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Dextran synthesized by Leuconostoc mesenteroides BD1710 in tomato juice supplemented with sucrose

•The growth characteristic of Leuconostoc mesenteroides BD1710 in tomato juice supplemented with 15% sucrose was investigated.•L. mesenteroides BD1710 synthesized 32gL−1 dextran in the tomato juice sucrose medium, comparable to the yield in chemical defined medium.•The L. mesenteroides BD1710 dextra...

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Bibliographic Details
Published in:Carbohydrate polymers 2014-11, Vol.112, p.556-562
Main Authors: Han, Jin, Hang, Feng, Guo, Benheng, Liu, Zhenmin, You, Chunpin, Wu, Zhengjun
Format: Article
Language:English
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Summary:•The growth characteristic of Leuconostoc mesenteroides BD1710 in tomato juice supplemented with 15% sucrose was investigated.•L. mesenteroides BD1710 synthesized 32gL−1 dextran in the tomato juice sucrose medium, comparable to the yield in chemical defined medium.•The L. mesenteroides BD1710 dextran was with a peak molecular weight of 6.35×105Da, a linear backbone composed of consecutive α-(1→6)-linked d-glucopyranosyl units and approximately 6% α-(1→3) branches.•The BD1710 dextran could be easily solubilized in deionized water at 0.1%, and formed glutinous, translucent solution at higher concentrations. The characteristics of the growth of Leuconostoc mesenteroides BD1710 and the synthesis of dextran in tomato juice supplemented with 15% sucrose were assayed. L. mesenteroides BD1710 could synthesize approximately 32gL−1 dextran in the tomato-juice–sucrose medium when cultured at 28°C for 48h, which was on the same level as the dextran yield in a chemically defined medium. The viscosity of the cultured tomato-juice–sucrose medium with various dextran contents was also measured. The results of the monosaccharide composition, molecular-weight distribution, Fourier transform infrared spectra (FTIR) and nuclear magnetic resonance spectra (NMR) showed that the polysaccharide synthesized by L. mesenteroides BD1710 in the tomato-juice–sucrose medium was dextran with a peak molecular weight of 6.35×105Da, a linear backbone composed of consecutive α-(1→6)-linked d-glucopyranosyl units and approximately 6% α-(1→3) branches.
ISSN:0144-8617
1879-1344
DOI:10.1016/j.carbpol.2014.06.035