The Limits of Enzyme Specificity and the Evolution of Metabolism

被引:59
|
作者
Peracchi, Alessio [1 ]
机构
[1] Univ Parma, Dept Chem Life Sci & Environm Sustainabil, I-43124 Parma, Italy
关键词
ESCHERICHIA-COLI; THERMOCOCCUS-KODAKARENSIS; UNDERGROUND METABOLISM; SUBSTRATE-SPECIFICITY; CATALYTIC PROMISCUITY; BIOSYNTHESIS PATHWAY; DIRECTED EVOLUTION; DEHYDROGENASE; MECHANISM; PERSPECTIVE;
D O I
10.1016/j.tibs.2018.09.015
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 substrate specificity of enzymes is bound to be imperfect, because of unavoidable physicochemical limits. In extant metabolic enzymes, furthermore, such limits are seldom approached, suggesting that the degree of specificity of these enzymes, on average, is much lower than could be attained. During biological evolution, the activity of a single enzyme with available alternative substrates may be preserved to a significant or even substantial level for different reasons - for example when the alternative reaction contributes to fitness, or when its undesirable products are nevertheless dispatched by metabolite repair enzymes. In turn, the widespread occurrence of promiscuous reactions is a consistent source of metabolic messiness, from which both liabilities and opportunities ensue in the evolution of metabolic systems.
引用
收藏
页码:984 / 996
页数:13
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