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A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi

BACKGROUND: The filamentous fungus Trichoderma reesei, the most widely used cellulase producer, also has promising applications in lignocellulose-based biorefinery: consolidated bioprocessing for the production of high value-added products. However, such applications are thwarted by the time-consumi...

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Autores principales: Wang, Guokun, Jia, Wendi, Chen, Na, Zhang, Ke, Wang, Lixian, Lv, Pin, He, Ronglin, Wang, Min, Zhang, Dongyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109270/
https://www.ncbi.nlm.nih.gov/pubmed/30159032
http://dx.doi.org/10.1186/s13068-018-1223-8
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author Wang, Guokun
Jia, Wendi
Chen, Na
Zhang, Ke
Wang, Lixian
Lv, Pin
He, Ronglin
Wang, Min
Zhang, Dongyuan
author_facet Wang, Guokun
Jia, Wendi
Chen, Na
Zhang, Ke
Wang, Lixian
Lv, Pin
He, Ronglin
Wang, Min
Zhang, Dongyuan
author_sort Wang, Guokun
collection PubMed
description BACKGROUND: The filamentous fungus Trichoderma reesei, the most widely used cellulase producer, also has promising applications in lignocellulose-based biorefinery: consolidated bioprocessing for the production of high value-added products. However, such applications are thwarted by the time-consuming metabolic engineering processes (design–build–test–learn cycle) for T. reesei, resulted from (i) the spore separation-mediated purification as the multinucleate hyphae, (ii) transformant screening for high expression levels since unavailable of episomal expression system, and (iii) cases of inexpressible heterologous proteins. RESULTS: In this study, a GFP-fusion coupled fluorescence-activated cell sorting (FACS) platform was established to speed up the build and test process of the DBTL cycle, by enabling rapid selection for expressible heterologous genes and bypassing both laborious spore separation and transformant screening. Here, the feasibility of flow cytometry in analyzing and sorting T. reesei cells harboring GFP-fused expressible protein was proven, as well as the application of the platform for constitutive promoter strength evaluation. As a proof-of-concept, the platform was employed to construct the first T. reesei strain producing fatty alcohol, resulting in up to 2 mg hexadecanol being produced per gram biomass. Pathway construction was enabled through rapid selection of functional fatty acyl-CoA reductase encoding gene Tafar1 from three candidate genes and strains with high expression level from spore pools. As a result of using this method, the total costed time for the build and test cycle using T. reesei, subsequently, reduced by approx. 75% from 2 months to 2 weeks. CONCLUSION: This study established the GFP-fusion coupling FACS platform and the first filamentous fungal fatty alcohol-producing cell factory, and demonstrated versatile applications of the platform in the metabolic engineering of filamentous fungi, which can be harnessed to potentially advance the application of filamentous fungi in lignocellulose-based biorefinery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1223-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-61092702018-08-29 A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi Wang, Guokun Jia, Wendi Chen, Na Zhang, Ke Wang, Lixian Lv, Pin He, Ronglin Wang, Min Zhang, Dongyuan Biotechnol Biofuels Research BACKGROUND: The filamentous fungus Trichoderma reesei, the most widely used cellulase producer, also has promising applications in lignocellulose-based biorefinery: consolidated bioprocessing for the production of high value-added products. However, such applications are thwarted by the time-consuming metabolic engineering processes (design–build–test–learn cycle) for T. reesei, resulted from (i) the spore separation-mediated purification as the multinucleate hyphae, (ii) transformant screening for high expression levels since unavailable of episomal expression system, and (iii) cases of inexpressible heterologous proteins. RESULTS: In this study, a GFP-fusion coupled fluorescence-activated cell sorting (FACS) platform was established to speed up the build and test process of the DBTL cycle, by enabling rapid selection for expressible heterologous genes and bypassing both laborious spore separation and transformant screening. Here, the feasibility of flow cytometry in analyzing and sorting T. reesei cells harboring GFP-fused expressible protein was proven, as well as the application of the platform for constitutive promoter strength evaluation. As a proof-of-concept, the platform was employed to construct the first T. reesei strain producing fatty alcohol, resulting in up to 2 mg hexadecanol being produced per gram biomass. Pathway construction was enabled through rapid selection of functional fatty acyl-CoA reductase encoding gene Tafar1 from three candidate genes and strains with high expression level from spore pools. As a result of using this method, the total costed time for the build and test cycle using T. reesei, subsequently, reduced by approx. 75% from 2 months to 2 weeks. CONCLUSION: This study established the GFP-fusion coupling FACS platform and the first filamentous fungal fatty alcohol-producing cell factory, and demonstrated versatile applications of the platform in the metabolic engineering of filamentous fungi, which can be harnessed to potentially advance the application of filamentous fungi in lignocellulose-based biorefinery. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-018-1223-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-24 /pmc/articles/PMC6109270/ /pubmed/30159032 http://dx.doi.org/10.1186/s13068-018-1223-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Guokun
Jia, Wendi
Chen, Na
Zhang, Ke
Wang, Lixian
Lv, Pin
He, Ronglin
Wang, Min
Zhang, Dongyuan
A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi
title A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi
title_full A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi
title_fullStr A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi
title_full_unstemmed A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi
title_short A GFP-fusion coupling FACS platform for advancing the metabolic engineering of filamentous fungi
title_sort gfp-fusion coupling facs platform for advancing the metabolic engineering of filamentous fungi
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6109270/
https://www.ncbi.nlm.nih.gov/pubmed/30159032
http://dx.doi.org/10.1186/s13068-018-1223-8
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