Article first published online: 21 NOV 2012
© 2012 The Authors New Phytologist © 2012 New Phytologist Trust
Volume 197, Issue 2, page 680, January 2013
How to Cite
(2013), Corrigendum. New Phytologist, 197: 680. doi: 10.1111/nph.12076
- Issue published online: 18 DEC 2012
- Article first published online: 21 NOV 2012
Vol. 192, Issue 3, 566–569, Article first published online: 19 OCT 2011
- indole glucosinolates;
- innate immunity;
- microbe-associated molecular pattern (MAMP);
- nonhost resistance;
New Phytologist 192 (2011), 566–569.
Since its publication, it has been brought to our attention that there is an error in Fig. 2 of Clay (2011), where the chemical structure of rapalexin A is incorrect in that the isothiocyanate group is attached to the indole ring via a methylene group; the isothiocyanate should be directly attached to the indole ring. The correct figure is printed below.
We apologize to our readers for this mistake.
- 2009. The multifunctional enzyme CYP71B15 (PHYTOALEIN DEFICIENT3) converts cysteine-indole-3-acetonitrile to camalexin in the indole-3-acetonitrile metabolic network of Arabidopsis thaliana. Plant Cell 21: 1830–1845. , , , , , .
- 2011. Chemical diversity on display in the plant innate immune systems of closely-related species. New Phytologist 192: 566–569. .
- 2008. Phytoalexins and phytoanticipins from the wild crucifers Thellungiella halophila and Arabidopsis thaliana: rapalexin A, wasalexins and camalexin. Phytochemistry 69: 889–893. , .