Lecture 12

Textbook Reading

9.6 Fermentation

  • fermentation — metabolic pathway that includes glycolysis and an additional set of reactions that oxidize stockpiles of NADH to regeneration NAD+

  • lactic acid fermentation — regenerates NAD+ by reducing pyruvate to form lactate

  • alcohol fermentation — yeast produces ethanol as waste

  • fermentation is extremely inefficient compared with cellular respiration

    • only 2 ATP produced per glucose molecule

  • facultative anaerobes — organisms that can switch between fermentation and aerobic cellular respiration

8.5 Enzymes Can Work Together in Metabolic Pathways

  • metabolic pathways — linked series of biochemical reactions that sequentially change an initial substrate to form a final product

    • A -(enzyme 1)→ B -(enzyme 2)→ C -(enzyme 3)→ D

  • feedback inhibition — regulate a metabolic pathway by using the final product of the reaction sequence to inactivate one of the pathway’s own enzymes

  • catabolic pathways — break down molecules for sources of energy/carbon building blocks

  • anabolic pathways — use energy/carbon building blocks to synthesize molecules

Lecture Slides

  • we followed the path of the C and H in glucose to complete oxidation in the presence of O2:

    • glycolysis first (1 glucose → 2 pyruvate)

    • krebs cycle next (carbons released as CO2)

    • ETC and oxidative phosphorylation last (hydrogens combine with oxygen to form H2O)

  • we followed the path of the energy in glucose (as electrons) to make ATP

    • some ATP generated by SLP in both glycolysis and Krebs Cycle

    • most electrons transferred to cofactors which carry them to the ETC, which uses them to create a proton gradient, which in turn powers ATP synthase to perform oxidative phosphorylation

  • what happens to aerobically-respiring cells under anaerobic conditions?

    • these cells can perform glycolysis, but no Krebs cycle, ETC, or oxidative phosphorylation — all ATP comes from glycolysis

    • the pyruvate undergoes a process called fermentation:

      • serves to regenerate the NAD+ which was reduced to NADH in glycolysis

      • no additional energy is released per molecule of glucose (because glucose is not completely oxidized), but the rate of glycolysis is increased to compensate for the loss of oxidative phosphorylation

      • fermentation products accumulate

  • fermentation in yeast

    • pyruvate -(pyruvate decarboxylase)→ acetaldehyde + CO2 -(alcohol dehydrogenase)→ ethanol

    • NADH gets oxidized to NAD+ in the process of making ethanol

  • fermentation in muscle cells and many bacteria

    • pyruvate -(lactace dehydrogenase)→ lactic acid (lactate)

    • NADH gets oxidized to NAD+ in the process

  • catabolic and biosynthetic pathways are regulated and coordinated

    • don’t use any more energy than necessary

    • coordination comes from two primary sources

      • amount of enzyme

      • activity of allosterically-regulated enzyme

  • some enzymes have binding sites other than the active site to which regulatory molecules (allosteric regulation) bind

    • noncompetitive enzyme inhibition = allosteric negative regulation

    • change conformation of active site

    • can either increase or decrease activity of enzyme

      • called positive regulator if it increases activity

      • called negative regulator if it decreases activity

  • sometimes, the allosteric regulator is a product of a later reaction in that pathway

    • called feedback inhibition — random collisions affect binding

    • low product (active)

      • substrate binds normally

    • high product (inactive)

      • allosteric binding results in feedback inhibition; enzyme 1 cannot bind substrate

  • example: feedback inhibition of glycolysis by ATP:

    • phosphofructokinase (PFK) — phosphorylates a phosphated fructose

    • if ATP binds to regulatory site, activity of PFK is decreased (negative regulation)

    • if ADP (or AMP) binds to regulatory site, active of PFK is increase (positive regulation)

    • whichever gets to the active site first binds, so if there is more ATP, there is less ATP produced because it binds more

    • allosteric binding sites: adenine nucleotide site

  • some allosteric regulators can turn “up” one reaction and turn “down” a different reaction

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