ライフサイエンスコーパス: laurate

1 acylated to produce chlorobactene glucoside laurate.

2 the production of oils containing up to 50% laurate.

3 d the highest activity towards 4-nitrophenyl laurate.

4 that accumulates 30% caprate (10:0) and 54% laurate (12:0) in seed storage lipids.

5 yl carrier proteins, the enzyme incorporated laurate 3-8 times faster than decanoate or myristate, re

6 s palmitic acid (a fatty acid) and isopropyl laurate (a fatty acid ester), respectively.

7 nut protein into BTE oilseed rape lines with laurate above 50 mol % further increases total laurate l

8 ing the intermediate (Kdo)2-lipid IVA as the laurate acceptor, extracts of strains with transposon in

9 MsbB transfers myristate or laurate, activated on ACP, to (Kdo)2-(lauroyl)-lipid IVA

10 cted between CYP4A4 and CYP4A7 indicate that laurate activity is affected by the residues within SRS1

11 to the bulk seawater composition when sodium laurate, an organic surfactant, is present in the seawat

12 A containing a secondary laurate chain or a laurate and a myristate chain, respectively.

13 ite-directed mutant proteins of CYP4A7 found laurate and arachidonate activity markedly diminished in

14 ther hand, exhibited remarkable increases in laurate and arachidonate metabolism (3-fold) above wild-

15 Steady-state turnover rates with both laurate and arachidonate showed the trend WT > F393Y >>

16 the stimulation of cytochrome c reduction by laurate and CO.

17 enzene, Tris buffer, lauric acid, and methyl laurate and epoxidations of styrene and 10-undecenoic ac

18 ed out a comparative study of the effects of laurate and its close analogue, undecanesulfonate.

19 tive analysis showed a comparable release of laurate and myristate but no release of 3-hydroxymyrista

20 d disaccharide of glucosamine with secondary laurate and myristate chains on the distal unit.

21 f 27-hydroxyoctacosanoate and the absence of laurate and myristate in R. leguminosarum.

22 ation as the loss of radiolabeled secondary (laurate and myristate) and primary fatty acids (3-hydrox

23 Laurate and other substrates stimulate cytochrome c redu

24 vities were monitored on p-NP-butyrate, p-NP-laurate and p-NP-palmitate.

25 Both laurate and undecanesulfonate inhibited Cl- with competi

26 We show that undecanesulfonate and laurate are mutually competitive inhibitors, supporting

27 with a Km value similar to that observed for laurate as it activated H+ transport.

28 Laurate binding induces conformational changes in the fl

29 hydrolytic activity against caprylate (C8), laurate (C12) and myristate (C14).

30 (i) Laurate caused uncoupling protein-mediated H+ transport,

31 to nascent lipid A in place of the secondary laurate chain normally added by LpxL(HtrB).

32 acylated free lipid A containing a secondary laurate chain or a laurate and a myristate chain, respec

33 ichia coli LpxL, which transfers a secondary laurate chain to the 2' position of lipid A, in Yersinia

34 We show that laurate-dependent oxidation of NADPH and oxygen consumpt

35 BTE oilseed rape seeds facilitates efficient laurate deposition at the sn-2 position, resulting in th

36 x- and 30-fold higher, respectively, in high-laurate developing seeds.

37 Undecanesulfonate and laurate differed in two important respects.

38 The oxidations of lauric acid and methyl laurate displayed saturation kinetic behavior, which per

39 in At4g14070 (AAE15) was reduced 80% in 14C-laurate elongation into 16- and 18-carbon FAs.

40 Laurate elongation was 85% inhibited by 50 microm cerule

41 cyl-CoA intermediates were formed during 14C-laurate elongation, whereas 14C-acyl-ACP accumulated to

42 12 degrees C is accompanied by a decline in laurate from approximately 18% to approximately 5.5%.

43 ns in msbB are not defective in transferring laurate from lauroyl acyl carrier protein to (Kdo)2-lipi

44 h encodes the enzyme that normally transfers laurate from lauroyl-ACP to Kdo2-lipid IVA are not defec

45 The inner membrane enzyme LpxL transfers laurate from lauroyl-acyl carrier protein to the 2'- R-3

46 The laurate hydroxylase activities of cytochrome P450 2C2 or

47 ubstituted for the linker, had no detectable laurate hydroxylase activity in COS-1 cells, and minor a

48 3 catalyzes single-turnover and steady-state laurate hydroxylation with near stoichiometric product f

49 rome c has no effect on the K(m) and Vmax of laurate hydroxylation.

50 lipid A of cold-adapted MKV11 contained only laurate in amounts comparable with those seen in wild ty

51 e mature seed, resulting in up to 60 mol% of laurate in triacylglycerols.

52 The rate of laurate incorporation was reduced by several orders of m

53 Laurate induced tighter binding (Kd for the C12 azole lo

54 Undecanesulfonate inhibited laurate-induced H+ transport with competitive kinetics.

55 In these BTE oils, laurate is found almost exclusively at the sn-1 and sn-3

56 urate above 50 mol % further increases total laurate levels.

57 including the aggregation pheromones methyl laurate, methyl myristate, and methyl palmitate, attract

58 SNs) detect the fly-produced odorants methyl laurate (ML), methyl myristate, and methyl palmitate.

59 Saturated fatty acids (SFAs) such as laurate, myristate, and palmitate increased cellular tri

60 l-trans-, 13-cis-, and 9-cis-), fatty acids (laurate, myristate, palmitate, oleate, linoleate, arachi

61 ly acylated A. tequilana fructans with vinyl laurate, obtaining products with different degrees of po

62 erovar Typhimurium, removal of the secondary laurate or myristate chain in lipid A results in bacteri

63 P. aeruginosa PE did not contain either laurate or oleate, implying that the native attractant s

64 ncreasing the Km and decreasing the kcat for laurate oxidation.

65 The fatty acids fed in random order were laurate, palmitate, stearate, oleate, elaidate (the tran

66 the purified enzyme rapidly incorporated one laurate residue into (Kdo)2-lipid IVA.

67 to threefold at midstage development in high-laurate seeds.

68 duction of cytochrome c and hydroxylation of laurate simultaneously.

69 st ranged from a high of 41% of the dose for laurate to a low of 13% of the dose for stearate.

70 d, but infected HeLa cell cultures elongated laurate to myristate and palmitate.

71 l caprylate, vanillyl decanoate and vanillyl laurate) was obtained.

72 degrees C contained palmitoleate in place of laurate, whereas the lipid A of cold-adapted MKV11 conta

73 The replacement of laurate with palmitoleate in lipid A may reflect the des