Enzymes
| UniProtKB help_outline | 195 proteins |
Reaction participants Show >> << Hide
- Name help_outline 7-methylmellein Identifier CHEBI:192524 (CAS: 1799965-79-9) help_outline Charge 0 Formula C11H12O3 InChIKeyhelp_outline SLYRNFYMGDTQEZ-UHFFFAOYSA-N SMILEShelp_outline CC1CC2=CC=C(C)C(O)=C2C(=O)O1 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
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Namehelp_outline
reduced [NADPH—hemoprotein reductase]
Identifier
RHEA-COMP:11964
Reactive part
help_outline
- Name help_outline FMNH2 Identifier CHEBI:57618 (Beilstein: 6258176) help_outline Charge -2 Formula C17H21N4O9P InChIKeyhelp_outline YTNIXZGTHTVJBW-SCRDCRAPSA-L SMILEShelp_outline Cc1cc2Nc3c([nH]c(=O)[nH]c3=O)N(C[C@H](O)[C@H](O)[C@H](O)COP([O-])([O-])=O)c2cc1C 2D coordinates Mol file for the small molecule Search links Involved in 852 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline O2 Identifier CHEBI:15379 (CAS: 7782-44-7) help_outline Charge 0 Formula O2 InChIKeyhelp_outline MYMOFIZGZYHOMD-UHFFFAOYSA-N SMILEShelp_outline O=O 2D coordinates Mol file for the small molecule Search links Involved in 2,851 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline 7-carboxymellein Identifier CHEBI:192525 Charge -1 Formula C11H9O5 InChIKeyhelp_outline POPKYYDFBOZZGX-UHFFFAOYSA-M SMILEShelp_outline C(C=1C(O)=C2C(CC(C)OC2=O)=CC1)([O-])=O 2D coordinates Mol file for the small molecule Search links Involved in 2 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
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Namehelp_outline
oxidized [NADPH—hemoprotein reductase]
Identifier
RHEA-COMP:11965
Reactive part
help_outline
- Name help_outline FMN Identifier CHEBI:58210 Charge -3 Formula C17H18N4O9P InChIKeyhelp_outline ANKZYBDXHMZBDK-SCRDCRAPSA-K SMILEShelp_outline C12=NC([N-]C(C1=NC=3C(N2C[C@@H]([C@@H]([C@@H](COP(=O)([O-])[O-])O)O)O)=CC(=C(C3)C)C)=O)=O 2D coordinates Mol file for the small molecule Search links Involved in 861 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline H2O Identifier CHEBI:15377 (CAS: 7732-18-5) help_outline Charge 0 Formula H2O InChIKeyhelp_outline XLYOFNOQVPJJNP-UHFFFAOYSA-N SMILEShelp_outline [H]O[H] 2D coordinates Mol file for the small molecule Search links Involved in 6,485 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
- Name help_outline H+ Identifier CHEBI:15378 Charge 1 Formula H InChIKeyhelp_outline GPRLSGONYQIRFK-UHFFFAOYSA-N SMILEShelp_outline [H+] 2D coordinates Mol file for the small molecule Search links Involved in 9,932 reaction(s) Find molecules that contain or resemble this structure Find proteins in UniProtKB for this molecule
Cross-references
| RHEA:72771 | RHEA:72772 | RHEA:72773 | RHEA:72774 | |
|---|---|---|---|---|
| Reaction direction help_outline | undefined | left-to-right | right-to-left | bidirectional |
| UniProtKB help_outline |
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| MetaCyc help_outline |
Publications
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A consensus ochratoxin A biosynthetic pathway: insights from the genome sequence of Aspergillus ochraceus and a comparative genomic analysis.
Wang Y., Wang L., Wu F., Liu F., Wang Q., Zhang X., Selvaraj J.N., Zhao Y., Xing F., Yin W.B., Liu Y.
Ochratoxin A (OTA) is a toxic secondary metabolite produced by <i>Aspergillus</i> and <i>Penicillium</i> species that widely contaminates food and feed. We sequenced and assembled the complete ∼37-Mb genome of <i>Aspergillus</i><i>ochraceus</i> fc-1, a well-known producer of OTA. Key genes of the ... >> More
Ochratoxin A (OTA) is a toxic secondary metabolite produced by <i>Aspergillus</i> and <i>Penicillium</i> species that widely contaminates food and feed. We sequenced and assembled the complete ∼37-Mb genome of <i>Aspergillus</i><i>ochraceus</i> 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: <i>A. carbonarius</i>, <i>A. niger</i>, <i>A. steynii</i>, <i>A. westerdijkiae</i>, and <i>Penicillium nordicum</i> OTA production was completely inhibited in the deletion mutants (Δ<i>otaA</i>, Δ<i>otaB</i>, Δ<i>otaC</i>, Δ<i>otaD</i>, and Δ<i>otaR1</i>), and OTA biosynthesis was restored by feeding a postblock substrate to the corresponding mutant. The OTA biosynthetic pathway was unblocked in the Δ<i>otaD</i> 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 <i>otaABCD</i> genes were expressed at low levels in the Δ<i>otaR1</i> mutant. A second regulator, <i>otaR2</i>, which is adjacent to the biosynthetic gene, could modulate only the expression of <i>otaA</i>, <i>otaB</i>, and <i>otaD</i> 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.<b>IMPORTANCE</b> 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 <i>Aspergillus</i> and <i>Penicillium</i> 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. << Less
Appl. Environ. Microbiol. 84:0-0(2018) [PubMed] [EuropePMC]
This publication is cited by 3 other entries.
Comments
The reaction has only been inferred from deletion experiments.