was calculated by FBA simulation; then, with the objective function fixed at the optimal value, for each reaction the maximum and minimum possible fluxes were computed. The two values calculated for each reaction characterize its variability.
Metabolic Reconstruction Process
Based on the conceptual reviews [19, 18, 22] and published protocol , a non-automated but iterative three-stage process was designed to reconstruct a genome-scale metabolic network of the halophilic bacterium C. salexigens DSM 3043.
In the first stage, a draft catalog of gene-enzyme-reaction associations was prepared via coupling genome annotation data [48, 49] with biochemical information databases [50–54]. The genome annotation resources for C. salexigens[48, 49] not only include genetic information such as genome position, coding region, locus tag, gene product function, but also represent assignments of gene products to PRIAM categories, COG functional groups, KEGG orthologies and pathways, and Enzyme Commission (EC) numbers. All these information were assembled and analyzed manually to identify candidate metabolic functions. In the first step, the pathway databases, namely KEGG  and BiGG , were systematically searched for the associations of the metabolic reactions to the enzymes. At this step, KEGG pathway assignments and EC numbers, which represent a hierarchical classification of enzymatic reactions and are commonly utilized as identifiers of enzymes in the analysis of complete genomes, played important role in bridging the genomic repertoire of gene models to the chemical repertoire of metabolic pathways. However, several EC numbers were assigned to signaling or regulatory proteins, whose functions are not normally considered in metabolic reconstructions. For instance, Csal2070 gene was assigned for a repressor protein LexI (EC 126.96.36.199) functioning in SOS regulation. Therefore, these assignments were carefully checked and not included in the draft reconstruction. Another important point to be emphasized is the incompleteness of pathway databases. Although very high percentages (66.6%) of the enzymes were associated with the reactions, there were missing reactions that were not represented in these databases. In the second step, enzyme information databases, namely ExPASy , BioCyc  and BRENDA  were explored to include the missing reactions to the model. Since EC numbers were known from previously obtained gene-annotation data, enzymes could be connected with accurate metabolic reactions. For example, the reactions for carbonyl reductase (EC 188.8.131.52), malate synthase (EC 184.108.40.206) and creatinase (EC 220.127.116.11) were obtained from ExPASy, BRENDA and BioCyc databases, respectively. The outcome of the first stage was an initial catalog of gene-enzyme-reaction associations.
Second stage comprised of semi-automatically refinements of the draft reconstruction through gap analysis. Using the draft catalog of gene-enzyme-reaction associations, the stoichiometric matrix, the reaction and metabolite adjacency matrices were constructed, metabolic maps were drawn and topological analysis was performed [55, 56] Analysis of the preliminary version of the network indicated the occurance of metabolites not connected with the overall metabolic network, i.e. the presence of dead-end metabolites. Their presence might be due to a misassignment of a gene function or to missing reactions linking these metabolites with the overall network. The resulting shortage was overcome mostly by manually searching other biochemical information databases, namely ExPASy , BioCyc  and BRENDA . In addition for these enzyme-reaction associations, the required information was obtained from literature. For instance, in the utilization pathway of tagatose, tagatose-6-phosphate kinase reaction (EC 18.104.22.168) was present in the model; but, an essential intermediate step, i.e. the formation reaction of tagatose 6-phosphate from tagatose, was missing in the model. Subsequently, tagatose kinase reaction (EC 22.214.171.124) was included to the model. In some cases, gap analysis indicated the lack of numerous steps in several pathways. For example, in arabinose metabolism 5 additional metabolic reactions (EC 126.96.36.199, EC 188.8.131.52, EC 184.108.40.206, EC 220.127.116.11 and EC 18.104.22.168) were required to link dead-end metabolites to the metabolic model. At this stage, stoichiometrically unbalanced reactions were also checked. Normally, there are two common errors causing unbalanced reactions : Missing proton and/or water, or when the stoichiometric coefficient of at least one metabolite is wrong. All the metabolic reactions were tested for mass and charge balancing and several reactions required corrections. For example, in the reaction catalyzed by glucokinase (EC 22.214.171.124, Csal0935), which was obtained from KEGG , a proton was missing.
