Protease, for one.
Because the organs are layered with mucus.
The lysosomal membrane is protected from the lysosomal enzymes due to the presence of a protective glycoprotein layer on its surface. This layer acts as a shield, preventing the enzymes from damaging the membrane and leaking out into the cytoplasm. Additionally, the low pH inside the lysosome helps to keep the enzymes inactive until they are needed for breaking down cellular materials.
extra cellular digestion takes place by lysosomal enzymes.when there is no lysosomal enzyme then extra cellular digestion cannot tak place.
Yes, where? The first R in 'RER' stands for rough as in 'rough endoplasmic reticulum'. Compare this to 'SER' - smooth endoplasmic reticulum. Yes, the rough designation reflects the existence of endoplasmic bound ribosome entities/particles that are the main sites of cellular protein synthesis.
Autolysis is caused by enzymes known as autolytic enzymes, such as lysosomal enzymes, that break down cellular components. These enzymes are released when cells are damaged or die, leading to the breakdown of cell membranes and organelles.
Hydrocortisone stabilizes lysosomal membranes by reducing the release of enzymes that can damage the lysosomal membrane. It also helps to decrease inflammation and limit the immune response that can contribute to lysosomal membrane damage. Overall, hydrocortisone's anti-inflammatory properties help to protect the lysosomal membrane and maintain its integrity.
The MPS disorders are caused by absent or insufficient production of proteins known as lysosomal enzymes The specific enzyme that is deficient or absent distinguishes one type of MPS from another
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.
monocytes. WRONG.Neutrophils, also called polymorphonuclear leukocytes, phagocytize bacteria with lysosomal enzymes.
RNA polymerase
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A major fat digesting enzyme is called pancreatic lipase. This enzyme is produced in the pancreas and is responsible for breaking down fats into smaller molecules like fatty acids and glycerol, which can then be absorbed by the body.