戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

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 to a Phe residue found in the active site of isoprene synthases.
2 ively high K(m)s that have been reported for isoprene synthases (0.5-8 mM).
3 all enzymes encoded by the 34 TPS genes: one isoprene synthase, 10 exclusively or predominantly monot
4  as a second Phe residue that closes off the isoprene synthase active site.
5 l soluble (i.e. stromal) and thylakoid-bound isoprene synthase activities.
6 ge and light, do not alter the percentage of isoprene synthase activity in the bound or soluble form.
7             It was found that an increase in isoprene synthase activity is primarily responsible for
8  supply of DMADP rather than from changes in isoprene synthase activity.
9 comparable with that observed for angiosperm isoprene synthases and 3 orders of magnitude higher than
10                                  Willow leaf isoprene synthase appears to be plastidic, with whole-le
11  terpene synthase gene family indicated that isoprene synthases are either within the monoterpene syn
12 ing two Phe residues do not have homologs in isoprene synthases but occupy the same space as a second
13                                              Isoprene synthase converts dimethylallyl diphosphate, de
14  The solubilized thylakoid-bound and stromal isoprene synthases exhibit similar catalytic properties,
15     It was found that genes encoding stromal isoprene synthase exist as a small gene family, the memb
16 ray crystal structure of recombinant PcISPS (isoprene synthase from gray poplar hybrid Populusxcanesc
17 the isolation of thylakoid-bound and soluble isoprene synthases from a single willow (Salix discolor
18                      Expression of the kudzu isoprene synthase gene in Arabidopsis caused Arabidopsis
19               Heterologous expression of the isoprene synthase gene in the cyanobacterium Synechocyst
20 asured in cyanobacteria transformed with the isoprene synthase gene only.
21                                              Isoprene synthase gene structure was analysed in three p
22                                              Isoprene synthase genes of kudzu and aspen (Populus trem
23 iously, thylakoid-bound and soluble forms of isoprene synthase had been isolated separately, each fro
24 soprene emission is controlled by the enzyme isoprene synthase; however, there is still relatively li
25               Heterologous expression of the isoprene synthase in combination with the MVA pathway en
26     In Arabidopsis, the gene most similar to isoprene synthase is a myrcene/ocimene (acyclic monoterp
27                                          The isoprene synthase is cytosolic; six monoterpene synthase
28                                              Isoprene synthase is the enzyme responsible for the foli
29                     Although thylakoid-bound isoprene synthase is tightly bound to the thylakoid memb
30                 The relationship between the isoprene synthase isoforms and the implications for func
31 ean were thought to have evolutionarily lost isoprene synthase (ISPS) and are typically considered no
32 ms of (E)-beta-farnesene synthase (EBFS) and isoprene synthase (ISPS), enzymes that catalyze a formal
33                    In immature leaves, where isoprene synthase levels are variable, emission levels a
34  phenylalanine residues found exclusively in isoprene synthases make the active site smaller than oth
35                              Accumulation of isoprene synthase protein is developmentally regulated,
36  levels are also influenced by the amount of isoprene synthase protein.
37 efore starting to decrease; in contrast, the isoprene synthase rate constant increased up to 40 degre
38 ount of DMADP fell but the rate constant for isoprene synthase remained constant, indicating that the