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Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway
BACKGROUND: The oleaginous yeast, Yarrowia lipolytica, has been utilized as an industrial host for about 60 years for various applications. Recently, the metabolic engineering of this host has become increasingly popular due to its ability to accumulate lipids as well as improvements made toward dev...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955270/ https://www.ncbi.nlm.nih.gov/pubmed/27446238 http://dx.doi.org/10.1186/s13068-016-0562-6 |
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author | Rodriguez, Gabriel M. Hussain, Murtaza Shabbir Gambill, Lauren Gao, Difeng Yaguchi, Allison Blenner, Mark |
author_facet | Rodriguez, Gabriel M. Hussain, Murtaza Shabbir Gambill, Lauren Gao, Difeng Yaguchi, Allison Blenner, Mark |
author_sort | Rodriguez, Gabriel M. |
collection | PubMed |
description | BACKGROUND: The oleaginous yeast, Yarrowia lipolytica, has been utilized as an industrial host for about 60 years for various applications. Recently, the metabolic engineering of this host has become increasingly popular due to its ability to accumulate lipids as well as improvements made toward developing new genetic tools. Y. lipolytica can robustly metabolize glucose, glycerol, and even different lipid classes. However, little is known about its xylose metabolizing capability. Given the desirability of having a robust xylose utilizing strain of Y. lipolytica, we performed a comprehensive investigation and elucidation of the existing components of its xylose metabolic pathway. RESULTS: A quick and efficient means of determining functionality of the candidate xylose pathway genes (XYR, XDH, and XKS) from Y. lipolytica was desirable. We challenged Escherichia coli mutants lacking either the xylose isomerase (xylA) gene or the xylulose kinase (xylB) gene to grow on xylose minimal media by expressing the candidate genes from Y. lipolytica. We showed that the XKS of Y. lipolytica is able to rescue xylose growth of E. coli ΔxylB, and the XDH enabled growth on xylitol, but not on xylose, of E. coli ΔxylA. Overexpression of XKS and XDH in Y. lipolytica improved growth on xylitol, indicating that expression of the native enzymes was limiting. Overexpression of XKS and XDH in Y. lipolytica also enables robust growth on xylose under high nitrogen conditions without the need for adaptation. These results prove that a complete xylose pathway exists in Y. lipolytica, but the pathway is poorly expressed. To elucidate the XYR gene, we applied the E. coli ΔxylA xylose growth challenge with 14 candidate XYR genes and XDH. The XYR2 candidate was able to rescue growth of E. coli ΔxylA xylose on minimal media. CONCLUSIONS: While a native xylose pathway exists in Y. lipolytica, the microorganism’s inability to grow robustly on xylose is an effect of cryptic genetic circuits that control expression of key enzymes in the metabolic pathway. We have characterized the key enzymes associated with xylose metabolism and demonstrated that gene regulatory issues can be overcome using strong hybrid promoters to attain robust growth on xylose without adaptation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0562-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4955270 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49552702016-07-22 Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway Rodriguez, Gabriel M. Hussain, Murtaza Shabbir Gambill, Lauren Gao, Difeng Yaguchi, Allison Blenner, Mark Biotechnol Biofuels Research BACKGROUND: The oleaginous yeast, Yarrowia lipolytica, has been utilized as an industrial host for about 60 years for various applications. Recently, the metabolic engineering of this host has become increasingly popular due to its ability to accumulate lipids as well as improvements made toward developing new genetic tools. Y. lipolytica can robustly metabolize glucose, glycerol, and even different lipid classes. However, little is known about its xylose metabolizing capability. Given the desirability of having a robust xylose utilizing strain of Y. lipolytica, we performed a comprehensive investigation and elucidation of the existing components of its xylose metabolic pathway. RESULTS: A quick and efficient means of determining functionality of the candidate xylose pathway genes (XYR, XDH, and XKS) from Y. lipolytica was desirable. We challenged Escherichia coli mutants lacking either the xylose isomerase (xylA) gene or the xylulose kinase (xylB) gene to grow on xylose minimal media by expressing the candidate genes from Y. lipolytica. We showed that the XKS of Y. lipolytica is able to rescue xylose growth of E. coli ΔxylB, and the XDH enabled growth on xylitol, but not on xylose, of E. coli ΔxylA. Overexpression of XKS and XDH in Y. lipolytica improved growth on xylitol, indicating that expression of the native enzymes was limiting. Overexpression of XKS and XDH in Y. lipolytica also enables robust growth on xylose under high nitrogen conditions without the need for adaptation. These results prove that a complete xylose pathway exists in Y. lipolytica, but the pathway is poorly expressed. To elucidate the XYR gene, we applied the E. coli ΔxylA xylose growth challenge with 14 candidate XYR genes and XDH. The XYR2 candidate was able to rescue growth of E. coli ΔxylA xylose on minimal media. CONCLUSIONS: While a native xylose pathway exists in Y. lipolytica, the microorganism’s inability to grow robustly on xylose is an effect of cryptic genetic circuits that control expression of key enzymes in the metabolic pathway. We have characterized the key enzymes associated with xylose metabolism and demonstrated that gene regulatory issues can be overcome using strong hybrid promoters to attain robust growth on xylose without adaptation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13068-016-0562-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-21 /pmc/articles/PMC4955270/ /pubmed/27446238 http://dx.doi.org/10.1186/s13068-016-0562-6 Text en © The Author(s) 2016 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 Rodriguez, Gabriel M. Hussain, Murtaza Shabbir Gambill, Lauren Gao, Difeng Yaguchi, Allison Blenner, Mark Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway |
title | Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway |
title_full | Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway |
title_fullStr | Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway |
title_full_unstemmed | Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway |
title_short | Engineering xylose utilization in Yarrowia lipolytica by understanding its cryptic xylose pathway |
title_sort | engineering xylose utilization in yarrowia lipolytica by understanding its cryptic xylose pathway |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955270/ https://www.ncbi.nlm.nih.gov/pubmed/27446238 http://dx.doi.org/10.1186/s13068-016-0562-6 |
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