Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchari
Abstract Background Despite its ability to grow and produce high-value molecules using renewable carbon sources, two main factors must be improved to use Burkholderia sacchari as a chassis for bioproduction at an industrial scale: first, the lack of molecular tools to engineer this organism and seco...
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doaj-5bceb1e5787a4b02a1d08e37505a07bb2020-11-25T02:01:48ZengBMCMicrobial Cell Factories1475-28592018-05-0117111110.1186/s12934-018-0924-9Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchariLinda P. Guamán0Carlos Barba-Ostria1Fuzhong Zhang2Edmar R. Oliveira-Filho3José Gregório C. Gomez4Luiziana F. Silva5Universidad Tecnológica Equinoccial, Centro de Investigación Biomédica, Facultad de Ciencias de la Salud Eugenio EspejoDepartment of Microbiology, Institute of Biomedical Sciences, University of São PauloDepartment of Energy, Environmental and Chemical Engineering, Washington University in St. LouisDepartment of Microbiology, Institute of Biomedical Sciences, University of São PauloDepartment of Microbiology, Institute of Biomedical Sciences, University of São PauloDepartment of Microbiology, Institute of Biomedical Sciences, University of São PauloAbstract Background Despite its ability to grow and produce high-value molecules using renewable carbon sources, two main factors must be improved to use Burkholderia sacchari as a chassis for bioproduction at an industrial scale: first, the lack of molecular tools to engineer this organism and second, the inherently slow growth rate and poly-3-hydroxybutyrate [P(3HB)] production using xylose. In this work, we have addressed both factors. Results First, we adapted a set of BglBrick plasmids and showed tunable expression in B. sacchari. Finally, we assessed growth rate and P(3HB) production through overexpression of xylose transporters, catabolic or regulatory genes. Overexpression of xylR significantly improved growth rate (55.5% improvement), polymer yield (77.27% improvement), and resulted in 71% of cell dry weight as P(3HB). Conclusions These values are unprecedented for P(3HB) accumulation using xylose as a sole carbon source and highlight the importance of precise expression control for improving utilization of hemicellulosic sugars in B. sacchari.http://link.springer.com/article/10.1186/s12934-018-0924-9BurkholderiaXyloseP(3HB)xylRBglBricks |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Linda P. Guamán Carlos Barba-Ostria Fuzhong Zhang Edmar R. Oliveira-Filho José Gregório C. Gomez Luiziana F. Silva |
spellingShingle |
Linda P. Guamán Carlos Barba-Ostria Fuzhong Zhang Edmar R. Oliveira-Filho José Gregório C. Gomez Luiziana F. Silva Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchari Microbial Cell Factories Burkholderia Xylose P(3HB) xylR BglBricks |
author_facet |
Linda P. Guamán Carlos Barba-Ostria Fuzhong Zhang Edmar R. Oliveira-Filho José Gregório C. Gomez Luiziana F. Silva |
author_sort |
Linda P. Guamán |
title |
Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchari |
title_short |
Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchari |
title_full |
Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchari |
title_fullStr |
Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchari |
title_full_unstemmed |
Engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium Burkholderia sacchari |
title_sort |
engineering xylose metabolism for production of polyhydroxybutyrate in the non-model bacterium burkholderia sacchari |
publisher |
BMC |
series |
Microbial Cell Factories |
issn |
1475-2859 |
publishDate |
2018-05-01 |
description |
Abstract Background Despite its ability to grow and produce high-value molecules using renewable carbon sources, two main factors must be improved to use Burkholderia sacchari as a chassis for bioproduction at an industrial scale: first, the lack of molecular tools to engineer this organism and second, the inherently slow growth rate and poly-3-hydroxybutyrate [P(3HB)] production using xylose. In this work, we have addressed both factors. Results First, we adapted a set of BglBrick plasmids and showed tunable expression in B. sacchari. Finally, we assessed growth rate and P(3HB) production through overexpression of xylose transporters, catabolic or regulatory genes. Overexpression of xylR significantly improved growth rate (55.5% improvement), polymer yield (77.27% improvement), and resulted in 71% of cell dry weight as P(3HB). Conclusions These values are unprecedented for P(3HB) accumulation using xylose as a sole carbon source and highlight the importance of precise expression control for improving utilization of hemicellulosic sugars in B. sacchari. |
topic |
Burkholderia Xylose P(3HB) xylR BglBricks |
url |
http://link.springer.com/article/10.1186/s12934-018-0924-9 |
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