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Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria
Cyanobacteria can convert CO(2) to chemicals such as 2,3-butanediol (2,3-BDO), rendering them promising for renewable production and carbon neutralization, but their applications are limited by low titers. To enhance cyanobacterial 2,3-BDO production, we developed a combinatorial CRISPR interference...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253771/ https://www.ncbi.nlm.nih.gov/pubmed/35800335 http://dx.doi.org/10.3389/fbioe.2022.913820 |
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author | Li, Hung Pham, Nam Ngoc Shen, Claire R. Chang, Chin-Wei Tu, Yi Chang, Yi-Hao Tu, Jui Nguyen, Mai Thanh Thi Hu, Yu-Chen |
author_facet | Li, Hung Pham, Nam Ngoc Shen, Claire R. Chang, Chin-Wei Tu, Yi Chang, Yi-Hao Tu, Jui Nguyen, Mai Thanh Thi Hu, Yu-Chen |
author_sort | Li, Hung |
collection | PubMed |
description | Cyanobacteria can convert CO(2) to chemicals such as 2,3-butanediol (2,3-BDO), rendering them promising for renewable production and carbon neutralization, but their applications are limited by low titers. To enhance cyanobacterial 2,3-BDO production, we developed a combinatorial CRISPR interference (CRISPRi) library strategy. We integrated the 2,3-BDO pathway genes and a CRISPRi library into the cyanobacterium PCC7942 using the orthogonal CRISPR system to overexpress pathway genes and attenuate genes that inhibit 2,3-BDO formation. The combinatorial CRISPRi library strategy allowed us to inhibit fbp, pdh, ppc, and sps (which catalyzes the synthesis of fructose-6-phosphate, acetyl-coenzyme A, oxaloacetate, and sucrose, respectively) at different levels, thereby allowing for rapid screening of a strain that enhances 2,3-BDO production by almost 2-fold to 1583.8 mg/L. Coupled with a statistical model, we elucidated that differentially inhibiting all the four genes enhances 2,3-BDO synthesis to varying degrees. fbp and pdh suppression exerted more profound effects on 2,3-BDO production than ppc and sps suppression, and these four genes can be repressed simultaneously without mutual interference. The CRISPRi library approach paves a new avenue to combinatorial metabolic engineering of cyanobacteria. |
format | Online Article Text |
id | pubmed-9253771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92537712022-07-06 Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria Li, Hung Pham, Nam Ngoc Shen, Claire R. Chang, Chin-Wei Tu, Yi Chang, Yi-Hao Tu, Jui Nguyen, Mai Thanh Thi Hu, Yu-Chen Front Bioeng Biotechnol Bioengineering and Biotechnology Cyanobacteria can convert CO(2) to chemicals such as 2,3-butanediol (2,3-BDO), rendering them promising for renewable production and carbon neutralization, but their applications are limited by low titers. To enhance cyanobacterial 2,3-BDO production, we developed a combinatorial CRISPR interference (CRISPRi) library strategy. We integrated the 2,3-BDO pathway genes and a CRISPRi library into the cyanobacterium PCC7942 using the orthogonal CRISPR system to overexpress pathway genes and attenuate genes that inhibit 2,3-BDO formation. The combinatorial CRISPRi library strategy allowed us to inhibit fbp, pdh, ppc, and sps (which catalyzes the synthesis of fructose-6-phosphate, acetyl-coenzyme A, oxaloacetate, and sucrose, respectively) at different levels, thereby allowing for rapid screening of a strain that enhances 2,3-BDO production by almost 2-fold to 1583.8 mg/L. Coupled with a statistical model, we elucidated that differentially inhibiting all the four genes enhances 2,3-BDO synthesis to varying degrees. fbp and pdh suppression exerted more profound effects on 2,3-BDO production than ppc and sps suppression, and these four genes can be repressed simultaneously without mutual interference. The CRISPRi library approach paves a new avenue to combinatorial metabolic engineering of cyanobacteria. Frontiers Media S.A. 2022-06-21 /pmc/articles/PMC9253771/ /pubmed/35800335 http://dx.doi.org/10.3389/fbioe.2022.913820 Text en Copyright © 2022 Li, Pham, Shen, Chang, Tu, Chang, Tu, Nguyen and Hu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Li, Hung Pham, Nam Ngoc Shen, Claire R. Chang, Chin-Wei Tu, Yi Chang, Yi-Hao Tu, Jui Nguyen, Mai Thanh Thi Hu, Yu-Chen Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria |
title | Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria |
title_full | Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria |
title_fullStr | Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria |
title_full_unstemmed | Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria |
title_short | Combinatorial CRISPR Interference Library for Enhancing 2,3-BDO Production and Elucidating Key Genes in Cyanobacteria |
title_sort | combinatorial crispr interference library for enhancing 2,3-bdo production and elucidating key genes in cyanobacteria |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9253771/ https://www.ncbi.nlm.nih.gov/pubmed/35800335 http://dx.doi.org/10.3389/fbioe.2022.913820 |
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