TY - JOUR
T1 - Pyrone polyketides synthesized by a type III polyketide synthase from Drosophyllum lusitanicum
AU - Jindaprasert, Aphacha
AU - Springob, Karin
AU - Schmidt, Jürgen
AU - De-Eknamkul, Wanchai
AU - Kutchan, Toni M.
N1 - Funding Information:
We thank Verona Dietl, Christine Kuhnt and Dagmar Knöfel (Leibniz-Institut für Pflanzenbiochemie, Halle, Germany) for technical assistance and Dr. Joseph M. Jez (Donald Danforth Plant Science Center, St. Louis, MO, USA) for his help in preparing the models of DluHKS and PinHKS. A. Jindaprasert was supported by the Royal Golden Jubilee Ph.D. program, Thailand Research Fund (RGJ-TRF), the German Academic Exchange Service (DAAD), and Thailand’s National Center for Genetic Engineering and Biotechnology (BIOTEC, Grant No. 2/2545). Financial support by the DFG priority program SPP1152: “Evolution of metabolic diversity” (KU990/5-2) is gratefully acknowledged.
PY - 2008/12
Y1 - 2008/12
N2 - To isolate cDNAs involved in the biosynthesis of acetate-derived naphthoquinones in Drosophyllum lusitanicum, an expressed sequence tag analysis was performed. RNA from callus cultures was used to create a cDNA library from which 2004 expressed sequence tags were generated. One cDNA with similarity to known type III polyketide synthases was isolated as full-length sequence and termed DluHKS. The translated polypeptide sequence of DluHKS showed 51-67% identity with other plant type III PKSs. Recombinant DluHKS expressed in Escherichia coli accepted acetyl-coenzyme A (CoA) as starter and carried out sequential decarboxylative condensations with malonyl-CoA yielding α-pyrones from three to six acetate units. However, naphthalenes, the expected products, were not isolated. Since the main compound produced by DluHKS is a hexaketide α-pyrone, and the naphthoquinones in D. lusitanicum are composed of six acetate units, we propose that the enzyme provides the backbone of these secondary metabolites. An involvement of accessory proteins in this biosynthetic pathway is discussed.
AB - To isolate cDNAs involved in the biosynthesis of acetate-derived naphthoquinones in Drosophyllum lusitanicum, an expressed sequence tag analysis was performed. RNA from callus cultures was used to create a cDNA library from which 2004 expressed sequence tags were generated. One cDNA with similarity to known type III polyketide synthases was isolated as full-length sequence and termed DluHKS. The translated polypeptide sequence of DluHKS showed 51-67% identity with other plant type III PKSs. Recombinant DluHKS expressed in Escherichia coli accepted acetyl-coenzyme A (CoA) as starter and carried out sequential decarboxylative condensations with malonyl-CoA yielding α-pyrones from three to six acetate units. However, naphthalenes, the expected products, were not isolated. Since the main compound produced by DluHKS is a hexaketide α-pyrone, and the naphthoquinones in D. lusitanicum are composed of six acetate units, we propose that the enzyme provides the backbone of these secondary metabolites. An involvement of accessory proteins in this biosynthetic pathway is discussed.
KW - Drosophyllaceae
KW - Drosophyllum lusitanicum link
KW - Hexaketide synthase
KW - Naphthoquinone
KW - Pyrone synthase
KW - Type III polyketide synthase
UR - http://www.scopus.com/inward/record.url?scp=57049181405&partnerID=8YFLogxK
U2 - 10.1016/j.phytochem.2008.03.013
DO - 10.1016/j.phytochem.2008.03.013
M3 - Article
C2 - 18466932
AN - SCOPUS:57049181405
SN - 0031-9422
VL - 69
SP - 3043
EP - 3053
JO - Phytochemistry
JF - Phytochemistry
IS - 18
ER -