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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
8 in gonococci encodes for a late-functioning lauroyl acyl transferase that adds a lauric acid at posi
10 membrane enzyme LpxL transfers laurate from lauroyl-acyl carrier protein to the 2'- R-3-hydroxymyris
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
16 yl-CoA substrates, and product inhibition by lauroyl-CoA suggest that this region is important for co
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
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
28 oring msbB+ bearing plasmids acylate (Kdo)2-(lauroyl)-lipid IVA very rapidly compared with wild type.
31 um tuberculosis, FabH catalyzes extension of lauroyl, myristoyl and palmitoyl groups from which cell
33 r hexaacylated lipid A, we overexpressed the lauroyl- or the myristoyltransferase of lipid A biosynth
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
40 and lambda233) capable of overexpressing the lauroyl transferase that functions after 3-deoxy-D-manno
42 nhibitor of steroid sulfatase activity was n-lauroyl tryamine phosphate with a Ki of 3.6 microM and 5
44 s deduced (oleoyl dopamine, oleoyl tyramine, lauroyl tryptamine, oleoyl aminovaleric acid, a-linoleno