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弗氏柠檬酸杆菌酪氨酸酚裂解酶中His343突变为Ala的定点诱变。对动力学机制和速率决定步骤的影响。

Site-directed mutagenesis of His343-->Ala in Citrobacter freundii tyrosine phenol-lyase. Effects on the kinetic mechanism and rate-determining step.

作者信息

Chen H, Gollnick P, Phillips R S

机构信息

Department of Biochemistry, University of Georgia, Athens, USA.

出版信息

Eur J Biochem. 1995 Apr 15;229(2):540-9.

PMID:7744078
Abstract

His343 in Citrobacter freundii tyrosine phenol-lyase is conserved in all known sequences of both tyrosine phenol-lyase and tryptophan indole-lyase; it is located near the active-site Lys257 in C. freundii tyrosine phenol-lyase [Antson, A. A., Demidkina, T. V., Gollnick, P., Danter, Z., Von Tersch, R.L., Long, J., Berezhnoy, S. N., Phillips, R. S., Harutyunyan, E. H. & Wilson, K. S. (1993) Biochemistry 32, 4195--4206]. In order to evaluate the role of His343 in the reaction mechanism of tyrosine phenol-lyase and tryptophan indole-lyase, we have mutated it to Ala; the former mutant is referred to as [H343A]tyrosine phenol lyase. All substrates for alpha, beta-elimination (except S-ethyl-L-cysteine) exhibited lower kcat (10-30%) and kcat/Km (1-10%) values with [H343A]tyrosine phenol-lyase than with the wild-type enzyme. The mutant also shows slower rates of deuterium isotope exchange for L-phenylalanine and L-methionine than does the wild type. The pH-dependent behavior in the reaction of 3-fluoro-L-tyrosine with wild-type tyrosine phenol-lyase is identical to that of L-tyrosine described previously [Kiick, D. M. & Phillips, R. S. (1988) Biochemistry 27, 7333-7338]. The pH profile of kcat/Km for this reaction exhibits two pKa values with an average of 7.7 +/- 0.2, indicating that the catalytic mechanism requires two essential basic groups. The pH profile of kcat/Km for 3-fluoro-L-tyrosine with [H343A]tyrosine phenol-lyase also exhibits two pKa values with an average of 7.8 +/- 0.3. However, kcat for 3-fluoro-L-tyrosine is pH-dependent for the mutant, exhibiting two pKa values with an average of about 7.8, whereas it is pH-independent for the wild type. Steady-state kinetic isotope effects on the reactions with wild-type and [H343A]tyrosine phenol-lyase were examined at various pH values. For the wild type, the values of the isotope effects on kcat and kcat/Km for 3-fluoro-L-[alpha-2H]-tyrosine are independent of pH and equal to 3.9 +/- 0.2 and 2.2 +/- 0.3, respectively, while the corresponding values for [H343A]tyrosine phenol-lyase are 5.4 +/- 0.2 and 3.8 +/- 0.3, respectively.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

弗氏柠檬酸杆菌酪氨酸酚裂解酶中的His343在酪氨酸酚裂解酶和色氨酸吲哚裂解酶的所有已知序列中均保守;它位于弗氏柠檬酸杆菌酪氨酸酚裂解酶的活性位点Lys257附近[Antson, A. A., Demidkina, T. V., Gollnick, P., Danter, Z., Von Tersch, R.L., Long, J., Berezhnoy, S. N., Phillips, R. S., Harutyunyan, E. H. & Wilson, K. S. (1993) Biochemistry 32, 4195 - 4206]。为了评估His343在酪氨酸酚裂解酶和色氨酸吲哚裂解酶反应机制中的作用,我们将其突变为丙氨酸;前一个突变体称为[H343A]酪氨酸酚裂解酶。与野生型酶相比,[H343A]酪氨酸酚裂解酶对所有α,β-消除的底物(除S-乙基-L-半胱氨酸外)表现出较低的kcat(10 - 30%)和kcat/Km(1 - 10%)值。该突变体对L-苯丙氨酸和L-甲硫氨酸的氘同位素交换速率也比野生型慢。3-氟-L-酪氨酸与野生型酪氨酸酚裂解酶反应的pH依赖性行为与先前描述的L-酪氨酸相同[Kiick, D. M. & Phillips, R. S. (1988) Biochemistry 27, 7333 - 7338]。该反应的kcat/Km的pH曲线呈现两个pKa值,平均值为7.7±0.2,表明催化机制需要两个必需的碱性基团。3-氟-L-酪氨酸与[H343A]酪氨酸酚裂解酶反应的kcat/Km的pH曲线也呈现两个pKa值,平均值为7.8±0.3。然而,3-氟-L-酪氨酸的kcat对该突变体是pH依赖性的,呈现两个pKa值,平均值约为7.8,而对野生型则是pH非依赖性的。在不同pH值下研究了野生型和[H343A]酪氨酸酚裂解酶反应的稳态动力学同位素效应。对于野生型,3-氟-L-[α-2H]-酪氨酸对kcat和kcat/Km的同位素效应值与pH无关,分别为3.9±0.2和2.2±0.3,而[H343A]酪氨酸酚裂解酶的相应值分别为5.4±0.2和3.8±0.3。(摘要截断于400字)

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