- Research article
- Open Access
Complete genome sequence of the sugarcane nitrogen-fixing endophyte Gluconacetobacter diazotrophicus Pal5
BMC Genomics volume 10, Article number: 450 (2009)
Gluconacetobacter diazotrophicus Pal5 is an endophytic diazotrophic bacterium that lives in association with sugarcane plants. It has important biotechnological features such as nitrogen fixation, plant growth promotion, sugar metabolism pathways, secretion of organic acids, synthesis of auxin and the occurrence of bacteriocins.
Gluconacetobacter diazotrophicus Pal5 is the third diazotrophic endophytic bacterium to be completely sequenced. Its genome is composed of a 3.9 Mb chromosome and 2 plasmids of 16.6 and 38.8 kb, respectively. We annotated 3,938 coding sequences which reveal several characteristics related to the endophytic lifestyle such as nitrogen fixation, plant growth promotion, sugar metabolism, transport systems, synthesis of auxin and the occurrence of bacteriocins. Genomic analysis identified a core component of 894 genes shared with phylogenetically related bacteria. Gene clusters for gum-like polysaccharide biosynthesis, tad pilus, quorum sensing, for modulation of plant growth by indole acetic acid and mechanisms involved in tolerance to acidic conditions were identified and may be related to the sugarcane endophytic and plant-growth promoting traits of G. diazotrophicus. An accessory component of at least 851 genes distributed in genome islands was identified, and was most likely acquired by horizontal gene transfer. This portion of the genome has likely contributed to adaptation to the plant habitat.
The genome data offer an important resource of information that can be used to manipulate plant/bacterium interactions with the aim of improving sugarcane crop production and other biotechnological applications.
In recent years, concerns about fossil fuel supplies and prices have motivated the search for renewable biofuels. With the existing technologies and current costs of fuel transportation, ethanol from sugarcane is the most viable alternative. In some countries, including Brazil, sugarcane is planted with low amounts of nitrogen fertilizers and there is evidence that the use of low levels of nitrogen can be compensated by Biological Nitrogen Fixation (BNF) . Although several organisms are capable of contributing to BNF, it has been shown that the diazotroph Alphaproteobacteria Gluconacetobacter diazotrophicus Pal5 (GDI), present in large numbers in the intercellular space of sugarcane roots, stem and leaves, fixes N2 inside sugarcane plants, without causing apparent disease [2, 3]. Remarkable characteristics of this bacterium are the acid tolerance, the inability to use nitrate as sole nitrogen source and the ability to fix nitrogen in the presence of ammonium in medium with high sugar concentration . Although isolation of GDI from the sugarcane rhizosphere has been reported , its poor survival soil and complete absence in soil samples collected between sugarcane rows strongly support the endophytic nature of this nitrogen fixing bacterium [5–7]. In addition to BNF, GDI has other characteristics that contribute to its biotechnological importance: 1-) A nif- mutant enhances plant growth, particularly in roots, indicating that GDI secretes plant growth-promoting substances ; 2-) It produces a lysozyme-like bacteriocin that inhibits the growth of the sugarcane pathogen Xanthomonas albilineans ; 3-) It has antifungal activity against Fusarium sp. and Helminthosporium carbonum ; 4-) GDI promotes an increase in the solubility of phosphate and zinc . Besides its biotechnological features, the genome is especially interesting be-cause is the third diazotrophic endophytic bacteria to be completed sequenced. The first two diazotrophic endophytes to be sequenced, Azoarcus sp. strain BH72  and Klebsiella pneumoniae 342 , belong to the Betaproteobacteria and Gammaproteobacteria classes, respectively. Thus, the genome of GDI is the first to be completely sequence from Alphaproteobacteria class. Here we report the complete genome sequence of the G. diazotrophicus strain Pal5. Sequence analyzes show the existence of a large accessory genome, probably originated by extensive Horizontal Gene Transfer (HGT). Moreover, experimental results reveal differences in Genomic Islands (GI) among G. diazotrophicus strains. The knowledge of the metabolic routes, organization and regulation of genes involved in nitrogen fixation, establishment of successful plant association and other processes should allow a better understanding of the role played by this bacterium in plant-bacteria interaction.
Overview of the G. diazotrophicus PAL5 genome
The complete genome of GDI is composed of one circular chromosome of 3,944,163 base pairs (bp) with an average G+C content of 66.19%, and two plasmids of 38,818 and 16,610 bp, respectively (table 1). The circular chromosome has a total of 3,864 putative coding sequences (CDS), with an overall coding capacity of 90.67%. Among the predicted genes, 2,861 were assigned a putative function, and 1,077 encode hypothetical proteins. Regarding noncoding RNA genes, 12 rRNAs (four rRNA operons) and 55 tRNAs were identified. The larger plasmid (pGD01) has 53 CDS; approximately 70% encode hypothetical or conserved hypothetical proteins and five encode proteins involved in plasmid-related functions. The remaining 11 CDS encode putative components of the Type IV secretion system (T4SS). The small plasmid (pGD02) has 21 CDS, and around 50% are hypothetical proteins.
Although today the genome databases have more than 800 complete microbial genomes, only nine are endophytes (Azoarcus sp. BH72, Burkholderia phytofirmans PsJN, Enterobacter sp. 638, Methylobacterium populi BJ001, Pseudomonas putida W619, Serratia proteamaculans 568, Klebsiella pneumoniae 342, Stenotrophomonas maltophilia R551-3 and Gluconacetobacter diazotrophicus Pal5) . The complete genomes of endophytic bacteria reveal remarkably few mobile elements in its genome (Additional file 1), an observation that led to the proposal that this could denote an adaptation to a more stable life style . In contrast, GDI contains 190 transposable elements, more than any other endophytic bacteria (Additional file 1). The large number of mobile elements could be a signature of a recent evolutionary bottleneck and consequent relaxation of selection, perhaps due to a recent change in niche . Alternatively, because GDI is found in low frequency at the rhizosphere, the transposable elements could have been acquired from other bacteria inhabiting the same environment. In order to identify possible specific characteristics of the genome, the Predicted Highly Express Genes (PHX) genes were identified . PHX analysis identified 658 CDS (17% of the chromosome) in GDI with E(g) (general expression level) > 1,0. Combining this information with the proteomic results , which sequenced peptides from 541 genes, we identified 318 of these genes PHX. As expected, ribosomal proteins, translation/transcription factors and chaperone/degradation genes are among the top 30 E(g) values within the 318 CDS, (Additional file 2). However, some unexpected CDS also appear as PHX. For instance, there are 50 transporter proteins or transporter-related proteins with high E(g) value, of which 27 are putative ABC transporter proteins and six are putative TonB-dependent receptors. The genome has two ammonium transporter proteins (GDI0706 and GDI2352) and both with high E(g) values. Two other proteins related to ammonium metabolism are also PHX: a putative glutamate-ammonia-ligase adenyltransferase (GDI3425) and a putative histidine-ammonia-lyase (GDI0550). This finding is consistent with the fact that ammonium is the preferred nitrogen source for GDI when it is available.
Core and accessory regions
Analysis of the core and accessory regions of GDI is important in order to understand its evolution and adaptation to the plant environment . Even though Pal5 is the first Gluconacetobacter diazotrophicus strain to be sequenced, it is possible to identify the core genome by comparing with closely related species. The closest completed genomes available in the database were identified by phylogenetic analysis (Additional file 3). These include Acidiphilium cryptum JF-5 (ACC), Gluconobacter oxydans 621H (GOX) and Granulibacter bethesdensis CGDNIH (GRB). Using quartops analysis (quartets of orthologous proteins ) we identified 894 CDS as core. Most of these CDS are related to metabolism, information transfer and energy metabolism, as illustrated in figure 1. As CDS with low GC3 (G+C content of synonymous third position) are potential accessory genes, the mean and standard deviation of the non-quartops were used as cut-offs to identify possible accessory genes. We found that 1,352 CDS have a GC3 percentage lower than 80% (figure 2). Interpolated Variable Order Motifs  (IVOMs) were used to complement the accessory genome analysis, revealing that 1,164 CDS have an "Alien score" greater than the threshold, 11,134. The group of CDS in common between GC3 and IVOMs (851 CDS) was used to define the accessory genes in the genome. The percentages of conserved hypothetical proteins, hypothetical proteins, phage/IS elements and pseudo genes are higher in the putative accessory regions than in the core regions and in the genome (figure 1), suggesting that the putative accessory regions have been transferred horizontally into the genome. Overall, the putative accessory regions cover approximately 24% of the GDI genome and are separated into 28 distinct regions, of which seven are classified as phage regions (Additional file 4). A third and completely independent method, PHX, also supports the assignment of the predicted accessory regions (figure 3).
