Previous studies have shown that the hyperthermophilic archaeon Pyrococcus furiosus contains four distinct cytoplasmic 2-ketoacid oxidoreductases (ORs) which differ in their substrate specificities, while the hyperthermophilic bacterium Thermotoga maritima contains only one, pyruvate ferredoxin oxidoreductase (POR). These enzymes catalyze the synthesis of the acyl (or aryl) coenzyme A derivative in a thiamine PPi-dependent oxidative decarboxylation reaction with reduction of ferredoxin. We report here on the molecular analysis of the POR (por) and 2-ketoisovalerate ferredoxin oxidoreductase (vor) genes from P. furiosus and of the POR gene from T. maritima, all of which comprise four different subunits. The operon organization for P. furiosu...
Hyperthermophilic bacteria Thermotoga maritima and Thermotoga hypogea produce ethanol as a metabolic...
金沢大学理工研究域自然システム学系A ferredoxin was purfied from the hyperthermophilic archaeon, Pyrobaculum islandicu...
Protists that live in low oxygen conditions often oxidize pyruvate to acetate via anaerobic ATP-gene...
Previous studies have shown that the hyperthermophilic archaeon Pyrococcus furiosus contains four di...
Previous studies have shown that the hyperthermophilic archaeon Pyrococcus furiosus contains four di...
The hyperthermophilic archaea Pyrococcus furiosus and Thermococcus litoralis contain the tungstoenzy...
The hyperthermophilic archaeon Thermococcus guaymasensis produces ethanol as a metabolic end product...
The hyperthermophilic archaea Pyrococcus furiosus and Thermococcus litoralis contain the tungstoenzy...
The hyperthermophilic archaeon Thermococcus guaymasensis produces ethanol as a metabolic end product...
Pyruvate:ferredoxin oxidoreductase (PFOR) is a key enzyme in bacterial anaerobic metabolism. Since a...
AbstractPyruvate-ferredoxin oxidoreductase oxidises pyruvate in many fermentative microorganisms. Th...
A gene coding for the ferredoxin of the primordial, strictly anaerobic and hyperthermophilic bacteri...
Pyruvate:ferredoxin oxidoreductase (PFOR) is a microbial enzyme that uses thiamine pyrophosphate (TP...
Crystal structures of formaldehyde ferredoxin oxidoreductase (FOR), a tungstopterin-containing prote...
Pyruvate:ferredoxin oxidoreductase (PFOR) catalyzes the Coenzyme A (CoA)-dependent oxidative decarbo...
Hyperthermophilic bacteria Thermotoga maritima and Thermotoga hypogea produce ethanol as a metabolic...
金沢大学理工研究域自然システム学系A ferredoxin was purfied from the hyperthermophilic archaeon, Pyrobaculum islandicu...
Protists that live in low oxygen conditions often oxidize pyruvate to acetate via anaerobic ATP-gene...
Previous studies have shown that the hyperthermophilic archaeon Pyrococcus furiosus contains four di...
Previous studies have shown that the hyperthermophilic archaeon Pyrococcus furiosus contains four di...
The hyperthermophilic archaea Pyrococcus furiosus and Thermococcus litoralis contain the tungstoenzy...
The hyperthermophilic archaeon Thermococcus guaymasensis produces ethanol as a metabolic end product...
The hyperthermophilic archaea Pyrococcus furiosus and Thermococcus litoralis contain the tungstoenzy...
The hyperthermophilic archaeon Thermococcus guaymasensis produces ethanol as a metabolic end product...
Pyruvate:ferredoxin oxidoreductase (PFOR) is a key enzyme in bacterial anaerobic metabolism. Since a...
AbstractPyruvate-ferredoxin oxidoreductase oxidises pyruvate in many fermentative microorganisms. Th...
A gene coding for the ferredoxin of the primordial, strictly anaerobic and hyperthermophilic bacteri...
Pyruvate:ferredoxin oxidoreductase (PFOR) is a microbial enzyme that uses thiamine pyrophosphate (TP...
Crystal structures of formaldehyde ferredoxin oxidoreductase (FOR), a tungstopterin-containing prote...
Pyruvate:ferredoxin oxidoreductase (PFOR) catalyzes the Coenzyme A (CoA)-dependent oxidative decarbo...
Hyperthermophilic bacteria Thermotoga maritima and Thermotoga hypogea produce ethanol as a metabolic...
金沢大学理工研究域自然システム学系A ferredoxin was purfied from the hyperthermophilic archaeon, Pyrobaculum islandicu...
Protists that live in low oxygen conditions often oxidize pyruvate to acetate via anaerobic ATP-gene...