Chapter 7. Energy Generation in Mitochondria and Chloroplasts. (1) Mitochondria: in all eukaryotic cells The relationship between the structure and function of mit. (2) Chloroplasts: in plant cells The relationship between the structure and function of chl.
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Energy Generation in Mitochondria and Chloroplasts
(1) Mitochondria: in all eukaryotic cells
The relationship between the structure and function of mit.
(2) Chloroplasts: in plant cells
The relationship between the structure and function of chl.
Mit: Oxidative phosphorylation → ATP
Chl: Photosynthesis → ATP + NADPH → Sugar
1. Mitochondria and oxidative phosphorylation
A. Mitochondrial structure and function
Figure7-4Relationship between mitochondria and microtubules.
Figure7-3Mitochondrial plasticity.Rapid changes of shape are observed when a mitochondrion is visualized in a living cell.
Figure7-5Localization of mitochondria near sites of high ATP utilization in cardiac muscle and a sperm tail.
Outer membrane the matrix and intermembrane space.:
Contains channel-forming protein, called Porin. Permeable to all molecules of 5000 daltons or less.
Inner membrane (Impermeability):
Contains proteins with three types of functions:
(1) Electron-transport chain: Carry out oxidation reactions; (2) ATP synthase: Makes ATP in the matrix; (3) Transport proteins: Allow the passage of metabolites
Contains several enzymes use ATP to phosphorylate other nucleotides.
Matrix: Enzymes; Mit DNA, Ribosomes, etc.
B. Specific functions localized within the Mit by disruption of the organelle and fractionation
Figure14-6Fractionation of purified mitochondria into separate components.These techniques have made it possible to study the different proteins in each mitochondrial compartment. The method shown, which allows the processing of large numbers of mitochondria at the same time, takes advantage of the fact that in media of low osmotic strength water flows into mitochondria and greatly expands the matrix space (yellow). While the cristae of the inner membrane allow it to unfold to accommodate the expansion, the outer membranewhich has no folds to begin withbreaks, releasing a structure composed of only the inner membrane and the matrix.
Inner membrane: of the organelle and fractionation
Localization of metabolic functions within the mitochondrion
fatty acid desaturation
Fatty acid elongation
ß oxidation of fats
DNA replication, RNA transcription,
A. Molecular basis of oxidation: Electron- of the organelle and fractionation
B. Molecular basis of phosphorylation:
F1 particle is the catalytic subunit;
The F0 particle attaches to F1 and is embedded in the inner membrane.
F1: 5 subunits in the ratio 3:3:1:1:1
Boyer proposed in 1979, and was greatly stimulated by the publication in 1994 of the structure for F1 complex (X-ray) from bovine heart mitochondria
Japan researcher, Nature 386: 300, 1997.
addition to ATP synthase
C. Mithchell’s Chemiosmotic theory (1961)
More than 21026 molecules (>160kg) of ATP per day in our bodies.
Electrons pass from NADH or FADH protons links oxidation to phosphorylation.2 to O2, the terminal electron acceptor, through a chain of carriers in the inner membrane (FMN, Fe-S center, Heme group Fe, CoQ);
As electrons move through the electron-transport chain, H+ are pumped out across the inner membrane, and form Proton motive force;
Electrons move through the inner membrane via a series of carriers of decreasing redox potential
Figure protons links oxidation to phosphorylation.7-26An experiment demonstrating that the ATP synthase is driven by proton flow.By combining a light-driven bacterial proton pump (bacteriorhodopsin), an ATP synthase purified from ox heart mitochondria, and phospholipids, vesicles were produced that synthesized ATP in response to light.
If not all the detergent is removed, what will happen?
