首页> 外文期刊>Antonie van Leeuwenhoek: Journal of Microbiology and serology >Improvement of Aspergillus oryzae NRRL 3484 by mutagenesis and optimization of culture conditions in solid-state fermentation for the hyper-production of extracellular cellulase
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Improvement of Aspergillus oryzae NRRL 3484 by mutagenesis and optimization of culture conditions in solid-state fermentation for the hyper-production of extracellular cellulase

机译:通过诱变改良米曲霉NRRL 3484并优化固态发酵中培养条件的培养条件以超量生产细胞外纤维素酶

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摘要

Spore suspensions of Aspergillus oryzae NRRL 3484 were subjected to mutagenesis using ultraviolet-irradiation followed by chemical treatments to improve the biosynthesis of cellulase. Ten mutant strains namely UEAC7, UEAR5, UNAC4, UNAC16, UNAR19, UNBC7, UNBR3, UNBR10, UNBR23 and UNBR25 were selected and their extracellular cellulase activities were assayed. Mutant UNAC4 gave the highest cellulase production [2,455 ± 28 U/g-dry substrate (ds) for filter paper-ase (FP-ase)] in a yield 4-fold exceeding that of the wild type strain (578 ± 5.0 U/g-ds for FP-ase). Rice straw (RS) was used as a sole carbon source for the enzyme production at a concentration of 10 % (w/v). Maximum cellulase production was achieved at initial medium pH 5.5, initial moisture content 77 % and an incubation temperature 28 °C on the fifth day of growth. NH4Cl proved to be the suitable added nitrogen source for maximum enzyme production followed by peptone. These results clearly indicate the cost-effectiveness of solid state fermentation technology in the economic production of extracellular cellulase. The hyper-production of cellulase by mutant strain UNAC4 has potential for industrial processes that convert lignocellulosic material (e.g. RS) into products of commercial value such as glucose and biofuels.
机译:将米曲霉NRRL 3484的孢子悬浮液进行紫外线诱变,然后进行化学处理以改善纤维素酶的生物合成。选择了10个突变株,即UEAC7,UEAR5,UNAC4,UNAC16,UNAR19,UNBC7,UNBR3,UNBR10,UNBR23和UNBR25,并测定了它们的细胞外纤维素酶活性。突变UNAC4产生的纤维素酶产量最高[2,455±28 U / g干滤纸酶(FP-ase)的干底物(ds)],其产量是野生型菌株的(578±5.0 U / g)的4倍。 FP酶的g-ds)。稻草(RS)被用作酶生产的唯一碳源,浓度为10%(w / v)。在生长的第五天,在初始培养基pH 5.5,初始水分含量77%和孵育温度28°C时,纤维素酶的产量最高。事实证明,NH4Cl是增加酶产量的合适氮源,其次是蛋白ept。这些结果清楚地表明了固态发酵技术在细胞外纤维素酶的经济生产中的成本效益。突变菌株UNAC4过量生产纤维素酶具有将木质纤维素材料(例如RS)转化成具有商业价值的产品(例如葡萄糖和生物燃料)的工业过程的潜力。

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