EC Number | Application | Comment | Organism |
---|---|---|---|
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Escherichia coli |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Starkeya novella |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Azospirillum brasilense |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Streptomyces violaceoruber |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Xanthomonas sp. |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Xanthobacter flavus |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Cupriavidus oxalaticus |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Methylorubrum extorquens |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Methylobacterium organophilum |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Variovorax paradoxus |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Azospirillum lipoferum |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Oxalobacter formigenes |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Cupriavidus necator |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Rhodopseudomonas palustris |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Shigella flexneri |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Streptomyces avermitilis |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Streptomyces coelicolor |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Xanthobacter autotrophicus |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Ancylobacter polymorphus |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Ancylobacter oerskovii |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Bradyrhizobium japonicum |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Methylorubrum thiocyanatum |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Pandoraea sp. |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Oxalicibacterium flavum |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Bradyrhizobium sp. |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Arquibacter sp. |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Herminiimonas saxobsidens |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Azorhizobium sp. |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Paraburkholderia xenovorans |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Herminiimonas arsenicoxydans |
2.8.3.16 | environmental protection | bacterial oxalate-degrading function, microbiological processes are considered as the main oxalate sinks in natural environments, in soil oxalate from fungi, plant root exudates and decaying plant tissues display powerful metal chelating properties. Oxalate takes part in plant nutrition status by increasing the availability of phosphate and other poorly soluble micro-nutriments, through its ability to complex and remove excess metal cations. It also plays an important role in the detoxification of heavy metals in the vicinity of plant roots. | Janthinobacterium sp. Marseille |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Escherichia coli |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Starkeya novella |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Azospirillum brasilense |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Streptomyces violaceoruber |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Xanthomonas sp. |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Xanthobacter flavus |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Cupriavidus oxalaticus |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Methylorubrum extorquens |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Methylobacterium organophilum |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Variovorax paradoxus |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Azospirillum lipoferum |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Oxalobacter formigenes |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Cupriavidus necator |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Rhodopseudomonas palustris |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Shigella flexneri |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Streptomyces avermitilis |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Streptomyces coelicolor |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Xanthobacter autotrophicus |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Ancylobacter polymorphus |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Ancylobacter oerskovii |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Bradyrhizobium japonicum |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Methylorubrum thiocyanatum |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Pandoraea sp. |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Oxalicibacterium flavum |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Bradyrhizobium sp. |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Arquibacter sp. |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Herminiimonas saxobsidens |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Azorhizobium sp. |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Paraburkholderia xenovorans |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Herminiimonas arsenicoxydans |
2.8.3.16 | medicine | bacterial oxalate-degrading function, in humans an accumulation of oxalic acid can result in a number of pathologic conditions, including hyperoxaluria, urolithiasis, renal failure, cardiomyopathy and cardiac conductance disorders | Janthinobacterium sp. Marseille |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Escherichia coli |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Starkeya novella |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Azospirillum brasilense |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Streptomyces violaceoruber |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Xanthomonas sp. |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Xanthobacter flavus |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Cupriavidus oxalaticus |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Methylorubrum extorquens |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Methylobacterium organophilum |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Variovorax paradoxus |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Azospirillum lipoferum |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Oxalobacter formigenes |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Cupriavidus necator |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Rhodopseudomonas palustris |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Shigella flexneri |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Streptomyces avermitilis |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Streptomyces