High and efficient isomaltulose production using an engineered Yarrowia lipolytica strain

[Display omitted] •Exogenous sucrose isomerase was successfully expressed in Y. lipolytica.•SIase in Y. lipolytica showed high activity, stability, and product specificity.•Isomaltulose concentration was highest (572.1 g/L) in a 10-L fermentor.•Recombinant SIase secretion was coupled to enzymatic ca...

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Veröffentlicht in:Bioresource technology 2018-10, Vol.265, p.577-580
Hauptverfasser: Zhang, Peng, Wang, Zhi-Peng, Sheng, Jun, Zheng, Yuan, Ji, Xiao-Feng, Zhou, Hai-Xiang, Liu, Xiao-Yan, Chi, Zhen-Ming
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Sprache:eng
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Zusammenfassung:[Display omitted] •Exogenous sucrose isomerase was successfully expressed in Y. lipolytica.•SIase in Y. lipolytica showed high activity, stability, and product specificity.•Isomaltulose concentration was highest (572.1 g/L) in a 10-L fermentor.•Recombinant SIase secretion was coupled to enzymatic catalysis in a 2-stage process. Isomaltulose is an ideal functional sweetener and has been approved as a safe sucrose substitute. It is produced mainly through sucrose isomerization catalyzed by sucrose isomerase. Here, to produce food-grade isomaltulose and improve its yield, the sucrose isomerase gene from Pantoea dispersa UQ68J was overexpressed in the non-pathogenic yeast Yarrowia lipolytica. When the engineered strain, S47, was fermented on 600 g/L sucrose in a 10-L bioreactor, a maximum isomaltulose concentration of 572.1 g/L was achieved. Sucrose isomerase activity was 7.43 U/mL, and yield reached 0.96 g/g. Moreover, monosaccharide byproducts were simultaneously transformed into intracellular lipids, thus reducing the production of undesirable compounds and resulting in high isomaltulose purity (97.8%) in the final broth. In summary, the bioprocess employed in this study provides an efficient alternative strategy for isomaltulose production.
ISSN:0960-8524
1873-2976
DOI:10.1016/j.biortech.2018.06.081