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Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus
BACKGROUND: Itaconic acid is on the DOE (Department of Energy) top 12 list of biotechnologically produced building block chemicals and is produced commercially by Aspergillus terreus. However, the production cost of itaconic acid is too high to be economically competitive with the petrochemical-base...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145239/ https://www.ncbi.nlm.nih.gov/pubmed/25162619 http://dx.doi.org/10.1186/s12934-014-0108-1 |
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author | Huang, Xuenian Chen, Mei Lu, Xuefeng Li, Yueming Li, Xia Li, Jian-Jun |
author_facet | Huang, Xuenian Chen, Mei Lu, Xuefeng Li, Yueming Li, Xia Li, Jian-Jun |
author_sort | Huang, Xuenian |
collection | PubMed |
description | BACKGROUND: Itaconic acid is on the DOE (Department of Energy) top 12 list of biotechnologically produced building block chemicals and is produced commercially by Aspergillus terreus. However, the production cost of itaconic acid is too high to be economically competitive with the petrochemical-based products. Itaconic acid is generally produced from raw corn starch, including three steps: enzymatic hydrolysis of corn starch into a glucose-rich syrup by α-amylase and glucoamylase, fermentation, and recovery of itaconic acid. The whole process is very time-consuming and energy-intensive. RESULTS: In order to reduce the production cost, saccharification and fermentation were integrated into one step through overexpressing the glucoamylase gene in A. terreus under the control of the native PcitA promoter. The transformant XH61-5 produced higher itaconate titer from liquefied starch than WT. To further increase the titer by enhancing the secretion capacity of overexpressed glucoamylase, a stronger signal peptide was selected based on the major secreted protein ATEG_02176 (an acid phosphatase precursor) by A. terreus under the itaconate production conditions. Under the control of the stronger signal peptide, the transformant XH86-8 showed higher itaconate production level than XH61-5 from liquefied starch. The itaconate titer was further enhanced through a two-step process involving the vegetative and production phase, and the transformant XH86-8 produced comparable itaconate titer from liquefied starch to current one (~80 g/L) from saccharified starch hydrolysates in industry. The effects of the new signal peptide and the two-step process on itaconate production were investigated and discussed. CONCLUSIONS: Itaconic acid could be efficiently produced from liquefied corn starch by overexpressing the glucoamylase gene in A. terreus, which will be helpful for constructing a highly efficient microbial cell factory for itaconate production and for further lowering the production cost of itaconic acid. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-014-0108-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4145239 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41452392014-08-28 Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus Huang, Xuenian Chen, Mei Lu, Xuefeng Li, Yueming Li, Xia Li, Jian-Jun Microb Cell Fact Research BACKGROUND: Itaconic acid is on the DOE (Department of Energy) top 12 list of biotechnologically produced building block chemicals and is produced commercially by Aspergillus terreus. However, the production cost of itaconic acid is too high to be economically competitive with the petrochemical-based products. Itaconic acid is generally produced from raw corn starch, including three steps: enzymatic hydrolysis of corn starch into a glucose-rich syrup by α-amylase and glucoamylase, fermentation, and recovery of itaconic acid. The whole process is very time-consuming and energy-intensive. RESULTS: In order to reduce the production cost, saccharification and fermentation were integrated into one step through overexpressing the glucoamylase gene in A. terreus under the control of the native PcitA promoter. The transformant XH61-5 produced higher itaconate titer from liquefied starch than WT. To further increase the titer by enhancing the secretion capacity of overexpressed glucoamylase, a stronger signal peptide was selected based on the major secreted protein ATEG_02176 (an acid phosphatase precursor) by A. terreus under the itaconate production conditions. Under the control of the stronger signal peptide, the transformant XH86-8 showed higher itaconate production level than XH61-5 from liquefied starch. The itaconate titer was further enhanced through a two-step process involving the vegetative and production phase, and the transformant XH86-8 produced comparable itaconate titer from liquefied starch to current one (~80 g/L) from saccharified starch hydrolysates in industry. The effects of the new signal peptide and the two-step process on itaconate production were investigated and discussed. CONCLUSIONS: Itaconic acid could be efficiently produced from liquefied corn starch by overexpressing the glucoamylase gene in A. terreus, which will be helpful for constructing a highly efficient microbial cell factory for itaconate production and for further lowering the production cost of itaconic acid. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12934-014-0108-1) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-17 /pmc/articles/PMC4145239/ /pubmed/25162619 http://dx.doi.org/10.1186/s12934-014-0108-1 Text en © Huang et al. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Huang, Xuenian Chen, Mei Lu, Xuefeng Li, Yueming Li, Xia Li, Jian-Jun Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus |
title | Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus |
title_full | Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus |
title_fullStr | Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus |
title_full_unstemmed | Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus |
title_short | Direct production of itaconic acid from liquefied corn starch by genetically engineered Aspergillus terreus |
title_sort | direct production of itaconic acid from liquefied corn starch by genetically engineered aspergillus terreus |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4145239/ https://www.ncbi.nlm.nih.gov/pubmed/25162619 http://dx.doi.org/10.1186/s12934-014-0108-1 |
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