Abstract
The diversity of opines from 43 naturally occurring crown gall tumors on several plant species was analyzed for the presence of agropine, chrysopine, iminodiacid, an unidentified leucinopine-like iminodiacid (IDA-B), mannopine, octopine, nopaline, DL- and LL-succinamopine, leucinopine and heliopine. Opine utilization patterns of agrobacteria and fluorescent pseudomonads resident in a tumor were then analyzed and compared for agreement with the opine isolated from that tumor. Nopaline was the most common opine found and was detected in tumors from cherry, blackberry, grape, and plum. Octopine was not found, although octopine-catabolizing bacteria were isolated from several tumors. A new, previously undescribed iminodiacid of the succinamopine-leucinopine type (provisionally designated IDA-B) was isolated from tumors of wild blackberry. Field tumors from apple, blueberry and grape yielded no detectable opines, even though opine-utilizing bacteria were present. Bacterial isolates from plum and cherry showed the best correspondence between the opine in tumors (nopaline) and the presence of bacteria that catabolized that opine. However, several unusual opine catabolic combinations were identified, including isolates that catabolized a variety of opines but were nonpathogenic. More variability was observed among isolates from field tumors on the remaining plant species. We isolated novel mannopine-nopaline type agrobacteria from field tumors of cherry, plum and blackberry that induced tumors containing either mannopine (plus agropine) or nopaline, but not both. Epidemiologically, the galled plants from an area were not of clonal origin (same Ti plasmid), indicating that the field tumors from a small area were incited by more than one type of Ti plasmid.
Full Text
The Full Text of this article is available as a PDF (195.1 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Beauchamp C. J., Chilton W. S., Dion P., Antoun H. Fungal catabolism of crown gall opines. Appl Environ Microbiol. 1990 Jan;56(1):150–155. doi: 10.1128/aem.56.1.150-155.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bell C. R., Cummings N. E., Canfield M. L., Moore L. W. Competition of Octopine-Catabolizing Pseudomonas spp. and Octopine-Type Agrobacterium tumefaciens for Octopine in Chemostats. Appl Environ Microbiol. 1990 Sep;56(9):2840–2846. doi: 10.1128/aem.56.9.2840-2846.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bell C. R., Moore L. W., Canfield M. L. Growth of Octopine-Catabolizing Pseudomonas spp. under Octopine Limitation in Chemostats and Their Potential To Compete with Agrobacterium tumefaciens. Appl Environ Microbiol. 1990 Sep;56(9):2834–2839. doi: 10.1128/aem.56.9.2834-2839.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Blocquel H., Justin J., Lafforgue P., Petit S. Etude comparative de la maturation de la seconde molaire supérieure et inférieure selon le sexe de l'enfant. J Int Assoc Dent Child. 1983 Dec;14(2):61–68. [PubMed] [Google Scholar]
- Bouzar H., Chilton W. S., Nesme X., Dessaux Y., Vaudequin V., Petit A., Jones J. B., Hodge N. C. A new Agrobacterium strain isolated from aerial tumors on Ficus benjamina L. Appl Environ Microbiol. 1995 Jan;61(1):65–73. doi: 10.1128/aem.61.1.65-73.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bouzar H., Moore L. W. Isolation of different agrobacterium biovars from a natural oak savanna and tallgrass prairie. Appl Environ Microbiol. 1987 Apr;53(4):717–721. doi: 10.1128/aem.53.4.717-721.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bélanger C., Canfield M. L., Moore L. W., Dion P. Genetic analysis of nonpathogenic Agrobacterium tumefaciens mutants arising in crown gall tumors. J Bacteriol. 1995 Jul;177(13):3752–3757. doi: 10.1128/jb.177.13.3752-3757.