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Molecular Biology of the Cell by Bruce Alberts, Alexander Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter by by Bruce Alberts, Alexander Johnson, Julian Lewis, David Morg

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HOW CELLS OBTAIN ENERGY FROM FOOD

73

HEAD POLYMERIZATION (e.g., PROTEINS, FATTY ACIDS)

TAIL POLYMERIZATION (e.g., DNA, RNA, POLYSACCHARIDES)

6 +

7

1

+

7

6

each monomer carries a high-energy

bond that will be used for the

addition of the next monomer

7

each monomer carries

a high-energy bond

for its own addition

7

1

growing polymer, and it must therefore be regenerated each time that a monomer

is added. In this case, each monomer brings with it the reactive bond that will be

used in adding the next monomer in the series. In tail polymerization, the reactive

bond carried by each monomer is instead used immediately for its own addition

(Figure 2–44).

We shall see in later chapters that both of these types of polymerization are

used. The synthesis of polynucleotides and some simple polysaccharides occurs

by tail polymerization, for example, whereas the synthesis MBoC6 m2.68/2.44 of proteins occurs by a

head polymerization process.

Figure 2–44 The orientation of the

active intermediates in the repetitive

condensation reactions that form

biological polymers. The head growth of

polymers is compared with its alternative,

tail growth. As indicated, these two

mechanisms are used to produce different

types of biological macromolecules.

Summary

Living cells need to create and maintain order within themselves to survive and

grow. This is thermodynamically possible only because of a continual input of

energy, part of which must be released from the cells to their environment as heat

that disorders the surroundings. The only chemical reactions possible are those that

increase the total amount of disorder in the universe. The free-energy change for a

reaction, ∆G, measures this disorder, and it must be less than zero for a reaction

to proceed spontaneously. This ∆G depends both on the intrinsic properties of the

reacting molecules and their concentrations, and it can be calculated from these

concentrations if either the equilibrium constant (K) for the reaction or its standard

free-energy change, ∆G°, is known.

The energy needed for life comes ultimately from the electromagnetic radiation

of the sun, which drives the formation of organic molecules in photosynthetic organisms

such as green plants. Animals obtain their energy by eating organic molecules

and oxidizing them in a series of enzyme-catalyzed reactions that are coupled to the

formation of ATP—a common currency of energy in all cells.

To make possible the continual generation of order in cells, energetically favorable

reactions, such as the hydrolysis of ATP, are coupled to energetically unfavorable

reactions. In the biosynthesis of macromolecules, ATP is used to form reactive

phosphorylated intermediates. Because the energetically unfavorable reaction of

biosynthesis now becomes energetically favorable, ATP hydrolysis is said to drive

the reaction. Polymeric molecules such as proteins, nucleic acids, and polysaccharides

are assembled from small activated precursor molecules by repetitive condensation

reactions that are driven in this way. Other reactive molecules, called either

activated carriers or coenzymes, transfer other chemical groups in the course of

biosynthesis: NADPH transfers hydrogen as a proton plus two electrons (a hydride

ion), for example, whereas acetyl CoA transfers an acetyl group.

HOW CELLS OBTAIN ENERGY FROM FOOD

The constant supply of energy that cells need to generate and maintain the biological

order that keeps them alive comes from the chemical-bond energy in food

molecules.

The proteins, lipids, and polysaccharides that make up most of the food we eat

must be broken down into smaller molecules before our cells can use them—either

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