4.5 Article

Elicitation of defense response by transglycosylated chitooligosaccharides in rice seedlings

Journal

CARBOHYDRATE RESEARCH
Volume 510, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.carres.2021.108459

Keywords

Chitinase; Transglycosylation; Chitooligosaccharides; Elicitor activity; Defense mechanism

Funding

  1. University Grants Commission (UGC) [F.4-2/2006 (BSR)/BL/14-15/0063]
  2. DST, Govt. of India [JCB/2017/000053]
  3. CSIR (India) [09/414 (1149)/2017-EMR-I]
  4. European Union [613931]
  5. DST-FIST
  6. UGC-SAP
  7. DBT-CREBB

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Long-chain chitooligosaccharides with degree of polymerization greater than 4 have potential biological activities. A mutant endo-chitinase was used to synthesize COS with DP6 and DP7, inducing defense response in rice seedlings and affecting gene expression levels, possibly through phosphorylation signaling pathways.
Long-chain chitooligosaccharides (COS) with degree of polymerization (DP) more than 4 are known to have potential biological activities. A hyper-transglycosylating mutant of an endo-chitinase from Serratia proteamaculans (SpChiD-Y28A) was used to synthesize COS with DP6 and DP7 using COS DP5 as substrate. Purified COS with DP5-7 were tested to elicit the defense response in rice seedlings. Among the COS used, DP7 strongly induced oxidative burst response as well as peroxidase, and phenylalanine ammonia lyase activites. A few selected marker genes in salicylic acid (SA)- and jasmonic acid-dependent pathways were evaluated by real-time PCR. The expression levels of pathogenesis-related (PR) genes PR1a and PR10 and defense response genes (chitinase1, peroxidase and 13 -1,3-glucanase) were up regulated upon COS treatment in rice seedlings. The DP7 induced Phenylalanine ammonia lyase and Isochorismate synthase 1 genes, with concomitant increase of Mitogenactivated protein kinase 6 and WRKY45 transcription factor genes indicated the possible role of phosphorylation in the transmission of a signal to induce SA-mediated defense response in rice.

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