A Consensus Ochratoxin A Biosynthetic Pathway: Insights from the Genome Sequence of Aspergillus ochraceus and a Comparative Genomic Analysis
Ochratoxin A (OTA) is a significant mycotoxin that contaminates cereal products, coffee, grapes, wine, cheese, and meat. OTA is nephrotoxic, carcinogenic, teratogenic, and immunotoxic. OTA contamination is a serious threat to food safety, endangers human health, and can cause huge economic losses. A...
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Published in | Applied and environmental microbiology Vol. 84; no. 19 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
01.10.2018
|
Subjects | |
Online Access | Get full text |
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Summary: | Ochratoxin A (OTA) is a significant mycotoxin that contaminates cereal products, coffee, grapes, wine, cheese, and meat. OTA is nephrotoxic, carcinogenic, teratogenic, and immunotoxic. OTA contamination is a serious threat to food safety, endangers human health, and can cause huge economic losses. At present, >20 species of the genera
Aspergillus
and
Penicillium
are known to produce OTA. Here we demonstrate that a consensus OTA biosynthetic pathway exists in all OTA-producing fungi and is encoded by a gene cluster containing four highly conserved biosynthetic genes and a bZIP transcription factor.
Ochratoxin A (OTA) is a toxic secondary metabolite produced by
Aspergillus
and
Penicillium
species that widely contaminates food and feed. We sequenced and assembled the complete ∼37-Mb genome of
Aspergillus
ochraceus
fc-1, a well-known producer of OTA. Key genes of the OTA biosynthetic pathway were identified by comparative genomic analyses with five other sequenced OTA-producing fungi:
A. carbonarius
,
A. niger
,
A. steynii
,
A. westerdijkiae
, and
Penicillium nordicum
. OTA production was completely inhibited in the deletion mutants (Δ
otaA
, Δ
otaB
, Δ
otaC
, Δ
otaD
, and Δ
otaR1
), and OTA biosynthesis was restored by feeding a postblock substrate to the corresponding mutant. The OTA biosynthetic pathway was unblocked in the Δ
otaD
mutant by the addition of heterologously expressed halogenase. OTA biosynthesis begins with a polyketide synthase (PKS), OtaA, utilizing acetyl coenzyme A (acetyl-CoA) and malonyl-CoA to synthesize 7-methylmellein, which is oxidized to OTβ by cytochrome P450 monooxygenase (OtaC). OTβ and
l
-β-phenylalanine are combined by a nonribosomal peptide synthetase (NRPS), OtaB, to form an amide bond to synthesize OTB. Finally, OTB is chlorinated by a halogenase (OtaD) to OTA. The
otaABCD
genes were expressed at low levels in the Δ
otaR1
mutant. A second regulator,
otaR2
, which is adjacent to the biosynthetic gene, could modulate only the expression of
otaA
,
otaB
, and
otaD
. Thus, we have identified a consensus OTA biosynthetic pathway that can be used to prevent and control OTA synthesis and will help us understand the variation and production of the intermediate components in the biosynthetic pathway.
IMPORTANCE
Ochratoxin A (OTA) is a significant mycotoxin that contaminates cereal products, coffee, grapes, wine, cheese, and meat. OTA is nephrotoxic, carcinogenic, teratogenic, and immunotoxic. OTA contamination is a serious threat to food safety, endangers human health, and can cause huge economic losses. At present, >20 species of the genera
Aspergillus
and
Penicillium
are known to produce OTA. Here we demonstrate that a consensus OTA biosynthetic pathway exists in all OTA-producing fungi and is encoded by a gene cluster containing four highly conserved biosynthetic genes and a bZIP transcription factor. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Citation Wang Y, Wang L, Wu F, Liu F, Wang Q, Zhang X, Selvaraj JN, Zhao Y, Xing F, Yin W-B, Liu Y. 2018. A consensus ochratoxin A biosynthetic pathway: insights from the genome sequence of Aspergillus ochraceus and a comparative genomic analysis. Appl Environ Microbiol 84:e01009-18. https://doi.org/10.1128/AEM.01009-18. Y.W. and L.W. contributed equally to this work. |
ISSN: | 0099-2240 1098-5336 1098-5336 |
DOI: | 10.1128/AEM.01009-18 |