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Microbial strain improvement for enhanced polygalacturonase production by Aspergillus sojae

机译:微生物菌株改良,以提高大豆曲霉产生的半乳糖醛酸酶的产量

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摘要

Strain improvement is a powerful tool in commercial development of microbial fermentation processes. Strains of Aspergillus sojae which were previously identified as polygalacturonase producers were subjected to the costeffective mutagenesis and selection method, the so-called random screening. Physical (ultraviolet irradiation at 254 nm) and chemical mutagens (N-methyl-N′-nitro-Nnitrosoguanidine) were used in the development and implementation of a classical mutation and selection strategy for the improved production of pectic acid-degrading enzymes. Three mutation cycles of both mutagenic treatments and also the combination of them were performed to generate mutants descending from A. sojae ATCC 20235 and mutants of A. sojae CBS 100928. Pectinolytic enzyme production of the mutants was compared to their wild types in submerged and solid-state fermentation. Comparing both strains, higher pectinase activity was obtained by A. sojae ATCC 20235 and mutants thereof. The highest polygalacturonase activity (1,087.2±151.9 U/g) in solid-state culture was obtained by mutant M3, which was 1.7 times increased in comparison to the wild strain, A. sojae ATCC 20235. Additional, further mutation of mutant M3 for two more cycles of treatment by UV irradiation generated mutant DH56 with the highest polygalacturonase activity (98.8±8.7 U/mL) in submerged culture. This corresponded to 2.4-fold enhanced polygalacturonase production in comparison to the wild strain. The results of this study indicated the development of a classical mutation and selection strategy as a promising tool to improve pectinolytic enzyme production by both fungal strains.
机译:菌株改良是微生物发酵工艺商业开发中的有力工具。以前被鉴定为多聚半乳糖醛酸酶生产者的大豆曲霉菌株经过了具有成本效益的诱变和选择方法,即所谓的随机筛选。物理的(在254 nm处进行紫外线照射)和化学的诱变剂(N-甲基-N'-硝基-亚硝基胍)被用于开发和实施经典的突变和选择策略,以提高果胶酸降解酶的产量。进行了三种诱变处理以及它们的组合的三个突变周期,以产生源自大豆曲霉ATCC 20235和大豆曲霉CBS 100928的突变体。比较了该突变体的果胶酶生产与淹没和固态的野生型。状态发酵。比较这两种菌株,通过大豆芽孢杆菌ATCC 20235及其突变体获得更高的果胶酶活性。突变体M3获得了固态培养物中最高的半乳糖醛酸酶活性(1,087.2±151.9 U / g),这是野生菌株A. sojae ATCC 20235的1.7倍。另外,突变体M3进一步突变了两个通过紫外线照射的更多处理周期,在水下培养物中产生了具有最高半乳糖醛酸酶活性(98.8±8.7 U / mL)的突变体DH56。与野生株相比,这相当于多聚半乳糖醛酸酶产量提高了2.4倍。这项研究的结果表明,经典的突变和选择策略的发展是提高两种真菌菌株产生的果胶分解酶产量的有前途的工具。

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