A new study by an international team of scientists has revealed conditions under which a body produces more superoxide — a dangerous form of oxygen with the capability to destruct DNA.
Human mutations in a gene encoding the DHTKD1 protein result in a range of neurological disturbances. On molecular level, the mutations cause accumulation of the reactive oxygen species (ROS) and degradation products of lysine and tryptophan, said the study published recently in the journal Free Radical Biology and Medicine.
The structure of the DHTKD1 protein is similar to an enzyme, 2-oxoglutarate dehydrogenase, which is able to produce superoxide.
According to the researcher, a cell combats the “poisonous” forms of oxygen with a help of antioxidants, and antioxidant defence system proteins.
But disturbed metabolism may cause a shortage of amino acids (the bricks for building proteins) lysine and tryptophan which may result into physical, neurologic and mental malfunctions, and even lead to death.
Those amino acids belong to irreplaceable and cannot be produced from other substances in human body, so they should come from food, the researchers noted.
According to the study, 2-aminoadipate and 2-oxoadipate are the degradation products of lysine, tryptophan and hydroxylysine.