FADH2 O2 : 2ATP/2e
in a mitochondrion生物氧化产生ATP的统计 一个葡萄糖分子经过细胞呼吸全过程产生多少ATP？ 糖酵解：底物水平磷酸化产生 4 ATP（细胞质） 己糖分子活化消耗 2 ATP（细胞质） 产生 2NADH，经电子传递产生 4或 6 ATP （线粒体）净积累 6或8 ATP丙酮酸氧化脱羧：产生 2NADH（线粒体），生成 6ATP三羧酸循环：底物水平的磷酸化产生（线粒体）2ATP；产生 6NADH（线粒体），生成18ATP；产生 2FADH2（线粒体），生成 4 ATP总计生成 36或38 ATP
A. Comparison of a mitochondrion and a chloroplast.
Figure in a mitochondrion14-39The chloroplast.This photosynthetic organelle contains three distinct membranes (the outer membrane, the inner membrane, and the thylakoid membrane) that define three separate internal compartments (the intermembrane space, the stroma, and the thylakoid space). The thylakoid membrane contains all of the energy-generating systems of the chloroplast. In electron micrographs this membrane appears to be broken up into separate units that enclose individual flattened vesicles (see Figure 14-40), but these are probably joined into a single, highly folded membrane in each chloroplast. As indicated, the individual thylakoids are interconnected, and they tend to stack to form aggregates called grana.
(A) A wheat leaf cell in which a thin rim of cytoplasm containing chloroplasts surrounds a large vacuole. (B) A thin section of a single chloroplast, showing the starch granules and lipid droplets that have accumulated in the stroma as a result of the biosyntheses occurring there. (C) A high-magnification view of a granum, showing its stacked thylakoid membrane. (Courtesy of K. Plaskitt.)
Figure containing chloroplasts surrounds a large vacuole. (B) A thin section of a single chloroplast, showing the starch granules and lipid droplets that have accumulated in the stroma as a result of the biosyntheses occurring there. (C) A high-magnification view of a granum, showing its stacked thylakoid membrane. (Courtesy of K. Plaskitt.) 7-42Photosynthesis in a chloroplast.Water is oxidized and oxygen is released in the photosynthetic electron-transfer reactions, while carbon dioxide is assimilated (fixed) to produce carbohydrate in the carbon-fixation reactions.
B. Photosynthesis containing chloroplasts surrounds a large vacuole. (B) A thin section of a single chloroplast, showing the starch granules and lipid droplets that have accumulated in the stroma as a result of the biosyntheses occurring there. (C) A high-magnification view of a granum, showing its stacked thylakoid membrane. (Courtesy of K. Plaskitt.)
Light-dependent reaction: Electron transport in the thylakoid membrane and noncyclic photophosphorylation:
Cyclic thylakoid membrane and noncyclic photophosphorylationphotophosphorylation:
Changes in redox potential during photosynthesis. thylakoid membrane and noncyclic photophosphorylation
Figure C3 plants (Calvin cycle)14-43The initial reaction in carbon fixation.This reaction, in which carbon dioxide is converted into organic carbon, is catalyzed in the chloroplast stroma by the abundant enzyme ribulose bisphosphate carboxylase. The product, 3-phosphoglycerate, is also an important intermediate in glycolysis: the two carbon atoms shaded in blue are used to produce phosphoglycolate when the enzyme adds oxygen instead of CO2。
The structure and function in C4 plants C3 plants (Calvin cycle)
A. Organelle DNA
Products of mt genes are not exported
The organization of the liverwort proteins(地钱)Chl genome
Mit and Chl are organelles semiautocephaly.
The synthesis of mt proteins is coordinated
C. The transport protein into Mit. And Chl.
N-terminal signal sequence is recognized by receptors of TOM; The protein is translocated across both Mit membranes at or near special contact sites.
Translocation into thylakoid space or thylakoid M can occur by any one of at least four routes.
5. Thylakoid membrane in Chl.The proliferation and origin of Mit and Chl.
A.Organelle growth and division determine the number of Mitochondria and Plastids in a cell
B. Origin: The endosymbiont theory Thylakoid membrane in Chl.
Suggested evolutionary pathway for the origin of Mit. Thylakoid membrane in Chl.