Difference between revisions of "Citric acid cycle" - New World Encyclopedia

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A high-concept description of the the '''citric acid cycle''' (also known as the [[tricarboxylic acid cycle]], the [[TCA cycle]], and the [[Krebs cycle]] would be that it is the the process of controlled buring that all living things use to power their activities. The energy of this controlled oxygen buring oxygen is captured in high-energy [[ATP]] molecules that drive all the rest of the cell's activities. This method of is called cellular respiration.  
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The '''citric acid cycle''' (also known as the [[tricarboxylic acid cycle]], the [[TCA cycle]], and the [[Krebs cycle]] ) plays a central role in the manipulation of small carbon-oxygen-hydrogen molecules.This cycle plays two key roles in metabolism.  
  
This key metabolic cycle was established very early in God's unfolding plan of creation. The molecules involved, and the set of [[enzyme]]s that run the cycle, are essentially the same in all bacteria, fungi, plants and animals. The implication being that the cycle was well-established in creation well before the last universal ancestor of life. The current consensus is that this cycle predated the advent of free oxygen where it was 'run in reverse' (energy was put into the cycle) to assemble, rather than disassemble, important molecules.
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Running in one direction, the cycle constructs many basic molecules on which the rest of metabolism is based. Running in the opposite direction, the cycle combines small molecules with oxygen and capture the liberated energy to run all of metabolism. In practice, a cell runs billions of such cycles simultaneiously; most in the energy generating direction. Bacteriaial procaryotes run the cycle both ways in their cytoplasm, in the eukaryote cells such as ours, this energy-generating cellular respiration is constrained to within the mitochondria, the bacteria-like power houses of the cell.
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This key metabolic cycle was established very early in God's unfolding plan of creation as the molecules involved, and the set of [[enzyme]]s that run the cycle, are essentially the same in all bacteria, fungi, plants and animals. The implication being that the cycle was well-established in creation well before the last universal ancestor of all life. The current consensus is that this cycle predated the advent of free oxygen where it was 'run in reverse' (energy was put into the cycle) to assemble important molecules.
  
 
The citric acid cycle has food molecules fed into it by a preprocessing pathway called fermentation. A basic food molecule such as glucose is first broken down, without oxygen, by a series of steps, into two smalled molecules. Some energy is captured as a few ATP molecules during this fermentation stage. In the absence of oxygen, no more energy can be extracted, and the waste is converted into molecules such as ethanol (a yeast cell in wine) or lactic acid (a muscle cell in cramp).
 
The citric acid cycle has food molecules fed into it by a preprocessing pathway called fermentation. A basic food molecule such as glucose is first broken down, without oxygen, by a series of steps, into two smalled molecules. Some energy is captured as a few ATP molecules during this fermentation stage. In the absence of oxygen, no more energy can be extracted, and the waste is converted into molecules such as ethanol (a yeast cell in wine) or lactic acid (a muscle cell in cramp).
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In essence, this highly-efficient process is a very simple cycle of molecules being transformed under the guidance of the enzymes:
 
In essence, this highly-efficient process is a very simple cycle of molecules being transformed under the guidance of the enzymes:
• The glucose fragment from the fermentation step is combined with molecule AA to form molecule BB.  
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• The glucose fragment from the fermentation step is combined with molecule X to form molecule Y.  
• A carbon atom is removed from BB—and its energy captured—to make molecule CC.  
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• A carbon atom is removed from Y—and its energy captured—to make molecule Z....  
• A carbon atom is removed from CC—and its energy captured—to make molecule DD...  
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• A carbon atom is removed from Z—and its energy captured—to make molecule X. Repeat
• A carbon atom is removed from ZZ—and its energy captured—to make molecule AA. Repeat
 
 
   
 
   
 
The cycle continues, thousands of times a second. One turn of the cycle turns the glucose fragment into carbon dioxide and water, just as if it had burnt in a flame.
 
The cycle continues, thousands of times a second. One turn of the cycle turns the glucose fragment into carbon dioxide and water, just as if it had burnt in a flame.
  
