Mitochondira And Peroxisomes Flashcards
Mitochondria are thought to have originated when _________ was engulfed by a larger ________.
Aerobic prokaryote; anaerobic eukaryote
Mitochondria have their own DNA and ribosomes. T/F
True
Number of mitochondria are the same throughout all cells. T/F
False
Number of mitochondria matches the cells requirement to energy
Why do cardiac muscles have lots of mitochondria?
To supply ATP for actin-myosin contraction
Kidney cells have mitochondria in order to
Provide energy to move water from the lumen to the tubule to the underlying blood capillaries
How many membranes to mitochondria have?
2
Transmembrane Proteins on the outer membrane of the mitochondria are called________and they allow small molecules such as ________ to pass from the cytoplasm to the inter membrane space
Porins; pyruvate
The inner membrane of the mitochondria forms folds called
Cristae
The function of cristae on the inner membrane of the mitochondria is to increase the ________
Surface area
Transmembrane proteins on the inner membrane allow the mitochondria to
Carry out oxidation reactions of the ETC
ATP synthase
ADP/ATP carrier
Mitochondrial DNA is different than nucleus DNA in that
Mitochondrial DNA is circular and not packaged by histones
All protein destined for the mitochondria must carry
Mitochondrial targeting sequence
Mitochondrial division is linked to cell division. T/F
False
Mitochondria divide independently
All mitochondria come from which parent
The mother
Mitochondria is not passed from the father because sperm mitochorarra are tagged with
Ubequitin
Mitochondrial diseases tend to affect which part of the body
Brain and muscle
3 parent babies involve having a second mother donate their healthy ________to the first mothers cytoplasm
Mitochondria
The main function of the mitochondria is to produce
ATP
Mitochondria produce ATP through
Oxidative phosphorylation
The cytoplasm uses______ to produce ATP which is _____ process
Glycolysis; anaerobic
Pyruvate and fatty acids in the inner membrane of the inner membrane are converted into
Acetyl CoA
The inner membrane of the mitochondria contains high energy electrons carried by
NADH and FADH2
The main driver of ATP synthase is
H+ (Hydrogen Ion)
The release of which proteins from the mitochondria to the cytosol initiate apoptosis?
Procaspases
Apoptosis initiatermfactor (AIF)
Cytochrome c
Mitochondria of steroid producing cells reveal______ which contain enzymes required for steroidogenesis
Tubular cristae
Mitochondria produces heat (thermogenesis) through the
Oxidation of fat
The main function of peroxisomes is to degrade
Hydrogen peroxide
Peroxisomes do not contain DNA. T/F
True
Peroxisomes are characterized in TEM by
Electron dense inclusions
Enzymes which contribute to peroxisomes function are known as
Peroxins
Peroxisomes targeting signals contain
3 amino acids
Serine lysine leucine
Peroxisomes divide through
Fission
De novo formation
De Novo Formation of peroxisomes involves pre-peroxisome budding off of the _______which contain_______that recognize PTS obtaining peroxins
ER; RECEPTORS
Peroxisomes breakdown very long fatty acid chains (VLCFA’s) through
Beta oxidation
What is the main difference between Beta oxidation in mitochondria and peroxisomes
Peroxisome oxidation are not coupled to ATP synthase
Peroxidases such ______break down h2o2 to water and oxygen
Catalase
Peroxisomes in liver cells participate in the synthesis of
Bile acids
Bile acids are made from
Cholesterol
Where are bile acids made ?
Peroxisomes
H2O2 of the peroxisome is used to convert cholesterol into
Bile acids
Peroxisomes are numerous in the liver and kidney since they rid the body of
Toxic substances (detoxification)
Myelin is a mixture of
Proteins and phospholipids
Peroxisome participate in the synthesis of phospholipids known as_____which contribute to the smooth endoplasmic reticulum
Plasmalogens
Adrenoleukodystrophy (ALD) refers to
The breakdown of myelin in the adrenal glands
ALD is directly correlated to a________which results in an accumulation of very long fatty acid chains in tissues throughout the body
Disorder of Peroxisome fatty acid beta oxidation
Zellweger sydrome Is a result of the reduction or absence of
Peroxisomes
The Zellweger syndrome is when patients are defective in either
Importing proteins into peroxisomes
‘Empty’ peroxisomes