Data from A Genetic Toolbox for Metabolic Engineering of Issatchenkia orientalis
Abstract
The nonconventional yeast Issatchenkia orientalis can grow under highly acidic conditions and has been explored for production of various organic acids. However, its broader application is hampered by the lack of efficient genetic tools to enable sophisticated metabolic manipulations. We recently constructed an episomal plasmid based on the autonomously replicating sequence (ARS) from Saccharomyces cerevisiae (ScARS) in I. orientalis and developed a CRISPR/Cas9 system for multiplexed gene deletions. Here we report three additional genetic tools including: (1) identification of a 0.8 kb centromere-like (CEN-L) sequence from the I. orientalis genome by using bioinformatics and functional screening; (2) discovery and characterization of a set of constitutive promoters and terminators under different culture conditions by using RNA-Seq analysis and a fluorescent reporter; and (3) development of a rapid and efficient in vivo DNA assembly method in I. orientalis, which exhibited ~100% fidelity when assembling a 7 kb-plasmid from seven DNA fragments ranging from 0.7 kb to 1.7 kb. As proof of concept, we used these genetic tools to rapidly construct a functional xylose utilization pathway in I. orientalis.
- Authors:
-
- Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Center for Advanced Bioenergy and Bioproducts Innovation (CABBI), Urbana, IL (United States)
- Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Department of Microbiology, Nankai University, Tianjin, China
- Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, United States; Center for Advanced Bioenergy and Bioproducts Innovation (CABBI), Urbana, IL (United States)
- Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States
- Genome Informatics Facility, Office of Biotechnology, Iowa State University, Ames, IA, 50011, United States
- Department of Chemical and Biological Engineering, Iowa State University, Ames, IA, 50011, United States; Center for Advanced Bioenergy and Bioproducts Innovation (CABBI), Urbana, IL (United States)
- Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, United States; U.S. Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, United States; Biological Systems Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, 94720, United States; Center for Advanced Bioenergy and Bioproducts Innovation (CABBI), Urbana, IL (United States)
- Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Carl R. Woese Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Center for Advanced Bioenergy and Bioproducts Innovation (CABBI), Urbana, IL (United States); Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Department of Biochemistry, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States; Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL, 61801, United States
- Publication Date:
- DOE Contract Number:
- SC0018420
- Research Org.:
- Center for Advanced Bioenergy and Bioproducts Innovation (CABBI), Urbana, IL (United States); University of Illinois Urbana-Champaign
- Sponsoring Org.:
- U.S. Department of Energy (DOE)
- Subject:
- Conversion; Genome Engineering; Genomics; Transcriptomics
- OSTI Identifier:
- 3013818
- DOI:
- https://doi.org/10.13012/B2IDB-8429399_V1
Citation Formats
Cao, Mingfeng, Fatma, Zia, Song, Xiaofei, Hsieh, Ping-Hung, Tran, Vinh G., Lyon, William L., Sayadi, Maryam, Shao, Zengyi, Yoshikuni, Yasuo, and Zhao, Huimin. Data from A Genetic Toolbox for Metabolic Engineering of Issatchenkia orientalis. United States: N. p., 2020.
Web. doi:10.13012/B2IDB-8429399_V1.
Cao, Mingfeng, Fatma, Zia, Song, Xiaofei, Hsieh, Ping-Hung, Tran, Vinh G., Lyon, William L., Sayadi, Maryam, Shao, Zengyi, Yoshikuni, Yasuo, & Zhao, Huimin. Data from A Genetic Toolbox for Metabolic Engineering of Issatchenkia orientalis. United States. doi:https://doi.org/10.13012/B2IDB-8429399_V1
Cao, Mingfeng, Fatma, Zia, Song, Xiaofei, Hsieh, Ping-Hung, Tran, Vinh G., Lyon, William L., Sayadi, Maryam, Shao, Zengyi, Yoshikuni, Yasuo, and Zhao, Huimin. 2020.
"Data from A Genetic Toolbox for Metabolic Engineering of Issatchenkia orientalis". United States. doi:https://doi.org/10.13012/B2IDB-8429399_V1. https://www.osti.gov/servlets/purl/3013818. Pub date:Fri Jan 31 00:00:00 UTC 2020
@article{osti_3013818,
title = {Data from A Genetic Toolbox for Metabolic Engineering of Issatchenkia orientalis},
author = {Cao, Mingfeng and Fatma, Zia and Song, Xiaofei and Hsieh, Ping-Hung and Tran, Vinh G. and Lyon, William L. and Sayadi, Maryam and Shao, Zengyi and Yoshikuni, Yasuo and Zhao, Huimin},
abstractNote = {The nonconventional yeast Issatchenkia orientalis can grow under highly acidic conditions and has been explored for production of various organic acids. However, its broader application is hampered by the lack of efficient genetic tools to enable sophisticated metabolic manipulations. We recently constructed an episomal plasmid based on the autonomously replicating sequence (ARS) from Saccharomyces cerevisiae (ScARS) in I. orientalis and developed a CRISPR/Cas9 system for multiplexed gene deletions. Here we report three additional genetic tools including: (1) identification of a 0.8 kb centromere-like (CEN-L) sequence from the I. orientalis genome by using bioinformatics and functional screening; (2) discovery and characterization of a set of constitutive promoters and terminators under different culture conditions by using RNA-Seq analysis and a fluorescent reporter; and (3) development of a rapid and efficient in vivo DNA assembly method in I. orientalis, which exhibited ~100% fidelity when assembling a 7 kb-plasmid from seven DNA fragments ranging from 0.7 kb to 1.7 kb. As proof of concept, we used these genetic tools to rapidly construct a functional xylose utilization pathway in I. orientalis.},
doi = {10.13012/B2IDB-8429399_V1},
journal = {},
number = ,
volume = ,
place = {United States},
year = {Fri Jan 31 00:00:00 UTC 2020},
month = {Fri Jan 31 00:00:00 UTC 2020}
}
