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1 vitro is regulated by the effector molecule 1,2-propanediol.
2 on under anoxic conditions in the absence of 1,2-propanediol.
3 latory region, allowing cellular growth on L-1,2-propanediol.
4 It contains the reactions for degrading 1,2-propanediol.
5 (OAc)]2(OTf)2-catalyzed aerobic oxidation of 1,2-propanediol.
6 romohydrin (EBH) to its vicinal diol 3-bromo-1,2-propanediol.
7 presence and absence of the substrate (R,S)-1,2-propanediol.
8 erial mutant for Ado-B12-dependent growth on 1,2-propanediol.
9 thogenicity-relevant carbon sources, such as 1,2-propanediol.
10 dies that are involved in the degradation of 1,2-propanediol.
11 r the coenzyme B(12)-dependent catabolism of 1,2-propanediol.
12 the propanediol utilization (pdu) operon by 1,2-propanediol.
13 pdu operon and its expression independent of 1,2-propanediol.
14 opentanediol > 2,3-dimethyl-2,3-butanediol > 1,2-propanediol.
19 ging of enzymes into a MCP that functions in 1,2-propanediol (1,2-PD) utilization (Pdu) by Salmonella
22 tion of the cobalamin biosynthetic (cob) and 1,2-propanediol (1,2-PDL) utilization (pdu) operons in S
24 markets including polyols (ethylene glycol, 1,2-propanediol, 1,3-propanediol, glycerol, 1,4-butanedi
25 ,3R)-3-(cis-2,6-dimethylpiperidino)-3-phenyl-1,2-propanediol (11) has been anchored to a 2-chlorotrit
26 s was probed using para-substituted 1-phenyl-1,2-propanediols 1g, 1m, and 1n and density functional t
29 he proposed hypothesis, whereas loading with 1,2-propanediol (76 Da) produces complete volume recover
30 In addition, the RiDD will utilize both (S)-1,2-propanediol and (R)-1,2-propanediol as a substrate,
31 the C(3) compounds, our results suggest that 1,2-propanediol and acetone follow the hydroxyacetone pa
33 e metabolic products, including resveratrol, 1,2-propanediol and mevalonate were increased as a funct
34 ionyl-CoA) as the common intermediate in the 1,2-propanediol and propionate catabolic pathways of Sal
35 xpression: the pdu operon for utilization of 1,2-propanediol and the eut operon for ethanolamine cata
38 be using carbon sources, such as propionate, 1,2-propanediol, and ethanolamine, in addition to melibi
39 a transcription factor that is activated by 1,2-propanediol, and subsequently activates expression o
41 elles formed by S. enterica during growth on 1,2-propanediol are not involved in the concentration of
42 e utilization of fucose fermentation product 1,2-propanediol, are increased in the microbiome of CD p
44 stool of infected mice, suggesting a role of 1,2-propanediol as a carbon and energy source of listeri
45 Co(III)TFA/PPNTFA binary catalyst system and 1,2-propanediol as a chain transfer agent, providing an
47 ill utilize both (S)-1,2-propanediol and (R)-1,2-propanediol as a substrate, with an observed prefere
49 enterica LT2 retained the ability to grow on 1,2-propanediol as the sole carbon source when a Pdu enz
51 resolution, Rcryst = 21%, Rfree = 24%), and 1,2-propanediol-bound (2.4 A resolution, Rcryst = 20%, R
53 he wild-type strain at low concentrations of 1,2-propanediol but exhibited a period of interrupted gr
55 lla to grow anaerobically on ethanolamine or 1,2-propanediol by using endogenously synthesized B12.
58 lization (pdu) operon, which when induced by 1,2-propanediol compensated for the lack of CobB during
60 roteinaceous organelle that is essential for 1,2-propanediol degradation and enteric pathogenesis.