coelicolor |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Xanthobacter autotrophicus |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Ancylobacter polymorphus |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Ancylobacter oerskovii |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Bradyrhizobium japonicum |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Methylorubrum thiocyanatum |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Pandoraea sp. |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Oxalicibacterium flavum |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Bradyrhizobium sp. |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Arquibacter sp. |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Herminiimonas saxobsidens |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Azorhizobium sp. |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Paraburkholderia xenovorans |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Herminiimonas arsenicoxydans |
2.8.3.16 | molecular biology | use of the frc gene as template for PCR to detect oxalotrophic bacteria | Janthinobacterium sp. Marseille |
EC Number | Cloned (Comment) | Organism |
---|---|---|
2.8.3.16 | expression in Escherichia coli XL1 | Escherichia coli |
2.8.3.16 | expression in Escherichia coli XL1 | Starkeya novella |
2.8.3.16 | expression in Escherichia coli XL1 | Azospirillum brasilense |
2.8.3.16 | expression in Escherichia coli XL1 | Streptomyces violaceoruber |
2.8.3.16 | expression in Escherichia coli XL1 | Xanthomonas sp. |
2.8.3.16 | expression in Escherichia coli XL1 | Xanthobacter flavus |
2.8.3.16 | expression in Escherichia coli XL1 | Cupriavidus oxalaticus |
2.8.3.16 | expression in Escherichia coli XL1 | Methylorubrum extorquens |
2.8.3.16 | expression in Escherichia coli XL1 | Methylobacterium organophilum |
2.8.3.16 | expression in Escherichia coli XL1 | Variovorax paradoxus |
2.8.3.16 | expression in Escherichia coli XL1 | Azospirillum lipoferum |
2.8.3.16 | expression in Escherichia coli XL1 | Oxalobacter formigenes |
2.8.3.16 | expression in Escherichia coli XL1 | Cupriavidus necator |
2.8.3.16 | expression in Escherichia coli XL1 | Rhodopseudomonas palustris |
2.8.3.16 | expression in Escherichia coli XL1 | Shigella flexneri |
2.8.3.16 | expression in Escherichia coli XL1 | Streptomyces avermitilis |
2.8.3.16 | expression in Escherichia coli XL1 | Streptomyces coelicolor |
2.8.3.16 | expression in Escherichia coli XL1 | Xanthobacter autotrophicus |
2.8.3.16 | expression in Escherichia coli XL1 | Ancylobacter polymorphus |
2.8.3.16 | expression in Escherichia coli XL1 | Ancylobacter oerskovii |
2.8.3.16 | expression in Escherichia coli XL1 | Bradyrhizobium japonicum |
2.8.3.16 | expression in Escherichia coli XL1 | Methylorubrum thiocyanatum |
2.8.3.16 | expression in Escherichia coli XL1 | Pandoraea sp. |
2.8.3.16 | expression in Escherichia coli XL1 | Oxalicibacterium flavum |
2.8.3.16 | expression in Escherichia coli XL1 | Bradyrhizobium sp. |
2.8.3.16 | expression in Escherichia coli XL1 | Arquibacter sp. |
2.8.3.16 | expression in Escherichia coli XL1 | Herminiimonas saxobsidens |
2.8.3.16 | expression in Escherichia coli XL1 | Azorhizobium sp. |
2.8.3.16 | expression in Escherichia coli XL1 | Paraburkholderia xenovorans |
2.8.3.16 | expression in Escherichia coli XL1 | Herminiimonas arsenicoxydans |
2.8.3.16 | expression in Escherichia coli XL1 | Janthinobacterium sp. Marseille |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.8.3.16 | formyl-CoA + oxalate | Escherichia coli | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Starkeya novella | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Azospirillum brasilense | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Streptomyces violaceoruber | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Xanthomonas sp. | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Xanthobacter flavus | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Cupriavidus oxalaticus | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Methylorubrum extorquens | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Methylobacterium organophilum | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Variovorax paradoxus | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Azospirillum lipoferum | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Oxalobacter formigenes | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Cupriavidus necator | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Rhodopseudomonas palustris | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Shigella flexneri | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Streptomyces avermitilis | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Streptomyces coelicolor | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Xanthobacter autotrophicus | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Ancylobacter polymorphus | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Ancylobacter oerskovii | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Bradyrhizobium japonicum | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Methylorubrum thiocyanatum | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Pandoraea sp. | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Oxalicibacterium flavum | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Bradyrhizobium sp. | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Arquibacter sp. | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Herminiimonas saxobsidens | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Azorhizobium sp. | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Paraburkholderia xenovorans | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Herminiimonas arsenicoxydans | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Janthinobacterium sp. Marseille | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | Cupriavidus necator JMP 134-1 | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | formate + oxalyl-CoA | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
2.8.3.16 | Ancylobacter oerskovii | - |
- |
- |
2.8.3.16 | Ancylobacter polymorphus | B3VMH8 | fragment | - |
2.8.3.16 | Arquibacter sp. | - |
- |
- |
2.8.3.16 | Azorhizobium sp. | - |
- |
- |
2.8.3.16 | Azospirillum brasilense | - |
- |
- |
2.8.3.16 | Azospirillum lipoferum | - |
- |
- |
2.8.3.16 | Bradyrhizobium japonicum | Q89QH2 | USDA 110, gene frc, no detection of the frc-gene in Klebsiella oxytoca, Bacillus subtilis, Micrococcus luteus, Microvirgula aerodenitrificans, Paracoccus denitrificans, Rhodococcus opacus, Xanthobacter agilis and Pseudomonas aeruginosa | - |
2.8.3.16 | Bradyrhizobium sp. | A5EGD7 | BTAi1, frc gene | - |
2.8.3.16 | Cupriavidus necator | Q0K0H8 | H16 gene | - |
