4.6 Article

Ergot Alkaloid Synthesis Capacity of Penicillium camemberti

Journal

APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 84, Issue 19, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.01583-18

Keywords

specialized metabolism; aldehyde dehydrogenase; Camembert cheese; rugulovasines

Funding

  1. National Institutes of Health, National Institute of General Medical Sciences [R15GM114774]
  2. Hatch project from the United States Department of Agriculture, National Institute of Food and Agriculture [WVA00669]
  3. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R15GM114774] Funding Source: NIH RePORTER

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Ergot alkaloids are specialized fungal metabolites with potent biological activities. They are encoded by well-characterized gene clusters in the genomes of producing fungi. Penicillium camembert) plays a major role in the ripening of Brie and Camembert cheeses. The P. camembert) genome contains a cluster of five genes shown in other fungi to be required for synthesis of the important ergot alkaloid intermediate chanoclavine-I aldehyde and two additional genes (easH and easQ) that may control modification of chanoclavine-I aldehyde into other ergot alkaloids. We analyzed samples of Brie and Camembert cheeses, as well as cultures of P. camembert), and did not detect chanoclavine-I aldehyde or its derivatives. To create a functioning facsimile of the P. camembert) eas cluster, we expressed P. camembert) easH and easQ in a chanoclavine-I aldehyde-accumulating easA knockout mutant of Neosartorya fumigata. The easH-easQ-engineered N. fumigata strain accumulated a pair of compounds of m/z 269.1288 in positive-mode liquid chromatography-mass spectrometry (LC-MS). The analytes fragmented in a manner typical of the stereoisomeric ergot alkaloids rugulovasine A and B, and the related rugulovasine producer Penicillium biforme accumulated the same isomeric pair of analytes. The P. camembert! eas genes were transcribed in culture, but comparison of the P. camembert) eas cluster with the functional cluster from P. biforme indicated 11 polymorphisms. Whereas other P. camembert) eas genes functioned when expressed in N. fumigata, P. camembert) easC did not restore ergot alkaloids when expressed in an easC mutant. The data indicate that P. camembert) formerly had the capacity to produce the ergot alkaloids rugulovasine A and B. IMPORTANCE The presence of ergot alkaloid synthesis genes in the genome of Penicillium camemberti is significant, because the fungus is widely consumed in Brie and Camembert cheeses. Our results show that, although the fungus has several functional genes from the ergot alkaloid pathway, it produces only an early pathway intermediate in culture and does not produce ergot alkaloids in cheese. Penicillium biforme, a close relative of P. camembert), contains a similar but fully functional set of ergot alkaloid synthesis genes and produces ergot alkaloids chanoclavine-I, chanoclavine-I aldehyde, and rugulovasine A and B. Our reconstruction of the P. camembert) pathway in the model fungus Neosartorya fumigata indicated that P. camembert) formerly had the capacity to produce these same ergot alkaloids. Neither P. camembert) nor P. biforme produced ergot alkaloids in cheese, indicating that nutritionally driven gene regulation prevents these fungi from producing ergot alkaloids in a dairy environment.

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