Mutations produced by DNA polymerase III holoenzyme of Escherichia coli after in vitro synthesis in the absence of single‐strand binding protein

Summary Single‐stranded plasmid DNA, containing the mnt gene, was replicated in vitro with DNA polymerase III holoenzyme. Escherichia colimutH bacteria, defective in mismatch repair, were transformed with the products of in vitro synthesis. Mutations in mnt were readily identified and 33 out of 65 i...

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Veröffentlicht in:Molecular microbiology 1990-10, Vol.4 (10), p.1645-1652
Hauptverfasser: Carraway, M., Rewinski, C., Marinus, M. G.
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container_title Molecular microbiology
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creator Carraway, M.
Rewinski, C.
Marinus, M. G.
description Summary Single‐stranded plasmid DNA, containing the mnt gene, was replicated in vitro with DNA polymerase III holoenzyme. Escherichia colimutH bacteria, defective in mismatch repair, were transformed with the products of in vitro synthesis. Mutations in mnt were readily identified and 33 out of 65 isolates were single base changes including transition, transversion and frameshift mutations. The remaining 32 isolates were deletions of apparently random length and substitutions (deletion/insertions). The intergenic deletions as well as the transition and frameshift mutations were identical to those previously isolated from mismatch repair‐defective cells in vivo.
doi_str_mv 10.1111/j.1365-2958.1990.tb00541.x
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G.</creatorcontrib><title>Mutations produced by DNA polymerase III holoenzyme of Escherichia coli after in vitro synthesis in the absence of single‐strand binding protein</title><title>Molecular microbiology</title><addtitle>Mol Microbiol</addtitle><description>Summary Single‐stranded plasmid DNA, containing the mnt gene, was replicated in vitro with DNA polymerase III holoenzyme. Escherichia colimutH bacteria, defective in mismatch repair, were transformed with the products of in vitro synthesis. Mutations in mnt were readily identified and 33 out of 65 isolates were single base changes including transition, transversion and frameshift mutations. The remaining 32 isolates were deletions of apparently random length and substitutions (deletion/insertions). The intergenic deletions as well as the transition and frameshift mutations were identical to those previously isolated from mismatch repair‐defective cells in vivo.</description><subject>Bacteriology</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Chromosome Deletion</subject><subject>DNA Polymerase III - metabolism</subject><subject>DNA Replication</subject><subject>DNA Transposable Elements</subject><subject>DNA, Bacterial - biosynthesis</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Single-Stranded - biosynthesis</subject><subject>Escherichia coli</subject><subject>Escherichia coli - enzymology</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Bacterial</subject><subject>Genetics</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>Mutation</subject><subject>Plasmids</subject><subject>Templates, Genetic</subject><subject>Tetracycline Resistance - genetics</subject><issn>0950-382X</issn><issn>1365-2958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUU2P0zAQtRBoKQs_AclCYm8NdvxRhwtaLQtE2sIFJG6W40yoq9QudgKbPe1PQPxEfgkOrYAbwpcZvXkzb8YPoSeUFDS_Z9uCMimWZSVUQauKFENDiOC0uL6DFr9Ld9GCVIIsmSo_3kcPUtoSQhmR7ASd0EqyilYL9H09DmZwwSe8j6EdLbS4mfDLt-d4H_ppB9EkwHVd403oA_ibDOHQ4ctkNxCd3TiDbegdNt0AETuPv7ghBpwmP2wguTRDOcOmSeDtr97k_Kceftx-S0M0Pus532ZoXmAA5x-ie53pEzw6xlP04dXl-4s3y6t3r-uL86ulZTyfKEXHuWwpka0pV0J1dpWvzglhBoA1RgmzkpwTpkC0ghrStEpZ4LZpqKSGnaKzw9ys-3mENOidSxb63ngIY9KK5Hl8tfonkcqSEFbyTHx-INoYUorQ6X10OxMnTYmendNbPdujZ3v07Jw-Oqevc_Pjo8rY7KD903qwKtefHusmWdN3-eusS3_ROC8VVZn34sD76nqY_mMDvV7XVHLBfgI9wLju</recordid><startdate>199010</startdate><enddate>199010</enddate><creator>Carraway, M.</creator><creator>Rewinski, C.</creator><creator>Marinus, M. 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G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mutations produced by DNA polymerase III holoenzyme of Escherichia coli after in vitro synthesis in the absence of single‐strand binding protein</atitle><jtitle>Molecular microbiology</jtitle><addtitle>Mol Microbiol</addtitle><date>1990-10</date><risdate>1990</risdate><volume>4</volume><issue>10</issue><spage>1645</spage><epage>1652</epage><pages>1645-1652</pages><issn>0950-382X</issn><eissn>1365-2958</eissn><abstract>Summary Single‐stranded plasmid DNA, containing the mnt gene, was replicated in vitro with DNA polymerase III holoenzyme. Escherichia colimutH bacteria, defective in mismatch repair, were transformed with the products of in vitro synthesis. Mutations in mnt were readily identified and 33 out of 65 isolates were single base changes including transition, transversion and frameshift mutations. 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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Bacteriology
Base Sequence
Biological and medical sciences
Chromosome Deletion
DNA Polymerase III - metabolism
DNA Replication
DNA Transposable Elements
DNA, Bacterial - biosynthesis
DNA, Bacterial - genetics
DNA, Single-Stranded - biosynthesis
Escherichia coli
Escherichia coli - enzymology
Escherichia coli - genetics
Escherichia coli - metabolism
Fundamental and applied biological sciences. Psychology
Genes, Bacterial
Genetics
Microbiology
Molecular Sequence Data
Mutation
Plasmids
Templates, Genetic
Tetracycline Resistance - genetics
title Mutations produced by DNA polymerase III holoenzyme of Escherichia coli after in vitro synthesis in the absence of single‐strand binding protein
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