Genome Islands: Variation among G. diazotrophicus strains
Because HGT is an important source of intra-specific genetic variation in bacteria , we investigated whether there are differences in putative genome islands among 19 G. diazotrophicus strains and one G. johannae strain, using PCR with primers designed against 39 single-copy genes in 20 Genome Islands (GIs), and 17 CDS from the core genome. There was a complex variation among the strains, with gene content of eleven GIs - 1, 3, 7, 8, 9, 11, 15, 16, 17, 18, 19 - either almost entirely conserved or less than 50% variable (Additional file 5). In two GIs - 12 and 14 - there was high variability in a group of genes, while other genes were conserved in most strains. The remaining seven GIs, representing approximately 7% of the genome, were highly variable, especially GIs 4 and 21, which are 78 and 242 kb long, and encode 80 and 242 CDS, respectively. Furthermore, a considerable number of CDS in these two GIs encode genes involved in processes that could confer a competitive edge, such as oxidative stress, proteases, biosynthesis of antimicrobial agents, amino acid metabolism and secondary metabolites, as well a large number of transport systems and transcriptional regulators. Both GI4 and GI21 also contain complete copies of the T4SS operon. As it has been suggested that T4SS can increase host adaptability in Bartonella , we suspected that they could be a source of intraspecific variation among G. diazotrophicus strains. A Southern blot used to probe the trbE gene shows that indeed the T4SS copy number varies from one to four depending on the strain (Additional file 6). These GIs could be especially important for bacterial adaptation to the endophytic lifestyle and may confer adaptation advantages to G. diazotrophicus in comparison with other microbes that colonize the same niche.
As the experimental results support the prediction of accessory regions in GDI, another interesting question concerns which regions of the genome resembles genomes from the database. For this purpose, a Reciprocal Best Hits (RBH) comparison was used . The RBH analysis indicates that only 2,966 CDSs of GDI generate a hit with a completed bacterial genome. Among them, 2,470 CDSs have best hit with the Alphaproteobacteria class, 190 with the Betaproteobacteria class, 188 CDS with the Gammaproteobacteria class and 118 with other groups. The distribution of all RBHs demonstrated that even genes from phylogenetically distant related organisms can exhibit high percent identity (Additional file 7). The organism with the highest number of best hits is GOX, with 1,099. However, in figure 1, it is possible to observe that most of the hits occur in core regions. In the three organisms closest to GDI, around 90% of the best hits occur in core regions, with 10% in accessories regions. On the other hand, among rhizobiales and other Alphaproteobacteria orders, 56% of the best hits occur in core regions and 44% in accessory regions (Additional file 8). Curiously, complete genomes from the Betaproteobacteria class, Gammaproteobacteria class and other groups have a significant number (65-70%) of RBHs in core regions, and low percentage (30-35%) in accessory regions. In addition, the number of RBHs with phytopathogenic organisms is higher in Betaproteobacteria and Gammaproteobacteria than in Alphaproteobacteria (68%, 55% and 8%, respectively).
Comparisons with other endophytic bacteria
Currently, there are only nine complete genome sequences of endophytic bacteria, and all are Proteobacteria. Using the complete genomes, we searched for common and exclusive CDS among endophytic bacteria in order to identify genes that could explain the endophytic capacity. However, we found only five CDS that are exclusively conserved (Additional file 9). The comparison among the endophytic organisms indicates that GDI has more CDS exclusively conserved with Methylobacterium populi BJ001 (133 genes) than with the others, which is consistent with the fact that M. populi BJ001 is also an Alphaproteobacteria. Most of these genes (Additional file 10) occur in an accessory region (GI4, GI9, GI12, GDI13, GDI14, GDI19 and GI21), and many are putative transcriptional regulators and putative T4SS (Additional file 9), which could also be involved in bacteria-host interactions. We also searched for exclusively conserved CDS between GDI and Azoarcus sp. BH72, as these two bacteria are currently the only diazotrophs among the endophytes sequenced. The result confirmed the presence in both endophytes of the nif cluster (figure 2, around 0.5 MB) and genes from the putative gum cluster are only conserved within Azoarcus sp. BH72 and GDI (Additional file 10). An assessment of the classes and frequency of signaling CDS in both diazotrophs shows that Azoarcus sp. BH72 has acquired a far more complex set of regulators (Additional file 11). In contrast, GDI has many more transport systems than Azoarcus sp. BH72 (Additional file 12). Altogether, the strategy developed by GDI to interact with plants seems to be more similar to Methylobacterium populi BJ001 then to other endophytes. However, the result suggests that there is not only one strategy and probably there are different ways in which bacteria can interact with plants.
After we completed this work, a second genome sequence of Gluconacetobacter diazotrophicus strain Pal5 was deposited. We carried out extensive comparisons between the two sequences. The comparison is summarized in Additional file 13. The results show significant differences between the two versions. GDI-BR has 309 more CDS than GDI-US, although this number is significantly reduced when small ORFs are annotated as CDSs in GDI-US. Likewise, the number of unique genes in both genomes decreases from 747 and 438 to 624 and 110, respectively, when the small CDSs are taken into account. The results show that the transposases, integrases and hypothetical proteins can explain the majority of the differences between the two sequences. Furthermore, 67% of the genes unique to GDI-BR are located in Genome Islands. On the other hand, 85% BBH among the two sequences are found outside the GIs. The results of the genomic comparisons between the two sequences are compatible with the PCR results reported here, that showed that most of the genic differences among GDI strains are situated in the GIs. Furthermore, when GIs from the two sequences are compared, most of the genic variation is found in the same more variable GIs (data not shown). Altogether, these analyzes suggest that the two sequences deposited as G. diazotrophicus Pal5 strain may represent either two different strains or a fast diverging strain.
In addition, our results were corroborated by at least three independent approaches. First, Southern Blot analyzes confirmed that the genomic sequence we have deposited has 4 copies of the TSS4 secretion system. Furthermore, PCR with primers that amplified genes in the GIs verified the presence of all CDS in our sequence, while some like GDI2782 which encodes a putative H(+)/Cl(-) exchange transporter, is absent from the second sequence. Finally, over 500 CDS in our sequence were validated by proteomics . Some of these CDS may confer unique biological properties and competitiveness to Gluconacetobacter diazotrophicus Pal5, such as a Bacteriocin (GDI0415). Additional file 14 contains the list of Blast Best Hits among the two Gluconacetobacter diazotrophicus Pal5 genomic sequences, a list of unique CDS found in chromosome from GeneBank file CP001189 and a list of unique genes found in chromosome from GeneBank file AM889285 (this work).
Genome Features in Core Regions
GDI supports high sugar concentrations, being able to tolerate up to 30% sucrose, but is sensitive to salt . This shows its adaptation to sugarcane tissues, where the sucrose content is frequently high. Several osmoprotection systems were found (figure 4). There is a Kdp sensor system kdpABCDE, which regulates potassium flux (GDI1564-1568) . One putative proline/betaine transporter gene was detected (GDI2530), but transporter genes proU, betT and opuA were not found. Pathways for glycine/betaine production are incomplete and genes necessary for conversion from choline to betaine are absent. The GDI genome harbors three Dpp ABC transporters that facilitate the uptake of di- and tripeptides (GDI0246-0250, GDI0454-0458 and GDI3540-3544). Two ORFs encoding a DtpT transporter, also involved in the uptake of di- and tripeptides, are present (GDI3819 and GDI0829). The presence of otsA, otsB and treA homologs (GDI0917, GDI0916 and GDI1341) suggests that GDI may synthesize and use the osmolytic disaccharide trehalose, although experiments on solid culture medium have shown that GDI is able to grow poorly on trehalose as a carbon source (data not shown). The hyperosmotic sensing in GDI may occur through the two-component system envZ/ompR (GDI3087 and GDI3088). However, the envZ-regulated porins ompF and ompC are not present. In bacteria, two porins (aqpZ and glpF) regulate the movement of water and aliphatic alcohols across cell membranes . Homologs of aqpZ are missing in GDI, although two sets of glyceroporin genes were found in two clusters: one containing glpRDFK (GDI1751-1754) and the other composed of glpDKF (GDI0262, GDI0266, and GDI0267). The mechanisms shown in figure 4 and discussed here are similar to those found in bacteria without the high level of tolerance to high sugar concentrations observed for G. diazotrophicus. Therefore, unknown mechanisms that protect the bacteria specifically against high sugar concentrations may act in GDI. However, GDI seems to have a larger number of isoforms of enzymatic systems involved in osmotolerance. These differences may be explained by the different niches inhabited by GDI and Azoarcus sp BH72. While GDI is found in plants with elevated concentration of sugars, Azoarcus sp BH72 lives in association with plants that do not accumulate carbon sources in high concentration in vegetative tissues, rice and Kallar grass, and thus Azoarcus sp BH72 may not need a large number of enzymes.
