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9.7 The Biochemistry of movement: 10. Sprinting and anaerobic respiration

Syllabus reference (October 2002 version)
10. Sprinting involves muscles contracting powerfully and rapidly and utilises type 2 muscles
Students learn to: Students:
Extract from Chemistry Stage 6 Syllabus (Amended October 2002) © Board of Studies, NSW.
[Edit: 27 Jun 08]

solve problems and process information from a simplified flow chart of biochemical pathways to summarise the steps in anaerobic glycolysis and analyse the total energy output from this process

  1. The number of ATP quickly produced in the cytoplasm from conversion of one glucose to two pyruvic acid (do not include ATP later released from the NADH as this requires oxygen and many more steps, mostly in mitochondria)

    Answer

    This number of ATP represents the energy released from one glucose without any oxygen.


  2. Subtract the number you obtained above for energy released by one glucose without oxygen from the total number of ATP released from one glucose (you worked this out in the table in subsection 9).

    38 - __ = __ ATP released from glucose in the many steps beyond pyruvic acid.

    Answer

outline the problems associated with the supply and use of fuels during sprinting and relate this to the sprinting muscles’ reliance on non-oxygen/non-mitochondrial based ATP production

Note that this is the only reversible reaction shown in the Biochemical Pathways Flowchart:

CH3 – CO – COOH + NADH + H+  arrows   CH3 – CHOH – COOH + NAD+

pyruvic acid                                        lactic acid

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explain the relationship between the production of 2–hydroxypropanoic (lactic) acid during anaerobic respiration and the impairment of muscle contractions by changes in cellular pH

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use available evidence and process information from a simplified flow chart of biochemical pathways to trace the path of lactic acid formation and compare this with the process of fermentation

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process information to discuss the use of multiple naming systems in chemistry using lactic acid (2-hydroxypropanoic acid or 2-hydroxypropionic acid) as an example

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