ライフサイエンスコーパス: cadaverine

1 s 1,3-diaminopropane and 1,5-diaminopentane (cadaverine).

2 molar for spermine to tens of millimolar for cadaverine.

3 c environments, as lysine decarboxylation to cadaverine.

4 n dento-gingival biofilms converts lysine to cadaverine.

5 trans-UCA, 2.23 mg/kg cis-UCA and 1.86 mg/kg cadaverine.

6 putrescine, histamine, phenylethylamine and cadaverine.

7 tially enhanced by addition of the polyamine cadaverine.

8 e enzyme and a soluble desthiobiotin-labeled cadaverine.

9 e-3, in a manner suppressible by mono-dansyl cadaverine.

10 the transglutaminase inhibitor, mono-dansyl cadaverine.

11 ted in vitro in the presence of biotinylated cadaverine.

12 nes (100%), followed by putrescine (77%) and cadaverine (14%).

13 an increase in polyamines including N-acetyl-cadaverine (2.9-fold), N-acetylputrescine (1.8-fold), pu

14 escine (1.8-fold), putrescine (2.7-fold) and cadaverine (28-fold), which depending on context can be

15 eating TIG3-expressing cells with monodansyl cadaverine, a competitive transglutaminase substrate, at

16 at acidic pH, Escherichia coli cells secrete cadaverine, a polyamine known to inhibit porin-mediated

17 Our recent studies demonstrated that cadaverine, a polyamine, specifically acts to abrogate t

18 The enterotoxin inhibitor was identified as cadaverine, a product of the reaction catalyzed by LDC.

19 Here, we show that the addition of exogenous cadaverine allows wild-type cells to survive a 30-min ex

20 taminyl substrate) is cross-linked to dansyl cadaverine (amine substrate).

21 Histamine, putrescine cadaverine and cis-urocanic acid (UCA) have all been imp

22 ed by the transglutaminase inhibitors dansyl-cadaverine and cystamine, indicating that apoptosis of M

23 involved in the decarboxylation of lysine to cadaverine and in cadaverine excretion.

24 s of significant production of the polyamine cadaverine and increased sensitivity to acidified nitrit

25 Furthermore, olfactory receptors that detect cadaverine and putrescine have not been identified in an

26 -mediated avoidance behavior of zebrafish to cadaverine and related diamines, and concomitant activat

27 cine, histamine, tyramine, phenylethylamine, cadaverine and serotonin) were determined by LC-UV after

28 idine (Kd=430 nM), but the related compounds cadaverine and spermine did not bind.

29 Increased cadaverine and tyramine contents were found in samples w

30 Putrescine, cadaverine and tyramine showed very good correspondence

31 Putrescine, cadaverine and tyramine showed very good correspondence

32 of various biogenic amines (i.e. putrescine, cadaverine) and in the monitoring of spoilage in raw mea

33 henylethylamine, tryptamine, putrescine, and cadaverine) and two polyamines (spermidine and spermine)

34 ration of fluorescein isothiocyanate-labeled cadaverine, and a threefold increase in acetic acid-extr

35 s polyamines such as putrescine, spermidine, cadaverine, and homospermidine present in both PBCV-1 an

36 trates for this exporter include putrescine, cadaverine, and monoacetyl spermidine and have the gener

37 ase in intracellular contents of putrescine, cadaverine, and N8-acetylspermidine, in unstressed proli

38 polyamines, including spermidine, spermine, cadaverine, and putrescine, strongly inhibited opening a

39 proline, glycine, lysine, serine, glutamate, cadaverine, and pyrophosphate.

40 e pathway will utilize 1,3-diaminopropane or cadaverine, and suggest that the majority of bacteria us

41 CadA (lysine decarboxylase) and CadB (lysine/cadaverine antiporter) in a lysine-rich environment.

42 ne in an operon with cadB, encoding a lysine/cadaverine antiporter.

