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   <subfield code="a">Expression of plectasin in Bacillus subtilis using SUMO technology by a maltose-inducible vector</subfield>
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   <subfield code="c">[Licong Zhang, Xiaodan Li, Dandan Wei, Jue Wang, Anshan Shan, Zhongyu Li]</subfield>
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   <subfield code="a">Plectasin, the first fungus defensin, is especially efficient against Gram-positive bacteria. To explore an effective approach for expressing plectasin in Bacillus subtilis, the sequence encoding plectasin fused with the small ubiquitin-like modifier (SUMO) gene, the 6×His gene and the signal peptide of SacB were cloned into an E. coli-B. subtilis shuttle vector pGJ148 in which the maltose utilization operon promoter Pglv directed the expression. The fusion protein successfully secreted in culture and approximately, 41mg of the recombinant fusion protein SUMO-plectasin was purified per liter of culture supernatant. After purification by Ni-NTA resin column and digestion by SUMO protease, 5.5mg of plectasin with a purity of 94% was obtained from 1L fermentation culture. Recombinant plectasin was found inhibition activity against S. pneumoniae, S. aureus and S. epidermidis. These results indicate that the maltose-induced expression system may be a safe and efficient way for the large-scale production of soluble peptides in B. subtilis.</subfield>
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