In oxygen using [[aerobic organism]]s, the citric acid cycle is the final step in the breakdown of [[carbohydrate]]s, [[fat]]s and [[protein]]s into [[carbon dioxide]] and [[water]] in order to generate energy. Lacking oxygen, cells can survive, usually for a short time, using two other metabolic pathways called [[glycolysis]] and [[oxidative phosphorylation]]. These are very inefficient compared to the cycle. The citric acid cycle also provides precursors for many compounds such as certain [[amino acid]]s, and some of its reactions are therefore important even in cells performing such [[fermentation]] reactions in the absence of oxygen. In this case, as on the pre-oxygen earth, energy (from fermentation) has to be pumped into the cycle to run it in reverse.
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In oxygen using [[aerobic organism]]s, the citric acid cycle is the final step in the breakdown of [[carbohydrate]]s, [[fat]]s and [[protein]]s into [[carbon dioxide]] and [[water]] in order to generate energy.
  
 
==History==
 
==History==

Revision as of 18:40, 14 January 2006

The citric acid cycle (also known as the tricarboxylic acid cycle, the TCA cycle, and the Krebs cycle ) plays a central role in the manipulation of small carbon-oxygen-hydrogen molecules.This cycle plays two key roles in metabolism.

Running in one direction, the cycle constructs many basic molecules on which the rest of metabolism is based. Running in the opposite direction, the cycle combines small molecules with oxygen and capture the liberated energy to run all of metabolism. In practice, a cell runs billions of such cycles simultaneiously; most in the energy generating direction. Bacteriaial procaryotes run the cycle both ways in their cytoplasm, in the eukaryote cells such as ours, this energy-generating cellular respiration is constrained to within the mitochondria, the bacteria-like power houses of the cell.

This key metabolic cycle was established very early in God's unfolding plan of creation as the molecules involved, and the set of enzymes that run the cycle, are essentially the same in all bacteria, fungi, plants and animals. The implication being that the cycle was well-established in creation well before the last universal ancestor of all life. The current consensus is that this cycle predated the advent of free oxygen where it was 'run in reverse' (energy was put into the cycle) to assemble important molecules.

The citric acid cycle has food molecules fed into it by a preprocessing pathway called fermentation. A basic food molecule such as glucose is first broken down, without oxygen, by a series of steps, into two smalled molecules. Some energy is captured as a few ATP molecules during this fermentation stage. In the absence of oxygen, no more energy can be extracted, and the waste is converted into molecules such as ethanol (a yeast cell in wine) or lactic acid (a muscle cell in cramp).

When these glucose fragments are fed into the cycle in the presense of oxygen and completely burned to carbon dioxide and water, however, a large number of ATP molecules are generated.

In essence, this highly-efficient process is a very simple cycle of molecules being transformed under the guidance of the enzymes: • The glucose fragment from the fermentation step is combined with molecule X to form molecule Y. • A carbon atom is removed from Y—and its energy captured—to make molecule Z.... • A carbon atom is removed from Z—and its energy captured—to make molecule X. Repeat

The cycle continues, thousands of times a second. One turn of the cycle turns the glucose fragment into carbon dioxide and water, just as if it had burnt in a flame.

In oxygen using aerobic organisms, the citric acid cycle is the final step in the breakdown of carbohydrates, fats and proteins into carbon dioxide and water in order to generate energy.

History

The citric acid cycle is also known as the Krebs cycle after Sir Hans Adolf Krebs (1900-1981), who proposed the key elements of this pathway in 1937 and was awarded the Nobel Prize in Medicine for its discovery in 1953. It is correctly written without a possessive apostrophe.

Location of cycle and inputs and outputs

The citric acid cycle takes place within the mitochondrial matrix in eukaryotes, and within the cytoplasm in prokaryotes.

The reactions of TCAC as they happen in a human cell.
The color scheme is as follows: enzymes, coenzymes, substrate names, metal ions, inorganic molecules, inhibition, stimulation .
* - FAD/FADH2 is covalently attached to SDH

Fuel molecule catabolism (including glycolysis) produces acetyl-CoA, a two-carbon acetyl group bound to coenzyme A. Acetyl-CoA is the main input to the citric acid cycle. Citrate is both the first and the last product of the cycle (Fig 1), and is regenerated by the condensation of oxaloacetate and acetyl-CoA.

