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Production optimization of a heat-tolerant alkaline pectinase from Bacillus subtilis ZGL14 and its purification and characterization

机译:枯草芽孢杆菌ZGL14耐热碱性果胶酶的生产优化及其纯化与表征

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Alkaline pectinase has important applications in the pretreatment of waste water from food processing and in both the fabric and paper industries. In this study, a 2-level factorial design was used to screen significant factors that affect the activity of alkaline pectinase, and the response surface methodology (RSM) with a Box-Behnken design (BBD) was used to optimize their concentrations. Starch, peptone, KH_(2)PO_(4) and K_(2)HPO_(4)·3H_(2)O were found to significantly affect the activity of alkaline pectinase. Their optimal concentrations were as follows: 4.68% starch, 1.6% peptone, 0.26% KH_(2)PO_(4) and 0.68% K_(2)HPO_(4)·3H_(2)O. Under the above conditions, the activity of alkaline pectinase was significantly improved to 734.11?U/mL. Alkaline pectinase was purified to homogeneity with a recovery rate of 9.6% and a specific activity of 52372.52?U/mg. Its optimal temperature and pH were 50°C and 8.6, respectively. The purified enzyme showed strong thermo-stability and good alkali resistance. In addition, the activity of alkaline pectinase was improved in the presence of Mg~(2+). Cu~(2+), Mn~(2+), and Co~(2+) significantly inhibited its activity. This study provides an important basis for the future development and use of a heat-tolerant alkaline pectinase from B. subtilis ZGL14.
机译:碱性果胶酶在食品加工废水以及织物和造纸行业的预处理中具有重要的应用。在这项研究中,采用2级因子设计来筛选影响碱性果胶酶活性的重要因子,并使用Box-Behnken设计(BBD)的响应面方法(RSM)来优化其浓度。发现淀粉,蛋白ept,KH_(2)PO_(4)和K_(2)HPO_(4)·3H_(2)O显着影响碱性果胶酶的活性。它们的最佳浓度如下:4.68%淀粉,1.6%蛋白ept,0.26%KH_(2)PO_(4)和0.68%K_(2)HPO_(4)·3H_(2)O。在上述条件下,碱性果胶酶的活性显着提高到734.11?U / mL。碱性果胶酶被纯化至均质,回收率为9.6%,比活性为52372.52?U / mg。其最佳温度和pH分别为50°C和8.6。纯化的酶显示出很强的热稳定性和良好的耐碱性。另外,在Mg〜(2+)存在下,碱性果胶酶的活性得到提高。 Cu〜(2 +),Mn〜(2+)和Co〜(2+)明显抑制其活性。这项研究为将来开发和使用B耐热碱性果胶酶提供了重要基础。枯草杆菌ZGL14。

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