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首页> 外文期刊>Jordan Journal of Biological Sciences >Screening Wild and Mutant Strains of Aspergillus flavus and Aspergillus niger Isolated from Plantain Stalks for Amylase Production
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Screening Wild and Mutant Strains of Aspergillus flavus and Aspergillus niger Isolated from Plantain Stalks for Amylase Production

机译:从车前草茎中分离出黄曲霉和黑曲霉野生和突变菌株生产淀粉酶

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摘要

This study is conducted to determine the amylase activity of wild and mutant strains of Aspergillus flavus and Aspergillus niger isolated from plantain stalks. The isolation of the fungal species was carried out using standard microbiological methods. Strain improvement of the fungal isolates was carried out by exposing the wild fungal species to ultraviolet (UV) radiation at 240nm for ten, twenty, and thirty minutes. The amylase production from the wild and mutant strains was examined quantitatively while the effects of pH and temperature on the amylase activities of the wild and mutant strains were determined. Three mutant strains were obtained from each of Aspergillus flavus and Aspergillus niger. The wild and mutant strains of the fungal isolates showed variations in the amylase production. The amount of amylase produced by the fungal strains ranged from 2.849 mg/mL/min to 3.263 mg/mL/min of which the mutant strains of Aspergillus niger, exposed for ten minutes showed the highest amylase production. Furthermore, the amylase activities of the wild and mutant strains of the fungal species were sensitive to changes in pH and temperature. Amylase was optimally produced from all the fungal strains at pH 6 and 25oC. This study has revealed the amylase producing potential of wild and mutant (irradiated) strains of Aspergillus flavus and Aspergillus niger. Therefore, the mutated strains of Aspergillus flavus and Aspergillus niger could be employed in the commercial production of amylase. Findings from this study are promising; however, further intensive studies are still needed on the improved strains as well as the purification and characterization of the enzyme.
机译:进行这项研究来确定从车前草茎中分离出的黄曲霉和黑曲霉的野生菌株和突变菌株的淀粉酶活性。真菌种类的分离使用标准的微生物学方法进行。通过将野生真菌种类在240nm的紫外线(UV)辐射下暴露10分钟,20分钟和30分钟来进行菌株分离株的菌株改良。定量检查从野生和突变菌株产生的淀粉酶,同时确定pH和温度对野生和突变菌株的淀粉酶活性的影响。从黄曲霉和黑曲霉中分别获得三个突变株。真菌分离株的野生株和突变株显示出淀粉酶产生的变化。由真菌菌株产生的淀粉酶的量在2.849mg / mL / min至3.263mg / mL / min的范围内,其中暴露十分钟的黑曲霉突变菌株显示出最高的淀粉酶产生。此外,真菌种类的野生和突变菌株的淀粉酶活性对pH和温度的变化敏感。在pH 6和25oC下,所有真菌菌株均可以最佳地产生淀粉酶。这项研究揭示了黄曲霉和黑曲霉的野生和突变(辐照)菌株产生淀粉酶的潜力。因此,黄曲霉和黑曲霉的突变菌株可用于淀粉酶的商业生产。这项研究的结果令人鼓舞;然而,仍需要对改进的菌株以及酶的纯化和表征进行进一步的深入研究。

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