Novel key metabolites reveal further branching of the roquefortine/ meleagrin biosynthetic pathway

Journal of Biological Chemistry

Volumn 288, Issue 52, 2013, Pages 37289-37295

  Ries, Marco I ^a   Ali, Hazrat ^b,c,f   Lankhorst, Peter P ^d   Hankemeier, Thomas ^a,e   Bovenberg, Roel A L ^b,d   Driessen, Arnold J M ^b,c   Vreeken, Rob J ^a,e  

^a LEIDEN UNIVERSITY   (Netherlands)

^b UNIVERSITY OF GRONINGEN   (Netherlands)

^c Kluyver Center for Genomics of Industrial Fermentation   (Netherlands)

^d DSM BIOTECHNOLOGY CENTER   (Netherlands)

^e LEIDEN UNIVERSITY   (Netherlands)

^f University of Swat   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

BIOACTIVE MOLECULES; BIOSYNTHETIC PATHWAY; GENE CLUSTERS; ROQUEFORTINE; SYNTHETASES;

BIOMOLECULES; BIOSYNTHESIS; GENES;

METABOLITES;

ARTICLE; BIOSYNTHESIS; CATALYSIS; CONTROLLED STUDY; ENZYME MODIFICATION; ENZYME SPECIFICITY; FUNGAL GENE; FUNGAL STRAIN; GENE CLUSTER; GENE EXPRESSION PROFILING; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROLYSIS; MELEAGRIN GENE; NEOXALINE GENE; NONHUMAN; PENICILLIUM CHRYSOGENUM; PLASMID; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTOPLAST; ROQUEFORTINE F GENE; ROQUEFORTINE GENE; ROQUEFORTINE L GENE; ROQUEFORTINE M GENE; ROQUEFORTINE N GENE; SIGNAL TRANSDUCTION;

EID: 84891416276     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M113.512665     Document Type: Article

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