Answer :
Thank you for posting your question here. I believe the answer is the below:
B) a defect in the mannose-6-phosphate receptor in the Golgi apparatus
D) a defect in a hydrolytic enzyme that breaks down polysaccharide
F) a defect in the mannose-6-phosphate receptor in the mitochondria
B) a defect in the mannose-6-phosphate receptor in the Golgi apparatus
D) a defect in a hydrolytic enzyme that breaks down polysaccharide
F) a defect in the mannose-6-phosphate receptor in the mitochondria
Answer:
B); D) and E)
Explanation:
B) a defect in the mannose-6-phosphate receptor in the Golgi apparatus.
Explanation: The mannose-6-phosphate receptors (MPR's) in the Golgi apparatus are essential for targeting the mannose-6-phosphate tagged lysosomal proteins to the lysosome.
D) a defect in a hydrolytic enzyme that breaks down polysaccharide.
Explanation: Lysosomes contain enzymes that hydrolyze polysaccharides, therefore any defects in these enzymes causes malfunctioning of the lysosome.
E) a defect in the process of adding a mannose-6-phosphate signal to lysosomal hydrolases.
Explanation: In the Golgi apparatus lysosomal proteins are tagged with mannose-6-phosphate so that they are specifically transported to the lysosomes.