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Isolation and Identification of a New Bacillus cereus Strain and Characterization of its Neopullulanase

机译:蜡状芽孢杆菌新菌株的分离鉴定及其新普洛聚糖酶的鉴定

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Identification and use of more efficient enzymes in the food and pharmaceutical industries is the focus of many researchers. The aim of this study was to search for a new bacterial strain capable of producing high levels of pullulanase applicable to biotechnology, the starch bioprocessing and food industries. A new pullulan hydrolyzing Bacillus strain was isolated and designated SDK2. Morphological and biochemical tests identified the strain as a putative Bacillus cereus strain, which was further characterized and confirmed through 16s rRNA sequencing, and was submitted to GeneBank, under the accession number FR6864500. Quantitative analysis of the strain’s pullulanase activity was carried out by the Dintrosalicyclic (DNS) acid-based assay. Thin layer chromatography (TLC) of the culture supernatant, identified the extracellular pullulanase as neopullulanase. Effects of temperature and pH on pullulanase activity were also studied. The optimum conditions for enzyme activity, as represented by 60°C and a pH of 7, resulted in an activity of 13.43 U/ml, which is much higher than some of the previously reported activities. However, growth of B. cereus SDK2 was also observed at a pH range of 5 to 10, and temperatures of 30°C to 50°C. The effect of metal ions and reagents, such as Mg+2, Ca+2, Zn+2, Cu+2, Fe+2, Ni+2 on enzyme activity showed that Ca+2 ions increased pullulan activity, whereas the other ions and reagents inhibited pullulanase activity. The ability of B. cereus SDK2 to produce high levels of neopullulanase stable at 60°C that can generate panose from pullulan, make this newly isolated strain a valuable source of debranching enzyme for biotechnology, the starch bioprocess and medical industries.
机译:在食品和制药行业中识别和使用更有效的酶是许多研究人员的重点。这项研究的目的是寻找一种能够产生高水平支链淀粉酶的新细菌菌株,适用于生物技术,淀粉生物加工和食品工业。分离了新的支链淀粉水解芽孢杆菌菌株并命名为SDK2。形态和生化测试确定该菌株为推定的蜡状芽孢杆菌菌株,通过16s rRNA测序对其进行了进一步表征和确认,并提交给GeneBank,登录号为FR6864500。该菌株的支链淀粉酶活性的定量分析是通过基于双脂环(DNS)酸的分析进行的。培养物上清液的薄层色谱法(TLC),鉴定出细胞外支链淀粉酶为新古支链淀粉酶。还研究了温度和pH对支链淀粉酶活性的影响。以60°C和7的pH值表示的最佳酶活性条件导致活性为13.43 U / ml,比以前报道的某些活性高得多。但是,在5至10的pH范围和30至50的温度下也观察到蜡状芽孢杆菌SDK2的生长。 Mg + 2,Ca + 2,Zn + 2,Cu + 2,Fe + 2,Ni + 2等金属离子和试剂对酶活性的影响表明,Ca + 2离子增加了支链淀粉的活性,而其他离子和试剂抑制支链淀粉酶活性。蜡状芽孢杆菌SDK2能够产生稳定在60°C的高水平新pululananase,能够从支链淀粉中产生panose,这使得这种新分离的菌株成为生物技术,淀粉生物工艺和医疗行业脱支酶的重要来源。

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