In the last stage, the reconstructed metabolic network was automatically converted into a mathematical model that could be analyzed through constraint-based approaches, and was validated through comparison of model predictions with phenotypic data. The biomass formation and transport reactions, which describe the intra- and extracellular exchange of metabolites, were added to the metabolic network predominantly based on the experimental evidence [5–9, 16, 58, 59] on phenotypic characterization of the strain and then FBA simulations on various carbon sources were performed to verify the model. For example, uptake of macro nutrients (e.g., amino acids, sucrose, glucose), secretion of by-products (e.g., lactate, ammonia, betaine), and exchange of free compounds (water, carbon dioxide, oxygen) were added since they represent essential cellular inputs and outputs. The metabolic model was updated iteratively using the above procedure until the in silico phenotypic characterizations were completely represented by the simulation results.
Characteristics of the Reconstructed Metabolic Network of C. salexigens
Network characteristics of the reconstructed metabolic network of C. salexigens
Protein-encoding gene models
Reactions with protein-encoding gene model assignments
A large amount of enzymes, which were included by the metabolic model, were monofunctional (80.65%) whereas the rest were multifunctional accepting several different substrates. Therefore, the published genome for their corresponding genes were carefully checked during reconstruction process in order not to lead to false gene-enzyme-reaction associations in the reconstructed genome-scale metabolic model.
Moreover, C. salexigens is known for its capability to utilize many amino acids as a carbon and nitrogen source [5, 6, 59]. The presence of high number of enzymes (13%) in the amino acid metabolism is in agreement with the fact that the de novo synthesis pathways for all 20 amino acids are present in C. salexigens' genome [14, 48]. To validate in silico amino acid utilization as a carbon and nitrogen source, FBA simulations were carried out and growth on all of the 20 amino acids were obtained. For instance, at a specific uptake rate (1 mmol/gDW/h) of isoleucine, growth rate was calculated as 0.129 h-1. Additionally, glycan biosynthesis and metabolism; and biosynthesis of secondary metabolites have the lowest number of enzymes (1%).
Throughout the reconstruction process, 584 protein-encoding gene models have been assigned to the metabolic reactions. The distribution of the ratios of number of reactions per number of gene models in each enzyme class [27, 32] was investigated in the reconstructed model i OA584 (Figure 1B). In the metabolic network of C. salexigens, hydrolases (EC 3) were positioned primarily, followed by transferases (EC 2), ligases (EC 6), oxidoreductases (EC 1), lyases (EC 4), and isomerases (EC 5). Hence ligases and transferases were less substrate specific than the other enzyme classes in C. salexigens, as in the case of E. coli, whereas in S. cerevisiae isomerases and transferases were found to be the least substrate-specific enzyme classes .
Related species of the same domain share a substantial amount of conserved reactions for essential biological processes [66–68]. The metabolic network i OA584 was also compared with previous metabolic models from different domains [27, 34, 35, 39, 42, 43, 46, 47] to identify the conserved reactions in i OA584. As expected, highest number of metabolic reactions were shared by E. coli (i AF1260) with 320 reactions, P. aeruginosa (i MO1056) with 309 reactions and P. putida (i JN746) with 282 reactions. Number of shared metabolic reactions for S. cerevisiae, S. aureus N315, B. subtilis, and H.salinarium were obtained as 274, 265, 260, and 221, respectively; while C. salexigens and M. barkeri association indicated the lowest number with 205 metabolic reactions.
Capabilities of the metabolic network - Phenotypic characterization in silico
In silic o predictions of the phenotypic features.
