Restriction enzyme analysis and localization of Bacillus subtilis chromosomal fragment partially suppressing recB recC mutations of Escherichia coli

Authors

  • F. Sh. Gizatullin V. I. Ulyanov-Lenin State University of Kazan, Kazan, USSR Author
  • B. I. Barabanschikov V. I. Ulyanov-Lenin State University of Kazan, Kazan, USSR Author

DOI:

https://doi.org/10.7124/bc.000095

Abstract

The original plasmid pKUl partially suppressing recB21 recC22 mutations of E. coli contains a 6.9 kb chromosomal fragment of B. subtilis. Using this plasmid an inte-grative vector for B. subtilis was constructed. The complementation analysis revealed that the cloned fragment contained a new B. subtilis gene, which codes the exonuclease activity of ATP-dependent DNAse and differs from recE5 and recH genes. The new gene, designated as recQ, has been located in glyB region on 75° of the B. subtilis genetic map.

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Published

1989-01-20

Issue

Section

Gene-Engineering Biotechnology