61 Genes needed for organelle formation and for 1,2-propanediol degradation are located at the 1,2-propa
63 nzyme is to support coenzyme B(12)-dependent 1,2-propanediol degradation, and bioinformatic analysis
72 ted by this system supported the activity of 1,2-propanediol dehydratase as effectively as authentic
73 RM signature enzyme, the GRE, is a dedicated 1,2-propanediol dehydratase with a new type of intramole
75 Salmonella typhimurium is able to catabolize 1,2-propanediol for use as the sole carbon and energy so
76 ine) and the hydrogen bond donors (glycerol, 1,2-propanediol, formic acid, and acetic acid) in varyin
78 he unique capability of this species to make 1,2-propanediol from sugars was described decades ago, b
79 r sulfonic acid (2:1 H-PFESA) and hexafluoro-1,2-propanediol (HFPrD), were detected in 42% and 56% of
80 oup of natural 3-(indol-2-yl)-3-(indol-3-yl)-1,2-propanediol (IIPDO) analogues containing two stereog
81 ment contains the reactions for metabolizing 1,2-propanediol in certain enteric bacteria, including S
82 directly observe conformational dynamics of 1,2-propanediol in cold (6 K) collisions with atomic hel
85 onfirmed the production of formate, acetate, 1,2-propanediol, lactate and cleaving of fucose from 2'-
86 base substitute approach by the (S)-3-amino-1,2-propanediol linker allows placing two fluorophores i
88 A pduO double mutants were unable to grow on 1,2-propanediol minimal medium supplemented with vitamin
90 iol are not involved in the concentration of 1,2-propanediol or coenzyme B(12), but are consistent wi
93 yatomic alcohol (ethylene glycol, EgO(2), 1; 1,2-propanediol, PrO(2), 2; 1,2-butanediol, BuO(2), 3; 1
94 tants suggested EutF was somehow involved in 1,2-propanediol, propionate, and succinate utilization.
96 anthal, extracted with ChCl/xylitol and ChCl/1,2-propanediol showed an increase of 20-33% and 67.9-68
97 gars (glucose, fructose), polyols (glycerol, 1,2-propanediol, sorbitol), and an amide (urea) as hydro
98 t a mathematical bound, in terms of external 1,2-propanediol substrate concentration and diffusive ra
99 dings also implicate active transport of the 1,2-propanediol substrate under conditions of low extern
101 This effect did not require catabolism of 1,2-propanediol, suggesting that a Pdu protein, not a ca
102 n mechanism for hydroxyacetone, acetone, and 1,2-propanediol synthesis from CO(2)RR and gives insight
103 ly permeable pore tailored for the influx of 1,2-propanediol (the substrate of the Pdu microcompartme
104 s Pdu protein depends on the availability of 1,2-propanediol, the cell solves the problem faced in an
105 ion pathway for hydroxyacetone, acetone, and 1,2-propanediol through CO((2))RR, which are minor produ
106 fects on the kinetics for the dehydration of 1,2-propanediol to propanal and for the hydrolysis of ce
108 o growth uncoupled production of acetate and 1,2-propanediol upon growth cessation, producing up to 6
114 2-propanediol degradation are located at the 1,2-propanediol utilization (pdu) locus, but the specifi
115 are able to target reporter proteins to the 1,2-propanediol utilization (Pdu) MCP, and that this loc
116 that the hexameric PduA shell protein of the 1,2-propanediol utilization (Pdu) microcompartment forms
117 e the existence of a function encoded by the 1,2-propanediol utilization (pdu) operon, which when ind
118 ate proteins involved in the assembly of the 1,2-propanediol utilization bacterial microcompartment f
119 the Citrobacter freundii BMC associated with 1,2-propanediol utilization can be transferred into Esch
121 the loading of heterologous proteins to the 1,2-propanediol utilization microcompartment of Salmonel
122 a mathematical model of the function of the 1,2-propanediol utilization microcompartment of Salmonel
124 n initiation site of cob mRNA in response to 1,2-propanediol was identified and shown to be different
125 ting that a Pdu protein, not a catabolite of 1,2-propanediol, was responsible for the observed effect
126 lane) or bonding with aminoalcohols (3-amino-1,2-propanediol) were found to significantly improve the
127 he problem faced in an environment devoid of 1,2-propanediol where propionate is the sole carbon and
128 ropan-1-ol (3) by treating (+/-)-3-benzyloxy-1,2-propanediol with a mesylated phytol derivative throu