GDI has high tolerance to low pH and organic acids and is able to fix nitrogen at pH values as low as 2.5 . The acidophile Acetobacter aceti has an unusual citric acid cycle (CAC) that is important for acetic acid resistance at low pH . Genome analyses revealed the presence in the GDI genome of homologs of the alternative A. aceti citrate synthase gene aarA (GDI1830) and the gene for an acetyl-CoA hydrolase family protein gene with succinyl-CoA:acetate CoA-transferase activity, called aarC (GDI1836). In GDI, the aarAC homologs occur in a cluster similar to that of A. aceti, contrasting with the organization of these genes in non-acidophilic species, thus indicating that the same mechanisms of acid tolerance involving the CAC may be acting in both organisms. We also found a homolog of an ABC-transporter gene aatA (GDI1739) that, in A. aceti, constitutes an organic acid efflux pump mediating resistance to several acids . An unusual observation is the presence in the GDI genome of two copies of the chaperonin genes groES (GDI2050, GDI2648) and groEL (GDI2049, GDI2647), which are usually present as single copy in bacteria. In A. aceti, overexpression of the groESL operon led to augmented resistance to acetic acid , which may be explained by the fact that chaperonins protect proteins under denaturing conditions such as low pH .
Polysaccharides: CPS, EPS and LPS
Cell-surface components that are commonly involved in plant-bacteria interactions include capsular polysaccharides (CPS), exopolysaccharides (EPS), and lipopolysaccharide (LPS). On the GDI chromosome we found nine CDS related to polysaccharide encapsulation (GDI2398 to GDI2402 and GDI2409 to GDI2413). The GDI genome contains several CDS related to lipopolysaccharide biosynthesis. Five CDS (GDI3265, GDI1647, GDI1652, GDI1447 and GDI0495) encode glycosyltransferases, three CDS (GDI2535, GDI2549 and GDI2493) may be involved in lipopolysaccharide transport, one CDS (GDI2975) encodes an O-antigen polymerase, and there is an ADP-heptose synthase (GDI1133) and a nucleotidyl transferase (GDI0713). Seven CDS (GDI2490, GDI2971, GDI2492, GDI2544, GDI2549, GDI1898 and GDI1899) related to the synthesis of other EPS such as beta-glucans and exooligosaccharides were also identified. These CDS are dispersed over the GDI genome and encode exoF, exoZ, exoY, exoO, exoP, exoN and exoC, respectively. Homologs of these CDS are involved in the interaction between rhizobia and their host plants . GDI has a cluster (GDI2535-GDI2552) containing 14 CDSs that is similar to the gum cluster of Azoarcus sp.BH72, X. campestris and X. fastidiosa. The gum cluster in X. campestris is responsible for the synthesis of an EPS that is involved in host plant colonization and virulence . However, not all genes from the gum operon are present in GDI. We found eight CDSs (GDI2552, GDI2549, GDI2547, GDI2538, GDI2550, GDI2535, GDI2542 and GDI2548) which represent the genes gumB, C, D, E, H, J, K and M, respectively. The genes gumF, G, I and L are not present in the GDI genome. As GDI is not virulent, this cluster may be related with colonization and survival. In addition, it is proposed that the viscous nature of EPS helps localize and stabilize hydrolytic enzymes produced by the bacteria . We found a putative endoglucanase protein (GDI2537) in the gum cluster that may degrade plant cell walls in order to facilitate the active penetration of the bacteria and thereafter the colonization. In addition, the production of hydrolytic enzymes by GDI has been observed .
Biological Nitrogen Fixation (BNF)
The genetics and biochemistry of BNF and nitrogen utilization by G. diazotrophicus have been previously investigated to some extent. Corroborating previous studies , we have found that the GDI structural genes for nitrogenase nifHDK are arranged in a cluster (GDI0425-GDI0454), which also contains other N2 fixation-related genes, such as fixABCX, modABC and nifAB. Other related genes, ntrX, ntrY and ntrC (GDI2263, GDI2264, and GDI2265) are localized elsewhere in the chromosome in a 5.2 kb cluster. There are three copies of nifU homologous genes, one localized in the nif cluster (GD0447), and the other two scattered on the GDI chromosome (GDI1392 and GDI3055). No draT or draG homologs were found in GDI, confirming that nitrogenase activity is not regulated at the post-translational level. It has been suggested that post-translational modulation in G. diazotrophicus might be mediated by a FeSII Shethna protein , but no such CDS was identified. However, many other FeSII protein genes are present, and they possible candidates for this role. The apparent absence of nifL as a nifA activity modulator in response to the cell O2 status in GDI  is in agreement with the lack of a nifL homolog on the genome. The nifA protein appears to be inherently sensitive to O2. In G. diazotrophicus, the main route for assimilation of ammonia is believed to occur through the glutamine synthetase/glutamate synthase pathway (GS/GOGAT encoded by glnA and gltDB, respectively) . However, the genome analysis suggests the existence of alternative routes, where the putative enzymes NAD-synthase (GDI0919), aminomethyltransferase (GDI2317), histidine ammonia-lyase (GDI0550) and D-amino acid dehydrogenase (GDI2422) would incorporate ammonia into different compounds. The enzymatic activity of GS is known to be regulated by an adenylyltransferase enzyme, which is probably encoded by glnE (GDI3425). The glutamate dehydrogenase gene was not found in GDI, although its activity was demonstrated for G. diazotrophicus strain Pal3 .
Signaling and quorum sensing
The GDI genome contains 16 GGDEF family genes that are involved in the synthesis of the second messenger cyclic di-GMP, which has been shown to regulate cellulose synthesis and other processes such as transitions between sessile and planktonic lifestyle and pathogenesis . There are three cytoplasmic and 14 membrane-bound histidine kinase signaling proteins, the majority of which form two-component signaling systems with a neighboring response regulator gene. Among these histidine kinases are homologs of the kdpD (GDI1566), envZ (GDI3079), chvG (GDI1265), ntrY (GDI2264), ntrB (GDI2266) and phoB (GDI3817) genes. In addition, there are two adjacent hybrid histidine kinase/response regulator genes that are organized in an apparent operon (GDI3283-3293) that contains several chemotaxis genes and a proteolytic system encoded by hslUV that is absent in GOX. Chemotaxis enables microorganisms to move towards beneficial or away from harmful substances in their environments by means of flagellar motility. The G. diazotrophicus genome contains nine methyl-accepting proteins (MCPs, chemotaxis sensor proteins), the majority of which have close homologs in rhizobia, but not in the phylogenetically related non-endophyte GOX, which has only three MCP genes . Quorum sensing has been shown to be important in traits such as virulence, biofilm formation and swarming motility in many bacteria . In the Azoarcus sp BH72 genome, quorum sensing genes were not found, and it was suggested that this was compatible with a non-pathogenic interaction of Azoarcus sp BH72 with the host plant . Nevertheless, GDI, which inhabits a niche similar to Azoarcus sp BH72, has three quorum sensing genes: one luxI autoinducer synthase gene (GDI2836) and two luxR-type transcriptional regulator genes (GDI2837, GDI2838). Quorum sensing genes are also present in several rhizobial genomes, and they play roles in nodulation and nitrogen fixation .
Plant Growth-Promoting (PGP) Traits
There are several indications that GDI promotes plant growth by more than a few independent mechanisms besides nitrogen fixation, including synthesis of phytohormones and increased uptake of nutrients . Recent work has shown that mutations in two genes involved in cytochrome c biogenesis reduced auxin levels to 10% of the wild-type strain , suggesting their involvement in indole acetic acid (IAA) production, and indicating that GDI has at least two independent pathways for auxin biosynthesis. In addition, characterization of the IAA biosynthetic route in GDI has shown that auxin is mostly synthesized by the Indole-3-pyruvic acid (IPyA) pathway . Although no CDS encoding an indole 3-pyruvate carboxylase was found in GDI genome, we cannot rule out that the biochemical activity could be executed by one of the many putative decarboxylases identified in the genome. The presence of genes encoding enzymes such as aromatic-L-amino-acid decarboxylase (GDI1891), amine oxidase (GDI1716) and aldehyde dehydrogenases (GDI0311, GDI0461, GDI640) suggests that the bacteria might synthesize IAA via the trypamide pathway (TAM). Also, the presence of two genes coding for putative nitrilases (GDI0018, GDI3743) suggests that IAA might be produced by the indole-3-acetonitrile pathway (IAN). In addition to phytohormone production, some rhizosphere-associated bacteria can stimulate plant growth by secreting a mixture of plant volatiles, mainly 3-hydroxy-2-butanone (acetoin) and 2,3-butanediol . Although the role of GDI in PGP has been studied, no attention has been paid to the production of volatiles. We found GDI is likely to be capable to synthesize acetoin once the genome sequence encodes two enzymes of the pathway; acetolactate synthase (GDI0022, GDI0023) and acetoin diacetyl reductase (GDI2623). In addition, although an acetolactate decarboxylase has not been identified, 2-acetolactate can be converted to diacetyl spontaneously in the presence of oxygen (46). It has been shown for Azospirillum brasilense that the production and secretion of polyamines promote plant growth . The presence of genes coding for enzymes for the synthesis (GDI0476, GDI2322) and secretion (GDI2595) of spermidine in the G diazotrophicus Pal5 genome sequence suggests that this polyamine may also contribute to PGP. G. diazotrophicus has been shown to synthesize the gibberellins GA1 and GA3 . Although the gibberellin biosynthesis machinery in bacteria is largely unknown, recent studies have suggested likely biosynthetic mechanisms in Bradyrhizobium japonicum . The GDI genome contains genes for the synthesis of the diterpenoid precursor isopentenyl diphosphate through the non-mevalonate pathway. Condensation reactions of this precursor to form geranylgeranyl diphosphate may be performed by the geranyltranstransferase ispA (GDI1861). However, homologs of the genes responsible for the cyclization of geranylgeranyl diphosphate in B. japonicum (ent-copalyl diphosphate and ent-kaurene synthase) are apparently absent in the GDI genome and therefore the mechanism of cyclization of geranylgeranyl diphosphate to ent-kaurene remains unknown. However, a putative squalene cyclase (GDI1620) could fulfill such function, since a study with recombinant squalene cyclase has shown some cyclization of geranylgeraniol by this enzyme . Oxidation steps of ent-kaurene, necessary to produce GA1 and GA3, may be catalyzed by two cytochromes P450 (GDI2364 and GDI2593), homologs of which are absent in other acetobacteraceae genomes, thus suggesting a likely specific role in G. diazotrophicus. It has been reported that the capacity of G. diazotrophicus to antagonize diverse plant pathogens such as fungi, and bacteria contributes to increasing its ability to survive under environmental stress and leads to an improvement in plant fitness which may have important consequences for agricultural productivity [9, 10]. Its genome sequence encodes a large repertoire of genes whose products oppose attack from competing microbes, such as drug efflux systems, and acriflavin and fusaric acid resistance proteins. On the other hand, GDI may also produce a broad variety of proteins such as lytic enzymes and phospholipases and antibiotic biosynthetic pathways that could be toxic to other organisms. The secretion of a lysozyme-like bacteriocin by G. diazotrophicus, for instance, inhibits Xanthomonas albilineans growth . Indeed, GDI encodes a putative lysozyme-like bacteriocin (GDI0416 and GDI0415).
