Subcellular location of enzymes involved in oxidation of n-alkane by Cladosporium resinae |
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Authors: | P. Goswami J. J. Cooney |
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Affiliation: | (1) Environmental, Coastal and Ocean Sciences Department, University of Massachusetts Boston, Boston, 100 Morrissey Boulevard, MA 02125-3393, USA e-mail: jjc@capecod.net, US |
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Abstract: | More than 70% of n-hexadecane-grown cells of Cladosporium resinae ATCC 22711 were converted to spheroplasts when they were treated with chitinase and lytic enzyme from Trichoderma harziamum. The light mitochondrial fraction, containing microbodies, mitochondria and vacuoles, was isolated from spheroplasts. Vacuoles in cells were demonstrated by the inability of acridine orange to stain organelles previously treated with 2.5 μM Bafilomycin A1, a vacuolar ATPase inhibitor. Microbodies, mitochondria and vacuoles were separated from the light mitochondrial fraction by self-generated density-gradient ultracentrifugation using iodixanol as gradient medium. NADH-dependent n-alkane monooxygenase activity and fatty alcohol oxidase activity were located in the cytoplasm and mitochondrial fractions respectively. Received: 21 September 1998 / Received revision: 21 January 1999 / Accepted: 31 January 1999 |
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