(Q41821972)

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De novo sequencing, assembly and analysis of the genome of the laboratory strain Saccharomyces cerevisiae CEN.PK113-7D, a model for modern industrial biotechnology

scientific article published on 26 March 2012

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scholarly article

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Europe PubMed Central

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12 October 2017

De novo sequencing, assembly and analysis of the genome of the laboratory strain Saccharomyces cerevisiae CEN.PK113-7D, a model for modern industrial biotechnology (English)

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12 October 2017

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Saccharomyces cerevisiae

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Pascale Daran-Lapujade

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Jean-Marc Daran

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Jack T Pronk

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Wilbert H M Heijne

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Wilbert H M Heijne

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Marijke A H Luttik

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Marijke A Luttik

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Marcel A van den Broek

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Marcel van den Broek

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Marcel J T Reinders

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Marcel J T Reinders

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Jurgen F Nijkamp

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Dick de Ridder

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Lizanne Bosman

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Wanwipa Vongsangnak

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Erwin Datema

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Stefan de Kok

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Paul Klaassen

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Chris J Paddon

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Darren Platt

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Peter Kötter

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Roeland C van Ham

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publication date

26 March 2012

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Microbial Cell Factories

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MUMmer

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CZ Software Mentions: A large dataset of software mentions in the biomedical literature

https://scigraph.springernature.com/pub.10.1186/1475-2859-11-36

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Genome-wide analytical approaches for reverse metabolic engineering of industrially relevant phenotypes in yeast.

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Whole-genome sequencing of sake yeast Saccharomyces cerevisiae Kyokai no. 7.

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Hunger artists: yeast adapted to carbon limitation show trade-offs under carbon sufficiency

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Microbial laboratory evolution in the era of genome-scale science

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Unravelling evolutionary strategies of yeast for improving galactose utilization through integrated systems level analysis

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Linking genotype and phenotype of Saccharomyces cerevisiae strains reveals metabolic engineering targets and leads to triterpene hyper-producers.

1 reference

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6 June 2018

Whole-genome comparison reveals novel genetic elements that characterize the genome of industrial strains of Saccharomyces cerevisiae

1 reference

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Standard operating procedure for calculating genome-to-genome distances based on high-scoring segment pairs

1 reference

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Whole genome sequencing of Saccharomyces cerevisiae: from genotype to phenotype for improved metabolic engineering applications

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Unraveling condition-dependent networks of transcription factors that control metabolic pathway activity in yeast

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Variable tandem repeats accelerate evolution of coding and regulatory sequences.

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Key process conditions for production of C(4) dicarboxylic acids in bioreactor batch cultures of an engineered Saccharomyces cerevisiae strain.

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Elimination of glycerol production in anaerobic cultures of a Saccharomyces cerevisiae strain engineered to use acetic acid as an electron acceptor.

1 reference

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Genome structure of a Saccharomyces cerevisiae strain widely used in bioethanol production

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Eukaryote-to-eukaryote gene transfer events revealed by the genome sequence of the wine yeast Saccharomyces cerevisiae EC1118.

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Novel evolutionary engineering approach for accelerated utilization of glucose, xylose, and arabinose mixtures by engineered Saccharomyces cerevisiae strains.

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When transcriptome meets metabolome: fast cellular responses of yeast to sudden relief of glucose limitation.

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Co-utilization of L-arabinose and D-xylose by laboratory and industrial Saccharomyces cerevisiae strains.

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Intragenic tandem repeats generate functional variability

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based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1475-2859-11-36

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Europe PubMed Central

PMC publication ID

12 October 2017

Dimensions Publication ID

1 reference

9 September 2019

https://scigraph.springernature.com/pub.10.1186/1475-2859-11-36

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 October 2017

ResearchGate publication ID

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