Molecule Enzyme Reaction type Reactants/
Coenzymes
Products/
Coenzymes
I. Citrate 1. Aconitase Dehydration H2O
II. cis-Aconitate 2. Aconitase Hydration H2O
III. Isocitrate 3. Isocitrate dehydrogenase Oxidation NAD+ NADH + H+
IV. Oxalosuccinate 4. Isocitrate dehydrogenase Decarboxylation
V. α-Ketoglutarate 5. α-Ketoglutarate
dehydrogenase
Oxidative
decarboxylation
NAD+ +
CoA-SH
NADH + H+
+ CO2
VI. Succinyl-CoA 6. Succinyl-CoA synthetase Hydrolysis GDP
+ Pi
GTP +
CoA-SH
VII. Succinate 7. Succinate dehydrogenase Oxidation FAD FADH2
VIII. Fumarate 8. Fumarase Addition (H2O) H2O
IX. L-Malate 9. Malate dehydrogenase Oxidation NAD+ NADH + H+
X. Oxaloacetate 10. Citrate synthase Condensation
XI. Acetyl-CoA

To a biochemist, this intricate assembly is as much a testament to God's genius as a beautiful rose.

The sum of all reactions in the citric acid cycle is:

Acetyl-CoA + 3 NAD+ + FAD + GDP + Pi + 3 H2O →
CoA-SH + 3 NADH + H+ + FADH2 + GTP + 2 CO2 + 3 H+


Two carbons are oxidized to CO2, and the energy from these reactions is stored in GTP , NADH and FADH2. NADH and FADH2 are coenzymes (molecules that enable or enhance enzymes) that store energy and are utilized in oxidative phosphorylation.

A simplified view of the process: The process begins with pyruvate, producing one CO2, then one CoA. It begins with the six carbon sugar, glucose. It produces 2 CO2 and consumes 3 NAD+ producing 3NADH and 3H+. It consumes 3 H2O and consumes one FAD, producing one FADH+.

Regulation

Many of the enzymes in the TCA cycle are regulated by negative feedback from ATP when the energy charge of the cell is high. Such enzymes include the pyruvate dehydrogenase complex that synthesises the acetyl-CoA needed for the first reaction of the TCA cycle. Also the enzymes citrate synthase, isocitrate dehydrogenase and alpha-ketoglutarate dehydrogenase, that regulate the first three steps of the TCA cycle, are inhibited by high concentrations of ATP. This regulation ensures that the TCA cycle will not oxidise excessive amount of pyruvate and acetyl-CoA when ATP in the cell is plentiful. This type of negative regulation by ATP is by an allosteric mechanism.

Several enzymes are also negatively regulated when the level of reducing equivalents in a cell are high (high ratio of NADH/NAD+). This mechanism for regulation is due to substrate inhibition by NADH of the enzymes that use NAD+ as a substrate. This includes both the entry point enzymes pyruvate dehydrogenase and citrate synthase.

Major metabolic pathways converging on the TCA cycle

Most of the body's catabolic pathways converge on the TCA cycle, as the diagram shows. Reactions that form intermediates of the cycle are called anaplerotic reactions.

The citric acid cycle is the second step in carbohydrate catabolism (the breakdown of sugars). Glycolysis breaks glucose (a six-carbon-molecule) down into pyruvate (a three-carbon molecule). In eukaryotes, pyruvate moves into the mitochondria. It is converted into acetyl-CoA and enters the citric acid cycle.

In protein catabolism, proteins are broken down by protease enzymes into their constituent amino acids. These amino acids are brought into the cells and can be a source of energy by being funnelled into the citric acid cycle.

In fat catabolism, triglycerides are hydrolyzed to break them into fatty acids and glycerol. In the liver the glycerol can be converted into glucose via dihydroxyacetone phosphate and glyceraldehyde-3-phosphate by way of gluconeogenesis. In many tissues, especially heart tissue, fatty acids are broken down through a process known as beta oxidation which results in acetyl-CoA which can be used in the citric acid cycle. Sometimes beta oxidation can yield propionyl CoA which can result in further glucose production by gluconeogenesis in liver.

The citric acid cycle is always followed by oxidative phosphorylation. This process extracts the energy from NADH and FADH2, recreating NAD+ and FAD, so that the cycle can continue. The citric acid cycle itself does not use oxygen, but oxidative phosphorylation does.

The total energy gained from the complete breakdown of one molecule of glucose by glycolysis, the citric acid cycle and oxidative phosphorylation equals about 36 ATP molecules. The citric acid cycle is called an amphibolic pathway because it participates in both catabolism and anabolism.

See also

  • Oxidative decarboxylation
  • Citric acid
  • Glycolysis
  • Oxidative phosphorylation
  • Reverse (reductive) Krebs cycle

External links


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