Chapter 24: Introduction to Glycolysis (EMP)
Glycolysis, via the pathway named after its co-discoverers, is the primary route for glucose catabolism in mammalian cells leading to the cytoplasmic production of pyruvate, and its subsequent oxidation in the mitochondrial tricarboxylic acid (TCA) cycle through production of either acetyl-CoA, or oxaloacetate. Glycolysis is also a major pathway for the catabolism of fructose and galactose derived from dietary sucrose and lactose, respectively.
Of crucial biomedical importance is the ability of glycolysis to provide ATP for cells in the absence of oxygen (O2), thus allowing skeletal muscle, for example, to continue contracting when aerobic oxidation becomes insufficient. Anaerobic glycolysis also allows poorly perfused tissues to survive, and also those that lack mitochondria (e.g., mature erythrocytes). Conversely, heart muscle, which is adapted for sustained aerobic performance, has limited anaerobic glycolytic potential, and therefore does not perform well under conditions of ischemia. A small number of inherited hemolytic anemias occur among domestic animals, in which enzymes of glycolysis (e.g., pyruvate kinase or phosphofructokinase (PFK)), have reduced activity.
Glycolysis is a highly regulated process, with just enough glucose being metabolized at any one time to meet the cell's need for ATP. Metabolic intermediates between glucose and pyruvate are phosphorylated compounds, which promote their retention within the cytoplasm. Four molecules of ATP are generated from ADP in anaerobic glycolysis: two in the step catalyzed by phosphoglycerate kinase, and two in the step catalyzed by pyruvate kinase. However, two ATP molecules are consumed during earlier steps of this pathway: the first by the addition of a phosphate residue to glucose in the reaction catalyzed by hexokinase, and the second by the addition of a second phosphate to fructose 6-phosphate in the reaction catalyzed by PFK. Thus, there is a net gain of two ATP molecules in anaerobic glycolysis (when starting with glucose). Since the breakdown of glycogen through glucose 1- phosphate does not require ATP, the cytoplasmic phase of glycogenolysis can provide a net gain of 3 ATP molecules.
When oxygen becomes limited to cells, glucose cannot be oxidized completely to CO2 and H2O. Cells will thus "ferment" each glucose molecule to two moles of lactic acid -- again, with the net production of only two molecules of ATP from each glucose molecule. In fast-growing cancer cells, for example, glycolysis frequently proceeds at a much higher rate than can be accommodated by the mitochondrial TCA cycle. Many tumors are also poorly vascularized, thus reducing O2 availability. Thus, more pyruvate is produced than can be metabolized inside mitochondria. This, in turn, results in excessive production of lactic acid, which produces an acid environment in and around the tumor, a situation that may have implications for certain types of cancer therapy. Lactic acidosis results from other causes as well, including exercise, pyruvate dehydrogenase deficiency, or, for example, grain overload in ruminant animals.
The overall equation for anaerobic glycolysis (from glucose to lactate- ) is:
Glucose + 2 ADP + 2 Pi —> 2 Lactate- + 2 ATP + 2 H2O + 2 H+
The term lactic acid (CH3-CHOH-COOH) is often used interchangeably with lactate (CH3- CHOH-COO- ), which is an anion. Since lactic acid, like many organic acids, is largely dissociated in body fluids (CH3-CHOH-COOH —> CH3-CHOH-COO- + H+ ), use of the term "lactate" is more appropriate. It should be noted that when lactate accumulates in plasma, it displaces other important anions (e.g., HCO3 - and Cl- ) from extracellular fluids, thus having important implications in acid/base chemistry. When protons (H+ ) from lactic acid accumulate in muscle tissue, fatigue ensues because the Vmax of PFK is lowered, the release of Ca++ from the sarcoplasmic reticulum is compromised, actomyosin ATPase activity is reduced, and the conformation of muscle contractile proteins is affected, thus causing pain. Much of the lactate in blood normally passes into liver cells (where it can be converted to pyruvate, and then oxidized or used for glucose formation), or into cardiac muscle cells which can also convert it to pyruvate, and then oxidize it in mitochondria for energy purposes.
