Abstract
A plasmid able to transform and to be stably maintained both in Sulfolobus solfataricus and in Escherichia coli was constructed by insertion into an E. coli plasmid of the autonomously replicating sequence of the virus particle SSV1 and a suitable mutant of the hph (hygromycin phosphotransferase) gene as the transformation marker. The vector suffered no rearrangement and/or chromosome integration, and its copy number in Sulfolobus was increased by exposure of the cells to mitomycin C.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Base Sequence
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DNA Primers / genetics
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DNA Replication
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DNA, Archaeal / genetics
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Drug Resistance, Microbial / genetics
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Escherichia coli / genetics
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Escherichia coli / metabolism
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Genes, Archaeal
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Genetic Vectors*
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Hygromycin B / pharmacology
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Mutation
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Phosphotransferases (Alcohol Group Acceptor) / genetics
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Plasmids / genetics
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Sulfolobus / drug effects
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Sulfolobus / genetics*
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Sulfolobus / metabolism
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Transformation, Genetic*
Substances
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DNA Primers
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DNA, Archaeal
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Hygromycin B
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Phosphotransferases (Alcohol Group Acceptor)
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hygromycin-B kinase