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1  carboxamide intermediate 2 at carbon 6 with geranyl diphosphate.
2 e (C(50)) from isopentenyl diphosphate and E-geranyl diphosphate.
3 hosphate and isopentenyl diphosphate to form geranyl diphosphate.
4 ation of both geraniol and (R)-linalool from geranyl diphosphate.
5 for activity and produces only geraniol from geranyl diphosphate.
6 e, Rv1086, adds one isoprene unit to omega,E-geranyl diphosphate.
7 , respectively, as their major products from geranyl diphosphate.
8 ated as a possible C-methyltransferase, with geranyl diphosphate (1) and S-adenosylmethionine gave th
9                    Regiospecifically labeled geranyl diphosphates ((2E,6E)-[1,1,8,8,8-(2)H(5)]- and (
10 e the corresponding chlorinated analogues of geranyl diphosphate (3-ClGPP) and farnesyl diphosphate (
11 nzyme activity level (7-fold), and in planta geranyl diphosphate and geranylgeranyl diphosphate level
12 e overexpressed a bifunctional spruce IDS, a geranyl diphosphate and geranylgeranyl diphosphate synth
13 values of 21 and 51 microM were obtained for geranyl diphosphate and Mn2+, respectively.
14                                Incubation of geranyl diphosphate and S-adenosylmethionine with a mixt
15 CotB2, commencing with the substrate geranyl geranyl diphosphate and terminating with the carbocation
16 r isopentenyl diphosphate, 38 micrometer for geranyl diphosphate, and 16 micrometer for neryl diphosp
17 zyme was functionally expressed and produced geranyl diphosphate as its major product.
18 functional hybrid heterodimer that generated geranyl diphosphate as product in each case.
19 to all known monoterpene cyclases, which use geranyl diphosphate as substrate and invoke a cationic i
20 on in Escherichia coli and enzyme assay with geranyl diphosphate as substrate, subsequent analysis of
21 icate that, contrary to the textbook view of geranyl diphosphate as the "universal" substrate of mono
22 he monoterpene bornyl diphosphate (BPP) from geranyl diphosphate by BPP synthase using state of the a
23                                              Geranyl diphosphate C-methyltransferase (GPPMT) from Str
24 antly to beta-cubebene, while Mg17 converted geranyl diphosphate (C(5)) to alpha-terpineol.
25  in plants typically proceeds through either geranyl diphosphate (C10) or trans-farnesyl diphosphate
26 noid coupling reactions to give a mixture of geranyl diphosphate (chain elongation), chrysanthemyl di
27 rm yeast peroxisomes into microfactories for geranyl diphosphate-derived compounds, focusing on monot
28 mation of the prenyl diphosphate precursors, geranyl diphosphate, farnesyl diphosphate, and geranylge
29 phosphate synthase 1 (PcIDS1) yields 96% C10-geranyl diphosphate (GDP) and only 4% C15-farnesyl dipho
30 se in that it adds only one isoprene unit to geranyl diphosphate, generating the 15-carbon product (E
31 nd dimethylallyl diphosphate (DMAPP) to form geranyl diphosphate (GPP) and between IPP and GPP to giv
32 es, which are derived from linear precursors geranyl diphosphate (GPP) and lavandulyl diphosphate (LP
33 hosphate (BPP), which is itself derived from geranyl diphosphate (GPP) by the enzyme ( +)-bornyl diph
34             The TPS, termed LlTPS, converted geranyl diphosphate (GPP) into a mixture of monoterpenes
35 S1 catalyzing the irreversible conversion of geranyl diphosphate (GPP) to geraniol.
36 ed with dimethylallyl diphosphate (DMAPP) or geranyl diphosphate (GPP) to give the corresponding chlo
37              MoeN5 catalyzes the reaction of geranyl diphosphate (GPP) with the cis-farnesyl group in
38  is hypothesized to originate from 10-carbon geranyl diphosphate (GPP), 15-carbon farnesyl diphosphat
39 te (IPP), dimethylallyl diphosphate (DMAPP), geranyl diphosphate (GPP), farnesyl diphosphate (FPP), a
40 ere the C(10) product of the first addition, geranyl diphosphate (GPP), is the substrate for the seco
41 wers include three monoterpenes derived from geranyl diphosphate (GPP), myrcene, (E)-beta-ocimene and
42 (Humulus lupulus L.) trichomes, derives from geranyl diphosphate (GPP), the common precursor of monot
43                                              Geranyl diphosphate (GPP), the precursor of many monoter
44                                              Geranyl diphosphate (GPP), the precursor of most monoter
45  modifies an acyclic isoprenoid diphosphate, geranyl diphosphate (GPP), to yield a noncanonical acycl
46 imethylallyl diphosphate (DMAPP) and then to geranyl diphosphate (GPP).
47 solic NUDX1 hydrolase which dephosphorylates geranyl diphosphate (GPP).
