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1 ncia rettgeri and DptB for the gut mutualist Acetobacter.
2 10(10)/g), Propionibacterium (3 x 10(10)/g), Acetobacter (1 x 10(6)/g)) at a dose of 140 mg/kg (1.4 x
3 examined PurE from the acidophilic bacterium Acetobacter aceti (AaPurE), focusing on its adaptation t
4 s a seed broth for acetic fermentation using Acetobacter aceti as the inoculum for approximately 30da
5 (CAC) is linked to acetic acid resistance in Acetobacter aceti by several observations, among them th
6                                              Acetobacter aceti converts ethanol to acetic acid, and s
7  restriction endonuclease and methylase from Acetobacter aceti have been cloned and expressed in Esch
8 f a 151 kDa complex of uniformly 15N-labeled Acetobacter aceti PurE (AaPurE) and the active site liga
9 ith a role in a variant citric acid cycle in Acetobacter aceti.
10 s, Burkholderia, Bacteroides, Lactobacillis, Acetobacter, Allobaculum, Ruminococcus, and Nocardia.
11 ndance of key members of the gut microbiota (Acetobacter and Lactobacillus), suggesting that the acid
12 ecies, including Lactococcus, Lactobacillus, Acetobacter, and Lacticaseibacillus, enriched during fer
13           Drosophila prefers a Saccharomyces-Acetobacter co-culture to the same microorganisms grown
14 .5-kb cluster of nif and associated genes of Acetobacter diazotrophicus (syn. Gluconacetobacter diazo
15  colonization by unrelated commensals in the Acetobacter genus.
16 relates with the presence of Providencia and Acetobacter in their environment.
17 cus, one of Gluconobacter oxydans and one of Acetobacter malorum).
18                                              Acetobacter metabolism of Saccharomyces-derived ethanol
19 ics to show that in Drosophila melanogaster, Acetobacter pomorum (Ap) and Lactobacillus plantarum (Lp
20  to restore memory, while coinoculation with Acetobacter pomorum further enhanced memory performance.
21  microbiota, particularly from the commensal Acetobacter pomorum, which primes the NF-kB-dependent in
22 suppressed by mono-association with a single Acetobacter sp. isolate, through mechanisms involving bo
23 Co-culturing of Lactobacillus plantarum with Acetobacter species altered its tolerance to the transcr
24 tes and environmental pH, we determined that Acetobacter species counter the acidification driven by
25 se (SHC) genes and in particular to those of Acetobacter species.
26          The phosphodiesterase A1 protein of Acetobacter xylinum, AxPDEA1, is a key regulator of bact
27 r of beta-1,4-glucan (cellulose) synthase in Acetobacter xylinum.
28  analogues (bio-composite materials based on Acetobacter xylinus cellulose and xyloglucan).