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Lecture 2 August 3, 2005 Lehninger (4 th Edition), Chapter 6,
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ENZYME KINETICS LNC Chapter 6
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REACTANTS SUBSTRATES PRODUCTS k First order reactions:A P k Second order reactions:A + B P A + A P
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1 st order:ln[A] = ln[A o ] - kt or [A] = [A o ] exp(-kt) 2 nd order: 1/[A] = 1/[Ao] + kt
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TRANSITION STATE THEORY A C B D A C B D A C B D A catalyst serves in at least two ways: it binds and aligns the substrates it facilitates the redistribution of electrons (charges)
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k 1 k 2 E + S ES Products k -1 CHAPTER 6 Enzymes and Enzyme Kinetics
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Fig. 6-2
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Fig. 6-3
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Derivation of Michaelis-Menten equation 1. equilibrium assumption: k -1 >> k 2 2. steady state assumption:d[ES]/dt = 0 Note:[E] = [E] total – [ES]
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Hmmm..??
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when [S] >> K m then v v max and v max = k 2 [E] T k 2 x [E] T x [S] v = ------------------------- K m + [S]
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k -1 + k 2 K m = k 1
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d K m K d when k -1 >> k 2
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Fig. 6-11
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Fig. 6-12
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1 K m 1 1 = x + v o v max [S] v max y = ax + b
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Lineweaver-Burk Plot Double Reciprocal Plot box. 6-1
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- another definition : v max k 2 = k cat = ------------ [E] T TURNOVER NUMBER
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molecules of substrate / molecule of enzyme / second moles of substrate / mole of enzyme / second
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Reactions with more than one substrate (more typical) Overall reaction: S 1 + S 2 P 1 + P 2
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Fig. 6-13
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LNC 6-14 a Lines intersect: ternary complex is formed in the reaction
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LNC 6-13 b This case is also referred to as the Ping-Pong or double displacement mechanism
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LNC 6-14 b Lines do not intersect: no ternary complex is formed
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Enzyme Inhibitors
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Fig. 6-15a
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Competitive Inhibition = 1 + [I] / K I box. 6-2.1
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Fig. 6-15b
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Uncompetitive Inhibition ’ = 1 + [I] / K I box. 6-2.2
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Fig. 6-15c
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Mixed Inhibition When = ’, then we also speak of noncompetitive inhibition box 6-2.3
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LNC 6-28 FEEDBACK INHIBITION
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LNC 6-26
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LNC 6-27 ASPARTATE TRANSCARBAMYLASE
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LNC 6-29a
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LNC 6-29b
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LNC 6-29c
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Part III Bioenergetics and Metabolism Chapter 13 in LNC
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THE CARBON CYCLE
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urea THE NITROGEN CYCLE
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Types of Organic Reactions 1) Group transfer Glucose + ATP Glu-6-P + ADP H 2 O + ATP P i + ADP 2) Oxidation-reduction reactions Ethanol + NAH + acetaldehyde + NADH + H + 3) Eliminations, isomerizations, rearrangements aldose ketose 4) reactions involving making or breaking of C-C bonds Fru-1,6, bisphosphate dihydroxyacetone-phosphate + glyceraldehyde-3phosphate
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End of Lecture 2 Aug. 3, 2005
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