ライフサイエンスコーパス: straight chain

1 linear alpha-helices but less extended than straight chains.

2 lenic acids and are characterized by C17-C23 straight chains, 1-3 cis double bonds separated by methy

3 Exposure to straight-chain acids leads to a binary ligand shell that

4 methyldecanoyl-CoA, and isobutanoyl-CoA) and straight-chain acyl-CoA esters (decanoyl-CoA, octanoyl-C

5 pha)-inducible pathway capable of catalyzing straight-chain acyl-CoAs and a second noninducible pathw

6 ACX1A exhibited a preference for C12 and C14 straight-chain acyl-CoAs and also was active in the meta

7 ator-inducible pathway capable of catalyzing straight-chain acyl-CoAs by fatty acyl-CoA oxidase, L-bi

8 ding a broader range of acyl-HSLs, including straight-chain acyl-HSLs to which LuxR does not respond.

9 ant of LuxR-G2E that retains the response to straight-chain acyl-HSLs, but no longer responds to 3OC6

10 affinity with little difference between the straight-chain alcohol esters (from methyl to n-butyl).

11 ting ligands is increased through the use of straight chain alcohols, ROH, solvation of Pb(2+) is obs

12 e found to increase with the addition of the straight-chain alcohols ethanol, octanol, and to some ex

13 s of the series were those that could form a straight chain aldehyde intermediate after esterase-medi

14 Straight chain aldehydes and alcohols demonstrated signi

15 rs from a homologous series of iso-intensive straight-chain aldehydes that differed serially by only

16 re of fatty acids, an ester, and a series of straight-chain aldehydes.

17 raged peak areas for terpenes, pyrazines and straight-chained aldehydes.

18 ogressively by replacing W26 with non-coded, straight-chain aliphatic amino acids of increasing chain

19 Carbon chain length in several classes of straight-chain aliphatic odorants has been proposed as a

20 Patterns evoked by straight-chained aliphatic odorants confirmed an associa

21 rs have been functionalized with hydrophobic straight chain alkane units (C6, C12, and C18) while the

22 The mass spectrum for a straight-chain alkane mixture (C(21)-C(40)) shows compar

23 a membrane-spanning metalloenzyme, converts straight chain alkanes to alcohols in the first step of

24 Functionalization molecules included straight chain alkanes, anionically charged dye molecule

25 indrical capsule provides an environment for straight-chain alkanes that can properly fill the space

26 rential responses we observed previously for straight-chained alkanes of differing carbon number, the

27 lfactory responses to a homologous series of straight-chained alkanes that consisted of purely hydroc

28 A series of straight chain alkyl amides demonstrated that the optima

29 Two labile straight chain alkyl motifs were developed: a cysteine d

30 esterified with a variety of isoprenoid and straight-chain alkyl alcohols as in FAPs.

31 Straight-chain alkyl amides are one of the few classes o

32 isoflavone with a free 4'-OH function and a straight-chain alkyl substituent at the 7 position that

33 e study the interfacial behavior between the straight-chain alkyl surfactant sodium dodecyl sulfate (

34 Beginning with straight-chain alkyl, amine-terminated self-assembled mo

35 The thermochemistry of straight-chain alkynes and polyynes is very self-consist

36 ction that allowed stepwise incorporation of straight chain amino acid linkers and a bis-benzimidazol

37 ranched hydrophobic substrate but permit the straight-chain amino acids to be used as substrates.The

38 nstitution of acyltransferase activity using straight-chain analogues were unsuccessful, suggesting t

39 ct with residual -OH, whereas, on the longer straight chain anchor, reaction occurs exclusively at th

40 as comprised of a 20:80 (mol/mol) mixture of straight chain and iso-branched isomers, while the corre

41 ovides C.t. with the capacity to incorporate straight-chain and bacterial specific branched-chain fat

42 [M - H](+) is the dominant species for straight-chain and branched alkanes.

43 site discriminates the tertiary structure of straight-chain and branched-chain alcohols and appears t

44 representing 3 amine classes (alkanolamines, straight-chain and cyclic diamines, and amino acids), th

45 cture, the glucose sugar is observed in both straight-chain and ring forms.

46 u protein, arachidonic acid, and a series of straight chain anionic, cationic, and nonionic detergent

47 onization generates abundant ion signals for straight-chain, branched, and cycloalkanes with minimal

48 These straight-chained, branched, cyclic, and double-bonded mo

49 Hydrocarbon structural categories included straight-chained, branched, double-bonded, alicyclic, an

50 ultifold upregulation of almost all detected straight chain, but not branched, FAlc in MG lipidomes o

51 ylation was initially discovered as a normal straight chain butyrylation (Knbu).

52 aromatic (benzene, toluene, and xylene) and straight-chain (C(5) to C(12)) hydrocarbons present in p

53 pping effects resulting from branched versus straight-chain capping ligands were compared and a possi

54 interstellar medium (ISM) are organic with a straight-chain carbon backbone.

55 ve higher octane numbers compared with their straight-chain counterparts.

56 ulting lower net acetate supply rate towards straight chain elongation led to an increased selectivit

57 The formed acetate in turn stimulated straight chain elongation, but the resulting lower net a

58 The microbiome preferred straight-chain elongation over branched-chain elongation

59 The emission of straight-chain esters decreased under extremely low O(2)

60 molar K(d) values) in the order: cholesterol straight chain fatty acid > kinked chain fatty acid.

61 Straight chain fatty acid alpha-oxidation increases duri

62 nd suggested to catalyze the initial step of straight chain fatty acid alpha-oxidation.

