Characterisation of and changes to pro- and anti-oxidant enzyme activitiesduring the hypersensitive reaction in lettuce (Lactuca sativa L.)

Citation
Cs. Bestwick et al., Characterisation of and changes to pro- and anti-oxidant enzyme activitiesduring the hypersensitive reaction in lettuce (Lactuca sativa L.), PLANT SCI, 161(3), 2001, pp. 497-506
Citations number
49
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
PLANT SCIENCE
ISSN journal
01689452 → ACNP
Volume
161
Issue
3
Year of publication
2001
Pages
497 - 506
Database
ISI
SICI code
0168-9452(200108)161:3<497:COACTP>2.0.ZU;2-V
Abstract
Enzymes regulating aspects of reactive oxygen metabolism were characterised in expanded lettuce leaf tissue. Catalase (CAT) activity was optimal betwe en pH 7.0-8.0. predominantly located within peroxisomes and comprised two i soenzymes (pI 5.8 and 6.2). Of three principal superoxide dismutase (SOD) i soenzymes detected., CuZn SOD, (pI 4.90) represented 51.7%, Mn SOD (pI 4.75 ) 14.6% and a putative Fe SOD (pI 4.85), 33.7% of total activity. Lipoxygen ase (LOX) activity was optimal at pH 5. Activities were assessed following inoculation with Psendomonas syringae pv. phaseolicola and a related hrpD m utant. The wild-type bacterium induced a rapid hypersensitive reaction (HR) , associated with a progressive increase in thiobarbituric acid reactive su bstances (TBARS), indicative of lipid peroxidation, a sustained increase in LOX activity and a later increase in CAT activity. The hrp mutant induced a transitory increase in TBARS. a transient increase in LOX activity, again a later elevation in CAT activity but no macroscopic tissue collapse. In c omparison. water infiltration induced a rapid but transient increase in bot h SOD and CAT activities. From this and our previous work, it is concluded that lettuce cells undergoing an HR experience a prolonged oxidative stress . primarily through an increase in pro-oxidant activities initially occurri ng in the absence of enhanced antioxidant activities. (C) 2001 Elsevier Sci ence Ireland Ltd. All rights reserved.