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English: A simple diagram of a plant leaf cell, labelled with numbers. It shows the cytoplasm, nucleus, cell membrane, cell wall, mitochondria, permanent vacuole, and chloroplasts. Note going down the left the numbers are not sequential, this is to match the numbering on others in the series. Cytoplasm; Nucleus; Cell membrane; Mitochondrion ...
Nick Lane and William Martin have argued that mitochondria came first, on the grounds that energy had been the limiting factor on the size of the prokaryotic cell. [17] The phagotrophic model presupposes the ability to engulf food, enabling the cell to engulf the aerobic bacterium that became the mitochondrion. [12]
Mutually, post-translational alterations of mitochondrial apparatus and the development of transmembrane contact sites among mitochondria and other structures, which both have the potential to link signals from diverse routes that affect mitochondrial membrane dynamics substantially, [36] Mitochondria are wrapped by two membranes: an inner ...
In practice the efficiency may be even lower because the inner membrane of the mitochondria is slightly leaky to protons. [11] Other factors may also dissipate the proton gradient creating an apparently leaky mitochondria. An uncoupling protein known as thermogenin is expressed in some cell types and is a channel that can transport protons.
Mitochondrial dynamics in different cells are understood by the way in which these proteins regulate and bind to each other. [2] These GTPases in control of mitochondrial fusion are well conserved between mammals, flies, and yeast. Mitochondrial fusion mediators differ between the outer and inner membranes of the mitochondria.
To begin the process, mitochondria must first be separated from cultured cells. This is typically a two step process using homogenization to release the intercellular contents and differential centrifugation to separate the mitochondria from other organelles. Once the mitochondria are isolated, mitoplasts can then be formed.
Illustration of the malate–aspartate shuttle pathway. The malate–aspartate shuttle (sometimes simply the malate shuttle) is a biochemical system for translocating electrons produced during glycolysis across the semipermeable inner membrane of the mitochondrion for oxidative phosphorylation in eukaryotes.
The glycerol phosphate shuttle was first characterized as a major route of mitochondrial hydride transport in the flight muscles of blow flies. [5] [6] It was initially believed that the system would be inactive in mammals due to the predominance of lactate dehydrogenase activity over glycerol-3-phosphate dehydrogenase 1 (GPD1) [5] [7] until high GPD1 and GPD2 activity were demonstrated in ...