1887

Abstract

Dextransucrases are extracellular enzymes, which are exclusively expressed by lactic acid bacteria (LAB) and produce α−1→6 linked glucose polymers from sucrose. In this study, two dextransucrases derived from water kefir borne TMW 1.1822 and TMW 1.1827 were identified and comparatively investigated. Differences between both proteins mainly arise from an additional C-terminal glucan-binding domain and the presence of a signal motif in the TMW 1.1827 dextransucrase. TMW 1.1822 released the enzyme only in the presence of its substrate sucrose in contrast to TMW 1.1827, while both strains functionally expressed the dextransucrases independently of sucrose. Both enzymes could be recovered as crude protein extracts in culture supernatants, as they are not covalently bound to the cell surface. This enabled the formation of dextrans at equal reaction conditions as well as their subsequent structural analysis in terms of molecular structure and molecular weight. The volumetric transglycosylation and hydrolysis activities were distinctly different for both enzymes, which produced -branched dextrans with a comparable degree of branching. Moreover, identical oligosaccharides were obtained for both dextrans upon -dextranase digestion, while some differences in the polysaccharide fine structures could be identified from the varying portions of certain oligosaccharides. Dextrans synthesized by the dextransucrase released by exhibited an averaged molecular weight ( ) of 7.9×10 Da, while those produced by the dextransucrase released by exhibited an of 6.1×10 Da. Moreover, glycosylation of glucansucrases by LAB was identified for the first time for the released dextransucrase of TMW 1.1827. Our study therefore reveals new molecular insights into how dextransucrases released by water kefir borne TMW 1.1822 and TMW 1.1827 contribute to the complex formation of the traditional beverage water kefir.

Loading

Article metrics loading...

/content/journal/micro/10.1099/mic.0.000825
2019-09-01
2024-04-25
Loading full text...

Full text loading...

/deliver/fulltext/micro/165/9/956.html?itemId=/content/journal/micro/10.1099/mic.0.000825&mimeType=html&fmt=ahah

