ライフサイエンスコーパス: lauroyl

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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 eptor, whereas oleoyl-CoA was preferred over lauroyl-CoA as an acyl donor.

13 Lauroyl-CoA oxidase activity but not palmitoyl-CoA oxida

14 yl-CoA substrates, and product inhibition by lauroyl-CoA suggest that this region is important for co

15 The Km values of octanoyl-CoA and lauroyl-CoA were determined to be 1.1 +/- 0.3 and 10 +/-

16 ificantly reduce the reactivity of PhlD with lauroyl-CoA while still retaining its physiological acti

17 -CoAs, where the Hill coefficient is 3.8 for lauroyl-CoA, but decrease for long chain acyl-CoAs, wher

18 chaelis substrate complex of a FabH, that of lauroyl-coenzyme A with a catalytically disabled Cys-->A

19 between selectivity and yield: 40% yield for lauroyl glycine and less than 5% for dipeptide after 96h

20 Synthesis of lauroyl glycine lipoaminoacid was carried out with a lip

21 Results indicate that both enzymes favor the lauroyl glycine synthesis over the peptide synthesis, bu

22 ed not only the formation in vitro of Kdo 2-(lauroyl)-lipid IV A but also a slow second acylation, ge

23 MsbB acylates (KDO)(2)-(lauroyl)-lipid IV-A with myristate during lipid A biosyn

24 MsbB acylates (Kdo)2-(lauroyl)-lipid IVA about 100 times faster than (Kdo)2-li

25 oring msbB+ bearing plasmids acylate (Kdo)2-(lauroyl)-lipid IVA very rapidly compared with wild type.

26 e product formed by HtrB, designated (Kdo)2-(lauroyl)-lipid IVA.

27 ate or laurate, activated on ACP, to (Kdo)2-(lauroyl)-lipid IVA.

28 um tuberculosis, FabH catalyzes extension of lauroyl, myristoyl and palmitoyl groups from which cell

29 erculosis FabH, which catalyzes extension of lauroyl, myristoyl and palmitoyl groups.

30 r hexaacylated lipid A, we overexpressed the lauroyl- or the myristoyltransferase of lipid A biosynth

31 Sodium lauroyl sarcosinate (sarkosyl) was applied to enhance th

32 n bound to a micelle of the detergent sodium lauroyl sarcosinate (SLAS).

33 ccomplished in a single step with EDTA and N-lauroyl sarcosine (ES; pH 8.5 to 9.3) incubation at 50 d

34 roup region of the PLFE liposomes, while the lauroyl tail inserts into the hydrocarbon core of the me

35 insertions in htrB were found to contain no lauroyl transferase activity.

36 htrB encodes the lauroyl transferase of lipid A biosynthesis that acylate

37 and lambda233) capable of overexpressing the lauroyl transferase that functions after 3-deoxy-D-manno

38 d growth above 33 degrees C might encode the lauroyl transferase.

39 nhibitor of steroid sulfatase activity was n-lauroyl tryamine phosphate with a Ki of 3.6 microM and 5

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