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metabolism, there is a fundamental distinction between catabolism and anabolism. Catabolism is the degradation of organic matter (mostly polysaccharides, protein, and lipids) in order to provide chemical bonding energy through oxidation, which can be transferred to ATP. Polysaccharides are degraded to simple sugars such as glucose. Anabolism is the biosynthesis of monomers (e.g. amino acids, organic acids, and fatty acids) required for macromolecules and of macromolecules and other cell building blocks. Many catabolic and anabolic pathways involve the cytosol, but other compartments may also be involved (Figure 3.22).
Figure 3.22 Synopsis of the breakdown pathways and energy‐producing pathways in heterotrophic organisms (e.g. in humans).
The degradation of glucose to pyruvate is an important energy‐producing process. On balance, glycolysis produces 8 mol ATP per 1 mol glucose (2 mol NADH and 2 mol ATP). Pyruvate is transported into the mitochondria where it is transformed into acetyl CoA while producing NADH. In the mitochondria, acetyl CoA is further processed in the citric acid cycle, using up O2 and releasing CO2 and H2O (Figure 3.15). What matters for the energy balance is the provision of 4 mol NADH, 1 mol FADH2, and 1 mol GTP from 1 mol pyruvate. In the respiratory chain, they produce 12 mol ATP per mol acetyl CoA and 15 mol per 1 mol pyruvate. One mole of glucose, when completely oxidized, produces 38 mol ATP.
Lipids are hydrolyzed into fatty acids by lipases. Fatty acids are particularly rich in energy. During β‐oxidation, they are broken down into acetyl CoA in the mitochondria to provide NADH and FADH2. One mole of stearic acid yields 9 mol NADH, FADH2, and acetyl CoA, which is then further oxidized in the citric acid cycle. The total balance amounts to 9 × 5 + 9 × 12 = 153 mol ATP.
Proteins are broken down by proteases (pepsin, trypsin, and chymotrypsin) into amino acids. These can be entered into the degradation pathways at various stages, thus also producing ATP.
The synthetic pathways of the various low‐molecular‐weight building blocks are complex. They can often be derived from precursors in glycolysis or the citric acid cycle (Figure 3.23). In cell biology, physiology, medicine, and biotechnology, it is important to have a good understanding of these various pathways. This introduction can only scratch the surface, and readers should deepen their knowledge in the relevant textbooks.
Figure 3.23 Importance of glycolysis and the citric acid cycle as a point of departure for diverse biosynthetic pathways. IPP, isopentenyl pyrophosphate; DMAP, dimethylallyl pyrophosphate.
3.1.5 Cytoskeleton
The cytoplasm is by no means an unstructured, soup‐like fluid. It contains a complex network of thread‐shaped proteins, which are part of the cytoskeleton. These networks that can be made visible using antibodies coupled to a fluorescent dye or by electron microscopy. Also cell lines exist, which express tubulin or actin coupled to green fluorescent protein (GFP); thus the dynamics of the cytoskeleton can be directly studied under a fluorescence microscope (Chapter 19). The structural proteins are often connected to the cytoplasmic membrane or cellular organelles:
Actin filaments
Intermediary filaments
Microtubules
The most subtle filaments are the actin filaments (F actin) (Figure 3.24), consisting of G actin monomers. Actin filaments have a plus and a minus end. ATP favors the elongation of actin chains. Actin filaments are interconnected by a multitude of connecting and anchoring proteins. They are also in close contact with various membranes. When the cell crawls, they form lamellipodia and filopodia; strings of actin support these structures. The interaction of cytoskeletal proteins is particularly complex in muscle cells. The best studied cells are striated muscle cells. A single muscle fiber that has merged from several cells, thus containing several nuclei, contains many myofibrils. In these myofibrils, actin and myosin filaments cooperate, forming a highly organized nanomachine. Any contraction of a muscle is the result of highly coordinated interaction between actin filaments and myosin (Figure 3.25).
Figure 3.24 Schematic composition of actin filaments (microfilaments).
Figure 3.25 Mechanism of muscle contraction. (a) Molecular mechanism of muscle contraction.
Source: Voet et al. (2016). Adapted with permission of John Wiley and Sons.
(b) Contraction of myofibrils; the thin filaments are actin filaments, the thick filaments consist of myosin.
Source: Courtesy of Hugh Huxley, Brandeis University.
The thickness of intermediary filaments lies in the middle between actin filaments and microtubules. Their main task is to stabilize the cell. The filaments are interconnected with many other proteins to create complex networks that are firmly anchored to the cytoplasmic membrane.
The thickest filament in the cytoskeleton are the microtubules, which form hollow tube systems and may be looked at as polymers of tubulin dimers (α‐ and β‐tubulin) (Figure 3.26). Microtubules have a plus and a minus end. GTP favors the growth of microtubules; GDP lets it shrink. Microtubules play a special part in the intracellular transport of vesicles. During cell division, they form the spindle apparatus that transfers chromosomes into the daughter cells. During the metaphase, the condensed chromosomes line up along the equatorial plate of the cell (Figure 4.7). The microtubules bind to the centromeres of the chromatids (Figure 4.4) and pull them into the new daughter cells. The microtubules extend from polar‐bound centrioles.
Figure 3.26 Schematic view of microtubules and cilia structures. Tubulin dimers bind to GTP and then polymerize to form protofilaments. Thirteen protofilaments are required to form a microtubule. Cilia and flagella are composed of 9 + 2 microtubules.
Flagella