References

  1. Monsan P, Bozonnet S, Albenne C, Joucla G, Willemot RM et al. Homopolysaccharides from lactic acid bacteria. Int Dairy J 2001; 11:675–685 [View Article]
    [Google Scholar]
  2. van Geel-Schutten GH, Flesch F, ten Brink B, Smith MR, Dijkhuizen L. Screening and characterization of Lactobacillus strains producing large amounts of exopolysaccharides. Appl Microbiol Biotechnol 1998; 50:697–703 [View Article]
    [Google Scholar]
  3. De Vuyst L, Degeest B. Heteropolysaccharides from lactic acid bacteria. FEMS Microbiol Rev 1999; 23:153–177 [View Article]
    [Google Scholar]
  4. Leemhuis H, Pijning T, Dobruchowska JM, van Leeuwen SS, Kralj S et al. Glucansucrases: three-dimensional structures, reactions, mechanism, α-glucan analysis and their implications in biotechnology and food applications. J Biotechnol 2013; 163:250–272 [View Article]
    [Google Scholar]
  5. Sidebotham RL. Dextrans. In Tipson RS, Horton D. (editors) Advances in Carbohydrate Chemistry and Biochemistry 30 Academic Press; 1974 pp 371–444
    [Google Scholar]
  6. Cantarel BL, Coutinho PM, Rancurel C, Bernard T, Lombard V et al. The carbohydrate-active enzymes database (CAZy): an expert resource for glycogenomics. Nucleic Acids Res 2009; 37:D233–D238 [View Article]
    [Google Scholar]
  7. Monchois V, Willemot RM, Monsan P. Glucansucrases: mechanism of action and structure-function relationships. FEMS Microbiol Rev 1999; 23:131–151 [View Article]
    [Google Scholar]
  8. Mooser G. Glycosidases and glycosyltransferases. In Sigman DS. editor The Enzymes 20 Academic Press; 1992 pp 187–233
    [Google Scholar]
  9. Van Geel-Schutten GH, Faber EJ, Smit E, Bonting K, Smith MR et al. Biochemical and structural characterization of the glucan and fructan exopolysaccharides synthesized by the Lactobacillus reuteri wild-type strain and by mutant strains. Appl Environ Microbiol 1999; 65:3008–3014
    [Google Scholar]
  10. van Hijum SAFT, Kralj S, Ozimek LK, Dijkhuizen L, van Geel-Schutten IGH. Structure-function relationships of glucansucrase and fructansucrase enzymes from lactic acid bacteria. Microbiol Mol Biol Rev 2006; 70:157–176 [View Article]
    [Google Scholar]
  11. Funane K, Ookura T, Kobayashi M. Glucan binding regions of dextransucrase from Leuconostoc mesenteroides NRRL B-512F. Biosci Biotechnol Biochem 1998; 62:123–127 [View Article]
    [Google Scholar]
  12. Monchois V, Reverte A, Remaud-Simeon M, Monsan P, Willemot RM. Effect of Leuconostoc mesenteroides NRRL B-512F dextransucrase carboxy-terminal deletions on dextran and oligosaccharide synthesis. Appl Environ Microbiol 1998; 64:1644–1649
    [Google Scholar]
  13. Remaud-Simeon M, Willemot RM, Sarçabal P, Potocki de Montalk G, Monsan P. Glucansucrases: molecular engineering and oligosaccharide synthesis. J Mol Catal B Enzym 2000; 10:117–128 [View Article]
    [Google Scholar]
  14. Wong C, Hefta SA, Paxton RJ, Shively JE, Mooser G. Size and subdomain architecture of the glucan-binding domain of sucrose:3-alpha-D-glucosyltransferase from Streptococcus sobrinus . Infect Immun 1990; 58:2165–2170
    [Google Scholar]
  15. Prechtl RM, Wefers D, Jakob F, Vogel RF. Cold and salt stress modulate amount, molecular and macromolecular structure of a Lactobacillus sakei dextran. Food Hydrocoll 2018; 82:73–81 [View Article]
    [Google Scholar]
  16. Ua-Arak T, Jakob F, Vogel RF. Fermentation pH modulates the size distributions and functional properties of Gluconobacter albidus TMW 2.1191 Levan. Front Microbiol 2017; 8:807 [View Article]
    [Google Scholar]
  17. Stadie J, Gulitz A, Ehrmann MA, Vogel RF. Metabolic activity and symbiotic interactions of lactic acid bacteria and yeasts isolated from water kefir. Food Microbiol 2013; 35:92–98 [View Article]
    [Google Scholar]
  18. Gulitz A, Stadie J, Wenning M, Ehrmann MA, Vogel RF. The microbial diversity of water kefir. Int J Food Microbiol 2011; 151:284–288 [View Article]
    [Google Scholar]
  19. Pidoux M. The microbial flora of sugary kefir grain (the gingerbeer plant): biosynthesis of the grain fromLactobacillus hilgardii producing a polysaccharide gel. World J Microbiol Biotechnol 1989; 5:223–238 [View Article]
    [Google Scholar]
  20. Fels L, Jakob F, Vogel RF, Wefers D. Structural characterization of the exopolysaccharides from water kefir. Carbohydr Polym 2018; 189:296–303 [View Article]
    [Google Scholar]
  21. Laureys D, De Vuyst L. Microbial species diversity, community dynamics, and metabolite kinetics of water kefir fermentation. Appl Environ Microbiol 2014; 80:2564–2572 [View Article]
    [Google Scholar]
  22. Xu D, Fels L, Wefers D, Behr J, Jakob F et al. Lactobacillus hordei dextrans induce Saccharomyces cerevisiae aggregation and network formation on hydrophilic surfaces. Int J Biol Macromol 2018; 115:236–242 [View Article]
    [Google Scholar]
  23. De MAN JC, Rogosa M, Sharpe ME. A medium for the cultivation of lactobacilli. J Appl Bacteriol 1960; 23:130–135 [View Article]
    [Google Scholar]
  24. Blum H, Beier H, Gross HJ. Improved silver staining of plant proteins, RNA and DNA in polyacrylamide gels. Electrophoresis 1987; 8:93–99 [View Article]
    [Google Scholar]
  25. Frank A, Pevzner P. PepNovo: de novo peptide sequencing via probabilistic network modeling. Anal Chem 2005; 77:964–973 [View Article]
    [Google Scholar]
  26. Perkins DN, Pappin DJ, Creasy DM, Cottrell JS. Probability-based protein identification by searching sequence databases using mass spectrometry data. Electrophoresis 1999; 20:3551–3567 [View Article]
    [Google Scholar]
  27. Petersen TN, Brunak S, von Heijne G, Nielsen H. SignalP 4.0: Discriminating signal peptides from transmembrane regions. Nat Methods 2011; 8:785–786 [View Article]