(in vivo/in silico)
citrate synthase (126.96.36.199)
Nitrate reductase (188.8.131.52)
(in vivo/in silico)
rxn527, rxn559, rxn817
rxn136, rxn137, rxn243
rxn83, rxn107, rxn580
rxn328, rxn702, rxn726, rxn727
rxn62, rxn337, rxn433, rxn781
rxn877, rxn881, rxn882
rxn155, rxn156, rxn158 - rxn162, rxn720, rxn753 - rxn755
rxn182, rxn183, rxn257, rxn258, rxn605, rxn695, rxn802, rxn848, rxn859
rxn275, rxn616, rxn661, rxn753, rxn807
rxn175, rxn184, rxn389, rxn699, rxn806, rxn863, rxn868 - rxn872
rxn267, rxn268, rxn750
rxn37, rxn256, rxn257, rxn297, rxn298, rxn514 - rxn520, rxn721, rxn722, rxn751, rxn799, rxn800
rxn46, rxn47, rxn84, rxn85, rxn720
rxn97, rxn98, rxn156, rxn159, rxn160, rxn163, rxn700, rxn841
rxn883, rxn884, rxn885
The resultant metabolic model i OA584 has the ability to verify reported C. salexigens phenotypic features [5–9, 16, 58, 59] through in silico FBA simulations. C.salexigens is able to grow aerobically and has ability for anaerobic respiration with nitrate. This microorganism is catalase and citrate positive, oxidase negative. Nitrate can be reduced to nitrite in contrast nitrite cannot be reduced [5, 6, 59]. The in silico aerobic and anerobic growth simulations were performed with biomass as the objective function at a specific glucose uptake rate of 3 mmol/gDW/h and for anaerobic respiration with 1 mmol/gDW/h nitrate as an electron acceptor instead of O2. The growth rates were determined as 0.1934 h-1 and 0.0645 h-1 for aerobic and anaerobic conditions, respectively. As such, catalase, citrate, urease activities and nitrate reduction simulations were also consistent with literature data (Table 2). Acetoin, indole, lysine decarboxylase, ornithine decarboxylase and phenylalanine deaminase could not be produced by C. salexigens i OA584 as also reported in vivo. Literature data on the transport and use of 59 different substrates were also verified in silico by fixing the externally transport reaction of fluxes (3-10 mmol/gDW/h) and investigating the associated utilization reaction fluxes and objective function biomass flux to assess a positive growth. For example, 1 mmol/gDW/h uptakes of fructose and sucrose resulted in growth rates of 0.1290 h-1 and 0.0646 h-1, respectively.
Since the flux distribution of overall network map might be useful in investigating and improving FBA analysis, Omics Viewers Tool of BioCyc  was used to illustrate in silico flux distribution in C. salexigens metabolic pathways. Reaction flux data and gene information were provided for Omics Viewer to generate overall diagram colorized with flux data. The details of the connectivity aspects of the reconstructed metabolic network (Additional File 3), the overall map of the reconstructed network and its detailed batch images obtained were also supplemented (Additional File 4).
Case study on osmoadaptation
Generally, halophiles can adapt to the saline environment by either intracellular accumulation of salts, or exclusion of salts and production or accumulation of different classes of organic solutes (osmoprotectants) [71, 72]. C. salexigens has been used comprehensively as a model organism in osmoadaptation studies due to its ability to grow over a wide range of salinities [6–8]. Osmoadaptation in C. salexigens is mainly achieved by de novo synthesis of two compatible solutes, namely ectoine and hydroxyectoine, which are of industrial and biological interest due to their biostabilizing properties. In addition, when these solutes are provided externally, C. salexigens accumulates other osmoprotectants such as choline and glycine betaine. Besides the betaine exchange that is common in bacteria, the rarely encountered betaine biosynthesis pathway from choline has been characterized in C. salexigens to some extend at the biochemical level [5, 8, 59, 73, 74]. Further research on the genes and metabolic pathways responsible for the biosynthesis of compatible solutes will not only find numerous applications in biomedicine, agriculture, food and fermentation industries but also expand our knowledge on the prokaryotic adaptation mechanisms to abiotic stresses like high salinity .
Via integration of data from in vitro metabolic and genetic analyses, in further studies, the presented genome scale model iOA584 could be used to elucidate osmoadaptation mechanisms and to design strategies (i.e. optimizing culture media, genetical engineering of the microorganism) for optimum production of compatible solutes such as ectoine, which has industrial applications for cosmetics and dermopharmacy and is widely used in stabilizing enzymes for molecular biology.
