Metabolism/Citable Version

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Metabolism (from Greek μεταβολισμός "metabolismos") is the biochemical modification of chemical compounds by living organisms and cells. In common usage, the word is sometimes used to refer to the basal metabolic rate, the "set point" that each person has in breaking down food energy and building up their own body. Sometimes, in multicellular creatures like humans, it is also used to refer to the overall ingestion of food and excretion of wastes, and the building up of muscles and the growth of the body. This article describes the actual biology of metabolism at a cellular level, which explains just how those processes are carried out. In human and whole animal terms, metabolism also includes the chemical conversion of specific items other than food that may be ingested, like drugs and poisons (see Drug metabolism).

Metabolism includes: (1) anabolism, in which a cell uses energy and chemical reducing power to construct complex molecules, and perform such life functions as creating cellular structure; and (2) catabolism, in which a cell breaks down complex molecules to yield energy and chemical reducing power. Cell metabolism involves complex sequences of controlled chemical reactions called metabolic pathways. Just as the word metabolism can be used to describe processes in a whole organism, such as a person, the terms "anabolism" and "catabolism" can also be used in this way. For example, anabolic processes include building up muscle and adding body weight, and catabolic processes include loss of muscle mass and body fat.

History

Santorio Santorio (1561-1636) in his steelyard balance, from Ars de statica medecina, first published 1614.

The first controlled experiments on human metabolism were published by Santorio Santorio in 1614 in his book Ars de statica medecina, that made him famous throughout Europe. Santorio described his long series of personal experiments: in which he weighed himself in a chair suspended from a steelyard balance (see image), before and after eating, sleeping, working, sex, fasting, depriving from drinking, and excreting. He found that by far the greatest part of the food he took in was lost from the body through perspiratio insensibilis (insensible perspiration). In medicine and the health sciences today, the term "insensible losses" is still used to refer to the amount of fluid lost from the body through perspiration and processes that (unlike urine or feces) do not yield any obvious portion that can be weighed or measured.


At about the same time, Jan Baptist van Helmont made the first observations regarding photosynthesis, when he discovered that plant growth required (almost) no soil nutrients. In the 18th century, Priestley concluded that green plants use CO2 and release O2. In 1804, Nicolas de Saussure discovered that the increase in carbon content of plants (i.e. plant growth) arises from the fixation of atmospheric CO2.Between 1854 and 1864, Louis Pasteur discovered that glucose fermentation is due to microorganisms, and, in 1897, Eduard Buchner proved that cell-free yeast extracts could also perform these reactions, and so the ability to ferment was not limited to entire living creatures (cells)- but included certain portions of their physical contents. Subsequent investigations showed that (with a few exceptions) all living organisms metabolize glucose using the same mechanism, a biochemical pathway that breaks down sugar.

Overview: Harnessing energy and making chemical bonds

A few of the catabolic pathways in a cell. Proteins are broken down into amino acids, and fats into glycerol and fatty acids. Carbohydrates (mostly sugars and starch) are hydrolyzed into monosacharides like glucose. The mitochondrium (in green) contains the enzymes that catalyze the citric acid cycle and beta-oxidation, as well as the electron transport chain (where respiration occurs). ATP is a high-energy molecule. See text for details

Living things, like all things, obey the laws of thermodynamics. That means that energy and matter cannot be created out of nothing. That means that cool things always get colder and not warmer, and that means each fragment of something is always smaller, not the same size or bigger, than the thing itself. But, unlike inanimate things, cells and tissues are able to harness energy and matter to change in ways that at least give the illusion of defying those laws. A walrus' body is warmer than its icy surroundings. A baby does grow. An amoeba can divide and shortly be two amoebas, each one the same size of the original cell that split. The metabolism of the walrus, the baby, and the amoeba is responsible for all these processes. Of course, rather than defy the laws of physics, the chemical reactions that make up metabolic processes always obey them.

Enzymes present in cells can catalyze a large variety of chemical reactions with exquisite specificity. Sometimes these enzymes are floating free in the cytoplasm of the cell, other times they are bunched together within a compartment of the cell, a special organelle. For example, the mitochondrium of cells contains enzymes for oxidative phosphorylation (a catabolic process). The endoplasmic reticulum of cells contains some of the enzymes used for protein synthesis (an anabolic process).

Often, the chemical reactions needed to synthesize useful cell components need energy. Chemists describe these reactions as involving a positive change in free energy. Such chemical transformations are not spontaneous, but "uphill", requiring more than just the mixing together of the reactants. In these cases, enzymes may couple the "uphill" (non-spontaneous or energy requiring) reaction to a second, steep "downhill" (very spontaneous or energy releasing) reaction, so that the overall process goes on its own, as a spontaneous series of reactions.

ATP:the energy currency of cells

There is one particular energy-producing reaction that is repeatedly used to drive uphill reactions in metabolism. This reaction, hydrolysis of ATP into ADP and a phosphate ion, occurs again and again in many metabolic pathways. The breaking of that phosphate bond in ATP releases energy that can be coupled to drive other reactions. After the bond is broken, the cell has the materials, ADP and the phosphate group, to put the molecule back together, as long as more energy from other sources becomes available. To restore its supply of ATP, the high energy bond must be reformed by coupling to other "downhill" reactions. ATP synthesis from ADP and phosphate is one of the major tasks faced by cells.

