4.4 Article

Cloning and expression of an α-1,3-glucanase gene from Bacillus circulans KA-304:: The enzyme participates in protoplast formation of Schizophyllum commune

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BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY
卷 70, 期 7, 页码 1754-1763

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TAYLOR & FRANCIS LTD
DOI: 10.1271/bbb.60095

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Bacillus circulans KA-304; Schizophyllum commune; protoplast; alpha-1,3-glucanase; mutanase

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A culture filtrate of Bacillus circulans KA-304 grown on a cell-wall preparation of Schizophyllum commune has an activity to form protoplasts from S. commune mycelia, and a combination of alpha-1,3-glucanase and chitinase I, which were isolated from the filtrate, brings about the protoplast-forming activity. The gene of alpha-1,3-glucanase was cloned from B. circulans KA-304. It consists of 3,879 nucleotides, which encodes 1,293 amino acids including a putative signal peptide (31 amino acid residues), and the molecular weight of alpha-1,3-glucanase without the putative signal peptide was calculated to be 132,184. The deduced amino acid sequence of alpha-1,3-glucanase of B. circulans KA-304 showed approximately 80% similarity to that of mutanase (alpha-1,3-glucanase) of Bacillus sp. RM1, but no significant similarity to those of fungal mutanases. The recombinant alpha-1,3-glucanase was expressed in Escherichia coli Rosetta-gami B (DE 3), and significant alpha-1,3-glucanase activity was detected in the cell-free extract of the organism treated with isopropyl-beta-D-thiogalactopyranoside. The recombinant alpha-1,3-glucanase showed protoplast-forming activity when the enzyme was combined with chitinase I.

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