Mitochondria Flashcards
Mitochondrion
It is the energy-generating organelle of the cell
ATP production
NADH and flavin adenine dinucleotide ( FADH2), reduced coenzymes, generated by glycolysis, fatty acid metabolism and the tricarboxylic acid (TCA) cycle are oxidised via the electron transport chain to create the proton motor force required by ATP synthetase to make ATP (oxidative phosphorylation)
New Mitochondria
New mitochondria are generated by a division called mitochondrial fission
Mitochondrial fusion
M also have the ability to fuse together, joining membranes and compartments to yield a single larger mitochondrion
Different Mitochondria shapes
The dynamic flux between fusion and fission gives rise to diverse mitochondrial sizes and structures visible when observing mitochondrial morphology.
The difference in shape is due to different M having different functions.
Mitophagy
Old or depolarised/damaged M are removed
Mitochnodrial genome
mtDNA is histone-free, circular, double-stranded DNA molecule with around 16569 base pairs
-They are intronless genes
-It encodes rRNAs, tRNA’s and 13 proteins, these are subunits of the oxidative phosphorylation pathway
-Nuclear genes encode for many proteins required for Mt function such as DNA repair enzymes
Other critical roles of M
-Carbon skeletons
-Calcium buffering
-Nitrogen metabolism
-Programmed cell death
Carbon skeletons
They provide carbon skeletons for biomolecules such as amino acids, glucose and fatty acids
Calcium buffering
-Mitochondria serve as a critical store of intracellular calcium
-Ca enters into the M matrix via the mitochondrial calcium uniporter MCU due to the high electronegative potential of the membrane (-180mV) while its extrusion depends on the NA+/Ca2+ exchanger and H+/Ca2+
Nitrogen metabolism
it occurs via the metabolism of glutamate used in transamination reactions and the glutamine used to shuttle nitrogen around the body as well as the urea cycle
-Iron containing molecules such as heme are also synthesies in the M
Programmed Cell Death
M activate caspases through the release of Cytochrome C and other factors from the intermembrane space when pro-apoptotic stimuli trigger Bcl-2 family members and the permeability transition pore