1 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

2 examined PurE from the acidophilic bacterium Acetobacter aceti (AaPurE), focusing on its adaptation t

3 s a seed broth for acetic fermentation using Acetobacter aceti as the inoculum for approximately 30da

4 (CAC) is linked to acetic acid resistance in Acetobacter aceti by several observations, among them th

5                                              Acetobacter aceti converts ethanol to acetic acid, and s

6  restriction endonuclease and methylase from Acetobacter aceti have been cloned and expressed in Esch

7 f a 151 kDa complex of uniformly 15N-labeled Acetobacter aceti PurE (AaPurE) and the active site liga

8 ith a role in a variant citric acid cycle in Acetobacter aceti.

9 ndance of key members of the gut microbiota (Acetobacter and Lactobacillus), suggesting that the acid

10           Drosophila prefers a Saccharomyces-Acetobacter co-culture to the same microorganisms grown

11 .5-kb cluster of nif and associated genes of Acetobacter diazotrophicus (syn. Gluconacetobacter diazo

12 cus, one of Gluconobacter oxydans and one of Acetobacter malorum).

13                                              Acetobacter metabolism of Saccharomyces-derived ethanol

14  microbiota, particularly from the commensal Acetobacter pomorum, which primes the NF-kB-dependent in

15          The phosphodiesterase A1 protein of Acetobacter xylinum, AxPDEA1, is a key regulator of bact

16 r of beta-1,4-glucan (cellulose) synthase in Acetobacter xylinum.

17  analogues (bio-composite materials based on Acetobacter xylinus cellulose and xyloglucan).