Abstract
A protein from the cell lysate of Aspergillus oryzae was purified by column chromatography immobilized with a ferrichrysin (Fcy), which is one of the siderophores of A. oryzae. It is produced only in an iron-deficient culture and its molecular weight is estimated as 35,000 by SDS-PAGE. Two internal amino acid sequences of the protein obtained by lysylendopeptidase digestion were analyzed. Molecular cloning shows that it encodes 310 putative amino acid residues separated by 4 introns and is designated as fleA. It shows approximately 26% similarity with the gene encoding a fucose-specific lectin of Aleuria aurantia (AAL). The gene was overexpressed under control of the melO promoter in a submerged culture of A. oryzae. The fleA gene product showed hemagglutination activity against rabbit erythrocytes. A hemagglutination inhibition assay of monosaccharides showed that this lectin specifically binds to L-fucose and weakly reacts with mannose and N-acetyl-neuraminic acid. © 2002, Taylor & Francis Group, LLC. All rights reserved.
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Ishida, H., Moritani, T., Hata, Y., Kawato, A., Suginami, K., Abe, Y., & Imayasu, S. (2002). Molecular cloning and overexpression of fleA gene encoding a fucose-specific lectin of aspergillus oryzae. Bioscience, Biotechnology and Biochemistry, 66(5), 1002–1008. https://doi.org/10.1271/bbb.66.1002
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