WHAT METABOLITE LEVELS MAY BE EVOLUTIONARILY REACHED IN THE GLYCOLYTIC PATHWAY

被引:5
作者
PETTERSSON, G
机构
[1] Avdelningen for Biokemi, Kemicentrum, Lunds Universitet, Lund
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1990年 / 194卷 / 01期
关键词
D O I
10.1111/j.1432-1033.1990.tb19437.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
The thermodynamic and kinetic properties of the glycolytic pathway have been analyzed in order to characterize the ultimate limits for the metabolite concentrations that may be evolutionarily reached in response to a selective pressure in the direction of increased glycolytic reaction flux. The results indicate that the chemical potential for conversion of glucose into pyruvate at presently observed levels of these two metabolites (and of NADH, NAD+, ATP, ADP and inorganic phosphate) is high enough to allow ultimately for an accumulation of fructose 1,6‐bisphosphate at concentrations which may be considered as indefinitely high from a practical point of view. This means that non‐kinetic factors such as metabolite solubility put a definite limit to the glycolytic reaction flux that may be evolutionarily reached. With the reasonable assumption that evolution eventually may raise the concentration of fructose 1,6‐bisphosphate minimally to the same level as that presently attained by glucose, analytical evidence is presented to show that catalytic improvement of enzymes in the glycolytic pathway ultimately may result in glycerone phosphate levels that are at least two orders of magnitude higher than those presently observed. This argues strongly against the idea that triose‐phosphate isomerase represents a perfectly evolved catalyst in the sense that it should have reached the end of its evolutionary development. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:141 / 146
页数:6
相关论文
共 15 条
[1]   FREE-ENERGY PROFILE FOR REACTION CATALYZED BY TRIOSEPHOSPHATE ISOMERASE [J].
ALBERY, WJ ;
KNOWLES, JR .
BIOCHEMISTRY, 1976, 15 (25) :5627-5631
[2]   EVOLUTION OF ENZYME FUNCTION AND DEVELOPMENT OF CATALYTIC EFFICIENCY [J].
ALBERY, WJ ;
KNOWLES, JR .
BIOCHEMISTRY, 1976, 15 (25) :5631-5640
[3]   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-&
[4]  
COLOWICK SP, 1973, ENZYMES, V9, P1, DOI DOI 10.1016/S1874-6047(08)60113-4
[5]  
FROBERG CE, 1970, INTRO NUMERICAL ANAL
[6]   ISOTOPE-EXCHANGE EVIDENCE FOR AN ORDERED MECHANISM FOR RAT-LIVER GLUCOKINASE, A MONOMERIC COOPERATIVE ENZYME [J].
GREGORIOU, M ;
TRAYER, IP ;
CORNISHBOWDEN, A .
BIOCHEMISTRY, 1981, 20 (03) :499-506
[7]   THERMODYNAMIC CONSIDERATIONS OF ERYTHROCYTE GLYCOLYSIS [J].
MINAKAMI, S ;
YOSHIKAW, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1965, 18 (03) :345-&
[8]   MECHANISTIC ORIGIN OF THE SIGMOIDAL RATE BEHAVIOR OF GLUCOKINASE [J].
PETTERSSON, G .
BIOCHEMICAL JOURNAL, 1986, 233 (02) :347-350
[9]   ULTIMATE LIMITS FOR THE REACTION FLUX AND METABOLITE LEVELS THAT MAY BE EVOLUTIONARILY REACHED IN A LINEAR METABOLIC PATHWAY [J].
PETTERSSON, G ;
PETTERSSON, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 194 (01) :135-139
[10]   EFFECT OF EVOLUTION ON THE KINETIC-PROPERTIES OF ENZYMES [J].
PETTERSSON, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 184 (03) :561-566