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1 s 1,3-diaminopropane and 1,5-diaminopentane (cadaverine).
2 mg/mL for putrescine, and 0.1-6.0 mg/mL for cadaverine.
3 the transglutaminase inhibitor, mono-dansyl cadaverine.
4 ted in vitro in the presence of biotinylated cadaverine.
5 molar for spermine to tens of millimolar for cadaverine.
6 find that adults no longer show aversion to cadaverine.
7 s lysine and forms an alternative polyamine, cadaverine.
8 c environments, as lysine decarboxylation to cadaverine.
9 n dento-gingival biofilms converts lysine to cadaverine.
10 trans-UCA, 2.23 mg/kg cis-UCA and 1.86 mg/kg cadaverine.
11 putrescine, histamine, phenylethylamine and cadaverine.
12 tially enhanced by addition of the polyamine cadaverine.
13 e enzyme and a soluble desthiobiotin-labeled cadaverine.
14 e-3, in a manner suppressible by mono-dansyl cadaverine.
16 an increase in polyamines including N-acetyl-cadaverine (2.9-fold), N-acetylputrescine (1.8-fold), pu
17 escine (1.8-fold), putrescine (2.7-fold) and cadaverine (28-fold), which depending on context can be
18 anediol, erythritol, tryptophol, putrescine, cadaverine, 3-phenyllactate, 2-hydroxyisocaproate) were
19 metabolites, including phenylpropanoic acid, cadaverine, 9-10-methylenehexadecanoic acid, and 12-meth
20 eating TIG3-expressing cells with monodansyl cadaverine, a competitive transglutaminase substrate, at
21 at acidic pH, Escherichia coli cells secrete cadaverine, a polyamine known to inhibit porin-mediated
24 The enterotoxin inhibitor was identified as cadaverine, a product of the reaction catalyzed by LDC.
26 Here, we show that the addition of exogenous cadaverine allows wild-type cells to survive a 30-min ex
28 ader, whereas shorter C4 (putrescine) to C5 (cadaverine) analogs, found in mammalian cells, do not in
31 ed by the transglutaminase inhibitors dansyl-cadaverine and cystamine, indicating that apoptosis of M
33 s of significant production of the polyamine cadaverine and increased sensitivity to acidified nitrit
34 Furthermore, olfactory receptors that detect cadaverine and putrescine have not been identified in an
37 -mediated avoidance behavior of zebrafish to cadaverine and related diamines, and concomitant activat
38 cine, histamine, tyramine, phenylethylamine, cadaverine and serotonin) were determined by LC-UV after
41 lack these neurons are also less repelled by cadaverine and their behavioral response to alarm substa
46 of various biogenic amines (i.e. putrescine, cadaverine) and in the monitoring of spoilage in raw mea
47 henylethylamine, tryptamine, putrescine, and cadaverine) and two polyamines (spermidine and spermine)
48 ration of fluorescein isothiocyanate-labeled cadaverine, and a threefold increase in acetic acid-extr
49 s polyamines such as putrescine, spermidine, cadaverine, and homospermidine present in both PBCV-1 an
50 trates for this exporter include putrescine, cadaverine, and monoacetyl spermidine and have the gener
51 ase in intracellular contents of putrescine, cadaverine, and N8-acetylspermidine, in unstressed proli
52 polyamines, including spermidine, spermine, cadaverine, and putrescine, strongly inhibited opening a
54 e pathway will utilize 1,3-diaminopropane or cadaverine, and suggest that the majority of bacteria us
