ULTIMATE LIMITS FOR THE REACTION FLUX AND METABOLITE LEVELS THAT MAY BE EVOLUTIONARILY REACHED IN A LINEAR METABOLIC PATHWAY

被引:11
作者
PETTERSSON, G [1 ]
PETTERSSON, P [1 ]
机构
[1] UNIV LUND,INST MATEMAT,S-22101 LUND,SWEDEN
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1990年 / 194卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1990.tb19436.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A relationship is derived for the maximum steady‐state reaction rate that may be supported by an enzyme catalysing substrate/product interconversion by a generalized Michaelian mechanism for a single‐substrate reaction. This relationship is used to characterize the ultimate kinetic and thermodynamic limits for the evolutionary improvement of a linear metabolic sequence of reactions catalysed by Michaelian enzymes in response to a selective pressure in the direction of increased reaction flux. A mathematical analysis is presented which provides explicit expressions for the maximum reaction flux and metabolite concentrations that can be evolutionarily reached in such a pathway. These expressions may be used to obtain information on the reaction steps that represent ultimate bottlenecks for the attainment of high reaction flux in a certain pathway and to identify the enzymes that ultimately are likely to exert main flux control. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:135 / 139
页数:5
相关论文
共 14 条
[1]   EVOLUTION OF ENZYME FUNCTION AND DEVELOPMENT OF CATALYTIC EFFICIENCY [J].
ALBERY, WJ ;
KNOWLES, JR .
BIOCHEMISTRY, 1976, 15 (25) :5631-5640
[2]   FREE ENERGY CHANGES AND METABOLIC REGULATION IN STEADY-STATE PHOTOSYNTHETIC CARBON REDUCTION [J].
BASSHAM, JA ;
KRAUSE, GH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1969, 189 (02) :207-&
[3]   PRE-EMINENCE OF KCAT IN MANIFESTATION OF OPTIMAL ENZYMIC ACTIVITY DELINEATED BY USING BRIGGS-HALDANE 2-STEP IRREVERSIBLE KINETIC-MODEL [J].
BROCKLEHURST, K ;
CORNISHBOWDEN, A .
BIOCHEMICAL JOURNAL, 1976, 159 (01) :165-166
[4]   EVOLUTION OF ENZYME CATALYTIC POWER - CHARACTERISTICS OF OPTIMAL CATALYSIS EVALUATED FOR SIMPLEST PLAUSIBLE KINETIC-MODEL [J].
BROCKLEHURST, K .
BIOCHEMICAL JOURNAL, 1977, 163 (01) :111-116
[5]   EFFECT OF NATURAL-SELECTION ON ENZYMIC CATALYSIS [J].
CORNISHBOWDEN, A .
JOURNAL OF MOLECULAR BIOLOGY, 1976, 101 (01) :1-9
[6]   NATURAL-SELECTION AND MICHAELIS CONSTANT [J].
CROWLEY, PH .
JOURNAL OF THEORETICAL BIOLOGY, 1975, 50 (02) :461-475
[7]   CATALYSIS, BINDING AND ENZYME-SUBSTRATE COMPLEMENTARITY [J].
FERSHT, AR .
PROCEEDINGS OF THE ROYAL SOCIETY SERIES B-BIOLOGICAL SCIENCES, 1974, 187 (1089) :397-407
[8]  
HARRIS DA, 1986, BIOCHEM EDUC, V14, P2
[9]  
HEINRICH R, 1985, BIOMED BIOCHIM ACTA, V44, P959
[10]   EVOLUTION OF CATALYTIC PROTEINS OR ON THE ORIGIN OF ENZYME SPECIES BY MEANS OF NATURAL-SELECTION [J].
KACSER, H ;
BEEBY, R .
JOURNAL OF MOLECULAR EVOLUTION, 1984, 20 (01) :38-51