Comparison of 10,11-Dehydrocurvularin Polyketide Synthases fromAlternaria cinerariaeandAspergillus terreusHighlights Key Structural Motifs-Reference-Cited by-同舟云学术

Comparison of 10,11-Dehydrocurvularin Polyketide Synthases fromAlternaria cinerariaeandAspergillus terreusHighlights Key Structural Motifs

Published:2015-10-23 Issue:17 Volume:16 Page:2479-2483
ISSN:1439-4227
Container-title:ChemBioChem
language:en
Short-container-title:ChemBioChem

Author:

Cochrane Rachel V. K.¹,Gao Zhizeng¹,Lambkin Gareth R.¹,Xu Wei²,Winter Jaclyn M.³,Marcus Sandra L.¹,Tang Yi²,Vederas John C.¹

Affiliation:

1. Department of Chemistry; University of Alberta; Edmonton Alberta T6G 2G2 Canada

2. Department of Chemical and Biomolecular Engineering and; Department of Chemistry and Biochemistry; University of California; Los Angeles CA 90095 USA

3. Department of Medicinal Chemistry; The University of Utah; Salt Lake City Utah 84112 USA

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

Reference41 articles.

1. The Identification of a Major Phytotoxic Component from Alternaria macrospora as αβ-Dehydrocurvularin

2. βγ-Dehydrocurvularin and Related Compounds as Nematicides ofPratylenchus penetransfrom the FungusAspergillussp.

3. Alternariol Monomethyl Ether and α, β-Dehydrocurvularin from Endophytic Fungi Alternaria spp. Inhibit Appressorium Formation of Magnaporthe grisea

4. Isolation of .ALPHA..BETA.-dehydrocurvularin and .BETA.-hydroxycurvularin from Alternaria tomato as sporulation-suppressing factors.

5. Isolation and phytotoxicity of a metabolite from Curvularia eragrostidis and characterisation of its modes of action

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