scholarly journals Clostridium ultunense sp. nov., a Mesophilic Bacterium Oxidizing Acetate in Syntrophic Association with a Hydrogenotrophic Methanogenic Bacterium

1996 ◽  
Vol 46 (4) ◽  
pp. 1145-1152 ◽  
Author(s):  
A. SCHNURER ◽  
B. SCHINK ◽  
B. H. SVENSSON
1997 ◽  
Vol 36 (6-7) ◽  
pp. 133-140 ◽  
Author(s):  
Zhu Jianrong ◽  
Hu Jicui ◽  
Gu Xiasheng

The bacterial numeration and microbial observation were made on granular sludge from laboratory single and two-phase UASB reactors. It was shown that the fermentative bacteria (group I), H2-producing acetogenic bacteria (group II) and methanogenic bacteria (group III) of granular sludge in single UASB reactor were 9.3 × 108−4.3 × 109, 4.3 × 107−4.3 × 108, 2.0−4.3 × 108, respectively, during the granulation process. The sludge of methanogenic reactor exhibited the similar results. That indicates there is no big difference between suspended and granular sludge, and bacterial population for three groups of anaerobic bacteria are similar. The formation of granular sludge depends mainly on the organization and arrangement of bacteria. An observation of granular sludge using electron microscope revealed that the fermentative bacteria and hydrogenotrophic methanogens existed on outer surface of granules, and aceticlastic methanogens and H2-producing acetogenic bacteria occupied the inner layer. A new syntrophic association between Methanosaeta sp. and Syntrophomonas sp. (even plus Methanobrevibacter sp.) was observed. Because Methanosaeta can effectively convert the acetate (the end product of propionate and butyrate) to methane, such a new syntrophic association is supposed to support the degradation of short fatty acids and high methanogenic activity of granular sludge. Based on structural pattern, a hypothesis on mechanism of granulation called “crystallized nuclei formation” is proposed.


1983 ◽  
Vol 47 (12) ◽  
pp. 2941-2943 ◽  
Author(s):  
Silvia Yuko EGUCHI ◽  
Naomichi NISHIO ◽  
Shiro NAGAI

1991 ◽  
Vol 47 (5) ◽  
pp. 707-730 ◽  
Author(s):  
Z. Dauter ◽  
C. Betzel ◽  
N. Genov ◽  
N. Pipon ◽  
K. S. Wilson
Keyword(s):  
Eglin C ◽  

1998 ◽  
Vol 44 (12) ◽  
pp. 1142-1147 ◽  
Author(s):  
Nathalie Cabirol ◽  
Richard Villemur ◽  
Joseph Perrier ◽  
François Jacob ◽  
Bruno Fouillet ◽  
...  

RSC Advances ◽  
2015 ◽  
Vol 5 (16) ◽  
pp. 12052-12061 ◽  
Author(s):  
Samira Moradi ◽  
Seyed Hadi Razavi ◽  
Seyyed Mohammad Mousavi ◽  
Seyed Mohammad Taghi Gharibzahedi

A new aerobic mesophilic bacterium was isolated from the southern coastal waters of the Caspian Sea which substantially produced an extracellular lipase in solid-state fermentation using milled coriander seeds (MCS) as support substrate.


2007 ◽  
Vol 4 (1) ◽  
pp. 53-56 ◽  
Author(s):  
Brittany A Morrison ◽  
Daniel H Shain

Disparate psychrophiles (e.g. glacier ice worms, bacteria, algae and fungi) elevate steady-state intracellular ATP levels as temperatures decline, which has been interpreted as a compensatory mechanism to offset reductions in molecular motion and Gibb's free energy of ATP hydrolysis. In this study, we sought to manipulate steady-state ATP levels in the mesophilic bacterium, Escherichia coli , to investigate the relationship between cold temperature survivability and elevated intracellular ATP. Based on known energetic pathways and feedback loops, we targeted the AMP nucleotidase ( amn ) gene, which is thought to encode the primary AMP degradative enzyme in prokaryotes. By knocking out amn in wild-type E. coli DY330 cells using recombineering methodology, we generated a mutant (AMNk) that elevated intracellular ATP levels by more than 30% across its viable temperature range. As temperature was lowered, the relative ATP disparity between AMNk and DY330 cells increased to approximately 66% at 10°C, and was approximately 100% after storage at 0°C for 5–7 days. AMNk cells stored at 0°C for 7 days displayed approximately fivefold higher cell viability than wild-type DY330 cells treated in the same manner.


2016 ◽  
Vol 4 (2) ◽  
Author(s):  
Takashi Narihiro ◽  
Masaru K. Nobu ◽  
Hideyuki Tamaki ◽  
Yoichi Kamagata ◽  
Wen-Tso Liu

Syntrophomonas wolfei subsp. methylbutyratica strain 4J5 T (=JCM 14075 T ) is a mesophilic bacterium capable of degrading butyrate and 2-methylbutyrate through syntrophic cooperation with a partner methanogen. The draft genome sequence is 3.2 Mb, with a G+C content of 45.5%.


2001 ◽  
Vol 67 (9) ◽  
pp. 3846-3851 ◽  
Author(s):  
Mickaël Desvaux ◽  
Henri Petitdemange

ABSTRACT An investigation of cellulose degradation by the nonruminal, cellulolytic, mesophilic bacterium Clostridium cellulolyticum was performed in cellulose-fed chemostat cultures with ammonium as the growth-limiting nutrient. At any dilution rate (D), acetate was always the main product of the catabolism, with a yield of product from substrate ranging between 37.7 and 51.5 g per mol of hexose equivalent fermented and an acetate/ethanol ratio always higher than 1. AsD rose, the acetyl coenzyme A was rerouted in favor of ethanol pathways, and ethanol production could represent up to 17.7% of the carbon consumed. Lactate was significantly produced, but with increasing D, the specific lactate production rate declined, as did the specific rate of production of extracellular pyruvate. The proportion of the original carbon directed towards phosphoglucomutase remained constant, and the carbon surplus was balanced mainly by exopolysaccharide and glycogen biosyntheses at highD values, while cellodextrin excretion occurred mainly at lower ones. With increasing D, the specific rate of carbon flowing down catabolites increased as well, but when expressed as a percentage of carbon it declined, while the percentage of carbon directed through biosynthesis pathways was enhanced. The maximum growth and energetic yields were lower than those obtained in cellulose-limited chemostats and were related to an uncoupling between catabolism and anabolism leading to an excess of energy. Compared to growth on cellobiose in ammonium-limited chemostats (E. Guedon, M. Desvaux, and H. Petitdemange, J. Bacteriol. 182:2010–2017, 2000), (i) a specific consumption rate of carbon of as high as 26.72 mmol of hexose equivalent g of cells−1h−1 could not be reached and (ii) the proportions of carbon directed towards cellodextrin, glycogen, and exopolysaccharide pathways were not as high as first determined on cellobiose. While the use of cellobiose allows highlighting of metabolic limitation and regulation of C. cellulolyticumunder ammonium-limited conditions, some of these events should then rather be interpreted as distortions of the metabolism. Growth of cellulolytic bacteria on easily available carbon and nitrogen sources represents conditions far different from those of the natural lignocellulosic compounds.


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