Engineered ketol-acid reductoisomerase and alcohol dehydrogenase enable anaerobic 2-methylpropan-1-ol production at theoretical yield in Escherichia coli (Q39114191)

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scientific article published on May 2011

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English	Engineered ketol-acid reductoisomerase and alcohol dehydrogenase enable anaerobic 2-methylpropan-1-ol production at theoretical yield in Escherichia coli	scientific article published on May 2011

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scholarly article

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Europe PubMed Central

9 September 2017

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

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Europe PubMed Central

9 September 2017

Escherichia coli

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6

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Frances H Arnold

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Europe PubMed Central

9 September 2017

Christopher D Snow

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Christopher D Snow

4

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author name string

Sabine Bastian

1

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Europe PubMed Central

9 September 2017

Xiang Liu

2

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Europe PubMed Central

9 September 2017

Joseph T Meyerowitz

3

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Europe PubMed Central

9 September 2017

Mike M Y Chen

5

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Europe PubMed Central

9 September 2017

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publication date

1 May 2011

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Metabolic Engineering

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Europe PubMed Central

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13

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Europe PubMed Central

9 September 2017

345-352

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Europe PubMed Central

9 September 2017

3

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Europe PubMed Central

9 September 2017

Engineering for biofuels: exploiting innate microbial capacity or importing biosynthetic potential?

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Non-fermentative pathways for synthesis of branched-chain higher alcohols as biofuels

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Engineering the isobutanol biosynthetic pathway in Escherichia coli by comparison of three aldehyde reductase/alcohol dehydrogenase genes

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Xylose reductase from Pichia stipitis with altered coenzyme preference improves ethanolic xylose fermentation by recombinant Saccharomyces cerevisiae

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The crystal structure of plant acetohydroxy acid isomeroreductase complexed with NADPH, two magnesium ions and a herbicidal transition state analog determined at 1.65 A resolution

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Protein stability promotes evolvability

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Mechanism of ketol acid reductoisomerase--steady-state analysis and metal ion requirement

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Determinants of coenzyme specificity in glyceraldehyde-3-phosphate dehydrogenase: role of the acidic residue in the fingerprint region of the nucleotide binding fold.

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The expression of a Pichia stipitis xylose reductase mutant with higher K(M) for NADPH increases ethanol production from xylose in recombinant Saccharomyces cerevisiae

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Characteristics of alcohol/polyol dehydrogenases. The zinc-containing long-chain alcohol dehydrogenases.

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Expression of the Escherichia coli pntAB genes encoding a membrane-bound transhydrogenase in Corynebacterium glutamicum improves L-lysine formation.

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Computational design of Candida boidinii xylose reductase for altered cofactor specificity

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Rapid and efficient site-specific mutagenesis without phenotypic selection

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Genetic engineering of Escherichia coli for biofuel production

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Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I1-I2 regulatory elements

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Expression of protein engineered NADP+-dependent xylitol dehydrogenase increases ethanol production from xylose in recombinant Saccharomyces cerevisiae.

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Bioethanol production from xylose by recombinant Saccharomyces cerevisiae expressing xylose reductase, NADP(+)-dependent xylitol dehydrogenase, and xylulokinase

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Altering the coenzyme preference of xylose reductase to favor utilization of NADH enhances ethanol yield from xylose in a metabolically engineered strain of Saccharomyces cerevisiae

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Reversal of the nucleotide specificity of ketol acid reductoisomerase by site-directed mutagenesis identifies the NADPH binding site

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Effect of overexpression of a soluble pyridine nucleotide transhydrogenase (UdhA) on the production of poly(3-hydroxybutyrate) in Escherichia coli.

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Redesign of the coenzyme specificity of a dehydrogenase by protein engineering

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The crystal structure of a bacterial class II ketol-acid reductoisomerase: domain conservation and evolution.

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10.1016/J.YMBEN.2011.02.004

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Europe PubMed Central

9 September 2017

release_ssdn5mrzd5bflg7tukdgmfhkny

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