Elucidation of biosynthetic pathways of natural products.

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Safety of the fungal workhorses of industrial biotechnology: update on the mycotoxin and secondary metabolite potential of Aspergillus niger, Aspergillus oryzae, and Trichoderma reesei

P2860

Q57183197-0FA49625-4106-442F-A871-48377CCCA159

P2860

Elucidation of biosynthetic pathways of natural products.

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http://www.wikidata.org/entity/Q39226283

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

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2017年論文

@zh-tw

2017年论文

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2017年论文

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2017年论文

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name

Elucidation of biosynthetic pathways of natural products.

@en

Elucidation of biosynthetic pathways of natural products.

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type

Item

label

Elucidation of biosynthetic pathways of natural products.

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Elucidation of biosynthetic pathways of natural products.

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prefLabel

Elucidation of biosynthetic pathways of natural products.

@en

Elucidation of biosynthetic pathways of natural products.

@nl

P1476

Elucidation of biosynthetic pathways of natural products.

@en

P2093

Kenji Watanabe

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

Michio Sato

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

Shinji Kishimoto

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

P2860

A polyketide synthase-peptide synthetase gene cluster from an uncultured bacterial symbiont of Paederus beetles

Complexity generation during natural product biosynthesis using redox enzymes

The Catalytic Mechanism of a Natural Diels-Alderase Revealed in Molecular Detail

Human theta class glutathione transferase: the crystal structure reveals a sulfate-binding pocket within a buried active site

Synthetic biology to access and expand nature's chemical diversity

Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications

Glutathione catalysis and the reaction mechanisms of glutathione-dependent enzymes

Isolating "uncultivable" microorganisms in pure culture in a simulated natural environment.

Enzymatic processing of fumiquinazoline F: a tandem oxidative-acylation strategy for the generation of multicyclic scaffolds in fungal indole alkaloid biosynthesis.

Molecules of natural origin, semi-synthesis and synthesis with anti-inflammatory and anticancer utilities.

P31

scholarly article

P356

10.1002/TCR.201700015

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P50

Yuta Tsunematsu

P577

2017-04-07T00:00:00Z

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P698

28387469

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Elucidation of biosynthetic pathways of natural products.

about

P2860

P2860

Elucidation of biosynthetic pathways of natural products.

description

name

type

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P1433

P1476

P2093

P2860

P31

P356

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P31

P356

P50

P577

P698