Sugar metabolism and energy generation
Sucrose is the common carbon source used for isolation of Gluconacetobacter diazotrophicus from sugarcane and other plants in the semi-solid LGIP medium . However, sucrose is not directly metabolized by the bacteria. Experimental evidence has shown that there is a constitutively expressed levansucrase (LsdA GDI0471), secreted to the periplasm via a specific signal peptide-dependent pathway, that converts sucrose to beta-1,2 -oligofructans and levan . In addition, a fructose-releasing exo-levanase (LsdB GDI 0477) probably controlled by an antitermination inducer system converts polyfructans into fructose . A type II secretion operon (GDI481-GDI 490) is required for the transport o f LsdA across the outer membrane . The transport of LsdB to the periplasm involves the cleavage of the N-terminal peptide signal, and it is induced during growth of the bacteria with low fructose levels but repressed by glucose .
In G. diazotrophicus oxidation of glucose to gluconate in the periplasmic space is the first step in glucose metabolism by GDI . Gluconate may be synthesized by the product of three CDS encoding membrane-bound quinoprotein glucose dehydrogenases (GDI3277, GDI0325 and GDI0539) in accordance with the observed high activity of PQQ-GDH detected in glucose-containing batch culture of GDI strain Pal3 grown mainly under biological nitrogen fixation and/or C-limitation conditions . A NAD-GDH (GDI2625) also participates in the glucose oxidation (intracellularly) when glucose is in excess . Further periplasmic oxidation of gluconate to 2-ketogluconic acid occurs by a putative three-subunit flavin-dependent gluconate-2-dehydrogenase (GDI0854, GDI0855 and GDI0856). Gluconate dehydrogenases (extracellular, dye-linked and intracellular, NAD-Linked) activities have been demonstrated in GDI strain Pal3 grown in presence of gluconate with 2-ketogluconate the major compound accumulated (57). The production of 5-ketogluconate and 2,5 di-ketogluconate are probably mediated by a glucose/methanol/choline oxidoreductase (GDI0859) and a putative alcohol dehydrogenase cytochrome c/gluconate 2-dehydrogenase acceptor (GDI0860). High activities of 2-ketogluconate reductase (NAD linked) have been detected in a GDI Pal3 strain grown with gluconate .
CDS for transport (GDI3258) and phosphorylation (GDI0293) proteins indicate that gluconate can also be directly driven into the pentose phosphate route (PPP), supporting the experimental data . The presence of a kinase (GDI3115), a 2-ketogluconate reductase (GDI 3432) and a 6-phosphogluconate dehydrogenase-NAD (GDI2166) corroborates with the experimental data which shows that the PPP is the main C-metabolism route in GDI following the oxidation of glucose to gluconate .
Different from GOX, CDSs encoding a complete respiratory chain complex I (nuoA - nuoN or complex I proton-translocating NADH-quinone oxidoreductase; GDI2459-GDI2471) are present in the GDI genome . The GDI genome contains CDS that encode L-sorbosone dehydrogenases (GDI0574 and GDI3764), membrane-bound small and large subunits (GDI3280 and GDI3281) and the cytochrome c subunit (GDI3279) of aldehyde dehydrogenase, indicating that GDI may be able to synthesize the industrially important substances such as L-ascorbic acid (vitamin C) and its precursor 2-keto-L-gulonic acid .
Genome Features in Accessory Regions
Type IV secretion system
Type IV secretion systems (T4SS) are multi-subunit cell envelope-spanning structures, ancestrally related to bacterial conjugation machines, that transfer proteins, DNA and nucleoprotein complexes across membranes . Moreover, T4SSs have been described as essential pathogenicity factors and recently it has been indicated that TSS4 can also increase host adaptability in Bartonella sp. . GDI has 4 complete T4SS in the chromosome which are similar to bacterial conjugation machines (trb) of Agrobacterium tumefasciens  and Ti (tumor inducing) Enterobacter IncP plasmid R751 . Although the order of the trb genes in the operon is conserved (trbB, -C, -D, -E, -J, -L, -F, -G, -I), two genes are missing from the original trb operon (trbK and trbH). The gene trbK has been reported as non-essential but trbH has been reported as essential for conjugal transfer of Agrobacterium tumor inducing plasmid pTiC58 . Another difference is that, in Agrobacterium tumefasciens and Enterobacter IncP plasmid R751, the first gene in the operon is traI, which is an essential signal for the quorum-sensing regulation of the Ti plasmid conjugation transfer . In GDI the first gene in the operon is traG, which is essential for DNA transfer in bacterial conjugation. This gene is thought to mediate interactions between the DNA-processing (Dtr) and the mating pair-formation (Mpf) systems . T4SS have been found in many different organisms , from pathogenic to mutualistic endosymbiont organisms (for instance, Helicobacter pylori, Legionella pneumophila, Brucella spp, Bartonella spp, Rickettsia spp., Coxiella spp., Anaplasma marginale, Ehrlichia spp, Agrobacterium tumefaciens, Wolbachia spp). All four complete T4SS operons in the GDI chromosome were found in accessory regions (GI4, GI12, and twice in GI21), suggesting that the bacteria acquired the ability to translocate macromolecules across the cell envelope to the plant. The four copies of the T4SS operon diverge by the presence of a variable region between the traG and the trbB genes that include transcriptional regulators mucR and araC, a DNA-binding protein HU-beta, an aldo/keto reductase and hypothetical proteins. These genes might confer specific functions to each T4SS copy.
Flagella and pili
In many organisms, flagella are involved in motility, adherence, biofilm formation and host colonization . GDI has a large accessory region (GI15) with at least 40 genes predicted to encode functions related to motility. This observation is in accordance with the presence of peritrichous flagella on the GDI cell surface. Next to the motility cluster there is a putative tad locus (Flp-1, cpaABC, cpaEF, and tadBCDG) which probably encodes the machinery for the synthesis of Flp (fimbrial low-molecular-weight protein) pili, which form a subfamily in the type IVb pilus family. In Actinobacillus, Haemophilus, Pasteurella, Pseudomonas, Yersinia and Caulobacter. Flp pili are essential for biofilm formation, colonization and pathogenesis . Additionally, several pseudopilins (GDI0483, GDI0484, and GDI0485) were identified as part of a type II secretion system. Recently, it has been shown that flagella-less mutant of GDI was non-motile and displayed reduced capacity to form biofilm . These findings suggest that these genes were acquired by HGT and play an important role in the interaction with the plant.
Despite the potential impact of endophytes on the environment and on crop production, our current knowledge of their biology is limited. Analysis of the G. diazotrophicus PAL5 complete genome sequence provides important insights into the endophytic relationship, and suggests many interesting candidate genes for post-genomic experiments.
The genome reveals an unexpectedly high number of mobile elements for an endophytic bacterium; it is in fact the endophyte with the highest frequency of mobile genes per Mb of genome. The high number of mobile elements seems to be associated with a high number of HGT events. The analysis of HGT shows that most of the genes are more similar to genes from the order rhizobiales (40%), suggesting that a likely previous niche was located in the rhizosphere. Thus, a recent evolutionary bottleneck and consequent relaxation of selection, due to a possible change of niche, is probably the hypothesis that could best explain the high number of HGT .
