Mycobiota, Total Aflatoxins and Ochratoxin A of Cardamom Pods

Gherbawy, Youssuf A.; Shebany, Yassmin M.

doi:10.3136/fstr.24.87

Cited by 11 publications

(10 citation statements)

References 32 publications

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Section: Microorganism Secondary Metabolites Commentsmentioning

confidence: 99%

“…quinazolinones bioactive compound [112] roquefortine C mycotoxin [114,120,123,[131][132][133] rugulosin bioactive compound [134] secalonic acid mycotoxin [120,135] skyrin bioactive compound [134] Penicillium chrysogenum sorbicillactones A and B bioactive compound [114] sorbicillin bioactive compound [114] sorbicillinol bioactive compound [114] sorbivinetone bioactive compound [114] xanthocillin X bioactive compound [123] Penicilium citrinum (3S)-4,6-dihydro-8-mehoxy-3,5-dimethyl-6-oxo-3H-2-benzopyran bioactive compound [136] (3S)-6-hydroxy-8-methoxy-3,5-dimethylisochroman bioactive compound [136] 1,2,3,11b-tetrahydroquinolactacide bioactive compound [136] 2-(hept-5-enyl)-3-methyl-4-oxo-6,7,8,8a-tetrahydro-4H-pyrrolo[2,1-b]-1,3-oxazine bioactive compound [137] 2,4,5-trimethylbenzene-1,3-diol bioactive compound [137] 2,4-dihydroxy-3, 5,6-trimethylbenzoic acid bioactive compound [137] 3-methoxy-2-methyl-4H-pyran-4-one bioactive compound [137] 4-hydroxyquinolin-2(1H)-one bioactive compound [136] 5-methyl alternariol ether bioactive compound [137] Database on potential toxigenic capacities of microorganisms used for industrial production…”

Section: Microorganism Secondary Metabolites Commentsmentioning

confidence: 99%

“…anti-phytopathogenic compounds [105] nematicidal compounds [106] Penicillium camemberti cyclopiazonic acid mycotoxin [107] Penicillium chrysogenum (3R, 4R)-3,4,8-trihydroxy-3,4-dihydronaphthalen-1 (2H)-one bioactive compound [108] (9Z,12Z)-2,3-dihydroxypropyl octadeca-9,12-dienoate neuroprotective effect [109] (E)-N-(4-hydroxystyryl) formamide bioactive compound [108] (Z)-N-(4-hydroxy styryl) formamide bioactive compound [108] 1,2,4 dihydroxy 6 methylbenzoyl glycerol antifungal compound [110] 11 bromoroquefortine C bioactive compound [111] 2,2,4 dihydroxy 6 methylbenzoyl glycerol antifungal compound [110] 2-(4-hydroxyphenyl)acetamides bioactive compound [112] Database on potential toxigenic capacities of microorganisms used for industrial production…”

Section: Paenibacillus Maceransmentioning

confidence: 99%

“…2-(4-hydroxyphenyl) acetonitrile bioactive compound [108] 2,3-dihydrosorbicillin neuroprotective effect [109] 2-[(2-hydroxypropionyl) amino] benzamide neuroprotective effect [109] 24 epicyclocitrinol 9 steroid [113] 2S,3R oxaline bioactive compound [108] 4-(2-hydroxyethyl) benzene-1,2-diol bioactive compound [108] bisvertinolone bioactive compound [114] BMS 182123 TNF-alpha inhibitor [115] chrysogenamide A neuroprotective effect [109] chrysotriazoles A and B bioactive compound [112] circumdatin G neuroprotective effect [109] Penicillium chrysogenum citrinin mycotoxin [116][117][118] conidiogenones diterpenes [119] conidogenol diterpenes [119] cyclocitrinol steroid [113] emodin bioactive compound [108,120] ergosterol endoperoxide bioactive compound [121] erythro 11 hydroxyneocyclocitrinol steroid [113] linolenic acid bioactive compound [121] Database on potential toxigenic capacities of microorganisms used for industrial production…”

