ライフサイエンスコーパス: tripolyphosphate

1 anganese and are inept at cleaving inorganic tripolyphosphate.

2 0.05% and 3% sodium trimetaphosphate/sodium tripolyphosphate.

3 In fact, orthophosphate, inorganic tripolyphosphate (3polyP), adenosine triphosphate (ATP)

4 tive inhibitors of cvRtp1 (K(i) = 0.6 microm tripolyphosphate and 2.4 microm pyrophosphate, respectiv

5 ociated to the presence of adulterants NaCl, tripolyphosphate and carrageenan.

6 We found that tripolyphosphate and pyrophosphate were potent competiti

7 orthophosphate, adenosine triphosphate, and tripolyphosphate, and a simple binding model is develope

8 anions-orthosilicate, borate, pyrophosphate, tripolyphosphate, and dibasic phosphate-that when introd

9 = 13), demonstrated that Zn, orthophosphate, tripolyphosphate, and hexametaphosphate corrosion/scalin

10 ated with Fo and GDP, GTP, pyrophosphate, or tripolyphosphate, and the hydrolysis of F(420)-0 to Fo.

11 anisms of AdoMet formation and hydrolysis of tripolyphosphate are proposed.

12 o AdoMet, PP(i), and P(i), with formation of tripolyphosphate as a tightly bound intermediate.

13 Adenosine tripolyphosphate (ATP) is a small polyvalent anion that

14 licifolium were encapsulated in the chitosan-tripolyphosphate carrier.

15 he sulfur of methionine displaces the intact tripolyphosphate chain (PPP(i)) from ATP, and subsequent

16 This research explores the interactions of tripolyphosphate-chitosan-pea protein (TPP-CS-PP) in imp

17 omplex-forming model ligands (pyrophosphate, tripolyphosphate, ethylenediaminetetraacetic acid, oxala

18 ed either with chitosan (Ch) or using sodium tripolyphosphate for chitosan complexation (TPP-Ch).

19 P = Mg(2+); and for myosin V pyrophosphate = tripolyphosphate > ATP-Mg(2+) = ATP = AMP-PNP > ADP = te

20 adenylyl imidodiphosphate) > pyrophosphate = tripolyphosphate > tetrapolyphosphate = ADP > cAMP = Mg(

21 5*A enzyme has a 100-fold greater k(cat) for tripolyphosphate hydrolysis than the wild type enzyme, b

22 alytic impairment in the partial reaction of tripolyphosphate hydrolysis.

23 = 1 mM), pyrophosphate (I(0.5) = 0.4 mM) and tripolyphosphate (I(0.5) = 30 microM).

24 0-fold whereas the rate of hydrolysis of the tripolyphosphate intermediate is decreased by less than

25 We show that tripolyphosphate is a potent competitive inhibitor of Tb

26 substrate for AdoMet formation during which tripolyphosphate is produced.

27 le to those obtained from tetrapolyphosphate-tripolyphosphate mixtures.

28 m oil and beta-carotene with chitosan/sodium tripolyphosphate or chitosan/carboxymethylcellulose and

29 d from tetrapolyphosphate in the presence of tripolyphosphate or NH4NO3 at higher concentrations (app

30 r diphosphates but not AMP, cAMP, adenosine, tripolyphosphate, or pyrophosphate.

31 rsion steps [AdoMet formation and subsequent tripolyphosphate (PPP(i)) hydrolysis], and product relea

32 describes a nonhydrolyzable analogue of the tripolyphosphate (PPP(i)) reaction intermediate, diimido

33 hetase catalyzes the formation of AdoMet and tripolyphosphate (PPPi) from ATP and L-methionine and th

34 rase) catalyzes a two-step reaction in which tripolyphosphate (PPPi) is a tightly bound intermediate.

35 enzyme, EutT was not inhibited by inorganic tripolyphosphate (PPPi).

36 f the methionine segment of AdoMet or in the tripolyphosphate segment of AMPPNP, these portions of th

37 low stripe trevally surimi added with sodium tripolyphosphate (STPP) (0.25% and 0.5%, w/w) and protei

38 tudy, similarities and differences of sodium tripolyphosphate (STPP) and sodium trimetaphosphate (STM

39 rn leatherjacket, phosphorylated with sodium tripolyphosphate (STPP) at various concentrations (0.25%

40 zed by their ability to hydrolyze a range of tripolyphosphate substrates.

41 ) CthTTM is 150-fold more active in cleaving tripolyphosphate than ATP and (ii) the substrate specifi

42 on process using, as counter-ion, the sodium tripolyphosphate to form loaded nanoparticles with TPC.

43 ATP and l-methionine (Met) and hydrolysis of tripolyphosphate to PP(i) and P(i).

44 aginase CLEAs were prepared utilizing sodium tripolyphosphate (TPP) as a crosslinker (TA-CLEA).

45 It has been reported that tripolyphosphate (TPP) can enhance the oxygenation of na

46 ur of bovine serum albumin (BSA) in chitosan-tripolyphosphate (TPP) hydrogel beads.

47 Chitosan (CH)-tripolyphosphate (TPP) submicron particles were formed a

48 dy, Chitosan (CS) was cross-linked to sodium tripolyphosphate (TPP) to produce nano-sized polyelectro

49 The mass ratios of chitosan (Ch) to tripolyphosphate (TPP), 1:1, for unloaded ChNPs and 1:1:

50 n of additives such as dextran sulfate (DS), tripolyphosphate (TPP), and hyaluronic acid (HA) was exp

51 After spraying tripolyphosphate (TPP), crosslinking with CS and phospho

52 NPs) prepared by ionic gelation with sodium tripolyphosphate (TPP), further encapsulated in ZN micro

53 es with millimolar affinities that also bind tripolyphosphate (TPP).

54 lyphosphates [orthophosphate, pyrophosphate, tripolyphosphate, trimetaphosphate, and tetrapolyphospha

55 f microparticles coated with chitosan/sodium tripolyphosphate was approximately 55%, while that of mi

56 cts of increased fat content and addition of tripolyphosphate were observed.

57 ysis of all dNTPs to the deoxynucleoside and tripolyphosphate, which effectively depletes the dNTP su

58 ed by ionic gelation of chitosan with sodium tripolyphosphate, which presented a spherical morphology