Dissection of exopolysaccharide biosynthesis in Kozakia baliensis

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Abstract

Background: Acetic acid bacteria (AAB) are well known producers of commercially used exopolysaccharides, such as cellulose and levan. Kozakia (K.) baliensis is a relatively new member of AAB, which produces ultra-high molecular weight levan from sucrose. Throughout cultivation of two K. baliensis strains (DSM 14400, NBRC 16680) on sucrose-deficient media, we found that both strains still produce high amounts of mucous, water-soluble substances from mannitol and glycerol as (main) carbon sources. This indicated that both Kozakia strains additionally produce new classes of so far not characterized EPS. Results: By whole genome sequencing of both strains, circularized genomes could be established and typical EPS forming clusters were identified. As expected, complete ORFs coding for levansucrases could be detected in both Kozakia strains. In K. baliensis DSM 14400 plasmid encoded cellulose synthase genes and fragments of truncated levansucrase operons could be assigned in contrast to K. baliensis NBRC 16680. Additionally, both K. baliensis strains harbor identical gum-like clusters, which are related to the well characterized gum cluster coding for xanthan synthesis in Xanthomanas campestris and show highest similarity with gum-like heteropolysaccharide (HePS) clusters from other acetic acid bacteria such as Gluconacetobacter diazotrophicus and Komagataeibacter xylinus. A mutant strain of K. baliensis NBRC 16680 lacking EPS production on sucrose-deficient media exhibited a transposon insertion in front of the gumD gene of its gum-like cluster in contrast to the wildtype strain, which indicated the essential role of gumD and of the associated gum genes for production of these new EPS. The EPS secreted by K. baliensis are composed of glucose, galactose and mannose, respectively, which is in agreement with the predicted sugar monomer composition derived from in silico genome analysis of the respective gum-like clusters. Conclusions: By comparative sugar monomer and genome analysis, the polymeric substances secreted by K. baliensis can be considered as unique HePS. Via genome sequencing of K. baliensis DSM 14400 + NBRC 16680 we got first insights into the biosynthesis of these novel HePS, which is related to xanthan and acetan biosynthesis. Consequently, the present study provides the basis for establishment of K. baliensis strains as novel microbial cell factories for biotechnologically relevant, unique polysaccharides.

