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The secondary metabolism glycosyltransferases UGT73B3 and UGT73B5 are components of redox status in resistance of A rabidopsis to P seudomonas syringae pv. tomato
Author(s) -
SIMON CLARA,
LANGLOISMEURINNE MATHILDE,
DIDIERLAURENT LAURE,
CHAOUCH SEJIR,
BELLVERT FLORIANT,
MASSOUD KAMAL,
GARMIER MARIE,
THAREAU VINCENT,
COMTE GILLES,
NOCTOR GRAHAM,
SAINDRENAN PATRICK
Publication year - 2014
Publication title -
plant, cell and environment
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.646
H-Index - 200
eISSN - 1365-3040
pISSN - 0140-7791
DOI - 10.1111/pce.12221
Subject(s) - glycosyltransferase , biochemistry , mutant , chemistry , glycosylation , reactive oxygen species , microbiology and biotechnology , biology , gene
Secondary metabolism plant glycosyltransferases ( UGTs ) ensure conjugation of sugar moieties to secondary metabolites ( SMs ) and glycosylation contributes to the great diversity, reactivity and regulation of SMs . UGT73B3 and UGT73B5 , two UGTs of A rabidopsis thaliana ( A rabidopsis), are involved in the hypersensitive response ( HR ) to the avirulent bacteria P seudomonas syringae pv. tomato ( Pst‐AvrRpm1 ), but their function in planta is unknown. Here, we report that ugt73b3 , ugt73b5 and ugt73b3 ugt73b5 T‐DNA insertion mutants exhibited an accumulation of reactive oxygen species ( ROS ), an enhanced cell death during the HR to Pst‐AvrRpm1 , whereas glutathione levels increased in the single mutants. In silico analyses indicate that UGT73B3 and UGT73B5 belong to the early salicylic acid ( SA ) ‐ induced genes whose pathogen‐induced expression is co‐regulated with genes related to cellular redox homeostasis and general detoxification. Analyses of metabolic alterations in ugt mutants reveal modification of SA and scopoletin contents which correlate with redox perturbation, and indicate quantitative modifications in the pattern of tryptophan‐derived SM accumulation after Pst‐AvrRpm1 inoculation. Our data suggest that UGT73B3 and UGT73B5 participate in regulation of redox status and general detoxification of ROS ‐reactive SMs during the HR to Pst‐AvrRpm1 , and that decreased resistance to Pst‐AvrRpm1 in ugt mutants is tightly linked to redox perturbation.