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Applied and Environmental Microbiology, April 2004, p. 2110-2118, Vol. 70, No. 4
0099-2240/04/$08.00+0     DOI: 10.1128/AEM.70.4.2110-2118.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Root Nodule Bradyrhizobium spp. Harbor tfdA and cadA, Homologous with Genes Encoding 2,4-Dichlorophenoxyacetic Acid-Degrading Proteins

Faculty of Life and Environmental Science, Shimane University, Matsue, Shimane 690-8504,¹ Institute for Biological Resources and Functions, National Institute of Advanced Industrial Science and Technology (WAIST), Tsukuba, Ibaraki 305-8566, Japan²

Received 12 September 2003/ Accepted 10 December 2003

The distribution of tfdA and cadA, genes encoding 2,4-dichlorophenoxyacetate (2,4-D)-degrading proteins which are characteristic of the 2,4-D-degrading Bradyrhizobium sp. isolated from pristine environments, was examined by PCR and Southern hybridization in several Bradyrhizobium strains including type strains of Bradyrhizobium japonicum USDA110 and Bradyrhizobium elkanii USDA94, in phylogenetically closely related Agromonas oligotrophica and Rhodopseudomonas palustris, and in 2,4-D-degrading Sphingomonas strains. All strains showed positive signals for tfdA, and its phylogenetic tree was congruent with that of 16S rRNA genes in -Proteobacteria, indicating evolution of tfdA without horizontal gene transfer. The nucleotide sequence identities between tfdA and canonical tfdA in ß- and -Proteobacteria were 46 to 57%, and the deduced amino acid sequence of TfdA revealed conserved residues characteristic of the active site of -ketoglutarate-dependent dioxygenases. On the other hand, cadA showed limited distribution in 2,4-D-degrading Bradyrhizobium sp. and Sphingomonas sp. and some strains of non-2,4-D-degrading B. elkanii. The cadA genes were phylogenetically separated between 2,4-D-degrading and nondegrading strains, and the cadA genes of 2,4-D degrading strains were further separated between Bradyrhizobium sp. and Sphingomonas sp., indicating the incongruency of cadA with 16S rRNA genes. The nucleotide sequence identities between cadA and tftA of 2,4,5-trichlorophenoxyacetate-degrading Burkholderia cepacia AC1100 were 46 to 53%. Although all root nodule Bradyrhizobium strains were unable to degrade 2,4-D, three strains carrying cadA homologs degraded 4-chlorophenoxyacetate with the accumulation of 4-chlorophenol as an intermediate, suggesting the involvement of cadA homologs in the cleavage of the aryl ether linkage. Based on codon usage patterns and GC content, it was suggested that the cadA genes of 2,4-D-degrading and nondegrading Bradyrhizobium spp. have different origins and that the genes would be obtained in the former through horizontal gene transfer.

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