Deletion of theSaccharomyces cerevisiae ARO8gene, encoding an aromatic amino acid transaminase, enhances phenylethanol production from glucose-Reference-Cited by-同舟云学术

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Deletion of theSaccharomyces cerevisiae ARO8gene, encoding an aromatic amino acid transaminase, enhances phenylethanol production from glucose

Published:2014-05 Issue: Volume: Page:n/a-n/a
ISSN:0749-503X
Container-title:Yeast
language:en
Short-container-title:Yeast

Author:

Romagnoli Gabriele¹²,Knijnenburg Theo A.³,Liti Gianni⁴⁵,Louis Edward J.⁴⁶,Pronk Jack T.¹²⁷,Daran Jean-Marc¹²⁷

Affiliation:

1. Department of Biotechnology; Delft University of Technology; Delft The Netherlands

2. Kluyver Centre for Genomics of Industrial Fermentation; Delft The Netherlands

3. Institute for Systems Biology; Seattle WA USA

4. Centre for Genetics and Genomics, Queens Medical Centre; University of Nottingham; UK

5. Institute for Research on Cancer and Ageing; CNRS UMR 7284-INSERM U 1081- UNS NICE; Nice France

6. Centre for Genetic Architecture of Complex Traits, Department of Genetics; University of Leicester; UK

7. Platform Green Synthetic Biology; Delft The Netherlands

Publisher

Wiley

Subject

Genetics,Applied Microbiology and Biotechnology,Biochemistry,Bioengineering,Biotechnology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/yea.3015/fullpdf

Reference65 articles.

1. A suite of Gateway cloning vectors for high-throughput genetic analysis in Saccharomyces cerevisiae;Alberti;Yeast,2007

2. A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length;Askree;Proc Natl Acad Sci U S A,2004

3. Contribution of the Saccharomyces cerevisiae transcriptional regulator Leu3p to physiology and gene expression in nitrogen- and carbon-limited chemostat cultures;Boer;FEMS Yeast Res,2005

4. Transcriptional responses of Saccharomyces cerevisiae to preferred and nonpreferred nitrogen sources in glucose-limited chemostat cultures;Boer;FEMS Yeast Res,2007

5. Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications;Brachmann;Yeast,1998

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