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Updated: Aug 8, 2026

Detection of Toxin Translocation into the Host Cytosol by Surface Plasmon Resonance
Published on: January 3, 2012
The Active Site on the Phytotoxin of Corynebacterium sepedonicum
1Department of Botany and Microbiology, Montana State University, Bozeman, Montana 59715.
Abstract:
Corynebacterium sepedonicum produces an extracellular phytotoxic glycopeptide that possesses a capacity to wilt plant cuttings. It has been previously demonstrated that the integrity of some of the membranes of the host cells is destroyed, suggesting the possibility that a biologically active site is present on the toxin molecule. The toxin was chemically altered in the following ways and then tested for biological activity: (a) the NH(2)-terminal group on the peptide portion of the toxin was blocked by the dansylation technique; (b) the OH groups on the sugar and amino acid residues as well as the NH groups on the amino acid residues were blocked by exhaustive methylation; (c) the COO(-) groups were converted to their respective methyl esters; (d) the peptide moiety was removed by pronase digestion. Experimental results indicate that the carboxyl groups of the nonpeptide portion of the molecule are responsible for the biological activity of the toxin. Other experiments showed that the toxin does not affect the membranes of animal cells.The biological activity of the glycopeptide, as well as its chemically altered derivatives, was determined by an instrument designated as a wilt-o-meter that quantitatively measures the strength of plant cuttings. A description of this instrument, how it is used, and how it can be manufactured is also included in this report.
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