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Enzyme Recruitment and Its Role in Metabolic Expansion

[Image: see text] Although more than 10(9) years have passed since the existence of the last universal common ancestor, proteins have yet to reach the limits of divergence. As a result, metabolic complexity is ever expanding. Identifying and understanding the mechanisms that drive and limit the dive...

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Detalles Bibliográficos
Autores principales: Schulenburg, Cindy, Miller, Brian G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985712/
https://www.ncbi.nlm.nih.gov/pubmed/24483367
http://dx.doi.org/10.1021/bi401667f
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author Schulenburg, Cindy
Miller, Brian G.
author_facet Schulenburg, Cindy
Miller, Brian G.
author_sort Schulenburg, Cindy
collection PubMed
description [Image: see text] Although more than 10(9) years have passed since the existence of the last universal common ancestor, proteins have yet to reach the limits of divergence. As a result, metabolic complexity is ever expanding. Identifying and understanding the mechanisms that drive and limit the divergence of protein sequence space impact not only evolutionary biologists investigating molecular evolution but also synthetic biologists seeking to design useful catalysts and engineer novel metabolic pathways. Investigations over the past 50 years indicate that the recruitment of enzymes for new functions is a key event in the acquisition of new metabolic capacity. In this review, we outline the genetic mechanisms that enable recruitment and summarize the present state of knowledge regarding the functional characteristics of extant catalysts that facilitate recruitment. We also highlight recent examples of enzyme recruitment, both from the historical record provided by phylogenetics and from enzyme evolution experiments. We conclude with a look to the future, which promises fruitful consequences from the convergence of molecular evolutionary theory, laboratory-directed evolution, and synthetic biology.
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spelling pubmed-39857122015-01-21 Enzyme Recruitment and Its Role in Metabolic Expansion Schulenburg, Cindy Miller, Brian G. Biochemistry [Image: see text] Although more than 10(9) years have passed since the existence of the last universal common ancestor, proteins have yet to reach the limits of divergence. As a result, metabolic complexity is ever expanding. Identifying and understanding the mechanisms that drive and limit the divergence of protein sequence space impact not only evolutionary biologists investigating molecular evolution but also synthetic biologists seeking to design useful catalysts and engineer novel metabolic pathways. Investigations over the past 50 years indicate that the recruitment of enzymes for new functions is a key event in the acquisition of new metabolic capacity. In this review, we outline the genetic mechanisms that enable recruitment and summarize the present state of knowledge regarding the functional characteristics of extant catalysts that facilitate recruitment. We also highlight recent examples of enzyme recruitment, both from the historical record provided by phylogenetics and from enzyme evolution experiments. We conclude with a look to the future, which promises fruitful consequences from the convergence of molecular evolutionary theory, laboratory-directed evolution, and synthetic biology. American Chemical Society 2014-01-21 2014-02-11 /pmc/articles/PMC3985712/ /pubmed/24483367 http://dx.doi.org/10.1021/bi401667f Text en Copyright © 2014 American Chemical Society
spellingShingle Schulenburg, Cindy
Miller, Brian G.
Enzyme Recruitment and Its Role in Metabolic Expansion
title Enzyme Recruitment and Its Role in Metabolic Expansion
title_full Enzyme Recruitment and Its Role in Metabolic Expansion
title_fullStr Enzyme Recruitment and Its Role in Metabolic Expansion
title_full_unstemmed Enzyme Recruitment and Its Role in Metabolic Expansion
title_short Enzyme Recruitment and Its Role in Metabolic Expansion
title_sort enzyme recruitment and its role in metabolic expansion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985712/
https://www.ncbi.nlm.nih.gov/pubmed/24483367
http://dx.doi.org/10.1021/bi401667f
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