| Literature DB >> 26248039 |
Xin Zhan1, Søren Spanner Bach1, Nikolaj Lervad Hansen1, Christina Lunde1, Henrik Toft Simonsen2.
Abstract
The bifunctional diterpene synthase, copalyl diphosphate/kaurene synthase from the moss Physcomitrella patens (PpCPS/KS), catalyses the formation of at least four diterpenes, including ent-beyerene, ent-sandaracopimaradiene, ent-kaur-16-ene, and 16-hydroxy-ent-kaurene. The enzymatic activity has been confirmed through generation of a targeted PpCPS/KS knock-out mutant in P. patens via homologous recombination, through transient expression of PpCPS/KS in Nicotiana benthamiana, and expression of PpCPS/KS in E. coli. GC-MS analysis of the knock-out mutant shows that it lacks the diterpenoids, supporting that all are products of PpCPS/KS as observed in N. benthamiana and E. coli. These results provide additional knowledge of the mechanism of this bifunctional diterpene synthase, and are in line with proposed reaction mechanisms in kaurene biosynthesis.Entities:
Keywords: Copalyl diphosphate/kaurene synthase; Diterpene; Ent-beyerene; Ent-sandaracopimaradiene; Physcomitrella patens
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Year: 2015 PMID: 26248039 DOI: 10.1016/j.plaphy.2015.07.011
Source DB: PubMed Journal: Plant Physiol Biochem ISSN: 0981-9428 Impact factor: 4.270