Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocess

Abstract In bacterial system, direct conversion of xylose to xylonic acid is mediated through NAD-dependent xylose dehydrogenase (xylB) and xylonolactonase (xylC) genes. Heterologous expression of these genes from Caulobacter crescentus into recombinant Corynebacterium glutamicum ATCC 13032 and C. g...

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Main Authors: M. S. Lekshmi Sundar, Aliyath Susmitha, Devi Rajan, Silvin Hannibal, Keerthi Sasikumar, Volker F. Wendisch, K. Madhavan Nampoothiri
Format: Article
Language:English
Published: SpringerOpen 2020-04-01
Series:AMB Express
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13568-020-01003-9
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spelling doaj-9a50bcd12ff84cc3add71e80870355ef2020-11-25T02:01:14ZengSpringerOpenAMB Express2191-08552020-04-0110111110.1186/s13568-020-01003-9Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocessM. S. Lekshmi Sundar0Aliyath Susmitha1Devi Rajan2Silvin Hannibal3Keerthi Sasikumar4Volker F. Wendisch5K. Madhavan Nampoothiri6Microbial Processes and Technology Division, CSIR–National Institute for Interdisciplinary Science and Technology (NIIST)Microbial Processes and Technology Division, CSIR–National Institute for Interdisciplinary Science and Technology (NIIST)Microbial Processes and Technology Division, CSIR–National Institute for Interdisciplinary Science and Technology (NIIST)Genetics of Prokaryotes, Faculty of Biology & CeBiTec, Bielefeld UniversityMicrobial Processes and Technology Division, CSIR–National Institute for Interdisciplinary Science and Technology (NIIST)Genetics of Prokaryotes, Faculty of Biology & CeBiTec, Bielefeld UniversityMicrobial Processes and Technology Division, CSIR–National Institute for Interdisciplinary Science and Technology (NIIST)Abstract In bacterial system, direct conversion of xylose to xylonic acid is mediated through NAD-dependent xylose dehydrogenase (xylB) and xylonolactonase (xylC) genes. Heterologous expression of these genes from Caulobacter crescentus into recombinant Corynebacterium glutamicum ATCC 13032 and C. glutamicum ATCC 31831 (with an innate pentose transporter, araE) resulted in an efficient bioconversion process to produce xylonic acid from xylose. Process parameters including the design of production medium was optimized using a statistical tool, Response Surface Methodology (RSM). Maximum xylonic acid of 56.32 g/L from 60 g/L xylose, i.e. about 76.67% of the maximum theoretical yield was obtained after 120 h fermentation from pure xylose with recombinant C. glutamicum ATCC 31831 containing the plasmid pVWEx1 xylB. Under the same condition, the production with recombinant C. glutamicum ATCC 13032 (with pVWEx1 xylB) was 50.66 g/L, i.e. 69% of the theoretical yield. There was no significant improvement in production with the simultaneous expression of xylB and xylC genes together indicating xylose dehydrogenase activity as one of the rate limiting factor in the bioconversion. Finally, proof of concept experiment in utilizing biomass derived pentose sugar, xylose, for xylonic acid production was also carried out and obtained 42.94 g/L xylonic acid from 60 g/L xylose. These results promise a significant value addition for the future bio refinery programs.http://link.springer.com/article/10.1186/s13568-020-01003-9Corynebacterium glutamicumBiomassHeterologous expressionResponse surface methodology (RSM)XyloseXylonic acid
collection DOAJ
language English
format Article
sources DOAJ
author M. S. Lekshmi Sundar
Aliyath Susmitha
Devi Rajan
Silvin Hannibal
Keerthi Sasikumar
Volker F. Wendisch
K. Madhavan Nampoothiri
spellingShingle M. S. Lekshmi Sundar
Aliyath Susmitha
Devi Rajan
Silvin Hannibal
Keerthi Sasikumar
Volker F. Wendisch
K. Madhavan Nampoothiri
Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocess
AMB Express
Corynebacterium glutamicum
Biomass
Heterologous expression
Response surface methodology (RSM)
Xylose
Xylonic acid
author_facet M. S. Lekshmi Sundar
Aliyath Susmitha
Devi Rajan
Silvin Hannibal
Keerthi Sasikumar
Volker F. Wendisch
K. Madhavan Nampoothiri
author_sort M. S. Lekshmi Sundar
title Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocess
title_short Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocess
title_full Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocess
title_fullStr Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocess
title_full_unstemmed Heterologous expression of genes for bioconversion of xylose to xylonic acid in Corynebacterium glutamicum and optimization of the bioprocess
title_sort heterologous expression of genes for bioconversion of xylose to xylonic acid in corynebacterium glutamicum and optimization of the bioprocess
publisher SpringerOpen
series AMB Express
issn 2191-0855
publishDate 2020-04-01
description Abstract In bacterial system, direct conversion of xylose to xylonic acid is mediated through NAD-dependent xylose dehydrogenase (xylB) and xylonolactonase (xylC) genes. Heterologous expression of these genes from Caulobacter crescentus into recombinant Corynebacterium glutamicum ATCC 13032 and C. glutamicum ATCC 31831 (with an innate pentose transporter, araE) resulted in an efficient bioconversion process to produce xylonic acid from xylose. Process parameters including the design of production medium was optimized using a statistical tool, Response Surface Methodology (RSM). Maximum xylonic acid of 56.32 g/L from 60 g/L xylose, i.e. about 76.67% of the maximum theoretical yield was obtained after 120 h fermentation from pure xylose with recombinant C. glutamicum ATCC 31831 containing the plasmid pVWEx1 xylB. Under the same condition, the production with recombinant C. glutamicum ATCC 13032 (with pVWEx1 xylB) was 50.66 g/L, i.e. 69% of the theoretical yield. There was no significant improvement in production with the simultaneous expression of xylB and xylC genes together indicating xylose dehydrogenase activity as one of the rate limiting factor in the bioconversion. Finally, proof of concept experiment in utilizing biomass derived pentose sugar, xylose, for xylonic acid production was also carried out and obtained 42.94 g/L xylonic acid from 60 g/L xylose. These results promise a significant value addition for the future bio refinery programs.
topic Corynebacterium glutamicum
Biomass
Heterologous expression
Response surface methodology (RSM)
Xylose
Xylonic acid
url http://link.springer.com/article/10.1186/s13568-020-01003-9
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