Search: id:"swepub:oai:research.chalmers.se:bc558331-c2ff-47b8-838e-a7a71936c311" >
Improved Production...
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Liu, Zihe,1984Chalmers tekniska högskola,Chalmers University of Technology
(author)
Improved Production of a Heterologous Amylase in Saccharomyces cerevisiae by Inverse Metabolic Engineering
- Article/chapterEnglish2014
Publisher, publication year, extent ...
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American Society for Microbiology,2014
Numbers
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LIBRIS-ID:oai:research.chalmers.se:bc558331-c2ff-47b8-838e-a7a71936c311
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https://research.chalmers.se/publication/205394URI
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https://doi.org/10.1128/aem.00712-14DOI
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Language:English
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Summary in:English
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Subject category:art swepub-publicationtype
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Subject category:ref swepub-contenttype
Notes
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The increasing demand for industrial enzymes and biopharmaceutical proteins relies on robust production hosts with high protein yield and productivity. Being one of the best-studied model organisms and capable of performing posttranslational modifications, the yeast Saccharomyces cerevisiae is widely used as a cell factory for recombinant protein production. However, many recombinant proteins are produced at only 1% (or less) of the theoretical capacity due to the complexity of the secretory pathway, which has not been fully exploited. In this study, we applied the concept of inverse metabolic engineering to identify novel targets for improving protein secretion. Screening that combined UV-random mutagenesis and selection for growth on starch was performed to find mutant strains producing heterologous amylase 5-fold above the level produced by the reference strain. Genomic mutations that could be associated with higher amylase secretion were identified through whole-genome sequencing. Several single-point mutations, including an S196I point mutation in the VTA1 gene coding for a protein involved in vacuolar sorting, were evaluated by introducing these to the starting strain. By applying this modification alone, the amylase secretion could be improved by 35%. As a complement to the identification of genomic variants, transcriptome analysis was also performed in order to understand on a global level the transcriptional changes associated with the improved amylase production caused by UV mutagenesis.
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Liu, Lifang,1979Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)lifang
(author)
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Österlund, Tobias,1984Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)tobiaso
(author)
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Hou, Jin,1982Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)hjin
(author)
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Huang, Mingtao,1984Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)mingtao
(author)
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Fagerberg, L.Kungliga Tekniska Högskolan (KTH),Royal Institute of Technology (KTH)
(author)
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Petranovic Nielsen, Dina,1975Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)dinap
(author)
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Uhlen, M.Danmarks Tekniske Universitet,Technical University of Denmark,Kungliga Tekniska Högskolan (KTH),Royal Institute of Technology (KTH)
(author)
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Nielsen, Jens B,1962Chalmers tekniska högskola,Chalmers University of Technology(Swepub:cth)nielsenj
(author)
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Chalmers tekniska högskolaKungliga Tekniska Högskolan (KTH)
(creator_code:org_t)
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In:Applied and Environmental Microbiology: American Society for Microbiology80:17, s. 5542-55501098-53360099-2240
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