During hot and humid seasons, extensive rot of sour lime was observed to be caused by Aspergillus flavus. In view of this, investigations were undertaken to obtain data on the production of various toxins by A. flavus during post harvest pathogenesis of sour lime. Sixty percent of the pathogenic A. flavus isolates were detected to be aflatoxin B(1) producers in sour lime tissue. It was also noted that thirty three percent of aflatoxigenic A. flavus isolates had the potential to coproduce cyclopiazonic acid (CPA). Such aflatoxigenic isolates produced quantitatively more CPA (ranging from 250.0 to 2501.3 microg/kg) than aflatoxin B(1) (ranging from 141.3 to 811.7 microg/kg) in the affected sour lime. This study demonstrates for the first time that sour lime are a favourable substrate for aflatoxin B(1) and cyclopiazonic acid production by A. flavus isolates. This is of great concern to the health of consumers.
Mushroom cultivation is an economical biotechnological process for the conversion of various unused lignocellulosic wastes into protein rich food. The present study was conducted to assess the suitability of three different cereal grains viz., bajra (Pennisetum glaucum L.), wheat (Triticum aestivum L.) and maize (Zea mays L.) for spawn production of Macrocybe gigantea (Massee) Pegler & Lod. and further its cultivation on two agrowastes (wheat straw and paddy straw) for assessing biological efficacy. It was observed that among the three cereal grains tested, bajra grains took significantly (P?0.05) less time for spawn development. Moreover, a minimum period of spawn run (16.3 days), highest sporophore yield (343.6g/500g of dry substrate) and biological efficiency (68.7%) were also recorded from substrate bags inoculated with bajra grain spawn. These results suggest the use of bajra grain spawn for quick and successful cultivation of M. gigantea.
Myco-keratinophilic species have a predilection for different keratinous substrates but show variability in their affinity towards them. Keeping this in view, a survey was conducted in the Khardung and Khardung La soils of Ladakh (India) and 28 myco-keratinophilic species belonging to 15 fungal genera (Sarocladium, Aspergillus, Beauveria, Chrysosporium, Cladosporium, Alternaria, Epicoccum, Fusarium, Gibberella, Clonostachys, Paecilomyces, Purpureocillium, Metarhizium, Penicillium and Sagenomella) were isolated by using keratin bait technique. These isolated species were tested for their preferential utilization ability and colonization on different baits by morphological assessment. Different types of keratin baits used were feathers, human hair, human nails and wool. Overall assessment revealed that feathers were colonized and utilized by all the species (100 %), followed in decreasing order by nails (89.29 %), hair (85.71 %) and sheep wool (67.86 %). So, it is concluded that feather baiting technique, could be more useful in trapping keratinophilic fungi than the hair baiting technique which is till date regarded as the best method for the isolation of mycokeratinophiles. On the basis of succession on keratinous baits, the recovered keratinophilic species were also categorized into four categories: early successional species (pioneer colonizers), late successional species (final colonizers), persistent species and no-pattern species.
An investigation of mycoflora and associated mycotoxins was carried out from dried market samples of stem portions of Tinospora cordifolia, an important medicinal plant of India. These samples were collected from various wholesale and retail shops of eight districts of Jammu and Kashmir state viz., Kathua, Jammu, Udhampur, Rajouri, Poonch, Doda, Srinagar and Leh. A total of 39 fungal species representing 18 genera were recovered by using surface washing technique. Assessment of mycobial load of T. cordifolia showed the presence of many such fungal species that are widely acknowledged as the most important mycotoxin producers. Analyses of samples for mycotoxin contamination was done by multimycotoxin detection method. The dried samples of Tinospora cordifolia were detected to be contaminated with aflatoxin B1, aflatoxin B2, ochratoxin A, patulin and citrinin. Among the various mycotoxins detected, aflatoxins were present in maximum number of samples, which is probably because Aspergillus flavus was recovered from all the investigated samples. However, fusarial species and their toxins were not detected from the investigated samples. DOI: http://dx.doi.org/10.3329/ijarit.v3i2.17839 Int. J. Agril. Res. Innov. & Tech. 3 (2): 16-21, December, 2013
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