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Applied and Environmental Microbiology, December 2001, p. 5721-5728, Vol. 67, No. 12
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.12.5721-5728.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Differential Synthesis of Peritoxins and Precursors by Pathogenic Strains of the Fungus Periconia circinata

Alice C. L. Churchill,1,* Larry D. Dunkle,2 Walter Silbert,1,dagger Kevin J. Kennedy,1,Dagger and Vlado Macko1

Boyce Thompson Institute, Cornell University, Ithaca, New York 14853-1801,1 and USDA-Agricultural Research Service, Department of Botany and Plant Pathology, Purdue University, West Lafayette, Indiana 47907-11552

Received 7 March 2001/Accepted 20 September 2001

Pathogenic strains of the soilborne fungus Periconia circinata produce peritoxins with host-selective toxicity against susceptible genotypes of sorghum. The peritoxins are low-molecular-weight, hybrid molecules consisting of a peptide and a chlorinated polyketide. Culture fluids from pathogenic, toxin-producing (Tox+) and nonpathogenic, non-toxin-producing (Tox-) strains were analyzed directly by gradient high-performance liquid chromatography (HPLC) with photodiode array detection and HPLC-mass spectrometry to detect intermediates and final products of the biosynthetic pathway. This approach allowed us to compare the metabolite profiles of Tox+ and Tox- strains. Peritoxins A and B and the biologically inactive intermediates, N-3-(E-pentenyl)-glutaroyl-aspartate, circinatin, and 7-chlorocircinatin, were detected only in culture fluids of the Tox+ strains. The latter two compounds were produced consistently by Tox+ strains regardless of the amount of peritoxins produced under various culture conditions. In summary, none of the known peritoxin-related metabolites were detected in Tox- strains, which suggests that these strains may lack one or more functional genes required for peritoxin biosynthesis.


* Corresponding author. Mailing address: Boyce Thompson Institute, Cornell University, Tower Rd., Ithaca, NY 14853-1801. Phone: (607) 254-1355. Fax: (607) 254-2958. E-mail: acc7{at}cornell.edu.

dagger Present address: Department of Medicine, University of Rochester, Rochester, NY 14607.

Dagger Present address: Oridigm Corporation, Seattle, WA 98103-8012.


Applied and Environmental Microbiology, December 2001, p. 5721-5728, Vol. 67, No. 12
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.12.5721-5728.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.