    [Google Scholar]
  28. Kumar S, Stecher G, Tamura K. MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol Biol Evol 2016; 33:1870–1874 [View Article]
    [Google Scholar]
  29. Robert X, Gouet P. Deciphering key features in protein structures with the new ENDscript server. Nucleic Acids Res 2014; 42:W320–W324 [View Article]
    [Google Scholar]
  30. Jones DT, Taylor WR, Thornton JM. The rapid generation of mutation data matrices from protein sequences. Comput Appl Biosci 1992; 8:275–282 [View Article]
    [Google Scholar]
  31. Jakob F, Pfaff A, Novoa-Carballal R, Rübsam H, Becker T et al. Structural analysis of fructans produced by acetic acid bacteria reveals a relation to hydrocolloid function. Carbohydr Polym 2013; 92:1234–1242 [View Article]
    [Google Scholar]
  32. Yuryev V, Tomasik P, Bertoft E. Starch: Achievements in understanding of structure and functionality New York: Nova Science Publishers; 2007 pp 1–315
    [Google Scholar]
  33. Ua-Arak T, Jakob F, Vogel RF. Influence of levan-producing acetic acid bacteria on buckwheat-sourdough breads. Food Microbiol 2017; 65:95–104 [View Article]
    [Google Scholar]
  34. Münkel F, Wefers D. Fine structures of different dextrans assessed by isolation and characterization of endo-dextranase liberated isomalto-oligosaccharides. Carbohydr Polym 2019; 215:296–306 [View Article]
    [Google Scholar]
  35. Bechtner J, Xu D, Behr J, Ludwig C, Vogel RF. Proteomic analysis of Lactobacillus nagelii in the presence of Saccharomyces cerevisiae isolated from water kefir and comparison with Lactobacillus hordei . Front Microbiol 2019; 10:325 [View Article]
    [Google Scholar]
  36. Xu D, Bechtner J, Behr J, Eisenbach L, Geißler AJ et al. Lifestyle of Lactobacillus hordei isolated from water kefir based on genomic, proteomic and physiological characterization. Int J Food Microbiol 2019; 290:141–149 [View Article]
    [Google Scholar]
  37. Öner ET, Hernández L, Combie J. Review of levan polysaccharide: from a century of past experiences to future prospects. Biotechnol Adv 2016; 34:827–844 [View Article]
    [Google Scholar]
  38. Kralj S, van Geel-Schutten GH, Dondorff MMG, Kirsanovs S, van der Maarel MJEC et al. Glucan synthesis in the genus Lactobacillus: isolation and characterization of glucansucrase genes, enzymes and glucan products from six different strains. Microbiology 2004; 150:3681–3690 [View Article]
    [Google Scholar]
  39. Gagic D, Wen W, Collett MA, Rakonjac J. Unique secreted-surface protein complex of Lactobacillus rhamnosus , identified by phage display. MicrobiologyOpen 2013; 2:1–17 [View Article]
    [Google Scholar]
  40. Bensing BA, Seepersaud R, Yen YT, Sullam PM. Selective transport by SecA2: an expanding family of customized motor proteins. Biochim Biophys Acta 1843; 2014:1674–1686
    [Google Scholar]
  41. Langsford ML, Gilkes NR, Singh B, Moser B, Miller RC et al. Glycosylation of bacterial cellulases prevents proteolytic cleavage between functional domains. FEBS Letters 1987; 225:163–167 [View Article]
    [Google Scholar]
  42. Ogrydziak DM, Proteases YE. Yeast extracellular proteases. Crit Rev Biotechnol 1993; 13:1–55 [View Article]
    [Google Scholar]
  43. Rühmkorf C, Bork C, Mischnick P, Rübsam H, Becker T et al. Identification of Lactobacillus curvatus TMW 1.624 dextransucrase and comparative characterization with Lactobacillus reuteri TMW 1.106 and Lactobacillus animalis TMW 1.971 dextransucrases. Food Microbiol 2013; 34:52–61 [View Article]
    [Google Scholar]
  44. Kralj S, van Geel-Schutten GH, van der Maarel MJEC, Dijkhuizen L. Biochemical and molecular characterization of Lactobacillus reuteri 121 reuteransucrase. Microbiology 2004; 150:2099–2112 [View Article]
    [Google Scholar]
  45. Lis M, Shiroza T, Kuramitsu HK. Role of C-terminal direct repeating units of the Streptococcus mutans glucosyltransferase-S in glucan binding. Appl Environ Microbiol 1995; 61:2040–2042
    [Google Scholar]
  46. Porras-Domínguez JR, Ávila-Fernández Á, Miranda-Molina A, Rodríguez-Alegría ME, Munguía AL. Bacillus subtilis 168 levansucrase (SacB) activity affects average levan molecular weight. Carbohydr Polym 2015; 132:338–344 [View Article]
    [Google Scholar]
  47. Falconer DJ, Mukerjea R, Robyt JF. Biosynthesis of dextrans with different molecular weights by selecting the concentration of Leuconostoc mesenteroides B-512FMC dextransucrase, the sucrose concentration, and the temperature. Carbohydr Res 2011; 346:280–284 [View Article]
    [Google Scholar]
  48. Abo H, Matsumura T, Kodama T, Ohta H, Fukui K et al. Peptide sequences for sucrose splitting and glucan binding within Streptococcus sobrinus glucosyltransferase (water-insoluble glucan synthetase). J Bacteriol 1991; 173:989–996 [View Article]
    [Google Scholar]
  49. Kingston KB, Allen DM, Jacques NA. Role of the C-terminal YG repeats of the primer-dependent streptococcal glucosyltransferase, GtfJ, in binding to dextran and mutan. Microbiology 2002; 148:549–558 [View Article]
    [Google Scholar]
  50. Shah DSH, Joucla G, Remaud-Simeon M, Russell RRB. Conserved repeat motifs and glucan binding by glucansucrases of oral streptococci and Leuconostoc mesenteroides . J Bacteriol 2004; 186:8301–8308 [View Article]
    [Google Scholar]
  51. Janecek S, Svensson B, Russell RR. Location of repeat elements in glucansucrases of Leuconostoc and Streptococcus species. FEMS Microbiol Lett 2000; 192:53–57 [View Article]
    [Google Scholar]
http://instance.metastore.ingenta.com/content/journal/micro/10.1099/mic.0.000825
Loading
/content/journal/micro/10.1099/mic.0.000825
Loading

Data & Media loading...

Supplements

Supplementary material 1

PDF
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error