Abstract
A mutant Xanthomonas maltophilia BT-112 with high α-anomer-selective glycosylation activity was screened by a series of mutation methods including UV light, N-methyl-N-nitro-N-nitroso-guanidine treatment and quick neutron mutation. The α-arbutin titer increased 15-folds compared with the parent strain. The optimal conditions for culture medium and the operational conditions for lab-scale fermenter were investigated. Under optimized conditions, the maximal hydroquinone (HQ) tolerance of cells and yield of α-arbutin were 120 mM and 30.6 g/l, respectively. The molar conversion yield of α-arbutin based on the amount of HQ supplied reached 93.6 %. The product was identified as α-arbutin by 13C NMR and 1H NMR analysis. In conclusion, the results in this work provide a one-step and cost-effective method for the large-scale production of α-arbutin. © 2013 Springer Science+Business Media Dordrecht.
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Liu, C. Q., Deng, L., Zhang, P., Zhang, S. R., Liu, L., Xu, T., … Tan, T. W. (2013). Screening of high α-arbutin producing strains and production of α-arbutin by fermentation. World Journal of Microbiology and Biotechnology, 29(8), 1391–1398. https://doi.org/10.1007/s11274-013-1302-8
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