2.8.3.16 | Cupriavidus necator | Q46S66 | JMP134, Reut_B4669 gene | - |
2.8.3.16 | Cupriavidus necator | Q46S72 | JMP 134 | - |
2.8.3.16 | Cupriavidus necator JMP 134-1 | Q46S72 | JMP 134 | - |
2.8.3.16 | Cupriavidus oxalaticus | - |
- |
- |
2.8.3.16 | Escherichia coli | - |
B, frc gene, but no Ca-oxalat utilization | - |
2.8.3.16 | Escherichia coli | P69902 | K12, frc gene | - |
2.8.3.16 | Herminiimonas arsenicoxydans | A4G241 | frcA gene | - |
2.8.3.16 | Herminiimonas arsenicoxydans | A4G242 | frcB gene | - |
2.8.3.16 | Herminiimonas saxobsidens | - |
- |
- |
2.8.3.16 | Janthinobacterium sp. Marseille | A6T0J2 | caiB3 gene | - |
2.8.3.16 | Methylobacterium organophilum | - |
- |
- |
2.8.3.16 | Methylorubrum extorquens | - |
- |
- |
2.8.3.16 | Methylorubrum thiocyanatum | - |
- |
- |
2.8.3.16 | Oxalicibacterium flavum | - |
- |
- |
2.8.3.16 | Oxalobacter formigenes | O06644 | frc gene | - |
2.8.3.16 | Pandoraea sp. | - |
- |
- |
2.8.3.16 | Paraburkholderia xenovorans | Q13RQ4 | LB400, frc gene | - |
2.8.3.16 | Rhodopseudomonas palustris | Q6N8F8 | CGA009, frc gene | - |
2.8.3.16 | Shigella flexneri | P69903 | 2a strain 301, frc gene | - |
2.8.3.16 | Starkeya novella | - |
- |
- |
2.8.3.16 | Streptomyces avermitilis | Q82M40 | MA-4680, frc gene | - |
2.8.3.16 | Streptomyces coelicolor | O87838 | A3, frc gene | - |
2.8.3.16 | Streptomyces violaceoruber | - |
- |
- |
2.8.3.16 | Variovorax paradoxus | - |
- |
- |
2.8.3.16 | Xanthobacter autotrophicus | A7ICK2 | Py2, Xaut_0487 gene | - |
2.8.3.16 | Xanthobacter flavus | - |
- |
- |
2.8.3.16 | Xanthomonas sp. | - |
frc gene, but no Ca-oxalate utilization | - |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
2.8.3.16 | enrichment culture | oxalate enrichment culture | Escherichia coli | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Starkeya novella | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Azospirillum brasilense | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Streptomyces violaceoruber | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Xanthomonas sp. | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Xanthobacter flavus | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Cupriavidus oxalaticus | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Methylorubrum extorquens | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Methylobacterium organophilum | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Variovorax paradoxus | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Azospirillum lipoferum | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Oxalobacter formigenes | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Cupriavidus necator | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Rhodopseudomonas palustris | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Shigella flexneri | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Streptomyces avermitilis | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Streptomyces coelicolor | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Xanthobacter autotrophicus | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Ancylobacter polymorphus | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Ancylobacter oerskovii | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Bradyrhizobium japonicum | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Methylorubrum thiocyanatum | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Pandoraea sp. | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Oxalicibacterium flavum | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Bradyrhizobium sp. | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Arquibacter sp. | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Herminiimonas saxobsidens | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Azorhizobium sp. | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Paraburkholderia xenovorans | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Herminiimonas arsenicoxydans | - |
2.8.3.16 | enrichment culture | oxalate enrichment culture | Janthinobacterium sp. Marseille | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Escherichia coli | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Starkeya novella | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Azospirillum brasilense | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Streptomyces violaceoruber | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Xanthomonas sp. | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Xanthobacter flavus | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Cupriavidus oxalaticus | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Methylorubrum extorquens | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Methylobacterium organophilum | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Variovorax paradoxus | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Azospirillum lipoferum | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Oxalobacter formigenes | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Cupriavidus necator | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Rhodopseudomonas palustris | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Shigella flexneri | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Streptomyces avermitilis | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Streptomyces coelicolor | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Xanthobacter autotrophicus | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Ancylobacter polymorphus | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Ancylobacter oerskovii | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Bradyrhizobium japonicum | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Methylorubrum thiocyanatum | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Pandoraea sp. | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Oxalicibacterium flavum | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Bradyrhizobium sp. | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Arquibacter sp. | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Herminiimonas saxobsidens | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Azorhizobium sp. | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Paraburkholderia xenovorans | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Herminiimonas arsenicoxydans | - |
2.8.3.16 | soil | soil samples are collected below the Ca-oxalate producing trees Milicia excelsa and Afzelia africana and in a similar soil distant from trees | Janthinobacterium sp. Marseille | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
2.8.3.16 | formyl-CoA + oxalate | - |
