コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ization of geranylgeranyl diphosphate to (+)-copalyl diphosphate.
2 hosphate to the stable bicyclic intermediate copalyl diphosphate.
3 the characteristic 7,13 double bond of 7,13-copalyl diphosphate.
5 e monofunctional diterpene synthases for ent-copalyl diphosphate and ent-kaurene biosynthesis is simi
6 ctionally conserved, sequentially acting ent-copalyl diphosphate and ent-kaurene synthases (CPS and K
7 lgeranyl diphosphate to the intermediate (+)-copalyl diphosphate and the ionization-dependent cycliza
8 ization of geranylgeranyl diphosphate to (+)-copalyl diphosphate and the second for the cyclization o
9 onal class II active sites and converted (+)-copalyl diphosphate, but not GGPP, into isopimaradiene a
10 s in carbocation rearrangements derived from copalyl diphosphate (CPP) and its diastereomers syn-CPP
11 rpene cyclases that produce the intermediate copalyl diphosphate (CPP), along with the more surprisin
12 nd at least one allelopathic agent, from syn-copalyl diphosphate (CPP), representing the only known m
13 13-en-8-ol diphosphate (LPP, TcCPS2) and (+)-copalyl diphosphate (CPP, TcCPS4), and three class-I diT
14 of the TPS-c subfamily were characterized as copalyl diphosphate (diterpene) synthases, and those bel
15 inorum diterpene synthases (diTPSs), the ent-copalyl diphosphate (ent-CPP) synthase SdCPS1, and the c
17 The class II terpene synthase producing syn-copalyl diphosphate from the universal diterpenoid precu
18 ations, of geranylgeranyl diphosphate and of copalyl diphosphate, in the formation of a mixture of ab
19 n of GGPP followed by rearrangement of a (+)-copalyl diphosphate intermediate at two discrete class I
20 y complement each other, suggesting that the copalyl diphosphate intermediate diffuses between the tw
21 abietadiene (a complex process involving the copalyl diphosphate intermediate) and then three to oxid
22 hase with geranylgeranyl diphosphate and (+)-copalyl diphosphate provided evidence for two functional
23 mics approach was utilized to identify a syn-copalyl diphosphate specific 9beta-pimara-7,15-diene syn
24 previously described and closely related ent-copalyl diphosphate specific cassa-12,15-diene synthase
28 biosynthesis is catalyzed in plastids by ent-copalyl diphosphate synthase (CPS), whose substrate, (E,
30 nally, our RNA sequencing analysis uncovered copalyl diphosphate synthase (SrCPS) and kaurene synthas
31 pression of the tanshinone-biosynthetic gene COPALYL DIPHOSPHATE SYNTHASE 1 (SmCPS1) through its spec
32 bHLH25 switches to promote the expression of Copalyl Diphosphate Synthase 2 (CPS2), which increases p
33 ck-outs of the relevant diterpene synthases (copalyl diphosphate synthase 4 (OsCPS4) and kaurene synt
34 ighly up-regulated genes, as was An2, an ent-copalyl diphosphate synthase associated with production
35 ces platensis CB00739 was verified as an ent-copalyl diphosphate synthase involved in the biosynthesi
37 crystal structure of Grindelia robusta 7,13-copalyl diphosphate synthase, GrTPS2, at 2.1 angstrom of
40 part of the catalytic base group in the ent-copalyl diphosphate synthases found in all seed plants f
41 been utilized to identify two disparate ent-copalyl diphosphate synthases from rice (OsCPS1ent and O
42 geranyl diphosphate and the intermediate (+)-copalyl diphosphate to a nearly equal mixture of abietad
43 te and the second for the cyclization of (+)-copalyl diphosphate to diterpene end products, and demon
44 e class I terpene synthase that converts syn-copalyl diphosphate to the corresponding polycyclic hydr
45 tes encountered during the conversion of ent-copalyl diphosphate to the diterpenes beyerene, kaurene,
46 hate to the stable bicyclic intermediate (+)-copalyl diphosphate via protonation-initiated cyclizatio
47 the ionization-dependent cyclization of (+)-copalyl diphosphate, via a pimarenyl intermediate, to th