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Lesson One£¨4ѧʱ£©
Inside the Living Cell: Structure and Function of Internal Cell Parts
: The Dynamic, Mobile Factory ϸ°ûÖÊ£º¶¯Á¦¹¤³§
Most of the properties we associate with life are properties of the cytoplasm. Much of the mass of a cell consists of this semifluid substance, which is bounded on the outside by the plasma membrane. Organelles are suspended within it, supported by the filamentous network of the cytoskeleton. Dissolved in the cytoplasmic fluid are nutrients, ions, soluble proteins, and other materials needed for cell functioning.
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The eukaryotic cell nucleus is the largest organelle and houses the genetic material (DNA) on chromosomes. (In prokaryotes the hereditary material is found in the nucleoid.) The nucleus also contains one or two organelles-the nucleoli-that play a role in cell division. A pore-perforated sac called the nuclear envelope separates the nucleus and its contents from the cytoplasm. Small molecules can pass through the nuclear envelope, but larger molecules such as mRNA and ribosomes must enter and exit via the pores.
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: Specialized Work Units£¨Ï¸°ûÆ÷£ºÌØÊâµÄ¹¦Äܵ¥Î»£©
All eukaryotic cells contain most of the various kinds of organelles, and each organelle performs a specialized function in the cell. Organelles described in this section include ribosomes, the endoplasmic reticulum, the Golgi complex, vacuoles, lysosomes, mitochondria, and the plastids of plant cells.
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The number of ribosomes within a cell may range from a few hundred to many thousands. This quantity reflects the fact that, ribosomes are the sites at which amino acids are assembled into proteins for export or for use in cell processes. A complete ribosome is composed of one larger and one smaller subunit. During protein synthesis the two subunits move along a strand of mRNA, \the genetic sequence coded in it and translating that sequence into protein. Several ribosomes may become attached to a single mRNA strand; such a combination is called a polysome. Most cellular proteins are manufactured on ribosomes in the cytoplasm. Exportable proteins and membrane proteins are usually made in association with the endoplasmic reticulum.
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The endoplasmic reticulum, a lacy array of membranous sacs, tubules, and vesicles, may be either rough (RER) or smooth (SER). Both types play roles in the synthesis and transport of proteins. The RER, which is studded with polysomes, also seems to be the source of the nuclear envelope after a cell divides.
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SER lacks polysomes; it is active in the synthesis of fats and steroids and in the oxidation of toxic substances in the cell. Both types of endoplasmic reticulum serve as compartments within the cell where specific products can be isolated and subsequently shunted to particular areas in or outside the cell.
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Transport vesicles may carry exportable molecules from the endoplasmic reticulum to another membranous organelle, the Golgi complex. Within the Golgi complex molecules are modified and packaged for export out of the cell or for delivery else where in the cytoplasm.
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Vacuoles in cells appear to be hollow sacs but are actually filled with fluid and soluble molecules. The most prominent vacuoles appear in plant cells and serve as water reservoirs and storage sites for sugars and other molecules. Vacuoles in animal cells carry out phagocytosis (the intake of particulate matter) and pinocytosis (vacuolar drinking).
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A subset of vacuoles are the organelles known as lysosomes, which contain digestive enzymes (packaged in lysosomes in the Golgi complex) that can break down most biological macromolecules. They act to digest food particles and to degrade damaged cell parts.
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Mitochondria are the sites of energy-yielding chemical reactions in all cells. In addition, plant cells contain plastids that utilize light energy to manufacture carbohydrates in the process of photosynthesis. It is on the large surface area provided by the inner cristae of mitochondria that ATP-generating enzymes are located. Mitochondria are self-replicating, and probably they are the evolutionary descendants of what were once free-living prokaryotes.
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There are two types of plastids: leucoplasts, which lack pigments and serve as storage sites for starch, proteins, and oils; and chromoplasts, which contain pigments. The most important chromoplasts are chloroplasts-organelles that contain the chlorophyll used in photosynthesis. The internal structure of chloroplasts includes stacks of membranes called grana, which are embedded in a matrix called the stroma.
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All eukaryotic cells have a cytoskeleton, which is a convoluted latticework of filaments and tubules that appears to fill all available space in the cell and provides support for various other organelles. A large portion of the cytoskeleton consists of threadlike microfilaments composed mainly of the contractile protein actin. They are involved in many types of intracellular movements in plant and animal cells. A second protein, myosin, is involve in the contraction of muscle cells. Another main structural component of the cytoskeleton consists of microtubules, which are composed of the globular protein tubulin and together act as scaffolding that provides a stable cell shape. Cytoskeletal intermediate filaments appear to impart tensile strength to the cell cytoplasm. Mechanoenzymes such as myosin, dynein, and kinesin interact with the cytoskeletal filaments and tubules to generate forces that cause movements.
