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Glycolysis (Figure 1) is a process to breakdown of glucose to simpler molecules by releasing energy in every cell.
Phosphorylation of glucose to glucose-6-phosphate by enzyme hexokinase or glucokinase with utilization of one mole of ATP. Phosphorylation of fructose-6-phosphate to fructose-1,6-bisphosphate by phosphofructokinase with utilization of one more of ATP. Cleavage of fructose-1,6-bisphosphate to 3-carbon fragments, glyceraldehyde-3-phosphate and dihydroxyacetone phosphate by aldolase. Isomerization of dihydroxyacetone phosphate to glyceraldehyde-3-phosphate by triose phosphate isomerase.
Transfer of phosphate group from phosphoenolpyruvate to form pyruvate with production of one mole of ATP.
Activated carriers couple energy release from spontaneous, energetically favorable reactions to energetically unfavorable reactions.
All nucleoside triphosphates can readily interchange phosphates and transfer energy between them.
Glycolysis and subsequent processes (fermentation in prokaryotes and in vertebrate muscle and the citric acid cycle and electron transport chain in eukaryotes) operate by stepwise oxidation. Glycolysis involves "priming" steps which require energy, cleavage of the 6 carbon sugar into two three carbon molecules, and energy generation. The overall pathway of glycolysis includes steps which have standard free energies which are negative (favorable) and some which are positive (unfavorable). The cleavage of the six carbon fructose 1,6-biphosphate occurs asymmetrically to produce dihydroxyacetone phosphate and glyceraldehyde-3-phosphate.
The activated, "high energy" carriers NADH and ATP are produced in energy conserving steps. Glucose -> glucose 6-phosphate is catalyzed by glucokinase in the vertebrate liver but hexokinase elsewhere. In vertebrates, fructose 1,6-biphosphate -> dihydroxyacetone phosphate + glyceraldehyde-3-phosphate is catalyzed by an aldolase which uses -SH bonds to the substrate. Glyceraldehyde 3-phosphate -> 1,3-biphosphoglycerate is catalyzed by an allosteric enzyme in which the subunits are negatively cooperative - As each unit binds a substate molecule, the other units become less able to bind and catalyze subsequent substrate molecules. Free energy changes for sequential reactions are additive - favorable reactions can overcome unfavorable ones! Anaerobic breakdown of pyruvate permits prokaryotes, who don't have any mitochondria, to get rid of the NADH produced in glycolysis.
Gluconeogenesis regenerates PEP from Pyruvate, thus forcing the reactions of glycolysis backwards. All text and images, not attributed to others, including course examinations and sample questions, are Copyright, 2006, Thomas J.
Glucose is a highly adaptable metabolite found in many organisms, offering a free energy of -2830kJ mol when fully metabolised.

This energy is released in small portions via ATP, the body’s universal energy currency.
The diagram above shows the process and points where ATP is released or consumed during Glycolysis. On this diagram we see the steps again, and highlighted in green are the molecules which differ from the next. The hydrogen on the alcohol on carbon 6 of glucose is replaced by a phosphate group from the ATP by Hexokinase. Phosphoglucose isomerase changes the glucose structure to fructose by swapping the C=O and alcohol groups on carbons 1&2. Phosphofructokinase replaces the hydrogen on the alcohol group of C1 with another phosphate group. Aldolase splits the fructose-1,6-bisphosphate into two 3 carbon molecules, dihydroxyacetone phosphate and glyceraldehyde 3-phosphate. Triose phosphate isomerase converts DHAP into GLAP by changing the structural configuration. From here on there are two molecules at a time (2 x 3 carbon rather than 1 x 6 carbon) and so all ATP & NADH figures have been doubled. Pyruvate kinase removes the phosphate group from C2, double bond C=O alters structure below C2. In anaerobic conditions we find only 2 ATP’s are produced for every glucose molecule converted to 2 lactate molecules. This is because the cell needs to reoxidise the NADH, and one such way of doing this is reducing the pyruvate by lactate dehydrogenase with the NADH, producing lactate. Glycolysis is derived fro Greek words, glycos which means sugar or sweet and lysis which means dissolution or degradation. This step in glycolysis is a destabilization step, where a the action of the enzyme aldolase splits fructose 1,6-bisphosphate into two sugars.
Step 7 of glycolysis is a substrate-level phosphorylation step, where the enzyme phosphoglycerokinase transfers a phosphate group from 1,3-bisphosphoglycerate. Step 9This step of glycolysis is a lyase reaction, which occurs in the presence of enolase enzyme. Regulation of Glycolysis is done by slowing down or speeding up steps in the glycolytic pathway. Under aerobic condition, pyruvate is oxidized to form acety-CoA which enter Krebs cycle in mitochondria. Herbert and may not be used for any commercial purpose without the express written permission of Thomas J. It is important to remember that this pathway is only the first section of a larger process (metabolism), as Pyruvate from this chain is used later in Krebs cycle etc.
All pyruvate must be converted to lactate to allow ATP synthesis to continue; and the lack of oxygen means no energy is gained from the oxidation of NADH.

Glycolysis is a metabolic pathway that is a sequence of 10 reactions that are enzyme catalyzed. In this step the enzyme phosphofructokinase is transfers phosphate group to form fructose 1,6-bisphosphate. In the presence of the enzyme pyruvate kinase, there is transfer of a inorganic phosphate molecule from phosphoenol pyruvate molecule to ADP to form pyruvic acid and ATP. The regulation is accomplished by the enzymes that are involved, that are inhibiting or activating enzymes. The first five steps of the glycolysis reaction is known as the preparatory or investment phase.
The enzyme also adds a inorganic phosphate from the cytosol to the glyceraldehyde phosphate to form 1,3-bisphosphoglycerate. This process yields two molecules of 3-phosphoglycerate molecules and two molecules of ATP. During this metabolic process high-energy compounds ATP (Adenosine triphosphate) and NADH (nicotinamide adenine dinucleotide).
The glycolytic pathway flux is adjusted in response to the inside and outside conditions of the cell. This process is a anaerobic reaction, the presence or absence of oxygen does not alter the reaction.
When there is fall in blood sugar levels, glycolysis is halted to allow the reverse process gluconeogenesis. It is often referred as the EMP pathway, as the scheme was given by Gustav Embden, Otto Meyerhof, and J. The PFK is inhibited by ATP and citrate and is activated by AMP, ADP and fructose 2,6-bisphosphate. The movement of carbon is through is inhibited at PFK, this happens when the cell contains enough stores of ATP and oxidizable substrates. Also, the PFK is activated by the presence of AMP and ADP, as their presence indicates the low levels of ATP in the cell. Fructose 2,6-bisphosphate is a major activator of PFK because it reciprocally inhibits fructose 1,6-bisphosphate. The fructose 1,6-bisphosphate is the gluconeogenic enzyme, it catalyzes the reversal of this step.

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