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chang C. C., Jayaswal R. K., Chen C. M., Gelvin S. B. Altered imino diacid synthesis and transcription in crown gall tumors with transposon Tn5 insertions in the 3' end of the octopine synthase gene. J Bacteriol. 1989 Nov;171(11):5922–5927. doi: 10.1128/jb.171.11.5922-5927.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chilton M. D., Drummond M. H., Merio D. J., Sciaky D., Montoya A. L., Gordon M. P., Nester E. W. Stable incorporation of plasmid DNA into higher plant cells: the molecular basis of crown gall tumorigenesis. Cell. 1977 Jun;11(2):263–271. doi: 10.1016/0092-8674(77)90043-5. [DOI] [PubMed] [Google Scholar]
- Chilton W. S., Chilton M. D. Mannityl opine analogs allow isolation of catabolic pathway regulatory mutants. J Bacteriol. 1984 May;158(2):650–658. doi: 10.1128/jb.158.2.650-658.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chilton W. S., Tempé J., Matzke M., Chilton M. D. Succinamopine: a new crown gall opine. J Bacteriol. 1984 Feb;157(2):357–362. doi: 10.1128/jb.157.2.357-362.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dessaux Y., Tempé J., Farrand S. K. Genetic analysis of mannityl opine catabolism in octopine-type Agrobacterium tumefaciens strain 15955. Mol Gen Genet. 1987 Jun;208(1-2):301–308. doi: 10.1007/BF00330457. [DOI] [PubMed] [Google Scholar]
- Guyon P., Chilton M. D., Petit A., Tempé J. Agropine in "null-type" crown gall tumors: Evidence for generality of the opine concept. Proc Natl Acad Sci U S A. 1980 May;77(5):2693–2697. doi: 10.1073/pnas.77.5.2693. [DOI] [PMC free article] [PubMed] [Google Scholar]
- KING E. O., WARD M. K., RANEY D. E. Two simple media for the demonstration of pyocyanin and fluorescin. J Lab Clin Med. 1954 Aug;44(2):301–307. [PubMed] [Google Scholar]
- LaPointe G., Nautiyal C. S., Chilton W. S., Farrand S. K., Dion P. Spontaneous mutation conferring the ability to catabolize mannopine in Agrobacterium tumefaciens. J Bacteriol. 1992 Apr;174(8):2631–2639. doi: 10.1128/jb.174.8.2631-2639.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Montoya A. L., Chilton M. D., Gordon M. P., Sciaky D., Nester E. W. Octopine and nopaline metabolism in Agrobacterium tumefaciens and crown gall tumor cells: role of plasmid genes. J Bacteriol. 1977 Jan;129(1):101–107. doi: 10.1128/jb.129.1.101-107.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nautiyal C. S., Dion P. Characterization of the Opine-Utilizing Microflora Associated with Samples of Soil and Plants. Appl Environ Microbiol. 1990 Aug;56(8):2576–2579. doi: 10.1128/aem.56.8.2576-2579.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nautiyal C. S., Dion P., Chilton W. S. Mannopine and mannopinic acid as substrates for Arthrobacter sp. strain MBA209 and Pseudomonas putida NA513. J Bacteriol. 1991 May;173(9):2833–2841. doi: 10.1128/jb.173.9.2833-2841.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Schell J., Van Montagu M., De Beuckeleer M., De Block M., Depicker A., De Wilde M., Engler G., Genetello C., Hernalsteens J. P., Holsters M. Interactions and DNA transfer between Agrobacterium tumefaciens, the Ti-plasmid and the plant host. Proc R Soc Lond B Biol Sci. 1979 Apr 11;204(1155):251–266. doi: 10.1098/rspb.1979.0026. [DOI] [PubMed] [Google Scholar]
- Tremblay G., Gagliardo R., Chilton W. S., Dion P. Diversity among Opine-Utilizing Bacteria: Identification of Coryneform Isolates. Appl Environ Microbiol. 1987 Jul;53(7):1519–1524. doi: 10.1128/aem.53.7.1519-1524.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vaudequin-Dransart V., Petit A., Poncet C., Ponsonnet C., Nesme X., Jones J. B., Bouzar H., Chilton W. S., Dessaux Y. Novel Ti plasmids in Agrobacterium strains isolated from fig tree and chrysanthemum tumors and their opinelike molecules. Mol Plant Microbe Interact. 1995 Mar-Apr;8(2):311–321. doi: 10.1094/mpmi-8-0311. [DOI] [PubMed] [Google Scholar]