Shafique Sobiya, Bajwa Rukhsana, Shafique Shazia
Institute of Mycology and Plant Pathology, University of the Punjab, Quaid-e-Azam Campus 54590-Lahore, Pakistan.
Nat Prod Commun. 2009 Jul;4(7):977-80.
Aspergillus flavus FCBP-231, a filamentous fungus, was genetically modified for its ability to reveal extra cellular alpha-amylase activity. For strain improvement, the selected strains were subjected to UV irradiation (5-40 min exposure) and EMS treatment (50-300 microg mL(-1)) for hyper activity of an alpha-amylase enzyme. The mutants were quantitatively compared with the parental strain. UV and chemical mutagenesis brought about a dramatic enhancement in enzymatic activity. The mutant strains Af-UV-5.3 and Af-Ch-5.7 exhibited 79 and 110% more enzyme activity than the native strain A. flavus FCBP-231. This improvement in enzyme activity of the mutants suggests that they are suitable strains to be used in biotechnology. RAPD-PCR analysis revealed different patterns of amplicons of native as well as mutant derivatives, which suggested that the mutation imparted changes in the genetic make up of the mutants probably involved enzyme production control.
黄曲霉FCBP - 231是一种丝状真菌,因其具有分泌胞外α -淀粉酶活性的能力而进行了基因改造。为了改良菌株,对所选菌株进行紫外线照射(照射5 - 40分钟)和EMS处理(50 - 300微克/毫升),以提高α -淀粉酶的活性。将突变体与亲本菌株进行定量比较。紫外线和化学诱变使酶活性显著提高。突变菌株Af - UV - 5.3和Af - Ch - 5.7的酶活性比天然菌株黄曲霉FCBP - 231分别高出79%和110%。突变体酶活性的这种提高表明它们是适用于生物技术的菌株。RAPD - PCR分析揭示了天然菌株及其突变衍生物的扩增子具有不同模式,这表明突变可能改变了突变体的基因组成,可能涉及酶的生产控制。