Cargando…

Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B

BACKGROUND: Polylactic acid (PLA), a biodegradable polymer, has the potential to replace (at least partially) traditional petroleum-based plastics, minimizing “white pollution”. However, cost-effective production of optically pure L-lactic acid is needed to achieve the full potential of PLA. Current...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Jinfang, Xu, Liyuan, Wang, Yongze, Zhao, Xiao, Wang, Jinhua, Garza, Erin, Manow, Ryan, Zhou, Shengde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693985/
https://www.ncbi.nlm.nih.gov/pubmed/23758664
http://dx.doi.org/10.1186/1475-2859-12-57
_version_ 1782274784735789056
author Zhao, Jinfang
Xu, Liyuan
Wang, Yongze
Zhao, Xiao
Wang, Jinhua
Garza, Erin
Manow, Ryan
Zhou, Shengde
author_facet Zhao, Jinfang
Xu, Liyuan
Wang, Yongze
Zhao, Xiao
Wang, Jinhua
Garza, Erin
Manow, Ryan
Zhou, Shengde
author_sort Zhao, Jinfang
collection PubMed
description BACKGROUND: Polylactic acid (PLA), a biodegradable polymer, has the potential to replace (at least partially) traditional petroleum-based plastics, minimizing “white pollution”. However, cost-effective production of optically pure L-lactic acid is needed to achieve the full potential of PLA. Currently, starch-based glucose is used for L-lactic acid fermentation by lactic acid bacteria. Due to its competition with food resources, an alternative non-food substrate such as cellulosic biomass is needed for L-lactic acid fermentation. Nevertheless, the substrate (sugar stream) derived from cellulosic biomass contains significant amounts of xylose, which is unfermentable by most lactic acid bacteria. However, the microorganisms that do ferment xylose usually carry out heterolactic acid fermentation. As a result, an alternative strain should be developed for homofermentative production of optically pure L-lactic acid using cellulosic biomass. RESULTS: In this study, an ethanologenic Escherichia coli strain, SZ470 (ΔfrdBC ΔldhA ΔackA ΔpflB ΔpdhR ::pflBp6-acEF-lpd ΔmgsA), was reengineered for homofermentative production of L-lactic acid from xylose (1.2 mole xylose = > 2 mole L-lactic acid), by deleting the alcohol dehydrogenase gene (adhE) and integrating the L-lactate dehydrogenase gene (ldhL) of Pediococcus acidilactici. The resulting strain, WL203, was metabolically evolved further through serial transfers in screw-cap tubes containing xylose, resulting in the strain WL204 with improved anaerobic cell growth. When tested in 70 g L(-1) xylose fermentation (complex medium), WL204 produced 62 g L(-1) L-lactic acid, with a maximum production rate of 1.631 g L(-1) h(-1) and a yield of 97% based on xylose metabolized. HPLC analysis using a chiral column showed that an L-lactic acid optical purity of 99.5% was achieved by WL204. CONCLUSIONS: These results demonstrated that WL204 has the potential for homofermentative production of L-lactic acid using cellulosic biomass derived substrates, which contain a significant amount of xylose.
format Online
Article
Text
id pubmed-3693985
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-36939852013-06-27 Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B Zhao, Jinfang Xu, Liyuan Wang, Yongze Zhao, Xiao Wang, Jinhua Garza, Erin Manow, Ryan Zhou, Shengde Microb Cell Fact Research BACKGROUND: Polylactic acid (PLA), a biodegradable polymer, has the potential to replace (at least partially) traditional petroleum-based plastics, minimizing “white pollution”. However, cost-effective production of optically pure L-lactic acid is needed to achieve the full potential of PLA. Currently, starch-based glucose is used for L-lactic acid fermentation by lactic acid bacteria. Due to its competition with food resources, an alternative non-food substrate such as cellulosic biomass is needed for L-lactic acid fermentation. Nevertheless, the substrate (sugar stream) derived from cellulosic biomass contains significant amounts of xylose, which is unfermentable by most lactic acid bacteria. However, the microorganisms that do ferment xylose usually carry out heterolactic acid fermentation. As a result, an alternative strain should be developed for homofermentative production of optically pure L-lactic acid using cellulosic biomass. RESULTS: In this study, an ethanologenic Escherichia coli strain, SZ470 (ΔfrdBC ΔldhA ΔackA ΔpflB ΔpdhR ::pflBp6-acEF-lpd ΔmgsA), was reengineered for homofermentative production of L-lactic acid from xylose (1.2 mole xylose = > 2 mole L-lactic acid), by deleting the alcohol dehydrogenase gene (adhE) and integrating the L-lactate dehydrogenase gene (ldhL) of Pediococcus acidilactici. The resulting strain, WL203, was metabolically evolved further through serial transfers in screw-cap tubes containing xylose, resulting in the strain WL204 with improved anaerobic cell growth. When tested in 70 g L(-1) xylose fermentation (complex medium), WL204 produced 62 g L(-1) L-lactic acid, with a maximum production rate of 1.631 g L(-1) h(-1) and a yield of 97% based on xylose metabolized. HPLC analysis using a chiral column showed that an L-lactic acid optical purity of 99.5% was achieved by WL204. CONCLUSIONS: These results demonstrated that WL204 has the potential for homofermentative production of L-lactic acid using cellulosic biomass derived substrates, which contain a significant amount of xylose. BioMed Central 2013-06-07 /pmc/articles/PMC3693985/ /pubmed/23758664 http://dx.doi.org/10.1186/1475-2859-12-57 Text en Copyright © 2013 Zhao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Zhao, Jinfang
Xu, Liyuan
Wang, Yongze
Zhao, Xiao
Wang, Jinhua
Garza, Erin
Manow, Ryan
Zhou, Shengde
Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B
title Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B
title_full Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B
title_fullStr Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B
title_full_unstemmed Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B
title_short Homofermentative production of optically pure L-lactic acid from xylose by genetically engineered Escherichia coli B
title_sort homofermentative production of optically pure l-lactic acid from xylose by genetically engineered escherichia coli b
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3693985/
https://www.ncbi.nlm.nih.gov/pubmed/23758664
http://dx.doi.org/10.1186/1475-2859-12-57
work_keys_str_mv AT zhaojinfang homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib
AT xuliyuan homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib
AT wangyongze homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib
AT zhaoxiao homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib
AT wangjinhua homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib
AT garzaerin homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib
AT manowryan homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib
AT zhoushengde homofermentativeproductionofopticallypurellacticacidfromxylosebygeneticallyengineeredescherichiacolib