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Lysosomes are single, membrane-bound sacs that contain digestive enzymes.Throughout a cell's lifetime, the lysosomal enzymes digest old organelles to make room for newly formed organelles. The lysosomes allow cells to continually renew themselves and prevent the accumulation of cellular toxins.

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Tay-Sachs disease is a human genetic abnormality that results in cells accumulating and becoming clogged with very large and complex lipids Which cellular organelle must be involved in this condition?

The lysosome must be involved in Tay-Sachs disease. Lysosomes are responsible for breaking down cellular waste, including lipids. In Tay-Sachs disease, a deficiency in the enzyme beta-hexosaminidase A leads to the accumulation of lipids in cells, particularly in the lysosomes.


What part of the cell is defective in pompe's disease and Tay-Sachs disease?

In Pompe's disease, the defect lies in the lysosomal enzyme alpha-glucosidase, which leads to the accumulation of glycogen in lysosomes. In Tay-Sachs disease, the defect is in the enzyme hexosaminidase A, which leads to the accumulation of GM2 gangliosides in lysosomes.


What cellular structures is involved in intracellular digestion Golgi apparatus ribosomes lysosomes?

The main cellular structures involved in intracellular digestion are lysosomes and the Golgi apparatus. Lysosomes contain digestive enzymes that break down complex molecules, while the Golgi apparatus modifies and packages these enzymes for transport to the lysosomes. Ribosomes are responsible for protein synthesis and do not directly participate in intracellular digestion.


Where will you find a lysosome?

Lysosomes are organelles involved in breaking down unwanted things inside cells.


Which organelle is involved in the formation of lysosome?

Lysosomes are produced by golgi bodies.They involve in cellular digestion.

Related Questions

What cellular organelle is involved in Tay-sachs?

Tay-Sachs disease is a human genetic disorder which results in the accumulation of cells due to the clogging caused by undigested lipids. The organelle involved in this disease is the lysosome.


Tay-Sachs disease is a human genetic abnormality that results in cells accumulating and becoming clogged with very large and complex lipids Which cellular organelle must be involved in this condition?

The lysosome must be involved in Tay-Sachs disease. Lysosomes are responsible for breaking down cellular waste, including lipids. In Tay-Sachs disease, a deficiency in the enzyme beta-hexosaminidase A leads to the accumulation of lipids in cells, particularly in the lysosomes.


What part of the cell is defective in pompe's disease and Tay-Sachs disease?

In Pompe's disease, the defect lies in the lysosomal enzyme alpha-glucosidase, which leads to the accumulation of glycogen in lysosomes. In Tay-Sachs disease, the defect is in the enzyme hexosaminidase A, which leads to the accumulation of GM2 gangliosides in lysosomes.


What is the disease that results from malfunction of lysosomes?

Alzheimer


What part of the cell is defective in pompe's disease and Tay Sachs disease?

Lysosomes


What involved in the digestion of food within the cell?

Lysosomes are the digestive center within a cell.


What organelle does pompe disease affect in cell?

lysosomes


What organelle is involved in programmed cell death?

The organelle involved in programmed cell death is the mitochondria. Mitochondria release proteins that trigger a series of events leading to cell death, known as apoptosis. This process is tightly regulated and necessary for normal cellular development and tissue homeostasis.


Defective in pompe's disease and tay-sachs disease?

Lysosomes are the organelles that become defective in these diseases.


Which organelle is primarily involved in the synthesis of phospholipids and steroids?

Lysosomes


What cellular structures is involved in intracellular digestion Golgi apparatus ribosomes lysosomes?

The main cellular structures involved in intracellular digestion are lysosomes and the Golgi apparatus. Lysosomes contain digestive enzymes that break down complex molecules, while the Golgi apparatus modifies and packages these enzymes for transport to the lysosomes. Ribosomes are responsible for protein synthesis and do not directly participate in intracellular digestion.


What do lysosomes in an animal cell do?

Lysosomes are involved in the breakdown of cell unwanted cell organs and bacteria It's like a "clean up crew"