In addition, to change niche from rhizosphere to endophytic, the bacteria should have features that would allow it to penetrate the plant. The putative gum-like cluster containing an endoglucanase could be important in this regard. Moreover, the limited similarity with the gum-like cluster from X. campestris and the absence of some genes found in X. campestris may mean that the cluster adapted to a non-virulence profile. However, the ability to penetrate the plant is not enough to transform it into an endophyte; the bacteria must evolve together with the plant to create a more depended relationship. The genome has many features to enhance plant fitness such as BNF, phytohormones and biocontrol genes, and all of them lie in the core of the genome or have a very low "Alien score". We propose that these features were important to create a dependent relationship, and may have helped GDI to spread out and occupy this niche. In contrast, many features that may be related to bacteria-plant interaction are found in genome islands, including type IV secretion systems, flagella, pili, chemotaxis, biofilm, capsular polysaccharide and some transport proteins. The overall result suggests that it is more likely that GDI acquired many features that are important for an endophytic lifestyle. Thus, experimental analyses of genes from genome islands may reveal an important source of gene candidates that will enhance our understanding of bacteria-plant relationship.
Finally, comparison of genome sequences of Gluconacetobacter diazotrophicus and Azoarcus sp. BH72 shows that these endophytic diazotrophic bacteria adopted very different strategies to colonize plants. A limited number of genomic features, such as the large number of TonB receptors, the gum-like and nif clusters, and osmotolerance mechanisms are common to both endophytic diazotrophic bacteria. On the other hand, Gluconacetobacter diazotrophicus has a larger number of transport systems, and it is capable of growing on a wide variety of carbon sources, while Azoarcus sp. BH72 has rather complex signaling mechanisms to communicate with its plant host.
Gluconacetobacter diazotrophicus strain PAl 5 (type strain) was isolated from sugarcane roots collected in Alagoas Sate, Brazil using the nitrogen-free semi-solid LGIP medium . It was deposited at the Embrapa Agrobiologia Culture Collection and received the identification number BR 11281 (BR-stands for the Brazilian Nitrogen-fixing bacteria Culture Collection). Later on, this strain was deposited by Johanna Dobereiner at the American Type Culture Collection (ATCC 49037) and also at the Culture Collection Laboratorium von Microbiologie, Belgium (LMG 7603) .
Genome sequencing, assembly and annotation
All the libraries were prepared with total bulk DNA originated from a Pal 5 lyophilized tube culture provided by the Embrapa Agrobiologia Culture Collection. Pal5 was grown in 500 mL Erlenmeyer flasks containing 200 mL of DYGS medium (Rodrigues-Neto et al., 1986) during 48 h at 200 rpm and 30°C. DNA extraction was performed according with the CTAB method . Phenol: chloroform: iso-amilic alcohol (25:24:1) and chloroform: iso-amilic alcohol (24:1) washing steps were repeated 2 times to guarantee removal of cells debris and other contaminants during DNA extraction.
DNA shotgun libraries with insert sizes of 0.5-1 kb, 2-3 kb and 4-6 kb were constructed in pUC18 vectors and 10-17 kb in the cosmid pLARF3. Plasmid clones were end-sequenced on ABI377 and ABI3100 (Applied Biosystems) and MegaBACE 1000 (GE Healthcare) sequencers. A total of 103,506 high-quality reads were obtained and assembled into contigs using the Phrap assembly tool. For gap closure, 16,963 additional reads were obtained through PCR direct sequencing and primer-walking on plasmids. Manual editing was done using the GAP4 software package . Genome integrity was verified by a physical map constructed using PFGE and hybridization with 42 single-copy and rDNA probes . Initial automatic gene prediction was done using GLIMMER , and subsequently manually curated with reference to codon-specific positional base preferences. Before the manual annotation of each predicted gene, different tools were used. Similarity search was performed against different databases including Uniprot , PROSITE , nr, Pfam , and InterPro . Additionally, SignalP , TMHMM  and tRNAscan-SE  were applied. All the data were viewed within the Artemis  program where the function of each gene was manually curated.
Pathogenicity/Adaptation/Chaperones, dark blue; Energy metabolism (glycolysis, electron transport etc.), gray; Information transfer (transcription/translation, DNA/RNA modification), red; Surface structures (IM, OM, secreted, LPS)), green; Stable RNA, cyan; Degradation of large molecules, light blue; Degradation of small molecules, purple; Central/intermediary/miscellaneous metabolism, yellow; Unknown and conserved hypothetical, orange; Regulators, magenta; Pseudogenes and partial genes, black; Phage/IS elements, pink; miscellaneous information (e.g. Prosite but no function), brown.
Nucleotide sequence accession numbers
The genomic sequence reported in this article has been deposited in the EMBL database under accession numbers AM889285, AM889286 and AM889287. The genome annotation and features are available at http://www.bioqmed.ufrj.br/bertalan/.
Core and accessory regions
The core regions were determined by quartops analysis (quartets of orthologous proteins), using reciprocal best hit of Blastp. The accessory regions were determined by a combination of two different methods: GC3 and IVOMs. The GC3 analyzes the percent of GC in the third base of the codon in each gene. For both methods, the regions indicated as accessory genes were manually checked for integrases, tRNAs and repeats (direct and inverted). The beginning and end of each the accessory region were defined by both methods and, in the case of bacteriophages, the genome islands were extended when evidence of the insertion point was found.
Reciprocal Best Hits
Reciprocal best hits comparison was done using only the complete bacterial genomes publicly available at ftp://ftp.ncbi.nih.gov/genomes/Bacteria/all.faa.tar.gz. Only reciprocal best hits with identity greater of 30% and alignment greater than 70% were selected.
Plant Endophyte comparison
Six complete endophyte genomes were used to represent the endophyte group and three closest complete genomes phylogenetically to GDI were used to represent the core genome. Endophyte genomes were Azoarcus sp. BH72, Burkholderia phytofirmans PsJN, Enterobacter sp. 638, Methylobacterium populi BJ001, Pseudomonas putida W619 and Serratia proteamaculans 568. Core genome species were Acidiphilium cryptum JF-5, Gluconobacter oxydans 621H and Granulibacter bethesdensis CGDNIH. Only reciprocal best hits with more than 30% identity and 70% alignment were accepted.
Biological Nitrogen Fixation
Gluconacetobacter diazotrophicus PAL5
Horizontal Gene Transfer
Predicted Highly Expressed Genes
Type IV secretion system
Acidiphilium cryptum JF-5
Gluconobacter oxydans 621H
Granulibacter bethesdensis CGDNIH
G+C content of synonymous third position
Interpolated Variable Order Motifs
Blast Best Hit
fimbrial low-molecular-weight protein
mating pair formation
Reciprocal Best Hits.
Boddey RM, Döbereiner J: Nitrogen fixation associated with grasses and cereals: recent progress and perspectives for the future. Fertilizer Res. 1995, 42: 241-250. 10.1007/BF00750518.
Cavalcante VA, Dobereiner J: A new acid-tolerant nitrogen-fixing bacterium associated with sugarcane. Plant Soil. 1988, 1008: 23-31. 10.1007/BF02370096.
James EK, Reis VM, Olivares FL, Baldani JI, Döbereiner J: Infection of sugarcane by the nitrogen-fixing bacterium Acetobacter diazotrophicus. J Exp Bot. 1994, 45: 757-766. 10.1093/jxb/45.6.757.
Muthukumarasamy R, Cleenwerck I, Revathi G, Vadivelu M, Janssens D, Hoste B, Gum KU, Park KD, Son CY, Sa T, Caballero-Mellado : Natural association of Gluconacetobacter diazotrophicus and diazotrophic Acetobacter peroxydans with wetland rice. J Syst Appl Microbiol. 2005, 283: 277-286. 10.1016/j.syapm.2005.01.006.
Boddey RM, Urquiaga S, Reis VM, Döbereiner J: Biological nitrogen fixation associated with sugarcane. Plant Soil. 1991, 137: 111-117. 10.1007/BF02187441.
Baldani JI, Caruso LV, Baldani VLD, Goi SR, Döbereiner J: Recent advances in BNF with non-legume plants. Soil Biol Biochem. 1997, 29: 911-922. 10.1016/S0038-0717(96)00218-0.
Dong Z, Canny MJ, McCully ME, Roboredo MR, Cabadilla CF, Ortega E, Rodes R: A Nitrogen-Fixing Endophyte of Sugarcane Stems (A New Role for the Apoplast). Plant Physiology. 1994, 105: 1139-1147.
Sevilla M, Burris RH, Gunapala N, Kennedy C: Comparison of benefit to sugarcane plant growth and 15N2 incorporation following inoculation of sterile plants with Acetobacter diazotrophicus wildtype and Nif- mutant strains. Mol Plant Microbe Interact. 2001, 3: 358-366. 10.1094/MPMI.2001.14.3.358.
Blanco Y, Blanch M, Pin D, Legaz ME, Vicente C: Antagonism of Gluconacetobacter diazotrophicus (a sugarcane endosymbiont) against Xanthomonas albilineans (pathogen) studied in alginate-immobilized sugarcane stalk tissues. J Biosci Bio eng. 2005, 4: 366-371.
