TY - JOUR
T1 - Production and Characterization of a Novel Exopolysaccharide from Ramlibacter tataouinensis
AU - Jivkova, Desislava
AU - Sathiyanarayanan, Ganesan
AU - Harir, Mourad
AU - Hertkorn, Norbert
AU - Schmitt-Kopplin, Philippe
AU - Sanhaji, Ghislain
AU - Fochesato, Sylvain
AU - Berthomieu, Catherine
AU - Heyraud, Alain
AU - Achouak, Wafa
AU - Santaella, Catherine
AU - Heulin, Thierry
N1 - Funding Information:
D.J. has research fellowship from the ANRT (National Agency of Research and Technology) (CIFRE N° 2013/1063) and the ARD company.
Publisher Copyright:
© 2022 by the authors.
PY - 2022/10/24
Y1 - 2022/10/24
N2 - The current study examines the desiccation-resistant Ramlibacter tataouinensis TTB310T as a model organism for the production of novel exopolysaccharides and their structural features. This bacterium is able to produce dividing forms of cysts which synthesize cell-bound exopolysaccharide. Initial experiments were conducted on the enrichment of cyst biomass for exopolysaccharide production under batch-fed conditions in a pilot-scale bioreactor, with lactate as the source of carbon and energy. The optimized medium produced significant quantities of exopolysaccharide in a single growth phase, since the production of exopolysaccharide took place during the division of the cysts. The exopolysaccharide layer was extracted from the cysts using a modified trichloroacetic acid method. The biochemical characterization of purified exopolysaccharide was performed by gas chromatography, ultrahigh-resolution mass spectrometry, nuclear magnetic resonance, and Fourier-transform infrared spectrometry. The repeating unit of exopolysaccharide was a decasaccharide consisting of ribose, glucose, rhamnose, galactose, mannose, and glucuronic acid with the ratio 3:2:2:1:1:1, and additional substituents such as acetyl, succinyl, and methyl moieties were also observed as a part of the exopolysaccharide structure. This study contributes to a fundamental understanding of the novel structural features of exopolysaccharide from a dividing form of cysts, and, further, results can be used to study its rheological properties for various industrial applications.
AB - The current study examines the desiccation-resistant Ramlibacter tataouinensis TTB310T as a model organism for the production of novel exopolysaccharides and their structural features. This bacterium is able to produce dividing forms of cysts which synthesize cell-bound exopolysaccharide. Initial experiments were conducted on the enrichment of cyst biomass for exopolysaccharide production under batch-fed conditions in a pilot-scale bioreactor, with lactate as the source of carbon and energy. The optimized medium produced significant quantities of exopolysaccharide in a single growth phase, since the production of exopolysaccharide took place during the division of the cysts. The exopolysaccharide layer was extracted from the cysts using a modified trichloroacetic acid method. The biochemical characterization of purified exopolysaccharide was performed by gas chromatography, ultrahigh-resolution mass spectrometry, nuclear magnetic resonance, and Fourier-transform infrared spectrometry. The repeating unit of exopolysaccharide was a decasaccharide consisting of ribose, glucose, rhamnose, galactose, mannose, and glucuronic acid with the ratio 3:2:2:1:1:1, and additional substituents such as acetyl, succinyl, and methyl moieties were also observed as a part of the exopolysaccharide structure. This study contributes to a fundamental understanding of the novel structural features of exopolysaccharide from a dividing form of cysts, and, further, results can be used to study its rheological properties for various industrial applications.
KW - bioreactor
KW - biosynthesis
KW - characterization
KW - exopolysaccharide
KW - FT-ICR-MS
KW - FTIR
KW - GC
KW - NMR
KW - optimization
KW - Ramlibacter tataouinensis
U2 - 10.3390/molecules27217172
DO - 10.3390/molecules27217172
M3 - Article
C2 - 36364003
AN - SCOPUS:85141578718
SN - 1420-3049
VL - 27
JO - Molecules
JF - Molecules
IS - 21
M1 - 7172
ER -