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1 d indole-3-aldehyde, or the bacterial enzyme tryptophanase.
2 trosation of the indole that is generated by tryptophanase.
3 thylene-tetra-hydrofolate dehydrogenase, and tryptophanase.
4 ment of the sodium/proton antiporter NhaC-2, tryptophanase A, and two putative regulators/histidine k
5 the addition of nitrate to the medium and on tryptophanase activity in the cells.
6                                 Furthermore, tryptophanase activity was required for full activation
7  and the tryptophan permease TnaB coregulate tryptophanase activity, through mutually exclusive pathw
8 altering the abundance of bacteria harboring tryptophanase activity.
9 s are altered and become similar to those of tryptophanase and aspartate aminotransferase, enzymes in
10 sRNA that interacts directly with the enzyme tryptophanase and enhances its affinity for its substrat
11  coli(EPEC) requires the tnaA-encoded enzyme tryptophanase and its substrate tryptophan to synthesize
12 ein of unknown function; tnaA, which encodes tryptophanase; as well as a homologue of Pasteurella mul
13                                    Bacterial tryptophanases convert tryptophan to indole, which is ab
14                                              Tryptophanase converts tryptophan into indole, and as ex
15 s shown to be tryptophanase dependent, and a tryptophanase-deficient strain is resistant to growth in
16  of multicopy plasmids by Rcd is shown to be tryptophanase dependent, and a tryptophanase-deficient s
17               Thus, an unknown metabolite of tryptophanase, derived from EPEC or from commensal non-p
18 e, Devlin et al. (2016) identify a family of tryptophanases encoded by members of the human gut micro
19                Rcd increases the affinity of tryptophanase for its substrate tryptophan which causes
20 sence and absence of tryptophan identified a tryptophanase gene (tna) that showed strong induction in
21 of tryptophan in growth media or deletion of tryptophanase gene failed to paralyse or kill C. elegans
22 , we identify a widely distributed family of tryptophanases in the gut commensal Bacteroides and find
23                                              Tryptophanase is activated in the stationary phase by th
24 otein expression, we found that YafQ reduced tryptophanase levels (TnaA mRNA has 16 putative YafQ cle
25 han metabolites failed to complement an EPEC tryptophanase mutant when presented extracellularly, com
26     Conditioned medium prepared from a tnaA (tryptophanase) mutant, deficient in indole production, s
27 -tryptophan by commensal bacteria expressing tryptophanase, not only is an important intercellular si
28                            Expression of the tryptophanase operon of Escherichia coli is regulated by
29           Regulation of transcription of the tryptophanase operon requires that translation of its le
30  likely than hmw-containing isolates to have tryptophanase, ornithine decarboxylase, or lysine decarb
31 , since a mutation in the tnaA gene encoding tryptophanase prevented enhanced biofilm formation upon
32 C. elegans required tryptophan and bacterial tryptophanase, the enzyme catalysing the production of i
33                            Expression of the tryptophanase (tna) operon in Escherichia coli is regula
34                         Transcription of the tryptophanase (tna) operon of Escherichia coli is regula
35                            Expression of the tryptophanase (tna) operon of Escherichia coli is regula
36                            Expression of the tryptophanase (tna) operon of Escherichia coli is regula
37                Expression of the degradative tryptophanase (tna) operon of Escherichia coli is regula
38                            Expression of the tryptophanase (tna) operon of Escherichia coli is regula
39                            Expression of the tryptophanase (tna) operon of Escherichia coli is regula
40 ic H. influenzae which are homologous to the tryptophanase (tna) operon of Escherichia coli.
41 or basal-level and induced expression of the tryptophanase (tna) operon of Proteus vulgaris, short de
42 g the status or abundance of the Bacteroides tryptophanase, we can modulate IS levels in gnotobiotic
43 ne phenol-lyase and tryptophan indole-lyase (tryptophanase) were studied by rapid-scanning stopped-fl
44                           We have identified tryptophanase (which catabolizes tryptophan to pyruvate

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