Literature DB >> 31210628

Identification and comparison of two closely related dextransucrases released by water kefir borne Lactobacillus hordei TMW 1.1822 and Lactobacillus nagelii TMW 1.1827.

Julia Bechtner1, Daniel Wefers2, Jonas Schmid1, Rudi F Vogel1, Frank Jakob1.   

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 Lactobacillus hordei TMW 1.1822 and Lactobacillus nagelii 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 L. nagelii TMW 1.1827 dextransucrase. L. hordei TMW 1.1822 released the enzyme only in the presence of its substrate sucrose in contrast to L. nagelii 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 O3-branched dextrans with a comparable degree of branching. Moreover, identical oligosaccharides were obtained for both dextrans upon endo-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 L. nagelii exhibited an averaged molecular weight (M w) of 7.9×107 Da, while those produced by the dextransucrase released by L. hordei exhibited an M w of 6.1×107 Da. Moreover, glycosylation of glucansucrases by LAB was identified for the first time for the released dextransucrase of L. nagelii TMW 1.1827. Our study therefore reveals new molecular insights into how dextransucrases released by water kefir borne L. hordei TMW 1.1822 and L. nagelii TMW 1.1827 contribute to the complex formation of the traditional beverage water kefir.

Entities:  

Keywords:  Dextransucrase; Lactobacillus hordei; Lactobacillus nagelii; Native Enzymes; Water kefir

Mesh:

Substances:

Year:  2019        PMID: 31210628     DOI: 10.1099/mic.0.000825

Source DB:  PubMed          Journal:  Microbiology        ISSN: 1350-0872            Impact factor:   2.777


  5 in total

1.  Insights into the pH-dependent, extracellular sucrose utilization and concomitant levan formation by Gluconobacter albidus TMW 2.1191.

Authors:  Frank Jakob; Clara Gebrande; Regina M Bichler; Rudi F Vogel
Journal:  Antonie Van Leeuwenhoek       Date:  2020-03-04       Impact factor: 2.271

2.  Analysis of Structural and Functional Differences of Glucans Produced by the Natively Released Dextransucrase of Liquorilactobacillus hordei TMW 1.1822.

Authors:  Jonas Schmid; Daniel Wefers; Rudi F Vogel; Frank Jakob
Journal:  Appl Biochem Biotechnol       Date:  2020-08-21       Impact factor: 2.926

3.  A systematic approach to study the pH-dependent release, productivity and product specificity of dextransucrases.

Authors:  Jonas Schmid; Julia Bechtner; Rudi F Vogel; Frank Jakob
Journal:  Microb Cell Fact       Date:  2019-09-10       Impact factor: 5.328

Review 4.  Exopolysaccharides Produced by Lactic Acid Bacteria: From Biosynthesis to Health-Promoting Properties.

Authors:  Dominika Jurášková; Susana C Ribeiro; Celia C G Silva
Journal:  Foods       Date:  2022-01-08

5.  The C-Terminal Domain of Liquorilactobacillus nagelii Dextransucrase Mediates the Production of Larger Dextrans Compared to Liquorilactobacillus hordei.

Authors:  Julia Bechtner; Verena Hassler; Daniel Wefers; Matthias Ehrmann; Frank Jakob
Journal:  Gels       Date:  2022-03-09
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.