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1 d the highest activity towards 4-nitrophenyl laurate.
2  acylated to produce chlorobactene glucoside laurate.
3  the production of oils containing up to 50% 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 axanthin 3-O-palmitate, (all-E)-violaxanthin laurate and (all-E)-violaxanthin palmitate.
13  A containing a secondary laurate chain or a laurate and a myristate chain, respectively.
14 ite-directed mutant proteins of CYP4A7 found laurate and arachidonate activity markedly diminished in
15 ther hand, exhibited remarkable increases in laurate and arachidonate metabolism (3-fold) above wild-
16        Steady-state turnover rates with both laurate and arachidonate showed the trend WT > F393Y >>
17 the stimulation of cytochrome c reduction by laurate and CO.
18 enzene, Tris buffer, lauric acid, and methyl laurate and epoxidations of styrene and 10-undecenoic ac
19 ed out a comparative study of the effects of laurate and its close analogue, undecanesulfonate.
20 tive analysis showed a comparable release of laurate and myristate but no release of 3-hydroxymyrista
21 d disaccharide of glucosamine with secondary laurate and myristate chains on the distal unit.
22 f 27-hydroxyoctacosanoate and the absence of laurate and myristate in R. leguminosarum.
23 ation as the loss of radiolabeled secondary (laurate and myristate) and primary fatty acids (3-hydrox
24                                              Laurate and other substrates stimulate cytochrome c redu
25 vities were monitored on p-NP-butyrate, p-NP-laurate and p-NP-palmitate.
26                                         Both laurate and undecanesulfonate inhibited Cl- with competi
27           We show that undecanesulfonate and laurate are mutually competitive inhibitors, supporting
28 with a Km value similar to that observed for laurate as it activated H+ transport.
29                                              Laurate binding induces conformational changes in the fl
30  hydrolytic activity against caprylate (C8), laurate (C12) and myristate (C14).
31 kin S. epidermidis, in the presence of PEG-8 Laurate, can mediate cyclophilin A to elicit an electric
32                                          (i) Laurate caused uncoupling protein-mediated H+ transport,
33 to nascent lipid A in place of the secondary laurate chain normally added by LpxL(HtrB).
34 acylated free lipid A containing a secondary laurate chain or a laurate and a myristate chain, respec
35 ichia coli LpxL, which transfers a secondary laurate chain to the 2' position of lipid A, in Yersinia
36                                 We show that laurate-dependent oxidation of NADPH and oxygen consumpt
37 BTE oilseed rape seeds facilitates efficient laurate deposition at the sn-2 position, resulting in th
38 x- and 30-fold higher, respectively, in high-laurate developing seeds.
39                        Undecanesulfonate and laurate differed in two important respects.
40     The oxidations of lauric acid and methyl laurate displayed saturation kinetic behavior, which per
41  in At4g14070 (AAE15) was reduced 80% in 14C-laurate elongation into 16- and 18-carbon FAs.
42                                              Laurate elongation was 85% inhibited by 50 microm cerule
43 cyl-CoA intermediates were formed during 14C-laurate elongation, whereas 14C-acyl-ACP accumulated to
44  12 degrees C is accompanied by a decline in laurate from approximately 18% to approximately 5.5%.
45 ns in msbB are not defective in transferring laurate from lauroyl acyl carrier protein to (Kdo)2-lipi
46 h encodes the enzyme that normally transfers laurate from lauroyl-ACP to Kdo2-lipid IVA are not defec
47     The inner membrane enzyme LpxL transfers laurate from lauroyl-acyl carrier protein to the 2'- R-3
48 r head group, an ester linkage, and a single laurate group at any position are all necessary for GML
49  group, linkage of acyl chain, and number of laurate groups.
50                                          The laurate hydroxylase activities of cytochrome P450 2C2 or
51 ubstituted for the linker, had no detectable laurate hydroxylase activity in COS-1 cells, and minor a
52 3 catalyzes single-turnover and steady-state laurate hydroxylation with near stoichiometric product f
53 rome c has no effect on the K(m) and Vmax of laurate hydroxylation.
54 lipid A of cold-adapted MKV11 contained only laurate in amounts comparable with those seen in wild ty
55 e mature seed, resulting in up to 60 mol% of laurate in triacylglycerols.
56                                  The rate of laurate incorporation was reduced by several orders of m
57                                              Laurate induced tighter binding (Kd for the C12 azole lo
58                  Undecanesulfonate inhibited laurate-induced H+ transport with competitive kinetics.
59 on of C. acnes and S. epidermidis plus PEG-8 Laurate into the mouse ear considerably suppressed the g
60                           In these BTE oils, laurate is found almost exclusively at the sn-1 and sn-3
61 urate above 50 mol % further increases total laurate levels.
62  including the aggregation pheromones methyl laurate, methyl myristate, and methyl palmitate, attract
63 n-Hp), isopropyl myristate (IPM), and methyl laurate (ML) were used.
64 SNs) detect the fly-produced odorants methyl laurate (ML), methyl myristate, and methyl palmitate.
65         Saturated fatty acids (SFAs) such as laurate, myristate, and palmitate increased cellular tri
66 l-trans-, 13-cis-, and 9-cis-), fatty acids (laurate, myristate, palmitate, oleate, linoleate, arachi
67 ly acylated A. tequilana fructans with vinyl laurate, obtaining products with different degrees of po
68 after pipetting S. epidermidis plus 2% PEG-8 Laurate onto anodes.
69 erovar Typhimurium, removal of the secondary laurate or myristate chain in lipid A results in bacteri
70      P. aeruginosa PE did not contain either laurate or oleate, implying that the native attractant s
71 ncreasing the Km and decreasing the kcat for laurate oxidation.
72     The fatty acids fed in random order were laurate, palmitate, stearate, oleate, elaidate (the tran
73 the purified enzyme rapidly incorporated one laurate residue into (Kdo)2-lipid IVA.
74 to threefold at midstage development in high-laurate seeds.
75 duction of cytochrome c and hydroxylation of laurate simultaneously.
76 st ranged from a high of 41% of the dose for laurate to a low of 13% of the dose for stearate.
77 d, but infected HeLa cell cultures elongated laurate to myristate and palmitate.
78 ncubated with 2% polyethylene glycol (PEG)-8 Laurate to yield electricity which was measured by a vol
79 at LpxO catalyzes the 2-hydroxylation of the laurate transferred by A. baumannii LpxL.
80 l caprylate, vanillyl decanoate and vanillyl laurate) was obtained.
81 degrees C contained palmitoleate in place of laurate, whereas the lipid A of cold-adapted MKV11 conta
82                           The replacement of laurate with palmitoleate in lipid A may reflect the des