Figures

  • Fig. 1 Monomer composition of the HePS isolated from K. baliensis strains DSM 14400 and NBRC 16680. HPLC profiles of the perchloric acid hydrolysates of HePS from K. baliensis DSM 14400 (a) and K. baliensis NBRC 16680 (b) in comparison with a 25 mM standard mix (dotted line) composed of d-glucose (13,43 min), d-galactose (15,21 min) and d-mannose (16,74 min). The retention times of the detected sugar monomers in the respective acid hydrolysates were consistent with the retention times of the standards
  • Fig. 2 Genome comparison and general features of K. baliensis strains DSM 14400 and NBRC 16680. Starting from inside: circle 1 shows the general genomic position in kilobases; circle 2 depicts the varying G+ C-content of K. baliensis DSM 14400 at different genetic loci; circle 3 is composed of the seven contigs of K. baliensis DSM 14400 [main chromosome and additional (partial) plasmids]; circle 4 reflects the coding density of K. baliensis DSM 14400; circle 5 shows the blast identities (red) of K. baliensis NBRC 16680 in comparison to K. baliensis DSM 14400 (note the low identity in plasmid regions)
  • Fig. 3 Genetic organization of HePS biosynthesis encoding gum-like clusters. The gum-like clusters of K. baliensis strains DSM 14400 + NBRC 16680 are depicted in (a). The cluster has an overall size of ~25 kb and involves 19 genes, including glycosyltransferases (gt), hypothetical proteins (hp), and eight gum like genes (gumB, -C, -D, -E, -H, -J, -K, and –M), which are marked in grey. Furthermore, the cluster contains a putative endoglucanase (e.g.), oxidoreductase (ox) and a UDP-glucose dehydrogenase (ugd). b, c show the related gum like clusters of the AAB strains Ga. diazotrophicus PAI5 and Komagataeibacter xylinus E25. The Ga. diazotrophicus cluster exhibits, in comparison to both K. baliensis clusters, an additional gumF gene, that could putatively incorporate acetyl-residues at specific positions into the related HePS. The so called acetan cluster of Ko. xylinus harbors—besides an additional gumF gene—a rhamnosyl transferase, coded by aceR, as well as a mannose-phosphate-guanyltransferase (mpg). The nomenclature for the acetan cluster in (c) is based on Griffin AM, Morris VJ and Gasson MJ [44], while brackets under the particular genes mark the homologous gum genes. In (d) the gum cluster of X. campestris, which consists of gumB, -C, -D, -E, -F, -G, -H, -I, -J, -K, -L, -M, -N and –P, is depicted. The dotted squares in the particular gum-clusters of B, C and D mark genes, which alter between the specific clusters (relative to both K. baliensis gum-like clusters). The corresponding monomer compositions of the respective HePSs are shown at the right. The putative functions of the corresponding annotated genes are as follows (derived from Pühler et al. [26] and Griffin et al. [45]): aceA UDP-glucosyltransferase, aceC GDP-mannosyltransferase, aceP glucosyltransferase, aceQ glucosyltransferase, aceR rhamnosyltransferase, gumJ export protein, gumE polymerization or export protein, gumK catalyzes the addition of glucuronic acid, gumD catalyzes the addition of glucose-1-phosphate, gumM catalyzes the addition of glucose in β-1,4-position, gumC polymerization and export protein, gumG acetyl transferase, gumL pyruvyl transferase, gumH catalyzes the addition of internal mannose, gumI β-mannosyltransferase, gumB polymerization and export protein, RE dTDP-4-dehydrorhamnose 3,5-epimerase, manB Mannose-1-phosphate guanylyltransferase, tp transporter
  • Table 1 Homology comparison between Gum proteins of K. baliensis DSM 14400 and Gum proteins of HePS biosynthesis related bacteria
  • Table 2 Overview of gum-genes and their corresponding predicted protein functions involved in xanthan biosynthesis in X. campestris [26]
  • Fig. 4 Schematic representation of the proposed nucleotide sugar biosynthesis related to EPS production in K. baliensis. Starting with the phosphorylation of fructose to fructose-6-phosphate (6) or glucose to glucose-6-phosphate (1), these intermediates can be converted into mannose-6-phosphate (7) or glucose-1-phosphate (2), respectively. Mannose-6-phosphate can be further converted into mannose1-phosphate (8) and finally into GDP-mannose. UGP (3) catalyzes the synthesis of UDP-glucose from glucose-1-phosphate. UDP-glucose can be further isomerized to UDP-galactose (4) or UDP-glucuronic acid (5). The proposed pathway for the biosynthesis of activated nucleotide sugar precursors is based on publications from Kornmann et al. [18] and Pühler et al. [26]. The corresponding genomic locations of these respective genes are listed in Additional file 2: Table S2: gk-gene coding for a Glucokinase (EC 2.7.1.2); 2: pgm-gene coding for a Phosphoglucomutase (EC 5.4.2.2); 3: ugp-gene coding for an UDP-glucose-1-phosphate uridylyltransferase (EC 2.7.7.9); 4: galE-gene coding for an UDP-glucose-4-epimerase (EC 5.1.3.2); 5: ugd-gene coding for an UDP-glucose dehydrogenase (EC 1.1.1.22); 6: fk-gene coding for a Fructokinase (EC 2.7.1.4); 7: mpi-gene coding for a Mannose-6-phosphate isomerase (EC 5.3.1.8); 8: pmm-gene coding for a Phosphomannomutase (EC 5.4.2.8); 9: mpg-gene coding for a Mannose-1-phosphate guanyltransferase (EC 2.7.7.22)
  • Fig. 5 Overview of additional EPS forming enzymes and clusters in K. baliensis. Figure (a) shows the levansucrase genes (ls) (EC 2.4.1.10) of K. baliensis DSM 14400 and NBRC 16680, flanked by a cysteine desulfurase (EC 2.8.1.7) (cd) and a ferric uptake regulation protein (fur), respectively. In (b) the genetic organization of the chromosomally located pol cluster of K. baliensis DSM 14400 is exemplarily depicted. The pol cluster contains 5 genes (polABCDE), which are functionally designated as polA: dTDP-glucose 4,6-dehydratase (EC 4.2.1.46), polB: glucose-1-phosphate thymidylyltransferase (EC 2.7.7.24), polC: dTDP-4-dehydrorhamnose 3,5-epimerase (EC 5.1.3.13), polD: dTDP-4-dehydrorhamnose reductase (EC 1.1.1.133), polE: alpha-L-Rha alpha-1,3-l-rhamnosyltransferase (EC 2.4.1.-). c Shows an additional plasmid located levansucrase gene (EC 2.4.1.10) of K. baliensis DSM 14400. It shares highest similarity to Ga. diazotrophicus levansucrase lsdA and is flanked by a (partial) type II dependent secretion operon [45]). In (d) is the genetic organization of the K. baliensis DSM 14400 cellulose synthase operon illustrated. The operon consists of six genes: dgc/pd diguanylate cyclase/phosphodiesterase (GGDEF & EAL domains) with PAS/PAC sensor(s), dgc diguanylate cyclase, bcsZ endoglucanase precursor (EC 3.2.1.4), bcsQ NTPase, bcsAB cellulose synthase catalytic subunit [UDP-forming] (EC 2.4.1.12), bcsC cellulose synthase operon protein C
  • Fig. 6 Comparison of K. baliensis NBRC 16680 wildtype and a HePS deficient mutant strain. a Phenotyps of K. baliensis NBRC 16680 rough (left, mutant) and smooth strain (right, wildtype); b isolatable polymeric substances from supernatants of K. baliensis NBRC 16680 wildtype strain (left) and K. baliensis NBRC 16680 mutant strain (right); c growth behavior of K. baliensis NBRC 16680 wildtype (left) and mutant strain (right) in static culture. The mutant strain exhibits a transposon insertion in its gum-like cluster (Fig. 7)

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Brandt, J. U., Jakob, F., Behr, J., Geissler, A. J., & Vogel, R. F. (2016). Dissection of exopolysaccharide biosynthesis in Kozakia baliensis. Microbial Cell Factories, 15(1). https://doi.org/10.1186/s12934-016-0572-x

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