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How come the enzyme inside the lysosome does not digest the wall of lysosome?
because the lysosome cannot release its contents unless nearby cells allow it.
What organelle lacks enzyme needed for lipid breakdown in tay Sahs Syndrome?
The lysosome is the organelle that lacks the enzyme needed for lipid breakdown in Tay-Sachs disease. This genetic disorder results in the accumulation of lipid molecules in the lysosomes, leading to cellular dysfunction and damage, particularly in nerve cells.
Which organelle is likely to be the one that lacks the proper enzyme needed for lipid breakdown?
The organelle likely lacking the proper enzyme for lipid breakdown is the lysosome. Lysosomes contain hydrolytic enzymes that are essential for breaking down lipids, proteins, and carbohydrates. If these enzymes are deficient or malfunctioning, the lysosome cannot effectively degrade lipids, leading to their accumulation and potential cellular dysfunction. Disorders such as Tay-Sachs disease illustrate the consequences of such enzyme deficiencies in lysosomes.
Where do you store a cell's waste?
its an enzyme
What breaks down substances in a cell?
The lysosome.
How come the enzyme inside the lysosome does not digest the wall of lysosome?
because the lysosome cannot release its contents unless nearby cells allow it.
Where is the lipase enzyme found in the cell?
Lipase is found in the organelle called a lysosome.
Which organelle is likely to be the one that lacks the proper enzyme needed for lipid brakedown?
lysosome
What is a real life example of a lysosome?
Lysosomes are found in only plant cells. The lysosome is like a mouth. Like a lysosome, the mouth contains an enzyme (amalase, lysosomes contain enzymes that break down polysaccharides, proteins and nucleic acids.
What is the porpouse lysosome?
The lysosome is called the recycle bin on the cell. This organelle is essentially a pouch filled with hydrolytic digestive enzyme that break down unused proteins, worn out organelles and ingested bacteria and viruses.
What organelle lacks enzyme needed for lipid breakdown in tay Sahs Syndrome?
The lysosome is the organelle that lacks the enzyme needed for lipid breakdown in Tay-Sachs disease. This genetic disorder results in the accumulation of lipid molecules in the lysosomes, leading to cellular dysfunction and damage, particularly in nerve cells.
What organelle has the problem if lactose digestive enzymes not produced?
Lysosome. Which fails to produce the enzyme lactase. (source : medical forum)
How do lysosomes work as digestive bags and suicidal bags?
A lysosome has a digestive enzyme inside of it; this enzyme can be used for breaking down food, but it could also be used to destroy worn down organelles. If there is a problem with the cell itself, the lysosome could simply burst, and the digestive enzymes would "eat" away at the cell.
What is the organelle of Gaucher's disease?
The organelle associated with Gaucher's disease is the lysosome. This genetic disorder is caused by a deficiency of the enzyme glucocerebrosidase, leading to the accumulation of a fatty substance called glucocerebroside within the lysosomes of cells, particularly in macrophages.
Which organelle is likely to be the one that lacks the proper enzyme needed for lipid breakdown?
The organelle likely lacking the proper enzyme for lipid breakdown is the lysosome. Lysosomes contain hydrolytic enzymes that are essential for breaking down lipids, proteins, and carbohydrates. If these enzymes are deficient or malfunctioning, the lysosome cannot effectively degrade lipids, leading to their accumulation and potential cellular dysfunction. Disorders such as Tay-Sachs disease illustrate the consequences of such enzyme deficiencies in lysosomes.
Where do you store a cell's waste?
its an enzyme
What might happen if some lysosome enzymes are absent?
extra cellular digestion takes place by lysosomal enzymes.when there is no lysosomal enzyme then extra cellular digestion cannot tak place.
