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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
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
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
14 .5-kb cluster of nif and associated genes of Acetobacter diazotrophicus (syn. Gluconacetobacter diazo
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