ライフサイエンスコーパス: sn-2 position

1 hospholipids" containing "acyl 20:4" at the "sn-2 position".

2 a-linolenic, or docosahexaenoic acid) in the sn-2 position.

3 n positions of PC, with a preference for the sn-2 position.

4 pids through PC acyl editing, largely at the sn-2 position.

5 ere synthesized with perdeuterated SA at the sn-2 position.

6 line with a preference for hydrolysis at the sn-2 position.

7 f concentrated fatty acids esterified at the sn-2 position.

8 (5), 18:1Delta(5), and SA was present at the sn-2 position.

9 spholipid formation and was localized in the sn-2 position.

10 C18 FAs, palmitic acid was typically in the sn-2 position.

11 d head groups and acyl chains located at the sn-2 position.

12 40%, respectively, more arachidonate in the sn-2 position.

13 ere antigenic whether oxidized or not in the sn-2 position.

14 ocosahexaenoic acid (DHA, 22:6omega3) at the sn-2 position.

15 and a N-(DNP)-8-amino-octanoyl group at the sn-2 position.

16 generated by a PLA with specificity for the sn-2 position.

17 ing mechanism that operates at both sn-1 and sn-2 positions.

18 ., the larger branched acyl chain) is in the sn-2 position, a dramatic increase in binding affinity i

19 In particular, occurrence at the sn-2 position allows optimal intestinal absorption condi

20 analogs with a BODIPY-pentanoyl group at the sn-2 position and DNP linked to the amino head group.

21 s are cleaved by pPLAIIalpha at the sn-1 and sn-2 positions, and galactolipids, including those conta

22 on from fragment ions unique to the sn-1 and sn-2 positions, and the positions of carbon-carbon doubl

23 onalized phenyl groups at either the sn-1 or sn-2 position are consistent with the proposed binding m

24 B expression generated TAGs with 14:0 at the sn-2 position, but not 10:0.

25 ydrolyzes phospholipids at both the sn-1 and sn-2 positions, but prefers galactolipids to phospholipi

26 synthetase(s), and re-esterification to the sn-2 position by sn-2 acyltransferase activity (i.e. the

27 of PS-containing linoleic acid in either the sn-2 position (C(18:0)/C(18:2)) or in both sn-1 and sn-2

28 sition (C(18:0)/C(18:2)) or in both sn-1 and sn-2 positions (C(18:2)/C(18:2)), formed in the cytochro

29 holine (PC) substrate containing 20:4 in the sn-2 position compared with the wild-type enzyme, result

30 he presence of a diacylglycerol lipid, whose sn-2 position contains almost exclusively an C18:1 acyl

31 -valuable polyunsaturated fatty acids at the sn-2 position) could be very attractive for food industr

32 at meals rich in palmitic acid (16:0) in the sn-2 position decrease lipemia.

33 a higher proportion of palmitic acid in the sn-2 position decrease postprandial lipemia in healthy s

34 However, the DPA and DHA content in the sn-2 position did not vary significantly among the vario

35 2%) and DHA (28.83%) content, along with the sn-2 positioned EPA (3.25%), DPA (1.36%) and DHA (16.35%

36 DHA was found to predominate in the sn-2 position for gurnard head and snapper head.

37 n and either 22:6 or 20:2 fatty acids in the sn-2 position for MS1 and MS2, respectively.

38 ity, with polyunsaturated fatty acids at the sn-2 position generating polyunsaturated sn-2-acyl lysop

39 increasing chain length and exchanging sn-1/sn-2 position had only small effects.

40 DHA was preferentially located at the sn-2 position in both DHA-containing TAGs studied, while

41 pholipids containing arachidonic acid at the sn-2 position in comparison to oleic acid.

42 fatty acids are preferentially esterified in sn-2 position in hazelnut oil, while no significant pref

43 Fatty acids at sn-2 position in modified products were: C10:0, 4%; C16:

44 ances the probability that DHA chains at the sn-2 position in SDPC rise up to the bilayer surface, wh

45 n alpha,beta-unsaturated fatty acid from the sn-2 position in the second.

