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Journal of Bacteriology, April 2001, p. 2576-2585, Vol. 183, No. 8
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.8.2576-2585.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Genetic Organization of the Region Encoding Regulation,
Biosynthesis, and Transport of Rhizobactin 1021, a Siderophore
Produced by Sinorhizobium meliloti
Damien
Lynch,1
John
O'Brien,2
Timothy
Welch,3
Paul
Clarke,1
Páraic
Ó
Cuív,1
Jorge H.
Crosa,3 and
Michael
O'Connell1,*
School of Biotechnology, Dublin City
University, Dublin 9, Ireland1; Max
Planck Institute for Molecular Genetics, D14195 Berlin,
Germany2; and Department of Molecular
Microbiology and Immunology, Oregon Health Sciences University,
Portland, Oregon 97201-30983
Received 26 May 2000/Accepted 26 January 2001
Eight genes have been identified that function in the
regulation, biosynthesis, and transport of rhizobactin 1021, a
hydroxamate siderophore produced under iron stress by
Sinorhizobium meliloti. The genes were sequenced, and
transposon insertion mutants were constructed for phenotypic analysis.
Six of the genes, named rhbABCDEF, function in the
biosynthesis of the siderophore and were shown to constitute an
operon that is repressed under iron-replete conditions. Another
gene in the cluster, named rhtA, encodes the outer membrane receptor protein for rhizobactin 1021. It was shown to be regulated by
iron and to encode a product having 61% similarity to IutA, the outer
membrane receptor for aerobactin. Transcription of both the
rhbABCDEF operon and the rhtA gene was
found to be positively regulated by the product of the eighth gene in
the cluster, named rhrA, which has characteristics of an
AraC-type transcriptional activator. The six genes in the
rhbABCDEF operon have interesting gene junctions
with short base overlaps existing between the genes. Similarities
between the protein products of the biosynthesis genes and other
proteins suggest that rhizobactin 1021 is synthesized by the formation of a novel siderophore precursor, 1,3-diaminopropane, which is then modified and attached to citrate in steps resembling those of the aerobactin biosynthetic pathway. The cluster of genes is
located on the pSyma megaplasmid of S. meliloti 2011. Reverse transcription-PCR with RNA isolated from mature alfalfa
nodules yielded no products for rhbF or rhtA at
a time when the nifH gene was strongly expressed,
indicating that siderophore biosynthesis and transport genes are not
strongly expressed when nitrogenase is being formed in root nodules.
Mutants having transposon insertions in the biosynthesis or transport
genes induced effective nitrogen-fixing nodules on alfalfa plants.
*
Corresponding author. Mailing address: School of
Biotechnology, Dublin City University, Glasnevin, Dublin 9, Ireland.
Phone: 353-1-7005318. Fax: 353-1-7005412. E-mail:
michael.oconnell{at}dcu.ie.
Journal of Bacteriology, April 2001, p. 2576-2585, Vol. 183, No. 8
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.8.2576-2585.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
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