13.3 Peroxisomes Flashcards
() are single-membrane organelles containing enzymes involved in many metabolic reactions
peroxisomes
what are the functions of peroxisomes
- oxidation of fatty acids
- lipid synthesis (in animal cells)
- carbohydrate synthesis
oxidative reactions in peroxisomes lead to the production of ()
hydrogen peroxide
oxidative reactions in peroxisome are efficient and effective due to the presence of (), which is an enzyme that converts hydrogen peroxide to water or uses it to oxidize another organic compound
catalase
in animal cells, fatty acids are oxidized both in peroxisomes and mitochondria; but in yeast and plant cells, this only occurs in ()
peroxisomes
what are the lipids synthesized in peroxisomes
- cholesterol
- dolichol
() are a family of phospholipids synthesized in peroxisomes that are important membrane components in tissues like the heart and brain; one of the hydrocarbon chains is joined to glycerol by an ether bond
plasmalogens
peroxisomes in seeds are responsible for the conversion of (), this aids in growth of plant tissue from seeds
stored fatty acids to carbohydrates
peroxisomes in leaves function in coordination with chloroplasts to metabolize a side product of the Calvin cycle that allowed for the () during photosynthesis
conversion of CO2 to carbohydrates
peroxisome assembly is mediated by the intersection of ()
proteins synthesized by free ribosomes and proteins transported to peroxisomes from the ER
() are transmembrane proteins invovled in peroxisome assembly
peroxins/Pex proteins
some peroxins form () through which internal (matrix) peroxisome proteins are imported
membrane channels
() are conditions that result from the mutations in the genes that code for peroxins → lead to defective peroxisome assembly
peroxisome biogenesis disorders
peroxins are exported from a specialized region in the ER called the ()
peroxisomal ER
what makes the vesicles budding off from the peroxisomal ER unique?
- they do not have a COPII coat; formation may be driven by peroxins
- instead of going to the Golgi, they may fuse to form peroxisomes into which matrix proteins can be imported
passage of large proteins and complexes into peroxisome lumen are mediated by ()
protein translocation
targeting of peroxisome matrix proteins can be done through 2 pathways (conserved from yeasts to humans), presence of either:
- PTS1 (peroxisome targeting signal 1)
- PTS2 (peroxisome targeting signal 2)
describe PTS1 and its cytosolic receptor
- simple amino acid sequence Ser-Lys-Leu at the C-terminus of a polypeptide
- recognized by Pex5
describe PTS2 and its cytosolic receptor
- a sequence of 9 amino acids at the N-terminus of a polypeptide
- recognized by Pex7
describe the mechanism for importing proteins with PTS1
- the Pex5/cargo complex binds to a docking complex (consisting of Pex13, Pex14, and Pex17) on the peroxisome membrane
- Pex5 and Pex14 then form a pore in the membrane through which the cargo is translocated into the peroxisome
- Pex5 is then recycled into the cytosol
formation of peroxisomes is done in response to the cell’s metabolic needs and can be done by either:
- formation by vesicle budding from ER, followed by import of peroxisomal matrix proteins
- de novo formation yields peroxisomes with entirely new contents
- growth and division of existing peroxisomes
- new peroxisomes are formed more rapidly by this division of old ones