scholarly journals Hugonella massiliensis gen. nov., sp. nov., genome sequence, and description of a new strictly anaerobic bacterium isolated from the human gut

2017 ◽  
Vol 6 (4) ◽  
pp. e00458 ◽  
Author(s):  
Ziena Elsawi ◽  
Amadou Hamidou Togo ◽  
Mamadou Beye ◽  
Grégory Dubourg ◽  
Claudia Andrieu ◽  
...  
2016 ◽  
Vol 4 (6) ◽  
Author(s):  
Sebastian Flüchter ◽  
Anja Poehlein ◽  
Bettina Schiel-Bengelsdorf ◽  
Rolf Daniel ◽  
Peter Dürre

Here, we report the genome sequence of Clostridium acetireducens (DSM 10703 T ), a strictly anaerobic bacterium capable of fermenting acetate and leucine to butyrate, isovalerate, and poly-3-hydroxybutyrate. The draft genome consists of a circular chromosome with a size of 2.4 Mb and harbors 2,239 predicted protein-encoding genes.


2016 ◽  
Vol 4 (1) ◽  
Author(s):  
Xiaoqiong Li ◽  
Ole Højberg ◽  
Samantha Joan Noel ◽  
Nuria Canibe ◽  
Bent Borg Jensen

Olsenella scatoligenesSK9K4Tis a strictly anaerobic bacterium isolated from pig feces that produces the malodorous compounds 3-methylindole (skatole) and 4-methylphenol (p-cresol). Here, we report the 2.47 Mbp draft genome sequence of SK9K4T, exploring pathways for the synthesis of skatole andp-cresol from the amino acids tryptophan and tyrosine, respectively.


2016 ◽  
Vol 4 (1) ◽  
Author(s):  
Bharat K. C. Patel ◽  
Valentino Setoa Junior Te'o

The genome sequence of Caloramator mitchellensis strain VF08, a rod-shaped, heterotrophic, strictly anaerobic bacterium isolated from the free-flowing waters of a Great Artesian Basin (GAB) bore well located in Mitchell, an outback Queensland town in Australia, is reported here. The analysis of the 2.42-Mb genome sequence indicates that the attributes of the genome are consistent with its physiological and phenotypic traits.


2016 ◽  
Vol 4 (2) ◽  
Author(s):  
Matthias H. Beck ◽  
Anja Poehlein ◽  
Frank R. Bengelsdorf ◽  
Bettina Schiel-Bengelsdorf ◽  
Rolf Daniel ◽  
...  

Here, we report the draft genome sequence of Clostridium neopropionicum X4 (DSM 3847 T ), a strictly anaerobic bacterium capable of fermenting ethanol and CO 2 to propionate, acetate, and propanol. The genome consists of a single chromosome (3.19 Mb).


2019 ◽  
Vol 31 ◽  
pp. 100571 ◽  
Author(s):  
S. Ndongo ◽  
M.L. Tall ◽  
I.I. Ngom ◽  
P.-E. Fournier ◽  
A. Levasseur ◽  
...  

2020 ◽  
Vol 9 (14) ◽  
Author(s):  
Emma Bertran ◽  
Lewis M. Ward ◽  
David T. Johnston

Here, we describe the genome of Desulfobacter hydrogenophilus DSM 3380, a bacterium that belongs to the Desulfobacterales. The genome of this strictly anaerobic bacterium capable of sulfate reduction expands our understanding of microbial sulfate reduction in a wide range of environmental conditions.


2015 ◽  
Vol 3 (5) ◽  
Author(s):  
Matthias H. Beck ◽  
Anja Poehlein ◽  
Frank R. Bengelsdorf ◽  
Bettina Schiel-Bengelsdorf ◽  
Rolf Daniel ◽  
...  

Here, we report the draft genome sequence ofClostridium homopropionicumLuHBu1 (DSM 5847T), a strictly anaerobic bacterium, which performs propionate fermentation and is capable of growing with 2-, 3-, or 4-hydroxybutyrate as its sole substrate. The genome consists of a single chromosome of 3.65 Mb.


2008 ◽  
Vol 74 (15) ◽  
pp. 4847-4852 ◽  
Author(s):  
Anastasia Matthies ◽  
Thomas Clavel ◽  
Michael Gütschow ◽  
Wolfram Engst ◽  
Dirk Haller ◽  
...  

ABSTRACT The metabolism of isoflavones by gut bacteria plays a key role in the availability and bioactivation of these compounds in the intestine. Daidzein and genistein are the most common dietary soy isoflavones. While daidzein conversion yielding equol has been known for some time, the corresponding formation of 5-hydroxy-equol from genistein has not been reported previously. We isolated a strictly anaerobic bacterium (Mt1B8) from the mouse intestine which converted daidzein via dihydrodaidzein to equol as well as genistein via dihydrogenistein to 5-hydroxy-equol. Strain Mt1B8 was a gram-positive, rod-shaped bacterium identified as a member of the Coriobacteriaceae. Strain Mt1B8 also transformed dihydrodaidzein and dihydrogenistein to equol and 5-hydroxy-equol, respectively. The conversion of daidzein, genistein, dihydrodaidzein, and dihydrogenistein in the stationary growth phase depended on preincubation with the corresponding isoflavonoid, indicating enzyme induction. Moreover, dihydrogenistein was transformed even more rapidly in the stationary phase when strain Mt1B8 was grown on either genistein or daidzein. Growing the cells on daidzein also enabled conversion of genistein. This suggests that the same enzymes are involved in the conversion of the two isoflavones.


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