Here, C. salexigens i OA584 was used to simulate the experimental observations on osmoadaptation of C. salexigens, in order to demonstrate that the model could be used for further studies in understanding the metabolic pathways behind osmoadaptation and to design or improve the adaptation mechanisms in extromophiles.
For validation of the model's predictive potential, in silico model simulations of the choline - betaine pathway of the osmoadaptation mechanism were compared with these experimental observations [5, 7–9, 59]. FBA simulations were performed with biomass as the objective function and 1 to 3 mmol/gDW/h glucose uptake rate (Figure 4). Via restriction of uptake of exogeneous choline to various values between 1 to 2 mmol/gDW/h, monotonic increase in the biomass flux (from 0.065 to 0.129 h-1) and in betaine production flux (from 0.45 to 0.89 mmol/gDW/h) were observed; hence stimulation of growth by the presence of choline was predicted, which is in agreement with the reported experimental observations . It is known that the resulting solution of FBA especially when applied to genome scale models is normally not unique . Therefore, the flux variability analysis was performed to observe the alternate optimal flux distributions in FBA simulations. Results showed that the fluxes are in general not affected since the range of variabilities for each flux were lower than 0.1%.
To simulate metabolic model in the view of ectoine synthesis, the required conditions were implemented and the resulting flux values were investigated. To demonstrate high-level ectoine production when the other external osmoprotectants are not accessible, as stated by Vargas and co-workers (2008); under the absence of exogenous osmoprotectants (i.e. choline and betaine uptake as well as choline oxidation fluxes were constrained to zero), FBA simulations were performed for 3-10 mmol/gDW/h glucose uptake rates. Ectoine production increased from 1.4975 up to 4.9722 mmol/gDW/h with a yield within a range of 49 - 50% mmol ectoine/mmol glucose with concomitant increase in biomass (0.1934 to 0.642 h-1) demonstrating the high level ectoine production when glucose was the only carbon source. In addition, Fallet and coworkers (2010) reported batch cultivation data for ectoine production with glucose as the sole carbon source. The performed FBA simulations with 1.5 mmol/gDW/h glucose uptake resulted in an ectoine production rate of 0.75 mmol/gDW/h, which was comparable with the reported experimental result of 0.72 mmol/gDW/h .
Comprehensive analysis of the ectoine biosynthesis (Figure 5) revealed the importance of aspartate, glutamate and alanine in directing fluxes through ectoine synthesis pathway. Moreover, key enzymes of the pathway (i.e. aspartate kinase, diaminobutyrate-2-oxoglutarate transaminase, diaminobutyrate--pyruvate transaminase and DA acetyltransferase) link the pathway to the central metabolism. In FBA simulations, the presence of glutamate and alanine in the medium significantly affected both growth and ectoine production. For instance, constraining the glucose and NaCl uptake rates at 1 mmol/gDW/h and 1.1 mmol/gDW/h, respectively; the presence of alanine in the medium was simulated by an uptake rate of 1.2 mmol/gDW/h and the growth was stimulated by 9.01% (from 0.0710 to 0.0774 h-1), whereas the ectoine production was improved 9.08% (from 0.5497 to 0.5996 mmol/gDW/h).
A non-automated but iterative decision-making process was employed in order to reconstruct the first comprehensive genome-scale metabolic model of a halophilic bacterium, C. salexigens DSM 3043. The in silico model was able not only to represent the potential of the network in terms of phenotypic characterization but also to predict metabolic fluxes during osmoadaptation, both of which were consistent with the experimental observations. The reconstructed model will accelarate the research on halophilic bacteria towards application of systems biology approaches, design of optimal culture conditions and metabolic engineering strategies for improved production of biological and industrially important products.
This research has been supported by Turkish State Planning Organization (DPT) through grant no, DPT09K120520 and TUBITAK MAG/110M613. Fellowship of Ozlem Ates provided by Italian and Turkish governments through TBAG-U/192(106T756) is gratefully acknowledged.
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