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Molecular cloning and nucleotide sequence of the mutT mutator of Escherichia coli that causes A:T to C:G transversion
Authors:Masahiro Akiyama   Takashi Horiuchi  Mutsuo Sekiguchi
Affiliation:(1) Department of Biology, Faculty of Science, Kyushu University 33, 812 Fukuoka, Japan;(2) Department of Molecular Biology, Graduate School of Medical Science, Kyushu University 33, 812 Fukuoka, Japan;(3) Department of Biochemistry, Faculty of Medicine, Kyushu University 33, 812 Fukuoka, Japan
Abstract:Summary The Escherichia coli mutator gene mutT, which causes A:TrarrC:G transversion, was cloned in pBR 322. mutT+ plasmids carry a 0.9 kb PvuII DNA fragment derived from the E. coli chromosome. Specific labelling of plasmid-encoded proteins by the maxicell method revealed that mutT codes for a polypeptide of about 15,000 daltons. The protein was overproduced when the mutT gene was placed under the control of the lac regulatory region on a multicopy runaway plasmid. The nucleotide sequence of the mutT gene was determined by the dideoxy method.Abbreviations Ap ampicillin - IPTG isopropyl-beta-d-thiogalactopyranoside - kb kilobase pair(s) - kDa kilodalton(s) - SDS sodium dodecyl sulphate - Tc tetracycline
Keywords:mutT mutator  Escherichia coli  A:T  /content/r13328u667325261/xxlarge8594.gif"   alt="  rarr"   align="  BASELINE"   BORDER="  0"  >C:G transversion  Molecular cloning  Nucleotide sequence
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