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1 It contains the reactions for degrading 1,2-propanediol.
2 thogenicity-relevant carbon sources, such as 1,2-propanediol.
3 (OAc)]2(OTf)2-catalyzed aerobic oxidation of 1,2-propanediol.
4 romohydrin (EBH) to its vicinal diol 3-bromo-1,2-propanediol.
5 presence and absence of the substrate (R,S)-1,2-propanediol.
6 erial mutant for Ado-B12-dependent growth on 1,2-propanediol.
7 dies that are involved in the degradation of 1,2-propanediol.
8 r the coenzyme B(12)-dependent catabolism of 1,2-propanediol.
9 the propanediol utilization (pdu) operon by 1,2-propanediol.
10 pdu operon and its expression independent of 1,2-propanediol.
11 opentanediol > 2,3-dimethyl-2,3-butanediol > 1,2-propanediol.
12 vitro is regulated by the effector molecule 1,2-propanediol.
13 on under anoxic conditions in the absence of 1,2-propanediol.
18 ging of enzymes into a MCP that functions in 1,2-propanediol (1,2-PD) utilization (Pdu) by Salmonella
21 tion of the cobalamin biosynthetic (cob) and 1,2-propanediol (1,2-PDL) utilization (pdu) operons in S
22 ,3R)-3-(cis-2,6-dimethylpiperidino)-3-phenyl-1,2-propanediol (11) has been anchored to a 2-chlorotrit
23 s was probed using para-substituted 1-phenyl-1,2-propanediols 1g, 1m, and 1n and density functional t
24 he proposed hypothesis, whereas loading with 1,2-propanediol (76 Da) produces complete volume recover
25 In addition, the RiDD will utilize both (S)-1,2-propanediol and (R)-1,2-propanediol as a substrate,
27 e metabolic products, including resveratrol, 1,2-propanediol and mevalonate were increased as a funct
28 ionyl-CoA) as the common intermediate in the 1,2-propanediol and propionate catabolic pathways of Sal
29 xpression: the pdu operon for utilization of 1,2-propanediol and the eut operon for ethanolamine cata
31 be using carbon sources, such as propionate, 1,2-propanediol, and ethanolamine, in addition to melibi
32 a transcription factor that is activated by 1,2-propanediol, and subsequently activates expression o
34 elles formed by S. enterica during growth on 1,2-propanediol are not involved in the concentration of
36 stool of infected mice, suggesting a role of 1,2-propanediol as a carbon and energy source of listeri
38 ill utilize both (S)-1,2-propanediol and (R)-1,2-propanediol as a substrate, with an observed prefere
40 enterica LT2 retained the ability to grow on 1,2-propanediol as the sole carbon source when a Pdu enz
42 resolution, Rcryst = 21%, Rfree = 24%), and 1,2-propanediol-bound (2.4 A resolution, Rcryst = 20%, R
43 he wild-type strain at low concentrations of 1,2-propanediol but exhibited a period of interrupted gr
45 lla to grow anaerobically on ethanolamine or 1,2-propanediol by using endogenously synthesized B12.
48 lization (pdu) operon, which when induced by 1,2-propanediol compensated for the lack of CobB during
50 Genes needed for organelle formation and for 1,2-propanediol degradation are located at the 1,2-propa
52 nzyme is to support coenzyme B(12)-dependent 1,2-propanediol degradation, and bioinformatic analysis
61 ted by this system supported the activity of 1,2-propanediol dehydratase as effectively as authentic
62 RM signature enzyme, the GRE, is a dedicated 1,2-propanediol dehydratase with a new type of intramole
64 Salmonella typhimurium is able to catabolize 1,2-propanediol for use as the sole carbon and energy so
65 ment contains the reactions for metabolizing 1,2-propanediol in certain enteric bacteria, including S
66 directly observe conformational dynamics of 1,2-propanediol in cold (6 K) collisions with atomic hel
69 base substitute approach by the (S)-3-amino-1,2-propanediol linker allows placing two fluorophores i
71 A pduO double mutants were unable to grow on 1,2-propanediol minimal medium supplemented with vitamin
73 iol are not involved in the concentration of 1,2-propanediol or coenzyme B(12), but are consistent wi
76 tants suggested EutF was somehow involved in 1,2-propanediol, propionate, and succinate utilization.
78 anthal, extracted with ChCl/xylitol and ChCl/1,2-propanediol showed an increase of 20-33% and 67.9-68
79 t a mathematical bound, in terms of external 1,2-propanediol substrate concentration and diffusive ra
80 dings also implicate active transport of the 1,2-propanediol substrate under conditions of low extern
82 This effect did not require catabolism of 1,2-propanediol, suggesting that a Pdu protein, not a ca
83 ly permeable pore tailored for the influx of 1,2-propanediol (the substrate of the Pdu microcompartme
84 s Pdu protein depends on the availability of 1,2-propanediol, the cell solves the problem faced in an
85 fects on the kinetics for the dehydration of 1,2-propanediol to propanal and for the hydrolysis of ce
92 2-propanediol degradation are located at the 1,2-propanediol utilization (pdu) locus, but the specifi
93 are able to target reporter proteins to the 1,2-propanediol utilization (Pdu) MCP, and that this loc
94 that the hexameric PduA shell protein of the 1,2-propanediol utilization (Pdu) microcompartment forms
95 e the existence of a function encoded by the 1,2-propanediol utilization (pdu) operon, which when ind
96 the Citrobacter freundii BMC associated with 1,2-propanediol utilization can be transferred into Esch
97 a mathematical model of the function of the 1,2-propanediol utilization microcompartment of Salmonel
98 the loading of heterologous proteins to the 1,2-propanediol utilization microcompartment of Salmonel
100 n initiation site of cob mRNA in response to 1,2-propanediol was identified and shown to be different
101 ting that a Pdu protein, not a catabolite of 1,2-propanediol, was responsible for the observed effect
102 he problem faced in an environment devoid of 1,2-propanediol where propionate is the sole carbon and
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