Anaerobic glycolysis is nearly universal among all cell types, although the end products may vary. That is, lactate (of mammals) may be replaced by a variety of different substances such as propionate in bacteria, or ethanol in yeast. As pyruvate is converted to lactate (or ethanol), the NADH produced in the initial stages of glycolysis is reoxidized to NAD+ , thus allowing anaerobic glycolysis to proceed (note: conversion of glyceraldehyde 3-phosphate to 1,3- bisphosphoglycerate requires NAD+ ). This anaerobic fermentation of carbohydrate in yeast forms the basis of the beer and wine industry.
Although anaerobic glycolysis produces only about 5% of the ATP provided during the catabolism of glucose, there are a number of reasons why it is necessary:
Mature red blood cells have no mitochondria, so all of their energy needs are supplied by anaerobic glycolysis. The space is needed for other molecules, in this case hemoglobin, which occupies about 33% of the cell interior. Also, red blood cells are located in a medium (blood plasma), that always has glucose available. On the other hand, heart muscle is an example of a tissue that has retained its aerobic capacity (many mitochondria), but lacks the ability to exhibit powerful contractile forces (like type IIB anaerobic skeletal muscle fibers that have many more actin and myosin filaments (and fewer mitochondria) per unit area).
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SUMMARY
Glycolysis is the primary pathway for glucose catabolism in mammalian cells, leading to the production of pyruvate. It is also important for the catabolism of fructose and galactose. Glycolysis can provide ATP for cells in the absence of oxygen, allowing tissues to survive in low oxygen conditions. It is a highly regulated process, with just enough glucose being metabolized to meet the cell's ATP needs. Anaerobic glycolysis produces two molecules of ATP from each glucose molecule, but also consumes two ATP molecules in earlier steps. Lactic acid is produced when oxygen is limited, and excessive production of lactic acid can create an acidic environment in tumors. Anaerobic glycolysis is necessary in certain situations where quick energy is needed, such as during sprinting or in tissues with limited blood supply. It is also important in skeletal muscle, which receives less oxygen compared to other organs. Some tissues, like the cornea and lens, rely heavily on anaerobic glycolysis due to their need for high efficiency in transmitting light signals. Mature red blood cells rely solely on anaerobic glycolysis for energy, while heart muscle retains its aerobic capacity but lacks powerful contractile forces.
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OUTLINE
I. Glycolysis as the primary route for glucose catabolism in mammalian cells
II. Importance of glycolysis in providing ATP in the absence of oxygen
III. Inherited hemolytic anemias and reduced activity of glycolytic enzymes
IV. Regulation of glycolysis
V. ATP production and consumption in anaerobic glycolysis
VI. Fermentation of glucose to lactic acid in the absence of oxygen
VII. Overall equation for anaerobic glycolysis
VIII. Use of the term "lactate" instead of "lactic acid" in body fluids
IX. Implications of lactate accumulation in plasma and muscle tissue
X. Anaerobic glycolysis in different organisms and end products
XI. Reasons for the necessity of anaerobic glycolysis
XII. Examples of tissues with high reliance on anaerobic glycolysis: cornea, lens, and mature red blood cells
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QUESTIONS
Qcard 1:
Question: What is the primary route for glucose catabolism in mammalian cells?
Answer: Glycolysis
Qcard 2:
Question: What is the net gain of ATP molecules in anaerobic glycolysis?
Answer: 2 ATP molecules
Qcard 3:
Question: What is the end product of anaerobic glycolysis?
Answer: Lactate
Qcard 4:
Question: Why is anaerobic glycolysis necessary?
Answer: It provides quick energy in situations where aerobic oxidation is not sufficient.
Qcard 5:
Question: What is the major source of energy in white, fast-twitch glycolytic muscle fibers?
Answer: Anaerobic glycolysis
Qcard 6:
Question: What is the primary source of energy for mature red blood cells?
Answer: Anaerobic glycolysis
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