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How did the peroxisome get its name?

How did the peroxisome get its name?

The peroxisome derives its name from the fact that many metabolic enzymes that generate hydrogen peroxide as a by-product are sequestered here because peroxides are toxic to cells. Within peroxisomes, hydrogen peroxide is degraded by the enzyme, catalase, to water and oxygen.

How was peroxisome discovered?

Peroxisomes (originally called microbodies) were discovered in 1954 using electron microscopy in mouse kidney (Rhodin 1954), 4 years before the first issue of this Journal (which in 1995 became Histochemistry and Cell Biology) was published.

Who discovered peroxisomes and Glyoxysomes?

They were reported in plants by Porter and Caulfield in 1958 (3) and by Mollenhauer et al. in 1966 (4). Microbodies are now recognized as ubiquitous subcellular respiratory organelles in eukaryotic cells.

What is the peroxisome?

Peroxisomes are small, membrane-enclosed organelles (Figure 10.24) that contain enzymes involved in a variety of metabolic reactions, including several aspects of energy metabolism.

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Who first discovered peroxisome?

Christian de Duve
Christian de Duve: Explorer of the cell who discovered new organelles by using a centrifuge. Christian de Duve, whose laboratory in Louvain discovered lysosomes in 1955 and defined peroxisomes in 1965, died at his home in Nethen, Belgium at the age of 95, on May 4, 2013.

Who first discovered chloroplast?

Discovery. The first definitive description of a chloroplast (Chlorophyllkörnen, “grain of chlorophyll”) was given by Hugo von Mohl in 1837 as discrete bodies within the green plant cell.

Why do peroxisomes produce hydrogen peroxide?

Peroxisomes contain enzymes that oxidize certain molecules normally found in the cell, notably fatty acids and amino acids. Those oxidation reactions produce hydrogen peroxide, which is the basis of the name peroxisome. In that way peroxisomes provide a safe location for the oxidative metabolism of certain molecules.

What do peroxisomes mean?

Definition of peroxisome : a cytoplasmic cell organelle containing enzymes (such as catalase) which act in oxidative reactions and especially in the production and decomposition of hydrogen peroxide.

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What is peroxisome made of?

Peroxisome Structure Peroxisomes vary in shape, size and number depending upon the energy requirements of the cell. These are made of a phospholipid bilayer with many membrane-bound proteins. The enzymes involved in lipid metabolism are synthesised on free ribosomes and selectively imported to peroxisomes.

Why is the peroxisome important?

Peroxisomes are indispensable for human health and development. They represent ubiquitous subcellular organelles which compartmentalize enzymes responsible for several crucial metabolic processes such as β-oxidation of specific fatty acids, biosynthesis of ether phospholipids and metabolism of reactive oxygen species.

Why is hydrogen peroxide called a peroxisome?

Those oxidation reactions produce hydrogen peroxide, which is the basis of the name peroxisome. However, hydrogen peroxide is potentially toxic to the cell, because it has the ability to react with many other molecules. Therefore, peroxisomes also contain enzymes such as catalase that convert hydrogen peroxide to water and oxygen,…

What are the different types of peroxisomes in plants?

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Specialized types of peroxisomes have been identified in plants, among them the glyoxysome, which functions in the conversion of fatty acids to carbohydrates. Peroxisomes contain enzymes that oxidize certain molecules normally found in the cell, notably fatty acids and amino acids.

What is the difference between a peroxisome and a vacuole?

Peroxisome s specialize in metabolically breaking down certain organic molecules and dangerous compounds, such as hydrogen peroxide, that may be produced during some biochemical reactions. Vacuoles are membranous sacs that store many different substances, depending on the organism and its metabolic state.

What is the function of peroxisome in cell membrane?

Peroxisomes are cytoplasmic organelles that play a central role in the catabolism of very-long-chain fatty acids and other compounds through the process of beta-oxidation. They also are critical in the biosynthesis of important cellular membrane constituents (plasmalogens), cholesterol, and bile acids.