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Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli

BACKGROUND: A multi-monocistronic synthetic vector was used to assemble multiple genes of a nucleotide diphosphate (NDP)-sugar biosynthetic pathway to construct robust genetic circuits for the production of valuable flavonoid glycosides in Escherichia coli. Characterized functional genes involved in...

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Autores principales: Parajuli, Prakash, Pandey, Ramesh Prasad, Trang, Nguyen Thi Huyen, Chaudhary, Amit Kumar, Sohng, Jae Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459062/
https://www.ncbi.nlm.nih.gov/pubmed/26051114
http://dx.doi.org/10.1186/s12934-015-0261-1
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author Parajuli, Prakash
Pandey, Ramesh Prasad
Trang, Nguyen Thi Huyen
Chaudhary, Amit Kumar
Sohng, Jae Kyung
author_facet Parajuli, Prakash
Pandey, Ramesh Prasad
Trang, Nguyen Thi Huyen
Chaudhary, Amit Kumar
Sohng, Jae Kyung
author_sort Parajuli, Prakash
collection PubMed
description BACKGROUND: A multi-monocistronic synthetic vector was used to assemble multiple genes of a nucleotide diphosphate (NDP)-sugar biosynthetic pathway to construct robust genetic circuits for the production of valuable flavonoid glycosides in Escherichia coli. Characterized functional genes involved in the biosynthesis of uridine diphosphate (UDP)-glucose and thymidine diphosphate (TDP)-rhamnose from various microbial sources along with glucose facilitator diffusion protein (glf) and glucokinase (glk) from Zymomonas mobilis were assembled and overexpressed in a single synthetic multi-monocistronic operon. RESULTS: The newly generated NDP-sugars biosynthesis circuits along with regiospecific glycosyltransferases from plants were introduced in E. coli BL21 (DE3) to probe the bioconversion of fisetin, a medicinally important polyphenol produced by various plants. As a result, approximately 1.178 g of fisetin 3-O-glucoside and 1.026 g of fisetin 3-O-rhamnoside were produced in UDP-glucose and TDP-rhamnose biosynthesis systems respectively, after 48 h of incubation in 3 L fermentor while supplementing 0.9 g of fisetin. These yields of fisetin glycosides represent ~99% of bioconversion of exogenously supplemented fisetin. The systems were also found to be highly effective in bio-transforming other flavonols (quercetin, kaempferol, myricetin) into their respective glycosides, achieving over 95% substrate conversion. CONCLUSION: The construction of a synthetic expression vector for bacterial cell factory followed by subsequent re-direction of metabolic flux towards desirable products have always been revolutionized the biotechnological processes and technologies. This multi-monocistronic synthetic vector in a microbial platform is customizable to defined task and would certainly be useful for applications in producing and modifying such therapeutically valued plant secondary metabolites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0261-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-44590622015-06-09 Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli Parajuli, Prakash Pandey, Ramesh Prasad Trang, Nguyen Thi Huyen Chaudhary, Amit Kumar Sohng, Jae Kyung Microb Cell Fact Research BACKGROUND: A multi-monocistronic synthetic vector was used to assemble multiple genes of a nucleotide diphosphate (NDP)-sugar biosynthetic pathway to construct robust genetic circuits for the production of valuable flavonoid glycosides in Escherichia coli. Characterized functional genes involved in the biosynthesis of uridine diphosphate (UDP)-glucose and thymidine diphosphate (TDP)-rhamnose from various microbial sources along with glucose facilitator diffusion protein (glf) and glucokinase (glk) from Zymomonas mobilis were assembled and overexpressed in a single synthetic multi-monocistronic operon. RESULTS: The newly generated NDP-sugars biosynthesis circuits along with regiospecific glycosyltransferases from plants were introduced in E. coli BL21 (DE3) to probe the bioconversion of fisetin, a medicinally important polyphenol produced by various plants. As a result, approximately 1.178 g of fisetin 3-O-glucoside and 1.026 g of fisetin 3-O-rhamnoside were produced in UDP-glucose and TDP-rhamnose biosynthesis systems respectively, after 48 h of incubation in 3 L fermentor while supplementing 0.9 g of fisetin. These yields of fisetin glycosides represent ~99% of bioconversion of exogenously supplemented fisetin. The systems were also found to be highly effective in bio-transforming other flavonols (quercetin, kaempferol, myricetin) into their respective glycosides, achieving over 95% substrate conversion. CONCLUSION: The construction of a synthetic expression vector for bacterial cell factory followed by subsequent re-direction of metabolic flux towards desirable products have always been revolutionized the biotechnological processes and technologies. This multi-monocistronic synthetic vector in a microbial platform is customizable to defined task and would certainly be useful for applications in producing and modifying such therapeutically valued plant secondary metabolites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-015-0261-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-09 /pmc/articles/PMC4459062/ /pubmed/26051114 http://dx.doi.org/10.1186/s12934-015-0261-1 Text en © Parajuli et al. 2015 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
Parajuli, Prakash
Pandey, Ramesh Prasad
Trang, Nguyen Thi Huyen
Chaudhary, Amit Kumar
Sohng, Jae Kyung
Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli
title Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli
title_full Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli
title_fullStr Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli
title_full_unstemmed Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli
title_short Synthetic sugar cassettes for the efficient production of flavonol glycosides in Escherichia coli
title_sort synthetic sugar cassettes for the efficient production of flavonol glycosides in escherichia coli
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459062/
https://www.ncbi.nlm.nih.gov/pubmed/26051114
http://dx.doi.org/10.1186/s12934-015-0261-1
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