Mehnaz S, Lazarovits G: Inoculation effects of Pseudomonas putida, Gluconacetobacter azotocaptans, and Azospirillum lipoferum on corn plant growth under greenhouse conditions. Microb Ecol. 2006, 3: 326-335. 10.1007/s00248-006-9039-7.
Saravanan VS, Kalaiarasan P, Madhaiyan M, Thangaraju M: Solubilization of insoluble zinc compounds by Gluconacetobacter diazotrophicus and the detrimental action of zinc ion (Zn2+) and zinc chelates on root knot nematode Meloidogyne incognita. Lett Appl Microbiol. 2007, 3: 235-241. 10.1111/j.1472-765X.2006.02079.x.
Krause A, Ramakumar A, Bartels D, Battistoni F, Bekel T, Boch J, Boehm M, Friedrich F, Hurek T, Krause L, et al: Complete genome of the mutualistic, N2-fixing grass endophyte Azoarcus sp. strain BH72. Nat Biotechnol. 2008, 24: 1385-1391. 10.1038/nbt1243.
Fouts DE, Tyler HL, De Boy RT, Daugherty S, Ren Q, Badger JH, Durkin AS, Huot H, Shrivastava S, Kothari S, et al: Complete genome sequence of the N2-fixing broad host range endophyte Klebsiella pneumoniae 342 and virulence predictions verified in mice. PLoS Genet. 2008, 47: e1000141-10.1371/journal.pgen.1000141.
Hapmap: Endopyte complete bacterial genomes. [http://www.expasy.ch/sprot/hamap/interactions.html]
Parkhill J, Sebaihia M, Preston A, Murphy LD, Thomson N, Harris DE, Holden MT, Churcher CM, Bentley SD, Mungall KL, et al: Comparative analysis of the genome sequences of Bordetella pertussis, Bordetella parapertussis and Bordetella bronchiseptica. Nat Genet. 2003, 35: 32-40. 10.1038/ng1227.
Karlin S, Barnett MJ, Campbell AM, Fisher RF, Mrazek J: Predicting gene expression levels from codon biases in alpha-proteobacterial genomes. Proc Natl Acad Sci. 2003, 100: 7313-7318. 10.1073/pnas.1232298100.
Lery LM, Coelho A, von Kruger WM, Gonçalves MS, Santos MF, Valente RH, Santos EO, Rocha SL, Perales J, Domont GB, et al: Protein expression profile of Gluconacetobacter diazotrophicus PAL5, a sugarcane endophytic plant growth promoting bacterium. Proteomics. 2008, 8: 1631-1644. 10.1002/pmic.200700912.
Wernegreen JJ: Genome evolution in bacterial endosymbionts of insects. Nat Rev Genet. 2002, 3: 850-861. 10.1038/nrg931.
Zhaxybayeva O, Gogarten JP: Bootstrap, and Bayesian probability and maximum likelihood mapping: exploring new tools for comparative genome analyses. BMC Genomics. 2002, 3: 4-19. 10.1186/1471-2164-3-4.
Vernikos GS, Parkhill J: Interpolated variable order motifs for identification of horizontally acquired DNA: revisiting the Salmonella pathogenicity islands. Bioinformatics. 2006, 22: 2196-2203. 10.1093/bioinformatics/btl369.
Ochman H, Lawrence JG, Groisman EA: Lateral gene transfer and the nature of bacterial innovation. Nature. 2000, 405: 299-304. 10.1038/35012500.
Saenz HL, Engel P, Stoeckli MC, Lanz C, Raddatz G, Vayssier-Taussat M, Birtles R, Schuster SC, Dehio C: Genomic analysis of Bartonella identifies type IV secretion systems as host adaptability factors. Nat Genet. 2007, 39: 1469-1476. 10.1038/ng.2007.38.
Moreno-Hagelsieb G, Latimer K: Choosing BLAST options for better detection of orthologs as reciprocal best hits. Bioinformatics. 2008, 24: 319-324. 10.1093/bioinformatics/btm585.
Reis VM, Döbereiner J: Effect of high sugar concentration on nitrogenase activity of Acetobacter diazotrophicus. Arch Microbiol. 1998, 171: 13-18. 10.1007/s002030050672.
Epstein W: The roles and regulation of potassium in bacteria. Prog Nucleic Acid Res Mol Biol. 2003, 75: 293-320. full_text.
Wood JM: Bacterial osmosensing transporters. Methods Enzymol. 2007, 428: 77-107. 10.1016/S0076-6879(07)28005-X.
Tejera NA, Ortega E, González-López J, Lluch C: Effect of some abiotic factors on the biological activity of Gluconacetobacter diazotrophicus. J Appl Microbiol. 2003, 95: 528-535. 10.1046/j.1365-2672.2003.02007.x.
Mullins EA, Francois JA, Kappock TJ: A specialized citric acid cycle requiring succinyl-coenzyme A (CoA):acetate CoA-transferase (AarC) confers acetic acid resistance on the acidophile Acetobacter aceti. J Bacteriol. 2008, 190: 4933-4940. 10.1128/JB.00405-08.
Nakano S, Fukaya M, Horinouchi S: Putative ABC transporter responsible for acetic acid resistance in Acetobacter aceti. Appl Environ Microbiol. 2006, 72: 497-505. 10.1128/AEM.72.1.497-505.2006.
Okamoto-Kainuma A, Yan W, Kadono S, Tayama K, Koizumi Y, Yanagida F: Cloning and characterization of groESL operon in Acetobacter aceti. J Biosci Bioeng. 2002, 94: 140-147. 10.1263/jbb.94.140.
Nakano S, Fukaya M: Analysis of proteins responsive to acetic acid in Acetobacter: molecular mechanisms conferring acetic acid resistance in acetic acid bacteria. Int J Food Microbiol. 2008, 125: 54-59. 10.1016/j.ijfoodmicro.2007.05.015.
Skorupska A, Janczarek M, Marczak M, Mazur A, Król J: Rhizobial exopolysaccharides: genetic control and symbiotic functions. Microb Cell Fact. 2006, 16: 5-7.
Katzen F, Ferreiro DU, Oddo CG, Ielmini MV, Becker A, Puhler A, Ielpi L: Xanthomonas campestris pv campestris gum mutants: effects on xanthan biosynthesis and plant virulence. J Bacteriol. 1998, 180: 1607-1617.
Roper MC, Greve LC, Warren JG, Labavitch JM, Kirkpatrick BC: Xylella fastidiosa requires polygalacturonase for colonization and pathogenicity in Vitis vinifera grapevines. Mol Plant Microbe Interact. 2007, 204: 411-419. 10.1094/MPMI-20-4-0411.
Adriano-Anayal M, Salvador-Figuero M, A OJ, García-Romera I: Plant cell-wall degrading hydrolytic enzymes of Gluconacetobacter diazotrophicus. Symbiosis. 2005, 40: 151-156.
Lee S, Reth A, Meletzus D, Sevilla M, Kennedy C: Characterization of a major cluster of nif, and fix, and and associated genes in a sugarcane endophyte, and Acetobacter diazotrophicus. J Bacteriol. 2000, 182: 7088-7091. 10.1128/JB.182.24.7088-7091.2000.
Ureta A, Nordlund S: Evidence for conformational protection of nitrogenase against oxygen in Gluconacetobacter diazotrophicus by a putative FeSII protein. J Bacteriol. 2002, 184: 5805-5809. 10.1128/JB.184.20.5805-5809.2002.
Perlova O, Nawroth R, Zellermann EM, Meletzus D: Isolation and characterization of the glnD gene of Gluconacetobacter diazotrophicus, encoding a putative uridylyltransferase/uridylyl-removing enzyme. Gene. 2002, 297: 159-168. 10.1016/S0378-1119(02)00881-8.
Dow JM, Fouhy Y, Lucey JF, Ryan RP: The HD-GYP domain, cyclic di-GMP signaling, and bacterial virulence to plants. Mol Plant Microbe Interact. 2006, 19: 1378-1384. 10.1094/MPMI-19-1378.
Prust C, Hoffmeister M, Liesegang H, Wiezer A, Fricke WF, Ehrenreich A, Gottschalk G, Deppenmeier U: Complete genome sequence of the acetic acid bacterium Gluconobacter oxydans. Nat Biotechnol. 2005, 23: 195-200. 10.1038/nbt1062.
Williams P, Winzer K, Chan WC, Cámara M, Philos Trans R: Look who's talking: communication and quorum sensing in the bacterial world. Soc Lond B Biol Sci. 2007, 362: 1119-1134. 10.1098/rstb.2007.2039.
Daniels R, De Vos DE, Desair J, Raedschelders G, Luyten E, Rosemeyer V, Verreth C, Schoeters E, Vanderleyden J, Michiels J: The cin quorum sensing locus of Rhizobium etli CNPAF512 affects growth and symbiotic nitrogen fixation. J Biol Chem. 2002, 277: 462-468. 10.1074/jbc.M106655200.
