Cargando…

Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture

BACKGROUND: Geraniol is an acyclic monoterpene alcohol, which exhibits good prospect as a gasoline alternative. Geraniol is naturally encountered in plants at low concentrations and an attractive target for microbial engineering. Geraniol has been heterologously produced in Escherichia coli, but the...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Wei, Xu, Xin, Zhang, Rubing, Cheng, Tao, Cao, Yujin, Li, Xiaoxiao, Guo, Jiantao, Liu, Huizhou, Xian, Mo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787002/
https://www.ncbi.nlm.nih.gov/pubmed/26973712
http://dx.doi.org/10.1186/s13068-016-0466-5
_version_ 1782420638570381312
author Liu, Wei
Xu, Xin
Zhang, Rubing
Cheng, Tao
Cao, Yujin
Li, Xiaoxiao
Guo, Jiantao
Liu, Huizhou
Xian, Mo
author_facet Liu, Wei
Xu, Xin
Zhang, Rubing
Cheng, Tao
Cao, Yujin
Li, Xiaoxiao
Guo, Jiantao
Liu, Huizhou
Xian, Mo
author_sort Liu, Wei
collection PubMed
description BACKGROUND: Geraniol is an acyclic monoterpene alcohol, which exhibits good prospect as a gasoline alternative. Geraniol is naturally encountered in plants at low concentrations and an attractive target for microbial engineering. Geraniol has been heterologously produced in Escherichia coli, but the low titer hinders its industrial applications. Moreover, bioconversion of geraniol by E. coli remains largely unknown. RESULTS: Recombinant overexpression of Ocimum basilicum geraniol synthase, Abies grandis geranyl diphosphate synthase, and a heterotic mevalonate pathway in E. coli BL21 (DE3) enabled the production of up to 68.6 ± 3 mg/L geraniol in shake flasks. Initial fed-batch fermentation only increased geraniol production to 78.8 mg/L. To further improve the production yield, the fermentation conditions were optimized. Firstly, 81.4 % of volatile geraniol was lost during the first 5 h of fermentation in a solvent-free system. Hence, isopropyl myristate was added to the culture medium to form an aqueous-organic two-phase culture system, which effectively prevented volatilization of geraniol. Secondly, most of geraniol was eventually biotransformed into geranyl acetate by E. coli, thus decreasing geraniol production. For the first time, we revealed the role of acetylesterase (Aes, EC 3.1.1.6) from E. coli in hydrolyzing geranyl acetate to geraniol, and production of geraniol was successfully increased to 2.0 g/L under controlled fermentation conditions. CONCLUSIONS: An efficient geraniol production platform was established by overexpressing several key pathway proteins in engineered E. coli strain combined with a controlled fermentation system. About 2.0 g/L geraniol was obtained using our controllable aqueous-organic two-phase fermentation system, which is the highest yield to date. In addition, the interconversion between geraniol and geranyl acetate by E. coli was first elucidated. This study provided a new and promising strategy for geraniol biosynthesis, which laid a basis for large-scale industrial application.
format Online
Article
Text
id pubmed-4787002
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-47870022016-03-12 Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture Liu, Wei Xu, Xin Zhang, Rubing Cheng, Tao Cao, Yujin Li, Xiaoxiao Guo, Jiantao Liu, Huizhou Xian, Mo Biotechnol Biofuels Research BACKGROUND: Geraniol is an acyclic monoterpene alcohol, which exhibits good prospect as a gasoline alternative. Geraniol is naturally encountered in plants at low concentrations and an attractive target for microbial engineering. Geraniol has been heterologously produced in Escherichia coli, but the low titer hinders its industrial applications. Moreover, bioconversion of geraniol by E. coli remains largely unknown. RESULTS: Recombinant overexpression of Ocimum basilicum geraniol synthase, Abies grandis geranyl diphosphate synthase, and a heterotic mevalonate pathway in E. coli BL21 (DE3) enabled the production of up to 68.6 ± 3 mg/L geraniol in shake flasks. Initial fed-batch fermentation only increased geraniol production to 78.8 mg/L. To further improve the production yield, the fermentation conditions were optimized. Firstly, 81.4 % of volatile geraniol was lost during the first 5 h of fermentation in a solvent-free system. Hence, isopropyl myristate was added to the culture medium to form an aqueous-organic two-phase culture system, which effectively prevented volatilization of geraniol. Secondly, most of geraniol was eventually biotransformed into geranyl acetate by E. coli, thus decreasing geraniol production. For the first time, we revealed the role of acetylesterase (Aes, EC 3.1.1.6) from E. coli in hydrolyzing geranyl acetate to geraniol, and production of geraniol was successfully increased to 2.0 g/L under controlled fermentation conditions. CONCLUSIONS: An efficient geraniol production platform was established by overexpressing several key pathway proteins in engineered E. coli strain combined with a controlled fermentation system. About 2.0 g/L geraniol was obtained using our controllable aqueous-organic two-phase fermentation system, which is the highest yield to date. In addition, the interconversion between geraniol and geranyl acetate by E. coli was first elucidated. This study provided a new and promising strategy for geraniol biosynthesis, which laid a basis for large-scale industrial application. BioMed Central 2016-03-11 /pmc/articles/PMC4787002/ /pubmed/26973712 http://dx.doi.org/10.1186/s13068-016-0466-5 Text en © Liu et al. 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
Liu, Wei
Xu, Xin
Zhang, Rubing
Cheng, Tao
Cao, Yujin
Li, Xiaoxiao
Guo, Jiantao
Liu, Huizhou
Xian, Mo
Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture
title Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture
title_full Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture
title_fullStr Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture
title_full_unstemmed Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture
title_short Engineering Escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture
title_sort engineering escherichia coli for high-yield geraniol production with biotransformation of geranyl acetate to geraniol under fed-batch culture
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787002/
https://www.ncbi.nlm.nih.gov/pubmed/26973712
http://dx.doi.org/10.1186/s13068-016-0466-5
work_keys_str_mv AT liuwei engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT xuxin engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT zhangrubing engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT chengtao engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT caoyujin engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT lixiaoxiao engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT guojiantao engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT liuhuizhou engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture
AT xianmo engineeringescherichiacoliforhighyieldgeraniolproductionwithbiotransformationofgeranylacetatetogeraniolunderfedbatchculture