TY - JOUR
T1 - The Amaryllidaceae alkaloids
T2 - biosynthesis and methods for enzyme discovery
AU - Kilgore, Matthew B.
AU - Kutchan, Toni M.
N1 - Publisher Copyright:
© 2015, Springer Science+Business Media Dordrecht.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - Amaryllidaceae alkaloids are an example of the vast diversity of secondary metabolites with great therapeutic promise. The identification of novel compounds in this group with over 300 known structures continues to be an area of active study. The recent identification of norbelladine 4′-O-methyltransferase (N4OMT), an Amaryllidaceae alkaloid biosynthetic enzyme, and the assembly of transcriptomes for Narcissus sp. aff. pseudonarcissus and Lycoris aurea highlight the potential for discovery of Amaryllidaceae alkaloid biosynthetic genes with new technologies. Recent technical advances of interest include those in enzymology, next generation sequencing, genetic modification, nuclear magnetic resonance spectroscopy, and mass spectrometry.
AB - Amaryllidaceae alkaloids are an example of the vast diversity of secondary metabolites with great therapeutic promise. The identification of novel compounds in this group with over 300 known structures continues to be an area of active study. The recent identification of norbelladine 4′-O-methyltransferase (N4OMT), an Amaryllidaceae alkaloid biosynthetic enzyme, and the assembly of transcriptomes for Narcissus sp. aff. pseudonarcissus and Lycoris aurea highlight the potential for discovery of Amaryllidaceae alkaloid biosynthetic genes with new technologies. Recent technical advances of interest include those in enzymology, next generation sequencing, genetic modification, nuclear magnetic resonance spectroscopy, and mass spectrometry.
KW - Galanthamine
KW - Haemanthamine
KW - Mass spectrometry
KW - Next generation sequencing
KW - Nuclear magnetic resonance spectroscopy
UR - https://www.scopus.com/pages/publications/84949944551
U2 - 10.1007/s11101-015-9451-z
DO - 10.1007/s11101-015-9451-z
M3 - Review article
AN - SCOPUS:84949944551
SN - 1568-7767
VL - 15
SP - 317
EP - 337
JO - Phytochemistry Reviews
JF - Phytochemistry Reviews
IS - 3
ER -