Skip to main content
. 2021 Aug 11;2:719420. doi: 10.3389/ffunb.2021.719420

Table 1.

Overview of fungal secondary metabolites detected in this study and their producing species in Aspergillus section Flavi.

Molecular Families graphic file with name ffunb-02-719420-i0001.jpg A.sojae A.pipericola A.oryzae A.flavus A.cerealis A.austwickii A.subflavus A.aflatoxiformans A.parasiticus A.arachidicola A.minisclerotigenes A.sergii A.transmontanensis A.novoparasiticus A.pseudotamarii A.caelatus A.tamarii A.pseudocaelatus A.pseudonomiae A.nomiae A. luteovirescens A.alliaceus A.vandermerwei A.albertensis A.neoalliaceus A.leporis A.aspearensis A.hancockii Abundance
Aflatoxins Aflatoxin B1 + + + + + + + + + + + 11
Aflatoxin B3 + + + + + + + + 8
Aflatoxin G1 + + + + + + + + + + + 11
Aflatoxin GM2 + + + 3
OMST a + + + + + + + + + + + 11
Sterigmatocystin + + + + 4
Dihydroaflatoxicol + + + + + + 6
Ochratoxins Ochratoxin A + + + + 4
Ochratoxin B + + + 3
Ochratoxin beta + + + 3
CTK3E9855 + + 2
CPAs CPA b + + + + + + + + + + + + + 13
Speradine A + + + + + + + + 8
Speradine F + + + + + + + + 8
2-oxo-CPA b + + + + + + + 7
3-OH-speradine A + + + + + + + 7
Fumifungins Fumifungin + + + + 4
Sphingofungin B + + + + 4
Sphingofungin C + + + + + 5
Sphingofungin D + + + + 4
Aflatrems Aflatrem + + + + + + 6
Paspalinine + + + + + + + + 8
Penerpenes + + + + + + + + 8
Asperindoles + 1
14-hydroxypaspalinine + + + 3
Paspaline + + + + 4
Aflavinines Aflavinine + + + + + + 6
14-hydroxyaflavinine + + + 3
Dihydroxyaflavinine + + 2
Tenuazonic acids Tenuazonic acid + + + + + + + + 8
Valine-tenuazonic acid + + + + + + 6
Aspergillicins Aspergillicin A + + + + + 5
Aspergillicin B + + + + 4
Aspergillicin C + + + + 4
Aspergillicin E/F + + + 3
Aspergillicin G + + + 3
Miyakamides Miyakamide A1/A2 + + + + + 5
Miyakamide Valine c + + + + 4
Miyakamide B1/B2 + + + + 4
Aspergillamide A/B + + + + + + + + + 9
Oryzamide A1/A2 + 1
Desertorins Desertorin A + + + + 4
Desertorin B + + + 3
Aspergillic acids Aspergillic acid + + + 3
Flavacol + 1
Lovastatins Lovastatin acid + 1
Lovastatin analog + 1
Lovastatin/mevinolin + 1
Parasiticolides Parasiticolide A + + + 3
Deacetylparasiticolide A + 1
Sphingosins Phytosphingosine + + + + + + + + + + + + + + + + + + + + + + + + + + + + 28
TMC TMC-95A + + 2
Ustilaginoidins ustilaginoidin C + + + + + + + + + + + + 12
Avenaciolides (-)-Canadensolide + + + + + + 6
Diketopiperazines Ditryptophenaline + + + + + + + 7
Ergot alkaloids Ergokonin B + + + + + + + + + + + + + + + + 16
Heptelidic acids Heptelidic acid + + + + 4
Kojic acids Kojic acid + + + + + + + + + + + + + 13
Chrysogines Chrysogine + + + + + + + + + 9

The rows indicate the known metabolites found in this study and the columns indicate the name of species. Abundance indicates the number of species producing the compound in this study. a OMST: O-methylsterigmatocystin. b CPA: Cyclopiazonic acid. c Miyakamide Valine: Miyakamide analogs with Valine.