Saravanan VS, Madhaiyan M, Osborne J, Thangaraju M, Sa TM: Ecological occurrence of Gluconacetobacter diazotrophicus and nitrogen-fixing Acetobacteraceae members: their possible role in plant growth promotion. Microb Ecol. 2008, 55: 130-140. 10.1007/s00248-007-9258-6.
Lee S, Flores-Encarnación M, Contreras-Zentella M, Garcia-Flores L, Escamilla JE, Kennedy C: Indole-3-acetic acid biosynthesis is deficient in Gluconacetobacter diazotrophicus strains with mutations in cytochrome c biogenesis genes. J Bacteriol. 2004, 186: 5384-5391. 10.1128/JB.186.16.5384-5391.2004.
Ryu CM, Farag MA, Hu CH, Reddy MS, Kloepper JW, Paré PW: Bacterial volatiles induce systemic resistance in Arabidopsis. Plant Physiol. 2004, 134: 1017-1026. 10.1104/pp.103.026583.
Carballo J, Martin R, Bernardo A, Gonzalez J: Purification, characterization and some properties of diacetyl(acetoin) reductase from Enterobacter aerogenes. Eur J Biochem. 1991, 198: 327-332. 10.1111/j.1432-1033.1991.tb16019.x.
Perrig D, Boiero ML, Masciarelli OA, Penna C, Ruiz OA, Cassán FD, Luna MV: Plant-growth-promoting compounds produced by two agronomically important strains of Azospirillum brasilense, and implications for inoculant formulation. Appl Microbiol Biotechnol. 2007, 75: 1143-1150. 10.1007/s00253-007-0909-9.
Bastian F, Cohen A, Piccoli P, Luna V, Baraldi R, Bottini R: Production of indole-3-acetic acid and gibberellins A(1) and A(3) by Acetobacter diazotrophicus and Herbaspirillum seropedicae in chemically-defined culture media. Plant Growth Regulation. 1998, 24: 7-11. 10.1023/A:1005964031159.
Morrone D, Chambers J, Lowry L, Kim G, Anterola A, Bender K, Peters RJ: Gibberellin biosynthesis in bacteria: separate ent-copalyl diphosphate and ent-kaurene synthases in Bradyrhizobium japonicum. FEBS Lett. 2009, 583: 475-480. 10.1016/j.febslet.2008.12.052.
Hoshino T, Kumai Y, Kudo I, Nakano S, Ohashi S: Enzymatic cyclization reactions of geraniol, farnesol and geranylgeraniol, and those of truncated squalene analogs having C20 and C25 by recombinant squalene cyclase. Org Biomol Chem. 2004, 2: 2650-2657. 10.1039/b407001a.
Baldani JI, Baldani VLD: History on the biological nitrogen fixation research in gramminaceous plants: special emphasis on the Brazilian experience. Anais da Academia Brasileira de Ciências. 2005, 77: 549-579. 10.1590/S0001-37652005000300014.
Hernandez L, Arrieta J, Menendez C, Vazquez R, Coego A, Suarez V, Selman G, Petit-Glatron MF, Chambert R: Isolation and enzymatic properties of levansucrase secreted by Acetobacter diazotrophicus SRT4, a bacterium associated with sugar cane. Biochem J. 1995, 309: 113-118.
Menéndez C, Hernández L, Banguela A, País J: Functional production and secretion of the Gluconacetobacter diazotrophicus fructose-releasing exo-levanase (LsdB) in Pichia pastoris. Enz Microbial Technol. 2004, 34: 446-452. 10.1016/j.enzmictec.2003.11.018.
Arrieta JG, Sotolongo M, Menéndez C, Alfonso D, Trujillo LE, Soto M, Ramírez R, Hernandez L: A Type II Protein Secretory Pathway Required for Levansucrase Secretion by Gluconacetobacter diazotrophicus. J Bacteriol. 2004, 186: 5031-5039. 10.1128/JB.186.15.5031-5039.2004.
Menéndez C, Banguela A, Caballero-Mellado J, Hernández L: Transcriptional Regulation and Signal-Peptide-Dependent Secretion of Exolevanase (LsdB) in the Endophyte Gluconacetobacter diazotrophicus. Appl Environ Microbiol. 2009, 75: 1782-1785. 10.1128/AEM.01887-08.
Attwood MM, van Dijken JP, Pronk JT: Glucose metabolism and gluconic acid production by Acetobacter diazotrophicus. J Ferment Bioeng. 1991, 72: 101-105. 10.1016/0922-338X(91)90317-A.
Luna MF, Bernardelli CE, Galar ML, Boiardi JL: Glucose metabolism in batch and continuous cultures of Gluconacetobacter diazotrophicus PAl 3. Cur Microbiol. 2006, 52: 163-168. 10.1007/s00284-005-4563-0.
Luna MF, Mignone CF, Boiardi JL: The carbon source influences the energetic efficiency of the respiratory chain of N2-fixing Acetobacter diazotrophicus. Appl Microbiol Biotechnol. 2000, 54: 564-569. 10.1007/s002530000425.
Matsushita K, Toyama H, Yamada M, Adachi O: Quinoproteins: structure, function, and biotechnological applications. Appl Microbiol Biotechnol. 2002, 58: 13-22. 10.1007/s00253-001-0851-1.
Miyazaki T, Sugisawa T, Hoshino T: Pyrroloquinoline quinone-dependent dehydrogenases from Ketogulonicigenium vulgare catalyze the direct conversion of L-sorbosone to L-ascorbic acid. Appl Environ Microbiol. 2006, 72: 1487-1495. 10.1128/AEM.72.2.1487-1495.2006.
Cascales E, Christie PJ: The versatile bacterial type IV secretion systems. Nat Rev Microbiol. 2003, 1: 137-149. 10.1038/nrmicro753.
Li PL, Hwang I, Miyagi H, True H, Farrand SK: Essential components of the Ti plasmid trb system, and a type IV macromolecular transporter. J Bacteriol. 1999, 181: 5033-5041.
Thorsted PB, Macartney DP, Akhtar P, Haines AS, Ali N, Davidson P, Stafford T, Pocklington MJ, Pansegrau W, Wilkins BM, et al: Complete sequence of the IncP beta plasmid R751: implications for evolution and organization of the IncP backbone. J Mol Biol. 1998, 282: 969-990. 10.1006/jmbi.1998.2060.
Mor M, Finger L, Stryker J, Fuqua C, Eberhard A, Winans S: Enzymatic synthesis of a quorum sensing autoinducer through use of defined substrates. Science. 1996, 272: 1655-8. 10.1126/science.272.5268.1655.
Dougherty BA, Hill C, Weidman JF, Richardson DR, Venter JC, Ross RP: Sequence and analysis of the 60 kb conjugative, and bacteriocin-producing plasmid pMRC01 from Lactococcus lactis DPC3147. Mol Microbiol. 1998, 29: 1029-1038. 10.1046/j.1365-2958.1998.00988.x.
Juhas M, Crook DW, Hood DW: Type IV secretion systems: tools of bacterial horizontal gene transfer and virulence. Cell Microbiol. 2008, 1012: 2377-2386. 10.1111/j.1462-5822.2008.01187.x.
Merritt PM, Danhorn T, Fuqua C: Motility and chemotaxis in Agrobacterium tumefaciens surface attachment and biofilm formation. J Bacteriol. 2007, 189: 8005-8014. 10.1128/JB.00566-07.
Tomich M, Planet PJ, Figurski DH: The tad locus: postcards from the widespread colonization island. Nat Rev Microbiol. 2007, 5: 363-375. 10.1038/nrmicro1636.
Rouws LF, Simões-Aráujo JL, Hemerly AS, Baldani JI: Validation of a Tn5 transposon mutagenesis system for Gluconacetobacter diazotrophicus through characterization of a flagellar mutant. Arch Microbiol. 2008, 189: 397-405. 10.1007/s00203-007-0330-x.
Gillis M, Kersters K, Hoste B, Janssens D, Kroppenstedt RM, Stephan MP, Teixeira KRS, Döbereiner J: Acetobacter diazotrophicus sp., a nitrogen-fixing acetic acid bacterium associated with sugarcane. Int J Systematic Bacteriol. 1989, 39: 361-364. 10.1099/00207713-39-3-361.
Rodrigues Neto J, Malavolta VA, Victor O: Meio simples para o isolamento e cultivo de Xanthomonas campestris pv. Citri Tipo B. Summa Phytopathologia. 1986, 12: 16-
Bonfield JK, Smith KF, Staden R: A new DNA sequence assembly program. Nucleic Acids Res. 1995, 23: 4992-4999. 10.1093/nar/23.24.4992.
Loureiro MM, Bertalan M, Turque AS, Franca LM, Pádua VLM, Baldani JI, Martins OB, Ferreira PCG: Physical and genetic map of the Gluconacetobacter diazotrophicus PAL5 chromosome. Rev Lat Microbiol. 2008, 50: 19-28.
Delcher AL, Bratke KA, Powers EC, Salzberg SL: Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics. 2007, 23: 673-679. 10.1093/bioinformatics/btm009.
