Article (Scientific journals)
Control of phenotypic diversification based on serial cultivations on different carbon sources leads to improved bacterial xylanase production
Romain, B.; Delvigne, Frank; Rémond, C. et al.
2022In Bioprocess and Biosystems Engineering, 45 (8), p. 1359 - 1370
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Keywords :
Lignocellulosic substrates; Phenotypic heterogeneity; Sporulation; Successive cultivations; Thermobacillus xylanilyticus; Xylanases; Bacteria; Carbon; Cytology; Enzymes; Esters; Metabolism; Straw; Substrates; Enzymatic activities; Enzyme production; Hemicellulases; Stationary phase; Successive cultivation; Thermobacillus xylanilyticu; Cells; acetylesterase; carbon; xylan 1,4 beta xylosidase; xylan endo 1,3 beta xylosidase; endo 1,4 beta xylanase; esterase; xylan; Article; carbon source; cell heterogeneity; controlled study; enzyme activity; enzyme synthesis; flow cytometry; Gram positive bacterium; nonhuman; phenotypic variation; wheat bran; bacterium; dietary fiber; metabolism; Dietary Fiber; Endo-1,4-beta Xylanases; Esterases; Xylans
Abstract :
[en] Thermobacillus xylanilyticus is a thermophilic and hemicellulolytic bacterium of interest for the production of thermostable hemicellulases. Enzymes’ production by this bacterium is challenging, because the proliferation of a cheating subpopulation of cells during exponential growth impairs the production of xylanase after serial cultivations. Accordingly, a strategy of successive cultivations with cells transfers in stationary phase and the use of wheat bran and wheat straw as carbon sources were tested. The ratio between subpopulations and their corresponding metabolic activities were studied by flow cytometry and the resulting hemicellulases production (xylanase, acetyl esterase and β-xylosidase) followed. During serial cultivations, the results pointed out an increase of the enzymatic activities. On xylan, compared to the first cultivation, the xylanase activity increases by 7.15-fold after only four cultivations. On the other hand, the debranching activities were increased by 5.88-fold and 57.2-fold on wheat straw and by 2.77-fold and 3.34-fold on wheat bran for β-xylosidase and acetyl esterase, respectively. The different enzymatic activities then stabilized, reached a plateau and further decreased. Study of the stability and reversibility of the enzyme production revealed cell-to-cell heterogeneities in metabolic activities which could be linked to the reversibility of enzymatic activity changes. Thus, the strategy of successive transfers during the stationary phase of growth, combined with the use of complex lignocellulosic substrates as carbon sources, is an efficient strategy to optimize the hemicellulases production by T. xylanilyticus, by preventing the selection of cheaters. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
Disciplines :
Biotechnology
Author, co-author :
Romain, B.;  Université de Reims Champagne-Ardenne, INRAE, FARE, UMR A 614, AFERE, Reims, France, Terra Research and Teaching Centre, Microbial Processes and Interactions (MiPI), Gembloux Agro‐Bio Tech, University of Liège, Gembloux, Belgium
Delvigne, Frank  ;  Université de Liège - ULiège > TERRA Research Centre > Microbial technologies
Rémond, C.;  Université de Reims Champagne-Ardenne, INRAE, FARE, UMR A 614, AFERE, Reims, France
Rakotoarivonina, H.;  Université de Reims Champagne-Ardenne, INRAE, FARE, UMR A 614, AFERE, Reims, France
Language :
English
Title :
Control of phenotypic diversification based on serial cultivations on different carbon sources leads to improved bacterial xylanase production
Publication date :
2022
Journal title :
Bioprocess and Biosystems Engineering
ISSN :
1615-7591
eISSN :
1615-7605
Publisher :
Springer Science and Business Media Deutschland GmbH
Volume :
45
Issue :
8
Pages :
1359 - 1370
Peer reviewed :
Peer Reviewed verified by ORBi
Funding text :
We are grateful to the material support of the MOBICYTE technical platform located at University of Reims Champagne-Ardennes (URCA) for the flow cytometer access. We are thankful to Damien Rioult from this technical platform for the different reservation and advice during the cytometry experiments. We are also grateful to Coralie Pierrot which performed different successive cultivations of Thermobacillus xylanilyticus described in this work. The work is part of a PhD grant provided by ULiège (Gembloux-Agro-Bio Tech) and a PhD contract in URCA. The authors are grateful to the French Region Grand Est and the Grand Reims for the financial support of the Chaire AFERE.
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