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Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux
Enzymatic reactions in living cells are highly dynamic but simultaneously tightly regulated. Enzyme engineers seek to construct multienzyme complexes to prevent intermediate diffusion, to improve product yield, and to control the flux of metabolites. Here we choose a pair of short peptide tags (RIAD...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751169/ https://www.ncbi.nlm.nih.gov/pubmed/31534134 http://dx.doi.org/10.1038/s41467-019-12247-w |
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author | Kang, Wei Ma, Tian Liu, Min Qu, Jiale Liu, Zhenjun Zhang, Huawei Shi, Bin Fu, Shuai Ma, Juncai Lai, Louis Tung Faat He, Sicong Qu, Jianan Wing-Ngor Au, Shannon Ho Kang, Byung Yu Lau, Wilson Chun Deng, Zixin Xia, Jiang Liu, Tiangang |
author_facet | Kang, Wei Ma, Tian Liu, Min Qu, Jiale Liu, Zhenjun Zhang, Huawei Shi, Bin Fu, Shuai Ma, Juncai Lai, Louis Tung Faat He, Sicong Qu, Jianan Wing-Ngor Au, Shannon Ho Kang, Byung Yu Lau, Wilson Chun Deng, Zixin Xia, Jiang Liu, Tiangang |
author_sort | Kang, Wei |
collection | PubMed |
description | Enzymatic reactions in living cells are highly dynamic but simultaneously tightly regulated. Enzyme engineers seek to construct multienzyme complexes to prevent intermediate diffusion, to improve product yield, and to control the flux of metabolites. Here we choose a pair of short peptide tags (RIAD and RIDD) to create scaffold-free enzyme assemblies to achieve these goals. In vitro, assembling enzymes in the menaquinone biosynthetic pathway through RIAD–RIDD interaction yields protein nanoparticles with varying stoichiometries, sizes, geometries, and catalytic efficiency. In Escherichia coli, assembling the last enzyme of the upstream mevalonate pathway with the first enzyme of the downstream carotenoid pathway leads to the formation of a pathway node, which increases carotenoid production by 5.7 folds. The same strategy results in a 58% increase in lycopene production in engineered Saccharomyces cerevisiae. This work presents a simple strategy to impose metabolic control in biosynthetic microbe factories. |
format | Online Article Text |
id | pubmed-6751169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-67511692019-09-20 Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux Kang, Wei Ma, Tian Liu, Min Qu, Jiale Liu, Zhenjun Zhang, Huawei Shi, Bin Fu, Shuai Ma, Juncai Lai, Louis Tung Faat He, Sicong Qu, Jianan Wing-Ngor Au, Shannon Ho Kang, Byung Yu Lau, Wilson Chun Deng, Zixin Xia, Jiang Liu, Tiangang Nat Commun Article Enzymatic reactions in living cells are highly dynamic but simultaneously tightly regulated. Enzyme engineers seek to construct multienzyme complexes to prevent intermediate diffusion, to improve product yield, and to control the flux of metabolites. Here we choose a pair of short peptide tags (RIAD and RIDD) to create scaffold-free enzyme assemblies to achieve these goals. In vitro, assembling enzymes in the menaquinone biosynthetic pathway through RIAD–RIDD interaction yields protein nanoparticles with varying stoichiometries, sizes, geometries, and catalytic efficiency. In Escherichia coli, assembling the last enzyme of the upstream mevalonate pathway with the first enzyme of the downstream carotenoid pathway leads to the formation of a pathway node, which increases carotenoid production by 5.7 folds. The same strategy results in a 58% increase in lycopene production in engineered Saccharomyces cerevisiae. This work presents a simple strategy to impose metabolic control in biosynthetic microbe factories. Nature Publishing Group UK 2019-09-18 /pmc/articles/PMC6751169/ /pubmed/31534134 http://dx.doi.org/10.1038/s41467-019-12247-w Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kang, Wei Ma, Tian Liu, Min Qu, Jiale Liu, Zhenjun Zhang, Huawei Shi, Bin Fu, Shuai Ma, Juncai Lai, Louis Tung Faat He, Sicong Qu, Jianan Wing-Ngor Au, Shannon Ho Kang, Byung Yu Lau, Wilson Chun Deng, Zixin Xia, Jiang Liu, Tiangang Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux |
title | Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux |
title_full | Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux |
title_fullStr | Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux |
title_full_unstemmed | Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux |
title_short | Modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux |
title_sort | modular enzyme assembly for enhanced cascade biocatalysis and metabolic flux |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751169/ https://www.ncbi.nlm.nih.gov/pubmed/31534134 http://dx.doi.org/10.1038/s41467-019-12247-w |
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