43 Cadaverine appears to promote a sustained inhibition of

44 s (PAs) spermidine, spermine, putrescine and cadaverine are an essential class of metabolites found t

45 lyamines such as putrescine, spermidine, and cadaverine are small, polycationic molecules that are re

46 Tg-1 activity was measured by a fluorescein cadaverine assay.

47 and GTM cells was studied by using a biotin cadaverine assay.

48 ovided into the cellular mechanisms by which cadaverine attenuates the ability of Shigella species to

49 For the cadaverine-based desferroxiamine E siderophore in Strept

50 hibition of receptor recycling by monodansyl cadaverine blocked association of BAD1 with Mphi and rev

51 monstrated that the product of LDC activity, cadaverine, blocks the action of Shigella enterotoxins a

52 sporters that recognized both putrescine and cadaverine but not spermidine or spermine.

53 r 1,3-diaminopropane or 1, 5-diaminopentane (cadaverine), but polyamine auxotrophy could not be overc

54 e inducible by diamines putrescine (PUT) and cadaverine (CAD) but not by diaminopropane.

55 No measurable amounts of cadaverine (CAD) or methylamine (MEA) were found, showin

56 h time, tyramine (TYR), putrescine (PUT) and cadaverine (CAD) were the most abundant.

57 ding diaminopropane (DAP), putrescine (Put), cadaverine (Cad), and spermidine (Spd), as carbon and/or

58 Furthermore, the demonstration that cadaverine can inhibit enterotoxin activity may lead to

59 Cadaverine mole fraction of lysine plus cadaverine (CF) indicated biofilm lysine decarboxylase a

60 that the lack of sensitivity of the porin to cadaverine confers a survival disadvantage to the mutant

61 Cooking process decreased putrescine and cadaverine content, both in conventionally and organical

62 is study are to determine biofilm lysine and cadaverine contents before oral hygiene restriction (OHR

63 Lysine and cadaverine contents discriminated PRs from GRs and HVs (

64 trophoresis was used to determine lysine and cadaverine contents in dental biofilm, tongue biofilm, a

65 Before OHR, lysine and cadaverine contents of dental biofilm were similar and 1

66 We report that increased levels of excreted cadaverine correlate with a decreased outer membrane per

67 ion of 5-dimethylaminonaphthalene-1-sulfonyl cadaverine (dansylcadaverine), [14C]putrescine, and dans

68 by desA that was suspected of producing the cadaverine (decarboxylated lysine) backbone.

69 Externally added polyamines, such as cadaverine, decrease porin-mediated fluxes of beta-lacta

70 understand the physiological significance of cadaverine excretion and the inhibition of porins, we is

71 carboxylation of lysine to cadaverine and in cadaverine excretion.

72 f neurons activated by low concentrations of cadaverine expresses a particular olfactory receptor, tr

73 tained three amines; there was prevalence of cadaverine followed by tyramine and putrescine; and tota

74 sively to study the export of putrescine and cadaverine from cultured mammalian cells.

75 Cadaverine had a slight effect on LDC-negative strain ad

76 A CEST agent, Tm-DO3A-cadaverine, has been designed to detect the catalytic ac

77 matter, with higher amounts, particularly of cadaverine, histamine and tyramine, in low-salt products

78 d for the analysis of eight biogenic amines (cadaverine, histamine, phenylethylamine, putrescine, spe

79 s (tryptamine, phenylethylamine, putrescine, cadaverine, histamine, serotonine, tyramine, spermidine

80 a macrocyclic trimer of N-hydroxy-N-succinyl-cadaverine (HSC).

81 , whereas marginally affected by filipin and cadaverine, implicating that CAM-endocytosis accounts fo

82 erocyclic compound formed from the polyamine cadaverine in the human intestine.

83 phenotype was independent of pH, lysine, or cadaverine in the media.

84 After 1 week of OHR, the biofilm content of cadaverine increased and that of lysine decreased, consi

85 Results indicate that cadaverine-induced compartmentalization of Shigella spec

86 The cadaverine-induced inhibition is sufficient to provide c

87 e to pH 3.6 better than cells expressing the cadaverine-insensitive OmpC porin.