Escherichia coli | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Starkeya novella | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Azospirillum brasilense | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Streptomyces violaceoruber | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Xanthomonas sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Xanthobacter flavus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Cupriavidus oxalaticus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Methylorubrum extorquens | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Methylobacterium organophilum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Variovorax paradoxus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Azospirillum lipoferum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Oxalobacter formigenes | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Cupriavidus necator | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Rhodopseudomonas palustris | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Shigella flexneri | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Streptomyces avermitilis | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Streptomyces coelicolor | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Xanthobacter autotrophicus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Ancylobacter polymorphus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Ancylobacter oerskovii | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Bradyrhizobium japonicum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Methylorubrum thiocyanatum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Pandoraea sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Oxalicibacterium flavum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Bradyrhizobium sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Arquibacter sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Herminiimonas saxobsidens | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Azorhizobium sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Paraburkholderia xenovorans | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Herminiimonas arsenicoxydans | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Janthinobacterium sp. Marseille | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Escherichia coli | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Starkeya novella | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Azospirillum brasilense | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Streptomyces violaceoruber | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Xanthomonas sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Xanthobacter flavus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Cupriavidus oxalaticus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Methylorubrum extorquens | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Methylobacterium organophilum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Variovorax paradoxus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Azospirillum lipoferum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Oxalobacter formigenes | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Cupriavidus necator | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Rhodopseudomonas palustris | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Shigella flexneri | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Streptomyces avermitilis | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Streptomyces coelicolor | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Xanthobacter autotrophicus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Ancylobacter polymorphus | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Ancylobacter oerskovii | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Bradyrhizobium japonicum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Methylorubrum thiocyanatum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Pandoraea sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Oxalicibacterium flavum | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Bradyrhizobium sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Arquibacter sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Herminiimonas saxobsidens | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Azorhizobium sp. | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Paraburkholderia xenovorans | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Herminiimonas arsenicoxydans | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Janthinobacterium sp. Marseille | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | - |
Cupriavidus necator JMP 134-1 | formate + oxalyl-CoA | - |
? | |
2.8.3.16 | formyl-CoA + oxalate | oxalate is a highly oxidized compound that may be used as C- and energy sources by oxalotrophic bacteria | Cupriavidus necator JMP 134-1 | formate + oxalyl-CoA | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
2.8.3.16 | formyl-CoA-transferase | - |
Escherichia coli |
2.8.3.16 | formyl-CoA-transferase | - |
Starkeya novella |
2.8.3.16 | formyl-CoA-transferase | - |
Azospirillum brasilense |
2.8.3.16 | formyl-CoA-transferase | - |
Streptomyces violaceoruber |
2.8.3.16 | formyl-CoA-transferase | - |
Xanthomonas sp. |
2.8.3.16 | formyl-CoA-transferase | - |
Xanthobacter flavus |
2.8.3.16 | formyl-CoA-transferase | - |
Cupriavidus oxalaticus |
2.8.3.16 | formyl-CoA-transferase | - |
Methylorubrum extorquens |
2.8.3.16 | formyl-CoA-transferase | - |
Methylobacterium organophilum |
2.8.3.16 | formyl-CoA-transferase | - |
Variovorax paradoxus |
2.8.3.16 | formyl-CoA-transferase | - |
Azospirillum lipoferum |
2.8.3.16 | formyl-CoA-transferase | - |
Oxalobacter formigenes |
2.8.3.16 | formyl-CoA-transferase | - |
Cupriavidus necator |
2.8.3.16 | formyl-CoA-transferase | - |
Rhodopseudomonas palustris |
2.8.3.16 | formyl-CoA-transferase | - |
Shigella flexneri |
2.8.3.16 | formyl-CoA-transferase | - |
Streptomyces avermitilis |
2.8.3.16 | formyl-CoA-transferase | - |
Streptomyces coelicolor |
2.8.3.16 | formyl-CoA-transferase | - |
Xanthobacter autotrophicus |
2.8.3.16 | formyl-CoA-transferase | - |
Ancylobacter polymorphus |
2.8.3.16 | formyl-CoA-transferase | - |
Ancylobacter oerskovii |
2.8.3.16 | formyl-CoA-transferase | - |
Bradyrhizobium japonicum |
2.8.3.16 | formyl-CoA-transferase | - |
Methylorubrum thiocyanatum |
2.8.3.16 | formyl-CoA-transferase | - |
Pandoraea sp. |
2.8.3.16 | formyl-CoA-transferase | - |
Oxalicibacterium flavum |
2.8.3.16 | formyl-CoA-transferase | - |
Bradyrhizobium sp. |
2.8.3.16 | formyl-CoA-transferase | - |
Arquibacter sp. |
2.8.3.16 | formyl-CoA-transferase | - |
Herminiimonas saxobsidens |
2.8.3.16 | formyl-CoA-transferase | - |
Azorhizobium sp. |
2.8.3.16 | formyl-CoA-transferase | - |
Paraburkholderia xenovorans |
2.8.3.16 | formyl-CoA-transferase | - |
Herminiimonas arsenicoxydans |
2.8.3.16 | formyl-CoA-transferase | - |
Janthinobacterium sp. Marseille |