ライフサイエンスコーパス: cineole

1 a series of terpene molecules, including 1,8-cineole.

2 ization reaction from alpha-terpineol to 1,8-cineole.

3 d (E)-beta-ocimene, and it does not form 1,8-cineole.

4 edione, and acetone, or the monoterpene, 1,8-cineole.

5 The main compounds of the REO were 1.8 cineole (52.2%), camphor (15.2%) and alpha-pinene (12.4%

6 s roots resulted in the rapid release of 1,8-cineole, a monoterpene that has not been previously repo

7 clade catalyzes the formation of mostly 1,8-cineole; a sesquiterpene synthase belonging to the TPS-a

8 ene synthase genes for the production of 1,8-cineole and alpha-pinene, and beta-pinene (which compris

9 Both 1,8-cineole and d-camphor are C(10) monoterpenes containing

10 bition caused by the natural monoterpene 1,4-cineole and its structurally related herbicide cinmethyl

11 enal was the most intense odorant, while 1,8-cineole and linalool were also revealed as important aro

12 N. obtusifolia emitted solely 1,8-cineole and no monoterpenes were found in floral scents

13 nthases produce (+)-bornyl diphosphate, 1, 8-cineole, and (+)-sabinene, respectively, as their major

14 yses identified linalool, hexyl acetate, 1,8-cineole, and butyl acetate as key aroma compounds of thi

15 ular monoterpenes, for example linalool, 1,8-cineole, and camphor.

16 on of plant tissue, the recent report of 1,8-cineole as an Arabidopsis root volatile suggests that th

17 n of cineole, enabling C. braakii to live on cineole as its sole source of carbon and energy.

18 tic 'cineole cassette' monoterpenes with 1,8-cineole as the dominant volatile product.

19 phor and a third one with high levels of 1,8-cineole, beta-pinene and sesquiterpenes.

20 cation of the hyp3 gene, responsible for 1,8-cineole biosynthesis, the first monoterpene synthase dis

21 he major constituents were alpha-pinene, 1,8-cineole, borneol, beta-bisabolene, and caryophyllene oxi

22 Cells were stimulated with the odour cineole by rapid exchange of the solution bathing the ol

23 thol:1,8-cineole (ME:EU) and 1:2 camphor:1,8-cineole (CA:EU) used at concentrations of 7.5 and 15 % i

24 es emit a characteristic blend including the cineole cassette monoterpenes.

25 A monoterpene synthase producing the set of 'cineole cassette' compounds was isolated from N. noctifl

26 To determine the origin of the 'cineole cassette' monoterpene phenotype other potential

27 characteristic floral scent comprising the' cineole cassette' monoterpenes 1,8-cineole, limonene, my

28 ynthesize simultaneously the characteristic 'cineole cassette' monoterpenes with 1,8-cineole as the d

29 All previously isolated 'cineole cassette'-monoterpene synthase genes are multi p

30 that synthesize the seven compounds of the 'cineole cassette'.

31 ent increased more gradually with increasing cineole concentration and did not saturate within the 10

32 id not saturate within the 100-fold range of cineole concentrations applied.When stimulated for 30 s

33 The LiCINS mRNA levels paralleled the 1,8-cineole content in mature flowers of the three lavender

34 atalytic mechanism of alpha-terpineol-to-1,8-cineole conversion is initiated by a catalytic dyad (his

35 This initiates the biodegradation of cineole, enabling C. braakii to live on cineole as its s

36 n the samples occurred in the amounts of 1,8-cineole, fenchone and trans-alpha-necrodyl acetate.

37 carvacrol for oregano, thymol for thyme, 1,8-cineole for rosemary, and citral for lemongrass.

38 that produce terpene molecules, such as 1,8-cineole, have been little explored in fungi, providing a

39 scence indicating that the production of 1,8 cineole in Lavandula is most likely controlled through t

40 tae, are rich in monoterpenes, including 1,8-cineole, limonene, beta-myrcene, alpha- and beta-pinene,

41 sing the' cineole cassette' monoterpenes 1,8-cineole, limonene, myrcene, beta-pinene, alpha-pinene, s

42 The natural mixtures of 1:1 menthol:1,8-cineole (ME:EU) and 1:2 camphor:1,8-cineole (CA:EU) used

43 ies to Arabidopsis roots did not produce 1,8-cineole nor any C6 wound-VOCs; compatible interactions b

44 zed by multiproduct enzymes, with either 1,8-cineole or alpha-terpineol contributing most to the vola

45 The presence of either 1,4-cineole or cinmethylin stimulated root uptake of [(14)C]

46 to the volatile spectrum, thus referring to cineole or terpineol synthase, respectively.

47 Cells were exposed to the odour cineole or to solutions of modified ionic content by rap

48 ns, including members of the p-menthane (1,8-cineole), pinane (alpha- and beta-pinene), thujane (isot

49 oterpenes from geranyl diphosphate, with 1,8-cineole predominating.

50 2)O, 2,2,5,5-tetramethyltetrahydrofuran, and cineole proceed via dimer-based transition structures [(

51 Through genome sequencing of cineole-producing isolate E7406B, we were able to identi

52 d 266 that determine the different terpineol-cineole ratios in Nicotiana suaveolens cineole synthase

53 is of the putative metabolite, 2-hydroxy-1,4-cineole, showed that the cis-enantiomer was much more ac

54 hemical formation of alpha-terpineol and 1,8-cineole, site-directed mutagenesis, in silico modeling,

55 rized cDNA with strong homology to known 1,8-cineole synthase (CINS) genes.

56 es) were functionally characterized as a 1,8-cineole synthase and a beta/alpha-pinene synthase.

57 ineol-cineole ratios in Nicotiana suaveolens cineole synthase and Nicotiana langsdorffii terpineol sy

58 nthase genes of e.g. N. alata rather than to cineole synthase genes of e.g. N. forgetiana.

59 The 1,8-cineole synthase produces significant amounts of (+)- an

60 ation-cyclization mechanism of action of 1,8-cineole synthase.

61 ee construction clustered the newly isolated cineole synthases (CIN) of section Alatae together with

62 cal for water capture and specificity during cineole synthesis, the same mechanism used in an unrelat

63 ible for aroma perception were limonene, 1,8-cineole, terpinen-4-ol, estragole and trans-anethole, an

64 braakii that catalyzes the hydroxylation of cineole to (S)-6beta-hydroxycineole.

65 noterpenoids, alpha-terpinyl acetate and 1,8-cineole, to which most of the quality of cardamom essent

66 alpha-pinene, beta-myrcene, borneol, and 1,8-cineole under deficit irrigation.

67 The GC-MS analysis of EO revealed that 1,8-Cineole was the main volatile compound.

68 P450cin catalyzes the monooxygenation of 1,8-cineole, which is structurally very similar to d-camphor

69 e laboratory-extracted TTO had higher of 1,8-cineole, while commercial TTO had more p-cymene.

70 near monoterpene precursor) primarily to 1,8-cineole with K ( m ) and k ( cat ) values of 5.75 muM an