The UniProt Consortium: The universal protein resource (UniProt). Nucleic Acids Res. 2008, 36: 190-195. 10.1093/nar/gkn141.
Hulo N, Bairoch A, Bulliard V, Cerutti L, Cuche B, De Castro E, Lachaize C, Langendijk-Genevaux PS, Sigrist CJA: The 20 years of PROSITE. Nucleic Acids Res. 2007, 36: D245-9. 10.1093/nar/gkm977.
Finn RD, Tate J, Mistry J, Coggill PC, Sammut JS, Hotz HR, Ceric G, Forslund K, Eddy SR, Sonnhammer EL, Bateman A: The Pfam protein families database. Nucleic Acids Res. 2008, 36: 281-288. 10.1093/nar/gkm960.
Hunter S, Apweiler R, Attwood TK, Bairoch A, Bateman A, Binns D, Bork P, Das U, Daugherty L, Duquenne L, et al: InterPro: the integrative protein signature database. Nucleic Acids Res. 2009, 37: 211-215. 10.1093/nar/gkn785.
Emanuelsson O, Brunak S, von Heijne G, Nielsen H: Locating proteins in the cell using TargetP, SignalP and related tools. Nat Protoc. 2007, 2: 953-971. 10.1038/nprot.2007.131.
Krogh A, Larsson B, von Heijne G, Sonnhammer EL: Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes. J Mol Biol. 2001, 305: 567-680. 10.1006/jmbi.2000.4315.
Lowe TM, Eddy SR: tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 1997, 25: 955-964. 10.1093/nar/25.5.955.
Carver T, Berriman M, Tivey A, Patel C, Böhme U, Barrell BG, Parkhill J, Rajandream MA: Artemis and ACT: viewing, annotating and comparing sequences stored in a relational database. Bioinformatics. 2008, 24: 2672-2676. 10.1093/bioinformatics/btn529.
This work is dedicated to the memory of. Johanna Döbereiner. This work was funded with grants from the Conselho Nacional de Desenvolvimento Cientifico e Tecnólogico (CNPq), Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro Carlos Chagas Filho (FAPERJ) and Coordenação de Aperfeiçoamento de Pessoal de Nivel Superior (CAPES). We are grateful to Julian Parkhill and Martha Sorenson for helpful discussions and for critical reading of the manuscript.
PF coordinated the study. MB, AP, DC, TU, WK, PB, LP, DF, HM, JJ, VF, BF, AB, ES, GA, AN, RA, DC, DO, TS, JM, AV, PG, EN, VP, JA, AO, LR, HG, ER, JB, LF, VM, RS, ML and PF conducted genome sequencing. MB and ML conducted genome assembly. MB, LL, PB, SR, GF, VF, MF, GM, AC, AN, RA, JM, HG, EN, VP, ML, LS, JM, KT, JA, MV, SS, AO, LR, JB, CM, AH, SA, AMC, WA, MD, RS, EO, AR, ML, OM and PF performed sequence annotation. MB performed bioinformatics analyses and comparative genome analyzes. MB, SS, VP, EN, AO, LR, JB, CR, AMC, and PF analyzed the results and participated in writing sections of the manuscript. MB and PF assembled and wrote the final version of the manuscript. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Distribution of mobile elements in plant endophyte complete genomes. The percentage column: Percentage of total number of mobile elements from all CDS annotated on the endophyte complete genomes. (PDF 13 KB)
Additional file 2: Predicted Highly Expressed (PHX) genes. The PHX and proteomic analysis was used to indicate potentially important genes in the GDI genome. (XLS 46 KB)
Additional file 3: 16S phylogenetic tree from Alphaproteobacteria. The Neighbor joining phylogenetic tree of 16S from Alphaproteobacteria was done using ClustalX. In blue are the three completed genomes closest to G. diazotrophicus PAL5 available in GenBank. (EPS 57 KB)
Additional file 4: The 28 genome islands (GI) identified by GC3 and IVOMs. The GI column has the ID for each genome island. The integrase column shows which kind of integrase was found in each genome island. The CDS column shows how many CDS are inside the genome island. The Alien+GC3 column show how many CDS in each genome island were identified as accessory by both methods. The Related column shows which kinds of genes were found in each genome island. (PDF 13 KB)
Additional file 5: Variation in G. diazotrophicus strains. 20 different strains were tested for gene variation. 37 CDS were selected from 21 putative genome islands and 17 CDS were selected from putative core regions of the chromossome as control. (+): PCR positive. (-): PCR negative. (PDF 66 KB)
Additional file 6: Presence of homologues of the trbE gene among G. diazotrophicus strains. Total DNA of 11 Gluconacetobacter strains was completely digested with restriction enzymes EcoRI (a.) or EcoRV (b.), separated on agarose gel and submitted to Southern blot analysis using a fragment of CDS GDI0133 (trbE, part of type IV secretion system) as a probe. Numbers 1-10 represent G. diazotrophicus strains: Pal5 (1), 3R2 (2), URU (3), 38f2 (4), PRJ50(5), Pal3 (6), AF3 (7), PCRI (8), PPe4 (9), CNFe-550 (10). Number 11 represents G. johannae. In strain Pal5, only 3 bands are present, although the genome sequence indicates the presence of four copies of the trbE gene. However, the fourth trbE paralog (GDI1016) is more dissimilar to the probe sequence then the other three (GDI0133, GDI2742 e GDI2911), which may have prevented hybridization. (JPEG 49 KB)
Additional file 7: Distribution of percent ID from RBH results. In red all the RBH from Rhodospirillales order. In yellow all RBH from other Alphaproteobacteria class and in blue RBH from other genomes beside Alphaproteobacteria class. (EPS 759 KB)
Additional file 8: Number of Reciprocal Best Hits (RBH) in accessory and core regions. The first column shows the number of RBH for each organism in parentheses. The RBH in columns show the total number of RBH for each organism. The RBH % by organism columns shows the percent of RBH in relation with the total number of RBH found in accessory and core regions. RBH result has 708 RBH in accessory regions and 2,258 in core regions. The RBH % by organism columns shows the percentage of RBH in accessory and core regions for each organism or group. GOX = Gluconobacter oxydans 621H, GBE = Granulibacter bethesdensis CGDNIH, ACR = Acidiphilium cryptum JF-5, Rhiz = All the complete genomes from Rhizobiales order, Other Alpha = All other complete genomes from Alphaproteobacteria class, Beta = All complete genomes from Betaproteobacteria class, Gamma = All complete genomes from Gammaproteobacteria class, Others = All other complete genomes. (PDF 9 KB)
Additional file 10: Endophyte comparison. In gray, genes similar to all genomes (core + endophyte, see Methods). In blue, genes present in all endophyte but not in core genomes. In red, genes only similar to GDI and Azoarcus sp BH72. In purple, genes only similar to GDI and Methylobacterium populi BJ001 and in green genes that are only present in GDI and at least two other endophyte genome. (EPS 1 MB)
Additional file 11: Comparison of main signalling protein categories. AT, Agrobacterium tumefaciens C58; BJ, Bradyrhizobium japonicum USDA110; ML, Mesorhizobium loti MAFF303099, SM, Sinorhizobium meliloti 1021, GO, Gluconobacter oxydans 621H; RP, Rickettsia prowazekii MadridE; AB, Azoarcus sp. BH72; AE, Azoarcus sp. EbN1; XF, Xylella fastidiosa 9a5c; EC, Escherichia coli K12-MG1655. (PDF 14 KB)
Additional file 12: Comparison of main transport-related protein categories. AT, Agrobacterium tumefaciens C58; BJ, Bradyrhizobium japonicum USDA110; ML, Mesorhizobium loti MAFF303099, SM, Sinorhizobium meliloti 1021, GO, Gluconobacter oxydans 621H; RP, Rickettsia prowazekii MadridE; AB, Azoarcus sp. BH72; AE, Azoarcus sp. BH72, XF, Xylella fastidiosa 9a5c; EC, Escherichia coli K12-MG1655. (PDF 14 KB)
Additional file 13: Comparison among the two Gluconacetobacter diazotrophicus Pal5 genomic sequences. GDI-BR, NCBI RefSeq NC_010125, GDI-US, NCBI RefSeq NC_011365, GIs, Genome Islands. (PDF 13 KB)
Additional file 14: CDS list of the two Gluconacetobacter diazotrophicus Pal5 sequences. Sheet 1: Blast best hits list of CDS found in both genomes. Sheet 2: List of unique CDS found in chromosome from GeneBank file CP001189. Sheet 3: List of unique genes found in chromosome from GeneBank file AM889285 (this work). (XLS 505 KB)
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Bertalan, M., Albano, R., de Pádua, V. et al. Complete genome sequence of the sugarcane nitrogen-fixing endophyte Gluconacetobacter diazotrophicus Pal5. BMC Genomics 10, 450 (2009). https://doi.org/10.1186/1471-2164-10-450
- Horizontal Gene Transfer
- Endophytic Bacterium
- Genome Island
- Biological Nitrogen Fixation
- Accessory Region