4.4 Article

Anthranilate-Activating Modules from Fungal Nonribosomal Peptide Assembly Lines

Journal

BIOCHEMISTRY
Volume 49, Issue 15, Pages 3351-3365

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/bi100198y

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Funding

  1. NIH [GM49338]
  2. National Institute of General Medical Sciences [F32GM090475]

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Fungal natural products containing benzodiazepinone- and quinazolinone-fused ring systems can be assembled by nonribosomal peptide synthetases (NRPS) using the conformationally restricted beta-amino acid anthranilate as one of the key building blocks. We validated that the first module of the acetylaszonalenin synthetase of Neosartorya fischeri NRRL 181 activates anthranilate to anthranilyl-AMP. With this as a starting point, we then used bioinformatic predictions about fungal adenylation domain selectivities to identify and confirm an anthranilate-activating module in the fumiquinazoline A producer Aspergillus fumigatus Af293 as well as a second anthranilate-activating NRPS in N. fischeri. This establishes an anthranilate adenylation domain code for fungal NRPS and should facilitate detection and cloning of gene clusters for benzodiazepine- and quinazoline-containing polycyclic alkaloids with a wide range of biological activities.

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