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Although the cytoskeleton provides some stabilityÎÈ¹Ì to cells, its microtubules
Ó¢[?maikr?u?tju:bju:l] and filaments ˿״Îï and their associated proteins enable cells to move by creeping ÅÀÐÐ or gliding »¬¶¯. Such movements require a solid¹ÌÌåµÄ substrate to which the cell can adhere¸½×Å and can be guided by the geometry d?i??mitri] ¼¸ºÎÐÎ×´of the surface. Some cells also exhibit [i¨À?zibit] Õ¹ÀÀ chemotaxis, kem??t?ksisÇ÷Ò©ÐÔ the ability to move toward or away from the source of a diffusing À©É¢ chemical.
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Certain eukaryotic cells can swim freely in liquid environments, propelled by whiplike cilia [?sili?]ÏËëor flagellaÓ¢[fl??d?el?±Þë. Both cilia and flagella have the same internal structure: nine doublets (pairs of microtubules) are arranged in a ring and extend the length of the cilium or flagellum, and two more microtubules run down the center of the ring. Every cilium or flagellum grows only from the cell surface where a basal body»ùÌåis located. Movement is based on the activities of tiny dynein¶¯Á¦µ°°× side arms that extend from one of the microtubules of each doublet³É¶ÔµÄ¶«Î÷.
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Lesson Two£¨2ѧʱ£©
Photosynthesis
Photosynthesis occurs only in the chlorophyllchlorophyllÒ¶ÂÌËØ-containing cells of green plants, algaeÔå, and certain protists ÔÉúÉúÎïand bacteria. Overall, it is a process that converts light energy into chemical energy that is stored in the molecular bonds. From the point of view of chemistry and energetics, it is the opposite of cellular respiration. Whereas È»¶ø cellularϸ°ûµÄ respiration ºôÎüis highly exergonicÎüÊÕÄÜÁ¿µÄ and releases energy, photosynthesis¹âºÏ×÷Óà requires energy and is highly endergonic.
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Photosynthesis starts with CO2 and H2O as raw materials and proceeds through two sets of partial reactions. In the first set, called the light-dependent reactions, water molecules are splitÁÑ¿ª (oxidized), 02 is released, and ATP and NADPH are formed. These reactions must take place in the presence of ÔÚÃæÇ° light energy. In the second set, called light-independent reactions, CO2 is reduced (via the addition of H atoms) to carbohydrate. These chemical events rely on the electron carrier NADPH and ATP generated by the first set of reactions.
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Both sets of reactions take place in chloroplasts. Most of the enzymes and pigments É«ËØfor the lightdependent reactions are embedded ÉîÈëµÄ ÄÚº¬µÄin the thylakoidÀàÄÒÌå membraneĤ ¸ôĤ of chloroplasts Ò¶ÂÌÌå. The dark reactions take place in the stroma.»ùÖÊ
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The energy in light photons in the visible part of the spectrum can be captured by biological molecules to do constructive work. The pigment chlorophyll in plant cells absorbs photons within a particular absorption spectrums statement of the amount of light absorbed by chlorophyll at different wavelengths. When light is absorbed it alters the arrangement of electrons in the absorbing molecule. The added energy of the photon boosts the energy condition of the molecule from a stable state to a less-stable excited state. During the light-dependent reactions of photosynthesis, as the absorbing molecule returns to the ground state, the \energy.
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All photosynthetic organisms contain various classes of chlorophylls and one or more carotenoid (accessory) pigments that also contribute to photosynthesis. Groups of pigment molecules called antenna complexes are present on thylakoids. Light striking any one of the pigment molecules is funneled to a special chlorophyll a molecule, termed a reaction-center chlorophyll, which directly participates in photosynthesis. Most photosynthetic organisms possess two types of reaction-center chlorophylls, P680 and P700, each associated with an electron acceptor molecule and an electron donor. These aggregations are known respectively as photosystem ¢ñ (P700) and photosystem ¢ò (P680).
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The Light-Dependent Reaction: Converting Solar Energy into Chemical-Bond Energy ¹â·´Ó¦£º¹âÄÜת»¯³É»¯Ñ§¼üÄÜ
The photosystems of the light-dependent reactions are responsible for the packaging of light energy in the chemical compounds ATP and NADPH. This packaging takes place through a series of oxidation reduction reactions set in motion when light strikes the P680 reaction center in photosystem ¢ò. In this initial event water molecules are cleaved, oxygen is released, and electrons are donated. These electrons are accepted first by plastoquinone and then by a series of carriers as they descend an electron transport chain. For each four electrons that pass down the chain, two ATPs are formed. The last acceptor in the chain is the P700 reaction center of photosystem ¢ñ. At this point incoming photons boost the energy of the electrons, and they are accepted by ferredoxin. Ferredoxin is then reoxidized, and the coenzyme NADP+ is reduced to the NADPH. The ATP generated previously and the NADPH then take part in the light independent reactions.
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