46 , DAG-sn-1 and DAG-sn-2, and both sn-1/3 and sn-2 positions in TAG.

47 r species, total fatty acids, and sn-1+3 and sn-2 positions in the two lipid pools are similar, excep

48 10:0 fatty acids in the Camelina sativa TAG sn-2 position, indicating a 10:0 CoA specificity that ha

49 cerophospholipids (SML) in which the sn-1 or sn-2 position is covalently attached to cholesterol and

50 currence of saturated fatty acids in the TAG sn-2 position is infrequent in seed oils.

51 se TAGs contained up to 40 mol % 10:0 in the sn-2 position, nearly double the amounts obtained from c

52 pholipids containing arachidonic acid at the sn-2 position occurs when a critical concentration of 's

53 ing AA from the stereospecifically numbered (sn) 2 position of phospholipids, and regional [3H]AA upt

54 lipase A2 (PLA2)-catalyzed hydrolysis at the sn-2 position of 1,2-dimyristoyl-sn-glycero-3-phosphocho

55 the transfer of a fatty acyl moiety from the sn-2 position of a phospholipid to the sn-3-position of

56 ncorporation of arachidonate, first into the sn-2 position of a preformed phosphatidylinositol (PI) m

57 Phospholipase A(2) (PLA(2)) hydrolyzes the sn-2 position of cell membrane phospholipids to release

58 l fatty acids were largely excluded from the sn-2 position of chloroplast galactolipids and seed tria

59 Delta6 desaturase utilised linoleate at the sn-2 position of exogenously supplied PtdCho presented t

60 lectively transfers a palmitoyl chain to the sn-2 position of G3P and sn-1-lysophosphatidic acid (LPA

61 is esterify acyl groups predominantly to the sn-2 position of G3P.

62 Remodeling occurs first at the sn-2 position of glycerol, involving removal of a longer

63 of cell membranes that is esterified to the sn-2 position of glycerophospholipids and is released fr

64 es a Delta(3-trans) hexadecenoic acid in the sn-2 position of its core glyceryl moiety.

65 T results in the incorporation of CPA at the sn-2 position of lysophosphatidic acid.

66 lly introduces polyunsaturated acyl onto the sn-2 position of lysophosphatidylcholine, thereby modula

67 ferase reaction by adding a palmitate to the sn-2 position of lysophospholipids.

68 role in liberating arachidonic acid from the sn-2 position of mammalian cellular phospholipids.

69 lective release of arachidonic acid from the sn-2 position of membrane phospholipids and has been sug

70 or linolenoyl than oleoyl moieties from the sn-2 position of PC to TAG.

71 in transferring acyl groups modified at the sn-2 position of PC to the sn-1 position of this molecul

72 ds were preferentially incorporated into the sn-2 position of PC, but the sn-1 position of de novo DA

73 e (LCAT), which is normally specific for the sn-2 position of phosphatidylcholine (PC), derives a sig

74 tes a preference for arachidonic acid at the sn-2 position of phosphatidylcholine as compared with pa

75 When 11,12-EET was esterified to the sn-2 position of phosphatidylcholine, restricting it to

76 In this pathway a fatty acid in the sn-2 position of phosphatidylethanolamine or phosphatidy

77 lective release of arachidonic acid from the sn-2 position of phospholipids and is believed to play a

78 ncorporated 20-[(3)H]HETE primarily into the sn-2 position of phospholipids through a coenzyme A-depe

79 catalyze hydrolysis of fatty acids from the sn-2 position of phospholipids.

80 poration of unsaturated acyl chains into the sn-2 position of phospholipids.

81 on by rapid turnover of acyl moieties at the sn-2 position of phospholipids.

82 ectively liberated arachidonic acid from the sn-2 position of plasmenylcholine substrates.

83 s able to hydrolyze the acetyl moiety at the sn-2 position of platelet-activating factor.

