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Journal of Bacteriology, December 1999, p. 7545-7551, Vol. 181, No. 24
Discovery Research Laboratory, Tanabe Seiyaku
Co., Ltd., Yodogawa-ku, Osaka 532-8505,1 and
Toda, Saitama 335-8505,2 Japan
Received 10 June 1999/Accepted 5 October 1999
Two ATP-binding cassette (ABC) exporters are present in
Pseudomonas fluorescens no. 33; one is the recently
reported AprDEF system and the other is HasDEF, which exports a heme
acquisition protein, HasA. The hasDEF genes were cloned by
DNA hybridization with a DNA probe coding for the LipB protein, one of
the components of the Serratia marcescens ABC exporter Lip
system. P. fluorescens HasA showed sequence identity of 40 to 49% with HasA proteins from Pseudomonas aeruginosa and
Serratia marcescens. The P. fluorescens Has
exporter secreted HasA proteins from P. fluorescens and
P. aeruginosa but not S. marcescens HasA in
Escherichia coli, whereas the Has exporter from S. marcescens allowed secretion of all three HasA proteins. The
P. fluorescens HasDEF system also promoted the secretion of
the lipase and alkaline protease of P. fluorescens. Hybrid
exporter analysis demonstrated that the HasD proteins, which are ABC
proteins, are involved in the discrimination of export substrates.
Chimeric HasA proteins containing both P. fluorescens and
S. marcescens sequences were produced and tested for
secretion through the Has exporters. The C-terminal region of HasA was
shown to be involved in the secretion specificity of the P. fluorescens Has exporter.
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Cloning and Characterization of the
Pseudomonas fluorescens ATP-Binding Cassette Exporter,
HasDEF, for the Heme Acquisition Protein HasA
*
Corresponding author. Mailing address: Discovery
Research Laboratory, Tanabe Seiyaku Co., Ltd., 2-50, Kawagishi-2-chome,
Toda, Saitama 335-8505, Japan. Phone: (81-48) 433-8069. Fax: (81-48) 433-8159. E-mail: k-omori{at}tanabe.co.jp.
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