Bioscience, Biotechnology, and Biochemistry
Online ISSN : 1347-6947
Print ISSN : 0916-8451
Sequence Analysis of Replication Origin of Plasmid pLS11 of Bacillus subtilis IFO 3022
Toshio HARAKazuhiko NAKAJIMAHiroyuki SAITOAyaaki ISHIZAKISeiya OGATASeinosuke UEDA
Author information
JOURNAL FREE ACCESS

1992 Volume 56 Issue 2 Pages 223-227

Details
Abstract
The structure of a 1.6-kb SphI-HindIII DNA sequence necessary and sufficient for the replication of a 8.6-kb plasmid pLS11 of Bacillus subtilis IFO 3022, which is responsible for γ-polyglutamate production, has been characterized by using a trimethoprim (Tmp)-resistance gene derived form B. subtilis TTK24 chromosomal DNA as a selective marker. The 1.6-kb DNA sequence contains a rep gene encoding the protein (333 amino acids) essential for initiation of replication and a possible origin of replication. The predicted REP protein of pLS11 has an overall homology with the REP proteins of pUH1 (74.8% identity), pBAA1 (92.8%), and pFTB14 (78.7%) in Bacillus spp., pLP1 (42.1%) and pLAB1000 (36.3%) in Lactobacillus spp., and pUB110 (35.3%) and pC194 (37.4) in Staphylococcus aureus, but has not any similarity with the REP protein of the staphylococcal plasmid pT181.
Content from these authors

This article cannot obtain the latest cited-by information.

© Japan Society for Bioscience, Biotechnology, and Agrochemistry
Previous article Next article
feedback
Top