Pseudomonas putida efficiently utilizes many different carbon sources without the formation of by products even under conditions of stress. This implies a high degree of flexibility to cope with conditions that require a significantly altered distribution of carbon to either biomass or energy in the form of NADH. In the literature, co-feeding of the reduced C1 compound formate to Escherichia coli heterologously expressing the NAD(+)-dependent formate dehydrogenase of the yeast Candida boidinii was demonstrated to boost various NADH-demanding applications. Pseudomonas putida as emerging biotechnological workhorse is inherently equipped with an NAD(+)-dependent formate dehydrogenase encouraging us to investigate the use of formate and its eff...
The understanding of how carbon fluxes are distributed through a metabolic network offers an overvie...
Metabolic control associated with diauxic growth of Pseudomonas oxalaticus in batch cultures on mixt...
WOS: 000366078800026Binay, Barış (Arel Author)NAD(+)-dependent formate dehydrogenase (FDH) enzyme ca...
Pseudomonas putida is a remarkable soil microorganism and emerges as biotechnological platform host,...
The soil bacterium and metabolic engineering platform Pseudomonas putida tolerates high levels of en...
Adenosine phosphate and NAD cofactors play a vital role in the operation of cell metabolism, and the...
Engineering the level of metabolic cofactors to manipulate metabolic flux is emerging as an attracti...
Engineering the level of metabolic cofactors to manipulate metabolic flux is emerging as an attracti...
As a frequent inhabitant of sites polluted with toxic chemicals, the soil bacterium and plant-root c...
Abstract Background Enzymatic NADH or NADPH-dependent reduction is a widely applied approach for the...
-dependent formate dehydrogenase (FDH) from methylotrophic bacterium Pseudomonas sp. 101 (EC 1.2.1.2...
Here, we report recent progress our laboratories have made in understanding the maturation and react...
Metabolic engineering studies have generally focused on manipulating enzyme levels. However, cofacto...
The obligate aerobic nature of Pseudomonas putida, one of the most prominent whole-cell biocatalysts...
We demonstrated that formaldehyde can be efficiently coutilized by an engineered Saccharomyces cerev...
The understanding of how carbon fluxes are distributed through a metabolic network offers an overvie...
Metabolic control associated with diauxic growth of Pseudomonas oxalaticus in batch cultures on mixt...
WOS: 000366078800026Binay, Barış (Arel Author)NAD(+)-dependent formate dehydrogenase (FDH) enzyme ca...
Pseudomonas putida is a remarkable soil microorganism and emerges as biotechnological platform host,...
The soil bacterium and metabolic engineering platform Pseudomonas putida tolerates high levels of en...
Adenosine phosphate and NAD cofactors play a vital role in the operation of cell metabolism, and the...
Engineering the level of metabolic cofactors to manipulate metabolic flux is emerging as an attracti...
Engineering the level of metabolic cofactors to manipulate metabolic flux is emerging as an attracti...
As a frequent inhabitant of sites polluted with toxic chemicals, the soil bacterium and plant-root c...
Abstract Background Enzymatic NADH or NADPH-dependent reduction is a widely applied approach for the...
-dependent formate dehydrogenase (FDH) from methylotrophic bacterium Pseudomonas sp. 101 (EC 1.2.1.2...
Here, we report recent progress our laboratories have made in understanding the maturation and react...
Metabolic engineering studies have generally focused on manipulating enzyme levels. However, cofacto...
The obligate aerobic nature of Pseudomonas putida, one of the most prominent whole-cell biocatalysts...
We demonstrated that formaldehyde can be efficiently coutilized by an engineered Saccharomyces cerev...
The understanding of how carbon fluxes are distributed through a metabolic network offers an overvie...
Metabolic control associated with diauxic growth of Pseudomonas oxalaticus in batch cultures on mixt...
WOS: 000366078800026Binay, Barış (Arel Author)NAD(+)-dependent formate dehydrogenase (FDH) enzyme ca...