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What compound accumulates in the blood of people who have PKU?
In individuals with phenylketonuria (PKU), the compound that accumulates in the blood is phenylalanine. This buildup occurs due to a deficiency in the enzyme phenylalanine hydroxylase, which is responsible for converting phenylalanine into tyrosine. If not managed through dietary restrictions, elevated levels of phenylalanine can lead to serious neurological damage and cognitive impairment. Regular monitoring of blood phenylalanine levels is crucial for individuals with PKU.
Is phenylalanine compound a element or mixture?
Phenylalanine is a compound, family of aminoacids.Additional answerYou obviously don't know what an element is. It is a substance that cannot be broken down into another substance by chemical processes. Hydrogen, neon, iron, cobalt, uranium are all examples of elements.
Which enzyme breaks down phenylalanine?
The enzyme phenylalanine hydroxylase breaks down phenylalanine into tyrosine. This enzyme is essential for the conversion of phenylalanine to tyrosine in the body. Deficiency in this enzyme can lead to a build-up of phenylalanine, which can result in a condition called phenylketonuria (PKU).
Phenylalanine C9H11NO2 is an amino acid used to make proteins It has a molar mass of 165.19 g mol What is the mass percent of oxygen in phenylalanine?
The molar mass of oxygen in phenylalanine is 16.00 g/mol. To calculate the mass percent of oxygen in phenylalanine, divide the molar mass of oxygen by the molar mass of phenylalanine, then multiply by 100. (16.00 g/mol / 165.19 g/mol) * 100 = 9.68% Therefore, the mass percent of oxygen in phenylalanine is approximately 9.68%.
Why is phenylalanine observed in the urine of a classical PKU patient?
PKU stands for phenylketonuria, the classic symptom of which (and the diagnostic test for the disease) is phenylalanine in the urine. This is a genetic disorder in which the body is unable to process phenylalalanine, so it is excreted in the urine.
How many elements are found in phenylalanine?
how many atoms are in this compound
What compound accumulates in the blood of people who have PKU?
In individuals with phenylketonuria (PKU), the compound that accumulates in the blood is phenylalanine. This buildup occurs due to a deficiency in the enzyme phenylalanine hydroxylase, which is responsible for converting phenylalanine into tyrosine. If not managed through dietary restrictions, elevated levels of phenylalanine can lead to serious neurological damage and cognitive impairment. Regular monitoring of blood phenylalanine levels is crucial for individuals with PKU.
What compound accumulates in the blood of people who have Phenylketonuria?
In people with Phenylketonuria (PKU), the compound that accumulates in the blood is phenylalanine. This occurs due to a deficiency in the enzyme phenylalanine hydroxylase, which is responsible for converting phenylalanine into tyrosine. Elevated levels of phenylalanine can lead to serious neurological issues if not managed through dietary restrictions. Early detection and treatment are crucial to prevent cognitive impairments associated with PKU.
Is phenylalanine compound a element or mixture?
Phenylalanine is a compound, family of aminoacids.Additional answerYou obviously don't know what an element is. It is a substance that cannot be broken down into another substance by chemical processes. Hydrogen, neon, iron, cobalt, uranium are all examples of elements.
Why Should phenylalanine give a yellow Color with concentrated nitric acid?
Phenylalanine gives a yellow color with concentrated nitric acid due to the formation of a nitro derivative. Nitric acid reacts with the aromatic ring of phenylalanine, leading to the formation of a yellow compound.
What is the mass percent of oxygen in phenylalanine?
The molecular formula of phenylalanine is C9H11NO2. To calculate the mass percent of oxygen in phenylalanine, we first need to calculate the molar mass of the compound. This molar mass is found to be 165.19 g/mol. The mass percent of oxygen in phenylalanine is then found to be (32.00 g/mol / 165.19 g/mol) * 100 ≈ 19.38%.
Which enzyme breaks down phenylalanine?
The enzyme phenylalanine hydroxylase breaks down phenylalanine into tyrosine. This enzyme is essential for the conversion of phenylalanine to tyrosine in the body. Deficiency in this enzyme can lead to a build-up of phenylalanine, which can result in a condition called phenylketonuria (PKU).
Does Phenylalanine have the same effect as Apartame does?
Phenylalanine is a component in aspartame.
How much phenylalanine does Dr Pepper 10 have?
It has 718mg of phenylalanine.
What is the molecular formula for Phenylalanine?
The molecular formula for phenylalanine is C9H11NO2.
What are the DNA codons for phenylalanine?
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
What codon codes for amino acids phenylalanine did scientist find?
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
