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Comparative sequence analysis of citrate synthase and 18S ribosomal DNA from a wild and mutant strains of Aspergillus niger with various fungi

机译:来自黑曲霉的野生和突变菌株与各种真菌的柠檬酸合酶和18S核糖体DNA的比较序列分析

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摘要

A mutation was induced in Aspergillus niger wild strain using ethidium bromide resulting in enhanced expression of citric acid by three folds and 112.42 mg/mL citric acid was produced under optimum conditions with 121.84 mg/mL of sugar utilization. Dendograms of 18S rDNA and citrate synthase from different fungi including sample strains were made to assess homology among different fungi and to study the correlation of citrate synthase gene with evolution of fungi. Subsequent comparative sequence analysis revealed strangeness between the citrate synthase and 18S rDNA phylogenetic trees. Furthermore, the citrate synthase movement suggests that the use of traditional marker molecule of 18S rDNA gives misleading information about the evolution of citrate synthase in different fungi as it has shown that citrate synthase gene transferred independently among different fungi having no evolutionary relationships. Random amplified polymorphic DNA (RAPD-PCR) analysis was also employed to study genetic variation between wild and mutant strains of A. niger and only 71.43% similarity was found between both the genomes. Keeping in view the importance of citric acid as a necessary constituent of various food preparations, synthetic biodegradable detergents and pharmaceuticals the enhanced production of citric acid by mutant derivative might provide significant boost in commercial scale viability of this useful product.AbbreviationsCS - Citrate synthase, CA - Citric acid, RAPD - Random amplified polymorphic DNA, TAF - Total amplified fragments, PAF - Polymorphic amplified fragments, CAF - Common amplified fragments.
机译:使用溴化乙锭在黑曲霉野生菌株中诱导突变,导致柠檬酸表达提高了三倍,在最佳条件下以121.84 mg / mL的糖利用量生产了112.42 mg / mL的柠檬酸。绘制了包括样品菌株在内的不同真菌的18S rDNA和柠檬酸合酶的树状图,以评估不同真菌之间的同源性,并研究柠檬酸合酶基因与真菌进化的相关性。随后的比较序列分析揭示了柠檬酸合酶和18S rDNA系统发育树之间的陌生性。此外,柠檬酸合酶的运动表明,传统的18S rDNA标记分子的使用提供了关于柠檬酸合酶在不同真菌中进化的误导性信息,因为它表明柠檬酸合酶基因在不同的真菌之间独立转移,没有进化关系。还使用随机扩增多态DNA(RAPD-PCR)分析来研究黑曲霉野生株和突变株之间的遗传变异,两个基因组之间仅发现71.43%的相似性。考虑到柠檬酸作为各种食品制剂,合成的可生物降解的清洁剂和药品中必不可少的组成部分的重要性,突变衍生物提高柠檬酸的产量可能会大大提高该有用产品的商业规模可行性.CS-柠檬酸合酶,CA -柠檬酸,RAPD-随机扩增的多态性DNA,TAF-总扩增片段,PAF-多态性扩增片段,CAF-普通扩增片段。

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