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Heterologous expression and characterization of Bacillus coagulans l-arabinose isomerase.

World J Microbiol Biotechnol.. 2012-05;  28(5):2205-2212
Zhou X, Wu JC. Institute of Chemical and Engineering Sciences, Agency for Science, Technology and Research (A STAR), 1 Pesek Road, Jurong Island 627833, Singapore.
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摘要

Bacillus coagulans has been of great commercial interest over the past decade owing to its strong ability of producing optical pure L: -lactic acid from both hexose and pentose sugars including L: -arabinose with high yield, titer and productivity under thermophilic conditions. The L: -arabinose isomerase (L-AI) from Bacillus coagulans was heterologously over-expressed in Escherichia coli. The open reading frame of the L-AI has 1,422 nucleotides encoding a protein with 474 amino acid residues. The recombinant L-AI was purified to homogeneity by one-step His-tag affinity chromatography. The molecular mass of the enzyme was estimated to be 56 kDa by SDS-PAGE. The enzyme was most active at 70°C and pH 7.0. The... More

关键词

l-arabinose; l-arabinose isomerase; Bacillus coagulans; l-ribulose; Bioconversion