Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation. - Wikidata - awgldk - TriplyDB

Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation.

Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation.

http://www.wikidata.org/entity/Q38082702

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NADPH-generating systems in bacteria and archaea High-yield anaerobic succinate production by strategically regulating multiple metabolic pathways based on stoichiometric maximum in Escherichia coli A new-generation of Bacillus subtilis cell factory for further elevated scyllo-inositol production.Complete genome sequence and analysis of Lactobacillus hokkaidonensis LOOC260(T), a psychrotrophic lactic acid bacterium isolated from silage.NADP+-Preferring D-Lactate Dehydrogenase from Sporolactobacillus inulinus.A novel approach to improve poly-γ-glutamic acid production by NADPH Regeneration in Bacillus licheniformis WX-02.Metabolic engineering of carbon and redox flow in the production of small organic acids.Guidelines for development and implementation of biocatalytic P450 processes.Malonyl-CoA pathway: a promising route for 3-hydroxypropionate biosynthesis.Cloning, expression, and characterization of a thermostable glucose-6-phosphate dehydrogenase from Thermoanaerobacter tengcongensis.Engineering cofactor flexibility enhanced 2,3-butanediol production in Escherichia coli.Production of 7α,15α-diOH-DHEA from dehydroepiandrosterone by Colletotrichum lini ST-1 through integrating glucose-feeding with multi-step substrate addition strategy.L-Methionine Production.Pyridine nucleotide transhydrogenases enable redox balance of Pseudomonas putida during biodegradation of aromatic compounds.Process limitations of a whole-cell P450 catalyzed reaction using a CYP153A-CPR fusion construct expressed in Escherichia coli.In silico model-driven cofactor engineering strategies for improving the overall NADP(H) turnover in microbial cell factories.Bacterial production of isobutanol without expensive reagents.Engineering class I cytochrome P450 by gene fusion with NADPH-dependent reductase and S. avermitilis host development for daidzein biotransformation.Understanding the impact of the cofactor swapping of isocitrate dehydrogenase over the growth phenotype of Escherichia coli on acetate by using constraint-based modeling.

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Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation.

http://www.wikidata.org/entity/Q38082702

description

article científic

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article scientifique

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articol științific

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articolo scientifico

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artigo científico

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artigo científico

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artigo científico

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artikel ilmiah

@id

artikull shkencor

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artículo científico

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name

Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation.

@en

type

label

Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation.

@en

prefLabel

Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation.

@en

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Applied Microbiology and Biotechnology

P1476

Engineering of NADPH regenerators in Escherichia coli for enhanced biotransformation.

@en

P2093

Jin-Ho Seo

http://www.w3.org/2001/XMLSchema#string

Myoung-Dong Kim

http://www.w3.org/2001/XMLSchema#string

Won-Heong Lee

http://www.w3.org/2001/XMLSchema#string

Yong-Su Jin

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P2860

A novel NADH kinase is the mitochondrial source of NADPH in Saccharomyces cerevisiae

Biochemical properties and physiological roles of NADP-dependent malic enzyme in Escherichia coli.

Overexpression and biochemical characterization of soluble pyridine nucleotide transhydrogenase from Escherichia coli.

The soluble and membrane-bound transhydrogenases UdhA and PntAB have divergent functions in NADPH metabolism of Escherichia coli.

Using proteins in their natural environment: potential and limitations of microbial whole-cell hydroxylations in applied biocatalysis.

Regeneration of cofactors for use in biocatalysis.

POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNA.

Minimizing acetate formation in E. coli fermentations.

Engineered ketol-acid reductoisomerase and alcohol dehydrogenase enable anaerobic 2-methylpropan-1-ol production at theoretical yield in Escherichia coli.

Cofactor regeneration by a soluble pyridine nucleotide transhydrogenase for biological production of hydromorphone.

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s00253-013-4750-z

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2761-2772

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scholarly article

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10.1007/S00253-013-4750-Z

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7

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97

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2013-02-19T00:00:00Z

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1049037431

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23420268

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