55 The concentrations of putrescine, histamine, cadaverine, and tyramine were reduced by about 15, 20, 2
56 CadA (lysine decarboxylase) and CadB (lysine/cadaverine antiporter) in a lysine-rich environment.
59 s (PAs) spermidine, spermine, putrescine and cadaverine are an essential class of metabolites found t
61 The polyamines putrescine, agmatine, and cadaverine are produced by pyridoxal 5'-phosphate-depend
62 lyamines such as putrescine, spermidine, and cadaverine are small, polycationic molecules that are re
65 ovided into the cellular mechanisms by which cadaverine attenuates the ability of Shigella species to
69 hibition of receptor recycling by monodansyl cadaverine blocked association of BAD1 with Mphi and rev
70 monstrated that the product of LDC activity, cadaverine, blocks the action of Shigella enterotoxins a
72 r 1,3-diaminopropane or 1, 5-diaminopentane (cadaverine), but polyamine auxotrophy could not be overc
77 ding diaminopropane (DAP), putrescine (Put), cadaverine (Cad), and spermidine (Spd), as carbon and/or
83 that the lack of sensitivity of the porin to cadaverine confers a survival disadvantage to the mutant
84 Cooking process decreased putrescine and cadaverine content, both in conventionally and organical
85 is study are to determine biofilm lysine and cadaverine contents before oral hygiene restriction (OHR
87 trophoresis was used to determine lysine and cadaverine contents in dental biofilm, tongue biofilm, a
89 We report that increased levels of excreted cadaverine correlate with a decreased outer membrane per
90 ion of 5-dimethylaminonaphthalene-1-sulfonyl cadaverine (dansylcadaverine), [14C]putrescine, and dans
94 understand the physiological significance of cadaverine excretion and the inhibition of porins, we is
96 f neurons activated by low concentrations of cadaverine expresses a particular olfactory receptor, tr
97 tained three amines; there was prevalence of cadaverine followed by tyramine and putrescine; and tota
101 matter, with higher amounts, particularly of cadaverine, histamine and tyramine, in low-salt products
102 d for the analysis of eight biogenic amines (cadaverine, histamine, phenylethylamine, putrescine, spe
103 s (tryptamine, phenylethylamine, putrescine, cadaverine, histamine, serotonine, tyramine, spermidine
104 ructural mimic of N(1)-hydroxy-N(1)-succinyl-cadaverine (HSC)-acyl-adenylate, the HSC-acyl sulfamoyl
106 ward genetic screen and isolated a mutation, cadaverine hypersensitive 3 (cdh3), which resulted in in
107 , whereas marginally affected by filipin and cadaverine, implicating that CAM-endocytosis accounts fo
111 these results revealed an unexpected role of cadaverine in the regulation of biotin biosynthesis, whi
112 After 1 week of OHR, the biofilm content of cadaverine increased and that of lysine decreased, consi
120 s, "in situ" by incorporation of fluorescein-cadaverine into the extracellular matrix or by changes i
121 , we incorporated an amine donor, thioacetyl cadaverine, into glutamine acceptor sites in fibrinogen
123 chlamydial AaxC transporter was resistant to cadaverine, L-lysine and L-ornithine, which inhibit the
131 olyamines N(1)-acetylspermidine, putrescine, cadaverine, N(1)-acetylspermine, spermidine, and spermin
132 ificant amounts of tyramine, putrescine, and cadaverine occurred especially in cheeses produced from
133 tested the effects of endogenously expressed cadaverine on the rate of permeation of cephaloridine th
135 composed of repeating units of N(1)-hydroxy-cadaverine (or N(1)-hydroxy-putrescine) and succinate.
137 In wild-type cells, the concentration of cadaverine produced per cell is substantially increased
139 e mere expression of cadC, in the absence of cadaverine production, leads to a reduction in the amoun
144 e (R(2) = 0.92; RMSEP = 0.41; RMSEC = 0.20), cadaverine (R(2) = 0.82; RMSEP = 1.58; RMSEC = 0.75) and
145 se that the inhibition of porins by excreted cadaverine represents a novel mechanism that provides ba
152 xamined, tyramine, putrescine, histamine and cadaverine showed high concentrations ranging from: 0 to
153 rated DM1 from T-DM1 and desulfurated dansyl-cadaverine-SMCC from SigmaMAb ADC mimic, respectively.
154 The effects of four polyamines (putrescine, cadaverine, spermidine, and spermine) on the activity of
155 the effects of four polyamines (putrescine, cadaverine, spermidine, and spermine) on two processes k
156 ontent of seven biogenic amines (putrescine, cadaverine, spermidine, spermine, histamine, tyramine an
157 ontent of eight biogenic amines (putrescine, cadaverine, spermidine, spermine, histamine, tyramine, t
158 molecules which have aliphatic (putrescine, cadaverine, spermine, spermidine), aromatic (tyramine, p
159 ,N-dimethylated casein by Gly-OMe and dansyl-cadaverine suggest a complex kinetic mechanism for both
160 ine synthesis by UPEC, and growth of UPEC in cadaverine-supplemented broth in the absence of ASN can
161 e stress, as generated by ASN, can stimulate cadaverine synthesis by UPEC, and growth of UPEC in cada
166 d at -9.2 ppm after TGase conjugated Tm-DO3A-cadaverine to albumin, which also caused a decrease in C
173 histamine, spermine, spermidine, putrescine, cadaverine, tyramine and tryptamine) on the recorded sig
177 in the 300MPa treatments, but putrescine and cadaverine were detected in the control and 100MPa treat
179 ed on the results, histamine, putrescine and cadaverine were selected as input variables and twelve q
180 two small aliphatic diamines, putrescine and cadaverine, which are generated by bacterial decarboxyla
181 ecarboxylase, CadA, which converts lysine to cadaverine while consuming a cytoplasmic proton, and the