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Mutation-Screening in Xylanase-Producing Strains by Ion Implantation

机译:通过离子注入对产木聚糖酶菌株的突变筛选

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摘要

With ion implantation (N~+, energy 10 keV and dosage 1.56 x 10~(15)N~+ cm~(-2)), a high xylanase-producing strain Aspergillus nlger N212 was selected. Based on an orthogonal experiment, an optimal fermentation condition was designed for this high-yield strain. The suitable medium was composed of 8% corncob; 1.0% wheat bran; 0.1% TWEEN20; 0.5% (NH_4)_2SO_4; 0.5%NaNO_3; 0.5%FeSO_4, 7.5 x 10~(-4); MnSO_4·H_2O, 2.5 x 10~(-4); ZnSO_4, 2.0 X 10~(-4); CoCl_2, 3.0 x 10~(-4) . At present, under our experiment condition, xylanase activity of Aspergillus niger N212 reached a level of 600 IU/ml, almost increased by 100% in xylanase production and the time of yielding xylanase was largely reduced to 12 h at 28℃.
机译:通过离子注入(N〜+,能量为10 keV,剂量为1.56 x 10〜(15)N〜+ cm〜(-2)),选择了高产木聚糖酶的菌株黑曲霉N212。基于正交试验,为该高产菌株设计了最佳发酵条件。合适的培养基由8%的玉米芯组成; 1.0%麦麸; 0.1%TWEEN20; 0.5%(NH_4)_2SO_4; 0.5%的NaNO_3; 0.5%FeSO_4,7.5 x 10〜(-4); MnSO_4·H_2O,2.5 x 10〜(-4); ZnSO_4,2.0 X 10〜(-4); CoCl_2,3.0×10〜(-4)。目前,在我们的实验条件下,黑曲霉N212的木聚糖酶活性达到600 IU / ml,木聚糖酶的产量几乎增加了100%,并且在28℃下木聚糖酶的生成时间大大减少了12 h。

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