Cargando…

Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts

BACKGROUND: Isoprene, a volatile C5 hydrocarbon, is an important platform chemical used in the manufacturing of synthetic rubber for tires and various other applications, such as elastomers and adhesives. RESULTS: In this study, Escherichia coli MG1655 harboring Populus trichocarpa isoprene synthase...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Jung-Hun, Wang, Chonglong, Jang, Hui-Jung, Cha, Myeong-Seok, Park, Ju-Eon, Jo, Seon-Yeong, Choi, Eui-Sung, Kim, Seon-Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5180398/
https://www.ncbi.nlm.nih.gov/pubmed/28010736
http://dx.doi.org/10.1186/s12934-016-0612-6
_version_ 1782485523817824256
author Kim, Jung-Hun
Wang, Chonglong
Jang, Hui-Jung
Cha, Myeong-Seok
Park, Ju-Eon
Jo, Seon-Yeong
Choi, Eui-Sung
Kim, Seon-Won
author_facet Kim, Jung-Hun
Wang, Chonglong
Jang, Hui-Jung
Cha, Myeong-Seok
Park, Ju-Eon
Jo, Seon-Yeong
Choi, Eui-Sung
Kim, Seon-Won
author_sort Kim, Jung-Hun
collection PubMed
description BACKGROUND: Isoprene, a volatile C5 hydrocarbon, is an important platform chemical used in the manufacturing of synthetic rubber for tires and various other applications, such as elastomers and adhesives. RESULTS: In this study, Escherichia coli MG1655 harboring Populus trichocarpa isoprene synthase (PtispS) and the exogenous mevalonate (MVA) pathway produced 80 mg/L isoprene. Codon optimization and optimal expression of the ispS gene via adjustment of the RBS strength and inducer concentration increased isoprene production to 199 and 337 mg/L, respectively. To augment expression of MVA pathway genes, the MVA pathway was cloned on a high-copy plasmid (pBR322 origin) with a strong promoter (P(trc)), which resulted in an additional increase in isoprene production up to 956 mg/L. To reduce the formation of byproducts derived from acetyl-CoA (an initial substrate of the MVA pathway), nine relevant genes were deleted to generate the E. coli AceCo strain (E. coli MG1655 ΔackA-pta, poxB, ldhA, dld, adhE, pps, and atoDA). The AceCo strain harboring the ispS gene and MVA pathway showed enhanced isoprene production of 1832 mg/L in flask culture with reduced accumulation of byproducts. CONCLUSIONS: We achieved a 23-fold increase in isoprene production by codon optimization of PtispS, augmentation of the MVA pathway, and deletion of genes involved in byproduct formation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0612-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5180398
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-51803982016-12-28 Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts Kim, Jung-Hun Wang, Chonglong Jang, Hui-Jung Cha, Myeong-Seok Park, Ju-Eon Jo, Seon-Yeong Choi, Eui-Sung Kim, Seon-Won Microb Cell Fact Research BACKGROUND: Isoprene, a volatile C5 hydrocarbon, is an important platform chemical used in the manufacturing of synthetic rubber for tires and various other applications, such as elastomers and adhesives. RESULTS: In this study, Escherichia coli MG1655 harboring Populus trichocarpa isoprene synthase (PtispS) and the exogenous mevalonate (MVA) pathway produced 80 mg/L isoprene. Codon optimization and optimal expression of the ispS gene via adjustment of the RBS strength and inducer concentration increased isoprene production to 199 and 337 mg/L, respectively. To augment expression of MVA pathway genes, the MVA pathway was cloned on a high-copy plasmid (pBR322 origin) with a strong promoter (P(trc)), which resulted in an additional increase in isoprene production up to 956 mg/L. To reduce the formation of byproducts derived from acetyl-CoA (an initial substrate of the MVA pathway), nine relevant genes were deleted to generate the E. coli AceCo strain (E. coli MG1655 ΔackA-pta, poxB, ldhA, dld, adhE, pps, and atoDA). The AceCo strain harboring the ispS gene and MVA pathway showed enhanced isoprene production of 1832 mg/L in flask culture with reduced accumulation of byproducts. CONCLUSIONS: We achieved a 23-fold increase in isoprene production by codon optimization of PtispS, augmentation of the MVA pathway, and deletion of genes involved in byproduct formation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-016-0612-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-12-23 /pmc/articles/PMC5180398/ /pubmed/28010736 http://dx.doi.org/10.1186/s12934-016-0612-6 Text en © The Author(s) 2016 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
Kim, Jung-Hun
Wang, Chonglong
Jang, Hui-Jung
Cha, Myeong-Seok
Park, Ju-Eon
Jo, Seon-Yeong
Choi, Eui-Sung
Kim, Seon-Won
Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts
title Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts
title_full Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts
title_fullStr Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts
title_full_unstemmed Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts
title_short Isoprene production by Escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts
title_sort isoprene production by escherichia coli through the exogenous mevalonate pathway with reduced formation of fermentation byproducts
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5180398/
https://www.ncbi.nlm.nih.gov/pubmed/28010736
http://dx.doi.org/10.1186/s12934-016-0612-6
work_keys_str_mv AT kimjunghun isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts
AT wangchonglong isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts
AT janghuijung isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts
AT chamyeongseok isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts
AT parkjueon isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts
AT joseonyeong isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts
AT choieuisung isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts
AT kimseonwon isopreneproductionbyescherichiacolithroughtheexogenousmevalonatepathwaywithreducedformationoffermentationbyproducts