Genetic Organization of the Region Encoding Regulation, Biosynthesis, and Transport of Rhizobactin 1021, a Siderophore Produced by Sinorhizobium meliloti
- 15 April 2001
- journal article
- research article
- Published by American Society for Microbiology in Journal of Bacteriology
- Vol. 183 (8) , 2576-2585
- https://doi.org/10.1128/jb.183.8.2576-2585.2001
Abstract
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.Keywords
This publication has 56 references indexed in Scilit:
- High efficiency transformation of Escherichia coli with plasmidsPublished by Elsevier ,2003
- High-Resolution Physical Map of the Sinorhizobium meliloti 1021 pSyma MegaplasmidJournal of Bacteriology, 2000
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- Siderophore‐mediated iron metabolism in growth and nitrogen fixation by alfalfa nodulated withRhizobium melilotiJournal of Plant Nutrition, 1996
- The Organization of Intercistronic Regions of the Aerobactin Operon of pCoIV-K30 may Account for the Differential Expression of the iucABCD iutA GenesJournal of Molecular Biology, 1994
- Versatile suicide vectors which allow direct selection for gene replacement in Gram-negative bacteriaGene, 1993
- Isolation and structure of rhizobactin 1021, a siderophore from the alfalfa symbiont Rhizobium meliloti 1021Journal of the American Chemical Society, 1993
- Physiological characteristics ofRhizobium meliloti1021 Tn5 mutants with altered rhizobactin activitiesJournal of Plant Nutrition, 1992
- Cloning a genomic region required for a high‐affinity iron‐uptake system in Rhizobium meliloti 1021Molecular Microbiology, 1989
- R Factor Transfer in Rhizobium leguminosarumMicrobiology, 1974