84 The sn-2 position of TAGs in hybrid palm oil was shown to be

85 ed, instead of saturated, fatty acids in the sn-2 position of the alkylacylglycerolipid component.

86 trate, CrDGTT1 preferred C16 over C18 in the sn-2 position of the glycerol backbone, but CrDGTT2 and

87 lysis of long-chain fatty acid esters at the sn-2 position of the glycerol backbone.

88 The reaction involves acyl transfer from the sn-2 position of the glyceryl moiety to the amino group

89 phy (GC) to determine FAs composition in the sn-2 position of the PC.

90 e subsite for the oxidized fatty acid at the sn-2 position of the phospholipid backbone.

91 Characterization of 5,6-trans-EET in the sn-2 position of the phospholipids was accomplished by h

92 The fatty acid in the sn-2 position of this biologically active isomer and its

93 C]fatty acids incorporated into the sn-1 and sn-2 positions of DAG through glycerol-3-phosphate acyla

94 tants, the esterification of both sn-1,3 and sn-2 positions of glycerol was impacted, and their cutin

95 acyl groups esterified at both the sn-1 and sn-2 positions of glycerol.

96 s a cycle that enriches CPA at both sn-1 and sn-2 positions of PC and results in increased accumulati

97 ould cleave acyl chains at both the sn-1 and sn-2 positions of PC, and displayed substrate selectivit

98 hatic groups readily from either the sn-1 or sn-2 positions of phospholipids.

99 anoyl and octyl lipid chains at the sn-1 and sn-2 positions of the glycerol backbone and phosphonoino

100 the fatty acyl substituents at the sn-1 and sn-2 positions of the glycerol backbone.

101 lysis of ester linkages at both the sn-1 and sn-2 positions of the glycerophospholipids.

102 nd MS/MS to show that AT1G78690 acylates the sn-2-position of 1-acyllyso-PE and 1-acyllyso-PG.

103 of cell membranes that is esterified to the sn-2-position of glycerophospholipids and is released fr

104 However, a ricinoleoyl group at the sn-2-position of PC was removed 4-6-fold faster than an

105 ransferase (LPAT) catalyzes acylation of the sn-2 position on lysophosphatidic acid by an acyl CoA su

106 - CH3](-) suggest favorable cleavage at the sn-2 position over the sn-1 due to distinct differences

107 ng alpha-phenylalkylidene side chains at the sn-2 position represent excellent scaffolds upon which t

108 2G2A) hydrolyzes glycerophospholipids at the sn-2 position resulting in the release of fatty acids an

109 ilitates efficient laurate deposition at the sn-2 position, resulting in the acccumulation of trilaur

110 Thus oleate at sn-1 and sn-2 positions served as substrate for the delta12 desat

111 son using PG with various acyl chains on the sn-2 position showed that oleate and linoleate were pref

112 rminal negatively charged carboxylate at the sn-2 position suffices to generate high binding affinity

113 hermore, analysis of acyl chains at sn-1 and sn-2 positions that accumulated in PC from S. foetida de

114 r, we found the fatty acid preference at the sn-2 position to be highly dependent upon substrate pres

115 beta) hydrolyzes glycerophospholipids at the sn-2-position to yield a free fatty acid and a 2-lysopho

116 The proportion of EPA in the sn-2 position was substantially higher in fish roe (12.6

117 mega 6, 20:5 omega 3, or 22:6 omega 3 at the sn-2 position were investigated in a matrix of dioleoylp

118 es C, the compounds with stigmasterol at the sn-2 position were more stable than those with stigmaste

119 at the sn-1 position and arachidonate at the sn-2 position were similar (kapp = 0.04 min-1 at 22 degr

120 ith oleic acid at sn-1,3 and stigmasterol at sn-2 position were the most stable compounds.

121 s that hydrolyze glycerophospholipids at the sn-2 position, which leads to the production of lipid me

122 tidylcholine (PC) esterified at the sn-1 and sn-2 positions, with alpha-eleostearic acid (9Z, 11E, 13