Cargando…

Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production

BACKGROUND: Cocoa butter (CB) extracted from cocoa beans (Theobroma cacao) is the main raw material for chocolate production, but CB supply is insufficient due to the increased chocolate demand and limited CB production. CB is mainly composed of three different kinds of triacylglycerols (TAGs), 1,3-...

Descripción completa

Detalles Bibliográficos
Autores principales: Wei, Yongjun, Bergenholm, David, Gossing, Michael, Siewers, Verena, Nielsen, Jens
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784687/
https://www.ncbi.nlm.nih.gov/pubmed/29370801
http://dx.doi.org/10.1186/s12934-018-0866-2
_version_ 1783295498436739072
author Wei, Yongjun
Bergenholm, David
Gossing, Michael
Siewers, Verena
Nielsen, Jens
author_facet Wei, Yongjun
Bergenholm, David
Gossing, Michael
Siewers, Verena
Nielsen, Jens
author_sort Wei, Yongjun
collection PubMed
description BACKGROUND: Cocoa butter (CB) extracted from cocoa beans (Theobroma cacao) is the main raw material for chocolate production, but CB supply is insufficient due to the increased chocolate demand and limited CB production. CB is mainly composed of three different kinds of triacylglycerols (TAGs), 1,3-dipalmitoyl-2-oleoyl-glycerol (POP, C16:0-C18:1-C16:0), 1-palmitoyl-3-stearoyl-2-oleoyl-glycerol (POS, C16:0-C18:1-C18:0) and 1,3-distearoyl-2-oleoyl-glycerol (SOS, C18:0-C18:1-C18:0). In general, Saccharomyces cerevisiae produces TAGs as storage lipids, which consist of C16 and C18 fatty acids. However, cocoa butter-like lipids (CBL, which are composed of POP, POS and SOS) are not among the major TAG forms in yeast. TAG biosynthesis is mainly catalyzed by three enzymes: glycerol-3-phosphate acyltransferase (GPAT), lysophospholipid acyltransferase (LPAT) and diacylglycerol acyltransferase (DGAT), and it is essential to modulate the yeast TAG biosynthetic pathway for higher CBL production. RESULTS: We cloned seven GPAT genes and three LPAT genes from cocoa cDNA, in order to screen for CBL biosynthetic gene candidates. By expressing these cloned cocoa genes and two synthesized cocoa DGAT genes in S. cerevisiae, we successfully increased total fatty acid production, TAG production and CBL production in some of the strains. In the best producer, the potential CBL content was eightfold higher than the control strain, suggesting the cocoa genes expressed in this strain were functional and might be responsible for CBL biosynthesis. Moreover, the potential CBL content increased 134-fold over the control Y29-TcD1 (IMX581 sct1Δ ale1Δ lro1Δ dga1Δ with TcDGAT1 expression) in strain Y29-441 (IMX581 sct1Δ ale1Δ lro1Δ dga1Δ with TcGPAT4, TcLPAT4 and TcDGAT1 expression) further suggesting cocoa GPAT and LPAT genes functioned in yeast. CONCLUSIONS: We demonstrated that cocoa TAG biosynthetic genes functioned in S. cerevisiae and identified cocoa genes that may be involved in CBL production. Moreover, we found that expression of some cocoa CBL biosynthetic genes improved potential CBL production in S. cerevisiae, showing that metabolic engineering of yeast for cocoa butter production can be realized by manipulating the key enzymes GPAT, LPAT and DGAT in the TAG biosynthetic pathway. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0866-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5784687
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-57846872018-02-07 Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production Wei, Yongjun Bergenholm, David Gossing, Michael Siewers, Verena Nielsen, Jens Microb Cell Fact Research BACKGROUND: Cocoa butter (CB) extracted from cocoa beans (Theobroma cacao) is the main raw material for chocolate production, but CB supply is insufficient due to the increased chocolate demand and limited CB production. CB is mainly composed of three different kinds of triacylglycerols (TAGs), 1,3-dipalmitoyl-2-oleoyl-glycerol (POP, C16:0-C18:1-C16:0), 1-palmitoyl-3-stearoyl-2-oleoyl-glycerol (POS, C16:0-C18:1-C18:0) and 1,3-distearoyl-2-oleoyl-glycerol (SOS, C18:0-C18:1-C18:0). In general, Saccharomyces cerevisiae produces TAGs as storage lipids, which consist of C16 and C18 fatty acids. However, cocoa butter-like lipids (CBL, which are composed of POP, POS and SOS) are not among the major TAG forms in yeast. TAG biosynthesis is mainly catalyzed by three enzymes: glycerol-3-phosphate acyltransferase (GPAT), lysophospholipid acyltransferase (LPAT) and diacylglycerol acyltransferase (DGAT), and it is essential to modulate the yeast TAG biosynthetic pathway for higher CBL production. RESULTS: We cloned seven GPAT genes and three LPAT genes from cocoa cDNA, in order to screen for CBL biosynthetic gene candidates. By expressing these cloned cocoa genes and two synthesized cocoa DGAT genes in S. cerevisiae, we successfully increased total fatty acid production, TAG production and CBL production in some of the strains. In the best producer, the potential CBL content was eightfold higher than the control strain, suggesting the cocoa genes expressed in this strain were functional and might be responsible for CBL biosynthesis. Moreover, the potential CBL content increased 134-fold over the control Y29-TcD1 (IMX581 sct1Δ ale1Δ lro1Δ dga1Δ with TcDGAT1 expression) in strain Y29-441 (IMX581 sct1Δ ale1Δ lro1Δ dga1Δ with TcGPAT4, TcLPAT4 and TcDGAT1 expression) further suggesting cocoa GPAT and LPAT genes functioned in yeast. CONCLUSIONS: We demonstrated that cocoa TAG biosynthetic genes functioned in S. cerevisiae and identified cocoa genes that may be involved in CBL production. Moreover, we found that expression of some cocoa CBL biosynthetic genes improved potential CBL production in S. cerevisiae, showing that metabolic engineering of yeast for cocoa butter production can be realized by manipulating the key enzymes GPAT, LPAT and DGAT in the TAG biosynthetic pathway. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-0866-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-01-25 /pmc/articles/PMC5784687/ /pubmed/29370801 http://dx.doi.org/10.1186/s12934-018-0866-2 Text en © The Author(s) 2018 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
Wei, Yongjun
Bergenholm, David
Gossing, Michael
Siewers, Verena
Nielsen, Jens
Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production
title Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production
title_full Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production
title_fullStr Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production
title_full_unstemmed Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production
title_short Expression of cocoa genes in Saccharomyces cerevisiae improves cocoa butter production
title_sort expression of cocoa genes in saccharomyces cerevisiae improves cocoa butter production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784687/
https://www.ncbi.nlm.nih.gov/pubmed/29370801
http://dx.doi.org/10.1186/s12934-018-0866-2
work_keys_str_mv AT weiyongjun expressionofcocoagenesinsaccharomycescerevisiaeimprovescocoabutterproduction
AT bergenholmdavid expressionofcocoagenesinsaccharomycescerevisiaeimprovescocoabutterproduction
AT gossingmichael expressionofcocoagenesinsaccharomycescerevisiaeimprovescocoabutterproduction
AT siewersverena expressionofcocoagenesinsaccharomycescerevisiaeimprovescocoabutterproduction
AT nielsenjens expressionofcocoagenesinsaccharomycescerevisiaeimprovescocoabutterproduction