博茨瓦纳传统非谷类酒精饮料khadi中的真菌毒素。

Microbiology insights Pub Date : 2022-11-25 eCollection Date: 2022-01-01 DOI:10.1177/11786361221139817
Koketso Motlhanka, Nerve Zhou, Malaki Kamakama, Monkgogi Masilo, Kebaneilwe Lebani
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引用次数: 0

摘要

霉菌毒素污染是影响食品商业化的主要食品安全问题。博茨瓦纳流行的发酵酒精饮料khadi的商业化需要对真菌毒素的存在进行调查。Khadi的酿造过程涉及对晒干的黄绿果进行不受控制和不规范的自发发酵,这可能是产生霉菌毒素的丝状真菌(霉菌)的来源。本研究旨在调查在博茨瓦纳中部和北部收集的18个khadi样品中产生真菌毒素的真菌和真菌毒素的存在。在18份khadi样品中鉴定出10份泰国周孢菌、枝孢子枝孢菌、赭曲霉、紫孢菌、土耳其绒球孢子菌、球精子枝孢菌、长毛毛菌和黄花黄酮。使用Myco-10 Randox Evidence Investigator生物芯片试剂盒检测真菌毒素,并使用UPLC-ESI-MS/MS进行确认。使用Myco-10 Randox Evidence Investigator生物芯片试剂盒检测霉菌毒素如paxilline、赭曲霉毒素A、麦角生物碱、黄曲霉毒素G1/G2和玉米赤霉烯酮。Myco-10结果显示,khadi样品中的真菌毒素低于FDA或欧盟委员会规定的监管限值。使用UPLC-ESI-MS/MS系统确认结果包括确认选定的真菌毒素(AFB1, DON;从选定的khadi样品(Palapye 1、Palapye 2、Letlhakane 2、Maun 3、Mmashoro 3和Tonota 3)中提取ZEA、FB1、FB2、FB3、NIV和OTA)。UPLC结果表明,所选khadi样品中上述真菌毒素均低于检测阈值。研究表明,虽然存在真菌分离株,但食用khadi后暴露于有毒真菌毒素的危险/风险几乎为零。为了商业化的努力,生产过程将需要最少的霉菌毒素监测和产品保存,但不需要解毒步骤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mycotoxins in khadi, A Traditional Non-Cereal Based Alcoholic Beverage of Botswana.

Mycotoxin contamination is a major food safety drawback towards the commercialization of food products. The commercialization of khadi, a popular fermented alcoholic beverage of Botswana necessitates the investigation of the presence of mycotoxins. Khadi brewing involves the uncontrolled and unstandardized spontaneous fermentation of sun-dried Grewia flava fruits, which could be a source of mycotoxin-producing filamentous fungi (molds). This study sought to investigate the presence of mycotoxins producing fungi and mycotoxins in 18 samples of khadi collected in Central and Northern Botswana. Periconia thailandica, Cladosporium cladosporioides, Aspergillus ochraceus, Phoma eupyrena, Setosphaeria turcica, Cladosporium sphaerospermum, Chaetomium longiciliata, and Flavodon ambrosius were identified in 10 out of 18 khadi samples. Mycotoxins were detected using the Myco-10 Randox Evidence Investigator biochip kit and confirmed using a UPLC-ESI-MS/MS. Mycotoxins such as paxilline, ochratoxin A, ergot alkaloids, aflatoxin G1/G2, and zearalenone were detected using the Myco-10 Randox Evidence Investigator biochip kit. The Myco-10 results revealed that the mycotoxins in the khadi samples were lower than the regulatory limits set by FDA or European Commission. Confirmation of results using an UPLC-ESI-MS/MS system involved confirming selected mycotoxins (AFB1, DON. ZEA, FB1, FB2, FB3, NIV, and OTA) from selected khadi samples (Palapye 1, Palapye 2, Letlhakane 2, Maun 3, Mmashoro 3, and Tonota 3). The UPLC results demonstrated that the aforementioned mycotoxins in the selected khadi samples were below the detection thresholds. The study shows that while fungal isolates were present, there is no to minimal danger/risk of exposure to toxic mycotoxins after consumption of khadi. Towards commercialization endeavors, the production process would necessitate minimal mycotoxin monitoring and product preservation but no detoxifying steps.

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