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1 ng this a hemiterpene synthase rather than a monoterpene synthase.
2 S-b subfamily that typically contains mostly monoterpene synthases.
3 at the produced GPP can be used by plastidic monoterpene synthases.
4 nd of monoterpenes, indicating that they are monoterpene synthases.
5  final cyclization reaction catalyzed by the monoterpene synthases.
6 brary that appeared to encode three distinct monoterpene synthases.
7 rtion of pathway genes into a region rich in monoterpene synthases.
8 d biosynthesis and others with activities as monoterpene synthases.
9 prene synthase is a myrcene/ocimene (acyclic monoterpenes) synthase.
10 ne synthase, 10 exclusively or predominantly monoterpene synthases, 17 sesquiterpene synthases and si
11 t has been shown to possess both sesqui- and monoterpene synthase activities resulted in increased le
12 ment with the results of cell-free assays of monoterpene synthase activity, followed by the coordinat
13 mechanism of GES is similar to that of other monoterpene synthases and is different from the action o
14  two that were functionally characterized as monoterpene synthases and three that preferred farnesyl
15 hase falls into the TPS-d1 group (gymnosperm monoterpene synthases) and is most closely related to li
16  residues in length (71.5 kDa); all of these monoterpene synthases appear to be translated as preprot
17                               Genes encoding monoterpene synthases are also prevalent, and they fall
18      The isoprene synthase is cytosolic; six monoterpene synthases are plastidic, and four are cytoso
19 owever, closer inspection indicates that the monoterpene synthases arise earlier, as shown by an abbr
20 dization using probes derived from the three monoterpene synthase cDNAs.
21 hat isoprene synthases are either within the monoterpene synthase clade or sister to it.
22 ible for 1,8-cineole biosynthesis, the first monoterpene synthase discovered in fungi.
23     Here we report the characterization of a monoterpene synthase encoded by two identical, closely l
24 imilar biochemical properties to other known monoterpene synthases, except for a relatively low K(m)
25 gene was created by a duplication event of a monoterpene synthase followed by a localized gene conver
26       The enzymes of clade III mainly act as monoterpene synthases, forming cyclic and acyclic monote
27 thases from conifers more closely than other monoterpene synthases from angiosperm species.
28      Sequence comparison revealed that these monoterpene synthases from grand fir resemble sesquiterp
29 solate the cDNAs encoding three multiproduct monoterpene synthases from this species that were functi
30   All previously isolated 'cineole cassette'-monoterpene synthase genes are multi product enzymes tha
31 elopmental, and rhythmic expression of these monoterpene synthase genes in snapdragon flowers reveale
32                                          The monoterpene synthase genes in the cluster likely evolved
33 method would allow the identification of new monoterpene synthase genes using transient expression in
34  to two P450s that were coexpressed with two monoterpene synthases in flowers and were thus predicted
35 ae), thus indicating gene diversification of monoterpene synthases in section Alatae.
36  diphosphate as the "universal" substrate of monoterpene synthases, in tomato glands neryl diphosphat
37 ray structure of the unique "head-to-middle" monoterpene synthase, lavandulyl diphosphate synthase (L
38 specific, methyl jasmonate (MeJA)-responsive monoterpene synthase (Li3CARS) from Lavandula x intermed
39 omated pipeline for the screening of diverse monoterpene synthase libraries, employing robotic liquid
40                                              Monoterpene synthases (MTSs) catalyze the first committe
41 ion of alternative product profiles of these monoterpene synthases of conifer defense against insects
42 nt enzymes resemble the corresponding native monoterpene synthases of wound-induced grand fir stem.
43 e nature of the branched reaction mechanism, monoterpene synthases often produce multiple products wh
44                                            A monoterpene synthase producing the set of 'cineole casse
45             Os02g02930 was found to encode a monoterpene synthase producing the single product S-lina
46 gesting that the reaction mechanism of Tps-g monoterpene synthase product formation does not proceed
47  Mg17 aligned more closely to the angiosperm monoterpene synthase subclass TPS-b.
48 haracteristic feature of the Tps-d and Tps-b monoterpene synthases, suggesting that the reaction mech
49 oded by three of these complementary DNAs: a monoterpene synthase that belongs to the TPS-b clade cat
50 dization to map the expression of a putative monoterpene synthase to the epithelium of glands and use
51              These newly isolated snapdragon monoterpene synthases, together with Arabidopsis AtTPS14
52  activated in response to wounding, with the monoterpene synthases up-regulated first (transcripts de
53 ound-induced accumulation of transcripts for monoterpene synthases was demonstrated by RNA blot hybri
54 es (R58R59) which is highly conserved in the monoterpene synthases, was removed.
55  availability of cDNA species encoding these monoterpene synthases will allow an understanding of the