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Light and scanning electron microscopic characterization of aflatoxins producing Aspergillus flavus in the maize crop

黄曲霉 黄曲霉毒素 分生孢子 生物 作物 孢子 植物 园艺 农学 食品科学
作者
Wajiha Seerat,Abida Akram,Rahmatullah Qureshi,Ghulam Yaseen,Tariq Mukhtar,Nafeesa Qudsia Hanif
出处
期刊:Microscopy Research and Technique [Wiley]
卷期号:85 (8): 2894-2903 被引量:8
标识
DOI:10.1002/jemt.24139
摘要

Abstract Maize ( Zea mays L.) is considered as one of the main cereals, used as a source of food, forage, and processed products. The loss of maize productivity is reported due to effect on roots, stalks, ears, and kernels mainly caused by many fungi. Among these fungal pathogens of maize, Aspergillus flavus ( A. flavus ) are the most prevalent that produces highly toxigenic aflatoxins that are highly carcinogenic to the consumers. The present study is confined to isolate and characterize the A. flavus from maize seeds for accurate identification that can be helpful for determination and management of aflatoxins in maize crop. Eighty stored seed samples of maize were collected from warehouses where seeds are stored for food and feeding purposes. For the isolation of A. flavus , Potato Dextrose Agar was used. Isolated fungi were identified macro and microscopically using light microscope and scanning electron microscope. A total of 212 Aspergillus isolates were identified based on macro‐morphological and micro‐morphological characteristics. The results showed that A. flavus colonies were granular, flat with yellow‐green to deep yellow‐green colony color having a white border and compact, spherical spore heads. Rapid rate of growth was observed maturing in about 3–5 days. In microscopic features, A. flavus have apically swollen conidiophores with various conidia bearing cells in long and dry chains. Spherical conidial heads were split into several columns ranging 300–400 μm in diameter. This will be helpful for farmers, researchers and traders in future for correct identification of sources of aflatoxins. Research Highlights Maize seed samples were collected from Pothohar region of Pakistan. The fungi were isolated on PDA. Aspergillus flavus was identified macro‐morphologically by observing growth rate, colony color and texture. Furthermore, these fungi were identified micro‐morphologically by using light and scanning electron microscope. The 212 Aspergillus flavus strains were isolated and identified.
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