Abstract
Co-expression of the two genes encoding the alpha- and beta-subunit of the Thermoplasma acidophilum thermosome in Escherichia coli yielded fully assembled hetero-oligomeric complexes (alpha+beta). Surprisingly, also separate expression of both genes resulted in formation of hexadecameric complexes (alpha, beta) in the bacterial cytoplasm. On electron micrographs these complexes were indistinguishable from each other and from the native thermosome. The recombinant alpha-complex as well as the native thermosome could be reconstituted in vitro from their dissociated subunits in the presence of Mg-ATP.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Adenosine Triphosphate / pharmacology
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Amino Acid Sequence
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Archaeal Proteins
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Base Sequence
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Blotting, Western
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Chromatography, Gel
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Cloning, Molecular
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Electrophoresis, Polyacrylamide Gel
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Escherichia coli / genetics
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Gene Expression Regulation, Bacterial / genetics
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Heat-Shock Proteins / chemistry
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Heat-Shock Proteins / genetics*
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Image Processing, Computer-Assisted
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Microscopy, Electron
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Molecular Chaperones / chemistry
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Molecular Chaperones / genetics*
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Molecular Sequence Data
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Protein Conformation
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Recombinant Proteins / genetics
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Recombinant Proteins / isolation & purification
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Thermoplasma / genetics*
Substances
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Archaeal Proteins
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Heat-Shock Proteins
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Molecular Chaperones
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Recombinant Proteins
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TF55 protein, Sulfolobus shibatae
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Adenosine Triphosphate