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A Proposed Biosynthetic Pathway of Picrosides Linked through the Detection of Biochemical Intermediates in the Endangered Medicinal Herb Picrorhiza kurroa
Author(s) -
Kumar Varun,
Sood Hemant,
Sharma Manu,
Chauhan Rajinder Singh
Publication year - 2013
Publication title -
phytochemical analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 72
eISSN - 1099-1565
pISSN - 0958-0344
DOI - 10.1002/pca.2437
Subject(s) - chemistry , biosynthesis , stereochemistry , catalpol , electrospray ionization , iridoid , biochemistry , enzyme , mass spectrometry , chromatography , glycoside
Picrorhiza kurroa Royle ex Benth is an important medicinal herb used in the preparation of several herbal drug formulations due to the presence of picroside‐I (P‐I) and picroside‐II (P‐II) along with other iridoid‐glucosides derivatives. Objective The endangered status of P. kurroa coupled with lack of information on biosynthesis of P‐I and P‐II necessitate deciphering the biosynthetic pathway for picrosides. Methods LC with electrospray ionisation (ESI) and quadrupole time of flight combined with MS/MS was used to detect intermediates and assemble the picrosides biosynthetic pathway in P. kurroa . Results The presence of catalpol and aucubin, the major backbone structures of picrosides, along with intermediate metabolites boschnaloside, bartsioside and mussaenosidic acid, was confirmed in ESI negative mode with pseudomolecular ion peaks, that is, m/z 361, m/z 343, m/z 345, m/z 329 and m/z 375 ions and their fragmentation patterns. Conclusion The picrosides biosynthetic pathway is expected to provide a reliable platform towards understanding the molecular components (genes/enzymes) of P‐I and P‐II biosynthesis in P. kurroa for their eventual utilisation in various applications. Copyright © 2013 John Wiley & Sons, Ltd.