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Purification and characterization of lipoxygenase from the thermophilic fungus Thermomyces lanuginosus

Published online by Cambridge University Press:  18 April 2001

Duo-Chuan LI
Affiliation:
Laboratory of Molecular Biology, Department of Plant Protection, Shandong Agricultural University, Taian, Shandong 271018, Peoples' Republic of China. E-mail [email protected]
Zhen-Wei LUI
Affiliation:
Laboratory of Molecular Biology, Department of Plant Protection, Shandong Agricultural University, Taian, Shandong 271018, Peoples' Republic of China. E-mail [email protected]
Jing LU
Affiliation:
Laboratory of Molecular Biology, Department of Plant Protection, Shandong Agricultural University, Taian, Shandong 271018, Peoples' Republic of China. E-mail [email protected]
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Abstract

A thermostable intracellular lipoxygenase from Thermomyces lanuginosus was purified to sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) homogeneity by ion-exchange chromatography on diethylaminoethyl (DEAE)-Sepharose, ion-exchange chromatography on carboxymethyl (CM)-Sepharose and Phenyl-Sepharose hydrophobic interaction chromatography. The molecular weight of the enzyme was estimated to be 100 kDa by SDS-PAGE. The lipoxygenase exhibited maximal activities at pH 6.0. The optimum temperature for the activity was 55 °C. The enzyme was thermostable at 50 ° with half-lives at 60 ° of 20 min and 70 ° of about 7 min. The lipoxygenase activity was completely lost by heating at 80 ° for 5 min. The lipoxygenase catalyzed the oxidation of linoleic acid into 13-L-hydroperoxy-9,11(Z,E)-octadecadienoic acid(13-HPOD) as the major product. The enzyme had an apparent Km of 8.5 μM and Vmax of 10.8 μmol mg−1 min−1 with linoleic acid as substrate.

Type
Research Article
Copyright
© The British Mycological Society 2001

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