TY - JOUR
T1 - Pullenvalenes A-D
T2 - Nitric Oxide-Mediated Transcriptional Activation (NOMETA) Enables Discovery of Triterpene Aminoglycosides from Australian Termite Nest-Derived Fungi
AU - Dewa, Amila Agampodi
AU - Khalil, Zeinab G.
AU - Hussein, Waleed M.
AU - Jin, Shengbin
AU - Wang, Yanan
AU - Cruz-Morales, Pablo
AU - Capon, Robert J.
N1 - Publisher Copyright:
© 2024 American Chemical Society and American Society of Pharmacognosy.
PY - 2024/4/26
Y1 - 2024/4/26
N2 - We report on the use of nitric oxide-mediated transcriptional activation (NOMETA) as an innovative means to detect and access new classes of microbial natural products encoded within silent biosynthetic gene clusters. A small library of termite nest- and mangrove-derived fungi and actinomyces was subjected to cultivation profiling using a miniaturized 24-well format approach (MATRIX) in the presence and absence of nitric oxide, with the resulting metabolomes subjected to comparative chemical analysis using UPLC-DAD and GNPS molecular networking. This strategy prompted study of Talaromyces sp. CMB-TN6F and Coccidiodes sp. CMB-TN39F, leading to discovery of the triterpene glycoside pullenvalenes A-D (1-4), featuring an unprecedented triterpene carbon skeleton and rare 6-O-methyl-N-acetyl-d-glucosaminyl glycoside residues. Structure elucidation of 1-4 was achieved by a combination of detailed spectroscopic analysis, chemical degradation, derivatization and synthesis, and biosynthetic considerations.
AB - We report on the use of nitric oxide-mediated transcriptional activation (NOMETA) as an innovative means to detect and access new classes of microbial natural products encoded within silent biosynthetic gene clusters. A small library of termite nest- and mangrove-derived fungi and actinomyces was subjected to cultivation profiling using a miniaturized 24-well format approach (MATRIX) in the presence and absence of nitric oxide, with the resulting metabolomes subjected to comparative chemical analysis using UPLC-DAD and GNPS molecular networking. This strategy prompted study of Talaromyces sp. CMB-TN6F and Coccidiodes sp. CMB-TN39F, leading to discovery of the triterpene glycoside pullenvalenes A-D (1-4), featuring an unprecedented triterpene carbon skeleton and rare 6-O-methyl-N-acetyl-d-glucosaminyl glycoside residues. Structure elucidation of 1-4 was achieved by a combination of detailed spectroscopic analysis, chemical degradation, derivatization and synthesis, and biosynthetic considerations.
UR - https://www.scopus.com/pages/publications/85189904602
U2 - 10.1021/acs.jnatprod.3c01233
DO - 10.1021/acs.jnatprod.3c01233
M3 - Article
C2 - 38575516
AN - SCOPUS:85189904602
SN - 0163-3864
VL - 87
SP - 935
EP - 947
JO - Journal of Natural Products
JF - Journal of Natural Products
IS - 4
ER -