Mohammed Hadi Wael Ali, Edwin Boby T, Jayakumaran Nair Ananthakrishnan
Inter University Center for Genomic and Gene Technology (IUCGGT), University of Kerala, Thiruvananthapuram-695 581, Kerala, India.
CEPCI Laboratory and Research Institute, Kollam-691 001, Kerala, India.
J Mar Bio Assoc India. 2021 Jul-Dec;63(2):43-48. doi: 10.6024/jmbai.2021.63.2.2195-06. Epub 2021 Oct 30.
L-asparaginase is a target for many researchers as its properties against cancer, especially leukaemia, and protective agents reduce acrylamide in fried food. In this study, the water samples from Thumba Arattuvazhi Beach in Kerala were screened for l-asparaginase producing microorganisms. This was followed by colourimetric screening using modified M9 media with 0.009% Phenol red dye and using l-asparagine as a sole nitrogen source. Then, the Nessler assay was performed to quantify the enzyme. Molecular identification was made by 16SrRNA sequencing and aligned the sequence with GeneBank for phylogenetic tree construction using BLAST. Seawater was serially diluted for 10 to 10 using nutrient agar plates. A total of 19 bacterial colonies were isolated. The colonies were evaluated to produce l-asparaginase according to the pink zone around the colonies on the modified M9 medium using a red phenol indicator. The KB1 sample was selected for further studies according to plate colour assay. Nessler assay of L-asparaginase quantified as 2.537 IU/ml. Molecular characterisation showed the sequence association with the sequence submitted in Genebank as strain. The l-asparaginase II gene (AnsB) was amplified based on the entire length of the hypothetical protein of annotated genome with accession number CP022319.2. The l-asparaginase activity in this study was 57% higher than the reference organism BITHSP010. The l-asparaginase producing bacterium KB1 from a marine source in Kerala can produce asparaginase, which can be utilised for biotechnology applications.
L-天冬酰胺酶是许多研究人员的目标,因为其抗癌特性,尤其是对白血病的作用,以及保护剂可减少油炸食品中的丙烯酰胺。在本研究中,对喀拉拉邦图姆巴阿拉图瓦齐海滩的水样进行了产L-天冬酰胺酶微生物的筛选。随后,使用添加0.009%酚红染料的改良M9培养基并以L-天冬酰胺作为唯一氮源进行比色筛选。然后,进行奈斯勒测定以定量该酶。通过16SrRNA测序进行分子鉴定,并使用BLAST将序列与基因库比对以构建系统发育树。使用营养琼脂平板将海水连续稀释至10到10 。总共分离出19个细菌菌落。根据改良M9培养基上菌落周围的粉红色区域,使用红色酚指示剂评估菌落是否产生L-天冬酰胺酶。根据平板颜色测定,选择KB1样本进行进一步研究。L-天冬酰胺酶的奈斯勒测定定量为2.537 IU/ml。分子表征显示该序列与基因库中提交的作为菌株的序列相关联。基于登录号为CP022319.2的注释基因组的假设蛋白的全长扩增了L-天冬酰胺酶II基因(AnsB)。本研究中的L-天冬酰胺酶活性比参考生物体BITHSP010高57%。来自喀拉拉邦海洋来源的产L-天冬酰胺酶细菌KB1可以产生天冬酰胺酶,可用于生物技术应用。