(Q28238654)

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Biotechnological production of plant-specific hydroxylated phenylpropanoids

scientific article (publication date: September 2014)

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title

Biotechnological production of plant-specific hydroxylated phenylpropanoids (English)

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Yuheng Lin

1

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Yajun Yan

series ordinal

2

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language of work or name

English

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publication date

September 2014

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published in

Biotechnology and Bioengineering

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volume

111

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issue

9

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page(s)

1895-9

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cites work

Resveratrol: a natural polyphenol with multiple chemopreventive properties.

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Caffeic acid production enhancement by engineering a phenylalanine over-producing Escherichia coli strain.

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Crystal structure of the oxygenase component (HpaB) of the 4-hydroxyphenylacetate 3-monooxygenase from Thermus thermophilus HB8

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High-yield resveratrol production in engineered Escherichia coli

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Combinatorial biosynthesis of plant-specific coumarins in bacteria

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Biosynthesis of caffeic acid in Escherichia coli using its endogenous hydroxylase complex

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Coordinated production and utilization of FADH2 by NAD(P)H-flavin oxidoreductase and 4-hydroxyphenylacetate 3-monooxygenase

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Inhibitory effects of esculetin on melanin biosynthesis

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Screening of bacterial cytochrome P450s responsible for regiospecific hydroxylation of (iso)flavonoids

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Biological activity of piceatannol: leaving the shadow of resveratrol.

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The cancer preventative agent resveratrol is converted to the anticancer agent piceatannol by the cytochrome P450 enzyme CYP1B1.

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Characterization of an Escherichia coli aromatic hydroxylase with a broad substrate range

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Cytochrome P450 monooxygenases: an update on perspectives for synthetic application.

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Genome-scale metabolic network modeling results in minimal interventions that cooperatively force carbon flux towards malonyl-CoA.

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Characterization of 4-hydroxyphenylacetate 3-hydroxylase (HpaB) of Escherichia coli as a reduced flavin adenine dinucleotide-utilizing monooxygenase

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Esculetin induces apoptosis and inhibits adipogenesis in 3T3-L1 cells

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Determination of the esculetin contents of medicinal plants by liquid chromatography-tandem mass spectrometry

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Identifiers

DOI

10.1002/BIT.25237

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4110405

OpenCitations bibliographic resource ID

4110405

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4110405

PubMed publication ID

24752627

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4110405

(Q28238654)

Biotechnological production of plant-specific hydroxylated phenylpropanoids

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