Summary of Cellular respiration

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Summary of Cellular respiration

  1. 1. CELLULAR RESPIRATION SUMMARY Cellular respiration is the enzymatic breakdown of glucose (C6H12O6) in the presence of oxygen (O2) to produce cellular energy (ATP): C6H12O6 + 6O2 6CO2 + 6H2O + 38 ATP THREE STAGES OF CELLULAR RESPIRATION 1. Glycolysis: A ten-step process that occurs in the cytoplasm Converts each molecule of glucose to two molecules of pyruvic acid (a 3-carbon molecule) An anaerobic process - proceeds whether or not O2 is present ; O2 is not required. Net yield of 2 ATP per glucose molecule Net yield of 2 NADH per glucose (NADH is nicotine adenine dinucleotide, a co-enzyme that serves as a carrier for H+ ions liberated as glucose is oxidized.) The pyruvic acid diffuses into the inner compartment of the mitochondrion where a transition reaction occurs that serves to prepare pyruvic acid for entry into the next stage of respiration:(a) pyruvic acid acetic acid + CO2 (a waste product of cell metabolism) + NADH+(b) acetic acid + co-enzyme A acetyl CoA
  2. 2. 2. Citric Acid or TCA Cycle: Occurs in the inner mitochondrial matrix The acetyl group detaches from the co-enzyme A and enters the reaction cycle an aerobic process; will proceed only in the presence of O2Net yield of 2 ATP per glucose molecule (per 2 acetyl CoA) Net yield of 6 NADH and 2 FADH2 (FAD serves the same purpose as NAD) In this stage of cellular respiration, the oxidation of glucose to CO2 is completed 3. Electron Transport System: Consists of a series of enzymes on the inner mitochondrial membrane Electrons are released from NADH and from FADH2 and as they are passed along the series of enzymes, they give up energy which is used to fuel a process called chemiosmosis by which H+ ions are actively transported across the inner mitochondrial membrane into the outer mitochondrial compartment. The H+ ions then flow back through special pores in the membrane, a process that is thought to drive the process of ATP synthesis. Net yield of 34 ATP per glucose molecule 6 H2O are formed when the electrons unite with O2* at the end of electron transport chain. [Note: This is the function of oxygen in living organisms!] GLUCOSE AS AN ENERGY SOURCE The above notes describe the process of carbohydrate (glucose) catabolism for the production of ATP. When glucose is in adequate supply, such as shortly after consumption of a meal, the hormone insulin which is secreted from the pancreas, increases glycogen formation (glycogenesis) in the liver. When glucose levels drop between meals, the hormone glucagon is released from the pancreas and stimulates the conversion of glycogen into glucose (by the process of glycogenolysis). If all
  3. 3. glycogen supplies are depleted, then other substances in the body are converted intoglucose or intermediate products that can enter the above-outlined cellular respirationpathway. The conversion of fatty acids (from lipids) or amino acids (from proteins)into glucose or intermediate products is called gluconeogenesis. FAT AS AN ENERGY SOURCEFats (lipids) are stored in adipose tissue. These stored fat molecules are synthesizedin the body from the breakdown products of fat digestion (glycerol and fatty acids),in a process known as lipogenesis. When needed as an energy source, the fatreserves are mobilized, moved out of adipose tissue, and broken down into glyceroland fatty acids in the liver by the process of lipolysis. Glycerol is changed into one ofthe intermediate products of glycolysis, so enters the cell respiration pathway. Fattyacids are changed in a series of reactions called beta-oxidation into acetyl CoAmolecules, which enter cell metabolism at the Krebs Cycle. When fats are beingused as the primary energy source such as in starvation, fasting or untreateddiabetes, an excess amount of acetyl CoA is produced, and is converted into acetoneand ketone bodies. This produces the sweet smell of acetone on the breath,noticeable in a diabetic state. PROTEIN AS AN ENERGY SOURCEProteins are used as an energy source only if protein intake is high, or if glucose andfat sources are depleted, in which case amino acids from protein breakdown areconverted into molecules that can enter the TCA Cycle. These molecules areproduced by either of two categories of reactions that alter the structure of aminoacids. Transamination transfers an amino group (NH2) from one amino acid toanother, whereas deamination removes an amino group from an amino acid. Asthey accumulate, the amino groups removed by the process of deamination arealtered to form a harmful waste product (ammonia), so are converted by the liverinto urea which is excreted by the kidneys.
  4. 4. FLOWCHART OF GLYCOLYSIS PATHWAY
  5. 5. FLOWCHART OF KREBS CYCLE

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