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 Previous Article

J Bacteriol, May 1998, p. 2796-2799, Vol. 180, No. 10
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Cloning and Physical Mapping of the EcoRI Fragments of the Giant Linear Plasmid SCP1

Matthias Redenbach,1,2 Kazuya Ikeda,1 Masayuki Yamasaki,1 and Haruyasu Kinashi1,*

Department of Molecular Biotechnology, Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527, Japan,1 and Genome Research Unit, Department of Genetics, Kaiserslautern University, D-67653 Kaiserslautern, Germany2

Received 25 November 1997/Accepted 10 March 1998

A cosmid library was constructed for the 350-kb giant linear plasmid SCP1 and aligned on a successive linear map. Only a 0.8-kb gap has remained uncloned in the terminal inverted repeats close to both ends. Partial digestion of the aligned cosmids with EcoRI and hybridization with the flanking fragments of the vector enabled physical mapping of all of the EcoRI fragments. On this map, the methylenomycin biosynthetic gene cluster, the insertion sequence IS466, and the sapCDE genes coding for spore-associated proteins were localized.


* Corresponding author. Mailing address: Department of Molecular Biotechnology, Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527, Japan. Phone: 81-824-7869. Fax: 81-824-24-7869. E-mail: kinashi{at}ipc.hiroshima-u.ac.jp.


J Bacteriol, May 1998, p. 2796-2799, Vol. 180, No. 10
0021-9193/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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