ATP is sometimes called "the energy currency" (money) of cells. It is used so widely by living things that organisms can be classified according to just how they derive energy for ATP synthesis. Organisms can be classified as:

Phototrophy

Phototrophic organisms can obtain energy from light. A typical example is provided by the light dependent reactions of photosynthesis: in these reactions, excitation of a photosystem caused by absorption of a light photon markedly lowers its redox potential. Since electron flow tends to occur from low potential species to high potential species, the excited photosystem transfers electrons to higher potential species in an electron transport chain present in the thylakoid membrane. These electrons eventually reduce NADP+ to NADPH. The energy released in the electron transfer steps is used to transport H+ across the thylakoid membrane, thereby creating a proton gradient across the thylakoid membrane. The energy stored in this proton gradient can be used to synthesize ATP from ADP and phosphate anion (see Chemiosmotic hypothesis).

A few of the anabolic pathways in a cell. Glucose can be stored as a glycogen polymer, or synthesized from lower molecular weight precursors. Excess acetyl-CoA can be stored as fatty acids, or converted into ketone bodies.

chemotrophic

Chemotrophic organisms obtain energy from chemical reactions. For example, glucose can be oxidized to pyruvate through glycolysis. This process yields two molecules of ATP for each molecule of glucose, and releases four electrons, which reduce NAD+ to NADH. As the NAD+ molecules are scarce, the electrons present in NADH must be transferred to another molecule in order to regenerate NAD+ and to allow the degradation of more glucose molecules. NADH may donate its electrons to pyruvate (or to a pyruvate derivative), in which case a fermentation is said to occur. Alternatively, the electron acceptor may be a molecule totally unrelated to the metabolic pathway that released the electrons now present in NADH, in which case a respiration is said to occur. In the presence of NAD+, pyruvate dehydrogenase may decarboxylate pyruvate into acetyl-CoA, a pivotal molecule in metabolism. Acetyl-CoA can also be formed through β-oxidation of fatty acids or through the catabolism of amino acids, and is oxidized to CO2 through the Krebs cycle. The Krebs cycle releases eight electrons from each acetyl-CoA molecule, which are used to reduce three NAD+ to three NADH and one FAD to FADH2. The energy released in electron transfer from NADH and FADH2 to oxygen (in aerobic organisms) or other electron acceptor (in organisms that perform anaerobic respiration) may be used to create a proton gradient across a membrane, and to synthesize ATP through dissipation of this gradient (see Chemiosmotic hypothesis).

Reducing Power: obtaining electrons for chemical bonds

Reducing power is an important input into may anabolic pathways, including the Calvin cycle of photosynthesis, biosynthesis of amino acids, and biosynthesis of fatty acids. Reducing power is usually supplied as hydrogen equivalents carried by NADPH. Organisms can be classified according to the primary source of this reducing power as:

organotrophic

These organisms use organic compounds (e.g. glucose) as the primary electron source.

lithotrophic

These organisms use inorganic compounds (e.g. Fe2+) as primary electron source.

Regulation of metabolism in animals

In animals, metabolism is controlled by the endocrine system through the secretion of a wide range of hormones. Some hormones have anabolic actions on the body, others have mainly catabolic actions. For example, testosterone is an anabolic hormone, and synthetic steroids that produce the anabolic actions are known as anabolic steroids. Cortisol on the other hand, which is a steroid hormone produced by the adrenal gland, is a catabolic hormone.

In mammals, and other warm blooded animals, metabolic process are ultimately controlled by the central nervous system, which regulates the endocrine system. They are influenced by the balance between the energy demands of the organism, and the energy stores (see also Hunger). For example, fat stores secrete a hormone called leptin that acts at the hypothalamus to regulate hormone secretion. The hypothalamus is also sensitive to circulating concentrations of glucose, and to body temperature. When the ambient temperature is low, the metabolic rate of an endothermic animal will increase in order to generate more body heat (thermogenesis).

Some ectothermic animals, like reptiles, regulate their body tempertaure by behavior. These "cold blooded" creatures, including lizards, snakes, and turtles, keep at an optimum body tempertaure by heating up in the sun (basking) and cooling down in the shade or the cool earth of a burrow. The metabolism of these animals also changes with body temperature, and explain the sluggish movements of an ectotherm in colder seasons or times of day.

Links to subtopics dealing with metabolism

General pathways

Anabolism

Anabolic pathways that create building blocks and compounds from simple precursors:

Catabolism

Drug metabolism

Drug metabolism pathways, the modification or degradation of drugs and other xenobiotic compounds through specialized enzyme systems:

Nitrogen metabolism

Nitrogen metabolism includes the pathways for turnover and excretion of nitrogen in organisms as well as the biological processes of the biogeochemical nitrogen cycle:

Other

See also

External links

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