Induction of auxin biosynthetic enzymes by jasmonic acid and in clubroot diseased Chinese cabbage plants

Citation
S. Grsic et al., Induction of auxin biosynthetic enzymes by jasmonic acid and in clubroot diseased Chinese cabbage plants, PHYSL PLANT, 105(3), 1999, pp. 521-531
Citations number
56
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
PHYSIOLOGIA PLANTARUM
ISSN journal
00319317 → ACNP
Volume
105
Issue
3
Year of publication
1999
Pages
521 - 531
Database
ISI
SICI code
0031-9317(199903)105:3<521:IOABEB>2.0.ZU;2-O
Abstract
Nitrilase (MT) and myrosinase are important enzymes for auxin biosynthesis in Brassicaceae, which is increased during clubroot disease, Therefore, NIT and myrosinase levels during club development and possible regulation mech anisms were investigated. In addition, the occurrence of different nitrilas e isoforms in Chinese cabbage has been shown. Nitrilase activity was enhanc ed in infected roots during later stages of club development (35-42 days af ter inoculation), However, no differences in nitrilase mRNA levels between infected and healthy roots were found during symptom development. Myrosinas e expression was increased in clubbed roots at slightly earlier time points (28 days after inoculation) and also at later time points during infection . The activities of tryptophan oxidizing enzyme (TrpOxE), which catalyzes t he first step in tryptophan-dependent auxin biosynthesis in Brassicaceae, a nd nitrilase were enhanced after treatment with jasmonic acid (JA) and meth yl jasmonate, Similarly, the amount of myrosinase mRNA was increased by JA, During clubroot disease the endogenous concentration of JA increased in in fected roots 3-5 weeks after inoculation. From our results it can be conclu ded that: (1) de novo indole-3-acetic acid (IAA) biosynthesis plays a role for symptom development of clubroot disease in Brassicaceae during later de velopmental stages; and (2) JA which increased during club development, may be involved in the up-regulation of three enzymes important for IAA synthe sis.