Section: Microorganism Secondary Metabolites Commentsmentioning

confidence: 99%

“…lovastatin bioactive compound [122] meleagrin bioactive compound [120,123] methyl 2-(4-hydroxyphenyl) acetate bioactive compound [108] N 4 hydroxystyryl formamides bioactive compound [112] neocyclocitrinols A-D steroid [113] norcyclocitrinol A steroid [113] ochratoxin A mycotoxin [124,125] oxosorbicillinol bioactive compound [114] penicillin G antibiotic [123] penicimonoterpene antifungal compound [110] penicisteroid A, B cytotoxic polyoxygenated steroids [126] Penicillium chrysogenum penicitide A, B cytotoxic and antimicrobial [110] penicitols A and C citrinin analogues [127] penimethavone A flavone [128] penixanacid A xanthone derivative [127] pesudocyclocitrinol A cytotoxic polyoxygenated steroids [113] phenoxyacetic acid antifungal compound [129] phenylacetic acid citrinin analogues [129] PR toxin sesquiterpenoid mycotoxin [130] Database on potential toxigenic capacities of microorganisms used for industrial production…”

Section: Microorganism Secondary Metabolites Commentsmentioning

confidence: 99%

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Database on the taxonomical characterisation and potential toxigenic capacities of microorganisms used for the industrial production of food enzymes and feed additives, which do not have a recommendation for Qualified Presumption of Safety

Benito

Ibáñez

Moncho

et al. 2017

EFSA Supporting Publications

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The present work constitutes the external scientific report of the EFSA open call OC/EFSA/FEED/2015/01. The aim of the call was to provide EFSA with a database from a review on the taxonomical description and potential toxigenic capacities of microorganisms used for the industrial production of feed additives and food enzymes. The review includes microorganisms used as source of feed additives and food enzymes for which EFSA has received or can potentially receive applications for safety assessment, and which have not been recommended for Qualified Presumption of Safety status. The database also comprises the molecular taxonomical identifiers and biosynthetic pathways involved in the production of toxic compounds and the responsible genes. The main result of the project is shown as a database developed according to the EFSA data structure. The methodological aspects and the queries used in the systematic search, as well as the procedure applied for the screening of scientific documents retrieved are described in this report. Details are available in supplementary appendices.In total, 22970 scientific documents were screened in the literature search, from which 411 were initially selected for providing pertinent data for the scope of the project. From the review of the selected articles, 474 bioactive secondary metabolites were recorded and 59 compounds were further studied in order to obtain data on their toxicology and the conditions in which they are produced by the microorganisms used in industrial fermentations. The database generated in this project comprises details that characterise, when available, the production conditions, genes involved and toxicity of these 59 compounds. This provides information that can be used to establish safety measures when using potentially toxigenic microorganisms in industrial fermentations Disclaimer: The present document has been produced and adopted by the bodies identified above as author(s). This task has been carried out exclusively by the author(s) in the context of a contract between the European Food Safety Authority and the author(s), awarded following a tender procedure. The present document is published complying with the transparency principle to which the Authority is subject. It may not be considered as an output adopted by the Authority. The European Food Safety Authority reserves its rights, view and position as regards the issues addressed and the conclusions reached in the present document, without prejudice to the rights of the authors. Acknowledgements:We thank the following EFSA satff: Jaime Aguilera, Margarita Aguilera-Gómez, Jane Richardson, Mario Monguidi and Davide Gibin for their valuable help and collaboration throughout the project. We also would like to thank the members of AINIA: Sonia Porta, Lidia Tomás, Joaquin Espí and Juan Antonio Nieto for providing expertise in biotechnology and molecular biology and contributing with their efforts to achieve the goals of this project, and Violeta Gómez from the University of Navarra for her colla...

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