48 th dimethylallyl diphosphate (DMAPP, C5) and geranyl diphosphate (GPP, C10) to give (E,E)-FPP (C15).
49 engineer their isoprene donor specificities (geranyl diphosphate [GPP] versus dimethylallyl diphospha
50 tene->xanthoxin->ABA)2(terpense->diterpense->geranyl diphosphate ->C20 ->GA).
51 lly synthesized as stable analogs of omega,E-geranyl diphosphate in which the labile diphosphate moie
52 , myrcene and (E)-beta-ocimene, derived from geranyl diphosphate, in addition to a major phenylpropan
53 catalyzed the formation of 18O-geraniol from geranyl diphosphate, indicating that the reaction mechan
54 enchol synthase, plant cyclases that convert geranyl diphosphate into products with closely related b
55    The data from both organisms suggest that geranyl diphosphate is the allylic substrate for two dis
56                                              Geranyl diphosphate is the precursor of monoterpenes, a
57 the coupled isomerization and cyclization of geranyl diphosphate, is reported at 2.7-A; resolution in
58 for rat farnesyl diphosphate (FPP) synthase (geranyl-diphosphate:isopentenyl-diphosphate geranyltrans
59 s the addition of isopentenyl diphosphate to geranyl diphosphate, neryl diphosphate, omega,E,E-farnes
60 , except for a relatively low K(m) value for geranyl diphosphate of 0.2 microm.
61 dition of isopentenyl diphosphate to omega,E-geranyl diphosphate or omega,Z-neryl diphosphate yieldin
62 terminal domain catalyzes the cyclization of geranyl diphosphate, orienting and stabilizing multiple
63                                FDS-1 prefers geranyl diphosphate over dimethylallyl diphosphate as an
64 r content of some compounds related with the geranyl-diphosphate pathway (neryl and geranyl acetates)
65 t cells overexpressing Rv1086 incubated with geranyl diphosphate showed a 5-fold increase of [(14)C]i
66                                              Geranyl diphosphate synthase (GPPS) catalyzes the conden
67  myrcene, in transgenic tobacco by elevating geranyl diphosphate synthase (GPS) activity.
68 erized Lavandula x intermedia cDNAs encoding geranyl diphosphate synthase (LiGPPS), geranylgeranyl di
69 phate synthase (SlDXS), Arabidopsis thaliana geranyl diphosphate synthase 1 (AtGPS) and Mentha x pipe
70                       The relative levels of geranyl diphosphate synthase and farnesyl diphosphate sy
71 the hybrid possesses characteristics of both geranyl diphosphate synthase and geranylgeranyl diphosph
72                                              Geranyl diphosphate synthase belongs to a subgroup of pr
73 synthases; yet it is absolutely required for geranyl diphosphate synthase catalysis.
74  diphosphate synthase, which are homodimers, geranyl diphosphate synthase from Mentha is a heterotetr
75  phosphate pathway were overexpressed, and a geranyl diphosphate synthase from the plant Abies grandi
76 nd recombinant enzymes, thus confirming that geranyl diphosphate synthase is a heterodimer.
77                       Immunogold labeling of geranyl diphosphate synthase occurred within secretory c
78 ate synthase 1 (AtGPS) and Mentha x piperita geranyl diphosphate synthase small subunit (MpGPS.SSU) o
79              These results indicate that the geranyl diphosphate synthase small subunit is capable of
80 expression in Escherichia coli of the Mentha geranyl diphosphate synthase small subunit with the phyl
81 l subunits of peppermint (Mentha x piperita) geranyl diphosphate synthase, spearmint (Mentha spicata)
82                                              Geranyl diphosphate synthase, which catalyzes the conden
83 sion of the two together produced functional geranyl diphosphate synthase.
84 sis suggested that the heterodimeric geranyl(geranyl)diphosphate synthase [G(G)PPS] is involved in my
85 ted L. x intermedia CINS (LiCINS), converted geranyl diphosphate (the linear monoterpene precursor) p
86 l diphosphate and isopentenyl diphosphate to geranyl diphosphate, the key precursor of monoterpene bi
87 proceed via an RR-dependent isomerization of geranyl diphosphate to 3S-linalyl diphosphate, as shown
88 terpene cyclase limonene synthase transforms geranyl diphosphate to a monocyclic olefin and constitut
89 ersion of the ubiquitous terpenoid precursor geranyl diphosphate to the iridoid loganic acid.
90 te; however, one truncated protein converted geranyl diphosphate to the monoterpene limonene.
91 en proposed to proceed by the cyclization of geranyl diphosphate to y-terpinene, followed by a series
92 ncapable of converting the natural substrate geranyl diphosphate, via the enzymatically formed tertia
93 ase (GES) activity, generating geraniol from geranyl diphosphate, was shown to be localized exclusive
94  additional product, the regular monoterpene geranyl diphosphate, when incubated with isopentenyl dip
95 e formation of 10 volatile monoterpenes from geranyl diphosphate, with 1,8-cineole predominating.