The same time, carbon dioxide that is dissolved in the blood comes out of the capillaries back into the air sacs, ready to be breathed out. Blood with fresh oxygen is carried from your lungs to the left side of your heart, which pumps blood around your body through the arteries.
When an acyl group is being transferred from the cytosol to the mitochondria for oxidation, the order of the enzymes it encounters is
CPT-I Carnitine Translocase : CPT -II
CPT-I and CPT-II are crucial for the beta-oxidation of long-chain fatty acids in the mitochondria by enabling their transport across the mitochondrial membrane.
To know more CPT I and CPT II about here
brainly.com/question/15047884
#SPJ4
Answer:
Its is a lysosomal storage disease!
Explanation:
<u>Hurler syndrome:-</u> is also known as mucopolysaccharidosis-I .
It Is due to the mutation on chromosome 4 .
There is a lack of of enzyme called alpha-L-iduronidase.This enzyme is present in lysosomes
It causes accumulation of mucopolysaccharides because of the absent of the enzyme in the lysosome
<u>Hunter syndrome:- </u>is also known as mucopolysaccharidosis-II
It occurs due to mutation in iduronate-2-sulfatase (IDS) gene.It is an X-linked disease
