Previous Article | Next Article ![]()
Journal of Bacteriology, August 2000, p. 4500-4504, Vol. 182, No. 16
Department of Biological Sciences, Louisiana
State University, Baton Rouge, Louisiana 70803,1
and Departments of Genetics and Medicine, Stanford University
School of Medicine, Stanford, California 943052
Received 17 March 2000/Accepted 24 May 2000
The tra gene of Streptomyces lividans
plasmid pIJ101 encodes a 621-amino-acid protein that can mediate both
plasmid transfer and the interbacterial transfer of chromosomal genes
(i.e., chromosome-mobilizing ability [Cma]) during mating. Here we
report the results of in-frame insertional mutagenesis studies aimed at
defining regions of Tra required for these functions. While hexameric
linker insertions throughout the tra gene affected plasmid
and chromosomal gene transfer, insertions in a 200-amino-acid region of
the Tra protein that contains presumed nucleotide-binding motifs and
that is widely conserved among a functionally diverse family of
bacterial and plasmid proteins (K. J. Begg, S. J. Dewar, and
W. D. Donachie, J. Bacteriol. 177:6211-6222, 1995) had especially
prominent effects on both functions. Insertions near the N terminus of
Tra reduced Cma for either circular or linear host chromosomes to a
much greater extent than pIJ101 plasmid transfer. Our results suggest
that Cma involves Tra functions incremental to those needed for plasmid DNA transfer.
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Mutational Analysis of the tra Locus of
the Broad-Host-Range Streptomyces Plasmid pIJ101
*
Corresponding author. Mailing address: Department of
Biological Sciences, Louisiana State University, 508 Life Sciences
Bldg., Baton Rouge, LA 70803. Phone: (225) 388-2798. Fax: (225)
388-2597. E-mail: gpettis{at}unixl.sncc.lsu.edu.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»