Enterobacter hormaechei Z8b-60: A Tannin Degrading Bacteria Isolated from Slaughterhouse Waste

Sharadamma Narayanaswamy, Lekhana Hanumegowda, Jayashree Sadhasivam, Nagesh Babu Rangappa
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Abstract

Tannases or Tannin acyl hydrolases (EC 3.1.1.20) are a family of esterases that catalyze the hydrolysis of ester and depside bonds present in hydrolyzable tannins to release gallic acid. Industrial applications of tannase in food, brewing, chemical, pharmaceutical, and bioremediation, have made it one of the most important enzymes in research. The aim of the present study focused on the degradation of tannic acid by novel bacterial tannase isolated from slaughterhouse waste-enriched soil. Soil containing ruminant microflora is cultured on MSM containing tannic acid. Among four bacterial isolates, a potent strain was cultivated for identification which are then analysed for biochemical characterization and physiological characterization. Bacteria use tannic acid as the sole carbon source for growth and showed maximum growth at 0.6%. The morphology of the isolate shows that it contains gram-negative rods that are nonmotile and capsulated. Based on 16S rRNA and phylogenetic analysis, the isolate was confirmed as Enterobacter hormaechei Z8b-60. Tannase production from bacteria was confirmed by a novel, sensitive plate assay by observing the zone of clearance around colonies and also by dye binding method using methyl gallate as substrate. During the study, TLC and HPLC were performed to analyze the accumulated gallic acid and other metabolites. Intracellular tannase production amplified from 14.98 U/mL to 102.7 U/mL as tannic acid concentration increases from 0.4% to 1.0%, respectively.
hormaechei肠杆菌Z8b-60:一种从屠宰场废弃物中分离的单宁降解菌
单宁酶或单宁酰基水解酶(EC 3.1.1.20)是一个酯酶家族,它催化水解存在于可水解单宁中的酯和深苷键以释放没食子酸。单宁酶在食品、酿造、化工、制药和生物修复等方面的工业应用使其成为研究中最重要的酶之一。本研究的目的是利用从屠宰场废物富集土壤中分离的新型细菌单宁酶降解单宁酸。在含单宁酸的MSM培养基上培养含有反刍动物菌群的土壤。在4株分离的细菌中,培养了一株强效菌株进行鉴定,然后进行了生化特性和生理特性分析。细菌以单宁酸为唯一的碳源生长,在0.6%时生长最快。分离物的形态显示它含有革兰氏阴性杆状细胞,这些杆状细胞不运动且被包膜。经16S rRNA和系统发育分析,该分离物为贺氏肠杆菌Z8b-60。通过观察菌落周围的清除区和以没食子酸甲酯为底物的染料结合法,一种新的灵敏平板试验证实了细菌产生鞣酶。在研究过程中,采用薄层色谱法和高效液相色谱法分析了没食子酸等代谢产物的积累。单宁酸浓度从0.4%增加到1.0%时,胞内单宁酶产量分别从14.98 U/mL增加到102.7 U/mL。
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