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首页> 外文期刊>Journal of Food Measurement and Characterization >Preliminary evaluation of irradiated medium and the optimization of conditions for a catalase produced by Bacillus firmus GL3
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Preliminary evaluation of irradiated medium and the optimization of conditions for a catalase produced by Bacillus firmus GL3

机译:辐照培养基的初步评价及芽孢杆菌淬火酶产生的过度酶条件的优化

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摘要

In this study, a hidden pitfall in the production of commercial tryptose soya agar (TSA) media sterilized with cobalt 60 irradiation was identified, and the applicability of TSA media was also determined. In addition, a strain of Bacillus firmus (B. firmus) with a high catalase activity, named GL3, was screened, and the conditions affecting the activity of its catalase were optimized. The 5 kinds of irradiated TSA media, named A, B, C, D, and E, were stored for 0 days, 15 days, 30 days, and 45 days, and their growth promoting ability, inhibitory properties, and sterility were analyzed to guarantee their suitability. The irradiated TSA media C had abnormal colony counts when Staphylococcus aureus (S. aureus) ATCC 6538 and Bacillus ginsengihumi (B. ginsengihumi) were used as the inocula, and both bacteria resumed normal growth when the media were stored for 15 days or the catalase was added. Screening of the significant variables and optimization of the catalase activity was performed using a Plackett-Burman design (PBD) and response surface methodology (RSM). The GL3 exhibited high catalase activity and stable catalase properties at 20-60 degrees and pH 7.0-10.0. Under optimal conditions, the activity of catalase reached 20,668 U/mL. The abnormal counts of plates can be eliminated by increasing the storage days of the irradiated media during the effective period or by adding optimal fermentation liquid from B. firmus GL3. The high catalase activity and stable enzymatic properties of B. firmus GL3 have potential uses in industrial food applications.
机译:在这项研究中,鉴定了用钴60辐射灭菌的商业胰蛋白酶大豆菌(TSA)培养基生产中的隐藏缺陷,并确定了TSA培养基的适用性。另外,筛选了具有高催化酶活性的芽孢杆菌(B. FirmuS),并筛选出称为GL3的高分子酶活性,并且优化了影响其过氧化氢酶活性的条件。将5种辐照的TSA培养基,命名为A,B,C,D和E,储存0天,15天,30天和45天,并分析其生长促进能力,抑制性能和无菌性保证他们的适用性。当使用金黄色葡萄球菌(S. aureus)ATCC 6538和Bacillusgihumi(B.Ginsengihumi)作为接种物时,辐照的TSA培养基C具有异常的菌落计数,并且当培养基储存15天或过氧化氢酶时,两种细菌恢复了正常生长加入。使用Plackett-Burman设计(PBD)和响应表面方法(RSM)进行显着变量和过氧化氢酶活性的优化。 GL3在20-60度和pH 7.0-10.0下表现出高的过氧化氢酶活性和稳定的过氧化氢酶性能。在最佳条件下,过氧化氢酶的活性达到20,668u / ml。通过在有效期内增加辐照介质的储存天或通过从B.Firmus GL3添加最佳发酵液来消除板的异常计数。 B. Firmus GL3的高碳酶活性和稳定的酶促性能在工业食品应用中具有潜在的用途。

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