Engineered bacteria are capable of converting phenylalanine and may serve as a potential therapy for phenylketonuria. Phenylketonuria, or PKU, is an inborn error of metabolism that is included in many newborn screening programs worldwide. The disease is caused by an inability to metabolize the amino acid phenylalanine (Phe). When left untreated, the accumulation of Phe can cause severe neurological disease, but early detection followed by a strict low-protein diet can mitigate these symptoms. Compliance with the diet is difficult, however, and the low-protein diet can lead to a failure to thrive. Alternative treatments are therefore eagerly awaited. Isabella and colleagues engineered bacteria capable of converting Phe, thereby reducing the ...
<div><p>Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenyl...
Phenylketonuria (PKU) is an inborn error of amino acid metabolism caused by phenylalanine hydroxylas...
Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenylalanine ...
The fields of synthetic biology and microbiome research developed greatly over the last decade. The ...
Phenylketonuria (PKU) is a genetic disease characterized by the inability to convert dietary phenyla...
<div><p>Phenylketonuria (PKU) is a genetic disease characterized by the inability to convert dietary...
The fields of synthetic biology and microbiome research developed greatly over the last decade. The ...
Mark Charbonneau et al. develop a mathematical model that describes the behavior of an engineered ba...
Orphan metabolic diseases are rare genetic defects that interfere with metabolism due to ineffective...
Inborn errors of metabolism (IEM) are a family of more than 500 potentially lethal congenital geneti...
Phenylketonuria (PKU) and related forms of non-PKU hyperphenylalaninemias (HPA) result from deficien...
Absence of functional phenylalanine hydroxylase results in phenylketonuria (PKU). Viable treatments ...
Phenylketonuria (PKU) is a rare metabolic disorder characterized by impaired conversion of phenylala...
The presence of an extensive enterorecirculation of amino acids between the intestine and the body, ...
PKU patients have elevated phenylalanine levels which can result in neurological impairment. Here th...
<div><p>Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenyl...
Phenylketonuria (PKU) is an inborn error of amino acid metabolism caused by phenylalanine hydroxylas...
Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenylalanine ...
The fields of synthetic biology and microbiome research developed greatly over the last decade. The ...
Phenylketonuria (PKU) is a genetic disease characterized by the inability to convert dietary phenyla...
<div><p>Phenylketonuria (PKU) is a genetic disease characterized by the inability to convert dietary...
The fields of synthetic biology and microbiome research developed greatly over the last decade. The ...
Mark Charbonneau et al. develop a mathematical model that describes the behavior of an engineered ba...
Orphan metabolic diseases are rare genetic defects that interfere with metabolism due to ineffective...
Inborn errors of metabolism (IEM) are a family of more than 500 potentially lethal congenital geneti...
Phenylketonuria (PKU) and related forms of non-PKU hyperphenylalaninemias (HPA) result from deficien...
Absence of functional phenylalanine hydroxylase results in phenylketonuria (PKU). Viable treatments ...
Phenylketonuria (PKU) is a rare metabolic disorder characterized by impaired conversion of phenylala...
The presence of an extensive enterorecirculation of amino acids between the intestine and the body, ...
PKU patients have elevated phenylalanine levels which can result in neurological impairment. Here th...
<div><p>Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenyl...
Phenylketonuria (PKU) is an inborn error of amino acid metabolism caused by phenylalanine hydroxylas...
Phenylketonuria (PKU) is a genetic metabolic disease in which the decrease or loss of phenylalanine ...