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Study of a High-Yield Cellulase System Created by Heavy-Ion Irradiation-Induced Mutagenesis of Aspergillus niger and Mixed Fermentation with Trichoderma reesei

机译:重离子辐照诱导黑曲霉诱变并与里氏木霉混合发酵产生高产纤维素酶系统的研究

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摘要

The aim of this study was to evaluate and validate the efficiency of 12C6+ irradiation of Aspergillus niger (A. niger) or mutagenesis via mixed Trichoderma viride (T. viride) culturing as well as a liquid cultivation method for cellulase production via mixed Trichoderma reesei (T. reesei) and A. niger culture fermentation. The first mutagenesis approach was employed to optimize yield from a cellulase-producing strain via heavy-ion mutagenesis and high-throughput screening, and the second was to effectively achieve enzymatic hydrolysis of cellulase from a mixed culture of mutant T. viride and A. niger. We found that 12C6+-ion irradiation induced changes in cellulase biosynthesis in A. niger but had no effect on the time course of the synthesis. It is notable that the exoglucanases (CBH) activities of A. niger strains H11-1 and H differed (6.71 U/mL vs. 6.01 U/mL) and were significantly higher than that of A. niger mutant H3-1. Compared with strain H, the filter paper assay (FPA), endoglucanase (EG) and β-glucosidase (BGL) activities of mutant strain H11-1 were increased by 250.26%, 30.26% and 34.91%, respectively. A mixed culture system was successfully optimized, and the best ratio of T. reesei to A. niger was 5:1 for 96 h with simultaneous inoculation. The BGL activity of the mixed culture increased after 72 h. At 96 h, the FPA and BGL activities of the mixed culture were 689.00 and 797.15 U/mL, respectively, significantly higher than those of monocultures, which were 408.70 and 646.98 U/mL for T. reesei and 447.29 and 658.89 U/mL for A. niger, respectively. The EG activity of the mixed culture was 2342.81 U/mL, a value that was significantly higher than that of monocultures at 2206.57 U/mL for T. reesei and 1727.62 U/mL for A. niger. In summary, cellulose production and hydrolysis yields were significantly enhanced by the proposed combination scheme.
机译:这项研究的目的是评估和验证黑曲霉(A. niger)的 12 C 6 + 辐射或通过混合木霉(Trichoderma viride)诱变的效率。 )以及通过里氏木霉(T. reesei)和黑曲霉(A.niger)混合发酵生产纤维素酶的液体培养方法。第一种诱变方法用于通过重离子诱变和高通量筛选来优化纤维素酶生产菌株的得率,第二种诱变方法是从突变型拟南芥和黑曲霉的混合培养物中有效地实现纤维素酶的酶促水解。 。我们发现 12 C 6 + 离子辐照诱导了黑曲霉纤维素酶生物合成的变化,但对时间的进程没有影响。合成。值得注意的是 A 的外切葡聚糖酶(CBH)活性。 niger 菌株H11-1和H不同(6.71 U / mL对6.01 U / mL),并且显着高于 A niger 突变体H3-1。与H菌株相比,突变菌株H11-1的滤纸测定(FPA),内切葡聚糖酶(EG)和β-葡萄糖苷酶(BGL)活性分别提高了250.26%,30.26%和34.91%,分别。成功地优化了混合培养系统,并优化了 T 的最佳比例。 reesei A niger 为5:1,持续接种96小时。混合培养物的BGL活性在72小时后增加。在96 h时,混合培养物的FPA和BGL活性分别为689.00和797.15 U / mL,明显高于单一培养物的 T 的408.70和646.98 U / mL。 reesei A 的447.29和658.89 U / mL。 niger 。混合培养物的EG活性为2342.81 U / mL,明显高于 T 的单一培养物的EG活性2206.57 U / mL。 reesei A 的1727.62 U / mL。 尼日尔。总之,通过所提出的组合方案,纤维素的生产和水解产率显着提高。

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