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2.23 Mechanism for enzyme catalyzed reactions. To explain the kinetics of enzyme-substrate
reactions, Michaelis and Menten (1913) came up with the following mechanism, which
uses an equilibrium assumption.
k1
A+E⇄X
k2 [X]
With K= , and with [Eo] = [E] + [X]
k3 [ A ] [ E]
X→R+E
and where [Eo] represents the total enzyme and [E] represents the free unattached
enzyme.
G. E. Briggs and J. B. S. Haldane, Biochem J., 19, 338 (1925), on the other hand,
employed a steady-state assumption in place of the equilibrium assumption
k1
A+E⇄X
k2 d[X]
With =0 , and with [Eo] = [E] + [X]
k3 dt
X→R+E
What final rate form -rA in terms of [A], [E0], k1, k2, and k3 does
(a) the Michaelis-Menten mechanism give?
(b) the Briggs-Haldane mechanism give?
Terjemahan soal:
Mekanisme reaksi yang dikatalisis oleh enzim. Untuk menjelaskan kinetika reaksi
enzim-substrat, Michaelis dan Menten (1913) mengemukakan mekanisme berikut, yang
menggunakan asumsi kesetimbangan
k1
A+E⇄X
k2 [X]
Dengan K= , dan dengan [Eo] = [E] + [X]
k3 [ A ] [ E]
X→R+E
dan di mana [Eo] mewakili enzim total dan [E] mewakili enzim bebas yang tidak
terikat.
G. E. Briggs dan J. B. S. Haldane, Biochem J., 19, 338 (1925), di sisi lain,
menggunakan asumsi kondisi mapan menggantikan asumsi keseimbangan
k1
A+E⇄X
k2 d[X]
Dengan =0 , dan dengan [Eo] = [E] + [X]
k3 dt
X→R+E
Bagaimana bentuk laju akhir rR dalam hal [A], [E0], k1, k2, dan k3
(a) mekanisme dari Michaelis-Menten?
(b) mekanisme dari Briggs-Haldane?
Jawab:
Reaksi:
k1
A + E ⇄ X .................(1)
k2
k3
X → R + E .................(2)
Dengan: [Eo] = [E] + [X] .....(3)
Michael-menten mengasumsikan bahwa reaksi (1) mencapai keadaan
kesetimbangan dengan cepat, dengan:
[X] k1
K= =
[ A ] [ E] k 2
Briggs-Haldane mengsumsikan
d[X]
=0
dt