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Peroxisome in Animal Cell

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| Peroxisome in animal cell | Life sciences, HAN university of applied science, Nijmegen, Netherlands | | Mohsen Ghanbari | 30-12-2012 |

Peroxisome in animal cell
Author: Mohsen Ghanbari
Abstract
Peroxisomes have an essential function in cell metabolism. [1] They are small, membrane bounded organelles that have at least fifty different enzymes for several metabolic reactions. [2] Their appearance is like lysosomes; however, their main function is oxidation reactions especially oxidation of hydrogen peroxide and producing oxygen and water. There are diseases related and caused by this organelle that can be classified in three groups. [2] First group is a disorder duo to overall dysfunction of peroxisomes, like zellweger …show more content…

[13] This organelle has the ability of division, proliferation and degradation in response to environment.
There are two types of divisions, constitutive and regulated:
During cell division, mitosis, or when the organelle is old constitutive division of peroxisomes which is for increasing the number or volume of the organelle will happen.
On the other hand when there is an external signal for proliferation of peroxisomes, regulated division will happen which is not connected with mitosis.
Illnesses related to dysfunction of proxisomes in humans
The human peroxisomal disorders are explained as genetic heterogeneous autosomal recessive diseases that are classified in three groups. [13] First one (group A) contain diseases like Zellweger syndrome, infantile Refsum disease and neonatal adrenoleukodystrophy which are characterized by severe neurological and hepatic dysfunction, craniofacial abnormalities and hypotonia, ending to an early death in this disease patients accumulate phytanic acid and very long chain fatty acids in circulation.
The patients in group B, rhizomelic chondrodysplasia punctata, rhizomelia, cataracts, epiphysial calcifications and ichthyosis accumulate higher levels of phytanic acid and in spite of group A, have a normal amount of very long chain fatty acids.
Group C shows a milder symptoms based on the mutated gene that as a result will change the activity or localization of single enzyme.
Disorder

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