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1                                SM containing lauroyl (12:0) acyl chains displayed only liquid-expande
2          The membrane fluorescence probes, 6-lauroyl-2-(dimethylamino) napthalene, 6-propionyl-2-(dim
3  effects of temperature and pH on Laurdan (6-lauroyl-2-(dimethylamino)naphthalene) fluorescence inten
4 ho-1'-rac-glycerol (LMPG, anionic) than in 1-lauroyl-2-hydroxy-sn-glycero-3-phosphocholine (LLPC, zwi
5  enzyme that normally transfers laurate from lauroyl-ACP to Kdo2-lipid IVA are not defective in the c
6                                         With lauroyl acyl carrier protein as the donor, the purified
7 e not defective in transferring laurate from lauroyl acyl carrier protein to (Kdo)2-lipid IVA.
8  in gonococci encodes for a late-functioning lauroyl acyl transferase that adds a lauric acid at posi
9               Expression of a California bay lauroyl-acyl carrier protein thioesterase (MCTE) in deve
10  membrane enzyme LpxL transfers laurate from lauroyl-acyl carrier protein to the 2'- R-3-hydroxymyris
11 zwitterionic and anionic membranes made from lauroyl (C12:0) or myristoyl (C14:0) lipids.
12 xovaleric acid, 3-methyl-2-oxobutanoic acid, lauroyl-carnitine) in response to AL and even more with
13  highest specificity for l-Tyr and l-Phe and lauroyl-CoA (k(cat)/K(M) = 5.9 +/- 0.8 x 10(3) M(-1)s(-1
14 eptor, whereas oleoyl-CoA was preferred over lauroyl-CoA as an acyl donor.
15                                              Lauroyl-CoA oxidase activity but not palmitoyl-CoA oxida
16 yl-CoA substrates, and product inhibition by lauroyl-CoA suggest that this region is important for co
17            The Km values of octanoyl-CoA and lauroyl-CoA were determined to be 1.1 +/- 0.3 and 10 +/-
18 ificantly reduce the reactivity of PhlD with lauroyl-CoA while still retaining its physiological acti
19 -CoAs, where the Hill coefficient is 3.8 for lauroyl-CoA, but decrease for long chain acyl-CoAs, wher
20 chaelis substrate complex of a FabH, that of lauroyl-coenzyme A with a catalytically disabled Cys-->A
21 between selectivity and yield: 40% yield for lauroyl glycine and less than 5% for dipeptide after 96h
22                                 Synthesis of lauroyl glycine lipoaminoacid was carried out with a lip
23 Results indicate that both enzymes favor the lauroyl glycine synthesis over the peptide synthesis, bu
24 itine, malonyl carnitine, glutarylcarnitine, lauroyl-L-carnitine, dodecenoylcarnitine, 3-hydroxytetra
25 ed not only the formation in vitro of Kdo 2-(lauroyl)-lipid IV A but also a slow second acylation, ge
26                      MsbB acylates (KDO)(2)-(lauroyl)-lipid IV-A with myristate during lipid A biosyn
27                        MsbB acylates (Kdo)2-(lauroyl)-lipid IVA about 100 times faster than (Kdo)2-li
28 oring msbB+ bearing plasmids acylate (Kdo)2-(lauroyl)-lipid IVA very rapidly compared with wild type.
29 e product formed by HtrB, designated (Kdo)2-(lauroyl)-lipid IVA.
30 ate or laurate, activated on ACP, to (Kdo)2-(lauroyl)-lipid IVA.
31 um tuberculosis, FabH catalyzes extension of lauroyl, myristoyl and palmitoyl groups from which cell
32 erculosis FabH, which catalyzes extension of lauroyl, myristoyl and palmitoyl groups.
33 r hexaacylated lipid A, we overexpressed the lauroyl- or the myristoyltransferase of lipid A biosynth
34                                       Sodium lauroyl sarcosinate (sarkosyl) was applied to enhance th
35 n bound to a micelle of the detergent sodium lauroyl sarcosinate (SLAS).
36 ccomplished in a single step with EDTA and N-lauroyl sarcosine (ES; pH 8.5 to 9.3) incubation at 50 d
37 roup region of the PLFE liposomes, while the lauroyl tail inserts into the hydrocarbon core of the me
38  insertions in htrB were found to contain no lauroyl transferase activity.
39                             htrB encodes the lauroyl transferase of lipid A biosynthesis that acylate
40 and lambda233) capable of overexpressing the lauroyl transferase that functions after 3-deoxy-D-manno
41 d growth above 33 degrees C might encode the lauroyl transferase.
42 nhibitor of steroid sulfatase activity was n-lauroyl tryamine phosphate with a Ki of 3.6 microM and 5
43                                              Lauroyl tryptamine is found to be an antagonist to the i
44 s deduced (oleoyl dopamine, oleoyl tyramine, lauroyl tryptamine, oleoyl aminovaleric acid, a-linoleno