Yassin Semira Nureddin, Jiru Tamene Milkessa, Indracanti Meera
Department of Biotechnology, Institute of Biotechnology, University of Gondar, P.O. Box: 196, Gondar, Ethiopia.
Department of Environmental and Industrial Biotechnology, Institute of Biotechnology, University of Gondar, P.O. Box: 196, Gondar, Ethiopia.
Int J Microbiol. 2021 May 10;2021:5592885. doi: 10.1155/2021/5592885. eCollection 2021.
Studying thermostable amylase-producing bacteria in extreme environments has a crucial role to overcome different industrial challenges. Afar Region is one of the hottest and salty areas, making it the home of extremophiles. This study aimed at screening and characterizing amylase-producing bacteria isolated from soil samples of Afdera, Afar Region, and detection of their amylase-coding genes. Thus, a total of 49 bacterial isolates were obtained from the collected soil samples. Out of these, three isolates (M2, M8, and M13) were selected on the basis of diameter of the average clear zone formation and time taken to decolorize iodine solution. Based on their morphological and biochemical characteristics, the isolates were identified as genus . PCR amplification and detection of the amylase-coding gene confirmed the presence of the amylase gene in the three bacterial isolates. Optimum amylase production time for these isolates was 48 hrs (M13 and M8) and 72 hrs (M2) corresponding to the amylase activity of 0.67 U/mL for M13, 0.74 U/mL for M8, and 0.73 U/mL for M2 with an optimum temperature of 55°C. Studies on the effect of temperature revealed that the crude enzyme had a maximum activity and stability at 75°C, 70°C, and 65°C for isolates M13, M8, and M2, respectively. Additionally, amylase produced from all isolates retained more than 66.41% of their original activity after incubating them at a temperature range from 55 to 80°C for 50 min. Optimum pH for the activity of all crude amylases was in the range from 5 to 9 with a peak activity at pH 8. Their activity decreased significantly by the presence of Zn and Mg; however, their activity increased by the presence of Ca. Moreover, the three crude amylases were stable (0-3 M) with NaCl concentration. Amylases of this finding with thermophilic and halophilic characteristics offer a wide range of applications in food, brewing, textile, starch, paper, and deterrent industries. Thus, identification of these isolates at a molecular level and purification as well as detailed characterization of the types of amylases are recommended for effective utilization in different industries.
研究极端环境中产生耐热淀粉酶的细菌对于克服不同的工业挑战具有至关重要的作用。阿法尔地区是最热且含盐量最高的地区之一,是极端微生物的家园。本研究旨在筛选和鉴定从阿法尔地区阿费德拉土壤样本中分离出的产淀粉酶细菌,并检测其淀粉酶编码基因。因此,从采集的土壤样本中总共获得了49株细菌分离株。其中,根据平均透明圈形成直径和碘溶液脱色所需时间,选择了三株分离株(M2、M8和M13)。根据其形态和生化特征,这些分离株被鉴定为属。淀粉酶编码基因的PCR扩增和检测证实了这三株细菌分离株中存在淀粉酶基因。这些分离株的最佳淀粉酶产生时间为48小时(M13和M8)和72小时(M2),对应的淀粉酶活性分别为M13的0.67 U/mL、M8的0.74 U/mL和M2的0.73 U/mL,最佳温度为55°C。温度影响研究表明,粗酶在75°C、70°C和65°C时分别对分离株M13、M8和M2具有最大活性和稳定性。此外,将所有分离株产生的淀粉酶在55至80°C的温度范围内孵育50分钟后,其保留的原始活性超过66.41%。所有粗淀粉酶活性的最佳pH值在5至9范围内,在pH 8时活性最高。锌和镁的存在会使其活性显著降低;然而,钙的存在会使其活性增加。此外,这三种粗淀粉酶在NaCl浓度为0 - 3 M时稳定。本研究中具有嗜热和嗜盐特性的淀粉酶在食品、酿造、纺织、淀粉、造纸和洗涤剂行业有广泛应用。因此,建议在分子水平上鉴定这些分离株,并对淀粉酶类型进行纯化和详细表征,以便在不同行业中有效利用。