88 Incorporation of fluorescein-cadaverine into matrix proteins was accompanied by the c

89 s, "in situ" by incorporation of fluorescein-cadaverine into the extracellular matrix or by changes i

90 , we incorporated an amine donor, thioacetyl cadaverine, into glutamine acceptor sites in fibrinogen

91 chlamydial AaxC transporter was resistant to cadaverine, L-lysine and L-ornithine, which inhibit the

92 nsmission electron microscopy to locate Au11-cadaverine-labeled gamma398/399 D domain sites.

93 Histamine, putrescine and cadaverine levels increased significantly (P value<0.05)

94 Biofilm cadaverine, lysine, and other amino acid (AA) contents w

95 s, in the presence or absence of mono-dansyl cadaverine (MDC), a TG inhibitor.

96 Cadaverine mole fraction of lysine plus cadaverine (CF)

97 Dansyl cadaverine (N-dansyl-1,5-diaminopentane) was used to stu

98 olyamines N(1)-acetylspermidine, putrescine, cadaverine, N(1)-acetylspermine, spermidine, and spermin

99 ificant amounts of tyramine, putrescine, and cadaverine occurred especially in cheeses produced from

100 tested the effects of endogenously expressed cadaverine on the rate of permeation of cephaloridine th

101 Exogenous addition of cadaverine or other polyamines rescues growth of cad mut

102 In wild-type cells, the concentration of cadaverine produced per cell is substantially increased

103 e mere expression of cadC, in the absence of cadaverine production, leads to a reduction in the amoun

104 se that the inhibition of porins by excreted cadaverine represents a novel mechanism that provides ba

105 It was found that cadaverine retards the lysis of the Shigella species-con

106 Incorporation of biotin cadaverine revealed a preference of MTG for the DAIP glu

107 xamined, tyramine, putrescine, histamine and cadaverine showed high concentrations ranging from: 0 to

108 The effects of four polyamines (putrescine, cadaverine, spermidine, and spermine) on the activity of

109 the effects of four polyamines (putrescine, cadaverine, spermidine, and spermine) on two processes k

110 ontent of seven biogenic amines (putrescine, cadaverine, spermidine, spermine, histamine, tyramine an

111 ontent of eight biogenic amines (putrescine, cadaverine, spermidine, spermine, histamine, tyramine, t

112 ontent of eight biogenic amines (putrescine, cadaverine, spermidine, spermine, histamine, tyramine, t

113 molecules which have aliphatic (putrescine, cadaverine, spermine, spermidine), aromatic (tyramine, p

114 ,N-dimethylated casein by Gly-OMe and dansyl-cadaverine suggest a complex kinetic mechanism for both

115 ine synthesis by UPEC, and growth of UPEC in cadaverine-supplemented broth in the absence of ASN can

116 e stress, as generated by ASN, can stimulate cadaverine synthesis by UPEC, and growth of UPEC in cada

117 Interestingly, the presence of a cadaverine tail confers to 7 the ability to target mitoc

118 ty to analogous gases such as putrscine, and cadaverine that will increase during storage.

119 ence of the reaction products putrescine and cadaverine to 1.7 and 2.15A, respectively.

120 d at -9.2 ppm after TGase conjugated Tm-DO3A-cadaverine to albumin, which also caused a decrease in C

121 Putrescine, cadaverine, tryptamine, beta-phenylethylamine spermidine

122 Fluorescein-cadaverine uptake was used to assess transglutaminase ac

123 Cadaverine was detected, but was not influenced by agein

124 s levels compared to sorghum with tannin and cadaverine was specific to samples without tannin.

125 in the 300MPa treatments, but putrescine and cadaverine were detected in the control and 100MPa treat

126 ed on the results, histamine, putrescine and cadaverine were selected as input variables and twelve q

127 two small aliphatic diamines, putrescine and cadaverine, which are generated by bacterial decarboxyla