Previous Article | Next Article 
J Bacteriol. 1994 May; 176(9): 2492-2501
The fas operon of Rhodococcus fascians encodes new genes required for efficient fasciation of host plants.
M Crespi,
D Vereecke,
W Temmerman,
M Van Montagu and
J Desomer
Laboratorium voor Genetica, Universiteit Gent, Belgium.
ABSTRACT
Three virulence loci (fas, att, and hyp) of Rhodococcus fascians D188 have been identified on a 200-kb conjugative linear plasmid (pFiD188). The fas locus was delimited to a 6.5-kb DNA fragment by insertion mutagenesis, single homologous disruptive recombination, and in trans complementation of different avirulent insertion mutants. The locus is arranged as a large operon containing six open reading frames whose expression is specifically induced during the interaction with host plants. One predicted protein is homologous to P-450 cytochromes from actinomycetes. The putative ferredoxin component is of a novel type containing additional domains homologous to transketolases from chemoautotrophic, photosynthetic, and methylotrophic microorganisms. Genetic analysis revealed that fas encodes, in addition to the previously identified ipt, at least two new genes that are involved in fasciation development, one of which is only required on older tobacco plants.
J Bacteriol. 1994 May; 176(9): 2492-2501
This article has been cited by other articles:
-
Uroz, S., Oger, P. M., Chapelle, E., Adeline, M.-T., Faure, D., Dessaux, Y.
(2008). A Rhodococcus qsdA-Encoded Enzyme Defines a Novel Class of Large-Spectrum Quorum-Quenching Lactonases. Appl. Environ. Microbiol.
74: 1357-1366
[Abstract]
[Full Text]
-
Vandeputte, O., Oden, S., Mol, A., Vereecke, D., Goethals, K., El Jaziri, M., Prinsen, E.
(2005). Biosynthesis of Auxin by the Gram-Positive Phytopathogen Rhodococcus fascians Is Controlled by Compounds Specific to Infected Plant Tissues. Appl. Environ. Microbiol.
71: 1169-1177
[Abstract]
[Full Text]
-
Seth-Smith, H. M. B., Rosser, S. J., Basran, A., Travis, E. R., Dabbs, E. R., Nicklin, S., Bruce, N. C.
(2002). Cloning, Sequencing, and Characterization of the Hexahydro-1,3,5-Trinitro-1,3,5-Triazine Degradation Gene Cluster from Rhodococcus rhodochrous. Appl. Environ. Microbiol.
68: 4764-4771
[Abstract]
[Full Text]
-
Brown, S. E., Knudson, D. L., Ishimaru, C. A.
(2002). Linear Plasmid in the Genome of Clavibacter michiganensis subsp. sepedonicus. J. Bacteriol.
184: 2841-2844
[Abstract]
[Full Text]
-
Vereecke, D., Cornelis, K., Temmerman, W., Jaziri, M., Van Montagu, M., Holsters, M., Goethals, K.
(2002). Chromosomal Locus That Affects Pathogenicity of Rhodococcus fascians. J. Bacteriol.
184: 1112-1120
[Abstract]
[Full Text]
-
Fernandes, P. J., Powell, J. A. C., Archer, J. A. C.
(2001). Construction of Rhodococcus random mutagenesis libraries using Tn5 transposition complexes. Microbiology
147: 2529-2536
[Abstract]
[Full Text]
-
Temmerman, W., Vereecke, D., Dreesen, R., Van Montagu, M., Holsters, M., Goethals, K.
(2000). Leafy Gall Formation Is Controlled by fasR, an AraC-Type Regulatory Gene in Rhodococcus fascians. J. Bacteriol.
182: 5832-5840
[Abstract]
[Full Text]
-
Saito, A., Iwabuchi, T., Harayama, S.
(2000). A Novel Phenanthrene Dioxygenase from Nocardioides sp. Strain KP7: Expression in Escherichia coli. J. Bacteriol.
182: 2134-2141
[Abstract]
[Full Text]
-
Bittinger, M. A., Handelsman, J.
(2000). Identification of Genes in the RosR Regulon of Rhizobium etli. J. Bacteriol.
182: 1706-1713
[Abstract]
[Full Text]
-
Kalogeraki, V. S., Winans, S. C.
(1998). Wound-Released Chemical Signals May Elicit Multiple Responses from an Agrobacterium tumefaciens Strain Containing an Octopine-Type Ti Plasmid. J. Bacteriol.
180: 5660-5667
[Abstract]
[Full Text]
-
Pisabarro, A., Correia, A., Martín, J. F.
(1998). Characterization of the rrnB Operon of the Plant Pathogen Rhodococcus fascians and Targeted Integrations of Exogenous Genes at rrn Loci. Appl. Environ. Microbiol.
64: 1276-1282
[Abstract]
[Full Text]
Copyright © 1994 by the American Society for Microbiology. All rights reserved.