63 xybutyric acid ((S)-3,4-DHBA), an endogenous straight chain fatty acid, is a normal human urinary met

64 alcohol acetates (HAAs) and ethyl esters of straight chain fatty acids (EEFAs) at the end of ferment

65 paralogue leading to a greater proportion of straight chain fatty acids in the membrane, and the upre

66 pathway involving, in the case of saturated straight chain fatty acids of even carbon number, at lea

67 in, the first two enzymes of the peroxisomal straight-chain fatty acid beta-oxidation pathway, exhibi

68 Initiation of straight-chain fatty acid biosynthesis by the type II FA

69 preferentially expressed candidate genes for straight-chain fatty acid biosynthesis confirmed their r

70 suggests that a FabH-independent pathway for straight-chain fatty acid biosynthesis operates in S. gl

71 othesis that TCDD dose-dependently repressed straight-chain fatty acid oxidation gene expression in m

72 cyl substituents (called phleic acids) and a straight-chain fatty acid residue and share a common bas

73 le butyryl-CoA was converted to palmitate (a straight-chain fatty acid).

74 ated 75 (Cys122Ala) to 500% (Cys122Gln) more straight-chain fatty acids (SCFA) than the corresponding

75 uch as Escherichia coli, which generate only straight-chain fatty acids (SCFAs), FabH has a substrate

76 and is applied to a mixture of branched- and straight-chain fatty acids derived from Bacillus subtili

77 ete acylsugars, which are branched-chain and straight-chain fatty acids esterified to Glu or Suc.

78 rial oxidation, and esterification of normal straight-chain fatty acids has been studied extensively,

79 efold increase in the cellular levels of the straight-chain fatty acids palmitate and myristate.

80 The production of straight-chain fatty acids produced was significantly co

81 stry-capable alkyne probes for branched- and straight-chain fatty acids uncovered 1,013 S-acylated pr

82 LS) showed that acetates and ethyl esters of straight-chain fatty acids were associated with floral a

83 higher concentrations of the ethyl esters of straight-chain fatty acids, ethyl, hexyl, isoamyl acetat

84 19-carbon fatty acids with 18- and 20-carbon straight-chain fatty acids.

85 OPDA and OPC-8:0, as well as medium-to-long straight-chain fatty acids.

86 Most of the known signals are straight-chain fatty acyl-HSLs, and evidence indicates t

87 reaction rate, the esterifications of C4-C18 straight-chain fatty alcohol with dihydrocaffeic acid (D

88 r 9c but only 33 for 9d, suggesting that the straight-chained fatty alcohol esters were more therapeu

89 thermophiles may use sugars in both ring and straight chain forms.

90 -bonded molecular junctions typically occupy straight-chain geometries due to steric effects.

91 eased hydrogenolysis rates relative to their straight-chain homologues in both homogeneous and hetero

92 These odorants had a common straight-chain hydrocarbon structure, but differed syste

93 ex food and environmental samples, including straight-chain hydrocarbons, primary alcohols, secondary

94 of alkanes (from six to 16 carbons) that are straight-chained hydrocarbons without functional groups.

95 ta participated in error-prone bypass of the straight-chain lesions, whereas Pol kappa preferentially

96 Unlike conventional PNCs capped with straight-chain ligands, APTES-capped PNCs show high stab

97 tylene spacer group, (2) either a two-carbon straight chain linker or a conformationally restricting

98 are examples synthesized with the two-carbon straight chain linker, whereas 26-31 are analogues prepa

99 SAM formation was also probed for straight-chain molecules, hexadecanethiol and hexadecane

100 dson's law states that the acute toxicity of straight-chain monohydroxy alcohols is directly proporti

101 -2 H-1-benzopyran linked to a 3-alkylindole (straight chain), more specifically substituted with a 5-

102 glycine was acylated almost exclusively with straight-chain myristic acid, whereas lysine was acylate

103 A series of straight-chain N5-aminoalkylacyl derivatives demonstrate

104 It exhibits straight chains of face-sharing [IrO(6)] octahedra, whic

105 structural analysis suggests the presence of straight chains of Te atoms ( approximately 3.0 A apart)

106 Straight chain peptide-bound aliphatic phosphates of the

107 orooctanoic acid, has been investigated on a straight-chain perfluorohexyl adsorbent.

108 ention mechanisms of perfluoroalkyl acids on straight-chain perfluorohexyl sorbents are discussed.

109 thyl-bridged organic/inorganic (BEH-C18) and straight-chain perfluorohexylpropyl silica (C6F13), have

110 ugh its B cell ligand has been identified as straight chain poly-N-acetyl-lactosamine (SC-PNAL), the

111 exclusively by either a branched-chain or a straight-chain probe, demonstrating acylation specificit

112 tive pathogen with phospholipids composed of straight chain saturated and monounsaturated fatty acids

113 led to the formation of wax monoesters from straight chain saturated, unsaturated, and polyunsaturat

114 h, rats were exposed to homologous series of straight-chained, saturated aliphatic aldehydes, ethyl e

115 distinction of branched chains from isomeric straight-chain species and the localization of branching

116 CN), with an abundance 0.4 times that of its straight-chain structural isomer.

117 The transition from ring form to straight-chain substrate is achieved through rotation of

118 sts that pyrococcal PGI has a preference for straight chain substrates and that metabolism in extreme

119 nylzinc reagents derived from both bulky and straight chain terminal alkynes.

120 er the other to form infinite ...Ti-O...Ti-O straight chains with alternating short and long Ti-O dis