Improved recovery of active recombinant laccase from maize seed

• Published in: Applied microbiology and biotechnology Vol. 63; no. 4; pp. 390 - 397
• Main Authors: BAILEY, M. R, WOODARD, S. L, VAN GASTEL, F, HOWARD, J. A, HOOD, E. E, CALLAWAY, E, BEIFUSS, K, MAGALLANES-LUNDBACK, M, LANE, J. R, HORN, M. E, MALLUBHOTLA, H, DELANEY, D. D, WARD, M
• Format: Journal Article
• Language: English
• Published: Berlin Springer 2004; Springer Nature B.V
• Subjects: Apoenzymes; Apoenzymes - isolation & purification; Apoenzymes - metabolism; Biological and medical sciences; Biotechnology; Chloride; Chlorides - metabolism; Copper; Copper - metabolism; Corn; Data processing; Enzyme engineering; Enzymes; Fundamental and applied biological sciences. Psychology; Fungal Proteins - genetics; Improved methods for extraction and purification of enzymes; Laccase; Laccase - biosynthesis; Laccase - genetics; Laccase - isolation & purification; Lignin - metabolism; Methods. Procedures. Technologies; Plants, Genetically Modified - enzymology; Plants, Genetically Modified - genetics; Polymerization; Polyporales - enzymology; Polyporales - genetics; Purification; Q1; Q2; Recombinant Proteins - biosynthesis; Recombinant Proteins - genetics; Recombinant Proteins - isolation & purification; Seeds; Seeds - enzymology; Zea mays; Zea mays - enzymology; Zea mays - genetics; Monocotyledones; Seeds; Purification; Zea mays; Enzyme; Fungi; Gramineae; Angiospermae; Spermatophyta; Oxidoreductases; Recombinant protein; Thallophyta; Laccase
• DOI: 10.1007/s00253-003-1362-z
• ISSN: 0175-7598

Lignolytic enzymes such as laccase have been difficult to over-express in an active form. This paper describes the expression, characterization, and application of a fungal laccase in maize seed. The transgenic seed contains immobilized and extractable laccase. Fifty ppm dry weight of aqueously extractable laccase was obtained, and the remaining solids contained a significant amount of immobilized laccase that was active. Although a portion of the extractable laccase was produced as inactive apoenzyme, laccase activity was recovered by treatment with copper and chloride. In addition to allowing the apoenzyme to regain activity, treatment with copper also provided a partial purification step by precipitating other endogenous corn proteins while leaving >90% of the laccase in solution. The data also demonstrate the application of maize-produced laccase as a polymerization agent. The apparent concentration of laccase in ground, defatted corn germ is approximately 0.20% of dry weight.