Engineering yeast artificial core promoter with designated base motifs

Abstract Background Synthetic biology requires toolbox of promoters to finely tune gene expression levels for building up efficient cell factories. Yeast promoters owned variable core promoter regions between the TATA-box and transcriptional starting site (TSS) at the length mostly around 20–80 base...

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Main Authors: Rui Liu, Lanqing Liu, Xia Li, Duo Liu, Yingjin Yuan
Format: Article
Language:English
Published: BMC 2020-02-01
Series:Microbial Cell Factories
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12934-020-01305-4
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author Rui Liu
Lanqing Liu
Xia Li
Duo Liu
Yingjin Yuan
author_facet Rui Liu
Lanqing Liu
Xia Li
Duo Liu
Yingjin Yuan
author_sort Rui Liu
collection DOAJ
description Abstract Background Synthetic biology requires toolbox of promoters to finely tune gene expression levels for building up efficient cell factories. Yeast promoters owned variable core promoter regions between the TATA-box and transcriptional starting site (TSS) at the length mostly around 20–80 bases. This region allowed flexible design of artificial promoter but potentially demand special base motifs to maintain or enhance the promoter’s strength. Results Here, we designed and screened the base motifs and tested the activities of yeast artificial core promoters. Different 30 bases of artificial sequences led to variable expression levels of CrtY enzyme which determined the lycopene–carotene compositions, represented in the colony-color spectrum of red–orange–yellow. The upstream sequences of two strong promoter PEXP1 and PGPD and two starting strains with distinguishable lycopene production levels were utilized to characterize the promoter sequences. Different partition designs of T-rich or G/C-rich base motifs led to distinguishable colony-color distributions. Finally, we screened a champion promoter with a highest 5.5-fold enhancement of lycopene–carotene transformation. Another selected promoter generated a highest beta-carotene production as 7.4 mg/g DCW. Conclusions This work offered an approach to redesign promoter with artificial sequences. We concluded that the core promoter region could be designated as 30 bases and different base motifs would enhance or weaken the promoter’s strength. Generally, more T-rich elements, higher %T and lower G/C percentage were beneficial to enhance the strength of artificial core promoter.
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spelling doaj.art-52aeacb18ea8455bb0cc4238e0f7ca652022-12-21T23:42:35ZengBMCMicrobial Cell Factories1475-28592020-02-011911910.1186/s12934-020-01305-4Engineering yeast artificial core promoter with designated base motifsRui Liu0Lanqing Liu1Xia Li2Duo Liu3Yingjin Yuan4Frontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin UniversityFrontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin UniversityFrontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin UniversityFrontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin UniversityFrontier Science Center for Synthetic Biology and Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin UniversityAbstract Background Synthetic biology requires toolbox of promoters to finely tune gene expression levels for building up efficient cell factories. Yeast promoters owned variable core promoter regions between the TATA-box and transcriptional starting site (TSS) at the length mostly around 20–80 bases. This region allowed flexible design of artificial promoter but potentially demand special base motifs to maintain or enhance the promoter’s strength. Results Here, we designed and screened the base motifs and tested the activities of yeast artificial core promoters. Different 30 bases of artificial sequences led to variable expression levels of CrtY enzyme which determined the lycopene–carotene compositions, represented in the colony-color spectrum of red–orange–yellow. The upstream sequences of two strong promoter PEXP1 and PGPD and two starting strains with distinguishable lycopene production levels were utilized to characterize the promoter sequences. Different partition designs of T-rich or G/C-rich base motifs led to distinguishable colony-color distributions. Finally, we screened a champion promoter with a highest 5.5-fold enhancement of lycopene–carotene transformation. Another selected promoter generated a highest beta-carotene production as 7.4 mg/g DCW. Conclusions This work offered an approach to redesign promoter with artificial sequences. We concluded that the core promoter region could be designated as 30 bases and different base motifs would enhance or weaken the promoter’s strength. Generally, more T-rich elements, higher %T and lower G/C percentage were beneficial to enhance the strength of artificial core promoter.http://link.springer.com/article/10.1186/s12934-020-01305-4Synthetic biologyPromoterCore promoterYarrowia lipolyticaLycopeneCarotene
spellingShingle Rui Liu
Lanqing Liu
Xia Li
Duo Liu
Yingjin Yuan
Engineering yeast artificial core promoter with designated base motifs
Microbial Cell Factories
Synthetic biology
Promoter
Core promoter
Yarrowia lipolytica
Lycopene
Carotene
title Engineering yeast artificial core promoter with designated base motifs
title_full Engineering yeast artificial core promoter with designated base motifs
title_fullStr Engineering yeast artificial core promoter with designated base motifs
title_full_unstemmed Engineering yeast artificial core promoter with designated base motifs
title_short Engineering yeast artificial core promoter with designated base motifs
title_sort engineering yeast artificial core promoter with designated base motifs
topic Synthetic biology
Promoter
Core promoter
Yarrowia lipolytica
Lycopene
Carotene
url http://link.springer.com/article/10.1186/s12934-020-01305-4
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AT duoliu engineeringyeastartificialcorepromoterwithdesignatedbasemotifs
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