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首页> 外文期刊>Brazilian Journal of Microbiology >Systematic mutagenesis method for enhanced production of bacitracin by Bacillus licheniformis mutant strain UV-MN-HN-6
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Systematic mutagenesis method for enhanced production of bacitracin by Bacillus licheniformis mutant strain UV-MN-HN-6

机译:地衣芽孢杆菌突变菌株UV-MN-HN-6提高杆菌肽产量的系统诱变方法

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The purpose of the current study was intended to obtain the enhanced production of bacitracin by Bacillus licheniformis through random mutagenesis and optimization of various parameters. Several isolates of Bacillus licheniformis were isolated from local habitat and isolate designated as GP-35 produced maximum bacitracin production (14±0.72 IU ml-1). Bacitracin production of Bacillus licheniformis GP-35 was increased to 23±0.69 IU ml-1 after treatment with ultraviolet (UV) radiations. Similarly, treatment of vegetative cells of GP-35 with chemicals like N-methyl N'-nitro N-nitroso guanidine (MNNG) and Nitrous acid (HNO2) increased the bacitracin production to a level of 31±1.35 IU ml-1 and 27±0.89 IU ml-1 respectively. Treatment of isolate GP-35 with combined effect of UV and chemical treatment yield significantly higher titers of bacitracin with maximum bacitracin production of 41.6±0.92 IU ml-1. Production of bacitracin was further enhanced (59.1±1.35 IU ml-1) by optimization of different parameters like phosphate sources, organic acids as well as temperature and pH. An increase of 4.22 fold in the production of bacitracin after mutagenesis and optimization of various parameters was achieved in comparison to wild type. Mutant strain was highly stable and produced consistent yield of bacitracin even after 15 generations. On the basis of kinetic variables, notably Yp/s (IU/g substrate), Yp/x (IU/g cells), Yx/s (g/g), Yp/s, mutant strain B. licheniformis UV-MN-HN-6 was found to be a hyperproducer of bacitracin.
机译:本研究的目的是通过随机诱变和优化各种参数来获得地衣芽孢杆菌提高杆菌肽的产量。从当地栖息地分离出了几种地衣芽孢杆菌分离株,命名为GP-35的分离株产生最大杆菌肽产量(14±0.72 IU ml-1)。用紫外线(UV)辐射处理后,地衣芽孢杆菌GP-35的杆菌肽产量增加至23±0.69 IU ml-1。同样,用N-甲基N'-硝基N-亚硝基胍(MNNG)和亚硝酸(HNO2)等化学试剂处理GP-35的营养细胞可使杆菌肽的产量增加到31±1.35 IU ml-1和27分别为±0.89 IU ml-1。用紫外线和化学处理相结合的方法处理分离株GP-35,可产生更高的杆菌肽效价,最大杆菌肽产量为41.6±0.92 IU ml-1。通过优化不同参数(如磷酸盐源,有机酸以及温度和pH),杆菌肽的产量进一步提高(59.1±1.35 IU ml-1)。与野生型相比,诱变后杆菌肽的产量增加了4.22倍,各种参数的优化。突变菌株高度稳定,即使经过15代后仍能产生一致的杆菌肽产量。根据动力学变量,尤其是Yp / s(IU / g底物),Yp / x(IU / g细胞),Yx / s(g / g),Yp / s,突变菌株B. licheniformis UV-MN-发现HN-6是杆菌肽的高产者。

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