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ENDO MEANS?
INSIDE
LYSO MEAN?
TO BREAK AKA “LYSIS”
lysosomes contain
enzymes that break things
there are both
early and late endosomes
endosomes can be
stable
transiental
a stable endosome mean?
structure does not change into anything
transient endosome means
it becomes something
both stable and transient endosomes are apart of
endocytic pathways (moving macromolecules within the cell)
early endosomes
sort proteins and recycle proteins
late endosomes
(will become lysosomes)
**final product of late endosomes*
lysosomes
rich in hydrolytic enzymes for intracellular digestion
lysosomes are most active in
leukocytes and phagocytes
hydrolytic is what?
uses water to break down molecules
leukocytes
white blood cells
lysosomes have…
unique membrane that is resistant to its own enzymes since the membrane is making some outside
(if it were to digest its own it would break)
lysosomes in lysosomal storage disease is
tay sacs disease
tay sac disease
there is a great accumulation lipids because the enzymes are not able to break them because they are defective.
rough endoplasmic reticulum
has basophilic bodies (takes basic dyes & attracted to acid molecules)
the RER basophilic bodies are called
ribosomes
rer is composed of
flattened sacs
continuous (attached to outer membrane of nuclear envelope)
rer function
protein synthesis and transportation to golgi complex
smoother er is
not rough
no ribosomes
tubular
form piplines
smooth er is mostly developed in
skeletal muscel
kidney tubules
steroid producing endocrine cells
when smooth er is homgenized it will break into
microsomes (smooth vesicles)
rough vesicles
smoother er has various functions
synthesis of different lipids
oils
phospholipids
steroids
detoxification and bioactivation (from inactive to active) of organic compounds
carbohydrate metabolism
membrane formation and recycling
sequesters and releases calcium in muscles
golgi appartus or complex function?
concentration site
modification
packaging and shipping if synthesized products
mitochondria
finger like organelles
powerhouse of the cell
double membraned
from cristae
has a HUGE amount of cells that generate ATP
what are the 3 main reaction cycles dealing with mitochondria
krebs cycle (reduced power in the cell)
B-oxidation of fatty acids
Electron transport chain
what reaction cycles are in the matrix of the mitochondria
krebs
b-oxidation of fatty acids
where is the electron transport chain located
in the membranes
mitocondria is
semiautonomous
this is due to it self duplicating and having its own DNA & Ribosomes
Peroxisomes
has single membrane with oxidative enzymes
peroxide reactions happen
what are the names of the oxidative enzymes in peroxisomes
urate oxidase
b-amino oxidase
catalase
(all 3 make peroxide)
nonfunctional peroxisomes cause
Zellweger syndrome
they simply dont work (early death is the outcome)